| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6009029-6009366 | Common:4; Rare:139; Clinvar:4; Clinvar (benign):15 | ||||
| chr7:6104627-6104938 | Common:5; Rare:117 | ||||
| chr7:6447919-6448066 | Common:1; Rare:51 | ||||
| chr7:6483981-6484249 | Common:2; Rare:122 | ||||
| chr7:7182353-7182735 | Common:3; Rare:138 | ||||
| chr7:7566806-7567037 | Common:4; Rare:94 | ||||
| chr7:8262109-8262298 | Rare:89 | ||||
| chr7:10973654-10973941 | Common:1; Rare:125 | ||||
| chr7:12211128-12211410 | Common:3; Rare:128 | ||||
| chr7:15686543-15686971 | Common:4; Rare:127 | ||||
| chr7:16645658-16646220 | Common:4; Rare:197 | ||||
| chr7:17298454-17298660 | Common:3; Rare:50 | ||||
| chr7:17940412-17940574 | Common:1; Rare:85 | ||||
| chr7:18509117-18509390 | Rare:49 | ||||
| chr7:21427788-21428146 | Common:3; Rare:133 |