chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85874804758748048AG36GENIChomozygous116509791
85874871658748717G23GENIChomozygous131048338
85875003458750035AG42GENIChomozygous116830161
85875078458750785AC32GENIChomozygous122978214
85875078558750786CA31GENIChomozygous122978215
85875238258752383CT27GENIChomozygous116830163
85875457558754576AG35GENIChomozygous116830165
85875509058755091CT32GENIChomozygous116830167
85875511458755115GA32GENIChomozygous116830169
85875524658755247TC28GENIChomozygous116509801
85875570258755703AC27GENIChomozygous116509803
85875623158756232GA43GENIChomozygous116830173
85875732758757328TG53GENICpossibly homozygous116830175
85875821958758220TA41GENIChomozygous116509805
85875876558758766A36GENIChomozygous131048339
85875879158758791G46GENIChomozygous131048340
85875879458758795AG46GENIChomozygous116830177
85875889258758893CT42GENIChomozygous116830179
85875942158759422CT44GENIChomozygous116830181
85876078358760784CT36GENIChomozygous116830183
85876575858765759CT34GENIChomozygous116830185
85876576758765768CT37GENIChomozygous116830187
85876674458766745TG43GENIChomozygous116830189
85876691058766911GC19GENIChomozygous117184499
85875679658756797GT42GENIChomozygous117928180
85876905858769058C27GENIChomozygous131048341
85876907358769074AG30GENIChomozygous116509819
85876912758769128TC34GENIChomozygous116830191
85877033258770333AG35GENIChomozygous116830193
85877048958770490CA39GENIChomozygous116830195
85877062458770625AG36GENIChomozygous116830197
85877091858770919CT37GENIChomozygous116830199
85877107758771078TC40GENIChomozygous116830201
85877175858771759CG34GENIChomozygous116830203
85877203758772038TG33GENIChomozygous116830205
85877213658772137TC38GENIChomozygous116830207