chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 87436646 87436647 G - 12 GENIC homozygous 696240540 13 87437570 87437571 A T 46 GENIC homozygous 532700429 13 87437693 87437694 C T 54 GENIC homozygous 532700430 13 87437877 87437878 A G 38 GENIC possibly homozygous 532700431 13 87437882 87437883 T C 40 GENIC possibly homozygous 532700432 13 87438264 87438265 G A 47 GENIC homozygous 532700433 13 87439019 87439020 G A 27 GENIC homozygous 532700434 13 87439202 87439203 G A 48 GENIC possibly homozygous 532700435 13 87439617 87439619 TC -- 33 GENIC heterozygous 696240541 13 87439621 87439623 TC -- 39 GENIC heterozygous 696240542 13 87439626 87439627 C G 57 GENIC heterozygous 536435011 13 87439953 87439957 TTAT ---- 8 GENIC homozygous 696240543 13 87440070 87440071 G A 36 GENIC homozygous 532700436 13 87441546 87441547 G A 59 GENIC homozygous 532700437 13 87444345 87444346 T - 25 GENIC homozygous 696240545 13 87445217 87445218 G GTGTA 26 GENIC homozygous 696240546 13 87445333 87445334 C T 38 GENIC homozygous 532700438 13 87448026 87448027 C CT 12 GENIC heterozygous 696240547 13 87448051 87448052 C T 27 GENIC heterozygous 536435012 13 87448072 87448073 T C 26 GENIC heterozygous 532700439