chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75846351458463516TC--5GENICheterozygous53930141
75847716758477168CCGT3GENICheterozygous54977338
75847716758477168CCGTGT3GENICheterozygous54977340
75847971958479720T-20GENICheterozygous55400185
75848871158488712CCA6GENICheterozygous54977342
75851438458514386CA--7GENICheterozygous54977344
75851952058519522TC--10GENICheterozygous54977346
75852417658524177CCTT2GENICheterozygous54977348
75852836658528368GT--10GENICheterozygous55024839
75852866358528664CT16GENIChomozygous53930161
75852923058529231TA20GENIChomozygous53930164
75854317658543177GA23GENIChomozygous56291953
75854390058543901GC3GENIChomozygous54977354
75854390158543902GA3GENIChomozygous54977356
75854390358543904GC3GENIChomozygous53930168
75855640758556409AA--1GENIChomozygous54905162
75855641058556411AAGTG1GENIChomozygous55141816
75856242558562426TTAC27GENIChomozygous53930175
75856334158563342AAT5GENICheterozygous55058506
75856334258563343T-5GENICheterozygous54977358
75857059458570595AAT24GENIChomozygous53930179
75858873958588740G-14GENIChomozygous53930189
75857093358570934G-20GENIChomozygous53930181
75857525058575252GT--7GENICheterozygous55024841
75858255558582556GGTAGA14GENICpossibly homozygous55024843
75858849258588493T-27GENIChomozygous53930185
75858853858588539TTA25GENIChomozygous53930187
75858888458588885AATG14GENICpossibly homozygous53930190
75859240458592405A-10GENICheterozygous53930192
75859556658595567CCACACACACACACACACACACACACACACACA3GENICheterozygous54977360