| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:65413190-65413432 | Rare:53 | ||||
| chr14:66507237-66507441 | Common:1; Rare:27 | ||||
| chr14:66507725-66508238 | Common:1; Rare:205 | ||||
| chr14:66508917-66509106 | Rare:62 | ||||
| chr14:66509244-66509272 | Rare:6 | ||||
| chr14:67241010-67241488 | Common:3; Rare:124 | ||||
| chr14:67241555-67241756 | Common:3; Rare:49 | ||||
| chr14:67359733-67360055 | Common:1; Rare:107 | ||||
| chr14:67360256-67360611 | Common:2; Rare:103 | ||||
| chr14:67488616-67488808 | Common:1; Rare:30 | ||||
| chr14:67488818-67488842 | Common:1; Rare:5 | ||||
| chr14:67600130-67600394 | Common:6; Rare:94; Clinvar (pathogenic):1 | ||||
| chr14:67619638-67619935 | Common:2; Rare:74 | ||||
| chr14:67674209-67674335 | Common:2; Rare:33 | ||||
| chr14:67674516-67675019 | Common:3; Rare:126 |