chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5122665391122665392TC65GENIChomozygous137607815
5122666478122666479TC58GENIChomozygous137607816
5122666716122666717CT66GENIChomozygous137607817
5122667283122667284CA45GENIChomozygous137607818
5122667600122667601GA49GENIChomozygous137607819
5122667667122667668TC50GENIChomozygous137607820
5122667900122667901CT31GENIChomozygous137607821
5122667997122667998CT42GENIChomozygous137607822
5122668191122668192GA49GENIChomozygous137607823
5122668375122668376AC51GENIChomozygous137607824
5122668509122668510TG41GENIChomozygous137607825
5122668774122668775GA52GENICpossibly homozygous137607826
5122669051122669052CT46GENIChomozygous137607827
5122670506122670507CT43GENIChomozygous137607828
5122671038122671038C50GENIChomozygous137338021
5122671117122671118GA55GENIChomozygous137607829
5122671236122671237CT33GENIChomozygous137607830
5122671517122671518GC58GENIChomozygous137607831
5122671583122671583T43GENICpossibly homozygous137338022
5122671863122671864AG48GENIChomozygous137607832
5122672027122672028TC44GENIChomozygous137607833
5122674416122674417GT43GENIChomozygous137607834
5122676706122676724CTTTCTCCTTTTCCTCCC14GENICpossibly homozygous137338023
5122679216122679217GA60GENIChomozygous137607835