| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:19240206-19240606 | Common:2; Rare:64 | ||||
| chr11:19240818-19241325 | Rare:690 | ||||
| chr11:19241562-19241962 | Common:4; Rare:394 | ||||
| chr11:19712580-19713007 | Common:10; Rare:528 | ||||
| chr11:20363506-20363906 | Common:21; Rare:253 | ||||
| chr11:20364030-20364244 | Common:26; Rare:220 | ||||
| chr11:20364332-20364752 | Common:1; Rare:181 | ||||
| chr11:20387319-20387786 | Common:45; Rare:680 | ||||
| chr11:20387940-20388340 | Common:2; Rare:158 | ||||
| chr11:22192803-22193203 | Rare:151 | ||||
| chr11:22624805-22625205 | Common:4; Rare:145; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr11:22625122-22625234 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):5 | ||||
| chr11:22625410-22625700 | Common:5; Rare:486; Clinvar:36; Clinvar (benign):16; Clinvar (pathogenic):10 | ||||
| chr11:22625681-22626081 | Common:19; Rare:553; Clinvar:21; Clinvar (benign):9; Clinvar (pathogenic):7 | ||||
| chr11:22755413-22755813 | Common:1; Rare:88 |