| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43638860-43639535 | Common:5; Rare:199 | ||||
| chr3:43689344-43689755 | Rare:72 | ||||
| chr3:43690093-43691138 | Common:42; Rare:1293; Clinvar:54; Clinvar (benign):18; Clinvar (pathogenic):4 | ||||
| chr3:43691077-43691800 | Common:13; Rare:497 | ||||
| chr3:43691885-43692829 | Common:1; Rare:170 | ||||
| chr3:44337860-44338205 | Common:12; Rare:335 | ||||
| chr3:44338190-44339000 | Common:49; Rare:1132 | ||||
| chr3:44477200-44477470 | Common:1; Rare:68 | ||||
| chr3:44477390-44478060 | Common:7; Rare:388 | ||||
| chr3:44510166-44511116 | Common:37; Rare:502 | ||||
| chr3:44584480-44584982 | Common:1; Rare:351 | ||||
| chr3:44624670-44625207 | Common:17; Rare:555 | ||||
| chr3:44625170-44625350 | Rare:52 | ||||
| chr3:44625306-44625706 | Rare:126 | ||||
| chr3:44648440-44648820 | Rare:175 |