chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 41801055 41801056 G A 16 GENIC homozygous 930636694 17 41801228 41801229 T C 28 GENIC homozygous 930636695 17 41801899 41801900 G A 21 GENIC homozygous 930636696 17 41802420 41802421 G A 11 GENIC homozygous 930636697 17 41802895 41802896 T C 29 GENIC homozygous 930636698 17 41803064 41803065 G A 52 GENIC homozygous 930636699 17 41803331 41803332 A G 49 GENIC homozygous 930636700 17 41803723 41803724 A G 41 GENIC homozygous 930636701 17 41804579 41804580 C A 27 GENIC homozygous 930636702 17 41804691 41804692 A T 42 GENIC homozygous 930636703 17 41805049 41805050 A G 24 GENIC homozygous 930636704 17 41805653 41805654 G A 20 GENIC homozygous 930636705 17 41805760 41805761 T C 32 GENIC homozygous 930636706 17 41806052 41806053 G T 38 GENIC homozygous 930636707 17 41807132 41807133 C T 43 GENIC possibly homozygous 930636708 17 41807849 41807850 T C 33 GENIC homozygous 930636709 17 41808996 41808997 A G 29 GENIC homozygous 930636710 17 41809399 41809400 C G 18 GENIC homozygous 930636711 17 41809606 41809607 C T 37 GENIC homozygous 930636712 17 41809607 41809608 T A 38 GENIC homozygous 930636713 17 41811273 41811274 T C 46 GENIC homozygous 930636714 17 41811480 41811481 G A 61 GENIC homozygous 930636715 17 41811519 41811520 T G 57 GENIC homozygous 930636716 17 41811800 41811801 T C 28 GENIC homozygous 930636717 17 41814826 41814827 G A 26 GENIC heterozygous 930636718 17 41815347 41815348 A C 35 GENIC homozygous 930636719 17 41815395 41815396 G A 37 GENIC homozygous 930636720