chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 18602431 18602432 C T 29 GENIC homozygous 116919022 10 18602724 18602725 G C 26 GENIC homozygous 116919024 10 18603551 18603552 T C 28 GENIC homozygous 116503475 10 18603707 18603708 A G 30 GENIC homozygous 116503477 10 18603709 18603710 T C 30 GENIC homozygous 116503479 10 18603741 18603742 C T 28 GENIC homozygous 116919026 10 18604342 18604343 T C 23 GENIC homozygous 116503485 10 18604575 18604576 T C 36 GENIC homozygous 116919028 10 18605073 18605074 G A 29 GENIC homozygous 116503489 10 18606496 18606497 G A 25 GENIC homozygous 116919030 10 18606518 18606519 C A 19 GENIC homozygous 116919032 10 18606634 18606635 A G 20 GENIC homozygous 116919034 10 18606973 18606974 G A 27 GENIC homozygous 116919036 10 18607008 18607009 C A 22 GENIC homozygous 116919038 10 18607204 18607205 G A 22 GENIC homozygous 116919040 10 18607826 18607827 G A 38 GENIC homozygous 116919042 10 18607903 18607904 A G 32 GENIC homozygous 116503497 10 18607981 18607982 G A 39 GENIC homozygous 116919044 10 18608476 18608477 G A 35 GENIC possibly homozygous 116919046 10 18608557 18608558 A G 21 GENIC homozygous 116503501 10 18608891 18608892 G A 41 GENIC homozygous 116919048