| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:55572617-55572639 | Rare:4 | ||||
| chr7:55572971-55573215 | Common:2; Rare:47 | ||||
| chr7:56051371-56051887 | Common:1; Rare:188; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56063789-56064375 | Common:2; Rare:239 | ||||
| chr7:56106364-56106671 | Common:8; Rare:117 | ||||
| chr7:65982158-65982328 | Common:3; Rare:60; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66114764-66114960 | Common:1; Rare:90 | ||||
| chr7:66115179-66115383 | Rare:49 | ||||
| chr7:66628640-66628983 | Common:2; Rare:126; Clinvar:5 | ||||
| chr7:66681948-66682200 | Common:6; Rare:106 | ||||
| chr7:66921102-66921460 | Common:1; Rare:104 | ||||
| chr7:66921716-66921844 | Rare:31 | ||||
| chr7:66995289-66995711 | Common:1; Rare:142; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr7:66996548-66996933 | Common:3; Rare:94 | ||||
| chr7:73521828-73522031 | Rare:69 |