chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103146176831461769TC32GENIChomozygous51391624
103146334731463348C-14GENIChomozygous51391625
103146349731463512AACAACAACAAAAAA---------------7GENIChomozygous52365297
103146423031464231GT13GENIChomozygous51391626
103146546331465464TG30GENIChomozygous51391627
103146577331465774TG22GENIChomozygous52315963
103146577631465777TG27GENIChomozygous51391629
103146745331467454TC17GENIChomozygous51391631
103146873231468733TA25GENIChomozygous51391632
103147000531470006TTG1GENIChomozygous51391633
103147016731470168A-12GENIChomozygous51391634
103147018131470182T-13GENIChomozygous51391635
103147041831470419TTCCC22GENIChomozygous51391636
103147109731471098TA31GENIChomozygous51391638
103147177031471771CCT16GENIChomozygous51391639
103147194731471948TC12GENIChomozygous51391640
103147281231472813TC16GENIChomozygous51391641
103147294531472946TA23GENIChomozygous51391642
103147307531473115TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTC----------------------------------------13GENIChomozygous52315964
103147329631473297CT30GENIChomozygous51391644
103147334031473341TG24GENIChomozygous51391645
103147362831473632CACA----16GENIChomozygous52365299
103147370031473701A-20GENIChomozygous51391648
103147419331474194A-9GENIChomozygous52185633
103147429731474298TTTTTC11GENICpossibly homozygous51391649
103147456231474563CCGTGTGT15GENICheterozygous51391650
103147456231474563CCGTGTGTGT15GENICpossibly homozygous51391651