chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18597930885979309TC14GENIChomozygous142842935
18597959385979594CG23GENIChomozygous145277521
18598487585984876TC19GENIChomozygous142842939
18598502085985021TC16GENIChomozygous142842940
18598547085985471CT30GENIChomozygous145277529
18598612285986123TA13GENIChomozygous142842941
18598618385986184GA16GENIChomozygous142842943
18598625785986258AC14GENIChomozygous145277530
18598653785986538GA18GENIChomozygous142842944
18598678385986784CT15GENIChomozygous142842945
18598734585987346TG14GENIChomozygous142842946
18598824285988243GC22GENIChomozygous142842948
18598884085988841AG12GENIChomozygous142842951
18597984385979844GA30GENIChomozygous147929007
18598760285987603CT19GENIChomozygous147929008
18598878985988790CT16GENIChomozygous147929009
18598881285988813TA11GENIChomozygous147929010
18597990385979903CACCTGTACCTGATGTACCTGCAAGTTCCCTGTGCATCTG18GENIChomozygous135412128
18598630785986308AG18GENIChomozygous144545986
18598773185987734TTC11GENIChomozygous147894602
18599112685991126TG27GENICpossibly homozygous142790336
18598030685980307C10GENICheterozygous402951676
18598030685980307CT10GENIChomozygous402951677
18599115485991154ATAG11GENICheterozygous147894603
18599122285991223CT18GENIChomozygous147929011
18599122485991225CT19GENIChomozygous147929012
18599122685991227CT20GENIChomozygous147929013
18599123485991236CA20GENIChomozygous147894604
18599124385991244GT23GENIChomozygous147929014
18599151585991516TA16GENIChomozygous142842953
18599197585991976TG19GENIChomozygous147929015
18599260685992607CA21GENIChomozygous147929016
18599322885993229CT20GENICpossibly homozygous147929017