chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108709243387092434TC22GENIChomozygous529744981
108709320887093209AG20GENIChomozygous529744982
108709380887093809CCA24GENIChomozygous694421923
108709412487094125TC7GENIChomozygous532398800
108709412487094125TTG4GENIChomozygous694421924
108709424487094245TC33GENIChomozygous529744983
108709436287094363GT29GENIChomozygous532398801
108709454387094544T-19GENICpossibly homozygous694421925
108709466787094668TG18GENIChomozygous529744984
108709469987094700AG20GENIChomozygous529744985
108709476587094766GA19GENIChomozygous529744986
108709508487095085CT18GENIChomozygous529744987
108709529587095297AT--8GENIChomozygous694421926
108709556987095570AG25GENICpossibly homozygous529744988
108709586287095863GA28GENIChomozygous529744989
108709589887095899GT22GENICheterozygous532398802
108709673287096733AG19GENIChomozygous529744990
108709673887096739TTA16GENIChomozygous694421927
108709710787097108GT23GENICpossibly homozygous532398803
108709746787097468TC12GENIChomozygous529744991
108709748287097483GA13GENIChomozygous529744992
108709757487097575T-12GENIChomozygous694421928
108709772087097721AC21GENIChomozygous529744993
108709885087098851AG25GENIChomozygous529744994
108709945687099457TC24GENIChomozygous529744995
108709955487099555GT25GENIChomozygous532398804
108709957187099572TC18GENIChomozygous529744996
108709963187099632TC23GENIChomozygous529744997
108709989987099900TC14GENIChomozygous529744998
108709991387099914AAACAC6GENIChomozygous694421929
108709994787099948TC13GENIChomozygous529744999
108709996587099966AG10GENIChomozygous529745000
108710003687100037CT18GENIChomozygous529745001
108710013487100135TA24GENIChomozygous529745002
108710054487100545CT20GENIChomozygous529745003