chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145361099145361100AG7GENIChomozygous561025921
5145361900145361901GC28GENIChomozygous561025922
5145363123145363126CCA---18GENIChomozygous707111029
5145363320145363321AC33GENIChomozygous561025923
5145364001145364002CT48GENIChomozygous559174379
5145364976145364977AG29GENIChomozygous561025924
5145365273145365274CCAGTT23GENIChomozygous707111030
5145365654145365655AT23GENIChomozygous561025925
5145365891145365892CT28GENIChomozygous559174380
5145366834145366835GA30GENIChomozygous559174381
5145367301145367302TG57GENIChomozygous559174382
5145368243145368244GGA17GENIChomozygous707111031
5145369071145369072AG38GENIChomozygous561025926
5145369147145369148TC37GENIChomozygous561025927
5145370295145370296A-3GENICheterozygous707111032
5145370312145370313CCA6GENICheterozygous707111034
5145370313145370314A-6GENICheterozygous707111033
5145371450145371458GTGTGTGT--------19GENICheterozygous707111035
5145371452145371458GTGTGT------19GENICheterozygous707111036
5145373072145373073CT35GENIChomozygous559174383
5145373159145373160TC30GENIChomozygous559174384
5145373253145373254TG34GENIChomozygous559174385
5145373669145373670CT34GENIChomozygous559174386
5145373689145373695TGTGTG------22GENICheterozygous707111039
5145373691145373695TGTG----22GENICpossibly homozygous707111040
5145374017145374021TTAT----2GENIChomozygous707111042
5145374274145374275CG32GENIChomozygous561025928
5145375208145375209CCT28GENIChomozygous707111045
5145376435145376436GA39GENIChomozygous559174387
5145376586145376587GA54GENIChomozygous559174388
5145377734145377735TG40GENIChomozygous561025929
5145377759145377760AG36GENIChomozygous561025930
5145377938145377939TC39GENIChomozygous561025931
5145378460145378461AG26GENIChomozygous559174389
5145378986145378987GA38GENIChomozygous559174390