chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145361099145361100AG4GENIChomozygous55767829
5145361900145361901GC13GENIChomozygous55767831
5145363320145363321AC22GENICpossibly homozygous55767841
5145364001145364002CT15GENICpossibly homozygous55767844
5145364976145364977AG17GENICpossibly homozygous55767847
5145365273145365274CCAGTT3GENIChomozygous55767850
5145365891145365892CT4GENIChomozygous55767855
5145366834145366835GA28GENIChomozygous55767858
5145367301145367302TG12GENICheterozygous55767860
5145369071145369072AG19GENIChomozygous55767866
5145369147145369148TC22GENIChomozygous55767869
5145373159145373160TC19GENICpossibly homozygous55767885
5145373253145373254TG14GENICpossibly homozygous55767887
5145373669145373670CT7GENIChomozygous55767890
5145373688145373689AATGTG1GENIChomozygous56291413
5145374274145374275CG18GENIChomozygous55767900
5145376435145376436GA19GENIChomozygous55767909
5145376586145376587GA22GENIChomozygous55767912
5145377734145377735TG26GENICpossibly homozygous55767915
5145377759145377760AG24GENIChomozygous55767918
5145377938145377939TC27GENIChomozygous55767921
5145378460145378461AG17GENICpossibly homozygous55767924
5145378986145378987GA3GENICheterozygous55767927