Genes with a similar H3K4me3 profile for Gene (Select 79905) - Gene

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Name/Gene ID	Description	Location	Aliases	MIM
Select item 79905 TMC7 ID: 79905	transmembrane channel like 7 [Homo sapiens (human)]	Chromosome 16, NC_000016.10 (18983934..19063942)		617198
Select item 3755 KCNG1 ID: 3755	potassium voltage-gated channel modifier subfamily G member 1 [Homo sapiens (human)]	Chromosome 20, NC_000020.11 (51003656..51023107, complement)	K13, KCNG, KV6.1, kH2	603788
Select item 23251 MINAR1 ID: 23251	membrane integral NOTCH2 associated receptor 1 [Homo sapiens (human)]	Chromosome 15, NC_000015.10 (79411400..79472304)	KIAA1024, UBTOR	618054
Select item 134285 TMEM171 ID: 134285	transmembrane protein 171 [Homo sapiens (human)]	Chromosome 5, NC_000005.10 (73120575..73131809)	PRP2
Select item 54620 FBXL19 ID: 54620	F-box and leucine rich repeat protein 19 [Homo sapiens (human)]	Chromosome 16, NC_000016.10 (30922851..30948783)	CXXC11, Fbl19, JHDM1C	609085
Select item 6785 ELOVL4 ID: 6785	ELOVL fatty acid elongase 4 [Homo sapiens (human)]	Chromosome 6, NC_000006.12 (79914814..79947553, complement)	ADMD, CT118, ISQMR, SCA34, STGD2, STGD3	605512
Select item 6567 SLC16A2 ID: 6567	solute carrier family 16 member 2 [Homo sapiens (human)]	Chromosome X, NC_000023.11 (74421493..74533916)	AHDS, DXS128, DXS128E, MCT 7, MCT 8, MCT7, MCT8, MRX22, XPCT	300095
Select item 57214 CEMIP ID: 57214	cell migration inducing hyaluronidase 1 [Homo sapiens (human)]	Chromosome 15, NC_000015.10 (80779370..80951771)	CCSP11, HYBID, KIAA1199, TMEM2L, CEMIP	608366
Select item 6000 RGS7 ID: 6000	regulator of G protein signaling 7 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (240774742..241357230, complement)		602517
Select item 130271 PLEKHH2 ID: 130271	pleckstrin homology, MyTH4 and FERM domain containing H2 [Homo sapiens (human)]	Chromosome 2, NC_000002.12 (43637260..43767987)	PLEKHH1L	612723
Select item 54796 BNC2 ID: 54796	basonuclin zinc finger protein 2 [Homo sapiens (human)]	Chromosome 9, NC_000009.12 (16409503..16870670, complement)	BSN2, LUTO, bn2	608669
Select item 11167 FSTL1 ID: 11167	follistatin like 1 [Homo sapiens (human)]	Chromosome 3, NC_000003.12 (120392293..120450992, complement)	FRP, FSL1, MIR198, OCC-1, OCC1, tsc36	605547
Select item 29800 ZDHHC1 ID: 29800	zinc finger DHHC-type containing 1 [Homo sapiens (human)]	Chromosome 16, NC_000016.10 (67394152..67416477, complement)	C16orf1, DHHC-1, HSU90653, ZNF377
Select item 286151 FBXO43 ID: 286151	F-box protein 43 [Homo sapiens (human)]	Chromosome 8, NC_000008.11 (100133351..100150569, complement)	EMI2, ERP1, FBX43, OOMD12, OZEMA12, SPGF64	609110
Select item 55068 ENOX1 ID: 55068	ecto-NOX disulfide-thiol exchanger 1 [Homo sapiens (human)]	Chromosome 13, NC_000013.11 (43213130..43786972, complement)	CNOX, PIG38, bA64J21.1, cCNOX	610914
Select item 5333 PLCD1 ID: 5333	phospholipase C delta 1 [Homo sapiens (human)]	Chromosome 3, NC_000003.12 (38007496..38029642, complement)	NDNC3, PLC-III	602142
Select item 122616 CLBA1 ID: 122616	clathrin binding box of aftiphilin containing 1 [Homo sapiens (human)]	Chromosome 14, NC_000014.9 (104985788..105001274)	C14orf79
Select item 64782 AEN ID: 64782	apoptosis enhancing nuclease [Homo sapiens (human)]	Chromosome 15, NC_000015.10 (88604683..88632281)	ISG20L1, pp12744	610177
Select item 9429 ABCG2 ID: 9429	ATP binding cassette subfamily G member 2 (JR blood group) [Homo sapiens (human)]	Chromosome 4, NC_000004.12 (88090264..88231626, complement)	ABC15, ABCP, BCRP, BCRP1, BMDP, CD338, CDw338, CDw388, EST157481, GOUT1, MRX, MXR, MXR-1, MXR1, UAQTL1	603756
Select item 3778 KCNMA1 ID: 3778	potassium calcium-activated channel subfamily M alpha 1 [Homo sapiens (human)]	Chromosome 10, NC_000010.11 (76869602..77637808, complement)	BKTM, CADEDS, IEG16, KCa1.1, LIWAS, MaxiK, PNKD3, SAKCA, SLO, SLO-ALPHA, SLO1, bA205K10.1, hSlo, mSLO1	600150