chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 10479345 10479346 C CTTT 1 GENIC homozygous 771625655 10 10479661 10479662 C - 8 GENIC homozygous 771625657 10 10479758 10479759 G T 2 GENIC homozygous 675823124 10 10480044 10480045 G C 8 GENIC homozygous 675823125 10 10480366 10480367 G C 5 GENIC homozygous 675823126 10 10481307 10481308 G A 11 GENIC homozygous 675823127 10 10481323 10481324 C A 12 GENIC homozygous 675823128 10 10481485 10481486 C CCTTT 7 GENIC homozygous 771625658 10 10481519 10481521 TT -- 5 GENIC homozygous 771625661 10 10484370 10484371 G A 6 GENIC homozygous 675823129 10 10486797 10486798 C T 6 GENIC homozygous 675823130 10 10487294 10487295 G C 11 GENIC homozygous 675823131 10 10489293 10489294 C T 9 GENIC homozygous 675823132 10 10491189 10491190 G T 5 GENIC homozygous 675823133 10 10491797 10491798 T TA 8 GENIC homozygous 771625663 10 10495466 10495467 A AGCACCAGATCTCATTACGGATGGTTGTGAGCCACCATGTGGTTGCTGGGGATTGAACTCATG 1 GENIC homozygous 771625664 10 10498866 10498867 A G 8 GENIC homozygous 675823134 10 10500281 10500282 T C 7 GENIC homozygous 675823135 10 10500294 10500295 T G 9 GENIC homozygous 675823136 10 10501769 10501770 T C 6 GENIC homozygous 675823137 10 10503177 10503178 G A 4 GENIC homozygous 675823138 10 10503977 10503978 T G 6 GENIC homozygous 675823139 10 10507184 10507185 A G 12 GENIC homozygous 675823140 10 10509105 10509113 CCTCTGCC -------- 5 GENIC homozygous 771625665 10 10510722 10510723 A G 8 GENIC homozygous 675823141 10 10511496 10511497 A C 9 GENIC homozygous 675823142 10 10511919 10511920 T C 5 GENIC homozygous 675823143