| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45253078-45253323 | Rare:69 | ||||
| chr14:45253443-45253482 | Rare:13 | ||||
| chr14:45253509-45253614 | Common:1; Rare:43 | ||||
| chr14:49586290-49586776 | Common:1; Rare:247; Clinvar (benign):1 | ||||
| chr14:49598731-49599023 | Common:1; Rare:107 | ||||
| chr14:49620563-49620848 | Common:2; Rare:118; Clinvar:4 | ||||
| chr14:49688201-49688266 | Rare:22 | ||||
| chr14:49767592-49767625 | Common:1; Rare:12 | ||||
| chr14:49767998-49768303 | Common:2; Rare:110 | ||||
| chr14:49892828-49893147 | Common:1; Rare:141 | ||||
| chr14:50116392-50116695 | Rare:147 | ||||
| chr14:50231861-50232005 | Common:1; Rare:57 | ||||
| chr14:50312055-50312380 | Common:1; Rare:142; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:50396265-50396374 | Common:1; Rare:19 | ||||
| chr14:50396730-50396995 | Common:4; Rare:77 |