| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31208045-31208421 | Common:2; Rare:95 | ||||
| chr14:31419922-31420212 | Common:2; Rare:70 | ||||
| chr14:31420463-31420810 | Common:6; Rare:115 | ||||
| chr14:31456863-31457002 | Rare:25 | ||||
| chr14:31457063-31457239 | Rare:48 | ||||
| chr14:31457368-31457607 | Common:2; Rare:80 | ||||
| chr14:31561081-31561529 | Common:5; Rare:125; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:32075862-32075892 | Rare:8 | ||||
| chr14:32076110-32076317 | Rare:57 | ||||
| chr14:32076472-32076877 | Common:1; Rare:86 | ||||
| chr14:32076925-32077128 | Common:1; Rare:84 | ||||
| chr14:32077269-32077366 | Rare:31 | ||||
| chr14:32077519-32077645 | Common:1; Rare:30 | ||||
| chr14:32077773-32078051 | Rare:75 | ||||
| chr14:32078058-32078270 | Common:1; Rare:52 |