chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 13091642 13091643 A G 19 GENIC homozygous 115259742 12 13092299 13092300 G T 20 GENIC homozygous 115259744 12 13092512 13092513 G A 19 GENIC homozygous 115259746 12 13092755 13092756 T A 17 GENIC homozygous 115259748 12 13096700 13096701 G A 12 GENIC possibly homozygous 115259750 12 13098210 13098211 G C 15 GENIC homozygous 115259752 12 13099650 13099651 T C 22 GENIC homozygous 115259754 12 13102473 13102474 T C 24 GENIC homozygous 115259756 12 13103676 13103677 C T 17 GENIC homozygous 115259758 12 13103844 13103845 A T 17 GENIC homozygous 115259760 12 13104281 13104282 G A 24 GENIC homozygous 115259762 12 13105348 13105349 C T 14 GENIC homozygous 115416645 12 13092357 13092358 T 17 GENIC homozygous 128961261 12 13097638 13097638 C 18 GENIC homozygous 128961262 12 13103001 13103001 GCTCA 19 GENIC possibly homozygous 128961263 12 13105295 13105295 T 13 GENIC homozygous 128961264 12 13094938 13094938 TTTTTTTT 17 GENIC heterozygous 132891623 12 13094943 13094943 ATATTTTATTTATTTATTATATATGAG 16 GENIC heterozygous 132891624 12 13105565 13105566 T G 9 GENIC homozygous 115259764 12 13105707 13105708 C G 18 GENIC homozygous 115259766 12 13106259 13106259 CTGGAACTCAAAGTTTACC 15 GENIC homozygous 128961265 12 13107182 13107183 C T 25 GENIC homozygous 115259768 12 13107640 13107641 C T 28 GENIC homozygous 115259770 12 13109211 13109212 C T 19 GENIC homozygous 115259772 12 13109316 13109317 G A 13 GENIC homozygous 115259774 12 13110695 13110696 T C 12 GENIC homozygous 115259776 12 13111748 13111749 A G 17 GENIC homozygous 115416647