| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22775832-22776167 | Common:3; Rare:82; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:22829741-22829915 | Rare:52 | ||||
| chr14:22871651-22871953 | Rare:78 | ||||
| chr14:22872054-22872222 | Common:2; Rare:39 | ||||
| chr14:22929357-22929609 | Rare:57 | ||||
| chr14:23095084-23095291 | Common:1; Rare:108 | ||||
| chr14:23095440-23095602 | Common:2; Rare:63 | ||||
| chr14:23154284-23154532 | Common:3; Rare:58 | ||||
| chr14:23286046-23286369 | Rare:85 | ||||
| chr14:23306712-23306895 | Common:1; Rare:42 | ||||
| chr14:23365120-23365306 | Rare:45 | ||||
| chr14:23555941-23556077 | Rare:38 | ||||
| chr14:23556246-23556334 | Common:1; Rare:21 | ||||
| chr14:23567737-23567829 | Rare:21 | ||||
| chr14:23953629-23953885 | Common:10; Rare:104 |