chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4170948283170948283TCTTTATATCCTATA20GENIChomozygous128104494
4170948631170948632TG17GENIChomozygous112951038
4170949316170949317AT24GENIChomozygous112951040
4170950052170950053AC15GENIChomozygous112951042
4170950128170950128TGTG10GENIChomozygous128104495
4170950258170950259AG21GENIChomozygous112951046
4170950341170950350TGTGTGTGT17GENIChomozygous128104496
4170951448170951449TG16GENIChomozygous112951048
4170952998170952999TC12GENIChomozygous112951050
4170954901170954902TC13GENIChomozygous112951082
4170954962170954963AG12GENIChomozygous112951084
4170955124170955124TG11GENIChomozygous128104497
4170955303170955304GA14GENIChomozygous112951086
4170955323170955324CG13GENIChomozygous112951088
4170956427170956428CT19GENIChomozygous112951090
4170956673170956674GT28GENIChomozygous112951092
4170957179170957180GA20GENIChomozygous112951094
4170957231170957232CT22GENIChomozygous112951096
4170957810170957811AG24GENIChomozygous112951099
4170957907170957908CT13GENIChomozygous112951101
4170958916170958916TT12GENIChomozygous128104498
4170959701170959703AC15GENIChomozygous128104499
4170960932170960933TG16GENIChomozygous112951113
4170957912170957913AG14GENIChomozygous112951103
4170959553170959554AG18GENIChomozygous112951107
4170960085170960086AG12GENIChomozygous112951109
4170960102170960103GC6GENIChomozygous112951111
4170961924170961925CT25GENIChomozygous112951117
4170961945170961946AG25GENIChomozygous112951119
4170962453170962454TC25GENIChomozygous112951121
4170962468170962480GTGTGCATGTGT13GENIChomozygous128104502
4170962550170962551GT19GENIChomozygous112951123
4170962567170962568CT17GENIChomozygous112951125
4170962579170962580CT13GENIChomozygous112951127
4170963007170963008GA6GENICheterozygous112951129