chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2229695898229695899AG15GENIChomozygous59430476
2229697378229697379AG12GENIChomozygous59430477
2229697679229697680GA14GENIChomozygous59430478
2229697689229697690GA11GENIChomozygous59430479
2229698055229698056GA10GENIChomozygous60357450
2229700753229700754CT15GENIChomozygous60357452
2229703835229703836GA14GENIChomozygous59430482
2229704215229704216GC7GENIChomozygous60357454
2229705654229705655GA14GENIChomozygous59430484
2229706174229706175CT16GENIChomozygous60357456
2229706345229706346AG13GENIChomozygous59430485
2229707257229707259AT--7GENIChomozygous60550413
2229707325229707326TC8GENIChomozygous62475433
2229707676229707677GA8GENIChomozygous62058551
2229708550229708551CT14GENIChomozygous59430487
2229708554229708555TC16GENIChomozygous60357470
2229709522229709523TC11GENIChomozygous59430488
2229713177229713178CCT16GENIChomozygous59430489
2229716679229716680GGT9GENICheterozygous59430492
2229717305229717309AAAC----9GENIChomozygous60168188
2229717317229717318A-8GENIChomozygous60168190
2229717506229717507GC14GENIChomozygous59430494
2229717765229717766GA16GENIChomozygous59430496
2229718429229718430AG15GENIChomozygous59430497
2229719214229719215AG9GENIChomozygous59430499
2229721428229721429TC12GENIChomozygous59430500
2229721833229721834CT16GENIChomozygous62058553
2229723735229723736AG18GENIChomozygous59430501
2229727567229727568CA16GENIChomozygous62058554
2229729163229729164GT9GENIChomozygous59430506
2229730049229730050TA19GENIChomozygous59430510
2229730741229730742CT15GENIChomozygous59430511
2229731397229731398GA17GENIChomozygous59430512
2229731998229732002TAGA----10GENICheterozygous59430518
2229732174229732175AATG17GENIChomozygous62434389
2229732201229732205TATA----11GENIChomozygous62434390