chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108709204787092048GA20GENIChomozygous650021298
108709221787092218AG18GENIChomozygous650021299
108709243387092434TC9GENIChomozygous650021300
108709380887093809CCA19GENIChomozygous757128394
108709406687094067CT13GENIChomozygous650021301
108709412487094125TC14GENIChomozygous650021302
108709412887094129GGGA14GENIChomozygous757128395
108709424487094245TC23GENIChomozygous650021303
108709454387094544T-14GENICpossibly homozygous757128396
108709466787094668TG20GENIChomozygous650021304
108709469987094700AG24GENIChomozygous650021305
108709476587094766GA16GENIChomozygous650021306
108709495987094960GT19GENIChomozygous650021307
108709508487095085CT21GENIChomozygous650021308
108709520287095203CA15GENIChomozygous650021309
108709529587095297AT--11GENIChomozygous757128398
108709556987095570AG26GENIChomozygous650021310
108709586287095863GA14GENIChomozygous650021311
108709588487095899CCTCCACCGAAGCTG---------------9GENIChomozygous757128399
108709673287096733AG11GENIChomozygous650021312
108709673887096739TTA8GENIChomozygous757128400
108709745387097454GA25GENIChomozygous650021313
108709746787097468TC21GENIChomozygous650021314
108709748287097483GA18GENIChomozygous650021315
108709751387097514CT25GENIChomozygous650021316
108709757487097575T-20GENIChomozygous757128401
108709885087098851AG24GENIChomozygous650021317
108709945687099457TC32GENIChomozygous650021318
108709957187099572TC25GENIChomozygous650021319
108709963187099632TC18GENIChomozygous650021320
108709989987099900TC26GENIChomozygous650021321
108709991487099916AC--11GENIChomozygous757128402
108709994787099948TC19GENIChomozygous650021322
108709996587099966AG21GENIChomozygous650021323
108710003687100037CT26GENIChomozygous650021324
108710013487100135TA19GENIChomozygous650021325