chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118330368118330369T-1GENIChomozygous54961157
6118337411118337412TTACACACAC5GENICheterozygous54961189
6118351693118351694C-13GENIChomozygous54667286
6118351735118351736GT6GENIChomozygous54667288
6118351741118351742TG5GENIChomozygous54667290
6118351744118351745CA5GENIChomozygous54667292
6118351759118351760AG11GENICpossibly homozygous54667294
6118352731118352732GGAGA6GENICheterozygous54667296
6118363663118363664CA10GENICheterozygous55265167
6118364366118364367CG1GENIChomozygous54667300
6118364371118364372TG2GENIChomozygous54667302
6118364380118364381A-6GENICheterozygous54667304
6118368243118368244AAC3GENIChomozygous54667312
6118368247118368248C-2GENIChomozygous54667314
6118368265118368266TC2GENICheterozygous54667316
6118368271118368272GGT2GENICheterozygous54667318