chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145361099145361100AG8GENIChomozygous55767829
5145361900145361901GC19GENIChomozygous55767831
5145363123145363126CCA---13GENICpossibly homozygous55767835
5145363320145363321AC19GENIChomozygous55767841
5145364001145364002CT34GENIChomozygous55767844
5145364976145364977AG28GENIChomozygous55767847
5145365273145365274CCAGTT15GENIChomozygous55767850
5145365654145365655AT10GENIChomozygous55767853
5145365891145365892CT28GENIChomozygous55767855
5145366834145366835GA21GENIChomozygous55767858
5145367301145367302TG28GENIChomozygous55767860
5145368243145368244GGA12GENIChomozygous55767863
5145369071145369072AG20GENIChomozygous55767866
5145369147145369148TC23GENIChomozygous55767869
5145370295145370296A-4GENICheterozygous55767871
5145370312145370313CCA2GENICheterozygous56494526
5145370313145370314A-2GENICheterozygous56458957
5145371450145371458GTGTGTGT--------9GENICheterozygous56458958
5145371452145371458GTGTGT------9GENICpossibly homozygous56458959
5145373072145373073CT29GENIChomozygous55767882
5145373159145373160TC23GENIChomozygous55767885
5145373253145373254TG28GENIChomozygous55767887
5145373669145373670CT17GENIChomozygous55767890
5145373689145373695TGTGTG------19GENICheterozygous55767893
5145373691145373695TGTG----19GENICpossibly homozygous55767894
5145374017145374021TTAT----1GENIChomozygous55767897
5145374274145374275CG13GENIChomozygous55767900
5145375208145375209CCT22GENIChomozygous55767903
5145376435145376436GA36GENIChomozygous55767909
5145376586145376587GA34GENIChomozygous55767912
5145377734145377735TG17GENIChomozygous55767915
5145377759145377760AG23GENIChomozygous55767918
5145377938145377939TC28GENIChomozygous55767921
5145378460145378461AG31GENIChomozygous55767924
5145378986145378987GA29GENIChomozygous55767927