| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:126704081-126704324 | Common:2; Rare:83 | ||||
| chr3:127598215-127598458 | Common:3; Rare:73 | ||||
| chr3:127628919-127629286 | Common:1; Rare:119 | ||||
| chr3:127822451-127822673 | Rare:48 | ||||
| chr3:127823175-127823340 | Common:3; Rare:32 | ||||
| chr3:128052184-128052525 | Common:2; Rare:117 | ||||
| chr3:128123767-128123968 | Rare:52 | ||||
| chr3:128879408-128879698 | Common:4; Rare:143; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129183821-129184079 | Common:2; Rare:87 | ||||
| chr3:129249545-129249746 | Common:1; Rare:56 | ||||
| chr3:129278761-129278905 | Common:4; Rare:46 | ||||
| chr3:129316245-129316300 | Rare:36 | ||||
| chr3:129439829-129440328 | Common:1; Rare:154; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893574-129893882 | Rare:129 | ||||
| chr3:130746792-130746934 | Common:3; Rare:41 |