| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52617389-52617518 | Rare:28 | ||||
| chr13:110870295-110870542 | Common:3; Rare:38 | ||||
| chr14:49633956-49634043 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49862713-49863005 | Rare:135 | ||||
| chr14:50001263-50001495 | Common:3; Rare:53 | ||||
| chr15:67148338-67148481 | Common:4; Rare:23 | ||||
| chr15:82750443-82750588 | Common:2; Rare:38 | ||||
| chr15:89115681-89115791 | Rare:23 | ||||
| chr15:90211928-90212061 | Rare:27 | ||||
| chr16:2603288-2603456 | Common:2; Rare:70 | ||||
| chr16:74368134-74368349 | Common:1; Rare:67 | ||||
| chr17:17836389-17836437 | Common:1; Rare:9 | ||||
| chr17:21286442-21286622 | Common:1; Rare:34 | ||||
| chr17:37708205-37708456 | Rare:47 | ||||
| chr17:41651508-41651885 | Common:1; Rare:90 |