| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6419360-6419930 | Common:7; Rare:143 | ||||
| chr11:6437465-6437865 | Common:2; Rare:250 | ||||
| chr11:6473811-6474211 | Common:3; Rare:459 | ||||
| chr11:6474230-6474630 | Common:2; Rare:98 | ||||
| chr11:6481155-6481631 | Common:34; Rare:939 | ||||
| chr11:6563280-6563743 | Common:8; Rare:255 | ||||
| chr11:6568008-6568974 | Common:2; Rare:387 | ||||
| chr11:6603481-6603914 | Common:27; Rare:631; Clinvar (benign):15 | ||||
| chr11:6604340-6604600 | Rare:129; Clinvar (benign):2 | ||||
| chr11:6606958-6607358 | Common:1; Rare:177 | ||||
| chr11:6611295-6612249 | Common:1; Rare:619 | ||||
| chr11:6612154-6612545 | Common:15; Rare:338 | ||||
| chr11:6612519-6612919 | Common:7; Rare:146; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:6619294-6619694 | Common:18; Rare:414; Clinvar:9; Clinvar (benign):38; Clinvar (pathogenic):4 | ||||
| chr11:6681904-6682304 | Common:6; Rare:128 |