| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24195420-24195727 | Common:1; Rare:71 | ||||
| chr14:24232308-24232475 | Common:6; Rare:41 | ||||
| chr14:24232770-24232942 | Common:1; Rare:38 | ||||
| chr14:24242295-24242433 | Rare:46; Clinvar (benign):1 | ||||
| chr14:24242561-24242747 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271496-24271604 | Common:1; Rare:26 | ||||
| chr14:24299738-24299869 | Common:4; Rare:35 | ||||
| chr14:24429861-24429980 | Rare:28 | ||||
| chr14:24442680-24443023 | Common:5; Rare:109 | ||||
| chr14:26597429-26597742 | Common:1; Rare:68 | ||||
| chr14:30622190-30622362 | Common:1; Rare:71 | ||||
| chr14:31025207-31025472 | Rare:64 | ||||
| chr14:31025558-31025662 | Common:1; Rare:24 | ||||
| chr14:31207588-31207862 | Common:2; Rare:96 | ||||
| chr14:31420529-31420737 | Common:3; Rare:66 |