chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 31893470 31893471 T C 15 GENIC homozygous 45521083 20 31894064 31894065 T C 27 GENIC homozygous 45740948 20 31894653 31894654 C T 37 GENIC homozygous 45740949 20 31894750 31894751 T C 33 GENIC homozygous 45740951 20 31895283 31895284 T TG 15 GENIC homozygous 45740953 20 31895296 31895297 T TTC 15 GENIC homozygous 45740955 20 31895540 31895541 A G 30 GENIC homozygous 45740957 20 31896042 31896043 C G 22 GENIC homozygous 45521087 20 31896321 31896322 A AATC 27 GENIC homozygous 45521089 20 31897519 31897520 G GGACA 21 GENIC homozygous 45521091 20 31897998 31897999 C - 2 GENIC heterozygous 45521097 20 31898003 31898009 AAAAAC ------ 2 GENIC heterozygous 45859731 20 31898029 31898030 C A 11 GENIC homozygous 45521103 20 31898250 31898251 T C 27 GENIC homozygous 45521105 20 31898708 31898709 G A 31 GENIC homozygous 45740959 20 31898950 31898951 C T 21 GENIC homozygous 45740961 20 31898992 31898993 C T 17 GENIC homozygous 45740963 20 31901809 31901810 C T 27 GENIC homozygous 45740965 20 31901862 31901863 G C 22 GENIC homozygous 45521115 20 31902038 31902039 G T 31 GENIC homozygous 45740967 20 31902222 31902223 C T 25 GENIC homozygous 45740969 20 31903751 31903752 T C 30 GENIC homozygous 45521121 20 31905147 31905148 A G 20 GENIC homozygous 45740970