ID: 130061106 | ATAC-STARR-seq lymphoblastoid silent region 8665 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (48997475..48997544) | | |
ID: 127887242 | H3K27ac hESC enhancer GRCh37_chr17:47202514-47203019 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49125152..49125657) | | |
ID: 127887241 | NANOG hESC enhancer GRCh37_chr17:47163998-47164523 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49086636..49087161) | | |
ID: 127887240 | H3K4me1 hESC enhancer GRCh37_chr17:47135543-47136044 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49058181..49058682) | | |
ID: 127887239 | H3K4me1 hESC enhancer GRCh37_chr17:47126439-47127348 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49049077..49049986) | | |
ID: 127887238 | H3K27ac hESC enhancer GRCh37_chr17:47110305-47110846 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49032943..49033484) | | |
ID: 127887237 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:47092958-47093511 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49015596..49016149) | | |
ID: 127887236 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:47091293-47091848 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49013931..49014486) | | |
ID: 127887235 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:47090183-47090738 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49012821..49013376) | | |
ID: 127887234 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:47089629-47090182 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49012267..49012820) | | |
ID: 127887233 | H3K4me1 hESC enhancer GRCh37_chr17:47081123-47081644 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49003761..49004282) | | |
ID: 127887232 | H3K4me1 hESC enhancer GRCh37_chr17:47044045-47044545 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (48966683..48967183) | | |
ID: 127887231 | H3K4me1 hESC enhancer GRCh37_chr17:47043544-47044044 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (48966182..48966682) | | |
ID: 127887230 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:47041863-47042412 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (48964501..48965050) | | |
ID: 124904116 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (48956650..48956753, complement) | | |
ID: 124904021 | uncharacterized LOC124904021 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49121905..49123879, complement) | | |
ID: 124904020 | uncharacterized LOC124904020 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (48999269..49014487, complement) | | |
ID: 121852938 | Sharpr-MPRA regulatory region 671 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49022447..49022741) | | |
ID: 106481717 | B4GALNT2 pseudogene 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49085511..49086702) | | |
ID: 106479931 | RNA, U6 small nuclear 826, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49036352..49036449) | | |