chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 30980840 30980841 T C 21 GENIC homozygous 110321597 18 30981049 30981050 A T 2 GENIC homozygous 110589456 18 30999541 30999542 T A 20 GENIC homozygous 110321605 18 31005834 31005835 T C 22 GENIC homozygous 110321619 18 31015083 31015084 G A 26 GENIC homozygous 110532834 18 31016650 31016651 T C 16 GENIC homozygous 110321632 18 31026994 31026995 G A 9 GENIC homozygous 110457569 18 31052674 31052675 G C 25 GENIC homozygous 110321705 18 31062674 31062675 A T 34 GENIC homozygous 110321719 18 31062966 31062967 T C 29 GENIC homozygous 110532836 18 31062992 31062993 G C 26 GENIC homozygous 110532838 18 31063326 31063327 G A 27 GENIC homozygous 110321721 18 31063344 31063345 C T 29 GENIC homozygous 110321723 18 31063362 31063363 T C 27 GENIC homozygous 110532840 18 31063512 31063513 C T 28 GENIC homozygous 110321725 18 31063875 31063876 A G 17 GENIC homozygous 110321727 18 31063981 31063982 A C 26 GENIC homozygous 110321731 18 31064406 31064407 T C 15 GENIC homozygous 110457577 18 31064698 31064699 C T 25 GENIC homozygous 110532842 18 31065013 31065014 C A 23 GENIC homozygous 110321735 18 31066365 31066366 T G 41 GENIC homozygous 110321741 18 31066439 31066440 A G 37 GENIC homozygous 110321743 18 31066877 31066878 C T 23 GENIC homozygous 110532844 18 31067184 31067185 C T 13 GENIC homozygous 110321746 18 31067369 31067370 T C 20 GENIC homozygous 110321748 18 31067451 31067452 C A 26 GENIC homozygous 110532846 18 31068044 31068045 A C 29 GENIC homozygous 110532848 18 31068647 31068648 T C 20 GENIC homozygous 110321756 18 31069585 31069586 A G 27 GENIC homozygous 110321758 18 31069940 31069941 G A 38 GENIC homozygous 110321760 18 31070801 31070802 C T 17 GENIC homozygous 110321762