chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6118347310118347311TTC11GENIChomozygous54667280
6118350915118350919ACAC----3GENIChomozygous54667282
6118351692118351693G-13GENIChomozygous54667284
6118351693118351694C-24GENIChomozygous54667286
6118351735118351736GT30GENIChomozygous54667288
6118351741118351742TG30GENICpossibly homozygous54667290
6118351744118351745CA30GENIChomozygous54667292
6118351759118351760AG32GENICpossibly homozygous54667294
6118352731118352732GGAGA30GENIChomozygous54667296
6118358705118358706G-14GENIChomozygous54667298
6118364366118364367CG27GENIChomozygous54667300
6118364371118364372TG28GENIChomozygous54667302
6118364380118364381A-27GENIChomozygous54667304
6118365689118365690TA34GENICheterozygous54667306
6118365700118365705AAAAT-----33GENICheterozygous54961267
6118366594118366595GGT6GENICheterozygous54667308
6118368243118368244AAC27GENIChomozygous54667312
6118368247118368248C-24GENIChomozygous54667314
6118368265118368266TC23GENIChomozygous54667316
6118368271118368272GGT23GENIChomozygous54667318