| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:70170454-70170676 | Common:3; Rare:75 | ||||
| chr10:70404103-70404182 | Rare:31 | ||||
| chr10:70888530-70888649 | Common:1; Rare:41; Clinvar:5; Clinvar (benign):1 | ||||
| chr10:71773494-71773658 | Common:2; Rare:51 | ||||
| chr10:71819537-71819801 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:71851181-71851452 | Common:5; Rare:117; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:71964168-71964499 | Common:1; Rare:92 | ||||
| chr10:72216227-72216318 | Rare:45 | ||||
| chr10:72273693-72273942 | Rare:66 | ||||
| chr10:72354883-72355023 | Common:2; Rare:69 | ||||
| chr10:72626019-72626354 | Common:2; Rare:83 | ||||
| chr10:73096764-73097028 | Common:3; Rare:81 | ||||
| chr10:73110177-73110534 | Rare:65 | ||||
| chr10:73167951-73168150 | Rare:52 | ||||
| chr10:73252552-73252834 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):2 |