| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24195316-24195379 | Rare:20 | ||||
| chr14:24195400-24195744 | Common:2; Rare:76 | ||||
| chr14:24213051-24213198 | Rare:28 | ||||
| chr14:24213431-24213612 | Common:1; Rare:58 | ||||
| chr14:24232312-24232477 | Common:6; Rare:41 | ||||
| chr14:24232527-24232776 | Rare:55 | ||||
| chr14:24232823-24232975 | Common:1; Rare:38 | ||||
| chr14:24242258-24242401 | Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24242561-24242779 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271453-24271692 | Common:2; Rare:69 | ||||
| chr14:24299714-24299890 | Common:4; Rare:56 | ||||
| chr14:24367862-24368196 | Common:2; Rare:59 | ||||
| chr14:24399138-24399228 | Rare:23 | ||||
| chr14:24429836-24430032 | Common:2; Rare:46 | ||||
| chr14:24430148-24430341 | Common:3; Rare:56 |