Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:47578967-47579093 | Rare:63; Clinvar:2 | ||||
chr11:57427082-57427219 | Common:1; Rare:39 | ||||
chr11:57514858-57514974 | Rare:21 | ||||
chr11:57712178-57712571 | Common:9; Rare:117 | ||||
chr11:61333026-61333251 | Rare:74 | ||||
chr11:61361833-61361973 | Common:1; Rare:36 | ||||
chr11:61362065-61362407 | Common:2; Rare:101; Clinvar:9; Clinvar (benign):1 | ||||
chr11:61429909-61430152 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):3 | ||||
chr11:61792559-61792951 | Common:6; Rare:111 | ||||
chr11:61816114-61816353 | Rare:66 | ||||
chr11:62646600-62646932 | Common:2; Rare:106 | ||||
chr11:62665147-62665312 | Common:3; Rare:73 | ||||
chr11:62727469-62727715 | Rare:85 | ||||
chr11:62728418-62728538 | Common:1; Rare:70 | ||||
chr11:62832003-62832226 | Rare:86 |