chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145361099145361100AG3GENIChomozygous607851715
5145361900145361901GC18GENIChomozygous607851716
5145363123145363126CCA---19GENICpossibly homozygous733293934
5145363320145363321AC28GENIChomozygous607851717
5145364001145364002CT26GENIChomozygous606004808
5145364976145364977AG24GENIChomozygous607851718
5145365273145365274CCAGTT37GENIChomozygous733293935
5145365654145365655AT24GENIChomozygous607851719
5145365891145365892CT38GENIChomozygous606004809
5145366834145366835GA23GENIChomozygous606004810
5145367301145367302TG24GENIChomozygous606004811
5145368243145368244GGA16GENIChomozygous733293936
5145369071145369072AG17GENIChomozygous607851720
5145369147145369148TC27GENIChomozygous607851721
5145370313145370314A-1GENIChomozygous733293937
5145371449145371450AAGT14GENICheterozygous733293942
5145371450145371458GTGTGTGT--------14GENICheterozygous733293939
5145371452145371458GTGTGT------14GENICheterozygous733293940
5145373159145373160TC10GENIChomozygous606004812
5145373253145373254TG24GENIChomozygous606004813
5145373669145373670CT25GENIChomozygous606004814
5145373689145373695TGTGTG------20GENIChomozygous733293943
5145374274145374275CG19GENIChomozygous607851722
5145375208145375209CCT14GENIChomozygous733293946
5145376435145376436GA24GENIChomozygous606004815
5145376586145376587GA28GENIChomozygous606004816
5145377734145377735TG19GENIChomozygous607851723
5145377759145377760AG20GENIChomozygous607851724
5145377938145377939TC14GENIChomozygous607851725
5145378460145378461AG29GENIChomozygous606004817
5145378986145378987GA26GENIChomozygous606004818