| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:61762143-61762489 | Common:5; Rare:144 | ||||
| chr14:63543273-63543705 | Common:5; Rare:123 | ||||
| chr14:63641478-63641627 | Common:1; Rare:39 | ||||
| chr14:63641784-63642239 | Common:7; Rare:136 | ||||
| chr14:63727996-63728266 | Common:2; Rare:113 | ||||
| chr14:63852887-63853047 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:63853090-63853360 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr14:63853444-63853648 | Common:1; Rare:55 | ||||
| chr14:64196942-64197053 | Rare:30 | ||||
| chr14:64197120-64197500 | Rare:74 | ||||
| chr14:64338100-64338462 | Common:2; Rare:119 | ||||
| chr14:64338561-64339077 | Common:7; Rare:147 | ||||
| chr14:64387835-64388410 | Common:2; Rare:178 | ||||
| chr14:64424046-64424149 | Rare:24 | ||||
| chr14:64465160-64465570 | Common:2; Rare:103 |