| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77097980-77098334 | Rare:111 | ||||
| chr14:77320869-77321094 | Rare:69; Clinvar:1 | ||||
| chr14:77377053-77377146 | Common:1; Rare:35 | ||||
| chr14:77457550-77457876 | Common:1; Rare:97 | ||||
| chr14:77708000-77708164 | Common:2; Rare:91 | ||||
| chr14:81220871-81221097 | Common:1; Rare:106 | ||||
| chr14:81221275-81221458 | Common:1; Rare:45 | ||||
| chr14:85530033-85530184 | Common:1; Rare:34 | ||||
| chr14:89954661-89954950 | Rare:88 | ||||
| chr14:90396870-90397183 | Common:5; Rare:152 | ||||
| chr14:90397220-90397223 | Rare:1 | ||||
| chr14:91510280-91510622 | Common:1; Rare:104 | ||||
| chr14:92040031-92040117 | Common:2; Rare:24; Clinvar (benign):1 | ||||
| chr14:92121658-92122000 | Common:4; Rare:115 | ||||
| chr14:92794002-92794380 | Rare:117 |