| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:96502245-96502603 | Common:2; Rare:151 | ||||
| chr14:99271963-99272351 | Rare:62 | ||||
| chr14:99971895-99972054 | Common:4; Rare:41 | ||||
| chr14:100019283-100019359 | Common:1; Rare:13 | ||||
| chr14:100019370-100019608 | Common:1; Rare:46 | ||||
| chr14:100238514-100238831 | Common:3; Rare:95 | ||||
| chr14:100376264-100376521 | Common:3; Rare:84 | ||||
| chr14:101809793-101809897 | Rare:21 | ||||
| chr14:101810294-101810436 | Common:2; Rare:34 | ||||
| chr14:102027777-102027951 | Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:102083544-102083983 | Common:3; Rare:179 | ||||
| chr14:102139654-102139936 | Rare:99 | ||||
| chr14:102305019-102305308 | Common:1; Rare:83 | ||||
| chr14:102362856-102363098 | Rare:106 | ||||
| chr14:102922831-102922950 | Common:1; Rare:47 |