chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 48288391 48288392 C G 21 GENIC homozygous 804456707 13 48289304 48289305 G A 13 GENIC homozygous 804456708 13 48289479 48289480 A C 18 GENIC homozygous 804456709 13 48289539 48289540 A G 19 GENIC homozygous 804456710 13 48289889 48289890 A G 30 GENIC homozygous 804456711 13 48290478 48290479 T A 10 GENIC homozygous 804456712 13 48291011 48291012 A G 10 GENIC homozygous 804456713 13 48291308 48291309 A T 14 GENIC homozygous 804456714 13 48291571 48291572 T C 15 GENIC homozygous 804456715 13 48291779 48291780 C T 12 GENIC homozygous 804456716 13 48291970 48291971 C A 8 GENIC homozygous 804456717 13 48292967 48292968 T C 15 GENIC homozygous 804456718 13 48294151 48294152 A G 14 GENIC homozygous 804456719 13 48296042 48296043 T A 6 GENIC homozygous 804456720 13 48296242 48296243 T C 10 GENIC homozygous 804456721 13 48296271 48296272 G A 6 GENIC homozygous 804456722 13 48296328 48296329 G T 22 GENIC homozygous 804456723 13 48296843 48296844 G A 21 GENIC homozygous 804456724 13 48297374 48297375 T C 16 GENIC homozygous 804456725 13 48297548 48297549 G A 20 GENIC homozygous 804456726