chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84941911749419118TTC24INTERGENIChomozygous52972159
84941924649419247TC13INTERGENIChomozygous52972160
84941948749419488GGAGA13INTERGENIChomozygous52972161
84941985149419852TC19INTERGENIChomozygous52972162
84942027749420278TC7INTERGENIChomozygous52972167
84942056449420565TG17INTERGENIChomozygous52972170
84942082749420830GCC---12INTERGENIChomozygous52972171
84942145749421458TG19INTERGENIChomozygous52972172
84942170449421705GGT10INTERGENIChomozygous52972173
84942290049422901CCT8INTERGENIChomozygous52625386
84942290549422906GA9INTERGENIChomozygous52972176
84942321949423220GGTCTATCTA8INTERGENIChomozygous53430186
84942335049423351CA19INTERGENIChomozygous52972181
84942400549424006AG19INTERGENIChomozygous52972182
84942460749424608AG9INTERGENIChomozygous52972183
84942502649425027GT14INTERGENIChomozygous52972184
84942551949425520CT11INTERGENIChomozygous52972186
84942569349425694A-22INTERGENIChomozygous52972187
84942569449425695CG22INTERGENIChomozygous53363576
84942771749427718TC15INTERGENIChomozygous52972193
84942813949428147GTGCGTGC--------11INTERGENIChomozygous52972194
84942836449428365GA11INTERGENIChomozygous52972196
84942907349429074GA12INTERGENIChomozygous52972198
84942931249429313CT13INTERGENIChomozygous52972199
84942290949422910AATCCATCATCTG8INTERGENIChomozygous54255085
84943008549430086CCCCCTCATCCTCTCTCT9INTERGENIChomozygous53363579
84943010249430103CT7INTERGENIChomozygous52972204
84943012549430126CCTT9INTERGENIChomozygous52972206
84943063249430633TC8INTERGENIChomozygous52972208