| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101092999-101093813 | Common:3; Rare:234 | ||||
| chr10:101095416-101095930 | Common:4; Rare:149 | ||||
| chr10:101111150-101111450 | Common:1; Rare:51 | ||||
| chr10:101141290-101141590 | Common:2; Rare:84 | ||||
| chr10:101213630-101214010 | Common:4; Rare:98 | ||||
| chr10:101310583-101311288 | Common:5; Rare:283 | ||||
| chr10:101401945-101402593 | Common:5; Rare:273 | ||||
| chr10:101569729-101570010 | Rare:68 | ||||
| chr10:101693736-101694151 | Common:2; Rare:98 | ||||
| chr10:101694247-101694519 | Rare:109; Clinvar:2 | ||||
| chr10:101830938-101831120 | Common:1; Rare:49 | ||||
| chr10:102065997-102066212 | Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:102119640-102119892 | Common:1; Rare:47 | ||||
| chr10:102133576-102133821 | Common:1; Rare:61 | ||||
| chr10:102133980-102135007 | Common:3; Rare:236 |