| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:120252606-120252945 | Common:3; Rare:111 | ||||
| chr2:121530317-121530906 | Common:10; Rare:230; Clinvar (pathogenic):3 | ||||
| chr2:121649382-121649855 | Common:3; Rare:132 | ||||
| chr2:121649953-121650163 | Rare:57 | ||||
| chr2:121736709-121737226 | Common:5; Rare:206 | ||||
| chr2:121755415-121755893 | Common:5; Rare:160 | ||||
| chr2:126655996-126656311 | Common:1; Rare:92; Clinvar:2 | ||||
| chr2:127294086-127294231 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387925-127388286 | Common:9; Rare:157 | ||||
| chr2:127526419-127526593 | Common:2; Rare:59 | ||||
| chr2:127526803-127526880 | Rare:14 | ||||
| chr2:127811139-127811264 | Rare:37 | ||||
| chr2:127858107-127858219 | Common:1; Rare:56 | ||||
| chr2:127884335-127884798 | Common:2; Rare:91 | ||||
| chr2:127885867-127885999 | Rare:34 |