chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2186702772186702773TC13GENIChomozygous110166426
2186705132186705133GA20GENIChomozygous111277707
2186711811186711812CT18GENIChomozygous111277709
2186712730186712731TC13GENIChomozygous110166437
2186714600186714601CT18GENIChomozygous111277711
2186714601186714602AG16GENIChomozygous111277713
2186714882186714883AG10GENIChomozygous110166438
2186716567186716568TA35GENICpossibly homozygous111277715
2186718058186718059CT6GENIChomozygous111277717
2186719649186719650CT34GENIChomozygous110166447
2186719815186719816CG11GENIChomozygous110166448
2186719921186719922GA13GENIChomozygous110166449
2186720592186720593TC22GENIChomozygous111277721
2186720851186720852AT15GENIChomozygous110803519
2186720871186720872AG17GENIChomozygous110803520
2186721558186721559CT28GENIChomozygous111277723
2186721886186721887TC16GENIChomozygous110166455
2186721894186721895CT18GENIChomozygous110166456
2186722027186722028TG21GENIChomozygous110166457
2186722277186722278GA21GENIChomozygous111277725
2186722493186722494CT17GENIChomozygous110803522
2186722555186722556GA19GENIChomozygous110166458
2186722559186722560CT19GENIChomozygous110166459
2186722741186722742TC19GENIChomozygous110803524
2186722825186722826AC21GENIChomozygous111277727
2186704072186704073AC29GENIChomozygous120129793