Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:63712447-63712608 | Rare:24 | ||||
chr10:63866460-63866720 | Common:2; Rare:54 | ||||
chr10:63887293-63887457 | Common:1; Rare:42 | ||||
chr10:63976676-63976776 | Common:3; Rare:14 | ||||
chr10:63977470-63977740 | Rare:61 | ||||
chr10:64468230-64468750 | Common:4; Rare:92 | ||||
chr10:65570352-65570557 | Common:2; Rare:56 | ||||
chr10:65570767-65570984 | Common:2; Rare:42 | ||||
chr10:67606307-67607229 | Common:5; Rare:333; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
chr10:67666445-67666845 | Common:5; Rare:81 | ||||
chr10:67763930-67764230 | Common:5; Rare:78 | ||||
chr10:67764381-67764588 | Common:1; Rare:82 | ||||
chr10:67779862-67780144 | Common:2; Rare:98 | ||||
chr10:67788505-67788698 | Common:3; Rare:33 | ||||
chr10:67791089-67791196 | Rare:14 |