chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51302055513020556AG9GENIChomozygous137381244
51302086713020868TA20GENIChomozygous137381245
51302159913021599T16GENIChomozygous137291211
51302312613023127GA15GENIChomozygous137381246
51302353513023536GA18GENIChomozygous137381247
51302599913026000AT19GENICheterozygous403132988
51302276113022762TC10GENICheterozygous154266890
51302276113022762T10GENIChomozygous403132987
51302599913026000AG19GENIChomozygous154266891
51302963013029631AG19GENIChomozygous137381248
51302992913029930GT24GENIChomozygous137381249
51303008613030087GA15GENIChomozygous137381250
51303119213031193T8GENIChomozygous137291212
51303234213032343GC21GENIChomozygous137381251
51303291913032920AT22GENIChomozygous137381252
51303342113033421T16GENIChomozygous137291213
51303623113036232GA23GENIChomozygous137381253
51303945313039454TG20GENIChomozygous137381254
51303970913039710T13GENIChomozygous137291215
51304006013040061GA19GENIChomozygous137381255
51304300613043007TA15GENIChomozygous137381258
51304315813043159AG19GENIChomozygous137381259
51304324513043246TC18GENIChomozygous137381260
51304338713043420ACATACCCCTTCATACAAGCTTCCTACACACAT15GENIChomozygous137291216
51304407713044078GT17GENIChomozygous137381263
51304440513044406CA11GENIChomozygous137381264
51304460813044609AC15GENIChomozygous137381265
51304462713044628TC16GENIChomozygous137381266
51304486813044869TA17GENIChomozygous137381267
51304512613045127AC18GENIChomozygous137381268
51304637313046374TC20GENIChomozygous137381269
51304664913046650CT17GENIChomozygous137381270
51304829313048294TC15GENIChomozygous137381272
51304861013048612AA14GENIChomozygous137291218
51304890113048902AG19GENIChomozygous137381273
51304928813049290GC22GENIChomozygous137291219
51304856313048563GA14GENIChomozygous141677738
51304245213042453AG15GENIChomozygous141703844
51303648713036488GA9GENIChomozygous141703841
51304165613041657CT16GENIChomozygous141703842
51304167213041673GT18GENIChomozygous141703843