chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064511110645112TC13GENIChomozygous46059628
191064519710645198AG12GENICheterozygous46059630
191064526210645263TG17GENICpossibly homozygous46486199
191064567010645671CG13GENIChomozygous46486202
191064577110645772GA19GENIChomozygous46486204
191064579210645793AG20GENIChomozygous46486206
191064621610646217TC7GENIChomozygous46059633
191064626510646266GA5GENIChomozygous46059634
191064643510646436TC13GENIChomozygous46486208
191064673710646738TC2GENIChomozygous46059639
191064674510646746TA4GENICheterozygous46059640
191064717710647192GGGGGGGGGGGGTGG---------------3GENICheterozygous46486212
191064740510647406TTC14GENIChomozygous46059643
191064832410648325CCA10INTERGENIChomozygous46486214
191064837910648380GC22INTERGENICpossibly homozygous46059648
191065129610651297AC23INTERGENIChomozygous46059650
191065159510651596CT15INTERGENIChomozygous46059651
191065183410651835CT10INTERGENIChomozygous46059653
191065223210652233TG12INTERGENIChomozygous46059658
191065325410653255TC8INTERGENIChomozygous46059661
191065325610653257CCG8INTERGENICheterozygous46486216