| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20669447-20669674 | Common:3; Rare:93 | ||||
| chr11:20770564-20770839 | Common:1; Rare:42 | ||||
| chr11:22625817-22626004 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27506731-27506898 | Common:1; Rare:75 | ||||
| chr11:28108096-28108461 | Common:2; Rare:105 | ||||
| chr11:30322930-30323197 | Common:3; Rare:77 | ||||
| chr11:31369737-31369888 | Rare:47 | ||||
| chr11:31509561-31509787 | Common:1; Rare:70 | ||||
| chr11:32583630-32583929 | Rare:105 | ||||
| chr11:33015784-33015942 | Common:1; Rare:60 | ||||
| chr11:33039669-33039770 | Rare:22 | ||||
| chr11:33161426-33161663 | Common:6; Rare:65 | ||||
| chr11:33257122-33257428 | Common:3; Rare:98 | ||||
| chr11:33736400-33736605 | Common:1; Rare:64 | ||||
| chr11:33774501-33774666 | Common:2; Rare:60 |