| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10026304-10026492 | Rare:58 | ||||
| chr3:10115512-10115743 | Common:4; Rare:85 | ||||
| chr3:10141678-10142009 | Common:1; Rare:156; Clinvar:39; Clinvar (benign):34 | ||||
| chr3:10142141-10142187 | Rare:17; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:11225853-11226047 | Rare:30 | ||||
| chr3:11272233-11272423 | Common:1; Rare:42 | ||||
| chr3:11643818-11644016 | Common:2; Rare:59 | ||||
| chr3:11719422-11719566 | Rare:46 | ||||
| chr3:11846814-11846996 | Common:1; Rare:53 | ||||
| chr3:12158902-12158995 | Rare:26 | ||||
| chr3:12287771-12287930 | Common:5; Rare:25 | ||||
| chr3:12484349-12484570 | Common:4; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556877-12557155 | Common:5; Rare:94 | ||||
| chr3:12664056-12664330 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13420213-13420458 | Common:1; Rare:72 |