| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100376060-100376637 | Common:12; Rare:368 | ||||
| chr14:100586660-100587321 | Common:9; Rare:290 | ||||
| chr14:100587270-100587966 | Common:17; Rare:293 | ||||
| chr14:101561184-101561584 | Common:3; Rare:302 | ||||
| chr14:101761384-101761812 | Common:21; Rare:301 | ||||
| chr14:101809647-101809928 | Rare:133 | ||||
| chr14:101810171-101810464 | Common:6; Rare:125 | ||||
| chr14:101964370-101964935 | Common:9; Rare:343; Clinvar:8; Clinvar (benign):13 | ||||
| chr14:102084451-102085046 | Common:1; Rare:377 | ||||
| chr14:102086322-102086629 | Common:4; Rare:279 | ||||
| chr14:102086922-102087498 | Common:20; Rare:616 | ||||
| chr14:102087493-102087830 | Common:4; Rare:151 | ||||
| chr14:102139230-102139485 | Rare:266 | ||||
| chr14:102139564-102140028 | Common:1; Rare:388 | ||||
| chr14:102304981-102305358 | Common:3; Rare:244 |