chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1526958552695856AG28GENIChomozygous124019093
1526958552695855GT30GENIChomozygous129224141
1526958642695865A29GENIChomozygous129224142
1526958672695868C30GENIChomozygous129224143
1526958752695876C35GENIChomozygous129224144
1526958812695881CCA38GENIChomozygous129224145
1526958842695884CTATTAATGATGAGCTTTTAA40GENIChomozygous129224146
1526958892695889ATAACAATAATTGTATA44GENIChomozygous129224147
1526958912695891CATTGCAAAAAAG49GENIChomozygous129224148
1526958962695896A48GENIChomozygous129224149
1526958982695898AAGGCTGG49GENIChomozygous129224150
1526959002695900G49GENIChomozygous129224151
1526959042695904GTGCAGTGTTTTC48GENIChomozygous129224152
1526976222697623T23GENIChomozygous129224153
1526976242697624TGGCTCAGCG23GENIChomozygous129224154
1526976262697626TAAGAGCA18GENIChomozygous129224155
1526976282697628CGACTGCTCTT14GENIChomozygous129224156
1526992162699216TTCGCCGGA32GENIChomozygous129224157
1526994402699441CG30GENIChomozygous112446186
1527175822717584GG16GENIChomozygous129224180
1526992502699250T29GENIChomozygous129224160
1526992542699254T26GENIChomozygous129224161
1526995122699512A19GENICheterozygous129224163
1526996152699616G37GENIChomozygous129224164
1526996182699618G39GENIChomozygous129224165
1527134022713404TC43GENIChomozygous129224173
1527175462717546A23GENIChomozygous129224177
1526993352699336AG10GENIChomozygous118860079
1527175852717586CG15GENIChomozygous124019140
1527175932717594G13GENIChomozygous129224181
1527176082717608C10GENIChomozygous129224182