chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228633554228633555TC21GENICpossibly homozygous565101736
1228634120228634121TC30GENICpossibly homozygous565101737
1228634427228634428CT37GENIChomozygous565101738
1228634918228634919C-3GENICheterozygous707678067
1228635748228635749AG8GENICheterozygous565101739
1228636362228636363GA21GENICpossibly homozygous565101740
1228637646228637654TTGGGGGG--------5GENICheterozygous707678068
1228638469228638470TC21GENIChomozygous565101741
1228639214228639215TC32GENICpossibly homozygous565101742
1228640028228640029GA26GENIChomozygous565101743
1228640461228640462T-4GENIChomozygous707678069
1228640467228640468TC6GENICheterozygous565101744
1228640924228640925CA24GENICpossibly homozygous565101745
1228640959228640960AG20GENICpossibly homozygous565101746
1228642100228642101AG32GENIChomozygous565101747
1228642501228642502CT22GENICpossibly homozygous565101748
1228644791228644792CT23GENICpossibly homozygous565101749
1228645658228645659AG15GENICpossibly homozygous565101750
1228646084228646086AA--8GENICpossibly homozygous707678070
1228646473228646474TC22GENICpossibly homozygous565101751
1228647502228647503CT26GENICpossibly homozygous565101752
1228647930228647931CT29GENIChomozygous565101753
1228648336228648337TC25GENICpossibly homozygous565101754
1228648904228648905TC37GENIChomozygous565101755
1228649507228649508TC21GENICpossibly homozygous565101756
1228649787228649788TG28GENICpossibly homozygous565101757
1228650664228650665GA28GENIChomozygous565101758
1228651492228651493TC15GENIChomozygous565101759
1228652292228652293CG26GENIChomozygous565101760
1228654072228654073GA27GENICpossibly homozygous565101761
1228654389228654390TC21GENICpossibly homozygous563088561
1228654498228654499TG22GENICpossibly homozygous563088562
1228654518228654519AG20GENICpossibly homozygous563088563