| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:173714876-173715063 | Common:1; Rare:44 | ||||
| chr1:173824402-173824702 | Rare:56; Clinvar:1 | ||||
| chr1:173867970-173868392 | Common:2; Rare:142 | ||||
| chr1:174022345-174022508 | Rare:42 | ||||
| chr1:174159265-174159681 | Common:4; Rare:132 | ||||
| chr1:174999344-174999483 | Common:1; Rare:38 | ||||
| chr1:174999679-175000145 | Common:3; Rare:144 | ||||
| chr1:176207226-176207345 | Common:1; Rare:61 | ||||
| chr1:178725168-178725340 | Common:9; Rare:64 | ||||
| chr1:178869127-178869332 | Common:1; Rare:35 | ||||
| chr1:178870988-178871138 | Rare:25 | ||||
| chr1:179081889-179082086 | Common:1; Rare:60 | ||||
| chr1:179293692-179293922 | Common:3; Rare:66 | ||||
| chr1:179882165-179882369 | Common:1; Rare:39 | ||||
| chr1:179882513-179882950 | Common:1; Rare:220; Clinvar:9; Clinvar (benign):4 |