| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62612361-62612666 | Common:4; Rare:96 | ||||
| chr11:62612733-62612914 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:62621879-62622322 | Common:3; Rare:138 | ||||
| chr11:62646569-62646817 | Common:1; Rare:101; Clinvar (pathogenic):1 | ||||
| chr11:62653241-62653436 | Common:1; Rare:71 | ||||
| chr11:62664951-62665521 | Common:6; Rare:251 | ||||
| chr11:62671515-62671716 | Rare:67; Clinvar (benign):1 | ||||
| chr11:62671778-62671958 | Common:1; Rare:72; Clinvar (benign):1 | ||||
| chr11:62672238-62672490 | Rare:59 | ||||
| chr11:62679038-62679251 | Rare:66 | ||||
| chr11:62706102-62706461 | Common:3; Rare:133; Clinvar (benign):6 | ||||
| chr11:62727072-62727270 | Common:1; Rare:72 | ||||
| chr11:62727413-62727578 | Rare:71 | ||||
| chr11:62727610-62727710 | Rare:30 | ||||
| chr11:62727888-62728249 | Common:7; Rare:101 |