chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 44092228 44092229 G A 14 GENIC homozygous 142738656 20 44092247 44092248 T C 12 GENIC homozygous 130114527 20 44092266 44092267 T C 12 GENIC homozygous 130114530 20 44096380 44096381 A G 20 GENIC homozygous 142738657 20 44096547 44096548 C A 15 GENIC homozygous 142738658 20 44096894 44096895 C A 17 GENIC homozygous 142738659 20 44097121 44097122 T C 22 GENIC homozygous 142738660 20 44097546 44097547 C T 22 GENIC homozygous 142738661 20 44097551 44097552 C A 22 GENIC homozygous 142738662 20 44099660 44099660 CAAGTTTAGTTACTGAACCATACTGAAG 8 GENIC homozygous 130000657 20 44101240 44101241 A G 25 GENIC homozygous 130114583 20 44101587 44101588 C G 14 GENIC homozygous 142738664 20 44102758 44102759 T C 17 GENIC homozygous 142738665 20 44102955 44102956 A G 19 GENIC homozygous 142738666 20 44103184 44103185 C T 18 GENIC homozygous 142738667 20 44103225 44103226 T C 10 GENIC homozygous 130114593 20 44103368 44103369 T G 18 GENIC homozygous 142738668 20 44103509 44103510 C T 18 GENIC homozygous 142738669 20 44103755 44103756 A G 18 GENIC homozygous 130114599 20 44106018 44106019 T C 23 GENIC homozygous 130114606 20 44106636 44106637 A G 12 GENIC homozygous 142738670 20 44107058 44107059 A T 10 GENIC homozygous 142738671 20 44107068 44107069 C T 10 GENIC homozygous 142738672 20 44107352 44107353 C A 17 GENIC homozygous 142738673 20 44107478 44107479 T A 22 GENIC homozygous 142738674 20 44108235 44108236 A G 12 GENIC homozygous 142738675 20 44109084 44109085 T G 12 GENIC homozygous 142738676 20 44098284 44098288 CTTT 11 GENIC homozygous 145194696 20 44103298 44103299 A 16 GENIC homozygous 142715530 20 44109081 44109081 A 11 GENIC homozygous 142715531 20 44099598 44099599 T 5 GENIC heterozygous 145086400 20 44099600 44099613 TCTCTCTCTCTCT 5 GENIC heterozygous 145086401