| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61792573-61792942 | Common:5; Rare:97 | ||||
| chr11:61917356-61917652 | Common:2; Rare:100 | ||||
| chr11:61950237-61950386 | Common:1; Rare:29; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:61954850-61955195 | Common:7; Rare:81; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:61967116-61967300 | Common:1; Rare:50 | ||||
| chr11:61967311-61967800 | Common:3; Rare:185; Clinvar:4 | ||||
| chr11:62545559-62546013 | Common:1; Rare:101 | ||||
| chr11:62546658-62546939 | Common:1; Rare:84 | ||||
| chr11:62591494-62591804 | Rare:101 | ||||
| chr11:62601634-62601706 | Rare:18 | ||||
| chr11:62611595-62611902 | Rare:71 | ||||
| chr11:62612453-62612997 | Common:6; Rare:157; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:62646589-62646665 | Rare:41 | ||||
| chr11:62665122-62665452 | Common:6; Rare:154 | ||||
| chr11:62678883-62679113 | Rare:77 |