chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1526958552695856AG7GENIChomozygous124019093
1526958552695855GT7GENIChomozygous129224141
1526958642695865A7GENIChomozygous129224142
1526958672695868C8GENIChomozygous129224143
1526958752695876C11GENIChomozygous129224144
1526958812695881CCA12GENIChomozygous129224145
1526958842695884CTATTAATGATGAGCTTTTAA13GENIChomozygous129224146
1526958892695889ATAACAATAATTGTATA15GENIChomozygous129224147
1526958912695891CATTGCAAAAAAG15GENIChomozygous129224148
1526958962695896A17GENIChomozygous129224149
1526958982695898AAGGCTGG16GENIChomozygous129224150
1526959002695900G15GENIChomozygous129224151
1526959042695904GTGCAGTGTTTTC15GENIChomozygous129224152
1526992162699216TTCGCCGGA11GENIChomozygous129224157
1526992502699250T8GENIChomozygous129224160
1526992542699254T8GENIChomozygous129224161
1526994402699441CG13GENIChomozygous112446186
1526996152699616G11GENIChomozygous129224164
1526996182699618G11GENIChomozygous129224165
1527134022713404TC16GENIChomozygous129224173
1527175462717546A12GENIChomozygous129224177
1527175822717584GG11GENIChomozygous129224180
1527175852717586CG11GENIChomozygous124019140
1527175932717594G13GENIChomozygous129224181
1527176082717608C9GENIChomozygous129224182
1526993352699336AG4GENIChomozygous118860079