| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:20091769-20091846 | Not yet | Common:1; Rare:23 | 116 | ||
| chr10:20091870-20092075 | Not yet | Common:1; Rare:39 | 312 | ||
| chr10:24591224-24591457 | Not yet | Common:2; Rare:53 | 317 | ||
| chr10:26735289-26735561 | Not yet | Common:2; Rare:75; Clinvar:2; Clinvar (pathogenic):1 | 340 | ||
| chr10:29473846-29474151 | Not yet | Common:1; Rare:93 | 306 | ||
| chr10:43401116-43401162 | Not yet | Rare:7 | 159 | ||
| chr10:45445394-45445555 | Not yet | Rare:45 | 227 | ||
| chr10:46556076-46556202 | Not yet | Common:4; Rare:4 | 237 | ||
| chr10:46786617-46786785 | Not yet | Rare:24 | 193 | ||
| chr10:46786831-46786899 | Not yet | Rare:3 | 137 | ||
| chr10:47553421-47553540 | Not yet | Rare:4 | 185 | ||
| chr10:47553569-47553776 | Not yet | Rare:30 | 211 | ||
| chr10:50622985-50623165 | Not yet | Common:2; Rare:44 | 181 | ||
| chr10:51698323-51698331 | Not yet | 1 | |||
| chr10:51698405-51698490 | Not yet | Common:1; Rare:27 | 177 |