| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57597535-57597714 | Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:57597717-57597995 | Common:1; Rare:55; Clinvar:1 | ||||
| chr11:57598013-57598539 | Common:7; Rare:223; Clinvar (benign):6 | ||||
| chr11:57649824-57650224 | Common:2; Rare:132 | ||||
| chr11:57657482-57657806 | Common:4; Rare:85 | ||||
| chr11:57667222-57667509 | Common:1; Rare:49 | ||||
| chr11:57667692-57668153 | Common:5; Rare:149 | ||||
| chr11:57712338-57712653 | Common:3; Rare:96 | ||||
| chr11:57741237-57741620 | Common:2; Rare:148 | ||||
| chr11:57741644-57741826 | Common:1; Rare:89 | ||||
| chr11:57761601-57761930 | Common:2; Rare:73 | ||||
| chr11:57763774-57763906 | Common:1; Rare:19 | ||||
| chr11:58578188-58578514 | Common:4; Rare:108 | ||||
| chr11:58578734-58579274 | Common:7; Rare:164 | ||||
| chr11:58579602-58579803 | Common:1; Rare:85 |