chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5117698989117698990TC56GENIChomozygous114523934
5117699310117699311GA48GENIChomozygous114523936
5117699579117699580GA46GENIChomozygous114523938
5117699617117699618CT47GENIChomozygous114523940
5117699722117699723AG53GENIChomozygous114523942
5117699763117699764CT56GENIChomozygous114523944
5117700348117700349TG57GENIChomozygous114523946
5117701237117701238AT50GENIChomozygous114523948
5117701403117701404AG46GENICpossibly homozygous114523950
5117701693117701694GA40GENIChomozygous114523952
5117702120117702121CT65GENIChomozygous114523954
5117702244117702245TC50GENIChomozygous114523956
5117702530117702531T57GENIChomozygous134547458
5117702569117702570CT54GENIChomozygous114523958
5117702700117702701AG53GENIChomozygous114523960
5117702721117702722TC50GENIChomozygous114523962
5117704007117704008TA42GENIChomozygous113976630
5117700526117700527C51GENIChomozygous128229347
5117702704117702705CT51GENIChomozygous113976629
5117704292117704293AG48GENIChomozygous114523964
5117704407117704408AG42GENIChomozygous114523966
5117705412117705413TC35GENIChomozygous113976633
5117705844117705845GA44GENIChomozygous114523968