Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:129009870-129010152 | Common:2; Rare:100 | ||||
chr9:129320748-129321013 | Rare:55 | ||||
chr9:134767170-134767376 | Common:1; Rare:40; Clinvar:1 | ||||
chr9:134774581-134774912 | Common:3; Rare:87; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr9:134811326-134811599 | Rare:82; Clinvar:7; Clinvar (benign):5 | ||||
chr9:136547362-136547617 | Common:2; Rare:72 | ||||
chr9:136724919-136725033 | Common:3; Rare:17 | ||||
chr9:136847654-136847991 | Rare:89 | ||||
chrM:404-561 | |||||
chrM:564-1407 | |||||
chrM:15390-15770 | |||||
chrM:15884-16000 | |||||
chrX:2609154-2609433 | Common:1; Rare:90 | ||||
chrX:7147233-7147291 | Rare:11 | ||||
chrX:11351657-11351878 | Common:2; Rare:27 |