chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38664954286649543TC25GENIChomozygous578629348
38665015886650159TG18GENIChomozygous578629349
38665044686650447AG16GENICpossibly homozygous578629350
38665155386651554CT26GENICpossibly homozygous578629351
38665196286651963CT6GENIChomozygous580587225
38665196586651998GCAGGCTTTGCCATGCCCATTCTCTCTAGAAAT---------------------------------4GENIChomozygous717496600
38665215986652160TC24GENIChomozygous578629352
38665264186652642AG9GENICpossibly homozygous578629353
38665270086652701AG15GENIChomozygous578629354
38665292586652926GA17GENIChomozygous578629355
38665356986653570CT10GENICpossibly homozygous578629356
38665420486654205TC27GENICpossibly homozygous578629357
38665546486655465TG6GENICheterozygous578629358
38665717186657172TTGTGC4GENICheterozygous717496602
38665774986657750TTTCC5GENIChomozygous717496603
38665775986657760AG8GENIChomozygous580587226
38665834786658348TC8GENIChomozygous578629359
38665901286659013GA19GENICheterozygous578629360
38665988686659887GC11GENIChomozygous578629361
38665999286659993GA16GENIChomozygous578629362
38666013686660137TC23GENICpossibly homozygous578629363
38666064686660647CCCA4GENICheterozygous717496604
38666077586660776GA9GENICpossibly homozygous578629364
38666086186660862GA13GENIChomozygous578629365
38666104686661049AAA---7GENIChomozygous717496606
38666139886661399CT15GENIChomozygous578629366
38666166886661669T-11GENICpossibly homozygous717496607
38666230186662303GG--8GENICheterozygous717496608
38666230286662303G-8GENICheterozygous717496609
38666349486663495AG17GENIChomozygous578629367
38666353486663535AG25GENIChomozygous578629368
38666406086664061AAAGACG4GENIChomozygous717496610
38666472886664729TC22GENIChomozygous578629369
38666497486664975AAT3GENIChomozygous717496611
38666665186666652AG14GENIChomozygous578629370