| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69398245-69398747 | Common:2; Rare:149 | ||||
| chr14:69611466-69611744 | Common:1; Rare:93 | ||||
| chr14:69767699-69768282 | Common:3; Rare:188 | ||||
| chr14:69770802-69771144 | Common:1; Rare:98 | ||||
| chr14:71320296-71320487 | Rare:59 | ||||
| chr14:71321776-71321936 | Common:1; Rare:26 | ||||
| chr14:72926160-72926552 | Common:7; Rare:99 | ||||
| chr14:73058309-73058632 | Common:3; Rare:98 | ||||
| chr14:73136252-73136541 | Common:4; Rare:89; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73287294-73287471 | Rare:34 | ||||
| chr14:73537124-73537228 | Rare:11 | ||||
| chr14:73568744-73569309 | Common:1; Rare:110 | ||||
| chr14:73726900-73727172 | Common:1; Rare:69 | ||||
| chr14:73787109-73787353 | Common:3; Rare:87 | ||||
| chr14:73790369-73790570 | Rare:41 |