| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100535858-100535952 | Common:6; Rare:50 | ||||
| chr10:100912726-100913031 | Common:1; Rare:96 | ||||
| chr10:100987229-100987584 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100996990-100997095 | Rare:31 | ||||
| chr10:101031102-101031259 | Common:1; Rare:36 | ||||
| chr10:101588195-101588339 | Rare:56 | ||||
| chr10:101818342-101818552 | Rare:68 | ||||
| chr10:102056109-102056326 | Common:1; Rare:53 | ||||
| chr10:102114958-102115128 | Common:2; Rare:48 | ||||
| chr10:102714271-102714662 | Common:2; Rare:128 | ||||
| chr10:102776078-102776215 | Common:1; Rare:20 | ||||
| chr10:103193250-103193387 | Common:4; Rare:45 | ||||
| chr10:103396411-103396699 | Rare:103 | ||||
| chr10:104338463-104338539 | Rare:18 | ||||
| chr10:109923425-109923660 | Common:2; Rare:90 |