| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23969867-23969976 | Common:4; Rare:50 | ||||
| chr14:23988766-23988917 | Common:8; Rare:61 | ||||
| chr14:24094007-24094377 | Common:3; Rare:100 | ||||
| chr14:24114478-24114840 | Common:1; Rare:88 | ||||
| chr14:24114998-24115280 | Common:2; Rare:78 | ||||
| chr14:24141455-24141884 | Common:2; Rare:108 | ||||
| chr14:24144201-24144402 | Common:2; Rare:54 | ||||
| chr14:24146553-24146741 | Rare:67 | ||||
| chr14:24195400-24195711 | Common:2; Rare:69 | ||||
| chr14:24213095-24213188 | Rare:18 | ||||
| chr14:24213431-24213646 | Common:2; Rare:72 | ||||
| chr14:24215958-24216154 | Common:1; Rare:62 | ||||
| chr14:24232312-24232742 | Common:8; Rare:99 | ||||
| chr14:24232823-24232961 | Common:1; Rare:31 | ||||
| chr14:24242249-24242413 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):2 |