| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:178725760-178725954 | Common:2; Rare:111 | ||||
| chr1:179025660-179026094 | Common:15; Rare:260 | ||||
| chr1:179026023-179026402 | Common:4; Rare:151 | ||||
| chr1:179081610-179081800 | Common:2; Rare:34 | ||||
| chr1:179081764-179082310 | Common:10; Rare:372 | ||||
| chr1:179082313-179082713 | Common:3; Rare:168 | ||||
| chr1:179228640-179229290 | Common:4; Rare:157 | ||||
| chr1:179229520-179229889 | Common:24; Rare:212 | ||||
| chr1:179293560-179293916 | Common:8; Rare:291 | ||||
| chr1:179293970-179294370 | Common:3; Rare:94 | ||||
| chr1:179365591-179366101 | Common:28; Rare:294 | ||||
| chr1:179591475-179592089 | Common:8; Rare:331 | ||||
| chr1:179877721-179877949 | Rare:82 | ||||
| chr1:179881992-179882352 | Common:8; Rare:163 | ||||
| chr1:179882375-179882897 | Rare:416; Clinvar:17; Clinvar (benign):4 |