chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 62845110 62845111 G A 20 GENIC homozygous 993443685 4 62845203 62845204 T C 28 GENIC homozygous 993443686 4 62846328 62846329 T C 31 GENIC homozygous 993443687 4 62846452 62846453 T C 27 GENIC possibly homozygous 993443688 4 62848124 62848125 T G 17 GENIC homozygous 993443689 4 62848583 62848584 T C 27 GENIC homozygous 993443690 4 62848699 62848700 C T 31 GENIC homozygous 993443691 4 62851003 62851004 T C 23 GENIC homozygous 993443692 4 62851339 62851340 C T 28 GENIC possibly homozygous 993443693 4 62851955 62851956 C T 36 GENIC possibly homozygous 993443694 4 62853526 62853527 G A 27 GENIC homozygous 993443695 4 62853655 62853656 G T 33 GENIC homozygous 993443696 4 62853656 62853657 T C 33 GENIC homozygous 993443697 4 62855641 62855642 T C 22 GENIC homozygous 993443698 4 62855748 62855749 T C 20 GENIC homozygous 993443699 4 62855846 62855847 C T 26 GENIC possibly homozygous 993443700 4 62856102 62856103 A G 20 GENIC homozygous 993443701 4 62856299 62856300 C T 30 GENIC homozygous 993443702 4 62856410 62856411 A C 37 GENIC homozygous 993443703 4 62856412 62856413 A G 35 GENIC homozygous 993443704 4 62856422 62856423 C T 34 GENIC homozygous 993443705 4 62856433 62856434 C T 35 GENIC homozygous 993443706 4 62856434 62856435 A G 35 GENIC homozygous 993443707 4 62856742 62856743 G A 29 GENIC homozygous 993443708 4 62857122 62857123 C T 28 GENIC possibly homozygous 993443709 4 62857195 62857196 C T 19 GENIC homozygous 993443710 4 62858669 62858670 C T 39 GENIC possibly homozygous 993443711 4 62860166 62860167 C G 20 GENIC homozygous 993443712