| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65662895-65663008 | Common:1; Rare:31 | ||||
| chr11:65860356-65860554 | Common:3; Rare:62 | ||||
| chr11:65888432-65888643 | Common:1; Rare:75 | ||||
| chr11:65919060-65919504 | Rare:163 | ||||
| chr11:66002105-66002567 | Common:3; Rare:132; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:66347590-66347800 | Common:3; Rare:51 | ||||
| chr11:66480244-66480440 | Common:1; Rare:51 | ||||
| chr11:66744658-66744880 | Common:3; Rare:89 | ||||
| chr11:67482910-67483164 | Rare:56; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:68271934-68272108 | Common:2; Rare:78 | ||||
| chr11:68460563-68460776 | Common:3; Rare:77 | ||||
| chr11:68903774-68903910 | Common:3; Rare:65; Clinvar (benign):2 | ||||
| chr11:69675300-69675519 | Rare:60 | ||||
| chr11:70398125-70398408 | Common:3; Rare:78 | ||||
| chr11:70398452-70398611 | Common:1; Rare:58 |