chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	205128834	205128835	G	A	24	GENIC	homozygous	57058213
4	205129264	205129265	A	G	25	GENIC	homozygous	57058214
4	205129586	205129587	T	TG	25	GENIC	homozygous	57058215
4	205129782	205129783	T	C	26	GENIC	homozygous	57058216
4	205129956	205129957	C	T	15	GENIC	homozygous	57058217
4	205130242	205130243	C	T	31	GENIC	possibly homozygous	57362815
4	205130304	205130305	C	T	26	GENIC	homozygous	57058218
4	205130305	205130306	T	C	26	GENIC	homozygous	57058219
4	205130578	205130579	C	T	15	GENIC	homozygous	57058220
4	205130927	205130928	C	G	26	GENIC	homozygous	57058221
4	205131056	205131057	T	C	18	GENIC	homozygous	57058222
4	205131067	205131068	A	G	20	GENIC	homozygous	57058223
4	205131439	205131440	G	C	53	GENIC	homozygous	57058224
4	205132645	205132646	G	A	27	GENIC	homozygous	57058225
4	205133026	205133027	G	A	22	GENIC	homozygous	57362817
4	205133039	205133040	A	G	22	GENIC	homozygous	57058226
4	205133447	205133448	G	A	22	GENIC	homozygous	57058227
4	205133966	205133967	C	T	17	GENIC	possibly homozygous	57362819
4	205134011	205134012	T	C	14	GENIC	homozygous	57058228
4	205134854	205134855	C	T	27	GENIC	homozygous	57362821
4	205135577	205135578	C	T	35	GENIC	homozygous	57362823
4	205137912	205137913	C	T	1	GENIC	homozygous	58410458
4	205138221	205138222	T	C	14	GENIC	possibly homozygous	57058230
4	205138227	205138228	G	GTT	13	GENIC	possibly homozygous	57362825
4	205149823	205149824	T	C	28	GENIC	homozygous	57058232
4	205149920	205149921	T	A	28	GENIC	homozygous	57058233