ID: 127885900 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:16386369-16387185 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16483055..16483871) | | |
ID: 127885899 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:16380699-16381609 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16477385..16478295) | | |
ID: 127885898 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:16379787-16380698 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16476473..16477384) | | |
ID: 127885897 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:16369025-16369816 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16465711..16466502) | | |
ID: 127885896 | H3K4me1 hESC enhancer GRCh37_chr17:16360197-16360696 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16456883..16457382) | | |
ID: 127885895 | H3K4me1 hESC enhancer GRCh37_chr17:16359695-16360196 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16456381..16456882) | | |
ID: 127885894 | H3K4me1 hESC enhancer GRCh37_chr17:16352475-16352974 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16449161..16449660) | | |
ID: 127885893 | H3K4me1 hESC enhancer GRCh37_chr17:16351973-16352474 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16448659..16449160) | | |
ID: 127885892 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:16347109-16348008 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16443795..16444694) | | |
ID: 127885891 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:16342605-16343506 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16439291..16440192) | | |
ID: 127885890 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:16341705-16342604 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16438391..16439290) | | |
ID: 127885889 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:16340803-16341704 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16437489..16438390) | | |
ID: 127885888 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:16339567-16340199 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16436253..16436885) | | |
ID: 125177428 | Sharpr-MPRA regulatory regions 7543 and 3494 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16463755..16464089) | | |
ID: 692106 | small nucleolar RNA, C/D box 65 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16441226..16441298) | HBII-135A, SNORD65 | |
ID: 692087 | small nucleolar RNA, C/D box 49B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16439509..16439556) | U49B | |
ID: 388341 | leucine rich repeat containing 75A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16441577..16492193, complement) | C17orf76, FAM211A | |
ID: 125144 | small nucleolar RNA host gene 29 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16438987..16470648) | C17orf45, C17orf76-AS1, FAM211A-AS1, LRRC75A-AS1, NCRNA00188, TSAP19 | |
ID: 51393 | transient receptor potential cation channel subfamily V member 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16415571..16437003) | VRL, VRL-1, VRL1 | 606676 |
ID: 26800 | small nucleolar RNA, C/D box 49A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (16440036..16440106) | RNU49, U49, U49A | |