chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
43461493034614931CT20GENIChomozygous57926072
43461708234617083TC26GENICpossibly homozygous56815549
43461781934617820TC19GENICpossibly homozygous57718508
43461803834618039TC16GENIChomozygous57718510
43461913934619140GA25GENICpossibly homozygous57718513
43461947634619477GT21GENICpossibly homozygous56815569
43462030134620302AG20GENIChomozygous56815573
43462032134620322CT19GENICpossibly homozygous57718515
43462048134620482CT6GENICheterozygous57718517
43462070434620705GA8GENICpossibly homozygous57718519
43462070934620710CA7GENICpossibly homozygous57718521
43462073734620738CT24GENICpossibly homozygous56815579
43462114734621148AG16GENIChomozygous57718523
43462115234621155AAA---14GENIChomozygous57718524
43462131434621315GT17GENICpossibly homozygous57718525
43462151934621520GGA3GENICheterozygous56815581
43462189634621897TC5GENICheterozygous57718527
43462243834622439CT26GENIChomozygous56815589
43462271834622719TTTG12GENICheterozygous56815593
43462276834622769GA16GENICpossibly homozygous56815595
43462291534622916TC10GENICpossibly homozygous56815599
43462308234623083A-5GENIChomozygous56815601
43462309034623091GA7GENIChomozygous56815603
43462356534623566AG24GENICpossibly homozygous56815607
43462403534624036GA15GENICpossibly homozygous56815609
43462423234624233TC21GENIChomozygous56815611