chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184060816540608166GT7GENIChomozygous46427624
184060913440609135AG9GENIChomozygous46427628
184060922040609221AG7GENIChomozygous46427630
184060963040609631AG3GENICheterozygous46427631
184061107540611076GGTTT1GENIChomozygous46427638
184061194540611946AG9GENIChomozygous46427640
184061304940613050CA16GENICpossibly homozygous46427645
184061710140617102GA7GENIChomozygous46427649
184061773440617735TC12GENICpossibly homozygous46427652
184061774840617749GT8GENIChomozygous46427654
184061833040618331GA12GENICpossibly homozygous46427656
184061875240618753GA24GENICpossibly homozygous46427658
184061904140619042AG24GENICpossibly homozygous46427659
184061928940619290AG21GENIChomozygous46427661
184062017040620171AG22GENIChomozygous46427663
184062099840620999GA12GENIChomozygous46427665
184062283840622839AG13GENICheterozygous46427667
184062301440623015GA18GENIChomozygous46427669
184062450740624508TTTC8GENICheterozygous46427676
184062465840624659GC20GENICpossibly homozygous46427677
184062819840628199GA13GENIChomozygous46427683
184062860140628602CT4GENIChomozygous46427684
184063123440631235GA10GENIChomozygous46427688
184063172440631725GA13GENICpossibly homozygous46427690
184063333540633336AC15GENICpossibly homozygous46427692
184063387540633876GA22GENICpossibly homozygous46427694