ID: 127823890 | H3K27ac hESC enhancer GRCh37_chr12:31226445-31226976 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31073511..31074042) | | |
ID: 127823889 | H3K4me1 hESC enhancer GRCh37_chr12:31141041-31141540 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30988106..30988605) | | |
ID: 127823888 | H3K4me1 hESC enhancer GRCh37_chr12:31140539-31141040 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30987604..30988105) | | |
ID: 127823887 | H3K4me1 hESC enhancer GRCh37_chr12:31134009-31134508 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30981074..30981573) | | |
ID: 127823886 | H3K4me1 hESC enhancer GRCh37_chr12:31133507-31134008 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30980572..30981073) | | |
ID: 127823885 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:31130578-31131412 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30977643..30978477) | | |
ID: 127823884 | H3K4me1 hESC enhancer GRCh37_chr12:31117766-31118266 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30964831..30965331) | | |
ID: 127823883 | H3K4me1 hESC enhancer GRCh37_chr12:31062613-31063113 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30909679..30910179) | | |
ID: 127823882 | H3K4me1 hESC enhancer GRCh37_chr12:31027609-31028110 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30874675..30875176) | | |
ID: 124902911 | uncharacterized LOC124902911 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30918507..30926689, complement) | | |
ID: 124902910 | TSPAN11 antisense RNA 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30978308..31005972, complement) | | |
ID: 124629339 | Sharpr-MPRA regulatory region 7044 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31066315..31066609) | | |
ID: 107984476 | uncharacterized LOC107984476 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30869147..30880389, complement) | | |
ID: 100506660 | DDX11 antisense RNA 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31020763..31073847, complement) | CONCR, SCAT4 | |
ID: 441631 | tetraspanin 11 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30926748..31016502) | VSSW1971 | |
ID: 1663 | DEAD/H-box helicase 11 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (31073860..31104799) | CHL1, CHLR1, KRG2, WABS | 601150 |