chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135209311752093118TG13GENIChomozygous976870693
135209358352093584GA17GENIChomozygous976870694
135209401952094020CT22GENIChomozygous976870695
135209457352094574CT23GENIChomozygous976870696
135209478952094790TC24GENIChomozygous976870697
135209546852095469CT13GENIChomozygous976870698
135209575552095756CT11GENIChomozygous976870699
135209591152095912AC21GENIChomozygous976870700
135209591252095913GA21GENIChomozygous976870701
135209750152097502CT10GENIChomozygous976870702
135209885352098854TC26GENIChomozygous976870703
135209892652098927TG27GENIChomozygous976870704
135210154452101545GT23GENIChomozygous976870705
135210237252102373AT16GENIChomozygous976870706
135210270752102708TC12GENIChomozygous976870707
135210476652104767GA22GENIChomozygous976870708
135210508952105090TA13GENIChomozygous976870709
135210583452105835TC12GENIChomozygous976870710
135210597752105978TC6GENIChomozygous976870711
135210604052106041TC9GENIChomozygous976870712
135210633352106334GT16GENIChomozygous976870713
135210634452106345CT16GENIChomozygous976870714
135210716152107162AT17GENIChomozygous976870715
135210756652107567GA16GENIChomozygous976870716
135210780152107802TG25GENIChomozygous976870717
135210825352108254AC10GENIChomozygous976870718
135210861652108617TC22GENIChomozygous976870719
135210910752109108AT27GENIChomozygous976870720
135210912952109130TA24GENIChomozygous976870721
135210918252109183CT25GENIChomozygous976870722
135210927752109278AG28GENIChomozygous976870723
135210985352109854TC15GENIChomozygous976870724
135211076752110768GA6GENIChomozygous976870725
135211139952111400AC12GENIChomozygous976870726
135211150052111501GA13GENIChomozygous976870727
135211501452115015TG26GENICheterozygous976870728