| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18634325-18634590 | Common:2; Rare:85 | ||||
| chr11:18698547-18698772 | Common:4; Rare:61 | ||||
| chr11:19116934-19117261 | Common:3; Rare:90 | ||||
| chr11:20363683-20363783 | Common:2; Rare:24 | ||||
| chr11:20387450-20387771 | Common:7; Rare:105 | ||||
| chr11:22625518-22625622 | Rare:56; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626004 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26994001-26994188 | Common:1; Rare:32 | ||||
| chr11:27363128-27363390 | Rare:112 | ||||
| chr11:27506714-27506863 | Common:1; Rare:69 | ||||
| chr11:28108106-28108414 | Common:1; Rare:92 | ||||
| chr11:30322930-30323195 | Common:3; Rare:77 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509567-31509814 | Common:1; Rare:81 | ||||
| chr11:32829653-32830004 | Common:5; Rare:67 |