| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67482913-67483154 | Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67508056-67508443 | Common:1; Rare:85 | ||||
| chr11:67508640-67508772 | Common:3; Rare:50 | ||||
| chr11:68010130-68010359 | Common:1; Rare:61 | ||||
| chr11:68030399-68030737 | Common:3; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038921-68039064 | Rare:41; Clinvar:1 | ||||
| chr11:68271871-68272031 | Common:1; Rare:73 | ||||
| chr11:68460223-68460410 | Common:3; Rare:66 | ||||
| chr11:68903770-68903943 | Common:4; Rare:81; Clinvar (benign):6 | ||||
| chr11:69640952-69641199 | Rare:56 | ||||
| chr11:69675290-69675515 | Rare:62 | ||||
| chr11:70398353-70398596 | Common:2; Rare:85 | ||||
| chr11:71448306-71448720 | Common:5; Rare:109; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928907-71929079 | Common:1; Rare:55 | ||||
| chr11:72041056-72041323 | Common:1; Rare:47 |