| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99780265-99780371 | Rare:20 | ||||
| chr10:99784473-99784873 | Rare:158; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:99785176-99785351 | Rare:38 | ||||
| chr10:99785877-99786035 | Rare:29 | ||||
| chr10:99906581-99906715 | Common:2; Rare:23 | ||||
| chr10:99927039-99927209 | Common:2; Rare:29 | ||||
| chr10:99930859-99931126 | Common:3; Rare:55 | ||||
| chr10:99931200-99931710 | Common:2; Rare:93 | ||||
| chr10:99966352-99966604 | Common:1; Rare:39 | ||||
| chr10:100006431-100006813 | Common:4; Rare:54 | ||||
| chr10:100022295-100022695 | Common:4; Rare:112 | ||||
| chr10:100043280-100043640 | Common:3; Rare:59 | ||||
| chr10:100044465-100044865 | Common:6; Rare:78 | ||||
| chr10:100045707-100046001 | Common:1; Rare:43 | ||||
| chr10:100338417-100339490 | Common:11; Rare:256 |