| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134986469-134986556 | Common:3; Rare:40 | ||||
| chr7:135148045-135148129 | Rare:25 | ||||
| chr7:135170651-135170882 | Common:3; Rare:83 | ||||
| chr7:139036022-139036214 | Rare:50 | ||||
| chr7:141738033-141738432 | Common:4; Rare:126 | ||||
| chr7:143380846-143381409 | Common:2; Rare:168 | ||||
| chr7:155644384-155644702 | Common:2; Rare:101 | ||||
| chr7:157336936-157337013 | Rare:22 | ||||
| chr8:6406543-6406668 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708189-6708422 | Common:3; Rare:101 | ||||
| chr8:15540200-15540306 | Common:1; Rare:50; Clinvar:6 | ||||
| chr8:17246810-17247042 | Common:2; Rare:96 | ||||
| chr8:19817287-19817486 | Common:3; Rare:72 | ||||
| chr8:22245026-22245150 | Rare:64 | ||||
| chr8:26382956-26383119 | Common:1; Rare:74 |