| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24135943-24136299 | Common:1; Rare:114 | ||||
| chr14:24146537-24146912 | Common:1; Rare:122 | ||||
| chr14:24147304-24147672 | Common:4; Rare:89 | ||||
| chr14:24195324-24195357 | Rare:11 | ||||
| chr14:24195393-24195744 | Common:2; Rare:76 | ||||
| chr14:24213431-24213601 | Common:1; Rare:56 | ||||
| chr14:24232284-24232707 | Common:8; Rare:109 | ||||
| chr14:24232847-24232970 | Rare:32 | ||||
| chr14:24242268-24242401 | Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24242571-24242767 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271453-24271748 | Common:2; Rare:90 | ||||
| chr14:24299689-24299862 | Common:4; Rare:49 | ||||
| chr14:24429850-24429970 | Rare:27 | ||||
| chr14:24442631-24443043 | Common:6; Rare:125 | ||||
| chr14:24508263-24508515 | Common:3; Rare:48 |