| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24232248-24232707 | Common:8; Rare:116 | ||||
| chr14:24232754-24232949 | Common:1; Rare:43 | ||||
| chr14:24235498-24235794 | Common:2; Rare:63 | ||||
| chr14:24236997-24237300 | Common:2; Rare:92 | ||||
| chr14:24242295-24242436 | Rare:46; Clinvar (benign):1 | ||||
| chr14:24242539-24242750 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24271453-24271645 | Common:1; Rare:53 | ||||
| chr14:24299738-24299890 | Common:4; Rare:48 | ||||
| chr14:24399077-24399228 | Common:1; Rare:52 | ||||
| chr14:24429855-24429978 | Rare:30 | ||||
| chr14:24429984-24430323 | Common:4; Rare:82 | ||||
| chr14:24430926-24431021 | Common:1; Rare:39 | ||||
| chr14:24442213-24442626 | Common:4; Rare:146 | ||||
| chr14:24442644-24443043 | Common:6; Rare:124 | ||||
| chr14:26597571-26597612 | Rare:3 |