| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:72926215-72926524 | Common:4; Rare:72 | ||||
| chr14:73058322-73058595 | Common:3; Rare:87 | ||||
| chr14:73136319-73136534 | Common:4; Rare:70; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:73458504-73458870 | Common:5; Rare:96 | ||||
| chr14:73490870-73491000 | Common:4; Rare:50 | ||||
| chr14:73644900-73645030 | Common:2; Rare:37; Clinvar:2 | ||||
| chr14:73851724-73851980 | Common:4; Rare:83 | ||||
| chr14:73950080-73950324 | Common:5; Rare:97; Clinvar (benign):3 | ||||
| chr14:74019263-74019411 | Common:1; Rare:58 | ||||
| chr14:74084638-74084970 | Common:7; Rare:108 | ||||
| chr14:74348182-74348517 | Rare:68 | ||||
| chr14:74493568-74493813 | Common:3; Rare:98; Clinvar (benign):4 | ||||
| chr14:74713043-74713213 | Rare:96 | ||||
| chr14:74763231-74763402 | Rare:64 | ||||
| chr14:75126968-75127140 | Common:1; Rare:66 |