| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17200096-17200496 | Common:3; Rare:64 | ||||
| chr10:17201048-17201660 | Common:38; Rare:552 | ||||
| chr10:17201606-17201910 | Common:11; Rare:304 | ||||
| chr10:17228030-17228456 | Common:10; Rare:265 | ||||
| chr10:17228370-17228901 | Common:8; Rare:457 | ||||
| chr10:17228916-17229428 | Common:16; Rare:389 | ||||
| chr10:17229405-17229898 | Rare:223; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr10:17229863-17230740 | Common:17; Rare:1037; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr10:17453820-17455292 | Common:39; Rare:1188 | ||||
| chr10:17617173-17617851 | Common:19; Rare:501; Clinvar:1 | ||||
| chr10:17643810-17644304 | Common:14; Rare:891 | ||||
| chr10:17644517-17644917 | Rare:78 | ||||
| chr10:18651342-18651943 | Common:8; Rare:734 | ||||
| chr10:18658417-18658817 | Common:3; Rare:83 | ||||
| chr10:18658970-18659580 | Common:20; Rare:742 |