| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12158902-12159222 | Rare:88 | ||||
| chr3:12484389-12484522 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:12664075-12664318 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12796517-12796718 | Common:5; Rare:59 | ||||
| chr3:13420222-13420466 | Common:1; Rare:72 | ||||
| chr3:13480040-13480324 | Common:2; Rare:67 | ||||
| chr3:14124706-14125185 | Common:4; Rare:143; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178474-14178861 | Common:3; Rare:186; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402393-14402636 | Common:1; Rare:67 | ||||
| chr3:14947402-14947576 | Common:2; Rare:87 | ||||
| chr3:14948017-14948208 | Rare:86 | ||||
| chr3:15206066-15206279 | Rare:85 | ||||
| chr3:15427471-15427629 | Common:1; Rare:57 | ||||
| chr3:15601512-15601810 | Common:4; Rare:127; Clinvar:2 | ||||
| chr3:15859800-15860027 | Common:1; Rare:76 |