Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58551913-58552173 | Rare:114 | ||||
chr2:12715950-12716075 | Common:2; Rare:21 | ||||
chr2:13006982-13006998 | Common:1; Rare:3 | ||||
chr2:19348006-19348107 | Common:1; Rare:41 | ||||
chr2:20450931-20450975 | Rare:15 | ||||
chr2:23617373-23617683 | Rare:58 | ||||
chr2:23617993-23618236 | Rare:49 | ||||
chr2:26193584-26194052 | Common:2; Rare:125; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr2:27735605-27735825 | Common:1; Rare:49 | ||||
chr2:28391691-28391939 | Common:3; Rare:49 | ||||
chr2:28394655-28394729 | Rare:17 | ||||
chr2:28607283-28607288 | Rare:1 | ||||
chr2:28625365-28625465 | Rare:16 | ||||
chr2:36544223-36544498 | Common:1; Rare:76 | ||||
chr2:36548345-36548584 | Common:1; Rare:77 |