| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:72926219-72926524 | Common:3; Rare:71 | ||||
| chr14:73058309-73058656 | Common:3; Rare:103 | ||||
| chr14:73463622-73463672 | Common:1; Rare:6 | ||||
| chr14:73568790-73569088 | Common:1; Rare:45 | ||||
| chr14:73569104-73569292 | Rare:48 | ||||
| chr14:73591954-73592163 | Common:3; Rare:76 | ||||
| chr14:73759827-73760163 | Common:1; Rare:50 | ||||
| chr14:73787110-73787355 | Common:3; Rare:87 | ||||
| chr14:73790079-73790375 | Common:2; Rare:50 | ||||
| chr14:73886768-73886869 | Common:1; Rare:31 | ||||
| chr14:73950039-73950351 | Common:6; Rare:140; Clinvar (benign):5 | ||||
| chr14:74019233-74019423 | Common:1; Rare:74 | ||||
| chr14:74084397-74084622 | Common:2; Rare:60 | ||||
| chr14:74493367-74493788 | Common:4; Rare:129; Clinvar (benign):4 | ||||
| chr14:74713058-74713213 | Rare:84 |