| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:776705-776737 | Rare:4 | ||||
| chr11:776813-777138 | Common:4; Rare:86 | ||||
| chr11:777382-777812 | Common:3; Rare:158 | ||||
| chr11:796175-796383 | Rare:58; Clinvar:1 | ||||
| chr11:797334-797687 | Common:1; Rare:101 | ||||
| chr11:797827-798109 | Common:3; Rare:85 | ||||
| chr11:798147-798332 | Common:2; Rare:77 | ||||
| chr11:805170-805455 | Common:8; Rare:101 | ||||
| chr11:809161-809667 | Common:7; Rare:128 | ||||
| chr11:809703-810058 | Common:2; Rare:143 | ||||
| chr11:818647-818987 | Common:1; Rare:74; Clinvar:1 | ||||
| chr11:819280-819877 | Common:3; Rare:201; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:827263-827325 | Common:2; Rare:13 | ||||
| chr11:832808-833070 | Common:7; Rare:80 | ||||
| chr11:833135-833263 | Common:5; Rare:26 |