chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3153574853153574854TC28GENIChomozygous136843620
3153575667153575668CT23GENIChomozygous136843621
3153576250153576251GA25GENIChomozygous136843622
3153576660153576660ACACACACCATACATACACACCACATACAAAACACCACACAGACCATACATAA12GENIChomozygous136596613
3153576979153576979CA18GENIChomozygous136596614
3153577090153577092AC19GENICheterozygous146071047
3153579293153579294GA20GENIChomozygous136843623
3153579706153579712TGTCTG15GENIChomozygous136596615
3153579716153579718TG15GENIChomozygous136596616
3153579739153579740GC15GENIChomozygous136843624
3153579757153579758CG15GENIChomozygous136843625
3153579761153579762GC15GENIChomozygous136843626
3153579770153579776TCTCTG15GENIChomozygous136596617
3153580675153580676TC21GENIChomozygous136843627
3153581435153581436TC19GENIChomozygous136843628
3153583764153583765AG24GENIChomozygous136843629
3153583801153583802GA19GENIChomozygous136843630
3153585388153585389TA19GENIChomozygous136843631
3153586708153586709TC20GENIChomozygous136843632
3153587950153587951TC20GENIChomozygous136843633
3153588379153588380G15GENIChomozygous136596618
3153588980153588981CG16GENIChomozygous136843634
3153589370153589371TA20GENIChomozygous136843635
3153590737153590738TA26GENIChomozygous136843636
3153590799153590800AG24GENIChomozygous136843637
3153591056153591057TG15GENIChomozygous136843638
3153591091153591103CAGACATACAGG20GENIChomozygous136596619
3153591129153591131AC35GENIChomozygous136596620
3153591241153591241A19GENIChomozygous136596621
3153591251153591251TC13GENICpossibly homozygous136596622
3153591252153591253AT19GENIChomozygous136843639
3153591299153591300TC7GENIChomozygous136843640
3153591310153591311TC9GENIChomozygous136843641
3153591493153591494TC19GENIChomozygous136843642
3153592183153592184CT15GENIChomozygous136843643
3153592184153592185TG15GENIChomozygous136843644
3153592412153592413CT24GENIChomozygous136843645
3153592457153592458AG22GENIChomozygous136843646
3153583306153583307GA11GENICheterozygous144654066