chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191034059310340594CT24GENIChomozygous109633596
191034117810341179AC17GENIChomozygous109633598
191034130810341309AG17GENIChomozygous109764542
191034219110342192GA19GENIChomozygous109633600
191034284110342842AG19GENIChomozygous109633602
191034289110342892AG20GENIChomozygous109633604
191034577310345774CT16GENIChomozygous109633606
191034577810345779AG16GENIChomozygous109633608
191034659810346599GA13GENICheterozygous132512714
191034826310348264TC25GENIChomozygous109633610
191034956710349568CT18GENIChomozygous109633612
191035045210350453GA14GENIChomozygous109633614
191034659110346591TT13GENICheterozygous132918331
191034905510349062GGGGAGT22GENIChomozygous129583440
191035259510352596C21GENIChomozygous129583441
191035371710353723TCTCTC19GENIChomozygous129583442
191035372510353725G19GENIChomozygous129583443
191035372610353726ACATGAGC19GENIChomozygous129583444
191035496710354968TC27GENIChomozygous109633616
191035502110355022TC18GENIChomozygous109633618
191035552610355527GA17GENIChomozygous109633620
191035762910357630AG19GENIChomozygous109633622
191035848210358483CT15GENIChomozygous109633624
191035900410359005GT17GENIChomozygous109633626
191035921210359213AG19GENIChomozygous109633628