chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132936683029366831GA61GENIChomozygous149406633
132936686729366868AG63GENIChomozygous149406634
132936706329367064CT62GENIChomozygous149406635
132936828829368289CT56GENIChomozygous139264064
132936848529368486GA52GENIChomozygous149406636
132936875929368760AG56GENIChomozygous149406637
132936962429369625GT49GENIChomozygous149406638
132936983729369838CT49GENIChomozygous149406639
132937007729370078GT40GENIChomozygous149406640
132937015529370156TC41GENIChomozygous149406641
132937092429370925GA54GENIChomozygous149406642
132937175029371751CG32GENIChomozygous149406643
132937212629372127CT61GENIChomozygous149406644
132937222229372223AC73GENIChomozygous149406645
132937236429372365AG62GENIChomozygous149406646
132937275529372756TA50GENIChomozygous149406647
132937291629372917AG62GENIChomozygous149406648
132937300029373001GT53GENIChomozygous139264065
132937551329375514CT17GENIChomozygous149406649
132937551629375517GT17GENIChomozygous149406650
132937560629375607CT19GENIChomozygous139264066
132937616429376165CT55GENIChomozygous149406651
132937675429376755TA39GENICpossibly homozygous139264067
132937675529376756TA38GENIChomozygous139264068
132937237629372380ACAA58GENIChomozygous149396460
132937298529372986A47GENIChomozygous149396461
132937457929374579A51GENIChomozygous149396462
132937464129374642T46GENICpossibly homozygous149396463