chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3111326567111326568GA15GENIChomozygous111674351
3111327197111327198CT17GENIChomozygous112004930
3111328103111328104GA25GENIChomozygous111674353
3111328256111328256TG20GENIChomozygous130907945
3111328465111328466GA16GENIChomozygous111674355
3111328528111328528TTTTTAT10GENIChomozygous130907946
3111329213111329214GA10GENIChomozygous111674356
3111329959111329959CT15GENIChomozygous127918539
3111330068111330069AT11GENIChomozygous112004932
3111330705111330715GAAGCAGTAG22GENIChomozygous130907947
3111332060111332061CT23GENIChomozygous111674359
3111333526111333527AG15GENIChomozygous111674360
3111333679111333680AT15GENIChomozygous112004934
3111334201111334202AT15GENIChomozygous111674362
3111334504111334504G21GENIChomozygous127918540
3111335997111335998C6GENIChomozygous127918541
3111336005111336008TTA5GENICheterozygous127918542
3111337577111337578CA13GENIChomozygous111674371
3111335931111335932AG13GENIChomozygous111674364
3111336817111336818GA28GENIChomozygous111674366
3111337044111337045TC21GENIChomozygous111674367
3111337201111337202AG15GENIChomozygous111674369
3111330060111330061AT11GENIChomozygous119651130
3111338561111338562GA9GENIChomozygous111674373
3111338592111338593G10GENIChomozygous127918543
3111338618111338619TC10GENIChomozygous111674375
3111340796111340797AT19GENIChomozygous111674377
3111340808111340809TC17GENIChomozygous111674379
3111341442111341443TC23GENIChomozygous111674381
3111341524111341525GC17GENIChomozygous112004936
3111342111111342112AG20GENIChomozygous111674385
3111342284111342285TC7GENIChomozygous112004938
3111344870111344871TC18GENIChomozygous111674386
3111346731111346732TC14GENIChomozygous111674392
3111349259111349259AAAC13GENIChomozygous132459014
3111349384111349385TG12GENIChomozygous111674401
3111351275111351275TA8GENIChomozygous127918546
3111347747111347748GA12GENIChomozygous112139179
3111345621111345622CT13GENIChomozygous112139178