chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 48288391 48288392 C G 55 GENIC homozygous 980162069 13 48289539 48289540 A G 22 GENIC homozygous 980162070 13 48289683 48289684 G A 20 GENIC homozygous 980162071 13 48290461 48290462 C T 18 GENIC homozygous 980162072 13 48290478 48290479 T A 18 GENIC homozygous 980162073 13 48290648 48290649 G A 12 GENIC homozygous 980162074 13 48291011 48291012 A G 23 GENIC homozygous 980162075 13 48291308 48291309 A T 20 GENIC homozygous 980162076 13 48291571 48291572 T C 33 GENIC homozygous 980162077 13 48292967 48292968 T C 23 GENIC homozygous 980162078 13 48294489 48294490 T A 35 GENIC homozygous 980162079 13 48296042 48296043 T A 19 GENIC homozygous 980162080 13 48296843 48296844 G A 11 GENIC homozygous 980162081 13 48296865 48296866 T A 10 GENIC homozygous 980162082 13 48296866 48296867 G T 11 GENIC homozygous 980162083 13 48297374 48297375 T C 36 GENIC homozygous 980162084