| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102345085-102345542 | Common:1; Rare:81 | ||||
| chr4:102760903-102761052 | Rare:50; Clinvar:1 | ||||
| chr4:102825310-102825423 | Common:2; Rare:30 | ||||
| chr4:102826817-102826914 | Rare:23 | ||||
| chr4:102827041-102827197 | Common:3; Rare:58 | ||||
| chr4:102868814-102869087 | Common:2; Rare:93 | ||||
| chr4:103019621-103019788 | Common:1; Rare:51 | ||||
| chr4:104494833-104495022 | Common:1; Rare:46 | ||||
| chr4:105708626-105708852 | Common:2; Rare:74 | ||||
| chr4:106316161-106316660 | Common:5; Rare:160 | ||||
| chr4:107720182-107720486 | Common:7; Rare:123 | ||||
| chr4:107989693-107989995 | Common:5; Rare:134; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620388-108620727 | Common:6; Rare:148 | ||||
| chr4:108621993-108622202 | Common:1; Rare:53 | ||||
| chr4:108650284-108650674 | Common:2; Rare:127 |