chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145361099145361100AG19GENICpossibly homozygous55767829
5145361900145361901GC39GENIChomozygous55767831
5145363123145363126CCA---22GENICpossibly homozygous55767835
5145363320145363321AC27GENIChomozygous55767841
5145364001145364002CT38GENIChomozygous55767844
5145364976145364977AG36GENIChomozygous55767847
5145365273145365274CCAGTT17GENIChomozygous55767850
5145365654145365655AT21GENIChomozygous55767853
5145365891145365892CT25GENIChomozygous55767855
5145366834145366835GA57GENIChomozygous55767858
5145367301145367302TG28GENIChomozygous55767860
5145368243145368244GGA14GENIChomozygous55767863
5145369071145369072AG46GENIChomozygous55767866
5145369147145369148TC42GENIChomozygous55767869
5145370295145370296A-13GENICpossibly homozygous55767871
5145370312145370313CCA5GENICheterozygous56494526
5145370313145370314A-5GENICheterozygous56458957
5145371450145371458GTGTGTGT--------22GENICheterozygous56458958
5145371452145371458GTGTGT------22GENICheterozygous56458959
5145373072145373073CT37GENIChomozygous55767882
5145373159145373160TC31GENIChomozygous55767885
5145373253145373254TG39GENIChomozygous55767887
5145373669145373670CT34GENIChomozygous55767890
5145373689145373695TGTGTG------25GENICheterozygous55767893
5145373691145373695TGTG----25GENICpossibly homozygous55767894
5145374017145374021TTAT----8GENIChomozygous55767897
5145374274145374275CG51GENIChomozygous55767900
5145375208145375209CCT27GENIChomozygous55767903
5145376435145376436GA48GENIChomozygous55767909
5145376586145376587GA44GENIChomozygous55767912
5145377734145377735TG44GENIChomozygous55767915
5145377759145377760AG43GENIChomozygous55767918
5145377938145377939TC40GENIChomozygous55767921
5145378460145378461AG51GENIChomozygous55767924
5145378986145378987GA43GENIChomozygous55767927