| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20363682-20363735 | Rare:13 | ||||
| chr11:22625518-22625609 | Rare:46; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626005 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26993775-26993995 | Common:2; Rare:31 | ||||
| chr11:26994026-26994544 | Common:2; Rare:119 | ||||
| chr11:26994588-26995024 | Common:1; Rare:149 | ||||
| chr11:27506721-27506868 | Common:1; Rare:69 | ||||
| chr11:28108134-28108416 | Common:1; Rare:83 | ||||
| chr11:30016972-30017082 | Rare:32 | ||||
| chr11:30322983-30323156 | Common:1; Rare:50 | ||||
| chr11:31369728-31369882 | Rare:47 | ||||
| chr11:31509575-31509812 | Common:1; Rare:78 | ||||
| chr11:32583677-32583929 | Rare:92 | ||||
| chr11:32829647-32829975 | Common:4; Rare:66 | ||||
| chr11:33039975-33040051 | Rare:24 |