chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	21194662	21194663	A	C	26	GENIC	homozygous	113378814
14	21198624	21198625	A	G	12	GENIC	homozygous	113378816
14	21199420	21199421	A	G	14	GENIC	homozygous	113378818
14	21203873	21203874	A	G	7	GENIC	homozygous	113378820
14	21197117	21197118	T	C	16	GENIC	homozygous	113580684
14	21198037	21198038	T	G	3	GENIC	heterozygous	118681767
14	21202081	21202082	G	T	3	GENIC	heterozygous	126033131
14	21209302	21209303	A	C	9	GENIC	homozygous	113378822
14	21211603	21211604	G	A	13	GENIC	homozygous	113378824
14	21212431	21212432	A	C	17	GENIC	homozygous	113378826
14	21212499	21212500	G	C	19	GENIC	homozygous	113378828
14	21214179	21214180	G	A	9	GENIC	homozygous	113378830
14	21214472	21214473	G	C	25	GENIC	homozygous	113378832
14	21215390	21215391	C	T	8	GENIC	homozygous	114164130
14	21215566	21215567	T	C	12	GENIC	heterozygous	113378836
14	21215757	21215758	C	T	14	GENIC	homozygous	113378838
14	21216027	21216028	A	G	14	GENIC	homozygous	113378840
14	21217285	21217286	T	C	21	GENIC	homozygous	125906612
14	21207365	21207366	T	C	4	GENIC	heterozygous	125906608
14	21207366	21207367	A	G	4	GENIC	heterozygous	125906610
14	21217327	21217328	G	T	7	GENIC	homozygous	125906614
14	21218351	21218352	A	G	18	GENIC	homozygous	113378842
14	21218545	21218546	A	G	9	GENIC	homozygous	113378844