| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139359591-139359977 | Common:5; Rare:155 | ||||
| chr7:141551270-141551423 | Common:1; Rare:46; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:152025567-152025774 | Rare:83 | ||||
| chr7:155644384-155644719 | Common:2; Rare:112 | ||||
| chr7:157336778-157337061 | Common:2; Rare:133 | ||||
| chr7:158856423-158856632 | Common:5; Rare:73 | ||||
| chr8:232235-232377 | Common:2; Rare:56 | ||||
| chr8:6406540-6406663 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:11802470-11802791 | Common:6; Rare:174 | ||||
| chr8:17246810-17246965 | Rare:62 | ||||
| chr8:17692248-17692370 | Rare:35 | ||||
| chr8:21919572-21919763 | Common:2; Rare:82 | ||||
| chr8:22245026-22245164 | Rare:70 | ||||
| chr8:22669070-22669232 | Common:2; Rare:59 | ||||
| chr8:23457625-23457832 | Common:2; Rare:74 |