ID: 129662398 | ReSE screen-validated silencer GRCh37_chr8:144063636-144063766 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142982219..142982349) | | |
ID: 127460685 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:144073720-144074227 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142992303..142992810) | | |
ID: 127460684 | H3K4me1 hESC enhancer GRCh37_chr8:144070153-144070654 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142988736..142989237) | | |
ID: 127460683 | H3K4me1 hESC enhancer GRCh37_chr8:144033761-144034332 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142952344..142952915) | | |
ID: 121331313 | Sharpr-MPRA regulatory region 5092 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142934513..142934807) | | |
ID: 110673972 | CYP11B1 promoter [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142879723..142881144) | | |
ID: 110673971 | CYP11B2 promoter [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142917842..142919862) | | |
ID: 106799834 | CYP11B2 recombination region [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142903458..142918174) | | |
ID: 106799833 | CYP11B1 recombination region [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142874234..142879022) | | |
ID: 105375794 | uncharacterized LOC105375794 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142925293..142927173) | | |
ID: 100288248 | zinc finger HIT-type containing 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142858354..142858991) | | |
ID: 100133669 | LY6E divergent transcript [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142982031..143018390, complement) | | |
ID: 100128627 | CDC42 pseudogene 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142995828..142997663) | | |
ID: 1585 | cytochrome P450 family 11 subfamily B member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142910559..142917843, complement) | ALDOS, CPN2, CYP11B, CYP11BL, CYPXIB2, P-450C18, P450C18, P450aldo | 124080 |
ID: 1584 | cytochrome P450 family 11 subfamily B member 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (142872357..142879825, complement) | CPN1, CYP11B, FHI, P450C11 | 610613 |