| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:5288094-5288348 | Common:1; Rare:45 | ||||
| chr11:9758172-9758359 | Rare:52 | ||||
| chr11:14583472-14583641 | Rare:24 | ||||
| chr11:14644910-14644950 | Rare:16 | ||||
| chr11:14644964-14645014 | Rare:23 | ||||
| chr11:16381199-16381484 | Common:1; Rare:56 | ||||
| chr11:16604273-16604440 | Rare:36 | ||||
| chr11:18310817-18311041 | Rare:80; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:20035724-20036008 | Common:1; Rare:76 | ||||
| chr11:22624648-22625015 | Common:2; Rare:111; Clinvar:7; Clinvar (benign):6 | ||||
| chr11:27545223-27545272 | Rare:6 | ||||
| chr11:33881875-33882111 | Common:4; Rare:49 | ||||
| chr11:35360075-35360304 | Rare:38 | ||||
| chr11:46720710-46720836 | Rare:20 | ||||
| chr11:46744526-46744866 | Rare:65 |