| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:25049896-25050193 | Common:3; Rare:93 | ||||
| chr14:26597416-26597621 | Common:1; Rare:38 | ||||
| chr14:30559055-30559249 | Common:2; Rare:74 | ||||
| chr14:30622184-30622379 | Common:1; Rare:93 | ||||
| chr14:30874365-30874575 | Common:2; Rare:72 | ||||
| chr14:31025395-31025690 | Common:2; Rare:73 | ||||
| chr14:31026415-31026628 | Common:3; Rare:59 | ||||
| chr14:31207600-31207862 | Common:2; Rare:92 | ||||
| chr14:31420503-31420770 | Common:4; Rare:86 | ||||
| chr14:31457105-31457256 | Common:1; Rare:45 | ||||
| chr14:31457288-31457584 | Common:2; Rare:103 | ||||
| chr14:31561088-31561516 | Common:4; Rare:122; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076026-32076312 | Common:2; Rare:74 | ||||
| chr14:32076501-32077048 | Common:3; Rare:149 | ||||
| chr14:33951052-33951249 | Common:1; Rare:65 |