chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1219078759219078760GA8GENIChomozygous108540158
1219080398219080399TC19GENIChomozygous108540159
1219081614219081615TC31GENIChomozygous108540163
1219082445219082446AG28GENIChomozygous108540167
1219084675219084676CA27GENIChomozygous108540173
1219084931219084932AG20GENIChomozygous108540177
1219087061219087062TA26GENIChomozygous108540183
1219087318219087319GA31GENIChomozygous108540185
1219087843219087844GA19GENIChomozygous108540187
1219089732219089733CT31GENIChomozygous108540193
1219092027219092028TC20GENIChomozygous108540203
1219092862219092863GA31GENIChomozygous108540205
1219093131219093132GA29GENIChomozygous109195403
1219093897219093898GT21GENIChomozygous108540207
1219094817219094818AG27GENIChomozygous109195405
1219095622219095623GT17GENIChomozygous108540213
1219096516219096517TC24GENIChomozygous108540215
1219099249219099250TG25GENIChomozygous108540219
1219099568219099569AG17GENIChomozygous108540222
1219099927219099928AG21GENIChomozygous108540224
1219100002219100003AG18GENIChomozygous108540226
1219102600219102601CG54GENIChomozygous108540230
1219105119219105120CT13GENIChomozygous108540231
1219106237219106238GA33GENIChomozygous108540233
1219108739219108740AT27GENIChomozygous108540239
1219110849219110850AC34GENIChomozygous108540244
1219111286219111287CT21GENIChomozygous108540246
1219115141219115142AG20GENIChomozygous109195409
1219117186219117187CT28GENIChomozygous108540249
1219118695219118696CT11GENIChomozygous108540251
1219120520219120521TC25GENIChomozygous108540253
1219120830219120831AT17GENIChomozygous108540255
1219121097219121098TG21GENIChomozygous108540259
1219121466219121467GA27GENIChomozygous108540261
1219124371219124372GA17GENIChomozygous109195411