| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94129424-94129540 | Common:1; Rare:46 | ||||
| chr11:94493775-94494029 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973502-94973689 | Rare:64 | ||||
| chr11:95067438-95067643 | Common:1; Rare:90 | ||||
| chr11:95089725-95089878 | Common:3; Rare:61 | ||||
| chr11:95778902-95779062 | Rare:42 | ||||
| chr11:95789760-95789981 | Common:3; Rare:81 | ||||
| chr11:95790368-95790722 | Common:3; Rare:134; Clinvar:1 | ||||
| chr11:95923905-95924227 | Common:1; Rare:133; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:96342339-96342748 | Common:2; Rare:69 | ||||
| chr11:96389732-96390085 | Common:2; Rare:133 | ||||
| chr11:96390282-96390519 | Rare:45 | ||||
| chr11:101914869-101915028 | Common:2; Rare:41 | ||||
| chr11:102110288-102110472 | Common:1; Rare:65 | ||||
| chr11:102317206-102317499 | Rare:50 |