chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205672065205672066CT10GENICpossibly homozygous591612542
1205672498205672499TC4GENICheterozygous591612543
1205673037205673038GT13GENIChomozygous589676419
1205675052205675053AAC9GENIChomozygous723285388
1205676087205676088CT7GENICpossibly homozygous591612544
1205676803205676804AG4GENICheterozygous589676420
1205677344205677345TC1GENIChomozygous589676421
1205679667205679668CT7GENIChomozygous589676422
1205679712205679713TTA1GENIChomozygous723285389
1205680025205680026CT16GENICheterozygous589676423
1205680514205680515A-4GENIChomozygous723285390
1205680581205680582TC4GENIChomozygous589676424
1205680842205680843AG4GENICheterozygous591612545
1205681432205681433T-1GENIChomozygous723285392
1205681518205681519TC6GENIChomozygous589676425
1205682571205682572CT11GENIChomozygous589676426
1205682680205682681GC15GENICpossibly homozygous591612546
1205683062205683063GA4GENIChomozygous589676427
1205684050205684051AG13GENIChomozygous591612547
1205685744205685745AC9GENIChomozygous591612548
1205687116205687117AG13GENIChomozygous589676428
1205687228205687229GC5GENIChomozygous591612549
1205687559205687560AAAAC5GENICheterozygous723285393
1205687617205687618AG12GENICheterozygous591612550
1205688416205688417CT14GENIChomozygous589676429
1205688529205688530CT8GENIChomozygous591612551
1205689655205689656CT4GENICheterozygous591612552
1205690284205690285TC9GENICpossibly homozygous591612553
1205690876205690877TG8GENIChomozygous589676430
1205690924205690925G-12GENIChomozygous723285395
1205690975205690976TC18GENIChomozygous591612554
1205691392205691393TC15GENICpossibly homozygous591612555
1205691725205691726T-6GENIChomozygous723285396
1205691749205691750TA10GENICpossibly homozygous589676431
1205692043205692044AG17GENICpossibly homozygous589676432
1205692895205692896TC6GENICheterozygous589676433
1205693950205693951TC11GENIChomozygous589676434