| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61362232-61362404 | Common:2; Rare:50; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392527-61392652 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:61429912-61430144 | Common:1; Rare:103; Clinvar (benign):2 | ||||
| chr11:61792564-61792955 | Common:5; Rare:108 | ||||
| chr11:61816765-61817039 | Rare:74 | ||||
| chr11:61840440-61840696 | Common:1; Rare:53 | ||||
| chr11:61967311-61967552 | Rare:89; Clinvar:1 | ||||
| chr11:62123759-62124073 | Common:7; Rare:82 | ||||
| chr11:62545614-62545987 | Common:1; Rare:81 | ||||
| chr11:62591500-62591835 | Rare:110 | ||||
| chr11:62601615-62601657 | Rare:11 | ||||
| chr11:62653268-62653447 | Common:1; Rare:57 | ||||
| chr11:62665133-62665418 | Common:5; Rare:137 | ||||
| chr11:62678999-62679209 | Rare:68 | ||||
| chr11:62706231-62706418 | Common:2; Rare:83; Clinvar (benign):4 |