chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 43384883 43384884 G A 52 GENIC homozygous 139526647 14 43385350 43385351 G A 28 GENIC homozygous 139526648 14 43385824 43385825 C 38 GENIC homozygous 139395956 14 43386740 43386741 A G 50 GENIC homozygous 139526649 14 43387221 43387222 A C 42 GENIC homozygous 139526650 14 43387222 43387223 G A 42 GENIC homozygous 139526651 14 43387319 43387320 C T 44 GENIC homozygous 139526652 14 43388668 43388669 T C 46 GENIC homozygous 139526653 14 43388728 43388728 T 22 GENIC possibly homozygous 139395957 14 43389231 43389231 C 37 GENIC homozygous 139395958 14 43389496 43389500 CCCT 15 GENIC homozygous 139395959 14 43389565 43389566 A G 12 GENIC homozygous 139526654 14 43390378 43390379 G A 48 GENIC possibly homozygous 139526655 14 43392338 43392338 C 14 GENIC homozygous 139395960 14 43393241 43393242 G T 30 GENIC homozygous 139526656 14 43393825 43393826 C T 25 GENIC homozygous 139526657