chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 17681279 17681280 T A 19 GENIC homozygous 62915985 X 17682563 17682564 C G 24 GENIC homozygous 62915986 X 17683351 17683352 G A 17 GENIC homozygous 62915987 X 17686892 17686893 A T 13 GENIC homozygous 62915988 X 17690694 17690695 T C 25 GENIC homozygous 62915989 X 17695479 17695480 A G 15 GENIC homozygous 62915990 X 17697316 17697317 A G 3 GENIC heterozygous 63031008 X 17701458 17701459 A T 19 GENIC homozygous 62915991 X 17701835 17701836 A T 16 GENIC homozygous 62915992 X 17702707 17702708 A T 6 GENIC homozygous 62915993 X 17709886 17709887 T C 18 GENIC heterozygous 62915995 X 17713708 17713709 G A 12 GENIC homozygous 62916000 X 17722941 17722942 C T 19 GENIC homozygous 62916001 X 17724663 17724664 C T 13 GENIC heterozygous 62916002 X 17744540 17744541 A G 2 GENIC heterozygous 62916003 X 17737865 17737866 C A 9 GENIC heterozygous 63106838 X 17738971 17738972 T A 16 GENIC heterozygous 63106839 X 17741358 17741359 C A 7 GENIC heterozygous 63106840