| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61333773-61333852 | Rare:19 | ||||
| chr11:61334660-61334741 | Rare:21 | ||||
| chr11:61361504-61361667 | Rare:29 | ||||
| chr11:61361776-61362439 | Common:4; Rare:175; Clinvar:11; Clinvar (benign):1 | ||||
| chr11:61362682-61362767 | Rare:14 | ||||
| chr11:61392508-61392542 | Rare:8; Clinvar:1 | ||||
| chr11:61392569-61392685 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:61429093-61429367 | Common:2; Rare:83 | ||||
| chr11:61429465-61429592 | Common:1; Rare:41 | ||||
| chr11:61429843-61430208 | Common:2; Rare:154; Clinvar:3; Clinvar (benign):9 | ||||
| chr11:61430329-61430368 | Rare:5 | ||||
| chr11:61430389-61430411 | Rare:2 | ||||
| chr11:61580426-61580711 | Rare:62 | ||||
| chr11:61580987-61581342 | Common:2; Rare:115 | ||||
| chr11:61581393-61581493 | Rare:17 |