Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66924808-66925031 | Rare:96 | ||||
chr1:66925148-66925532 | Common:2; Rare:120 | ||||
chr1:67430273-67430580 | Rare:118 | ||||
chr1:67684931-67685247 | Common:3; Rare:83 | ||||
chr1:68496478-68496698 | Common:2; Rare:46 | ||||
chr1:68497016-68497214 | Common:2; Rare:68 | ||||
chr1:70205424-70205762 | Rare:125 | ||||
chr1:70221188-70221762 | Rare:218 | ||||
chr1:70231689-70231876 | Rare:26 | ||||
chr1:70246849-70247150 | Rare:59 | ||||
chr1:70354377-70354560 | Rare:54 | ||||
chr1:70354634-70354880 | Rare:76 | ||||
chr1:70354994-70355179 | Common:1; Rare:72 | ||||
chr1:70411053-70411311 | Common:2; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71066700-71066872 | Rare:61 |