chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 103657968 103657969 A G 29 GENIC homozygous 521099471 10 103658439 103658440 A G 46 GENIC homozygous 521099472 10 103659619 103659620 T G 42 GENIC homozygous 523781540 10 103659887 103659889 CC -- 10 GENIC heterozygous 691142404 10 103659899 103659900 G - 15 GENIC heterozygous 691142406 10 103662173 103662174 A C 36 GENIC homozygous 523781541 10 103662211 103662212 G GA 27 GENIC homozygous 691142407 10 103662344 103662345 C A 25 GENIC heterozygous 523781542 10 103662594 103662595 A G 50 GENIC possibly homozygous 523781543 10 103662601 103662602 C CT 28 GENIC heterozygous 691142408 10 103662715 103662719 TTTT ---- 15 GENIC homozygous 691142409 10 103664257 103664258 C T 46 GENIC homozygous 523781544 10 103664985 103664986 C T 26 GENIC heterozygous 523781545 10 103665312 103665313 C T 31 GENIC homozygous 523781546 10 103665617 103665618 C T 33 GENIC homozygous 523781547 10 103665767 103665768 A G 22 GENIC homozygous 521099473 10 103665802 103665803 C T 20 GENIC homozygous 523781548 10 103667631 103667632 C T 48 GENIC homozygous 523781549 10 103667793 103667794 A G 37 GENIC possibly homozygous 521099474 10 103667854 103667855 A G 33 GENIC homozygous 521099475 10 103668540 103668541 C CAA 14 GENIC homozygous 691142410 10 103669357 103669358 G A 34 GENIC possibly homozygous 523781550 10 103669648 103669649 A G 28 GENIC homozygous 523781551 10 103669968 103669969 C T 42 GENIC possibly homozygous 521099476 10 103670093 103670094 A T 31 GENIC homozygous 523781552 10 103670167 103670168 G A 39 GENIC homozygous 523781553 10 103670279 103670280 G A 32 GENIC homozygous 523781554