| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:60657819-60657867 | Rare:10 | ||||
| chr14:60734690-60734854 | Rare:54 | ||||
| chr14:60980960-60981295 | Common:1; Rare:126 | ||||
| chr14:61321549-61321646 | Common:2; Rare:24 | ||||
| chr14:61695135-61695635 | Common:3; Rare:153 | ||||
| chr14:61696196-61696297 | Rare:25 | ||||
| chr14:61762116-61762488 | Common:5; Rare:150 | ||||
| chr14:63542805-63542954 | Common:1; Rare:38 | ||||
| chr14:63543242-63543717 | Common:5; Rare:135 | ||||
| chr14:63543791-63543954 | Common:1; Rare:22 | ||||
| chr14:63641406-63641703 | Common:2; Rare:85 | ||||
| chr14:63641733-63642239 | Common:8; Rare:150 | ||||
| chr14:63642320-63642528 | Common:2; Rare:51 | ||||
| chr14:63727968-63728280 | Common:3; Rare:126 | ||||
| chr14:63852789-63853124 | Common:1; Rare:116; Clinvar:4; Clinvar (benign):2 |