chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6109914153109914154C-3GENIChomozygous54627994
6109914159109914160C-1GENIChomozygous54627996
6109914485109914486CT4GENIChomozygous54943392
6109917277109917278AG37GENIChomozygous54628006
6109917488109917489GT58GENICpossibly homozygous54628008
6109917937109917938CT35GENIChomozygous55096585
6109918006109918007TC34GENIChomozygous55096587
6109918503109918504GGTGC47GENIChomozygous54628012
6109919051109919052CT42GENIChomozygous54628014
6109919177109919178G-14GENICheterozygous54943396
6109919179109919188GAGAGAGAG---------16GENICheterozygous54943397
6109920957109920958AC26GENIChomozygous54943398
6109921079109921080GA35GENIChomozygous54628022
6109921138109921139GC36GENIChomozygous55096589
6109921748109921758GTGTGTGTGT----------1GENIChomozygous55096591
6109923146109923147TTTATTTGTA12INTERGENIChomozygous54628034
6109923291109923292TC41INTERGENIChomozygous54628036
6109924456109924457GA29INTERGENIChomozygous54943403
6109924468109924472TTGT----19INTERGENIChomozygous54628038
6109925472109925473TC50INTERGENIChomozygous54628046
6109926368109926369AT39INTERGENIChomozygous54628048
6109927387109927388CT37INTERGENIChomozygous55096593
6109927396109927397AG37INTERGENIChomozygous55096595
6109928230109928231TTGTA11INTERGENIChomozygous54628050
6109929204109929206TT--43INTERGENIChomozygous55096597
6109930268109930269TC22INTERGENIChomozygous55096599
6109931009109931010AAT23INTERGENICpossibly homozygous55048506
6109932728109932729GA26INTERGENICpossibly homozygous54628060
6109932784109932785TA27INTERGENICheterozygous54628066
6109932786109932787GGT23INTERGENICheterozygous54943408
6109932787109932788AT28INTERGENICheterozygous54943409
6109933008109933009G-30INTERGENIChomozygous54628070
6109934637109934638CT36INTERGENIChomozygous54628072
6109936178109936179AT44INTERGENIChomozygous54628076