| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73909096-73909288 | Common:1; Rare:37 | ||||
| chr10:73910547-73910630 | Rare:20 | ||||
| chr10:73910983-73911157 | Rare:52 | ||||
| chr10:73997695-73998249 | Common:2; Rare:148; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:73998448-73998716 | Common:1; Rare:53 | ||||
| chr10:74150305-74150402 | Rare:18 | ||||
| chr10:74150540-74150847 | Common:3; Rare:75 | ||||
| chr10:74150996-74151323 | Common:1; Rare:90 | ||||
| chr10:74151402-74151537 | Common:1; Rare:30 | ||||
| chr10:74151673-74151759 | Rare:19 | ||||
| chr10:74176376-74176665 | Common:1; Rare:74; Clinvar:1 | ||||
| chr10:74176681-74177079 | Common:1; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:74825264-74825608 | Rare:87 | ||||
| chr10:74825820-74825931 | Rare:28 | ||||
| chr10:74826072-74826464 | Common:2; Rare:96 |