chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8103512343103512344AG20GENIChomozygous52779044
8103513747103513748CG24GENIChomozygous52779045
8103517054103517055GA33GENIChomozygous52779046
8103517686103517688TT--2GENICheterozygous53453594
8103518156103518157GA28GENIChomozygous52779049
8103519323103519324CG23GENIChomozygous52779050
8103519399103519400GC12GENICpossibly homozygous52779051
8103522011103522012TTTA12GENICheterozygous52779053
8103522011103522012TTA12GENICheterozygous53406360
8103522024103522025AT18GENIChomozygous52779054
8103522747103522749TT--6GENICheterozygous52779055
8103525126103525130AAAC----7GENIChomozygous52779057
8103525860103525861AT33GENIChomozygous52779059
8103526054103526055AATT13GENIChomozygous52779060
8103527322103527323TTAC3GENIChomozygous52779062
8103528481103528497TGTGTGTGTGTGTGTG----------------5GENICheterozygous53406363
8103528483103528497TGTGTGTGTGTGTG--------------5GENICheterozygous53406364
8103529218103529219T-13GENIChomozygous52779063
8103531107103531109TC--4GENIChomozygous53406365
8103531110103531111T-4GENIChomozygous53406366
8103531582103531583GA29GENIChomozygous52779065
8103533781103533782CCTTTCTTTTTTTTTTTTTATTT8GENICheterozygous53406368
8103534473103534474TTCC3GENIChomozygous53406369
8103538569103538570A-21GENIChomozygous52779068
8103539417103539418AG47GENIChomozygous52779069
8103542658103542659CCT12GENIChomozygous52779071
8103543670103543671CT17GENIChomozygous52779073
8103545531103545532TTTGTGTGTGTGTG9GENIChomozygous53406372
8103545832103545833CT35GENIChomozygous52779075
8103548407103548408AG40GENIChomozygous52779077
8103548847103548848CCT26GENICpossibly homozygous52779078
8103549866103549867CT9GENIChomozygous52779084
8103551875103551887TGTTGCTGCTGC------------1GENIChomozygous53521329
8103552638103552639T-19GENIChomozygous52779086
8103552872103552873GA23GENIChomozygous52779087
8103552948103552949CT34GENIChomozygous52779088
8103553747103553748GA31GENIChomozygous52779089