chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5117698989117698990TC32GENIChomozygous114523934
5117699310117699311GA24GENIChomozygous114523936
5117699579117699580GA24GENIChomozygous114523938
5117699617117699618CT31GENIChomozygous114523940
5117699722117699723AG26GENIChomozygous114523942
5117699763117699764CT18GENIChomozygous114523944
5117700348117700349TG22GENIChomozygous114523946
5117701237117701238AT25GENIChomozygous114523948
5117701403117701404AG27GENIChomozygous114523950
5117701693117701694GA24GENIChomozygous114523952
5117702120117702121CT34GENIChomozygous114523954
5117702244117702245TC23GENIChomozygous114523956
5117702569117702570CT23GENIChomozygous114523958
5117702700117702701AG29GENIChomozygous114523960
5117702721117702722TC26GENIChomozygous114523962
5117704292117704293AG21GENIChomozygous114523964
5117704407117704408AG30GENIChomozygous114523966
5117705412117705413TC31GENIChomozygous113976633
5117700526117700527C30GENIChomozygous128229347
5117702704117702705CT29GENIChomozygous113976629
5117704007117704008TA27GENIChomozygous113976630
5117702530117702531T21GENIChomozygous134547458
5117705844117705845GA33GENIChomozygous114523968