| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102461047-102461442 | Common:1; Rare:96 | ||||
| chr10:102502607-102502965 | Common:1; Rare:103 | ||||
| chr10:102503766-102503999 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:102714171-102714505 | Common:2; Rare:116 | ||||
| chr10:102743635-102744078 | Common:4; Rare:119 | ||||
| chr10:102854184-102854299 | Common:1; Rare:44 | ||||
| chr10:102869353-102869560 | Common:5; Rare:52 | ||||
| chr10:102918469-102918558 | Rare:28 | ||||
| chr10:103193240-103193393 | Common:5; Rare:48; Clinvar (benign):1 | ||||
| chr10:103276682-103276723 | Rare:5 | ||||
| chr10:103276939-103277168 | Common:1; Rare:60 | ||||
| chr10:103277480-103278024 | Common:1; Rare:143; Clinvar (pathogenic):1 | ||||
| chr10:103350902-103351223 | Common:2; Rare:126 | ||||
| chr10:103367868-103367985 | Common:2; Rare:18 | ||||
| chr10:103396397-103396715 | Rare:112 |