| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95157957-95158016 | Common:1; Rare:15 | ||||
| chr14:95534568-95534650 | Rare:38 | ||||
| chr14:95714102-95714280 | Common:1; Rare:50 | ||||
| chr14:96363333-96363552 | Common:1; Rare:71 | ||||
| chr14:96502290-96502471 | Rare:67 | ||||
| chr14:99272001-99272122 | Rare:22 | ||||
| chr14:99480737-99480978 | Common:2; Rare:97 | ||||
| chr14:100238556-100238790 | Common:2; Rare:72 | ||||
| chr14:100375378-100375684 | Common:2; Rare:48 | ||||
| chr14:100376264-100376511 | Common:3; Rare:80 | ||||
| chr14:101809647-101809880 | Rare:46 | ||||
| chr14:101964319-101964642 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102086968-102087377 | Common:5; Rare:173 | ||||
| chr14:102087580-102087603 | Rare:4 | ||||
| chr14:102139292-102139435 | Rare:64 |