chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108709204787092048GA27GENIChomozygous553668348
108709221787092218AG16GENIChomozygous553668349
108709243387092434TC14GENIChomozygous553668350
108709380887093809CCA19GENICpossibly homozygous701608093
108709406687094067CT28GENIChomozygous553668351
108709412487094125TC17GENIChomozygous555419949
108709412887094129GGGA17GENIChomozygous701608094
108709424487094245TC27GENIChomozygous553668352
108709454387094544T-9GENIChomozygous701608095
108709466787094668TG19GENIChomozygous553668353
108709469987094700AG17GENIChomozygous553668354
108709476587094766GA29GENIChomozygous553668355
108709495987094960GT24GENIChomozygous553668356
108709508487095085CT26GENIChomozygous553668357
108709520287095203CA17GENIChomozygous553668358
108709529587095297AT--9GENIChomozygous701608097
108709556987095570AG33GENIChomozygous553668359
108709586287095863GA22GENIChomozygous553668360
108709588487095899CCTCCACCGAAGCTG---------------16GENIChomozygous701608098
108709673287096733AG15GENIChomozygous553668361
108709673887096739TTA13GENIChomozygous701608099
108709745387097454GA22GENIChomozygous553668362
108709746787097468TC22GENIChomozygous553668363
108709748287097483GA20GENIChomozygous553668364
108709751387097514CT16GENIChomozygous553668365
108709757487097575T-16GENIChomozygous701608100
108709885087098851AG21GENIChomozygous553668366
108709945687099457TC35GENIChomozygous553668367
108709957187099572TC24GENIChomozygous553668368
108709963187099632TC29GENIChomozygous553668369
108709989987099900TC25GENIChomozygous553668370
108709991487099916AC--19GENIChomozygous701608101
108709994787099948TC28GENIChomozygous553668371
108709996587099966AG24GENIChomozygous553668372
108710003687100037CT33GENIChomozygous553668373
108710013487100135TA19GENIChomozygous553668374