chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 15039893 15039894 G T 11 GENIC homozygous 108233016 X 15041831 15041832 C T 17 GENIC homozygous 108233018 X 15042314 15042315 A G 13 GENIC homozygous 108233020 X 15042671 15042672 A G 20 GENIC homozygous 108233022 X 15045759 15045760 G A 18 GENIC homozygous 108233024 X 15045760 15045761 A G 17 GENIC homozygous 108233026 X 15045784 15045785 G C 17 GENIC homozygous 108233028 X 15045786 15045787 T G 18 GENIC homozygous 108233030 X 15045787 15045788 G C 18 GENIC homozygous 108233032 X 15047190 15047191 T G 23 GENIC homozygous 108233034 X 15047282 15047283 C G 18 GENIC homozygous 108233036 X 15047290 15047291 C A 17 GENIC homozygous 108233038 X 15047316 15047317 A G 16 GENIC homozygous 108233040 X 15047374 15047375 G A 17 GENIC homozygous 108233042 X 15047384 15047385 C A 15 GENIC homozygous 108233044 X 15047385 15047386 G A 15 GENIC homozygous 108233046 X 15047392 15047393 C A 16 GENIC homozygous 108233048