| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:93976077-93976436 | Common:3; Rare:63 | ||||
| chr14:93976528-93976676 | Rare:32 | ||||
| chr14:93976710-93976886 | Rare:30 | ||||
| chr14:94080512-94080667 | Common:2; Rare:38 | ||||
| chr14:94081117-94081380 | Common:6; Rare:81 | ||||
| chr14:94129543-94129708 | Common:3; Rare:56 | ||||
| chr14:94173916-94174131 | Common:1; Rare:53 | ||||
| chr14:95157299-95157814 | Common:4; Rare:175; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:95157849-95157983 | Common:1; Rare:32 | ||||
| chr14:95158268-95158335 | Common:1; Rare:16 | ||||
| chr14:95534483-95535092 | Common:7; Rare:214; Clinvar (benign):4 | ||||
| chr14:95535628-95535781 | Common:1; Rare:39 | ||||
| chr14:95711581-95711812 | Rare:54 | ||||
| chr14:95714018-95714294 | Common:1; Rare:100 | ||||
| chr14:96363233-96363561 | Common:2; Rare:106 |