chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23078221730782218CT45GENIChomozygous109676205
23078252330782524AG37GENIChomozygous109676207
23078257130782572CT40GENIChomozygous109676209
23078261230782613GA49GENIChomozygous109676211
23078268230782683CA50GENIChomozygous109676213
23078276130782762TC46GENIChomozygous111098723
23078276230782763CG46GENIChomozygous120123046
23078290230782902GAAAATCTAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCCGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAAAAAAAAAA23GENIChomozygous127607635
23078322430783225CT53GENIChomozygous109676225
23078332330783324TC45GENIChomozygous109676227
23078338730783390ACT45GENIChomozygous127607637
23078345430783455TA49GENIChomozygous109676229
23078347630783477CT47GENIChomozygous109676231
23078356430783565AG50GENIChomozygous109676233
23078420330784204TC45GENIChomozygous109676235
23078428630784287AT53GENIChomozygous109676237
23078446630784467AG48GENIChomozygous109676239
23078447830784479TC49GENIChomozygous109676241
23078471030784711AG49GENIChomozygous109676243
23078477330784774C40GENIChomozygous127607638
23078489430784895GA58GENIChomozygous109676245
23078518130785181AAACA25GENIChomozygous127607639
23078520530785206AC28GENIChomozygous109676252
23078500830785009CA36GENIChomozygous109676246
23078507030785071GC41GENIChomozygous109676248
23078510130785102GA42GENIChomozygous109676250
23078521130785212C28GENIChomozygous127607640
23078551530785516GA45GENIChomozygous109676254
23078555230785553GA54GENIChomozygous109676256
23078557730785578TG53GENIChomozygous109676258
23078559930785600TC53GENIChomozygous109676260
23078563630785637GA51GENIChomozygous109676262
23078599430785995GA61GENIChomozygous109676264
23078667730786681CAAT53GENICpossibly homozygous127607641
23078677330786774TG34GENIChomozygous109676266
23078693230786933TC40GENIChomozygous109676270
23078726930787270CT41GENIChomozygous109676272
23078810730788112AACAA28GENIChomozygous127607642
23078831630788316AA36GENIChomozygous127607643
23078858830788589AG14GENIChomozygous109676280
23078752830787529GT45GENICpossibly homozygous109676274
23078778030787781TC52GENIChomozygous109676276
23078784230787843AG62GENIChomozygous109676278
23078867530788676CT17GENIChomozygous109676282
23078872230788722GGGGGGGGG31GENIChomozygous127607644
23078887130788871TTGTTA40GENIChomozygous127607645
23078891330788914GA35GENIChomozygous109676284
23078919730789197GT40GENICpossibly homozygous127607646
23078932130789322TC29GENICpossibly homozygous109676288
23078941330789414AG6GENIChomozygous109676290
23078941830789419CT5GENIChomozygous109676292
23078947430789475TC8GENIChomozygous110885755
23078950130789502TA9GENIChomozygous109676294
23078952230789527TATTT11GENIChomozygous127607647
23078969330789693T18GENICpossibly homozygous127607648
23078984230789843GA30GENIChomozygous109676296
23079032230790323AG41GENIChomozygous109676298
23079071830790719TC49GENIChomozygous109676300
23079075630790764TCTGGGCA40GENIChomozygous127607649
23079076630790777CAGACTCTGGG40GENIChomozygous127607650
23079082230790823CT35GENIChomozygous109676302
23079085930790860T26GENIChomozygous127607651