chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 2020583 2020584 C T 30 GENIC possibly homozygous 48936616 14 2020591 2020592 G A 27 GENIC homozygous 48936617 14 2022531 2022532 T C 35 GENIC homozygous 48936618 14 2022574 2022575 C CT 29 GENIC homozygous 48936619 14 2022703 2022704 T TAGGGTTCC 15 GENIC homozygous 48447480 14 2022752 2022753 A G 28 GENIC homozygous 48936620 14 2023204 2023205 G A 35 GENIC homozygous 48936621 14 2024012 2024013 C T 31 GENIC possibly homozygous 48936622 14 2026055 2026056 G A 38 GENIC homozygous 48936623 14 2026312 2026316 GGGG ---- 11 GENIC heterozygous 48936624 14 2026313 2026316 GGG --- 11 GENIC possibly homozygous 48936625 14 2026637 2026638 C T 35 GENIC homozygous 48936626 14 2026712 2026713 T C 31 GENIC homozygous 48447487 14 2029216 2029217 C T 45 INTERGENIC homozygous 48936627 14 2029891 2029892 A G 37 INTERGENIC homozygous 48936628 14 2031318 2031319 G T 38 INTERGENIC possibly homozygous 48936629