| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73885903-73887543 | Common:22; Rare:795 | ||||
| chr14:73949730-73950058 | Common:14; Rare:231 | ||||
| chr14:73950000-73950450 | Common:36; Rare:811; Clinvar:1; Clinvar (benign):24 | ||||
| chr14:73950510-73950820 | Common:1; Rare:159 | ||||
| chr14:74015922-74016322 | Common:2; Rare:102 | ||||
| chr14:74018196-74018947 | Common:5; Rare:156 | ||||
| chr14:74018960-74019600 | Common:17; Rare:737 | ||||
| chr14:74084251-74085100 | Common:60; Rare:1179 | ||||
| chr14:74085268-74085668 | Common:4; Rare:85 | ||||
| chr14:74302030-74302934 | Common:6; Rare:319; Clinvar (benign):3 | ||||
| chr14:74302856-74303280 | Common:9; Rare:437; Clinvar (benign):9 | ||||
| chr14:74493251-74494121 | Common:22; Rare:895; Clinvar:7; Clinvar (benign):24; Clinvar (pathogenic):2 | ||||
| chr14:74612517-74612928 | Common:3; Rare:264 | ||||
| chr14:74712939-74713339 | Common:3; Rare:799 | ||||
| chr14:74763070-74763450 | Rare:264 |