chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	81207952	81207953	C	T	29	GENIC	homozygous	112748235
4	81208413	81208414	T	C	16	GENIC	homozygous	112748239
4	81213132	81213133	A	T	23	GENIC	homozygous	112748243
4	81213399	81213400	T	C	28	GENIC	homozygous	112748245
4	81215801	81215802	G	A	10	GENIC	homozygous	113276909
4	81215803	81215804	G	A	10	GENIC	homozygous	112748249
4	81216563	81216564	A	G	12	GENIC	homozygous	112748251
4	81218371	81218372	T	A	36	GENIC	homozygous	112748253
4	81219204	81219205	T	C	6	GENIC	homozygous	112748255
4	81220000	81220001	A	G	29	GENIC	homozygous	112748259
4	81220013	81220014	G	A	28	GENIC	homozygous	112748261
4	81221243	81221244	G	A	21	GENIC	homozygous	112748265
4	81221261	81221262	C	T	22	GENIC	homozygous	112748267
4	81214618	81214619	T	C	24	GENIC	homozygous	119434796
4	81223921	81223922	A	G	11	GENIC	homozygous	112748271
4	81225283	81225284	G	A	18	GENIC	homozygous	112748275
4	81225292	81225293	A	T	16	GENIC	homozygous	119434797
4	81225656	81225657	A	C	13	GENIC	homozygous	112748277
4	81226875	81226876	T	C	30	GENIC	homozygous	112748279
4	81230253	81230254	C	A	18	GENIC	heterozygous	119434798
4	81230606	81230607	G	T	33	GENIC	homozygous	112748285
4	81231473	81231474	G	A	13	GENIC	homozygous	112748287