| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:101948057-101948381 | Common:2; Rare:96 | ||||
| chr14:102049817-102050132 | Common:2; Rare:118; Clinvar:3; Clinvar (benign):4 | ||||
| chr14:102370618-102370801 | Common:1; Rare:28 | ||||
| chr14:102776312-102776393 | Common:2; Rare:14 | ||||
| chr14:103094501-103094762 | Common:3; Rare:52 | ||||
| chr14:103121134-103121435 | Common:2; Rare:64 | ||||
| chr14:103319421-103319631 | Common:1; Rare:36 | ||||
| chr14:103680203-103680473 | Common:1; Rare:44 | ||||
| chr14:103694374-103694656 | Rare:55 | ||||
| chr14:103696767-103696900 | Common:2; Rare:31 | ||||
| chr14:104780101-104780489 | Common:4; Rare:107; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:105093927-105094150 | Common:1; Rare:49 | ||||
| chr14:105568445-105568618 | Common:2; Rare:57 | ||||
| chr14:105582128-105582238 | Rare:24 | ||||
| chr14:105587552-105587666 | Common:1; Rare:42 |