| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:98608323-98608708 | Common:3; Rare:272; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:98730913-98731382 | Common:10; Rare:271 | ||||
| chr2:99141124-99141783 | Common:6; Rare:432 | ||||
| chr2:99154836-99155134 | Common:8; Rare:220; Clinvar (benign):6 | ||||
| chr2:99180979-99181243 | Common:4; Rare:149 | ||||
| chr2:99181290-99181550 | Rare:90 | ||||
| chr2:99337209-99337564 | Rare:219 | ||||
| chr2:99489813-99490336 | Common:2; Rare:247 | ||||
| chr2:100417327-100417505 | Rare:66 | ||||
| chr2:100417504-100417695 | Rare:60 | ||||
| chr2:100562876-100563046 | Common:2; Rare:100 | ||||
| chr2:100819999-100820239 | Common:1; Rare:74 | ||||
| chr2:100820750-100821520 | Common:6; Rare:249 | ||||
| chr2:101002149-101002354 | Rare:149 | ||||
| chr2:101151300-101151703 | Common:10; Rare:195 |