ID: 127882533 | H3K4me1 hESC enhancer GRCh37_chr7:73995345-73995846 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74581016..74581517) | | |
ID: 127409572 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74031728-74032292 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74617409..74617973) | | |
ID: 127409571 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74031162-74031727 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74616843..74617408) | | |
ID: 127409570 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74002117-74002703 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74587788..74588374) | | |
ID: 127409569 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:74001529-74002116 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74587200..74587787) | | |
ID: 127409568 | H3K4me1 hESC enhancer GRCh37_chr7:73919312-73919812 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74504982..74505482) | | |
ID: 127409567 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:73909445-73910043 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74495115..74495713) | | |
ID: 127409566 | H3K4me1 hESC enhancer GRCh37_chr7:73892826-73893408 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74478496..74479078) | | |
ID: 127409565 | H3K4me1 hESC enhancer GRCh37_chr7:73892244-73892825 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74477914..74478495) | | |
ID: 127409564 | H3K4me1 hESC enhancer GRCh37_chr7:73849734-73850353 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74435404..74436023) | | |
ID: 123956164 | Sharpr-MPRA regulatory region 2459 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74581480..74581774) | | |
ID: 113218504 | microRNA 10525 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74595968..74596026) | | |
ID: 108254673 | CAGE-defined high expression enhancer upstream of GTF2IRD1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74452202..74452721) | | |
ID: 107986810 | Williams-Beuren syndrome chromosome region 23 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74532592..74533213) | | |
ID: 100873491 | RNA, 5S ribosomal pseudogene 233 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74487428..74487540, complement) | RN5S233 | |
ID: 9569 | GTF2I repeat domain containing 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74453906..74602605) | BEN, CREAM1, GTF3, MUSTRD1, RBAP2, WBS, WBSCR11, WBSCR12, hMusTRD1alpha1 | 604318 |