chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 127687303 127687304 C G 38 GENIC homozygous 968969332 2 127687717 127687718 T C 30 GENIC homozygous 968969333 2 127688367 127688368 G C 28 GENIC homozygous 968969334 2 127689696 127689697 A G 30 GENIC homozygous 968969335 2 127690819 127690820 A G 19 GENIC homozygous 968969336 2 127691546 127691547 A G 28 GENIC homozygous 968969337 2 127693426 127693427 T G 27 GENIC homozygous 968969338 2 127695088 127695089 C G 24 GENIC homozygous 968969339 2 127698127 127698128 C T 17 GENIC homozygous 968969340 2 127698529 127698530 G A 19 GENIC homozygous 968969341 2 127699869 127699870 G A 29 GENIC homozygous 968969342 2 127701576 127701577 G A 25 GENIC homozygous 968969343 2 127702177 127702178 T C 23 GENIC homozygous 968969344 2 127702495 127702496 A G 17 GENIC homozygous 968969345 2 127703817 127703818 A G 19 GENIC homozygous 968969346 2 127704976 127704977 G A 19 GENIC homozygous 968969347