| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322467-18322645 | Common:2; Rare:73 | ||||
| chr11:18394478-18394641 | Common:1; Rare:64; Clinvar (benign):1 | ||||
| chr11:18526824-18527018 | Common:1; Rare:94 | ||||
| chr11:18588656-18588827 | Common:1; Rare:64 | ||||
| chr11:18634283-18634590 | Common:3; Rare:107 | ||||
| chr11:18634785-18634874 | Rare:17 | ||||
| chr11:20387417-20387786 | Common:7; Rare:119 | ||||
| chr11:22625522-22625630 | Rare:60; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626004 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22829320-22829388 | Common:1; Rare:14 | ||||
| chr11:27363064-27363316 | Rare:112 | ||||
| chr11:27506729-27506864 | Common:1; Rare:62 | ||||
| chr11:28108080-28108437 | Common:2; Rare:107 | ||||
| chr11:30322966-30323194 | Common:2; Rare:63 | ||||
| chr11:31369737-31369887 | Rare:47 |