| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322447-18322624 | Common:2; Rare:69 | ||||
| chr11:18394439-18394619 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr11:18526866-18526977 | Rare:51 | ||||
| chr11:18588667-18588815 | Rare:53 | ||||
| chr11:18634317-18634588 | Common:2; Rare:88 | ||||
| chr11:20363650-20363770 | Common:2; Rare:24 | ||||
| chr11:20387410-20387774 | Common:8; Rare:117 | ||||
| chr11:22625813-22626004 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27363064-27363359 | Rare:129 | ||||
| chr11:27506754-27506864 | Common:1; Rare:45 | ||||
| chr11:28108110-28108410 | Common:1; Rare:91 | ||||
| chr11:30322971-30323173 | Common:1; Rare:60 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509544-31509790 | Common:2; Rare:76 | ||||
| chr11:32583663-32583921 | Rare:93 |