| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31561301-31561511 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076251-32076330 | Rare:23 | ||||
| chr14:32076650-32077045 | Common:3; Rare:117 | ||||
| chr14:32329179-32329402 | Rare:37 | ||||
| chr14:33951070-33951245 | Common:1; Rare:59 | ||||
| chr14:34462205-34462542 | Common:1; Rare:118 | ||||
| chr14:34539649-34539892 | Common:1; Rare:62 | ||||
| chr14:34630013-34630235 | Common:5; Rare:95 | ||||
| chr14:34714528-34714943 | Common:6; Rare:153 | ||||
| chr14:34875271-34875381 | Rare:46 | ||||
| chr14:34982372-34982709 | Common:1; Rare:136 | ||||
| chr14:35046139-35046580 | Common:1; Rare:150 | ||||
| chr14:35121950-35122781 | Common:4; Rare:235 | ||||
| chr14:35292179-35292471 | Common:5; Rare:106; Clinvar:1 | ||||
| chr14:35826347-35826465 | Rare:32 |