| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:78079604-78079759 | Common:2; Rare:51 | ||||
| chr11:78079761-78079942 | Common:2; Rare:56 | ||||
| chr11:78139584-78139805 | Common:3; Rare:88; Clinvar:2 | ||||
| chr11:78188597-78188941 | Common:2; Rare:107 | ||||
| chr11:78574761-78574970 | Common:2; Rare:85; Clinvar (benign):1 | ||||
| chr11:83071721-83072111 | Common:4; Rare:107 | ||||
| chr11:83157644-83157729 | Rare:34 | ||||
| chr11:83193619-83193811 | Common:1; Rare:90 | ||||
| chr11:83285931-83286127 | Common:3; Rare:90 | ||||
| chr11:85628324-85628632 | Common:7; Rare:105 | ||||
| chr11:86671874-86672242 | Common:2; Rare:85 | ||||
| chr11:86954909-86955105 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:86955386-86955634 | Common:1; Rare:73 | ||||
| chr11:87037793-87038080 | Common:2; Rare:130 | ||||
| chr11:88337661-88337888 | Common:4; Rare:109; Clinvar:6; Clinvar (benign):3 |