| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:560710-560978 | Common:5; Rare:123 | ||||
| chr11:615946-615978 | Rare:7 | ||||
| chr11:695731-695825 | Rare:32 | ||||
| chr11:747312-747583 | Rare:115; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:764130-764418 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:777460-777619 | Common:1; Rare:70 | ||||
| chr11:809503-809595 | Rare:28 | ||||
| chr11:809788-810037 | Common:2; Rare:113 | ||||
| chr11:818727-818976 | Rare:51; Clinvar:1 | ||||
| chr11:819357-819649 | Common:2; Rare:112; Clinvar:3 | ||||
| chr11:842456-842984 | Common:8; Rare:217 | ||||
| chr11:843954-844159 | Common:1; Rare:51 | ||||
| chr11:844178-844442 | Common:3; Rare:80 | ||||
| chr11:1309588-1309778 | Common:1; Rare:88 | ||||
| chr11:2138311-2138572 | Common:2; Rare:64 |