| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67508060-67508502 | Common:1; Rare:99 | ||||
| chr11:67583557-67583844 | Common:2; Rare:81 | ||||
| chr11:67611919-67612155 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr11:68030380-68030744 | Common:3; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039064 | Rare:44; Clinvar:1 | ||||
| chr11:68043613-68043827 | Common:1; Rare:72; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:68271895-68272171 | Common:2; Rare:118 | ||||
| chr11:68460201-68460516 | Common:3; Rare:107 | ||||
| chr11:68460560-68460816 | Common:3; Rare:87 | ||||
| chr11:68903734-68903955 | Common:5; Rare:97; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:69640884-69641338 | Common:1; Rare:106 | ||||
| chr11:69643773-69643873 | Rare:35 | ||||
| chr11:69675291-69675534 | Common:1; Rare:67 | ||||
| chr11:70398253-70398608 | Common:4; Rare:124 | ||||
| chr11:70662292-70662425 | Common:1; Rare:43 |