chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1526927012692702A21GENICheterozygous130438271
1526958552695856AG11GENIChomozygous124019093
1526958552695855GT11GENIChomozygous129224141
1526958642695865A13GENIChomozygous129224142
1526958672695868C13GENIChomozygous129224143
1526958752695876C13GENIChomozygous129224144
1526958812695881CCA12GENIChomozygous129224145
1526958842695884CTATTAATGATGAGCTTTTAA12GENIChomozygous129224146
1526958892695889ATAACAATAATTGTATA16GENIChomozygous129224147
1526958912695891CATTGCAAAAAAG15GENIChomozygous129224148
1526958962695896A16GENIChomozygous129224149
1526958982695898AAGGCTGG17GENIChomozygous129224150
1526959002695900G17GENIChomozygous129224151
1526959042695904GTGCAGTGTTTTC17GENIChomozygous129224152
1526992162699216TTCGCCGGA22GENIChomozygous129224157
1526992502699250T11GENIChomozygous129224160
1526992542699254T10GENIChomozygous129224161
1526994402699441CG19GENIChomozygous112446186
1526996152699616G29GENIChomozygous129224164
1526996182699618G29GENIChomozygous129224165
1527112252711226T3GENIChomozygous132899800
1527134022713404TC17GENIChomozygous129224173
1527175462717546A23GENIChomozygous129224177
1527175822717584GG20GENIChomozygous129224180
1527175852717586CG19GENIChomozygous124019140
1527175932717594G15GENIChomozygous129224181
1527176082717608C13GENIChomozygous129224182
1526993352699336AG3GENIChomozygous118860079