chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 6174916 6174917 G T 23 GENIC homozygous 970765756 14 6175387 6175388 A G 18 GENIC homozygous 970765757 14 6175388 6175389 G A 18 GENIC homozygous 970765758 14 6176768 6176769 A T 20 GENIC homozygous 970765759 14 6177149 6177150 T C 21 GENIC homozygous 970765760 14 6177400 6177401 G C 14 GENIC homozygous 970765761 14 6177456 6177457 T C 26 GENIC homozygous 970765762 14 6177559 6177560 A G 21 GENIC homozygous 970765763 14 6177626 6177627 A G 13 GENIC homozygous 970765764 14 6216600 6216601 C T 27 GENIC homozygous 970765765 14 6218929 6218930 C T 26 GENIC homozygous 970765766 14 6218963 6218964 C G 34 GENIC homozygous 970765767 14 6219311 6219312 C T 30 GENIC homozygous 970765768 14 6219445 6219446 G A 35 GENIC homozygous 970765769 14 6219600 6219601 G A 6 GENIC homozygous 970765770 14 6220214 6220215 C G 14 GENIC homozygous 970765771 14 6220223 6220224 C T 18 GENIC homozygous 970765772 14 6220406 6220407 G A 12 GENIC homozygous 970765773 14 6220714 6220715 A G 13 GENIC homozygous 970765774 14 6220747 6220748 T C 13 GENIC homozygous 970765775 14 6220981 6220982 A G 15 GENIC homozygous 970765776 14 6221230 6221231 T C 16 GENIC homozygous 970765777