chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121838534918385350TC10GENIChomozygous50091792
121838632718386328AG16GENIChomozygous50091812
121838648418386485TC15GENIChomozygous50091814
121838648518386486GA16GENIChomozygous50465590
121838696018386961TC30GENIChomozygous50091818
121838710418387105TC20GENIChomozygous50091820
121838713218387133AG19GENIChomozygous50091822
121838725718387261AAAA----17GENIChomozygous50465592
121838835618388357TC14GENIChomozygous50465594
121838846618388472CACACA------6GENICheterozygous50091826
121838871618388717TC20GENICpossibly homozygous50465596
121838872418388746ATATATATATATATATATATAT----------------------24GENICheterozygous50091836
121838872618388746ATATATATATATATATATAT--------------------24GENICpossibly homozygous50091838
121838880318388804GA26GENIChomozygous50465598
121838895118388952AG12GENIChomozygous50091842
121838902318389024TC16GENIChomozygous50091844
121838912218389123GA24GENIChomozygous50465600
121838957718389578CG25GENIChomozygous50465602
121839023218390233TC7GENIChomozygous50091858
121839057818390580TT--4GENICheterozygous50367931
121839057918390580T-4GENICheterozygous50091862
121839072518390726AG14GENIChomozygous50465606
121839072818390729AG17GENIChomozygous50091864
121839075618390757AG16GENIChomozygous50465608
121839087518390876GA25GENIChomozygous50091866
121839090818390909AG27GENIChomozygous50091868
121839018618390187AATGTGTGTGTGTGTGTGTGTG2GENICheterozygous50535947
121839039718390398GGTCTGTCTGTCTGTCTATCTA16GENIChomozygous50569147