chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31890657818906579CT41GENIChomozygous144636790
31890666218906662ACC24GENIChomozygous136551005
31890694118906942GA50GENIChomozygous136648901
31890712418907125AG48GENIChomozygous136648903
31890714618907147GA48GENIChomozygous136648904
31890737518907376TC76GENIChomozygous136648905
31890753218907533TA66GENICpossibly homozygous136648906
31890780418907805AG59GENIChomozygous136648907
31890810018908101AG55GENIChomozygous136648908
31890834618908347CT63GENIChomozygous144636791
31890840418908405TC55GENIChomozygous136648909
31890844818908449TC66GENIChomozygous136648910
31890904118909042AG60GENIChomozygous144636792
31890982118909822AG54GENIChomozygous144636793
31890986318909864TC50GENIChomozygous144636794
31891003718910038GA56GENIChomozygous144636795
31891014318910144GC48GENIChomozygous136648914
31891042318910424CT47GENIChomozygous144636796
31891092818910929GA41GENIChomozygous144636797
31891103418911035GA50GENIChomozygous144636798
31891109918911100TC49GENIChomozygous144636799
31891125618911257AC36GENIChomozygous136648915
31891169518911696GT50GENIChomozygous144636800
31891184218911843TC47GENIChomozygous136648916
31891282418912825AC46GENIChomozygous144636801
31891301818913019CA34GENIChomozygous136648921
31891302218913023AC31GENIChomozygous136648922
31891334718913348TG29GENICpossibly homozygous136648924
31891367718913678AC42GENIChomozygous144636802
31891384918913850GT43GENIChomozygous144636803
31891476418914765AG50GENIChomozygous144636804
31891478118914782CT50GENIChomozygous144636805
31891074318910744TC42GENIChomozygous141492254