| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:72836457-72836610 | Common:2; Rare:33 | ||||
| chr14:72926182-72926528 | Common:6; Rare:85 | ||||
| chr14:72926683-72926783 | Rare:27 | ||||
| chr14:73026990-73027239 | Common:1; Rare:66 | ||||
| chr14:73058295-73058650 | Common:3; Rare:106 | ||||
| chr14:73136390-73136569 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73237560-73237594 | Rare:8 | ||||
| chr14:73458251-73458360 | Rare:22 | ||||
| chr14:73458491-73458870 | Common:5; Rare:102 | ||||
| chr14:73491849-73492164 | Common:1; Rare:101 | ||||
| chr14:73567367-73567621 | Common:2; Rare:52 | ||||
| chr14:73568799-73569086 | Common:1; Rare:42 | ||||
| chr14:73569203-73569294 | Rare:28 | ||||
| chr14:73591962-73592176 | Common:3; Rare:82 | ||||
| chr14:73644881-73645065 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):1 |