| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127823105-127823406 | Common:4; Rare:67 | ||||
| chr3:128052170-128052543 | Common:2; Rare:127 | ||||
| chr3:128067234-128067592 | Rare:88 | ||||
| chr3:128153356-128153496 | Rare:39 | ||||
| chr3:128487908-128488063 | Common:1; Rare:39 | ||||
| chr3:128650756-128651091 | Common:1; Rare:99 | ||||
| chr3:128879404-128879694 | Common:4; Rare:144; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129183784-129184081 | Common:2; Rare:101 | ||||
| chr3:129249503-129249737 | Common:3; Rare:64 | ||||
| chr3:129278761-129278905 | Common:4; Rare:46 | ||||
| chr3:129315892-129316067 | Common:1; Rare:38 | ||||
| chr3:129316253-129316325 | Rare:38 | ||||
| chr3:129439819-129440393 | Common:1; Rare:175; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129893535-129893882 | Rare:135 | ||||
| chr3:130094249-130094352 | Rare:27 |