chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 15133931 15133932 A C 5 GENIC heterozygous 629233297 12 15134298 15134299 T TC 6 GENIC heterozygous 744939242 12 15134791 15134792 A G 24 GENIC homozygous 629233298 12 15135448 15135449 G T 14 GENIC possibly homozygous 629233299 12 15135506 15135507 T - 3 GENIC heterozygous 744939243 12 15135661 15135662 G A 20 GENIC possibly homozygous 629233300 12 15135904 15135905 T A 15 GENIC heterozygous 629233301 12 15139455 15139456 G GT 1 GENIC homozygous 744939246 12 15139849 15139850 G A 5 GENIC heterozygous 629233302 12 15140786 15140787 T TC 14 GENIC possibly homozygous 744939247 12 15141359 15141360 G C 19 GENIC possibly homozygous 629233303 12 15142134 15142135 G A 5 GENIC heterozygous 629233304 12 15142799 15142800 T C 14 GENIC homozygous 629233305 12 15145622 15145623 T C 23 GENIC possibly homozygous 629233306 12 15146149 15146150 T TGCTCA 1 GENIC homozygous 744939248 12 15146825 15146826 C T 25 GENIC homozygous 629233307 12 15146993 15146994 A T 19 GENIC possibly homozygous 629233308 12 15147430 15147431 G A 16 GENIC homozygous 629233309 12 15148244 15148245 C CATGTATGTATGTATGT 1 GENIC homozygous 744939250 12 15148497 15148498 C T 18 GENIC possibly homozygous 629233310 12 15148714 15148715 T G 15 GENIC homozygous 629233311 12 15148856 15148857 C G 14 GENIC homozygous 629233312 12 15150331 15150332 C T 12 GENIC heterozygous 629233313 12 15150789 15150790 C T 19 GENIC possibly homozygous 629233314 12 15152360 15152361 C T 19 GENIC homozygous 629233315 12 15152465 15152466 G A 13 GENIC possibly homozygous 629233316