chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173126315831263159GC43GENIChomozygous111025420
173126316031263161TG40GENIChomozygous111025422
173127758331277584G14GENIChomozygous130463017
173127759431277595C15GENIChomozygous130463018
173127760131277602A18GENIChomozygous130463019
173127762131277623GG20GENIChomozygous130463020
173127763131277631A20GENIChomozygous130463021
173127763431277638GAGT21GENIChomozygous130463022
173127765131277652C23GENIChomozygous130463023
173127765631277656G23GENIChomozygous130463024
173127766831277669G28GENIChomozygous130463025
173128724331287244C50GENIChomozygous129442713
173132332431323325TG1GENIChomozygous111573342
173132495831324958A1GENIChomozygous129442725
173132497231324973C3GENIChomozygous129442726
173132497731324977T3GENIChomozygous129442727
173132507731325077A4GENIChomozygous129442728
173132514531325146G1GENIChomozygous129442730
173132516331325164T3GENIChomozygous129442731
173132516931325169T3GENIChomozygous129442732
173132521731325218A8GENIChomozygous129442733
173132531631325317A4GENIChomozygous129442734
173134593931345939GGC43GENIChomozygous129442744
173134609931346100A51GENIChomozygous129442745
173134813531348135A48GENIChomozygous129442748
173135003931350039CCGTT20GENIChomozygous129442752
173127761731277618AG20GENIChomozygous130467389
173127761831277619CA20GENIChomozygous130467390
173132331831323318AG5GENICheterozygous132358330
173132832331328325TC42GENICheterozygous130794779