| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73781988-73782112 | Common:1; Rare:45 | ||||
| chr10:73785249-73785654 | Common:5; Rare:129 | ||||
| chr10:73874479-73874718 | Rare:56 | ||||
| chr10:73997773-73998300 | Common:2; Rare:138; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:73998329-73998374 | Rare:9; Clinvar:2 | ||||
| chr10:74083139-74083453 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:74150761-74151275 | Common:3; Rare:126 | ||||
| chr10:74176492-74176563 | Rare:11 | ||||
| chr10:74176573-74176855 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:74825267-74825610 | Rare:87 | ||||
| chr10:74826106-74826415 | Common:2; Rare:77 | ||||
| chr10:74826462-74826611 | Rare:33; Clinvar (benign):2 | ||||
| chr10:75099440-75099597 | Common:2; Rare:45 | ||||
| chr10:75111536-75111729 | Rare:61 | ||||
| chr10:75210460-75211030 | Common:2; Rare:193 |