chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 11694302 11694303 T C 45 GENIC homozygous 142035405 8 11695297 11695297 CCAT 17 GENIC possibly homozygous 146204673 8 11696436 11696437 T C 65 GENIC homozygous 142035406 8 11702703 11702703 AGGGG 13 GENIC homozygous 143374656 8 11700782 11700783 G C 36 GENIC homozygous 142035415 8 11697012 11697013 C G 57 GENIC homozygous 143385760 8 11699435 11699436 T C 49 GENIC homozygous 143385761 8 11700626 11700627 G T 35 GENIC homozygous 143385762 8 11702641 11702642 C T 42 GENIC homozygous 143385763 8 11697264 11697264 C 20 GENIC heterozygous 143374654 8 11702682 11702682 GAGAG 19 GENIC homozygous 143374655 8 11702735 11702736 G A 15 GENIC homozygous 143385764 8 11702744 11702744 G 15 GENIC homozygous 143374657 8 11702746 11702746 GAGGGAAGA 15 GENIC homozygous 143374658 8 11702754 11702755 G A 15 GENIC homozygous 143385765 8 11703216 11703217 T C 50 GENIC homozygous 143385766 8 11703219 11703220 T C 48 GENIC homozygous 142035422 8 11703360 11703361 A G 43 GENIC homozygous 143385767