chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206287530206287531TC25GENICheterozygous74683098
1206287760206287761AG38GENIChomozygous74683100
1206288017206288018CT53GENIChomozygous76205428
1206289812206289813CT25GENIChomozygous74683104
1206289863206289864AC24GENIChomozygous74683108
1206289916206289917GT32GENIChomozygous74683110
1206289934206289935AC33GENIChomozygous74683112
1206290013206290014TG24GENIChomozygous74683114
1206290098206290099CG36GENIChomozygous74683116
1206290151206290152TC37GENIChomozygous75478382
1206290275206290276AC32GENIChomozygous74683122
1206290345206290346TG11GENICpossibly homozygous74683124
1206295194206295195GA46GENIChomozygous74683126
1206309666206309667CA34GENICpossibly homozygous76205429
1206317832206317833TC43GENIChomozygous74683138
1206318531206318532GA50GENIChomozygous74683140
1206319282206319283CA39GENIChomozygous74683142
1206320455206320456GA48GENIChomozygous76205430
1206323084206323085AG55GENIChomozygous74683144
1206324839206324840GC18GENIChomozygous74683148
1206325111206325112GA32GENIChomozygous75206381
1206325920206325921GA37GENIChomozygous76205431
1206326162206326163GA36GENIChomozygous76205432
1206326325206326326CT55GENIChomozygous76205433
1206328300206328301GA44GENIChomozygous74683150
1206328864206328865AG22GENIChomozygous75206385
1206329506206329507AC57GENIChomozygous74683152
1206329809206329810AT48GENIChomozygous74683154
1206332270206332271AG44GENICpossibly homozygous74683156
1206332467206332468AG41GENIChomozygous74683158
1206333667206333668GC32GENIChomozygous75206393
1206334379206334380TG35GENIChomozygous74683162
1206335858206335859TC37GENIChomozygous75206395
1206336052206336053AG33GENIChomozygous75206397
1206337401206337402AG17GENIChomozygous74683168
1206340813206340814GC44GENIChomozygous76205434
1206341945206341946AG43GENIChomozygous76692517