| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73569595-73569693 | Common:1; Rare:51 | ||||
| chr14:73569779-73570078 | Common:6; Rare:132 | ||||
| chr14:73644530-73644678 | Rare:26 | ||||
| chr14:73644793-73645091 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73645423-73645515 | Rare:15 | ||||
| chr14:73713795-73714148 | Common:1; Rare:93 | ||||
| chr14:73714190-73714444 | Common:2; Rare:78 | ||||
| chr14:73755166-73755202 | Rare:13 | ||||
| chr14:73759827-73760637 | Common:4; Rare:143 | ||||
| chr14:73786665-73787520 | Common:9; Rare:235 | ||||
| chr14:73790309-73790461 | Common:1; Rare:32 | ||||
| chr14:73851652-73852130 | Common:8; Rare:135 | ||||
| chr14:73852202-73852323 | Common:1; Rare:31 | ||||
| chr14:73886329-73886433 | Rare:18 | ||||
| chr14:73886465-73887102 | Common:6; Rare:182 |