| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:26597370-26597681 | Common:2; Rare:58 | ||||
| chr14:28765234-28765433 | Common:1; Rare:33 | ||||
| chr14:30559055-30559216 | Common:2; Rare:62 | ||||
| chr14:30874284-30874565 | Common:4; Rare:88 | ||||
| chr14:31025207-31025515 | Rare:75 | ||||
| chr14:31207633-31207879 | Common:2; Rare:87 | ||||
| chr14:31420547-31420749 | Common:2; Rare:60 | ||||
| chr14:31457391-31457577 | Common:2; Rare:62 | ||||
| chr14:31561360-31561503 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076668-32077041 | Common:3; Rare:112 | ||||
| chr14:34462213-34462577 | Common:1; Rare:127 | ||||
| chr14:34539564-34539793 | Rare:82 | ||||
| chr14:34629991-34630256 | Common:5; Rare:108 | ||||
| chr14:34714538-34714966 | Common:6; Rare:149 | ||||
| chr14:34982372-34982656 | Common:1; Rare:109 |