| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49635169-49635310 | Common:1; Rare:28; Clinvar (benign):1 | ||||
| chr14:49688097-49688408 | Common:2; Rare:210 | ||||
| chr14:49692969-49693266 | Common:2; Rare:180 | ||||
| chr14:49693373-49693740 | Common:4; Rare:170 | ||||
| chr14:49767149-49767786 | Common:8; Rare:337 | ||||
| chr14:49767882-49768275 | Common:7; Rare:336 | ||||
| chr14:49768610-49769680 | Common:4; Rare:474 | ||||
| chr14:49851985-49852571 | Common:10; Rare:317 | ||||
| chr14:49852695-49852865 | Common:4; Rare:140 | ||||
| chr14:49853003-49853181 | Common:1; Rare:38 | ||||
| chr14:49892671-49893251 | Common:5; Rare:517 | ||||
| chr14:50116456-50116772 | Common:2; Rare:326 | ||||
| chr14:50231497-50232093 | Common:4; Rare:453 | ||||
| chr14:50311869-50311986 | Rare:32 | ||||
| chr14:50312021-50312472 | Common:6; Rare:439; Clinvar:4; Clinvar (benign):5 |