| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:83285874-83286120 | Common:3; Rare:112 | ||||
| chr11:85628399-85628620 | Common:3; Rare:66 | ||||
| chr11:85647908-85648081 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:86244939-86245244 | Common:1; Rare:125 | ||||
| chr11:86800360-86800648 | Common:1; Rare:107 | ||||
| chr11:86955369-86955634 | Common:1; Rare:80 | ||||
| chr11:88337687-88337892 | Common:4; Rare:97; Clinvar:4; Clinvar (benign):3 | ||||
| chr11:90223015-90223127 | Common:1; Rare:42 | ||||
| chr11:93741321-93741702 | Common:8; Rare:149 | ||||
| chr11:93784191-93784347 | Common:3; Rare:53 | ||||
| chr11:94493780-94494038 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973517-94973747 | Rare:72 | ||||
| chr11:95789555-95790014 | Common:4; Rare:187 | ||||
| chr11:95790347-95790707 | Common:3; Rare:142 | ||||
| chr11:96342704-96342947 | Rare:40 |