| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121649991-121650163 | Rare:47 | ||||
| chr2:121736728-121737291 | Common:5; Rare:225 | ||||
| chr2:121755342-121755814 | Common:6; Rare:153 | ||||
| chr2:126655848-126656477 | Common:1; Rare:188; Clinvar:2 | ||||
| chr2:126656642-126656771 | Rare:25 | ||||
| chr2:127294039-127294278 | Common:2; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:127387233-127387663 | Common:5; Rare:140 | ||||
| chr2:127387740-127388295 | Common:10; Rare:223 | ||||
| chr2:127526183-127526243 | Rare:18 | ||||
| chr2:127526348-127526657 | Common:2; Rare:121 | ||||
| chr2:127526746-127526959 | Rare:42 | ||||
| chr2:127701286-127701592 | Common:4; Rare:114 | ||||
| chr2:127701774-127701916 | Common:1; Rare:67 | ||||
| chr2:127811149-127811390 | Common:1; Rare:85 | ||||
| chr2:127811521-127811593 | Rare:6 |