chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121071083210710833TC23GENIChomozygous139082588
121071143410711435T7GENICheterozygous403316030
121071143410711435TA7GENICheterozygous403316031
121071267710712678AG21GENIChomozygous139082589
121071284210712843CT19GENIChomozygous139082590
121071322610713227GC10GENIChomozygous139082591
121071403510714036GC21GENIChomozygous139082594
121071537710715378GA10GENIChomozygous139082595
121071838510718386CT11GENIChomozygous139082596
121071893410718935CA11GENIChomozygous139082597
121071951310719514TG10GENIChomozygous139082598
121072067310720674AG11GENIChomozygous139082599
121072200210722024AGAGAGAGAGAGAGAGACAGAC13GENICheterozygous139040519
121072064610720647A11GENIChomozygous139040518
121071412210714164GGTGTGACACGGCCTGTCCCTGACACCACCCGGCAGGGCACC19GENIChomozygous139040516
121071978110719782A17GENIChomozygous139040517
121072373410723735CA15GENIChomozygous139082600
121072471210724713GA15GENIChomozygous139082601
121072559010725591GA11GENIChomozygous139082602
121072686710726868CT11GENIChomozygous139082603
121072694610726947G10GENIChomozygous139040520
121072705810727059CG16GENIChomozygous139082604
121072764110727642CT10GENIChomozygous139082605
121072765110727652AC11GENIChomozygous139082606
121072815210728152G2GENIChomozygous139040521
121073007410730075G6GENIChomozygous139040522
121073015510730156GA12GENIChomozygous139082607
121073019510730196TG13GENIChomozygous139082608
121073046810730469GA15GENIChomozygous139082609
121073056510730566AG17GENIChomozygous139082610
121073067410730675TC17GENIChomozygous139082611
121073117910731180TC14GENIChomozygous139082612
121073535110735352T13GENIChomozygous139040523
121073603710736038CT19GENIChomozygous139082613
121073658610736587TC20GENIChomozygous139082614
121073898510738985GA20GENIChomozygous139040524
121074028710740288GA17GENIChomozygous139082615
121074095310740953A16GENICpossibly homozygous139040525
121074296010742961TC13GENIChomozygous139082616
121074414810744149AG7GENIChomozygous139082618