| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56051439-56051857 | Common:1; Rare:162; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106384-56106591 | Common:6; Rare:79 | ||||
| chr7:66114792-66114955 | Common:1; Rare:73 | ||||
| chr7:66115177-66115354 | Common:1; Rare:41 | ||||
| chr7:66628678-66628973 | Common:2; Rare:108; Clinvar:4 | ||||
| chr7:66682009-66682207 | Common:6; Rare:94 | ||||
| chr7:66921130-66921229 | Rare:36 | ||||
| chr7:66995268-66995703 | Common:1; Rare:150; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr7:66996541-66996888 | Common:3; Rare:81 | ||||
| chr7:71131482-71131721 | Common:5; Rare:82 | ||||
| chr7:72828130-72828458 | Common:1; Rare:97 | ||||
| chr7:73557566-73557741 | Common:2; Rare:59 | ||||
| chr7:73683412-73683638 | Common:3; Rare:96 | ||||
| chr7:73738786-73739146 | Common:2; Rare:114 | ||||
| chr7:74027990-74028266 | Common:1; Rare:92; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 |