| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123270269-123270524 | Common:3; Rare:74 | ||||
| chr13:20773207-20773295 | Common:1; Rare:22 | ||||
| chr13:23888746-23888872 | Common:1; Rare:33 | ||||
| chr13:40921662-40921760 | Common:2; Rare:31 | ||||
| chr13:43055350-43055425 | Rare:16 | ||||
| chr13:48413088-48413239 | Rare:18 | ||||
| chr13:52194386-52194510 | Rare:38 | ||||
| chr13:102394517-102394654 | Common:1; Rare:52 | ||||
| chr14:32203265-32203616 | Common:13; Rare:148 | ||||
| chr14:49633956-49634070 | Common:1; Rare:45; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49862645-49863005 | Common:1; Rare:169 | ||||
| chr14:73245963-73246092 | Common:2; Rare:51 | ||||
| chr14:75259013-75259376 | Common:2; Rare:86 | ||||
| chr14:81219443-81219504 | Rare:17 | ||||
| chr14:95516638-95516791 | Common:2; Rare:36 |