| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66616422-66616676 | Common:2; Rare:77 | ||||
| chr11:66677773-66677926 | Common:1; Rare:63 | ||||
| chr11:66688725-66688985 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:66744502-66744631 | Common:1; Rare:34 | ||||
| chr11:66744680-66744892 | Common:2; Rare:83 | ||||
| chr11:67056762-67056923 | Common:1; Rare:48 | ||||
| chr11:67317767-67317877 | Rare:19 | ||||
| chr11:67353483-67353752 | Common:2; Rare:69 | ||||
| chr11:67443445-67443559 | Common:1; Rare:35 | ||||
| chr11:67482936-67483154 | Rare:50; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68030393-68030744 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68271900-68272105 | Common:2; Rare:87 | ||||
| chr11:68903800-68903943 | Common:4; Rare:63; Clinvar (benign):6 | ||||
| chr11:69675309-69675488 | Rare:50 | ||||
| chr11:70398427-70398611 | Common:2; Rare:71 |