chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3153574853153574854TC23GENIChomozygous136843620
3153575667153575668CT23GENIChomozygous136843621
3153576250153576251GA23GENIChomozygous136843622
3153576660153576660ACACACACCATACATACACACCACATACAAAACACCACACAGACCATACATAA6GENIChomozygous136596613
3153576979153576979CA16GENIChomozygous136596614
3153579293153579294GA17GENIChomozygous136843623
3153579706153579712TGTCTG7GENIChomozygous136596615
3153579716153579718TG7GENIChomozygous136596616
3153579739153579740GC7GENIChomozygous136843624
3153579757153579758CG7GENIChomozygous136843625
3153579761153579762GC7GENIChomozygous136843626
3153579770153579776TCTCTG7GENIChomozygous136596617
3153580675153580676TC8GENIChomozygous136843627
3153581435153581436TC14GENIChomozygous136843628
3153583764153583765AG31GENIChomozygous136843629
3153583801153583802GA26GENIChomozygous136843630
3153585388153585389TA12GENIChomozygous136843631
3153586708153586709TC17GENIChomozygous136843632
3153587950153587951TC25GENIChomozygous136843633
3153588379153588380G25GENIChomozygous136596618
3153588980153588981CG24GENIChomozygous136843634
3153589370153589371TA20GENIChomozygous136843635
3153590737153590738TA17GENIChomozygous136843636
3153590799153590800AG25GENIChomozygous136843637
3153591056153591057TG14GENIChomozygous136843638
3153591091153591103CAGACATACAGG18GENIChomozygous136596619
3153591129153591131AC19GENIChomozygous136596620
3153591241153591241A13GENIChomozygous136596621
3153591251153591251TC13GENIChomozygous136596622
3153591252153591253AT12GENIChomozygous136843639
3153591299153591300TC9GENIChomozygous136843640
3153591310153591311TC10GENIChomozygous136843641
3153591493153591494TC16GENIChomozygous136843642
3153592183153592184CT20GENIChomozygous136843643
3153592184153592185TG21GENIChomozygous136843644
3153592412153592413CT12GENIChomozygous136843645
3153592457153592458AG13GENIChomozygous136843646