| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31420511-31420777 | Common:4; Rare:81 | ||||
| chr14:31561353-31561503 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32075684-32075884 | Rare:37 | ||||
| chr14:32076245-32076352 | Rare:30 | ||||
| chr14:32076593-32077051 | Common:3; Rare:129 | ||||
| chr14:32494905-32495275 | Common:4; Rare:51 | ||||
| chr14:34462200-34462558 | Common:1; Rare:128 | ||||
| chr14:34539619-34539909 | Common:1; Rare:79 | ||||
| chr14:34629932-34630246 | Common:5; Rare:123 | ||||
| chr14:34714453-34714476 | Rare:7 | ||||
| chr14:34714524-34714795 | Common:4; Rare:102 | ||||
| chr14:34875304-34875344 | Rare:19 | ||||
| chr14:34875348-34875433 | Rare:31 | ||||
| chr14:34982373-34982682 | Common:1; Rare:121 | ||||
| chr14:35046139-35046623 | Common:1; Rare:167 |