chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2127635744127635745GA7GENIChomozygous120148019
2127636447127636448CT9GENIChomozygous110008760
2127640198127640199GT7GENIChomozygous120148021
2127640200127640201GA7GENIChomozygous120148023
2127652113127652114TG9GENIChomozygous120148025
2127652304127652305GT11GENIChomozygous110008777
2127652873127652874AG12GENIChomozygous120148027
2127655866127655867AG5GENIChomozygous110008779
2127656126127656127CT12GENIChomozygous110008780
2127656445127656446CG6GENIChomozygous120148029
2127657300127657301TA15GENIChomozygous110008781
2127657312127657313AG16GENIChomozygous120148031
2127659209127659210AT4GENIChomozygous120148033
2127659782127659783CG5GENIChomozygous111119528
2127660332127660333AG12GENIChomozygous111119530
2127662455127662456AG10GENIChomozygous111119536
2127662729127662730GA8GENIChomozygous111119538
2127663723127663724AC7GENIChomozygous111119540
2127664583127664584AG9GENIChomozygous110008786
2127666753127666754AC16GENIChomozygous110008788
2127667172127667173AC10GENIChomozygous120148035
2127667391127667392TC8GENIChomozygous110008789
2127667464127667465AG6GENIChomozygous111119546
2127669849127669850AG4GENIChomozygous110008791
2127670074127670075TC7GENIChomozygous111119548
2127670143127670144AT9GENIChomozygous111119550
2127670955127670956AG8GENIChomozygous110008792
2127673949127673950GA12GENIChomozygous120148037
2127674167127674168TC9GENIChomozygous110008795
2127674168127674169AG9GENIChomozygous110008796
2127679155127679156AT15GENICpossibly homozygous110008799
2127680020127680021AC8GENIChomozygous110008800
2127680610127680611AG7GENIChomozygous111119563