| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101761433-101761715 | Common:5; Rare:74 | ||||
| chr14:101809736-101810034 | Rare:71 | ||||
| chr14:101823773-101823859 | Rare:18 | ||||
| chr14:101964476-101964797 | Common:4; Rare:106; Clinvar:4; Clinvar (benign):6 | ||||
| chr14:102086987-102087314 | Common:4; Rare:131 | ||||
| chr14:102139651-102139923 | Rare:95 | ||||
| chr14:102362834-102363096 | Rare:120 | ||||
| chr14:102592412-102592658 | Common:1; Rare:98 | ||||
| chr14:102928477-102928688 | Rare:76 | ||||
| chr14:103123258-103123476 | Rare:40 | ||||
| chr14:103123710-103123942 | Common:1; Rare:61 | ||||
| chr14:103333969-103334257 | Common:1; Rare:120 | ||||
| chr14:103385631-103385778 | Rare:26 | ||||
| chr14:103521441-103521805 | Common:2; Rare:106 | ||||
| chr14:103529008-103529249 | Common:1; Rare:69 |