| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:132065858-132066022 | Common:2; Rare:34 | ||||
| chr10:132408458-132408622 | Rare:41 | ||||
| chr10:132464083-132464295 | Rare:38 | ||||
| chr10:132748708-132748798 | Common:1; Rare:14 | ||||
| chr10:132748880-132748993 | Common:1; Rare:26 | ||||
| chr10:133364668-133364818 | Common:1; Rare:33 | ||||
| chr10:133366063-133366305 | Common:2; Rare:70 | ||||
| chr10:133368921-133369123 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr11:311138-311307 | Rare:13 | ||||
| chr11:319572-319803 | Common:1; Rare:70 | ||||
| chr11:319948-320122 | Common:1; Rare:56 | ||||
| chr11:495003-495152 | Common:3; Rare:67 | ||||
| chr11:758852-759057 | Common:1; Rare:63; Clinvar:2 | ||||
| chr11:1225160-1225371 | Rare:38 | ||||
| chr11:1231176-1231436 | Common:1; Rare:69; Clinvar (benign):1 |