| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:126084022-126084223 | Common:2; Rare:78 | ||||
| chr3:126703947-126704324 | Common:4; Rare:117 | ||||
| chr3:127598190-127598458 | Common:3; Rare:78 | ||||
| chr3:127628955-127629217 | Common:1; Rare:86 | ||||
| chr3:128052170-128052525 | Common:2; Rare:120 | ||||
| chr3:128123702-128124020 | Rare:94 | ||||
| chr3:128153350-128153496 | Rare:39 | ||||
| chr3:128487892-128488036 | Common:1; Rare:37 | ||||
| chr3:128680637-128680800 | Common:2; Rare:44 | ||||
| chr3:128726056-128726242 | Common:1; Rare:54; Clinvar:3 | ||||
| chr3:128879408-128879698 | Common:4; Rare:143; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129160991-129161152 | Common:1; Rare:63 | ||||
| chr3:129183733-129184113 | Common:3; Rare:136 | ||||
| chr3:129249534-129249701 | Common:1; Rare:52 | ||||
| chr3:129278757-129278903 | Common:4; Rare:46 |