| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20363657-20363856 | Common:3; Rare:42 | ||||
| chr11:20364083-20364211 | Common:1; Rare:31 | ||||
| chr11:20387417-20387794 | Common:7; Rare:125 | ||||
| chr11:22625518-22625614 | Rare:51; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625801-22626016 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22829350-22829422 | Common:1; Rare:20 | ||||
| chr11:22829738-22830082 | Common:4; Rare:120 | ||||
| chr11:27506714-27506879 | Common:1; Rare:76 | ||||
| chr11:28108072-28108463 | Common:3; Rare:112 | ||||
| chr11:30322937-30323164 | Common:2; Rare:64 | ||||
| chr11:31369737-31369905 | Rare:52 | ||||
| chr11:31509535-31509940 | Common:2; Rare:150 | ||||
| chr11:31811073-31811491 | Rare:71; Clinvar:3 | ||||
| chr11:32091007-32091238 | Common:2; Rare:68 | ||||
| chr11:32091386-32091449 | Rare:13 |