chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	13131126	13131127	G	A	25	GENIC	homozygous	109394204
20	13131898	13131899	G	A	29	GENIC	homozygous	109492618
20	13132527	13132528	G	T	26	GENIC	homozygous	109394209
20	13133113	13133114	C	A	16	GENIC	homozygous	109492620
20	13133294	13133295	T	C	17	GENIC	homozygous	109099778
20	13133891	13133892	A	G	21	GENIC	homozygous	109492622
20	13134525	13134526	T	C	24	GENIC	possibly homozygous	109492624
20	13135065	13135066	T	C	38	GENIC	homozygous	109492626
20	13135811	13135812	C	A	25	GENIC	homozygous	109542822
20	13135863	13135864	G	T	19	GENIC	homozygous	109542824
20	13136823	13136824	G	A	14	GENIC	homozygous	109492628
20	13137200	13137201	A	G	34	GENIC	homozygous	109461698
20	13137281	13137282	C	T	24	GENIC	homozygous	109492632
20	13137359	13137360	A	G	21	GENIC	homozygous	109492634
20	13137385	13137386	A	T	19	GENIC	homozygous	109099782
20	13137593	13137594	G	A	31	GENIC	homozygous	109542826
20	13142127	13142128	C	T	19	GENIC	homozygous	109492636
20	13142763	13142764	C	T	29	GENIC	homozygous	109492638