| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49633956-49634043 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:71124243-71124549 | Common:1; Rare:64 | ||||
| chr15:24690713-24690989 | Common:3; Rare:43 | ||||
| chr15:28589233-28589495 | Common:1; Rare:9 | ||||
| chr15:35238696-35238971 | Common:6; Rare:45 | ||||
| chr15:41283750-41284015 | Common:2; Rare:69 | ||||
| chr16:9680134-9680342 | Common:1; Rare:46 | ||||
| chr16:56617392-56617504 | Common:2; Rare:20 | ||||
| chr16:72664947-72665133 | Common:1; Rare:52 | ||||
| chr16:74368134-74368367 | Common:1; Rare:69 | ||||
| chr17:16438934-16439054 | Common:1; Rare:35 | ||||
| chr17:35567873-35568139 | Common:2; Rare:83 | ||||
| chr17:45247761-45247934 | Common:1; Rare:30 | ||||
| chr17:64145764-64145973 | Common:2; Rare:55 | ||||
| chr17:64975564-64975688 | Common:1; Rare:39 |