chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1526958552695856AG17GENIChomozygous124019093
1526958552695855GT19GENIChomozygous129224141
1526958642695865A15GENIChomozygous129224142
1526958672695868C15GENIChomozygous129224143
1526958752695876C16GENIChomozygous129224144
1526958812695881CCA17GENIChomozygous129224145
1526958842695884CTATTAATGATGAGCTTTTAA19GENIChomozygous129224146
1526958892695889ATAACAATAATTGTATA24GENIChomozygous129224147
1526958912695891CATTGCAAAAAAG31GENIChomozygous129224148
1526958962695896A33GENIChomozygous129224149
1526958982695898AAGGCTGG32GENIChomozygous129224150
1526959002695900G32GENIChomozygous129224151
1526959042695904GTGCAGTGTTTTC30GENIChomozygous129224152
1526992162699216TTCGCCGGA28GENIChomozygous129224157
1526992502699250T19GENIChomozygous129224160
1526992542699254T17GENIChomozygous129224161
1526994402699441CG36GENIChomozygous112446186
1526996152699616G49GENIChomozygous129224164
1526996182699618G50GENIChomozygous129224165
1527134022713404TC34GENIChomozygous129224173
1527175462717546A32GENIChomozygous129224177
1527175822717584GG19GENIChomozygous129224180
1527175852717586CG19GENIChomozygous124019140
1527175932717594G20GENIChomozygous129224181
1527176082717608C18GENIChomozygous129224182
1526993352699336AG10GENIChomozygous118860079