| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:85647914-85648051 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:86244971-86245268 | Common:1; Rare:131 | ||||
| chr11:86955391-86955645 | Common:1; Rare:75 | ||||
| chr11:88337632-88337888 | Common:4; Rare:123; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:90223015-90223136 | Common:1; Rare:46 | ||||
| chr11:93741388-93741702 | Common:7; Rare:128 | ||||
| chr11:93784167-93784374 | Common:3; Rare:67 | ||||
| chr11:94493780-94494010 | Common:4; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973524-94973719 | Rare:61 | ||||
| chr11:95789484-95789595 | Common:1; Rare:57 | ||||
| chr11:95790359-95790674 | Common:3; Rare:118 | ||||
| chr11:95923780-95924164 | Common:2; Rare:159; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389857-96390043 | Common:1; Rare:75 | ||||
| chr11:102347111-102347317 | Common:2; Rare:69 | ||||
| chr11:102452623-102452943 | Common:2; Rare:100 |