| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:44897061-44897346 | Common:1; Rare:101 | ||||
| chr14:44961878-44962259 | Common:3; Rare:114 | ||||
| chr14:45095912-45096231 | Common:1; Rare:59 | ||||
| chr14:45131660-45131679 | Rare:2 | ||||
| chr14:45134194-45134541 | Rare:151 | ||||
| chr14:45231264-45231411 | Rare:39 | ||||
| chr14:45253049-45253321 | Rare:77 | ||||
| chr14:49598569-49599018 | Common:4; Rare:179 | ||||
| chr14:49620552-49620945 | Common:3; Rare:143; Clinvar:6; Clinvar (benign):1 | ||||
| chr14:49621187-49621301 | Rare:38 | ||||
| chr14:49767592-49767732 | Common:2; Rare:47 | ||||
| chr14:49892762-49893154 | Common:2; Rare:162 | ||||
| chr14:50231548-50231799 | Common:1; Rare:70 | ||||
| chr14:50312153-50312376 | Rare:98 | ||||
| chr14:50532446-50532632 | Common:3; Rare:53 |