chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145361099145361100AG5GENIChomozygous55767829
5145361900145361901GC18GENIChomozygous55767831
5145363123145363126CCA---14GENIChomozygous55767835
5145363320145363321AC27GENIChomozygous55767841
5145364001145364002CT31GENIChomozygous55767844
5145364976145364977AG30GENIChomozygous55767847
5145365273145365274CCAGTT32GENIChomozygous55767850
5145365654145365655AT15GENIChomozygous55767853
5145365891145365892CT23GENIChomozygous55767855
5145366834145366835GA31GENIChomozygous55767858
5145367301145367302TG29GENIChomozygous55767860
5145368243145368244GGA9GENIChomozygous55767863
5145369071145369072AG39GENIChomozygous55767866
5145369147145369148TC26GENIChomozygous55767869
5145370295145370296A-3GENICheterozygous55767871
5145370312145370313CCA6GENICheterozygous56494526
5145370313145370314A-6GENICheterozygous56458957
5145371450145371458GTGTGTGT--------15GENICheterozygous56458958
5145371452145371458GTGTGT------15GENICpossibly homozygous56458959
5145373072145373073CT25GENIChomozygous55767882
5145373159145373160TC32GENIChomozygous55767885
5145373253145373254TG24GENIChomozygous55767887
5145373669145373670CT21GENIChomozygous55767890
5145373689145373695TGTGTG------19GENICheterozygous55767893
5145373691145373695TGTG----19GENICpossibly homozygous55767894
5145374017145374021TTAT----1GENIChomozygous55767897
5145374274145374275CG17GENIChomozygous55767900
5145375208145375209CCT13GENIChomozygous55767903
5145376435145376436GA35GENIChomozygous55767909
5145376586145376587GA26GENIChomozygous55767912
5145377734145377735TG30GENIChomozygous55767915
5145377759145377760AG23GENIChomozygous55767918
5145377938145377939TC26GENIChomozygous55767921
5145378460145378461AG35GENIChomozygous55767924
5145378986145378987GA35GENIChomozygous55767927