chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118347308118347309GT37GENICpossibly homozygous54667278
6118347310118347311TTC31GENICheterozygous54667280
6118351692118351693G-24GENIChomozygous54667284
6118351693118351694C-44GENIChomozygous54667286
6118351735118351736GT62GENIChomozygous54667288
6118351741118351742TG59GENIChomozygous54667290
6118351744118351745CA59GENIChomozygous54667292
6118351759118351760AG60GENIChomozygous54667294
6118352731118352732GGAGA71GENIChomozygous54667296
6118358705118358706G-12GENIChomozygous54667298
6118360251118360252GC46GENICpossibly homozygous54844889
6118364366118364367CG70GENIChomozygous54667300
6118364371118364372TG71GENICpossibly homozygous54667302
6118364380118364381A-60GENIChomozygous54667304
6118368243118368244AAC35GENIChomozygous54667312
6118368247118368248C-34GENIChomozygous54667314
6118368265118368266TC38GENICpossibly homozygous54667316
6118368271118368272GGT39GENIChomozygous54667318