| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66480239-66480446 | Common:1; Rare:55 | ||||
| chr11:66616403-66616630 | Common:1; Rare:58 | ||||
| chr11:66638393-66638725 | Common:3; Rare:146 | ||||
| chr11:66677845-66678092 | Rare:88 | ||||
| chr11:67401760-67402075 | Common:3; Rare:115 | ||||
| chr11:67443458-67443598 | Common:1; Rare:51 | ||||
| chr11:67469234-67469444 | Common:1; Rare:59 | ||||
| chr11:68030381-68030733 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68903778-68903931 | Common:4; Rare:73; Clinvar (benign):6 | ||||
| chr11:69640875-69641204 | Rare:71 | ||||
| chr11:69675338-69675478 | Rare:36 | ||||
| chr11:70398465-70398611 | Common:1; Rare:52 | ||||
| chr11:71448321-71448703 | Common:4; Rare:102; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928889-71929058 | Common:1; Rare:58 | ||||
| chr11:72080471-72080784 | Common:1; Rare:69; Clinvar:5 |