chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106401073664010737TG14GENIChomozygous126384194
106401582064015821GC17GENIChomozygous126384195
106401635764016358AC13GENIChomozygous126384196
106401639764016398CA8GENIChomozygous126384197
106401643264016433CG13GENIChomozygous126384198
106401645064016451TC13GENIChomozygous126384199
106401651364016514CA26GENIChomozygous126384200
106401654564016546CA12GENIChomozygous126384201
106401655464016555CA7GENIChomozygous126384202
106401661164016612CA14GENIChomozygous126384203
106402732764027328AC18GENIChomozygous116616682
106402837264028373CT17GENIChomozygous116616684
106402946064029461GC6GENIChomozygous126384204
106402985864029859GA10GENIChomozygous116616686
106403115464031155AG19GENIChomozygous116616688
106403151564031516CT23GENIChomozygous116616690
106403155064031551GC19GENICpossibly homozygous116616692
106403166464031665AG7GENIChomozygous116616694
106403215864032159CT17GENIChomozygous116616698
106403294264032943CA14GENIChomozygous116616700
106403335264033353GC17GENIChomozygous116616702
106403343164033432CT17GENIChomozygous116616704
106403368864033689AG19GENIChomozygous116616706
106403399164033992GA15GENIChomozygous116616708
106403449164034492GA22GENIChomozygous116616710
106403475164034752CT19GENIChomozygous116616712
106403484164034842TC23GENIChomozygous116616714
106403503364035034AG19GENIChomozygous116616716
106403536364035364CA20GENIChomozygous116616718
106403558064035581CT14GENIChomozygous116616720
106403651264036513AT4GENIChomozygous126384205
106403651464036515AT5GENIChomozygous126384206
106403737064037371CA6GENIChomozygous126384207
106403737264037373CA4GENIChomozygous116616722