chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187219764187219765AT56GENICpossibly homozygous110167111
2187219969187219970CT41GENIChomozygous110167112
2187220403187220404TC48GENIChomozygous110167113
2187220467187220469TC41GENIChomozygous127716690
2187220522187220523GA39GENIChomozygous110167114
2187220535187220536CA42GENIChomozygous110614148
2187220539187220542ACA42GENIChomozygous127716691
2187220543187220558ATGGTTGTGAGCCAC42GENIChomozygous127716692
2187220561187220565GTGG42GENIChomozygous127716693
2187221430187221431AG37GENIChomozygous110167115
2187222044187222045CT26GENIChomozygous110167116
2187222179187222180TC36GENIChomozygous110167117
2187222259187222260AG34GENIChomozygous110167118
2187222361187222362CT45GENICpossibly homozygous110167119
2187222969187222970GA34GENIChomozygous110167120
2187220772187220794CTGCAGCTCCCGCTCCCTGCTA57GENIChomozygous133380423
2187223861187223862GA32GENIChomozygous110167123
2187223961187223962GT31GENIChomozygous110167124
2187224323187224324CT44GENIChomozygous110167125
2187224478187224479TC48GENIChomozygous110167126
2187224618187224619GA44GENIChomozygous110167127
2187224805187224806TA42GENIChomozygous110167128
2187224825187224826TC40GENIChomozygous110167129