| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103385233-103385456 | Common:1; Rare:89 | ||||
| chr14:103528996-103529274 | Common:1; Rare:76 | ||||
| chr14:103562581-103563053 | Common:14; Rare:333; Clinvar (benign):7 | ||||
| chr14:103628870-103629276 | Common:2; Rare:197 | ||||
| chr14:103715397-103715856 | Common:2; Rare:314 | ||||
| chr14:103847536-103847791 | Common:5; Rare:187 | ||||
| chr14:104689324-104689672 | Common:2; Rare:130; Clinvar (benign):1 | ||||
| chr14:104724058-104724233 | Common:1; Rare:66 | ||||
| chr14:104752704-104753450 | Common:9; Rare:362 | ||||
| chr14:104795687-104795834 | Rare:73 | ||||
| chr14:104800280-104800620 | Common:2; Rare:166 | ||||
| chr14:104864730-104865060 | Common:3; Rare:76 | ||||
| chr14:104865082-104865331 | Common:8; Rare:114 | ||||
| chr14:104978367-104978609 | Rare:70 | ||||
| chr14:105021041-105021510 | Common:4; Rare:299 |