| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:96502774-96502807 | Common:1; Rare:9 | ||||
| chr14:96502903-96503207 | Rare:77 | ||||
| chr14:99271667-99271778 | Rare:23 | ||||
| chr14:99271798-99272358 | Rare:83 | ||||
| chr14:99480731-99481013 | Common:2; Rare:109 | ||||
| chr14:99481275-99481525 | Common:1; Rare:71 | ||||
| chr14:99971700-99972055 | Common:6; Rare:107 | ||||
| chr14:100019292-100019608 | Common:1; Rare:59 | ||||
| chr14:100238504-100238848 | Common:3; Rare:101 | ||||
| chr14:100294289-100294376 | Rare:16 | ||||
| chr14:100376264-100376599 | Common:4; Rare:110 | ||||
| chr14:101761542-101761896 | Common:4; Rare:76 | ||||
| chr14:101809736-101809918 | Rare:40 | ||||
| chr14:101810268-101810375 | Rare:21 | ||||
| chr14:101964346-101964642 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):1 |