| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:202810756-202810985 | Common:2; Rare:135 | ||||
| chr1:202860769-202861169 | Common:8; Rare:152 | ||||
| chr1:202861485-202861795 | Common:2; Rare:173 | ||||
| chr1:205512169-205512369 | Common:1; Rare:54 | ||||
| chr1:205630850-205631310 | Common:6; Rare:193 | ||||
| chr1:207241190-207241570 | Common:2; Rare:104 | ||||
| chr1:207756801-207757301 | Common:3; Rare:206; Clinvar:8; Clinvar (pathogenic):2 | ||||
| chr1:207826801-207826998 | Common:1; Rare:46 | ||||
| chr1:209833049-209833498 | Common:4; Rare:193 | ||||
| chr1:211382639-211382858 | Common:3; Rare:161 | ||||
| chr1:211577700-211578150 | Common:1; Rare:208 | ||||
| chr1:213372120-213372590 | Rare:135 | ||||
| chr1:213376980-213377330 | Rare:63 | ||||
| chr1:213492150-213492530 | Common:3; Rare:145 | ||||
| chr1:213571530-213571750 | Common:3; Rare:63 |