Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174159332-174159588 | Common:2; Rare:96 | ||||
chr1:174999344-174999473 | Rare:36 | ||||
chr1:174999679-175000145 | Common:3; Rare:144 | ||||
chr1:178725017-178725335 | Common:10; Rare:109 | ||||
chr1:178869189-178869385 | Common:1; Rare:31 | ||||
chr1:178871037-178871337 | Rare:57 | ||||
chr1:179882201-179882303 | Rare:19 | ||||
chr1:179882478-179882852 | Rare:175; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954706-179954822 | Rare:24 | ||||
chr1:180502513-180502696 | Common:1; Rare:74 | ||||
chr1:180940877-180941051 | Common:7; Rare:48 | ||||
chr1:181088499-181088704 | Rare:66 | ||||
chr1:182391303-182391432 | Rare:26 | ||||
chr1:182789664-182789778 | Common:2; Rare:36 | ||||
chr1:182839229-182839399 | Common:1; Rare:73 |