chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 3882258 3882259 A G 5 GENIC homozygous 129706103 20 3883183 3883183 A 15 GENIC homozygous 129651578 20 3884388 3884389 A G 28 GENIC homozygous 109070199 20 3883756 3883757 T C 10 GENIC homozygous 109070185 20 3883858 3883859 G A 12 GENIC homozygous 109070187 20 3884061 3884062 T C 21 GENIC homozygous 109070189 20 3884223 3884224 C G 24 GENIC homozygous 109070191 20 3884297 3884298 G A 26 GENIC homozygous 109070193 20 3884304 3884305 T C 31 GENIC homozygous 109070195 20 3884342 3884343 A G 26 GENIC homozygous 109070197 20 3884394 3884395 A G 28 GENIC homozygous 109070201 20 3884411 3884412 T C 27 GENIC homozygous 109070203 20 3884423 3884424 A G 26 GENIC homozygous 109070205 20 3884471 3884473 TT 25 GENIC homozygous 129651579 20 3884474 3884490 CATCCTGACCCCGAGG 25 GENIC homozygous 129651580 20 3884495 3884496 A G 24 GENIC homozygous 109389160 20 3884514 3884515 G A 26 GENIC homozygous 109231924 20 3884541 3884542 A T 27 GENIC homozygous 109070207 20 3884550 3884551 A G 10 GENIC homozygous 109070209 20 3884575 3884576 T C 16 GENIC homozygous 109070211 20 3884590 3884591 G C 19 GENIC homozygous 109070213 20 3884595 3884596 T C 19 GENIC homozygous 109070215 20 3884632 3884632 AAG 25 GENIC homozygous 129651581 20 3884633 3884635 AC 25 GENIC homozygous 129651582 20 3884833 3884834 G T 29 GENIC homozygous 109070217 20 3884934 3884935 T G 25 GENIC homozygous 109070219 20 3884947 3884948 G A 24 GENIC homozygous 109070221 20 3884990 3884991 T C 29 GENIC homozygous 109070223 20 3884998 3884999 A C 28 GENIC homozygous 109070225 20 3885004 3885005 T C 28 GENIC homozygous 109070227 20 3885005 3885006 G A 28 GENIC homozygous 109070229