chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 9177260 9177261 G A 31 GENIC homozygous 975582211 5 9177508 9177509 G C 23 GENIC homozygous 975582212 5 9177521 9177522 T C 22 GENIC homozygous 975582213 5 9177712 9177713 T C 22 GENIC homozygous 975582214 5 9177908 9177909 T C 27 GENIC homozygous 975582215 5 9178462 9178463 G C 12 GENIC homozygous 975582216 5 9178690 9178691 G A 4 GENIC homozygous 975582217 5 9178691 9178692 G T 3 GENIC homozygous 975582218 5 9178968 9178969 C T 14 GENIC homozygous 975582219 5 9179223 9179224 G A 36 GENIC homozygous 975582220 5 9179291 9179292 T C 23 GENIC homozygous 975582221 5 9179532 9179533 G A 27 GENIC homozygous 975582222 5 9179756 9179757 G T 6 GENIC homozygous 975582223 5 9179837 9179838 C A 15 GENIC homozygous 975582224 5 9180731 9180732 G A 19 GENIC homozygous 975582225 5 9181024 9181025 T C 24 GENIC homozygous 975582226