chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2230368247230368248AG22GENIChomozygous815853495
2230368694230368695TA8GENIChomozygous815853496
2230368695230368696AC8GENIChomozygous815853497
2230369215230369216GA13GENIChomozygous815853498
2230369382230369383TC8GENIChomozygous815853499
2230370442230370443GT10GENIChomozygous815853500
2230370879230370880CT13GENIChomozygous815853501
2230371516230371517CT22GENIChomozygous815853502
2230376837230376838GA15GENIChomozygous815853503
2230377018230377019TC17GENIChomozygous815853504
2230377655230377656GA12GENIChomozygous815853505
2230378780230378781TC13GENIChomozygous815853506
2230381438230381440AC--23GENICheterozygous815853507
2230382465230382466TA22GENIChomozygous815853508
2230383135230383136TC15GENIChomozygous815853509
2230383623230383627AAAT----9GENIChomozygous815853510
2230384374230384375CT19GENIChomozygous815853511
2230385989230385990CT18GENIChomozygous815853512
2230387465230387466C-18GENIChomozygous815853513
2230388651230388652AAT19GENIChomozygous815853514
2230389275230389276TC22GENICpossibly homozygous815853515
2230391222230391223CG15GENIChomozygous815853516
2230391859230391860GC18GENIChomozygous815853517
2230391942230391943AG15GENIChomozygous815853518
2230392250230392251GA16GENIChomozygous815853519
2230392275230392276TTAA8GENIChomozygous815853520
2230392307230392308TTAGAC11GENIChomozygous815853521
2230392879230392880TG15GENIChomozygous815853522
2230394024230394025AG13GENIChomozygous815853523
2230394444230394445TC13GENIChomozygous815853524
2230394461230394462A-8GENIChomozygous815853525
2230394867230394868A-9GENIChomozygous815853526
2230396269230396271AG--21GENIChomozygous815853527
2230398591230398592AG13GENIChomozygous815853528
2230400552230400553AAT13GENIChomozygous815853529
2230401343230401346AAG---8GENIChomozygous815853530
2230401593230401594TC17GENIChomozygous815853531
2230402373230402374CA17GENIChomozygous815853532
2230403043230403044TA13GENIChomozygous815853533