| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14644922-14644986 | Rare:22 | ||||
| chr11:14852693-14852760 | Rare:7 | ||||
| chr11:15481986-15482269 | Rare:53 | ||||
| chr11:18232393-18232804 | Common:2; Rare:101 | ||||
| chr11:19976553-19976763 | Common:1; Rare:39 | ||||
| chr11:19981346-19981612 | Common:2; Rare:48 | ||||
| chr11:20002893-20003027 | Rare:20 | ||||
| chr11:20034680-20034774 | Common:2; Rare:19 | ||||
| chr11:20035721-20036017 | Common:1; Rare:80 | ||||
| chr11:35663315-35663601 | Rare:108; Clinvar (pathogenic):1 | ||||
| chr11:46720281-46720552 | Common:1; Rare:57 | ||||
| chr11:46720680-46720840 | Common:1; Rare:25 | ||||
| chr11:46726494-46726829 | Common:1; Rare:113; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr11:57327743-57328076 | Rare:79 | ||||
| chr11:57332457-57332689 | Rare:55 |