chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84094415740944158A-13GENICheterozygous771145552
84094417940944183TCGT----26GENICheterozygous771145553
84094446340944464AAT271GENICheterozygous771145554
84094471540944716G-129GENICheterozygous771145555
84094483540944836C-85GENICheterozygous771145556
84094537740945378TTG146GENICheterozygous771145557
84094773140947732C-120GENICheterozygous771145558
84094826440948265T-161GENICheterozygous771145559
84094984940949851AA--9GENICheterozygous771145560
84094985040949851A-9GENICheterozygous771145561
84095043640950437A-28GENICheterozygous771145562
84095794940957950GGCTT25GENICheterozygous771145563
84095844140958442T-57GENICheterozygous771145564
84096328240963283T-32GENICheterozygous771145565
84096347740963478CCT27GENICheterozygous771145566
84096380540963806CCTTT16GENICheterozygous771145569
84096380640963808TT--16GENICheterozygous771145567
84096539740965398CCA11GENICheterozygous771145571
84096629840966301CTT---59GENICheterozygous771145572
84096766740967668A-42GENICheterozygous771145573
84096832340968324AACATAGC31GENICheterozygous771145574
84096840440968405A-13GENICpossibly homozygous771145575
84096867240968673C-35GENICheterozygous771145576
84096902140969022C-9GENICheterozygous771145577
84096955640969557T-154GENICheterozygous771145578
84096998540969986G-154GENICheterozygous771145579
84097026040970261GGCAAGGA5GENICheterozygous771145580
84097608440976085T-125GENICheterozygous771145581
84097616940976170TTA75GENICheterozygous771145582
84098080840980809CCAT39GENICheterozygous771145583
84098087240980873TTC5GENICheterozygous771145584
84098213240982136TGAT----38GENICheterozygous771145585
84098246840982471AAC---20GENICheterozygous771145586