chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157648888157648891TTG19GENICheterozygous143064534
4157649696157649696G42GENIChomozygous136925257
4157650358157650359GA60GENIChomozygous143167507
4157651600157651601TG57GENIChomozygous143167508
4157653188157653191TCT31GENIChomozygous143064535
4157653970157653971GA53GENIChomozygous143167509
4157654118157654119AC41GENIChomozygous143167510
4157654350157654351GA36GENIChomozygous143167511
4157655099157655100AG28GENIChomozygous143167512
4157655215157655216AG14GENIChomozygous143167513
4157655219157655220GC15GENIChomozygous143167514
4157655917157655918CT8GENIChomozygous143167515
4157656408157656409AG40GENIChomozygous143167516
4157656654157656655AC43GENICpossibly homozygous143167517
4157656856157656857GT48GENIChomozygous143167518
4157656947157656948GA53GENIChomozygous143167519
4157656951157656952GC53GENIChomozygous143167520
4157657489157657489TGA28GENIChomozygous136925259
4157657523157657524G23GENIChomozygous143064536
4157655909157655910TC8GENIChomozygous154221631
4157657502157657503TG22GENICpossibly homozygous154221634
4157657755157657756AG7GENIChomozygous143167521
4157658248157658249TA51GENIChomozygous143167522
4157658655157658656GT36GENIChomozygous143167523
4157658809157658809CGGCAC44GENIChomozygous143064537
4157659834157659835AG48GENIChomozygous137248781
4157657502157657503T22GENICheterozygous403125165
4157654956157654957GA5GENICheterozygous403125163
4157654956157654957G5GENIChomozygous403125164
4157660105157660105GT18GENIChomozygous143064538
4157660697157660701TCTG34GENIChomozygous143064539
4157661066157661067GT37GENICpossibly homozygous143167524
4157661632157661633AG28GENIChomozygous137248782
4157657523157657524GT23GENICheterozygous403590786
4157660737157660737TCTG38GENIChomozygous143064540
4157661767157661767GG16GENIChomozygous143064541