| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:798262-798508 | Rare:71 | ||||
| chr11:805228-805432 | Common:5; Rare:73 | ||||
| chr11:809486-810038 | Common:5; Rare:206 | ||||
| chr11:821014-821267 | Rare:52 | ||||
| chr11:822219-822596 | Common:2; Rare:110; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:825823-826251 | Rare:95 | ||||
| chr11:827098-827365 | Common:3; Rare:72 | ||||
| chr11:827520-827647 | Common:3; Rare:37 | ||||
| chr11:827849-827960 | Common:2; Rare:28 | ||||
| chr11:829805-830004 | Common:1; Rare:47 | ||||
| chr11:832826-833018 | Common:7; Rare:63 | ||||
| chr11:842458-842984 | Common:8; Rare:216 | ||||
| chr11:844048-844442 | Common:4; Rare:110 | ||||
| chr11:1006338-1006620 | Rare:65 | ||||
| chr11:1020781-1021116 | Common:2; Rare:67 |