chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1127303329127303330CT16GENIChomozygous109135527
1127303805127303806CT29GENIChomozygous109135533
1127304264127304265CG28GENIChomozygous120569454
1127305326127305327CT29GENIChomozygous120569456
1127307399127307400GA30GENIChomozygous109135563
1127307708127307709CT27GENIChomozygous120569458
1127309122127309123GT26GENIChomozygous109135573
1127312964127312965GC28GENIChomozygous109135591
1127313081127313082TG31GENIChomozygous109135593
1127313769127313770TC21GENIChomozygous120569460
1127314475127314476AG12GENIChomozygous109135595
1127315466127315467AG27GENIChomozygous109135601
1127316917127316918AG27GENIChomozygous109135619
1127317094127317095TC32GENIChomozygous109135626
1127318274127318275AG22GENIChomozygous109135632
1127321250127321251AC25GENIChomozygous109135642
1127321579127321580AG25GENIChomozygous109135648
1127321641127321642GA22GENIChomozygous120569462
1127325133127325134GC28GENIChomozygous108223601
1127325078127325079CT37GENIChomozygous108223599
1127325443127325444AG16GENIChomozygous109135690
1127325708127325709AG17GENIChomozygous108223603
1127327632127327633GC20GENIChomozygous108223604
1127327648127327649GA20GENIChomozygous108223606
1127327719127327720TG6GENIChomozygous120514781
1127328157127328158TC2GENIChomozygous120514782
1127330962127330963AG25GENIChomozygous109135719
1127332045127332046CT22GENIChomozygous120569464
1127332723127332724AG27GENIChomozygous109135723
1127333523127333524GC27GENIChomozygous109135725
1127333794127333795TC26GENICpossibly homozygous109135727
1127334185127334186TC18GENIChomozygous109135729
1127335366127335367CT29GENIChomozygous109135731
1127335841127335842CT26GENIChomozygous109135733
1127337066127337067AG18GENIChomozygous109135735
1127337400127337401CT13GENIChomozygous109135737