chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124770613947706140AAGT17INTERGENICheterozygous50487456
124771296847712969AT16INTERGENICpossibly homozygous50223115
124771299047712991CA2INTERGENIChomozygous50223117
124771299247712993CA2INTERGENIChomozygous50223119
124771308947713090CA1INTERGENIChomozygous50223145
124771309447713095TC1INTERGENIChomozygous50223147
124771310147713102CA1INTERGENIChomozygous50223149
124771312547713126CA3INTERGENIChomozygous50223151
124771312747713128CA3INTERGENIChomozygous50223153
124771313247713133CA4INTERGENIChomozygous50223155
124771314647713147CA9INTERGENIChomozygous50223157
124771435747714358A-11INTERGENIChomozygous50223163
124771436047714361CG13INTERGENICpossibly homozygous50343210
124771440447714405GA14INTERGENIChomozygous50513490
124771450847714509CCT7INTERGENICheterozygous50223167
124771451147714512A-8INTERGENICheterozygous50223169
124771456747714568GT8INTERGENICheterozygous50223171
124771458347714584GA4INTERGENIChomozygous50223173
124771458447714585CA4INTERGENIChomozygous50513492
124771458647714587GC4INTERGENIChomozygous50513494
124771460847714609CT3INTERGENICheterozygous50223175
124771460947714610AT3INTERGENICheterozygous50223177
124773373947733740TTGAGCACAGGCACACCTGGGTATAGGGTACACCTG3INTERGENICheterozygous50513496
124773541447735417GTT---9INTERGENICheterozygous50223195