chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 101698380 101698381 G A 59 GENIC homozygous 114654737 13 101699756 101699757 G C 64 GENIC homozygous 114654738 13 101700248 101700249 C T 50 GENIC homozygous 114654739 13 101700642 101700643 C T 49 GENIC homozygous 114654740 13 101700740 101700741 G A 63 GENIC homozygous 114437832 13 101700743 101700744 A T 63 GENIC homozygous 114437834 13 101700782 101700783 C 60 GENIC homozygous 131921711 13 101701418 101701419 C G 53 GENIC homozygous 114654741 13 101703506 101703507 A 66 GENIC homozygous 131921712 13 101704705 101704706 G C 22 GENIC homozygous 123794899 13 101705376 101705380 CTTC 6 GENIC homozygous 133972887 13 101706137 101706137 C 5 GENIC homozygous 131921713 13 101707319 101707320 G A 3 GENIC homozygous 123794905 13 101707924 101707925 G A 27 GENIC homozygous 123794906 13 101700779 101700780 A 60 GENIC homozygous 129091082 13 101704768 101704768 TTGTTG 4 GENIC homozygous 129091083 13 101708094 101708095 C G 52 GENIC homozygous 114654742 13 101709006 101709007 G A 62 GENIC homozygous 114654743 13 101709027 101709028 T C 53 GENIC homozygous 114654744 13 101709524 101709525 C T 76 GENIC homozygous 114654745 13 101710531 101710532 T 23 GENIC homozygous 131921714 13 101711119 101711119 CTGC 37 GENIC homozygous 132174088 13 101711671 101711671 CT 73 GENIC homozygous 132174089 13 101711973 101711974 G A 51 GENIC homozygous 114654746 13 101712012 101712013 A G 46 GENIC homozygous 114654747 13 101712049 101712049 ACATTGCTACACGGACATGTGATCTCCACATGAAGTGATTGAT 34 GENIC homozygous 132174090 13 101714543 101714543 CCAGGACATAGGAC 64 GENIC homozygous 129091085 13 101719474 101719475 A C 63 GENIC homozygous 114654748 13 101720453 101720454 G 72 GENIC homozygous 129091086 13 101719530 101719531 A C 56 GENIC homozygous 114654749 13 101720220 101720221 G A 66 GENIC homozygous 114654750 13 101723319 101723320 T C 70 GENIC homozygous 114654751 13 101724644 101724645 A C 68 GENIC homozygous 114654752