| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121649394-121649679 | Common:2; Rare:85 | ||||
| chr2:121736736-121737261 | Common:5; Rare:212 | ||||
| chr2:121755410-121755800 | Common:5; Rare:129 | ||||
| chr2:124025166-124025320 | Common:2; Rare:53 | ||||
| chr2:127294092-127294212 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387904-127388217 | Common:6; Rare:141 | ||||
| chr2:127811131-127811259 | Rare:41 | ||||
| chr2:127858086-127858197 | Common:1; Rare:63 | ||||
| chr2:127885894-127885972 | Rare:18 | ||||
| chr2:128091038-128091387 | Common:8; Rare:113 | ||||
| chr2:130181546-130181797 | Common:3; Rare:111 | ||||
| chr2:130182087-130182374 | Common:2; Rare:112 | ||||
| chr2:130182424-130182569 | Common:1; Rare:53 | ||||
| chr2:130342118-130342279 | Rare:66; Clinvar:1 | ||||
| chr2:130342642-130342930 | Common:5; Rare:90 |