| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57741243-57741590 | Common:1; Rare:133 | ||||
| chr11:58578190-58578522 | Common:4; Rare:110 | ||||
| chr11:59142749-59142916 | Common:1; Rare:32 | ||||
| chr11:59668986-59669310 | Rare:113 | ||||
| chr11:59810729-59810869 | Common:3; Rare:41 | ||||
| chr11:60906522-60906673 | Rare:38 | ||||
| chr11:60914057-60914198 | Common:1; Rare:40 | ||||
| chr11:60924366-60924543 | Common:2; Rare:55 | ||||
| chr11:61333034-61333250 | Rare:71 | ||||
| chr11:61362258-61362410 | Common:1; Rare:44; Clinvar:7 | ||||
| chr11:61392527-61392649 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429920-61430149 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:61792569-61792962 | Common:5; Rare:108 | ||||
| chr11:61967313-61967553 | Rare:88; Clinvar:1 | ||||
| chr11:61967597-61967753 | Common:1; Rare:62; Clinvar:3 |