| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99438796-99439002 | Common:1; Rare:53 | ||||
| chr7:99439266-99439445 | Common:2; Rare:41 | ||||
| chr7:100088719-100089060 | Common:2; Rare:100 | ||||
| chr7:100101363-100101733 | Common:1; Rare:141; Clinvar (benign):1 | ||||
| chr7:100119335-100119717 | Rare:111 | ||||
| chr7:100428660-100428793 | Common:3; Rare:45 | ||||
| chr7:101217849-101218192 | Common:3; Rare:106 | ||||
| chr7:102464844-102465020 | Common:1; Rare:71 | ||||
| chr7:107563897-107563996 | Common:2; Rare:59; Clinvar (benign):2 | ||||
| chr7:108569654-108570043 | Common:1; Rare:121 | ||||
| chr7:118183961-118184169 | Common:1; Rare:75 | ||||
| chr7:123748953-123749230 | Common:2; Rare:100 | ||||
| chr7:130492220-130492283 | Rare:17 | ||||
| chr7:131109868-131110129 | Common:1; Rare:48 | ||||
| chr7:131327708-131327897 | Rare:65 |