chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 104623432 104623433 C T 16 GENIC homozygous 114932133 6 104623805 104623806 A G 22 GENIC homozygous 114932134 6 104625829 104625830 A T 18 GENIC homozygous 114932137 6 104626093 104626094 G A 22 GENIC homozygous 114932138 6 104626396 104626397 C A 23 GENIC homozygous 114932139 6 104626444 104626445 G A 16 GENIC homozygous 118733182 6 104626694 104626695 G A 13 GENIC homozygous 118733183 6 104626765 104626766 T C 13 GENIC homozygous 114932141 6 104627153 104627154 G T 22 GENIC homozygous 114932142 6 104627181 104627182 T G 22 GENIC homozygous 114932143 6 104627408 104627408 T 20 GENIC homozygous 128378122 6 104627514 104627515 G C 19 GENIC homozygous 114932145 6 104627519 104627520 A G 17 GENIC homozygous 114932146 6 104627558 104627559 C T 21 GENIC homozygous 114932147 6 104627599 104627600 C T 18 GENIC homozygous 118733184 6 104628005 104628006 C T 23 GENIC homozygous 118733185 6 104629531 104629532 C G 25 GENIC homozygous 114932154 6 104629621 104629622 C A 27 GENIC homozygous 118733186 6 104629720 104629721 G A 33 GENIC homozygous 118733187 6 104629802 104629803 G A 38 GENIC homozygous 118733188 6 104628711 104628711 T 26 GENIC homozygous 131412717