chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104541521245415213GA14GENIChomozygous51442430
104541562045415621CT12GENIChomozygous51442431
104541836345418364TC16GENIChomozygous51442434
104541883645418837AG14GENIChomozygous51442436
104541940545419406CT11GENIChomozygous51442438
104541948845419489TC13GENIChomozygous51442439
104542091445420915TC13GENIChomozygous51442440
104542121445421215GA14GENIChomozygous51442441
104542135245421353TC17GENIChomozygous51442442
104542303945423040GA14GENIChomozygous51442444
104542335045423351TC10GENIChomozygous51442445
104542351445423515AG15GENIChomozygous51442446
104542419745424198TC10GENIChomozygous51442447
104542433345424334AG13GENIChomozygous51442448
104542493445424935GA13GENIChomozygous51442449
104542778845427789AC14GENIChomozygous51636257
104542910545429106TC13GENIChomozygous51442461
104542942045429421CA16GENIChomozygous51636258
104543023645430237AG20GENIChomozygous51442463
104543067545430676AAT13GENIChomozygous51442464
104543213845432139AG10GENIChomozygous51442466
104543223545432236AG7GENIChomozygous51442467
104543254445432545AG10GENIChomozygous52193276
104543294445432945TTAATAATAAC12GENICheterozygous51873652
104543382745433828A-11GENIChomozygous51442471
104543386945433870TA15GENIChomozygous51442472
104543454445434545TG17GENIChomozygous51442475
104543472945434730GA10GENIChomozygous52052513
104543490645434907TC17GENIChomozygous52052517
104543545245435453AG15GENIChomozygous52052519
104543611745436118CT12GENIChomozygous52193280
104544052345440524CT16GENIChomozygous52193282
104544070745440708GT13GENIChomozygous52193284
104544114045441141GA14GENIChomozygous52052525
104543292145432922CCATA10GENICheterozygous53558800
104543431145434319TCCTTCCT--------7GENIChomozygous53558801