| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66616396-66616646 | Common:1; Rare:68 | ||||
| chr11:66638371-66638752 | Common:4; Rare:170 | ||||
| chr11:66677539-66677671 | Rare:35 | ||||
| chr11:66677765-66678071 | Common:1; Rare:112 | ||||
| chr11:66744627-66744887 | Common:3; Rare:106 | ||||
| chr11:67317734-67317881 | Rare:28 | ||||
| chr11:67353493-67353593 | Rare:31 | ||||
| chr11:67401789-67402055 | Common:2; Rare:95 | ||||
| chr11:67428347-67428531 | Rare:65 | ||||
| chr11:67443458-67443692 | Common:2; Rare:80 | ||||
| chr11:67482947-67483154 | Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68030381-68030743 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68213548-68213998 | Common:1; Rare:265 | ||||
| chr11:68271928-68272171 | Common:2; Rare:108 | ||||
| chr11:68903800-68903943 | Common:4; Rare:63; Clinvar (benign):6 |