| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66744656-66744832 | Common:1; Rare:70 | ||||
| chr11:67056792-67056908 | Rare:36 | ||||
| chr11:67353294-67353416 | Rare:33 | ||||
| chr11:67353443-67353863 | Common:2; Rare:101 | ||||
| chr11:67373576-67373838 | Rare:49 | ||||
| chr11:67401735-67402075 | Common:3; Rare:125 | ||||
| chr11:67428340-67428531 | Rare:65 | ||||
| chr11:67443445-67443598 | Common:1; Rare:54 | ||||
| chr11:67482920-67483192 | Rare:61; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67507820-67508113 | Rare:83 | ||||
| chr11:68038924-68039069 | Rare:42; Clinvar:1 | ||||
| chr11:68213548-68213946 | Common:1; Rare:229 | ||||
| chr11:68271881-68272134 | Common:2; Rare:105 | ||||
| chr11:68460223-68460516 | Common:3; Rare:95 | ||||
| chr11:68903734-68903943 | Common:4; Rare:91; Clinvar (benign):6 |