chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135209311752093118TG13GENIChomozygous998218874
135209358352093584GA22GENIChomozygous998218875
135209401952094020CT18GENIChomozygous998218876
135209457352094574CT19GENIChomozygous998218877
135209478952094790TC14GENIChomozygous998218878
135209546852095469CT33GENIChomozygous998218879
135209575552095756CT18GENIChomozygous998218880
135209591152095912AC18GENIChomozygous998218881
135209591252095913GA18GENIChomozygous998218882
135209750152097502CT22GENIChomozygous998218883
135209885352098854TC33GENIChomozygous998218884
135209892652098927TG37GENIChomozygous998218885
135210154452101545GT32GENIChomozygous998218886
135210237252102373AT22GENIChomozygous998218887
135210270752102708TC13GENIChomozygous998218888
135210476652104767GA32GENIChomozygous998218889
135210508952105090TA29GENIChomozygous998218890
135210583452105835TC23GENIChomozygous998218891
135210597752105978TC20GENIChomozygous998218892
135210604052106041TC23GENIChomozygous998218893
135210633352106334GT32GENIChomozygous998218894
135210634452106345CT30GENIChomozygous998218895
135210716152107162AT24GENIChomozygous998218896
135210756652107567GA33GENIChomozygous998218897
135210780152107802TG35GENIChomozygous998218898
135210825352108254AC17GENIChomozygous998218899
135210861652108617TC21GENIChomozygous998218900
135210882252108823AG21GENIChomozygous998218901
135210910752109108AT31GENIChomozygous998218902
135210912952109130TA27GENIChomozygous998218903
135210918252109183CT26GENIChomozygous998218904
135210927752109278AG33GENIChomozygous998218905
135210985352109854TC21GENIChomozygous998218906
135211139952111400AC6GENIChomozygous998218907
135211150052111501GA16GENIChomozygous998218908