chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110442376110442377AC16GENIChomozygous112292301
3110452494110452495TC23GENIChomozygous112292305
3110453246110453247GA19GENIChomozygous112292307
3110453430110453431AG18GENIChomozygous112292309
3110453556110453557AG20GENIChomozygous112292311
3110453686110453687CT4GENIChomozygous125939358
3110454023110454024CT20GENIChomozygous112292313
3110454715110454716AG21GENIChomozygous112138906
3110455267110455268AG8GENIChomozygous112292315
3110456058110456059AT15GENIChomozygous112292317
3110456080110456081GA11GENIChomozygous112292319
3110462720110462721GA13GENIChomozygous112003593
3110463051110463052GA15GENIChomozygous112138911
3110463066110463067AG15GENIChomozygous111672857
3110465091110465092TC5GENIChomozygous112003601
3110465447110465448AG25GENIChomozygous112003603
3110466543110466544CT7GENIChomozygous112003605
3110467748110467749GC4GENIChomozygous112003607
3110469248110469249TC7GENIChomozygous112003609
3110469574110469575AG22GENIChomozygous112138912
3110473730110473731CT12GENIChomozygous112292323
3110474579110474580CT7GENICheterozygous112255710
3110475728110475729TC15GENIChomozygous112003623
3110476491110476492GA7GENIChomozygous112138914
3110479203110479204CA15GENIChomozygous125831727
3110480114110480115GT15GENIChomozygous112003627
3110481041110481042GA5GENIChomozygous112003629
3110481403110481404TC26GENIChomozygous112003631
3110481916110481917CT8GENIChomozygous112003635
3110482841110482842AG14GENIChomozygous111672861