chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206287530206287531TC40GENICheterozygous74683098
1206287760206287761AG52GENIChomozygous74683100
1206288948206288949GA54GENIChomozygous74683102
1206289812206289813CT38GENIChomozygous74683104
1206289842206289843AG44GENIChomozygous74683106
1206289863206289864AC39GENIChomozygous74683108
1206289916206289917GT54GENIChomozygous74683110
1206289934206289935AC51GENIChomozygous74683112
1206290013206290014TG39GENICpossibly homozygous74683114
1206290098206290099CG34GENIChomozygous74683116
1206290247206290248GT4GENIChomozygous74683118
1206290250206290251GC5GENIChomozygous74683120
1206290275206290276AC16GENIChomozygous74683122
1206290345206290346TG13GENIChomozygous74683124
1206295194206295195GA48GENIChomozygous74683126
1206309801206309802GA28GENIChomozygous74683128
1206311309206311310AG37GENIChomozygous74683130
1206313757206313758GA40GENIChomozygous74683132
1206314877206314878GA50GENIChomozygous74683134
1206317750206317751TC25GENICpossibly homozygous74683136
1206317832206317833TC30GENIChomozygous74683138
1206318531206318532GA33GENIChomozygous74683140
1206319282206319283CA34GENICpossibly homozygous74683142
1206323084206323085AG29GENIChomozygous74683144
1206323340206323341AC36GENIChomozygous74683146
1206324839206324840GC10GENIChomozygous74683148
1206328300206328301GA53GENIChomozygous74683150
1206329506206329507AC43GENIChomozygous74683152
1206329809206329810AT57GENIChomozygous74683154
1206332270206332271AG54GENICpossibly homozygous74683156
1206332467206332468AG43GENIChomozygous74683158
1206333793206333794GT33GENICheterozygous74683160
1206334379206334380TG56GENICpossibly homozygous74683162
1206336771206336772GA43GENICpossibly homozygous74683164
1206337122206337123CT48GENIChomozygous74683166
1206337401206337402AG61GENIChomozygous74683168
1206341583206341584CT40GENIChomozygous74683170