| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:70907284-70907390 | Common:1; Rare:37 | ||||
| chr14:71320289-71320552 | Rare:81 | ||||
| chr14:71320814-71321177 | Common:3; Rare:110 | ||||
| chr14:71321754-71321911 | Common:1; Rare:29 | ||||
| chr14:72894085-72894260 | Common:4; Rare:60 | ||||
| chr14:72926237-72926535 | Common:2; Rare:71 | ||||
| chr14:73058309-73058607 | Common:3; Rare:90 | ||||
| chr14:73458504-73458853 | Common:5; Rare:90 | ||||
| chr14:73568729-73569104 | Common:1; Rare:57 | ||||
| chr14:73569132-73569303 | Rare:45 | ||||
| chr14:73592069-73592193 | Common:2; Rare:49 | ||||
| chr14:73644881-73645037 | Common:3; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73713794-73714023 | Rare:61 | ||||
| chr14:73787129-73787388 | Common:2; Rare:91 | ||||
| chr14:73851743-73851983 | Common:4; Rare:83 |