| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94493775-94494053 | Common:5; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94768058-94768429 | Common:2; Rare:97 | ||||
| chr11:94973519-94973707 | Rare:64 | ||||
| chr11:95789484-95789653 | Common:1; Rare:90 | ||||
| chr11:95789766-95789950 | Common:2; Rare:67 | ||||
| chr11:95790329-95790591 | Common:1; Rare:103 | ||||
| chr11:96389857-96390033 | Common:1; Rare:66 | ||||
| chr11:102347137-102347269 | Common:1; Rare:41 | ||||
| chr11:102452619-102452900 | Common:1; Rare:89 | ||||
| chr11:103092017-103092269 | Common:1; Rare:79 | ||||
| chr11:103109297-103109570 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:104164308-104164511 | Common:3; Rare:51 | ||||
| chr11:106077334-106077730 | Common:2; Rare:124 | ||||
| chr11:107457763-107457932 | Common:1; Rare:56 | ||||
| chr11:107591029-107591290 | Common:2; Rare:89 |