| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73950528-73950593 | Rare:21 | ||||
| chr14:74018735-74018952 | Common:2; Rare:48 | ||||
| chr14:74019105-74019423 | Common:3; Rare:110 | ||||
| chr14:74084342-74084565 | Common:1; Rare:73 | ||||
| chr14:74084622-74085060 | Common:8; Rare:134 | ||||
| chr14:74085185-74085290 | Common:2; Rare:15 | ||||
| chr14:74085363-74085470 | Rare:16 | ||||
| chr14:74085550-74085576 | Rare:5 | ||||
| chr14:74085620-74085647 | Rare:6 | ||||
| chr14:74302887-74303092 | Common:1; Rare:93; Clinvar (benign):3 | ||||
| chr14:74303116-74303143 | Common:1; Rare:7 | ||||
| chr14:74493245-74493387 | Rare:47; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:74493413-74493834 | Common:4; Rare:146; Clinvar (benign):4 | ||||
| chr14:74712992-74713248 | Common:1; Rare:134 | ||||
| chr14:74763025-74763447 | Rare:113 |