| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70146602-70146927 | Common:1; Rare:84 | ||||
| chr10:70170459-70170801 | Common:3; Rare:102 | ||||
| chr10:70233356-70233714 | Common:4; Rare:102 | ||||
| chr10:70382544-70382893 | Common:5; Rare:136 | ||||
| chr10:70403942-70404210 | Rare:101 | ||||
| chr10:70478501-70479007 | Rare:160 | ||||
| chr10:70672210-70672537 | Common:3; Rare:80 | ||||
| chr10:70815792-70816038 | Rare:94 | ||||
| chr10:70816295-70816471 | Rare:39 | ||||
| chr10:70887847-70888018 | Common:1; Rare:35 | ||||
| chr10:70888548-70888712 | Common:2; Rare:49; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:71212344-71212681 | Common:2; Rare:97 | ||||
| chr10:71319127-71319317 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:71773518-71773704 | Common:3; Rare:51 | ||||
| chr10:71851233-71851465 | Common:3; Rare:91; Clinvar:3; Clinvar (benign):6 |