| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34713356-34713892 | Common:1; Rare:135; Clinvar:3; Clinvar (benign):3 | ||||
| chr14:34714528-34714759 | Common:3; Rare:87 | ||||
| chr14:34875302-34875502 | Common:1; Rare:74 | ||||
| chr14:34982373-34982709 | Common:1; Rare:136 | ||||
| chr14:35046119-35046623 | Common:2; Rare:173 | ||||
| chr14:35121955-35122605 | Common:3; Rare:187 | ||||
| chr14:35292242-35292465 | Common:3; Rare:84 | ||||
| chr14:36320580-36320811 | Common:3; Rare:67 | ||||
| chr14:37197843-37198089 | Common:3; Rare:81 | ||||
| chr14:38256067-38256313 | Common:1; Rare:61 | ||||
| chr14:39170207-39170450 | Common:3; Rare:58 | ||||
| chr14:39267026-39267396 | Common:2; Rare:120 | ||||
| chr14:44961908-44962278 | Common:3; Rare:107 | ||||
| chr14:45253529-45253613 | Rare:34 | ||||
| chr14:49586327-49586719 | Common:1; Rare:205; Clinvar (benign):1 |