chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156215837156215838C-7GENICheterozygous55804265
5156215837156215838CA7GENICheterozygous55931304
5156223769156223771AC--20GENICheterozygous55931306
5156225813156225814CT5INTERGENICheterozygous55804266
5156238514156238515AG3INTERGENICheterozygous55804269
5156238521156238522AC4INTERGENIChomozygous55804270
5156238523156238524A-2INTERGENIChomozygous55804271
5156238533156238534AAG1INTERGENIChomozygous55804272
5156238555156238556A-3INTERGENIChomozygous55804275
5156238560156238561TTG3INTERGENIChomozygous55804276
5156242085156242086G-5INTERGENICheterozygous56070962
5156246373156246374T-12INTERGENICheterozygous55804278
5156246391156246392TC19INTERGENICheterozygous56192235
5156246567156246568T-10INTERGENICheterozygous55804279
5156263566156263567CT11GENICheterozygous56133019
5156266718156266719G-16INTERGENICheterozygous56133023
5156288125156288126GGT15INTERGENICpossibly homozygous55804282
5156288127156288128CCT14INTERGENIChomozygous55804284
5156291134156291135AG20INTERGENIChomozygous55804285
5156301143156301144TTATAC19GENICheterozygous55804288
5156301144156301148ATAC----19GENICpossibly homozygous55804289
5156301150156301152AC--31GENICheterozygous55804290
5156304444156304445CCTAT3GENIChomozygous55804291