chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	60526707	60526708	A	G	27	GENIC	homozygous	116155551
11	60528837	60528838	T	C	24	GENIC	homozygous	116399838
11	60530776	60530777	T	G	19	GENIC	homozygous	116155553
11	60533855	60533856	T	C	22	GENIC	homozygous	116155555
11	60534150	60534151	G	C	29	GENIC	possibly homozygous	116155557
11	60534466	60534467	A	C	28	GENIC	possibly homozygous	116155559
11	60537193	60537194	A	G	26	GENIC	homozygous	116399839
11	60537497	60537498	C	A	32	GENIC	possibly homozygous	116155561
11	60537765	60537766	G	A	24	GENIC	homozygous	116155563
11	60538176	60538177	A	G	35	GENIC	possibly homozygous	116399840
11	60538324	60538325	C	A	24	GENIC	homozygous	116155565
11	60538362	60538363	G	A	26	GENIC	homozygous	116155567
11	60538438	60538439	G	A	26	GENIC	possibly homozygous	116155569
11	60538588	60538589	A	G	36	GENIC	homozygous	116155571
11	60538707	60538708	A	G	30	GENIC	homozygous	116155573
11	60538755	60538756	C	T	32	GENIC	homozygous	116155575
11	60538873	60538874	C	T	19	GENIC	homozygous	116155577
11	60539323	60539324	G	T	34	GENIC	possibly homozygous	116155583
11	60539173	60539174	G	A	31	GENIC	possibly homozygous	116155579
11	60539293	60539294	G	A	34	GENIC	possibly homozygous	116155581
11	60539433	60539434	C	A	27	GENIC	possibly homozygous	116155585
11	60539512	60539513	G	A	29	GENIC	possibly homozygous	116155587
11	60539548	60539549	G	T	31	GENIC	possibly homozygous	116155589
11	60539794	60539795	A	G	25	GENIC	homozygous	116155591
11	60541395	60541396	G	C	23	GENIC	possibly homozygous	116155593
11	60542241	60542242	T	C	37	GENIC	homozygous	116155595
11	60546388	60546389	G	C	31	GENIC	possibly homozygous	116155597
11	60546971	60546972	G	C	15	GENIC	homozygous	116155599