chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31890666218906662ACC26GENIChomozygous136551005
31890694118906942GA20GENIChomozygous136648901
31890694418906945CT19GENIChomozygous136648902
31890712418907125AG42GENIChomozygous136648903
31890714618907147GA40GENIChomozygous136648904
31890737518907376TC55GENIChomozygous136648905
31890753218907533TA55GENIChomozygous136648906
31890780418907805AG54GENIChomozygous136648907
31890810018908101AG42GENIChomozygous136648908
31890840418908405TC54GENIChomozygous136648909
31890844818908449TC47GENIChomozygous136648910
31890859418908595AC35GENICpossibly homozygous136648911
31890885218908853CG43GENIChomozygous136648912
31890920218909203GA54GENIChomozygous136648913
31891014318910144GC40GENIChomozygous136648914
31891074318910743CTT29GENIChomozygous136551006
31891125618911257AC43GENIChomozygous136648915
31891184218911843TC40GENIChomozygous136648916
31891206218912063CT44GENIChomozygous136648917
31891235318912354TA47GENICpossibly homozygous136648918
31891241418912415AG51GENIChomozygous136648919
31891279218912793GT28GENIChomozygous136648920
31891301818913019CA29GENIChomozygous136648921
31891302218913023AC30GENIChomozygous136648922
31891317318913174CT36GENIChomozygous136648923
31891334718913348TG55GENIChomozygous136648924
31891393018913931GA34GENIChomozygous136648925
31891394718913947A34GENIChomozygous136551007