chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9100421014100421015TTA7GENICheterozygous735847575
9100421536100421537GT33GENIChomozygous610133949
9100422127100422128CT33GENIChomozygous610133950
9100423062100423063AG32GENIChomozygous610133951
9100426008100426009TTTTTTTTTTTTTTTTTTC4GENICheterozygous735847577
9100427518100427519TA31GENIChomozygous611162162
9100427755100427756TC23GENIChomozygous610133952
9100428241100428242CT25GENIChomozygous611162163
9100428446100428447AAGT6GENICheterozygous735847578
9100429133100429134CT23GENIChomozygous610133953
9100429739100429740GGA16GENICpossibly homozygous735847582
9100429740100429741A-16GENICheterozygous735847581
9100430571100430573AA--6GENICheterozygous735847583
9100430572100430573A-6GENICheterozygous735847584
9100430678100430679C-16GENIChomozygous735847585
9100430757100430758GT24GENIChomozygous610133954
9100430924100430925TA18GENIChomozygous610133955
9100431327100431328TC21GENIChomozygous611162164
9100432151100432152TC21GENIChomozygous611162165
9100432401100432402G-16GENIChomozygous735847586
9100432453100432455TT--14GENICpossibly homozygous735847587
9100432454100432455T-14GENICheterozygous735847588
9100432887100432888GA18GENIChomozygous611162166
9100433023100433024TTC31GENIChomozygous735847589
9100433284100433285GGCTCCGCCGCGAACCACAGACTCAGGACA42GENIChomozygous735847590