chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 12639973 12639974 T C 42 GENIC homozygous 935664959 9 12640207 12640208 T C 43 GENIC homozygous 935664960 9 12640322 12640323 A T 32 GENIC homozygous 935664961 9 12640329 12640330 G C 31 GENIC homozygous 935664962 9 12641114 12641115 G A 17 GENIC homozygous 935664963 9 12642081 12642082 T C 18 GENIC homozygous 935664964 9 12642925 12642926 C T 28 GENIC homozygous 935664965 9 12643650 12643651 C T 27 GENIC homozygous 935664966 9 12645453 12645454 A G 23 GENIC homozygous 935664967 9 12645711 12645712 G A 28 GENIC homozygous 935664968 9 12646113 12646114 G A 22 GENIC homozygous 935664969 9 12646217 12646218 T C 24 GENIC homozygous 935664970 9 12646961 12646962 A G 25 GENIC homozygous 935664971 9 12647216 12647217 A T 27 GENIC homozygous 935664972 9 12647877 12647878 A C 39 GENIC homozygous 935664973 9 12648245 12648246 A G 25 GENIC homozygous 935664974 9 12648554 12648555 G T 6 GENIC homozygous 935664975 9 12649024 12649025 G A 38 GENIC homozygous 935664976 9 12649428 12649429 T C 31 GENIC homozygous 935664977 9 12649787 12649788 A G 32 GENIC homozygous 935664978 9 12650995 12650996 T C 22 GENIC homozygous 935664979