| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:52730234-52731061 | Common:20; Rare:569 | ||||
| chr14:52791459-52791973 | Common:12; Rare:533 | ||||
| chr14:52792074-52792474 | Common:3; Rare:61 | ||||
| chr14:52950930-52951470 | Common:12; Rare:476 | ||||
| chr14:53149680-53150080 | Common:1; Rare:116 | ||||
| chr14:53152184-53153129 | Common:17; Rare:984; Clinvar:5; Clinvar (benign):27 | ||||
| chr14:53153129-53153529 | Common:18; Rare:606 | ||||
| chr14:54396664-54397086 | Common:8; Rare:409 | ||||
| chr14:54440844-54441750 | Common:6; Rare:610 | ||||
| chr14:54488494-54488894 | Common:2; Rare:103 | ||||
| chr14:54488916-54489305 | Common:7; Rare:372 | ||||
| chr14:54509523-54510014 | Common:14; Rare:356 | ||||
| chr14:54566547-54567494 | Common:7; Rare:643 | ||||
| chr14:54567470-54567810 | Common:4; Rare:114 | ||||
| chr14:54567751-54567981 | Common:1; Rare:52 |