chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103146176831461769TC25GENIChomozygous51391624
103146334731463348C-12GENIChomozygous51391625
103146349731463512AACAACAACAAAAAA---------------2GENIChomozygous52365297
103146423031464231GT9GENIChomozygous51391626
103146546331465464TG29GENIChomozygous51391627
103146577631465777TG12GENIChomozygous51391629
103146646431466465AAAGAGAGAG4GENIChomozygous51391630
103146745331467454TC18GENIChomozygous51391631
103146873231468733TA19GENIChomozygous51391632
103147000531470006TTG5GENICheterozygous51391633
103147016731470168A-26GENIChomozygous51391634
103147018131470182T-23GENIChomozygous51391635
103147041831470419TTCCC28GENIChomozygous51391636
103147109731471098TA20GENIChomozygous51391638
103147177031471771CCT7GENIChomozygous51391639
103147194731471948TC1GENIChomozygous51391640
103147281231472813TC18GENIChomozygous51391641
103147294531472946TA25GENIChomozygous51391642
103147329631473297CT18GENICpossibly homozygous51391644
103147334031473341TG26GENIChomozygous51391645
103147362831473632CACA----13GENIChomozygous52365299
103146577331465774TG9GENIChomozygous52315963
103147307531473115TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC----------------------------------------13GENIChomozygous52315964
103147370031473701A-29GENIChomozygous51391648
103147419331474194A-12GENIChomozygous52185633
103147429731474298TTTTTC9GENIChomozygous51391649
103147456231474563CCGTGTGTGT8GENICpossibly homozygous51391651