chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5120503	5120504	T	C	12	GENIC	homozygous	125210386
20	5120514	5120515	G	A	7	GENIC	homozygous	125221627
20	5120518	5120519	G	A	6	GENIC	homozygous	125221628
20	5122010	5122011	T	C	25	GENIC	possibly homozygous	125177244
20	5120567	5120568	T	C	14	GENIC	homozygous	125177238
20	5120643	5120644	T	C	15	GENIC	homozygous	125177239
20	5120789	5120790	C	T	20	GENIC	homozygous	125177240
20	5120851	5120852	T	C	14	GENIC	homozygous	125177241
20	5120889	5120890	G	C	21	GENIC	homozygous	125177242
20	5121474	5121475	G	A	15	GENIC	homozygous	125177243
20	5122060	5122061	T	C	25	GENIC	homozygous	125221629
20	5122177	5122178	C	T	14	GENIC	homozygous	125177245
20	5122374	5122375	T	A	24	GENIC	homozygous	125177247
20	5122395	5122396	G	A	15	GENIC	homozygous	125177248
20	5122616	5122617	C	T	20	GENIC	homozygous	125177249
20	5122641	5122642	C	T	18	GENIC	homozygous	125221630
20	5122713	5122714	T	C	7	GENIC	homozygous	125177250
20	5122719	5122720	A	C	9	GENIC	homozygous	125177251
20	5122905	5122906	T	C	16	GENIC	homozygous	125177253
20	5123060	5123061	A	G	34	GENIC	possibly homozygous	125177254