chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146501037146501038AC33GENICheterozygous925423187
4146501730146501731CT22GENICheterozygous925423188
4146502350146502351AG35GENICheterozygous925423189
4146503821146503822AG19GENICheterozygous925423190
4146503988146503989GA39GENICheterozygous925423191
4146503989146503990TC39GENICheterozygous925423192
4146504020146504025GTACT-----37GENICheterozygous925488561
4146504232146504233TC62GENICheterozygous925423193
4146505050146505051AG36GENICheterozygous925423194
4146515990146515991AAT32GENICheterozygous925488562
4146517794146517795AG42GENICheterozygous925423195
4146524824146524825TG20GENICheterozygous925423196
4146531680146531681GA33GENICheterozygous925423197
4146531724146531725AC26GENICheterozygous925423198
4146534492146534493GC34GENICheterozygous925423199
4146553231146553232GA52GENICheterozygous925423200
4146570351146570352T-27GENICheterozygous925488563
4146583422146583423TA40GENICheterozygous925423201
4146596037146596038CT27GENICheterozygous925423202
4146599737146599738AC16GENICheterozygous925423203
4146618063146618064CT20GENICheterozygous925423204
4146621855146621856GA40GENICheterozygous925423205