chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 21914295 21914296 T C 35 GENIC homozygous 978715772 4 21914812 21914813 A G 32 GENIC homozygous 978715773 4 21914944 21914945 G A 35 GENIC homozygous 978715774 4 21914970 21914971 A G 38 GENIC homozygous 978715775 4 21915021 21915022 T C 61 GENIC homozygous 978715776 4 21915109 21915110 A G 30 GENIC homozygous 978715777 4 21915265 21915266 A C 19 GENIC homozygous 978715778 4 21915271 21915272 A G 18 GENIC homozygous 978715779 4 21915327 21915328 C T 32 GENIC possibly homozygous 978715780 4 21915381 21915382 A G 29 GENIC homozygous 978715781 4 21915501 21915502 G A 59 GENIC homozygous 978715782 4 21915789 21915790 A G 25 GENIC homozygous 978715783 4 21915799 21915800 G A 23 GENIC homozygous 978715784 4 21916142 21916143 C G 14 GENIC homozygous 978715785 4 21916200 21916201 A C 32 GENIC homozygous 978715786 4 21916206 21916207 A T 35 GENIC homozygous 978715787 4 21916249 21916250 A G 41 GENIC homozygous 978715788 4 21916401 21916402 A T 17 GENIC homozygous 978715789 4 21916594 21916595 G T 20 GENIC homozygous 978715790 4 21917321 21917322 G A 31 GENIC homozygous 978715791 4 21918456 21918457 T G 40 GENIC homozygous 978715792 4 21918651 21918652 C T 55 GENIC homozygous 978715793 4 21918950 21918951 T C 27 GENIC homozygous 978715794