| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100373316-100373712 | Common:3; Rare:83 | ||||
| chr10:100373916-100374182 | Rare:44 | ||||
| chr10:100382956-100383079 | Rare:23 | ||||
| chr10:100523589-100523777 | Rare:34 | ||||
| chr10:101221687-101221810 | Rare:27 | ||||
| chr10:101781492-101781785 | Rare:61 | ||||
| chr10:101795602-101795634 | Rare:5 | ||||
| chr10:101796923-101797023 | Rare:18 | ||||
| chr10:101810630-101810658 | Rare:2 | ||||
| chr10:101857132-101857391 | Rare:44 | ||||
| chr10:102067634-102067865 | Common:1; Rare:91; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:102108840-102109153 | Rare:92 | ||||
| chr10:102113778-102113841 | Common:1; Rare:12 | ||||
| chr10:102286218-102286408 | Rare:32 | ||||
| chr10:102376372-102376630 | Common:1; Rare:67 |