chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101288104412881045AC8GENICheterozygous635462403
101288105112881052GC8GENICheterozygous635462404
101288108412881085AG15GENIChomozygous635462405
101288263112882635ATAT----12GENIChomozygous748123415
101288271712882721ATAT----7GENIChomozygous748123416
101288317012883171CCA22GENICpossibly homozygous748123417
101288342712883432AAAAC-----17GENICheterozygous748123418
101288342812883432AAAC----15GENICheterozygous748123419
101288555912885560GT43GENIChomozygous635462406
101288586912885870TC21GENIChomozygous635462407
101288598612885987CCT7GENICheterozygous748123420
101288620912886210TG17GENIChomozygous635462408
101288646712886468TC29GENIChomozygous635462409
101288653112886532GA23GENICpossibly homozygous635462410
101288682512886826AG35GENIChomozygous635462411
101288705512887056GA35GENIChomozygous635462412
101288788912887890CA31GENIChomozygous635462413
101288821012888211TTACACAC3GENICheterozygous748123422
101288821012888211TTACACACAC3GENICheterozygous748123423
101288872312888724TA28GENIChomozygous635462414
101288966612889667GC39GENIChomozygous635462415
101288993512889936CG42GENIChomozygous635462416
101288995712889958TC42GENIChomozygous635462417
101289005012890051AG24GENIChomozygous635462418
101289099212890993GA21GENIChomozygous635462419
101289122212891223TC36GENIChomozygous635462420