chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 131980042 131980043 G A 14 GENIC homozygous 53066594 8 131980294 131980295 C T 23 GENIC homozygous 53066595 8 131981991 131981992 A - 15 GENIC homozygous 53066597 8 131982277 131982278 G A 22 GENIC homozygous 53066598 8 131982552 131982553 G GA 15 GENIC possibly homozygous 53306554 8 131983919 131983920 T C 14 GENIC homozygous 52900404 8 131984040 131984041 G GCT 3 GENIC heterozygous 53172687 8 131984693 131984694 T - 22 GENIC homozygous 52900410 8 131985694 131985695 A G 29 GENIC homozygous 53066600 8 131986730 131986731 T C 23 GENIC homozygous 52900430 8 131986910 131986911 C CT 13 GENIC homozygous 53066601 8 131986947 131986948 C G 24 GENIC homozygous 53066602 8 131987092 131987093 A G 15 GENIC homozygous 53066603 8 131987200 131987201 A G 12 GENIC homozygous 53066604 8 131987352 131987353 G T 29 GENIC homozygous 52900432 8 131987559 131987560 G A 20 GENIC homozygous 53066605 8 131987639 131987640 G A 29 GENIC homozygous 53066606 8 131987650 131987651 C A 26 GENIC homozygous 53066607 8 131987708 131987709 A G 22 GENIC homozygous 53066608 8 131988002 131988003 T G 13 GENIC homozygous 53066609 8 131988274 131988275 A C 24 GENIC homozygous 53066610 8 131988296 131988297 T C 24 GENIC homozygous 53066611 8 131988654 131988655 T TTTAAGTAG 21 GENIC homozygous 53066612 8 131988849 131988850 A AT 15 GENIC homozygous 53066613 8 131989125 131989126 G T 19 GENIC homozygous 53066614 8 131989353 131989354 G A 26 GENIC homozygous 53066615 8 131989489 131989490 G A 23 GENIC homozygous 53066616 8 131989590 131989591 T C 26 GENIC homozygous 53066617 8 131989781 131989782 A T 28 GENIC homozygous 53066618 8 131990301 131990302 A AACTT 26 GENIC homozygous 53066619 8 131990357 131990358 C T 24 GENIC homozygous 53066620 8 131990473 131990474 T G 24 GENIC homozygous 52900434 8 131990701 131990702 T C 22 GENIC homozygous 53066621 8 131991741 131991742 T C 20 GENIC homozygous 53066622