chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 90763382 90763383 C G 15 GENIC homozygous 828549080 10 90763550 90763551 C T 10 GENIC homozygous 828549081 10 90763843 90763844 T C 12 GENIC homozygous 828549082 10 90763943 90763944 C G 16 GENIC homozygous 828549083 10 90764131 90764132 T A 13 GENIC homozygous 828549084 10 90764527 90764528 T C 10 GENIC homozygous 828549085 10 90764539 90764540 A C 10 GENIC homozygous 828549086 10 90764692 90764693 G C 16 GENIC homozygous 828549087 10 90765557 90765558 G A 16 GENIC homozygous 828549088 10 90765633 90765634 C CACTAGT 20 GENIC homozygous 828549089 10 90765724 90765725 A G 12 GENIC homozygous 828549090 10 90765994 90765995 C G 16 GENIC homozygous 828549091 10 90766309 90766310 G A 11 GENIC homozygous 828549092 10 90767191 90767192 G A 9 GENIC homozygous 828549093 10 90767365 90767366 C T 11 GENIC homozygous 828549094 10 90767574 90767575 G A 7 GENIC homozygous 828549095 10 90768111 90768112 A G 8 GENIC homozygous 828549096 10 90768215 90768216 T C 12 GENIC homozygous 828549097 10 90768892 90768893 C CA 14 GENIC homozygous 828549098 10 90769141 90769142 T C 13 GENIC homozygous 828549099 10 90769812 90769813 A G 11 GENIC homozygous 828549100 10 90770631 90770632 A G 7 GENIC homozygous 828549101 10 90771141 90771142 T A 11 GENIC homozygous 828549102 10 90771267 90771268 C T 12 GENIC homozygous 828549103 10 90771619 90771620 A G 12 GENIC homozygous 828549104