| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121530579-121530884 | Common:7; Rare:127 | ||||
| chr2:121649418-121649701 | Common:2; Rare:80 | ||||
| chr2:121736736-121737089 | Common:4; Rare:144 | ||||
| chr2:127294096-127294243 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387962-127388304 | Common:7; Rare:147 | ||||
| chr2:127526433-127526637 | Common:2; Rare:66 | ||||
| chr2:127811121-127811248 | Rare:41 | ||||
| chr2:127858112-127858352 | Common:3; Rare:85 | ||||
| chr2:127885886-127885991 | Rare:28 | ||||
| chr2:128091046-128091360 | Common:8; Rare:100 | ||||
| chr2:130181546-130181700 | Common:1; Rare:54 | ||||
| chr2:130182079-130182336 | Common:2; Rare:98 | ||||
| chr2:130342120-130342219 | Rare:42; Clinvar:1 | ||||
| chr2:130342648-130342924 | Common:5; Rare:85 | ||||
| chr2:130836755-130836947 | Common:2; Rare:75 |