chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110443548110443549GT19GENIChomozygous111672841
3110448513110448514GC49GENIChomozygous111672843
3110448584110448585TG15GENIChomozygous111672844
3110452888110452889GA27GENIChomozygous111672846
3110461437110461438GA51GENICheterozygous111672852
3110461443110461444AC46GENICheterozygous112349395
3110462720110462721GA29GENIChomozygous112003593
3110462748110462749GA23GENIChomozygous112003595
3110463066110463067AG22GENIChomozygous111672857
3110463562110463563GA34GENIChomozygous112003597
3110464459110464460AT24GENIChomozygous112003599
3110465091110465092TC30GENIChomozygous112003601
3110465447110465448AG24GENIChomozygous112003603
3110466543110466544CT17GENIChomozygous112003605
3110467748110467749GC31GENIChomozygous112003607
3110469248110469249TC44GENIChomozygous112003609
3110473122110473123CT34GENIChomozygous112003611
3110473578110473579GA21GENIChomozygous112003613
3110473956110473957GT22GENIChomozygous112003615
3110474591110474592TC28GENICheterozygous112003617
3110474599110474600CT29GENICheterozygous112003619
3110475248110475249GA35GENIChomozygous112003621
3110475728110475729TC32GENIChomozygous112003623
3110476366110476367GA47GENIChomozygous112003625
3110480114110480115GT47GENIChomozygous112003627
3110481041110481042GA33GENIChomozygous112003629
3110481403110481404TC26GENIChomozygous112003631
3110481451110481452TC24GENIChomozygous112003633
3110481916110481917CT39GENICpossibly homozygous112003635
3110482841110482842AG32GENIChomozygous111672861
3110482914110482915GA26GENIChomozygous112003637
3110484147110484148GA38GENIChomozygous112349397