chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46940774369407744TC23GENIChomozygous141628515
46940803969408040GT22GENIChomozygous141628516
46940888469408885CG16GENIChomozygous141628517
46941011269410113GA13GENIChomozygous141628518
46941202969412030TC18GENIChomozygous141628519
46941203269412033TA18GENIChomozygous154181251
46941203269412033T18GENICheterozygous403581983
46941211469412115CG22GENIChomozygous141628520
46941225969412260TC17GENIChomozygous141628521
46941226169412262AG18GENIChomozygous141628522
46941241969412420AG22GENIChomozygous141628523
46941242069412421AG22GENIChomozygous141628524
46941274869412749GT17GENIChomozygous141628525
46941303469413035AG20GENIChomozygous141628526
46941382469413825TC18GENIChomozygous141628527
46941407369414074GC14GENIChomozygous141628528
46941407769414078GC14GENIChomozygous141628529
46941516269415163TA30GENIChomozygous141628534
46941419869414199AG11GENIChomozygous141628530
46941427269414273CT14GENIChomozygous141628531
46941470069414701CT20GENIChomozygous141628532
46941500269415003GA24GENIChomozygous141628533
46941531069415311GA24GENIChomozygous141628535
46941564469415645TC20GENIChomozygous141628536
46941617769416178TC38GENIChomozygous141628537
46941627869416279TC28GENIChomozygous141628538
46941676769416768TC24GENIChomozygous141628539