chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84941911749419118TTC13INTERGENIChomozygous52972159
84941940449419407TCT---11INTERGENICheterozygous53112007
84941948749419488GGAGA17INTERGENIChomozygous52972161
84942027749420278TC8INTERGENICheterozygous52972167
84942056449420565TG12INTERGENICheterozygous52972170
84942082749420830GCC---17INTERGENIChomozygous52972171
84942145749421458TG12INTERGENIChomozygous52972172
84942170449421705GGT12INTERGENICheterozygous52972173
84942268449422685AAATCC11INTERGENIChomozygous52972174
84942296049422961TTATCC7INTERGENIChomozygous53506927
84942335049423351CA14INTERGENIChomozygous52972181
84942359249423593C-14INTERGENICheterozygous53112009
84942400549424006AG17INTERGENIChomozygous52972182
84942569349425694A-16INTERGENIChomozygous52972187
84942569449425695CG16INTERGENIChomozygous53363576
84942668949426690GA11INTERGENICheterozygous53112017
84942673349426734TC9INTERGENICheterozygous52972189
84942745549427456GC9INTERGENICheterozygous53112021
84942756649427567T-7INTERGENICheterozygous53112023
84942771749427718TC18INTERGENIChomozygous52972193
84942825349428254TA8INTERGENICheterozygous53112025
84942839649428418GTGTCTTTGTGTGAGTGTGTGT----------------------12INTERGENICheterozygous53112027
84942931249429313CT14INTERGENICheterozygous52972199
84942948049429481CCTCAAATGT8INTERGENIChomozygous52972201