chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109914153109914154C-3GENIChomozygous54627994
6109914485109914486CT6GENIChomozygous54943392
6109916110109916111AG26GENIChomozygous55048502
6109917277109917278AG19GENIChomozygous54628006
6109917488109917489GT12GENIChomozygous54628008
6109917542109917543AG27GENIChomozygous55048503
6109917786109917788AA--4GENICheterozygous54943395
6109918503109918504GGTGC11GENIChomozygous54628012
6109919051109919052CT13GENIChomozygous54628014
6109919400109919401T-5GENIChomozygous54628018
6109921079109921080GA23GENIChomozygous54628022
6109921747109921748CCGTGT5GENICheterozygous54628030
6109921831109921832CG25GENIChomozygous55048505
6109923146109923147TTTATTTGTA7INTERGENIChomozygous54628034
6109923291109923292TC14INTERGENIChomozygous54628036
6109924468109924472TTGT----12INTERGENICpossibly homozygous54628038
6109925472109925473TC24INTERGENIChomozygous54628046
6109926368109926369AT15INTERGENIChomozygous54628048
6109928230109928231TTGTA1INTERGENIChomozygous54628050
6109931009109931010AAT4INTERGENICheterozygous55048506
6109931020109931021AT5INTERGENIChomozygous55048507
6109932086109932087CT17INTERGENIChomozygous55048508
6109932728109932729GA14INTERGENICpossibly homozygous54628060
6109932786109932787GGT12INTERGENICpossibly homozygous54943408
6109932787109932788AT12INTERGENIChomozygous54943409
6109932787109932788AAGT12INTERGENICheterozygous54943410
6109933008109933009G-6INTERGENIChomozygous54628070
6109934637109934638CT24INTERGENIChomozygous54628072
6109934814109934815GC19INTERGENIChomozygous55048509
6109936178109936179AT15INTERGENIChomozygous54628076
6109936186109936187GA16INTERGENIChomozygous55048510
6109932748109932749CT16INTERGENICheterozygous55261901
6109932746109932747GA16INTERGENICheterozygous55261899