| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31025716-31025772 | Rare:16 | ||||
| chr14:31105608-31105847 | Rare:46 | ||||
| chr14:31121521-31121820 | Common:2; Rare:67 | ||||
| chr14:31207107-31207226 | Rare:34 | ||||
| chr14:31207415-31207752 | Common:2; Rare:110 | ||||
| chr14:31207781-31207841 | Rare:19 | ||||
| chr14:31208110-31208283 | Common:2; Rare:42 | ||||
| chr14:31420486-31420763 | Common:4; Rare:93 | ||||
| chr14:31457366-31457584 | Common:2; Rare:75 | ||||
| chr14:31561089-31561515 | Common:4; Rare:121; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076026-32076312 | Common:2; Rare:74 | ||||
| chr14:32076615-32077071 | Common:3; Rare:130 | ||||
| chr14:33950676-33950898 | Rare:61 | ||||
| chr14:34228097-34228283 | Common:3; Rare:29 | ||||
| chr14:34462194-34462558 | Common:1; Rare:132 |