ID: 127458046 | H3K4me1 hESC enhancer GRCh37_chr7:150672781-150673707 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150975693..150976619) | | |
ID: 127458045 | H3K4me1 hESC enhancer GRCh37_chr7:150669129-150669642 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150972041..150972554) | | |
ID: 127458044 | H3K4me1 hESC enhancer GRCh37_chr7:150658991-150659600 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150961903..150962512) | | |
ID: 127458043 | H3K4me1 hESC enhancer GRCh37_chr7:150654831-150655332 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150957743..150958244) | | |
ID: 127458042 | H3K4me1 hESC enhancer GRCh37_chr7:150651428-150652026 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150954340..150954938) | | |
ID: 127458041 | H3K4me1 hESC enhancer GRCh37_chr7:150645973-150646713 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150948885..150949625) | | |
ID: 127458040 | H3K4me1 hESC enhancer GRCh37_chr7:150643003-150643744 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150945915..150946656) | | |
ID: 127458039 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:150642260-150643002 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150945172..150945914) | | |
ID: 127458038 | H3K4me1 hESC enhancer GRCh37_chr7:150607062-150607562 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150909974..150910474) | | |
ID: 126860224 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr7:150698330-150699529 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (151001242..151002441) | | |
ID: 124901776 | uncharacterized LOC124901776 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150975318..150977355) | | |
ID: 121201618 | Sharpr-MPRA regulatory region 11983 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150898521..150898815) | | |
ID: 110973015 | NOS3 5' regulatory region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150988222..150994377) | | |
ID: 110121275 | VISTA enhancer hs2192 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150962513..150966344) | | |
ID: 4846 | nitric oxide synthase 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150991017..151014588) | ECNOS, eNOS | 163729 |
ID: 3757 | potassium voltage-gated channel subfamily H member 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150944961..150978321, complement) | ERG-1, ERG1, H-ERG, HERG, HERG1, Kv11.1, LQT2, SQT1 | 152427 |