chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5148926330148926333CTC56GENIChomozygous128255623
5148926336148926336TTC57GENIChomozygous128255624
5148929132148929132A49GENIChomozygous128255625
5148929677148929678AC39GENICheterozygous128301868
5148943146148943147T15GENIChomozygous128255626
5148943156148943157T16GENIChomozygous128255627
5148943165148943166T17GENIChomozygous128255628
5148943179148943180T17GENIChomozygous128255629
5148943200148943201T19GENIChomozygous128255630
5148943205148943208CAA13GENIChomozygous128255631
5148943212148943213T13GENIChomozygous128255632
5148943220148943221G13GENIChomozygous128255633
5148943225148943226A13GENIChomozygous128255634
5148943267148943268C58GENIChomozygous128255635
5148943282148943282T58GENIChomozygous128255636
5148943290148943291T60GENIChomozygous128255637
5148943351148943352C35GENIChomozygous128255638
5148943356148943357G36GENIChomozygous128255639
5148943359148943360A35GENIChomozygous128255640
5148943374148943375C47GENIChomozygous128255641
5148943437148943438C42GENIChomozygous128255642
5148944725148944726AG35GENIChomozygous114154368
5148944727148944728G34GENIChomozygous128255643
5148944735148944735TAAAT35GENIChomozygous128255644
5148944738148944743AGGCC33GENIChomozygous128255645
5148943177148943178CT17GENIChomozygous114049960
5148943201148943202AC13GENIChomozygous118943765
5148943228148943229TA16GENIChomozygous114538281
5148944747148944748CT33GENIChomozygous114049966
5148944729148944730CT34GENIChomozygous118846649
5148944745148944746CT33GENIChomozygous114049964