| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50116548-50116731 | Common:1; Rare:85 | ||||
| chr14:50312217-50312329 | Rare:35 | ||||
| chr14:50532522-50532755 | Common:3; Rare:76 | ||||
| chr14:50944356-50944558 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51651670-51651994 | Common:4; Rare:95 | ||||
| chr14:51989374-51989660 | Common:2; Rare:93 | ||||
| chr14:52707045-52707257 | Common:1; Rare:96 | ||||
| chr14:52791429-52791778 | Common:2; Rare:116 | ||||
| chr14:52951041-52951395 | Common:4; Rare:127 | ||||
| chr14:53152371-53152437 | Rare:25 | ||||
| chr14:53954449-53954628 | Common:1; Rare:28 | ||||
| chr14:55027031-55027290 | Common:2; Rare:73 | ||||
| chr14:55191495-55191747 | Common:5; Rare:54 | ||||
| chr14:55411800-55411970 | Common:2; Rare:83 | ||||
| chr14:55580088-55580352 | Common:2; Rare:111 |