chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 45318942 45318943 G - 12 GENIC homozygous 51442209 10 45319051 45319052 A - 14 GENIC homozygous 51442210 10 45322856 45322857 T C 23 GENIC homozygous 51636198 10 45324170 45324171 T TACTC 19 GENIC possibly homozygous 51442213 10 45324347 45324348 A G 22 GENIC possibly homozygous 52317951 10 45324869 45324870 G A 29 GENIC homozygous 51636199 10 45325072 45325075 GGT --- 13 GENIC homozygous 51442216 10 45328204 45328205 G A 20 GENIC homozygous 51636202 10 45328688 45328689 G A 19 GENIC homozygous 51636203 10 45329139 45329140 C T 24 GENIC homozygous 51442220 10 45329152 45329153 C A 25 GENIC homozygous 51636204 10 45330543 45330544 A - 6 GENIC homozygous 51442221 10 45330618 45330619 C CGT 1 GENIC homozygous 51442225 10 45332672 45332674 AA -- 3 GENIC homozygous 52439001 10 45333627 45333628 G GTAGCTAGC 37 GENIC homozygous 51442227 10 45324139 45324140 T TCAGATACTGTGTAGATCGCTTCTCGGCCTTTTGGCTAAGATCAAGTG 22 GENIC possibly homozygous 52372925 10 45332517 45332518 G GAAAA 14 GENIC heterozygous 52372930 10 45327370 45327372 AA -- 16 GENIC heterozygous 52459232