| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:65006638-65006878 | Common:3; Rare:72 | ||||
| chr7:65373672-65373954 | Rare:90 | ||||
| chr7:65982156-65982328 | Common:3; Rare:60; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66114753-66114952 | Common:1; Rare:88 | ||||
| chr7:66115153-66115354 | Common:1; Rare:46 | ||||
| chr7:66628664-66629002 | Common:2; Rare:121; Clinvar:6 | ||||
| chr7:66681979-66682192 | Common:6; Rare:96 | ||||
| chr7:66996555-66996974 | Common:2; Rare:112 | ||||
| chr7:72828130-72828488 | Common:1; Rare:102 | ||||
| chr7:73521880-73522107 | Rare:70 | ||||
| chr7:73557104-73557384 | Common:2; Rare:102 | ||||
| chr7:73578545-73578799 | Common:1; Rare:82 | ||||
| chr7:73683410-73683668 | Common:3; Rare:117 | ||||
| chr7:73738786-73739024 | Common:1; Rare:69 | ||||
| chr7:73842510-73842686 | Common:5; Rare:23 |