| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:60914105-60914240 | Rare:36 | ||||
| chr11:60951777-60951832 | Common:1; Rare:9 | ||||
| chr11:60952530-60952692 | Rare:25 | ||||
| chr11:61333034-61333258 | Rare:74 | ||||
| chr11:61356746-61356944 | Common:1; Rare:38 | ||||
| chr11:61357235-61357533 | Common:1; Rare:49 | ||||
| chr11:61361743-61361973 | Common:1; Rare:57 | ||||
| chr11:61362069-61362410 | Common:2; Rare:102; Clinvar:9; Clinvar (benign):1 | ||||
| chr11:61429852-61430161 | Common:1; Rare:129; Clinvar:3; Clinvar (benign):4 | ||||
| chr11:61792557-61792961 | Common:6; Rare:116 | ||||
| chr11:61880533-61880642 | Common:1; Rare:21 | ||||
| chr11:61967627-61967820 | Common:3; Rare:73; Clinvar:3 | ||||
| chr11:62591515-62591837 | Rare:102 | ||||
| chr11:62601228-62601298 | Rare:16 | ||||
| chr11:62622096-62622484 | Common:4; Rare:89 |