| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:85530032-85530205 | Common:1; Rare:38 | ||||
| chr14:87993024-87993294 | Common:4; Rare:128; Clinvar:13; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr14:88562880-88563154 | Rare:125 | ||||
| chr14:89619103-89619249 | Common:1; Rare:48 | ||||
| chr14:89955802-89955964 | Common:9; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90331921-90332235 | Common:1; Rare:87 | ||||
| chr14:90396870-90397232 | Common:5; Rare:171; Clinvar (benign):2 | ||||
| chr14:91510219-91510631 | Common:1; Rare:135 | ||||
| chr14:91836404-91836653 | Common:12; Rare:45 | ||||
| chr14:91946947-91947131 | Common:1; Rare:23 | ||||
| chr14:91947401-91947821 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):4 | ||||
| chr14:92039792-92040192 | Common:3; Rare:102; Clinvar:7; Clinvar (benign):2 | ||||
| chr14:92121647-92122000 | Common:5; Rare:118 | ||||
| chr14:92748497-92748850 | Rare:83 | ||||
| chr14:92793988-92794408 | Rare:135 |