chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 15063424 15063425 C T 13 GENIC heterozygous 628995670 10 15064392 15064393 C T 30 GENIC possibly homozygous 628995671 10 15066378 15066379 C T 18 GENIC homozygous 628995672 10 15066908 15066909 G GGAAA 7 GENIC possibly homozygous 744857095 10 15067567 15067568 A G 18 GENIC homozygous 628995673 10 15071819 15071820 G GAAAAAAAAAAAAAAAAAAAAA 3 GENIC heterozygous 744857097 10 15073246 15073247 G GTCAC 11 GENIC possibly homozygous 744857098 10 15074743 15074744 A G 15 GENIC homozygous 628995674 10 15076554 15076559 CTTTC ----- 2 GENIC heterozygous 744857099 10 15076774 15076775 C G 20 GENIC homozygous 628995675 10 15078242 15078243 C T 13 GENIC heterozygous 628995676 10 15080395 15080396 A T 2 GENIC homozygous 628995677 10 15080516 15080517 A - 16 GENIC possibly homozygous 744857100 10 15081772 15081773 C CT 11 GENIC homozygous 744857101 10 15083054 15083055 A - 6 GENIC heterozygous 744857102 10 15083066 15083067 A T 6 GENIC heterozygous 628995678 10 15084133 15084134 T - 9 GENIC possibly homozygous 744857103 10 15084363 15084364 T C 19 GENIC heterozygous 628995679 10 15086117 15086118 A - 7 GENIC possibly homozygous 744857104 10 15086801 15086816 AACAACAACAACAAC --------------- 2 GENIC homozygous 744857105 10 15087388 15087389 C G 9 GENIC homozygous 628995680 10 15087918 15087919 G T 21 GENIC possibly homozygous 628995681 10 15088556 15088557 T C 8 GENIC homozygous 628995682 10 15088684 15088685 G A 16 GENIC possibly homozygous 628995683 10 15089534 15089535 T C 14 GENIC possibly homozygous 628995684 10 15090695 15090697 AA -- 12 GENIC homozygous 744857108 10 15090780 15090781 C A 19 GENIC possibly homozygous 628995685 10 15091774 15091775 A AAC 19 GENIC homozygous 744857110 10 15092560 15092561 C T 10 GENIC possibly homozygous 628995686 10 15092790 15092791 G A 17 GENIC homozygous 628995687 10 15094566 15094567 G A 23 GENIC possibly homozygous 628995688 10 15095403 15095404 A AT 3 GENIC heterozygous 744857112