| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:2354056-2354098 | Rare:23 | ||||
| chr7:2354513-2354935 | Common:5; Rare:173 | ||||
| chr7:4775463-4775691 | Common:6; Rare:111; Clinvar:1 | ||||
| chr7:5423712-5424058 | Common:4; Rare:88 | ||||
| chr7:5424910-5425058 | Rare:52 | ||||
| chr7:5528004-5528384 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr7:6009030-6009350 | Common:4; Rare:135; Clinvar:3; Clinvar (benign):14 | ||||
| chr7:6026523-6026675 | Rare:39 | ||||
| chr7:6447897-6448078 | Common:1; Rare:72 | ||||
| chr7:6577329-6577571 | Common:1; Rare:80 | ||||
| chr7:7566666-7566993 | Common:5; Rare:127 | ||||
| chr7:7566994-7567037 | Rare:16 | ||||
| chr7:8262067-8262317 | Rare:104 | ||||
| chr7:12211145-12211390 | Common:3; Rare:112 | ||||
| chr7:12403654-12403766 | Common:2; Rare:53 |