| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67443776-67443837 | Rare:12 | ||||
| chr11:67469201-67469340 | Common:2; Rare:49 | ||||
| chr11:67482906-67483207 | Rare:72; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr11:67507782-67508454 | Common:1; Rare:172 | ||||
| chr11:67508591-67508779 | Common:3; Rare:60 | ||||
| chr11:68030381-68030751 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038733-68039117 | Rare:102; Clinvar:1 | ||||
| chr11:68213528-68213944 | Common:1; Rare:237 | ||||
| chr11:68271871-68272134 | Common:2; Rare:108 | ||||
| chr11:68460223-68460492 | Common:3; Rare:91 | ||||
| chr11:68460534-68460822 | Common:3; Rare:102 | ||||
| chr11:68903774-68903943 | Common:4; Rare:80; Clinvar (benign):6 | ||||
| chr11:69640983-69641294 | Common:1; Rare:73 | ||||
| chr11:69675289-69675503 | Rare:61 | ||||
| chr11:70326416-70326741 | Common:1; Rare:80 |