| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20387402-20387765 | Common:8; Rare:117 | ||||
| chr11:22625813-22626002 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27363071-27363381 | Rare:141 | ||||
| chr11:27506756-27506859 | Common:1; Rare:44 | ||||
| chr11:28108115-28108414 | Common:1; Rare:90 | ||||
| chr11:30322928-30323164 | Common:2; Rare:69 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509566-31509790 | Common:1; Rare:69 | ||||
| chr11:33161449-33161678 | Common:6; Rare:63 | ||||
| chr11:33257157-33257366 | Common:2; Rare:75 | ||||
| chr11:33736391-33736605 | Common:2; Rare:66 | ||||
| chr11:34052125-34052517 | Common:4; Rare:175 | ||||
| chr11:34105532-34105638 | Common:1; Rare:30 | ||||
| chr11:34916287-34916669 | Common:10; Rare:156; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139207 | Common:1; Rare:57 |