chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31890657818906579CT11GENIChomozygous144636790
31890666218906662ACC8GENIChomozygous136551005
31890694118906942GA10GENIChomozygous136648901
31890712418907125AG15GENIChomozygous136648903
31890714618907147GA12GENIChomozygous136648904
31890737518907376TC19GENIChomozygous136648905
31890753218907533TA15GENIChomozygous136648906
31890780418907805AG22GENIChomozygous136648907
31890810018908101AG24GENIChomozygous136648908
31890834618908347CT18GENICpossibly homozygous144636791
31890840418908405TC18GENIChomozygous136648909
31890982118909822AG16GENIChomozygous144636793
31890844818908449TC15GENIChomozygous136648910
31890904118909042AG21GENIChomozygous144636792
31890986318909864TC18GENIChomozygous144636794
31891003718910038GA14GENIChomozygous144636795
31891014318910144GC19GENIChomozygous136648914
31891042318910424CT18GENIChomozygous144636796
31891074318910744TC12GENIChomozygous141492254
31891092818910929GA11GENIChomozygous144636797
31891103418911035GA10GENIChomozygous144636798
31891109918911100TC13GENIChomozygous144636799
31891125618911257AC13GENIChomozygous136648915
31891169518911696GT22GENIChomozygous144636800
31891184218911843TC13GENIChomozygous136648916
31891282418912825AC6GENIChomozygous144636801
31891301818913019CA14GENIChomozygous136648921
31891302218913023AC13GENIChomozygous136648922
31891334718913348TG17GENIChomozygous136648924
31891367718913678AC16GENIChomozygous144636802
31891384918913850GT15GENIChomozygous144636803
31891476418914765AG16GENIChomozygous144636804
31891478118914782CT18GENIChomozygous144636805