chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103052078	103052079	A	-	11	GENIC	heterozygous	61299599
1	103054287	103054291	TGTG	----	13	GENIC	heterozygous	61487423
1	103054289	103054291	TG	--	13	GENIC	heterozygous	60780159
1	103055545	103055547	AC	--	12	GENIC	heterozygous	62147413
1	103060875	103060876	G	GTC	11	GENIC	heterozygous	62341903
1	103060875	103060876	G	GTCTC	11	GENIC	possibly homozygous	62553464
1	103066285	103066287	CT	--	13	GENIC	heterozygous	62147417
1	103074490	103074494	ATTT	----	1	GENIC	homozygous	60780185
1	103076300	103076302	GT	--	7	GENIC	heterozygous	62229340
1	103077583	103077584	A	C	23	GENIC	homozygous	60780186
1	103078006	103078009	AGT	---	16	GENIC	heterozygous	62311823
1	103078398	103078399	C	CA	13	GENIC	heterozygous	62147419
1	103078743	103078744	T	G	2	GENIC	homozygous	62147423
1	103084323	103084327	TGTG	----	12	GENIC	heterozygous	61487521
1	103084325	103084327	TG	--	12	GENIC	possibly homozygous	60780187