| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:20091769-20091846 | Common:1; Rare:23 | ||||
| chr10:20091870-20092075 | Common:1; Rare:39 | ||||
| chr10:24591224-24591457 | Common:2; Rare:53 | ||||
| chr10:26735289-26735561 | Common:2; Rare:75; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr10:29473846-29474151 | Common:1; Rare:93 | ||||
| chr10:43401116-43401162 | Rare:7 | ||||
| chr10:45445394-45445555 | Rare:45 | ||||
| chr10:46556076-46556202 | Common:4; Rare:4 | ||||
| chr10:46786617-46786785 | Rare:24 | ||||
| chr10:46786831-46786899 | Rare:3 | ||||
| chr10:47553421-47553540 | Rare:4 | ||||
| chr10:47553569-47553776 | Rare:30 | ||||
| chr10:50622985-50623165 | Common:2; Rare:44 | ||||
| chr10:51698323-51698331 | |||||
| chr10:51698405-51698490 | Common:1; Rare:27 |