| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75738860-75739370 | Common:5; Rare:257 | ||||
| chr7:75842894-75843182 | Common:4; Rare:82 | ||||
| chr7:75878832-75879152 | Common:24; Rare:208 | ||||
| chr7:75914895-75915207 | Common:7; Rare:204; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:75983380-75983843 | Common:7; Rare:271; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr7:75994497-75994797 | Common:9; Rare:288 | ||||
| chr7:76047770-76048215 | Common:6; Rare:250 | ||||
| chr7:76302462-76302715 | Common:4; Rare:154; Clinvar:5; Clinvar (benign):5 | ||||
| chr7:76303487-76303859 | Common:3; Rare:269; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):14 | ||||
| chr7:76358908-76359163 | Common:1; Rare:178 | ||||
| chr7:76359210-76359560 | Common:16; Rare:224 | ||||
| chr7:76392870-76393420 | Common:5; Rare:312 | ||||
| chr7:76397270-76397670 | Common:2; Rare:248 | ||||
| chr7:76397690-76398320 | Common:6; Rare:175 | ||||
| chr7:76510010-76510540 | Common:8; Rare:167 |