chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79866982998669830GA10GENICpossibly homozygous54489392
79867086498670865GA13GENICpossibly homozygous54489394
79867137698671377TC9GENIChomozygous54489406
79867166198671662CT14GENIChomozygous54489408
79867189598671896GA6GENIChomozygous54489410
79867322698673227GT16GENIChomozygous54489412
79867501798675018TTAA2GENICheterozygous54489414
79867501798675018TTA2GENICheterozygous54489416
79867614798676148G-2GENICheterozygous54033821
79867616198676162CG2GENIChomozygous54033822
79867617198676172G-1GENIChomozygous54033823
79867621098676211GA5GENIChomozygous54489420
79867634198676342CT13GENICheterozygous54489422
79867737298677373AG14GENIChomozygous54489424
79867859398678594CG10GENICpossibly homozygous54489426
79868186598681866GT25GENICpossibly homozygous54489430
79868339498683395TC11GENICheterozygous54489432
79868444398684444TG20GENICpossibly homozygous54489436
79868500098685001GC22GENICpossibly homozygous54489438
79868512698685127AATGTCC8GENICheterozygous54489440
79868541998685420GT23GENIChomozygous54489442
79868605898686059CA12GENIChomozygous54489448
79868756398687564CA11GENICheterozygous54489450
79868775698687757AC20GENICpossibly homozygous54489452
79868862698688627GA16GENIChomozygous54489454
79868903198689032GA23GENICpossibly homozygous54489456
79868990498689905CT26GENIChomozygous54489460
79869129298691293GA17GENICpossibly homozygous54489462
79869139098691391CT22GENICpossibly homozygous54489464
79869160498691605TC32GENICheterozygous54489466
79869269198692692GT13GENICpossibly homozygous54489468
79869275698692757GA16GENIChomozygous54489471
79869283298692833AT16GENICpossibly homozygous54489473
79869377098693771TC15GENICpossibly homozygous54489475
79869388798693888TC19GENIChomozygous54489477
79869476098694761AAAAACC1GENIChomozygous54489479
79869478798694788TC14GENIChomozygous54489481
79869484198694842TC13GENIChomozygous54489483
79869485298694853TC10GENIChomozygous54489485
79869496398694964CT12GENIChomozygous54489487
79869548998695490AG23GENIChomozygous54489489
79869570698695707TA5GENICheterozygous54489491
79869587998695880TC16GENICpossibly homozygous54489493
79869598198695982GGT4GENIChomozygous54033825
79869606298696063CT13GENIChomozygous54489495
79869609298696093GGCCTACTTC4GENICheterozygous54489497
79869612998696130TC15GENIChomozygous54489499
79869646298696463GC7GENIChomozygous54489501
79869652898696529TC9GENIChomozygous54489503
79869679898696802TGTC----8GENIChomozygous54489505
79869715798697158CT5GENICheterozygous54489509
79869721698697217AATC10GENIChomozygous54033828
79869727798697278AG14GENICheterozygous54489511
79869729198697292GA19GENIChomozygous54489513
79869762298697623TC22GENIChomozygous54489515
79869783198697832TG26GENICpossibly homozygous54489517
79869787898697879TC27GENIChomozygous54489519
79869801198698012CCAT4GENICheterozygous54489520
79869804998698050TC15GENICpossibly homozygous54489522
79869808498698085TC13GENIChomozygous54489524
79869809798698098GA23GENIChomozygous54489526
79869865298698653CCCTGCCT8GENIChomozygous54489528
79869891998698920AG10GENIChomozygous54489530
79869893298698933GT14GENIChomozygous54489532
79869900098699001AG22GENIChomozygous54489534
79869920498699205CA26GENICpossibly homozygous54489536
79869995498699955AG27GENICpossibly homozygous54489540
79870097198700972AC9GENICpossibly homozygous54489542