| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:81220579-81220793 | Common:2; Rare:35 | ||||
| chr14:81220855-81221059 | Common:1; Rare:98 | ||||
| chr14:81221275-81221567 | Common:1; Rare:90 | ||||
| chr14:81533716-81533902 | Common:1; Rare:66 | ||||
| chr14:85529974-85530290 | Common:2; Rare:66 | ||||
| chr14:88554668-88554821 | Common:3; Rare:35 | ||||
| chr14:88562922-88563139 | Rare:102 | ||||
| chr14:88824316-88824716 | Common:2; Rare:113; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89417096-89417326 | Rare:59 | ||||
| chr14:89954566-89954968 | Common:3; Rare:133 | ||||
| chr14:89955875-89956007 | Common:2; Rare:47; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90331892-90332408 | Common:1; Rare:133 | ||||
| chr14:90397127-90397233 | Common:3; Rare:38; Clinvar (benign):2 | ||||
| chr14:90816392-90816451 | Rare:14 | ||||
| chr14:91060298-91060365 | Rare:35 |