chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166431337166431338CT29GENIChomozygous108954822
1166435470166435471GA27GENICheterozygous108954823
1166436244166436245TC37GENICpossibly homozygous108356459
1166438511166438512CT33GENIChomozygous108954824
1166441142166441143GT32GENIChomozygous108356463
1166442761166442762GA35GENIChomozygous108954825
1166443025166443026CT37GENICheterozygous109051931
1166443029166443030TC38GENICheterozygous108954826
1166443351166443352TC21GENIChomozygous108356467
1166444993166444994AG32GENICheterozygous108356468
1166445011166445012CA31GENICheterozygous108356469
1166446094166446095AC31GENIChomozygous108954827
1166446134166446135AG40GENICheterozygous108954828
1166447973166447974TA20GENIChomozygous108356475
1166448210166448211AG23GENIChomozygous108356476
1166448396166448397GT48GENIChomozygous108954829
1166450576166450577GT28GENIChomozygous108356478
1166451271166451272TG40GENICpossibly homozygous108954830
1166453324166453325TC17GENIChomozygous108356480
1166456397166456398CT32GENIChomozygous108954832