| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:120012856-120013112 | Common:2; Rare:103 | ||||
| chr2:120223378-120223711 | Common:1; Rare:96 | ||||
| chr2:120252616-120252945 | Common:3; Rare:108 | ||||
| chr2:121530340-121530922 | Common:10; Rare:241; Clinvar (pathogenic):6 | ||||
| chr2:121649418-121649701 | Common:2; Rare:80 | ||||
| chr2:121649886-121650151 | Common:1; Rare:67 | ||||
| chr2:121736736-121737261 | Common:5; Rare:212 | ||||
| chr2:121755410-121755821 | Common:5; Rare:135 | ||||
| chr2:127064800-127065014 | Rare:54 | ||||
| chr2:127106963-127107343 | Common:2; Rare:119; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:127294077-127294256 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387962-127388256 | Common:7; Rare:128 | ||||
| chr2:127526404-127526607 | Common:2; Rare:75 | ||||
| chr2:127526795-127526821 | Rare:8 | ||||
| chr2:127811078-127811258 | Rare:58 |