| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:66507729-66508240 | Common:2; Rare:1153 | ||||
| chr14:66508230-66509431 | Common:5; Rare:630; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr14:67240990-67241810 | Common:16; Rare:714 | ||||
| chr14:67241830-67242200 | Common:3; Rare:86 | ||||
| chr14:67359627-67360591 | Common:22; Rare:1397 | ||||
| chr14:67360571-67360978 | Common:4; Rare:143 | ||||
| chr14:67533004-67533446 | Common:1; Rare:200 | ||||
| chr14:67599310-67599690 | Common:3; Rare:101 | ||||
| chr14:67599804-67599937 | Common:4; Rare:44 | ||||
| chr14:67600100-67600500 | Common:27; Rare:407; Clinvar (pathogenic):4 | ||||
| chr14:67619599-67619999 | Common:8; Rare:372 | ||||
| chr14:67674020-67674340 | Common:6; Rare:156 | ||||
| chr14:67674395-67675370 | Common:17; Rare:878 | ||||
| chr14:67695660-67695950 | Common:3; Rare:197 | ||||
| chr14:67816466-67817463 | Common:6; Rare:390; Clinvar:4 |