Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:48044694-48044793 | Rare:10 | ||||
chr11:57324883-57325169 | Common:1; Rare:95 | ||||
chr11:57335738-57335953 | Common:4; Rare:49 | ||||
chr11:57426896-57426995 | Rare:16 | ||||
chr11:57514858-57514974 | Rare:21 | ||||
chr11:57567597-57567767 | Rare:58 | ||||
chr11:57567857-57568113 | Common:2; Rare:51 | ||||
chr11:57606168-57606545 | Rare:99; Clinvar (benign):1 | ||||
chr11:57657556-57657801 | Common:3; Rare:60 | ||||
chr11:57712184-57712665 | Common:9; Rare:165 | ||||
chr11:57741264-57741598 | Common:1; Rare:124 | ||||
chr11:58577694-58577778 | Rare:14 | ||||
chr11:58578095-58578209 | Rare:30 | ||||
chr11:58578328-58578533 | Common:2; Rare:76 | ||||
chr11:58578650-58578743 | Common:1; Rare:31 |