chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 71211417 71211418 T A 9 GENIC homozygous 111606386 3 71213905 71213906 A T 13 GENIC homozygous 111606387 3 71215425 71215426 A G 24 GENIC homozygous 111606388 3 71218674 71218675 G A 28 GENIC homozygous 111606389 3 71219444 71219445 C T 30 GENIC homozygous 111606390 3 71219518 71219519 G A 23 GENIC homozygous 111606391 3 71219636 71219637 C T 26 GENIC homozygous 111606392 3 71219843 71219844 G A 17 GENIC homozygous 111606393 3 71219985 71219986 G A 15 GENIC homozygous 111606394 3 71221777 71221778 T A 33 GENIC homozygous 111606396 3 71222109 71222110 A G 33 GENIC homozygous 111606397 3 71223270 71223271 T G 14 GENIC homozygous 111606398 3 71223395 71223396 C T 35 GENIC homozygous 111606399 3 71223562 71223563 A T 25 GENIC homozygous 111606400 3 71225058 71225059 C T 25 GENIC homozygous 119649967 3 71244852 71244853 G A 19 GENIC homozygous 111606401 3 71247137 71247138 G A 38 GENIC homozygous 111606402