chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147532546147532547AG20GENIChomozygous112874536
4147534877147534878GA19GENIChomozygous112874542
4147535170147535171TC25GENIChomozygous113180243
4147535211147535211ATGGATACT20GENIChomozygous128088842
4147538539147538540GA29GENIChomozygous113180244
4147539958147539959AG23GENIChomozygous112874545
4147541091147541092T25GENIChomozygous128088844
4147541095147541097CT25GENIChomozygous128088845
4147544189147544190CT19GENIChomozygous113180245
4147547163147547164GA21GENIChomozygous113180246
4147553666147553667GA6GENIChomozygous132618573
4147558715147558715G17GENIChomozygous128088848
4147561539147561540CA24GENIChomozygous113180247
4147563893147563893C16GENIChomozygous128088849
4147570791147570792GA4GENIChomozygous113180248
4147570794147570795GA4GENIChomozygous113180249
4147572140147572141TC17GENIChomozygous112874575
4147573879147573880GA18GENIChomozygous113180250
4147575739147575740TC23GENIChomozygous112874577
4147578043147578044CT26GENIChomozygous113180251
4147584921147584922AG24GENIChomozygous112874581
4147587241147587242CT28GENIChomozygous113180253
4147591921147591922G24GENIChomozygous128088854
4147536662147536663G25GENIChomozygous132607069
4147590795147590796TC16GENIChomozygous112874584
4147585045147585047AG10GENIChomozygous132607070
4147588201147588203AC13GENIChomozygous132607071
4147541093147541094TA24GENIChomozygous119281740