Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882488-179882868 | Rare:181; Clinvar:8; Clinvar (benign):2 | ||||
chr1:179954464-179954939 | Common:3; Rare:111 | ||||
chr1:180912641-180912877 | Common:1; Rare:55 | ||||
chr1:180940877-180941050 | Common:7; Rare:48 | ||||
chr1:181088519-181088740 | Common:1; Rare:88 | ||||
chr1:182388400-182388835 | Common:2; Rare:101 | ||||
chr1:182389814-182390158 | Rare:59 | ||||
chr1:182390261-182390469 | Common:2; Rare:54 | ||||
chr1:182390662-182391254 | Common:7; Rare:137; Clinvar:7; Clinvar (benign):2 | ||||
chr1:182391273-182391521 | Common:1; Rare:59 | ||||
chr1:182391523-182391623 | Rare:36 | ||||
chr1:182391643-182391997 | Common:3; Rare:131; Clinvar:5; Clinvar (benign):3 | ||||
chr1:182789664-182789805 | Common:2; Rare:54 | ||||
chr1:182839251-182839399 | Common:1; Rare:66 | ||||
chr1:183023075-183023286 | Common:4; Rare:51 |