| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170584586-170584767 | Common:1; Rare:62 | ||||
| chr7:727245-727314 | Rare:23; Clinvar:1 | ||||
| chr7:868178-868393 | Common:3; Rare:68 | ||||
| chr7:1569962-1570117 | Common:1; Rare:53 | ||||
| chr7:2242176-2242261 | Common:2; Rare:49 | ||||
| chr7:2354605-2354946 | Common:4; Rare:148 | ||||
| chr7:5528004-5528400 | Common:1; Rare:124; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr7:5593254-5593380 | Rare:37 | ||||
| chr7:6009040-6009283 | Common:3; Rare:90; Clinvar:1; Clinvar (benign):9 | ||||
| chr7:6447922-6448057 | Common:1; Rare:48 | ||||
| chr7:6484073-6484247 | Common:1; Rare:89 | ||||
| chr7:16645622-16645929 | Rare:96 | ||||
| chr7:17940449-17940552 | Common:1; Rare:52 | ||||
| chr7:19117632-19118023 | Common:1; Rare:89 | ||||
| chr7:23105687-23105829 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):3 |