| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75878715-75879102 | Common:12; Rare:133 | ||||
| chr7:75914944-75915173 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994493-75994772 | Common:4; Rare:137 | ||||
| chr7:76047939-76048220 | Common:2; Rare:99 | ||||
| chr7:76302525-76303081 | Common:3; Rare:231; Clinvar:18; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:77696189-77696472 | Common:1; Rare:112 | ||||
| chr7:77798353-77798971 | Common:1; Rare:146 | ||||
| chr7:79452907-79453190 | Common:2; Rare:73; Clinvar (benign):2 | ||||
| chr7:79453560-79454179 | Common:3; Rare:148 | ||||
| chr7:82443551-82443885 | Common:2; Rare:105 | ||||
| chr7:87152307-87152648 | Common:2; Rare:101 | ||||
| chr7:87345455-87345730 | Common:5; Rare:88 | ||||
| chr7:87876224-87876646 | Common:2; Rare:180 | ||||
| chr7:90211625-90211944 | Common:4; Rare:98 | ||||
| chr7:90245099-90245221 | Rare:39 |