| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1662102-1662258 | Common:3; Rare:32 | ||||
| chr11:1665449-1665691 | Common:7; Rare:47 | ||||
| chr11:1672745-1672782 | Rare:10 | ||||
| chr11:1683285-1683455 | Common:4; Rare:45 | ||||
| chr11:1685517-1685916 | Common:12; Rare:68 | ||||
| chr11:1689880-1690165 | Common:3; Rare:68 | ||||
| chr11:1691176-1691399 | Rare:35 | ||||
| chr11:1995874-1996025 | Common:1; Rare:33 | ||||
| chr11:1996048-1996220 | Common:2; Rare:53 | ||||
| chr11:1996285-1996448 | Rare:55 | ||||
| chr11:2303607-2304003 | Common:5; Rare:75 | ||||
| chr11:3511483-3511697 | Common:4; Rare:50 | ||||
| chr11:5225348-5225596 | Common:2; Rare:68; Clinvar:12; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr11:5280686-5280874 | Common:3; Rare:30 | ||||
| chr11:5284759-5284943 | Common:1; Rare:33 |