chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91021647810216479CA24GENIChomozygous979669564
91022251410222515CT86GENIChomozygous979669565
91022284210222843CT30GENIChomozygous979669566
91022439010224391CA47GENIChomozygous979669567
91022637410226375AC19GENIChomozygous979669568
91023050210230503AG24GENIChomozygous979669569
91023361210233613TG27GENIChomozygous979669570
91023446010234461AC19GENIChomozygous979669571
91023561510235616GC26GENIChomozygous979669572
91023912110239122AG42GENIChomozygous979669573
91023982010239821TC68GENIChomozygous979669574
91023983310239834GC70GENIChomozygous979669575
91023983510239836GC70GENIChomozygous979669576
91023984210239843AC73GENIChomozygous979669577
91023984510239846AC72GENIChomozygous979669578
91024266110242662AC46GENIChomozygous979669579
91024309810243099TC73GENIChomozygous979669580
91024486110244862AG68GENIChomozygous979669581
91024592410245925TC55GENIChomozygous979669582
91024610910246110GT73GENIChomozygous979669583
91024859510248596CT79GENIChomozygous979669584
91024872610248727CT85GENIChomozygous979669585
91024957910249580AG28GENIChomozygous979669586
91024964710249648TC25GENIChomozygous979669587
91024999610249997CT68GENIChomozygous979669588
91025113810251139CT61GENIChomozygous979669589
91025343810253439GA38GENIChomozygous979669590
91025374710253748AG26GENIChomozygous979669591
91025415110254152CG22GENICpossibly homozygous979669592
91025571910255720CT19GENIChomozygous979669593
91025859510258596GT37GENIChomozygous979669594
91026048710260488CT13GENIChomozygous979669595
91026162810261629GC53GENIChomozygous979669596
91026706410267065AG21GENIChomozygous979669597
91026819110268192GA55GENIChomozygous979669598
91026852410268525AG39GENIChomozygous979669599
91027007010270071GA49GENIChomozygous979669600
91027011610270117TC46GENIChomozygous979669601
91027011810270119GA44GENIChomozygous979669602
91027091810270919CT52GENIChomozygous979669603
91027117910271180TC56GENIChomozygous979669604
91027947210279473TC45GENICpossibly homozygous979669605