chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 48288391 48288392 C G 19 GENIC homozygous 939102252 13 48289028 48289029 A G 25 GENIC homozygous 939102253 13 48289304 48289305 G A 39 GENIC homozygous 939102254 13 48289479 48289480 A C 39 GENIC homozygous 939102255 13 48289539 48289540 A G 29 GENIC homozygous 939102256 13 48289889 48289890 A G 28 GENIC homozygous 939102257 13 48290478 48290479 T A 17 GENIC homozygous 939102258 13 48291011 48291012 A G 28 GENIC homozygous 939102259 13 48291308 48291309 A T 18 GENIC homozygous 939102260 13 48291571 48291572 T C 16 GENIC homozygous 939102261 13 48291779 48291780 C T 33 GENIC homozygous 939102262 13 48291970 48291971 C A 27 GENIC homozygous 939102263 13 48292967 48292968 T C 43 GENIC homozygous 939102264 13 48294151 48294152 A G 25 GENIC homozygous 939102265 13 48296843 48296844 G A 33 GENIC homozygous 939102266 13 48296865 48296866 T A 34 GENIC homozygous 939102267 13 48296866 48296867 G T 34 GENIC homozygous 939102268 13 48297374 48297375 T C 22 GENIC homozygous 939102269 13 48297548 48297549 G A 19 GENIC homozygous 939102270