| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62621644-62621778 | Rare:34 | ||||
| chr11:62621834-62622421 | Common:4; Rare:179 | ||||
| chr11:62646171-62646348 | Common:3; Rare:50 | ||||
| chr11:62646554-62646823 | Common:1; Rare:109; Clinvar (pathogenic):1 | ||||
| chr11:62653240-62653545 | Common:1; Rare:90 | ||||
| chr11:62653548-62653646 | Rare:15 | ||||
| chr11:62664689-62664931 | Common:2; Rare:64 | ||||
| chr11:62665098-62665515 | Common:6; Rare:194 | ||||
| chr11:62665631-62665639 | Common:1 | ||||
| chr11:62671323-62671439 | Common:2; Rare:32 | ||||
| chr11:62671519-62671747 | Rare:79; Clinvar (benign):1 | ||||
| chr11:62671749-62671906 | Rare:59 | ||||
| chr11:62672219-62672444 | Rare:60 | ||||
| chr11:62678924-62679222 | Rare:99 | ||||
| chr11:62679321-62679368 | Rare:7 |