| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:71320192-71320491 | Rare:98 | ||||
| chr14:72926219-72926528 | Common:3; Rare:71 | ||||
| chr14:73027074-73027325 | Common:1; Rare:71 | ||||
| chr14:73058291-73058635 | Common:3; Rare:106 | ||||
| chr14:73136288-73136541 | Common:4; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73458513-73458879 | Common:5; Rare:96 | ||||
| chr14:73569254-73569292 | Rare:13 | ||||
| chr14:73644901-73645030 | Common:2; Rare:36; Clinvar:2 | ||||
| chr14:73787146-73787359 | Common:2; Rare:79 | ||||
| chr14:73851793-73851994 | Common:4; Rare:66 | ||||
| chr14:73886735-73886893 | Common:2; Rare:56 | ||||
| chr14:73950175-73950323 | Common:3; Rare:62; Clinvar (benign):1 | ||||
| chr14:74019233-74019406 | Common:1; Rare:69 | ||||
| chr14:74493275-74493458 | Common:1; Rare:43; Clinvar:2 | ||||
| chr14:74493570-74493781 | Common:3; Rare:79; Clinvar (benign):4 |