chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 15050336 15050337 A C 42 INTERGENIC homozygous 45095789 X 15050534 15050535 T C 42 INTERGENIC homozygous 45095790 X 15051033 15051034 A G 66 INTERGENIC homozygous 45095791 X 15052744 15052745 T C 61 INTERGENIC homozygous 45095792 X 15053027 15053028 T C 44 INTERGENIC possibly homozygous 45095793 X 15053459 15053460 T G 70 INTERGENIC homozygous 45095794 X 15054273 15054274 G A 39 GENIC homozygous 45095795 X 15054293 15054294 C T 56 GENIC heterozygous 45251983 X 15054337 15054338 C T 86 GENIC heterozygous 45095796 X 15054399 15054400 A G 107 GENIC possibly homozygous 45095797 X 15054544 15054545 G A 136 GENIC heterozygous 45095798 X 15054599 15054600 A G 110 GENIC heterozygous 45095799 X 15054615 15054616 A G 96 GENIC heterozygous 45095800 X 15054853 15054854 T C 4 GENIC homozygous 45095801 X 15055114 15055115 A G 42 GENIC homozygous 45095802 X 15055196 15055197 C T 54 GENIC possibly homozygous 45095803 X 15055410 15055411 A G 95 GENIC heterozygous 45095805 X 15055559 15055560 T C 96 GENIC possibly homozygous 45095806