chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 37784833 37784834 C T 18 GENIC homozygous 116563025 10 37785494 37785495 A T 22 GENIC homozygous 116563027 10 37785659 37785660 G A 14 GENIC homozygous 116563029 10 37785675 37785676 C T 15 GENIC homozygous 116563031 10 37785686 37785687 G A 15 GENIC homozygous 116563033 10 37785709 37785710 T G 15 GENIC homozygous 116563035 10 37787155 37787156 C T 13 GENIC homozygous 117057388 10 37787316 37787317 C T 13 GENIC homozygous 116563041 10 37787364 37787365 T G 10 GENIC homozygous 116563043 10 37787956 37787957 G A 19 GENIC homozygous 116563045 10 37788664 37788665 T A 28 GENIC homozygous 116563046 10 37788751 37788752 T C 29 GENIC homozygous 116563048 10 37788973 37788974 T C 15 GENIC homozygous 116563050 10 37789236 37789237 G C 24 GENIC homozygous 116563052 10 37789844 37789845 G A 22 GENIC possibly homozygous 116869047 10 37786565 37786566 T G 31 GENIC homozygous 116869039 10 37787564 37787565 C T 7 GENIC homozygous 116869041 10 37788226 37788227 G T 14 GENIC homozygous 116869043 10 37788227 37788228 G T 15 GENIC homozygous 116869045 10 37786643 37786644 T A 5 GENIC homozygous 117150856