chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191034059310340594CT22GENIChomozygous109633596
191034117810341179AC14GENIChomozygous109633598
191034219110342192GA16GENIChomozygous109633600
191034284110342842AG24GENIChomozygous109633602
191034289110342892AG18GENIChomozygous109633604
191034577310345774CT21GENIChomozygous109633606
191034577810345779AG21GENIChomozygous109633608
191034826310348264TC19GENIChomozygous109633610
191034956710349568CT19GENIChomozygous109633612
191035045210350453GA15GENICpossibly homozygous109633614
191034130810341309AG21GENIChomozygous109764542
191035371710353723TCTCTC22GENIChomozygous129583442
191035259510352596C16GENIChomozygous129583441
191034905510349062GGGGAGT13GENIChomozygous129583440
191035372510353725G22GENIChomozygous129583443
191035372610353726ACATGAGC20GENIChomozygous129583444
191035496710354968TC14GENIChomozygous109633616
191035502110355022TC16GENIChomozygous109633618
191035552610355527GA19GENIChomozygous109633620
191035762910357630AG18GENIChomozygous109633622
191035848210358483CT19GENIChomozygous109633624
191035900410359005GT21GENIChomozygous109633626
191035921210359213AG17GENIChomozygous109633628