| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143930165-143930537 | Common:2; Rare:146; Clinvar:21; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr8:143932131-143932582 | Common:1; Rare:195; Clinvar:18; Clinvar (benign):9 | ||||
| chr8:143933799-143933924 | Common:1; Rare:27 | ||||
| chr8:143935016-143935329 | Common:1; Rare:121; Clinvar:10; Clinvar (benign):10 | ||||
| chr8:143936837-143936895 | Rare:13 | ||||
| chr8:143936977-143937272 | Common:3; Rare:100; Clinvar:8; Clinvar (benign):6 | ||||
| chr8:143937749-143938021 | Common:1; Rare:72 | ||||
| chr8:143938855-143939070 | Common:1; Rare:60 | ||||
| chr8:144397392-144397507 | Rare:36 | ||||
| chr8:144461767-144461825 | Rare:22 | ||||
| chr8:145002821-145003047 | Common:2; Rare:83 | ||||
| chr9:528922-529013 | Rare:23 | ||||
| chr9:686360-686833 | Common:4; Rare:120 | ||||
| chr9:2015925-2016048 | Rare:41 | ||||
| chr9:4887672-4887690 | Rare:1 |