chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 59122767 59122768 T G 24 GENIC homozygous 111582739 3 59129284 59129285 A G 36 GENIC homozygous 111582740 3 59129475 59129476 T C 34 GENIC homozygous 111582741 3 59130212 59130213 T C 43 GENIC homozygous 111582742 3 59130247 59130248 A G 41 GENIC homozygous 111582743 3 59130454 59130455 C A 62 GENIC homozygous 111582744 3 59133746 59133747 A C 42 GENIC homozygous 111582745 3 59135394 59135395 A C 39 GENIC homozygous 111582746 3 59136012 59136013 A G 37 GENIC homozygous 111582747 3 59136091 59136092 G A 25 GENIC homozygous 111582748 3 59136347 59136348 A G 44 GENIC homozygous 111582749 3 59136595 59136596 T C 38 GENIC homozygous 111582750 3 59136812 59136813 A G 42 GENIC homozygous 111582751 3 59137088 59137089 A G 49 GENIC homozygous 111582752 3 59137218 59137219 G A 51 GENIC homozygous 111582753 3 59137436 59137437 C T 60 GENIC homozygous 111582754 3 59137622 59137623 A C 41 GENIC homozygous 111582755 3 59137801 59137802 A G 44 GENIC homozygous 111582756 3 59138127 59138128 C T 20 GENIC homozygous 111582757 3 59138583 59138584 T C 44 GENIC homozygous 111582758 3 59138979 59138980 C T 61 GENIC homozygous 111582759 3 59139667 59139668 T A 75 GENIC homozygous 111582760