chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 37830360 37830361 A G 40 GENIC homozygous 778021200 19 37830773 37830774 C T 32 GENIC homozygous 778021201 19 37832407 37832408 T C 30 GENIC homozygous 778021202 19 37833670 37833671 A T 26 GENIC homozygous 778021203 19 37833939 37833940 T C 50 GENIC homozygous 778021204 19 37834790 37834791 T C 28 GENIC homozygous 778021205 19 37836092 37836093 T C 36 GENIC homozygous 778021206 19 37836474 37836475 A G 47 GENIC homozygous 778021207 19 37837160 37837161 A G 49 GENIC possibly homozygous 778021208 19 37837766 37837767 G C 51 GENIC homozygous 778021209 19 37838077 37838078 T C 43 GENIC homozygous 778021210 19 37838079 37838080 A G 42 GENIC homozygous 778021211 19 37838923 37838924 T C 36 GENIC homozygous 778021212 19 37839601 37839602 C T 42 GENIC homozygous 778021213 19 37839610 37839611 A G 38 GENIC homozygous 778021214 19 37840352 37840353 A C 27 GENIC possibly homozygous 778021215 19 37840560 37840561 T C 30 GENIC homozygous 778021216 19 37841727 37841728 T G 29 GENIC heterozygous 778021217 19 37842122 37842123 G T 28 GENIC homozygous 778021218 19 37843078 37843079 G A 48 GENIC homozygous 778021219 19 37844555 37844556 A G 51 GENIC homozygous 778021220