| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:120012977-120013091 | Common:1; Rare:46 | ||||
| chr2:121530552-121530895 | Common:8; Rare:151; Clinvar (pathogenic):2 | ||||
| chr2:121649428-121649721 | Common:2; Rare:88 | ||||
| chr2:121649928-121650156 | Rare:63 | ||||
| chr2:121736810-121737092 | Common:4; Rare:108 | ||||
| chr2:121755419-121755755 | Common:4; Rare:111 | ||||
| chr2:127106863-127107351 | Common:5; Rare:142; Clinvar:10; Clinvar (benign):3 | ||||
| chr2:127294114-127294205 | Common:2; Rare:31; Clinvar (benign):2 | ||||
| chr2:127387956-127388257 | Common:7; Rare:130 | ||||
| chr2:127526431-127526607 | Common:2; Rare:55 | ||||
| chr2:127811153-127811270 | Common:1; Rare:34 | ||||
| chr2:127858042-127858228 | Common:2; Rare:94 | ||||
| chr2:127885946-127885982 | Rare:8 | ||||
| chr2:130172368-130172643 | Rare:90 | ||||
| chr2:130181531-130181784 | Common:4; Rare:113 |