chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5153022533153022534AC24GENIChomozygous149575444
5153023979153023979CC13GENIChomozygous149562943
5153024175153024176AG16GENIChomozygous143971188
5153024472153024473TC14GENIChomozygous143971189
5153027145153027146TC13GENIChomozygous143971194
5153028192153028193CT16GENIChomozygous149575445
5153028672153028674AG20GENIChomozygous143946939
5153030552153030553TC21GENIChomozygous143971201
5153030734153030735AG7GENICpossibly homozygous149575446
5153030760153030761AG9GENIChomozygous147263322
5153030773153030774GA12GENIChomozygous147263323
5153030774153030775GA12GENIChomozygous149575447
5153031194153031197GGA22GENIChomozygous143946945
5153031219153031220CT20GENIChomozygous149575448
5153031302153031303GA20GENIChomozygous143971202
5153031772153031772TA12GENIChomozygous149562944
5153031963153031964CT17GENIChomozygous149575449
5153032614153032615GT13GENIChomozygous149575453
5153032022153032023GA8GENIChomozygous149575450
5153032050153032051TC13GENIChomozygous143971203
5153032087153032088TA17GENIChomozygous149575451
5153032566153032567CT7GENIChomozygous149575452
5153032224153032225TG6GENIChomozygous141766614
5153033881153033881A13GENIChomozygous143946946
5153034231153034232TC16GENICpossibly homozygous143971206
5153034517153034518AG12GENIChomozygous143971207
5153035301153035302TA18GENIChomozygous149575454
5153035823153035823T16GENIChomozygous143946947
5153036037153036038GA14GENICpossibly homozygous149575455
5153036103153036104GT18GENIChomozygous149575456
5153036863153036864TC22GENIChomozygous149575457
5153037059153037060GC15GENIChomozygous149575458