| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69767683-69767780 | Common:1; Rare:61 | ||||
| chr14:70359599-70359843 | Common:1; Rare:45 | ||||
| chr14:70416998-70417115 | Rare:36 | ||||
| chr14:70600633-70600953 | Common:3; Rare:73 | ||||
| chr14:72926178-72926516 | Common:6; Rare:83 | ||||
| chr14:73027058-73027206 | Common:1; Rare:41 | ||||
| chr14:73058301-73058596 | Common:3; Rare:93 | ||||
| chr14:73458517-73458873 | Common:5; Rare:93 | ||||
| chr14:73644813-73645028 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73790311-73790540 | Common:1; Rare:46 | ||||
| chr14:73851741-73851983 | Common:4; Rare:84 | ||||
| chr14:73950106-73950322 | Common:5; Rare:83; Clinvar (benign):3 | ||||
| chr14:74019254-74019411 | Common:1; Rare:62 | ||||
| chr14:74302922-74303118 | Common:1; Rare:77; Clinvar (benign):1 | ||||
| chr14:74493406-74493783 | Common:4; Rare:122; Clinvar (benign):4 |