| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47426365-47426660 | Common:3; Rare:219 | ||||
| chr11:47553006-47553387 | Common:5; Rare:192 | ||||
| chr11:47565149-47565741 | Common:11; Rare:235 | ||||
| chr11:47566099-47566460 | Common:1; Rare:87 | ||||
| chr11:47578902-47579155 | Rare:315; Clinvar:6; Clinvar (pathogenic):3 | ||||
| chr11:47642374-47642869 | Rare:411 | ||||
| chr11:47715209-47715490 | Common:2; Rare:101 | ||||
| chr11:47767092-47767756 | Common:12; Rare:572 | ||||
| chr11:47847640-47848150 | Common:5; Rare:187 | ||||
| chr11:47848251-47848703 | Common:5; Rare:300 | ||||
| chr11:47980268-47980748 | Common:6; Rare:451 | ||||
| chr11:47980824-47980963 | Rare:41 | ||||
| chr11:47980889-47980990 | Rare:28 | ||||
| chr11:49208436-49208636 | Common:1; Rare:45 | ||||
| chr11:57311366-57311951 | Common:6; Rare:255 |