chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101288104412881045AC9GENIChomozygous541169259
101288105112881052GC10GENICheterozygous541169260
101288108412881085AG16GENIChomozygous541169261
101288263112882635ATAT----4GENICheterozygous697646653
101288317012883171CCA31GENIChomozygous697646654
101288555912885560GT42GENICpossibly homozygous538612385
101288586912885870TC26GENIChomozygous538612386
101288620912886210TG31GENIChomozygous538612387
101288646712886468TC18GENIChomozygous541169262
101288653112886532GA18GENIChomozygous538612388
101288682512886826AG36GENIChomozygous538612389
101288705512887056GA13GENIChomozygous538612390
101288788912887890CA29GENIChomozygous541169263
101288821012888211TTACAC11GENIChomozygous697646655
101288872312888724TA34GENIChomozygous538612391
101288966612889667GC48GENIChomozygous538612392
101288993512889936CG31GENIChomozygous538612393
101288995712889958TC32GENIChomozygous538612394
101289005012890051AG33GENIChomozygous538612395
101289099212890993GA28GENIChomozygous538612396
101289122212891223TC24GENIChomozygous538612397