| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61429915-61430169 | Common:1; Rare:115; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:61792573-61792947 | Common:5; Rare:99 | ||||
| chr11:61967116-61967807 | Common:4; Rare:237; Clinvar:4 | ||||
| chr11:62545614-62546013 | Common:1; Rare:86 | ||||
| chr11:62577249-62577429 | Common:1; Rare:39 | ||||
| chr11:62591494-62591837 | Rare:114 | ||||
| chr11:62601640-62601973 | Common:1; Rare:105 | ||||
| chr11:62611483-62611841 | Rare:94 | ||||
| chr11:62653273-62653436 | Common:1; Rare:51 | ||||
| chr11:62665129-62665418 | Common:5; Rare:139 | ||||
| chr11:62671752-62671985 | Common:1; Rare:85; Clinvar (benign):1 | ||||
| chr11:62678864-62679174 | Rare:104 | ||||
| chr11:62679222-62679298 | Rare:18 | ||||
| chr11:62706242-62706396 | Common:2; Rare:64; Clinvar (benign):4 | ||||
| chr11:62709501-62709830 | Common:1; Rare:113 |