| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:12066303-12066479 | Common:3; Rare:33 | ||||
| chr11:12075999-12076217 | Rare:31 | ||||
| chr11:16603980-16604112 | Rare:20 | ||||
| chr11:16604280-16604443 | Rare:33 | ||||
| chr11:20049346-20049537 | Rare:25 | ||||
| chr11:43943335-43943428 | Common:2; Rare:33 | ||||
| chr11:45734487-45734547 | Rare:5 | ||||
| chr11:45736633-45736947 | Common:3; Rare:46 | ||||
| chr11:45737268-45737434 | Common:1; Rare:29 | ||||
| chr11:62543300-62543441 | Common:1; Rare:25 | ||||
| chr11:62560082-62560450 | Rare:84 | ||||
| chr11:63997191-63997411 | Common:1; Rare:54 | ||||
| chr11:64746919-64747359 | Common:2; Rare:125; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr11:64755271-64755562 | Common:1; Rare:97; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:64758435-64758703 | Rare:98; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):5 |