| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49620567-49620820 | Common:2; Rare:101; Clinvar:1 | ||||
| chr14:49688199-49688283 | Rare:31 | ||||
| chr14:49692974-49693188 | Common:1; Rare:76 | ||||
| chr14:49767998-49768277 | Common:2; Rare:104 | ||||
| chr14:49852746-49853146 | Common:3; Rare:104 | ||||
| chr14:49892907-49893109 | Rare:82 | ||||
| chr14:50116422-50116641 | Rare:119 | ||||
| chr14:50312121-50312384 | Common:1; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:50532442-50532672 | Common:3; Rare:67 | ||||
| chr14:50559983-50560258 | Rare:48 | ||||
| chr14:50561075-50561198 | Rare:23 | ||||
| chr14:50627853-50628082 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr14:50668342-50668556 | Common:3; Rare:83 | ||||
| chr14:51095044-51095305 | Common:4; Rare:101 | ||||
| chr14:51240085-51240287 | Common:1; Rare:77 |