chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143783641143783642GGT9GENIChomozygous60878506
1143786235143786236CCTAT7GENIChomozygous61532450
1143787059143787060CT10GENIChomozygous61532451
1143787722143787723TA9GENICpossibly homozygous60878507
1143787750143787751A-11GENIChomozygous60878508
1143788785143788786GA14GENIChomozygous61532456
1143790450143790451CG6GENICheterozygous60878521
1143790615143790616A-4GENICheterozygous61532459
1143792403143792404TC4GENIChomozygous60878524
1143793598143793599GT11GENIChomozygous61532463
1143794620143794621CG11GENICpossibly homozygous60878528
1143797014143797015CT20GENIChomozygous62480962
1143797597143797598GT14GENICpossibly homozygous61532470
1143798503143798504GA9GENICheterozygous60878537
1143799164143799165TC22GENICpossibly homozygous60878538
1143799269143799270TG18GENICpossibly homozygous60878539
1143800356143800357TG12GENICpossibly homozygous60878541
1143800641143800642AAC6GENIChomozygous60878542
1143802015143802016AC13GENICpossibly homozygous60878545
1143802162143802163CT9GENIChomozygous60878546
1143805080143805081GGC16GENIChomozygous60878566
1143805117143805118AC2GENIChomozygous60878567
1143805170143805171T-1GENIChomozygous60878570
1143805174143805175AC5GENICheterozygous60878571
1143805272143805273AC2GENIChomozygous60878572
1143806055143806056TC18GENICpossibly homozygous60878575
1143806290143806291AAT5GENIChomozygous60878576
1143806333143806334GA13GENICpossibly homozygous60878577
1143807034143807035TG7GENIChomozygous60878579
1143807391143807392TC7GENICpossibly homozygous60878580
1143809430143809431TA16GENIChomozygous60878584
1143809939143809940CG13GENICheterozygous60878585
1143810121143810122TC15GENIChomozygous60878586
1143811045143811046GA14GENIChomozygous60878589
1143814952143814953TC16GENIChomozygous60878590