chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4168689596168689597TTA27INTERGENICpossibly homozygous59652038
4168690386168690387CA29INTERGENIChomozygous59652039
4168690454168690455TC32INTERGENIChomozygous57847216
4168690495168690496TC28INTERGENIChomozygous57847217
4168690730168690731CT23INTERGENIChomozygous59652040
4168690810168690811TC37INTERGENIChomozygous59652041
4168690909168690910AC28INTERGENIChomozygous59652042
4168690917168690918AG26INTERGENIChomozygous59652043
4168690949168690950CA26INTERGENIChomozygous59652044
4168690950168690951CT27INTERGENIChomozygous59652045
4168690964168690965TA28INTERGENIChomozygous59652046
4168691017168691018GC26INTERGENIChomozygous59652047
4168691159168691160TC29INTERGENIChomozygous59652048
4168691198168691199GA30INTERGENIChomozygous59652049
4168691808168691809TC24INTERGENIChomozygous57847219
4168693225168693247TCTGTCTCTGTCTCTGTCTCTG----------------------15INTERGENIChomozygous58290851
4168693307168693308CT27INTERGENIChomozygous59652050
4168693489168693490GA34INTERGENIChomozygous59652051
4168693640168693641AG26INTERGENIChomozygous57847222
4168693703168693704AG32INTERGENIChomozygous59652052
4168693780168693781CT19INTERGENIChomozygous58183651
4168693849168693850TC31INTERGENICpossibly homozygous59652053
4168693981168693982AG29INTERGENIChomozygous59652054
4168694053168694054CT18INTERGENIChomozygous59652055