chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 39365079 39365080 T C 31 GENIC heterozygous 52590983 8 39366176 39366177 C T 17 GENIC heterozygous 52590984 8 39412316 39412317 T C 11 GENIC heterozygous 52962503 8 39412421 39412422 A G 20 GENIC heterozygous 52591032 8 39413582 39413583 A G 23 GENIC heterozygous 52962509 8 39413646 39413647 C T 45 GENIC heterozygous 52962510 8 39421261 39421262 C A 21 GENIC heterozygous 52962523 8 39421824 39421825 T C 31 GENIC heterozygous 52591067 8 39426659 39426660 G A 36 GENIC heterozygous 52591075 8 39435918 39435919 T C 40 GENIC heterozygous 52962580 8 39438083 39438084 A G 23 GENIC heterozygous 52962589 8 39438101 39438102 A - 32 GENIC heterozygous 52962590 8 39445548 39445549 A C 31 GENIC heterozygous 52962599 8 39445553 39445563 GTCCCCGACG ---------- 28 GENIC heterozygous 52962600 8 39445963 39445964 T C 25 GENIC heterozygous 52962601 8 39446091 39446092 A G 14 GENIC heterozygous 52962602 8 39466743 39466744 C T 8 GENIC heterozygous 54797387 8 39467304 39467305 T C 9 GENIC heterozygous 52962621 8 39474715 39474716 G A 42 GENIC heterozygous 52962627 8 39474789 39474790 A ATT 45 GENIC heterozygous 52962628 8 39486910 39486911 C T 9 GENIC heterozygous 52962651 8 39500721 39500722 G T 27 GENIC heterozygous 52962671 8 39500773 39500774 A G 41 GENIC heterozygous 52962672 8 39501093 39501094 T C 42 GENIC heterozygous 52962673 8 39511407 39511408 A G 41 GENIC heterozygous 52962696 8 39526119 39526120 C CAGCTCA 13 GENIC heterozygous 52962728 8 39549526 39549527 C T 24 GENIC heterozygous 52962761 8 39553444 39553445 C A 42 GENIC heterozygous 52962765 8 39553579 39553580 G A 13 GENIC heterozygous 52962766