chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10362146	10362147	T	C	61	GENIC	homozygous	109090451
20	10362677	10362678	G	T	45	GENIC	homozygous	109090453
20	10363425	10363426	T	C	46	GENIC	homozygous	109090455
20	10363850	10363851	C	T	59	GENIC	heterozygous	119767957
20	10364209	10364210	C	T	62	GENIC	homozygous	109090457
20	10366603	10366604	A	G	48	GENIC	possibly homozygous	119767958
20	10368041	10368042	A	G	51	GENIC	homozygous	109090459
20	10368180	10368181	A	G	46	GENIC	homozygous	109090461
20	10368496	10368497	A	G	34	GENIC	possibly homozygous	109506883
20	10369350	10369351	T	C	44	GENIC	homozygous	109090463
20	10371043	10371044	A	T	26	GENIC	homozygous	109302031
20	10373371	10373372	G	C	40	GENIC	homozygous	109090465
20	10374364	10374365	G	A	36	GENIC	homozygous	109548614
20	10375272	10375273	C	A	45	GENIC	possibly homozygous	109090467
20	10377393	10377394	G	C	63	GENIC	heterozygous	119767959
20	10377397	10377398	G	C	57	GENIC	possibly homozygous	119767960
20	10377417	10377418	G	C	56	GENIC	homozygous	109527617
20	10377542	10377543	G	T	71	GENIC	possibly homozygous	109392562
20	10377835	10377836	A	G	57	GENIC	homozygous	109090469
20	10384154	10384155	G	T	30	GENIC	homozygous	109302035