| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69259970-69260210 | Common:2; Rare:62 | ||||
| chr14:69398251-69398381 | Rare:56 | ||||
| chr14:69398624-69398731 | Rare:28 | ||||
| chr14:69574849-69574991 | Common:1; Rare:28 | ||||
| chr14:69611478-69611708 | Common:1; Rare:80 | ||||
| chr14:69767689-69767918 | Common:1; Rare:98 | ||||
| chr14:70188901-70189124 | Common:3; Rare:44 | ||||
| chr14:70417025-70417115 | Rare:25 | ||||
| chr14:70600635-70600941 | Common:3; Rare:73 | ||||
| chr14:72926219-72926535 | Common:3; Rare:75 | ||||
| chr14:73058309-73058595 | Common:3; Rare:88 | ||||
| chr14:73458520-73458860 | Common:5; Rare:88 | ||||
| chr14:73644858-73645042 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73714353-73714462 | Common:1; Rare:41 | ||||
| chr14:73886754-73886897 | Common:2; Rare:50 |