| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:78139581-78139809 | Common:3; Rare:91; Clinvar:2 | ||||
| chr11:78188592-78188944 | Common:3; Rare:110 | ||||
| chr11:78574779-78574966 | Common:2; Rare:70; Clinvar (benign):1 | ||||
| chr11:83071791-83072111 | Common:4; Rare:91 | ||||
| chr11:83193629-83193800 | Common:1; Rare:80 | ||||
| chr11:83285915-83286128 | Common:3; Rare:101 | ||||
| chr11:83286331-83286542 | Rare:59 | ||||
| chr11:85628339-85628620 | Common:6; Rare:88 | ||||
| chr11:85647914-85648031 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:86069856-86069982 | Common:1; Rare:23 | ||||
| chr11:86244971-86245256 | Common:1; Rare:122 | ||||
| chr11:86302079-86302341 | Common:3; Rare:51 | ||||
| chr11:87037765-87038040 | Common:3; Rare:131 | ||||
| chr11:88175436-88175592 | Common:1; Rare:63 | ||||
| chr11:88337661-88337888 | Common:4; Rare:109; Clinvar:6; Clinvar (benign):3 |