chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177603210177603211GA38GENIChomozygous538213742
1177603640177603641GA34GENIChomozygous538213743
1177604146177604147TC28GENIChomozygous538213744
1177606006177606007CT23GENIChomozygous538213745
1177606686177606687CA36GENIChomozygous538213746
1177607561177607562AT18GENIChomozygous538213747
1177612088177612089AG46GENIChomozygous538213748
1177612817177612818CT36GENIChomozygous538213749
1177613540177613541CT43GENIChomozygous538213750
1177614914177614915CT47GENIChomozygous538213751
1177614961177614962TC52GENIChomozygous538213752
1177615613177615614TTGGG21GENIChomozygous696753773
1177615797177615798TC16GENIChomozygous538213753
1177616646177616647AG12GENIChomozygous538213754
1177616722177616723CA18GENIChomozygous538213755
1177616913177616914CT24GENIChomozygous538213756
1177617680177617681CT26GENIChomozygous538213757
1177619932177619933AG37GENIChomozygous538213758
1177621036177621037C-31GENIChomozygous696753775
1177621195177621196G-30GENIChomozygous696753776
1177621691177621692CT39GENIChomozygous538213759
1177622060177622061CT37GENIChomozygous538213760
1177622212177622213CT39GENIChomozygous538213761
1177624883177624884CT38GENIChomozygous538213762
1177625104177625105CT29GENIChomozygous538213763
1177626672177626673TG36GENIChomozygous538213764
1177627461177627462GA38GENIChomozygous538213765
1177627588177627589CCTT2GENIChomozygous696753778
1177628609177628610TC20GENIChomozygous538213766
1177628849177628853ACAC----21GENIChomozygous696753780
1177628952177628953TTG2GENIChomozygous696753781
1177631429177631430CT21GENIChomozygous538213767
1177632309177632310GA38GENIChomozygous538213768
1177632546177632558ACACACACACAT------------12GENICpossibly homozygous696753783
1177634280177634281TA46GENIChomozygous538213769
1177634420177634421GA41GENIChomozygous538213770
1177634489177634491CC--21GENIChomozygous696753784