chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	14559054	14559055	G	T	41	GENIC	homozygous	109102682
20	14561242	14561243	T	C	29	GENIC	possibly homozygous	109102704
20	14562007	14562008	G	A	38	GENIC	homozygous	109303526
20	14562161	14562162	G	A	38	GENIC	homozygous	109303528
20	14562371	14562372	A	T	36	GENIC	homozygous	109303530
20	14562490	14562491	G	A	32	GENIC	homozygous	109303532
20	14562779	14562780	T	C	27	GENIC	homozygous	109102714
20	14563523	14563524	A	G	47	GENIC	homozygous	109102728
20	14563633	14563634	A	C	22	GENIC	homozygous	109303534
20	14564052	14564053	T	C	38	GENIC	homozygous	109303544
20	14564056	14564057	C	T	35	GENIC	homozygous	109303546
20	14564448	14564449	T	C	36	GENIC	homozygous	109102736
20	14564951	14564952	C	T	29	GENIC	homozygous	109102742
20	14565065	14565066	T	G	32	GENIC	homozygous	109102744
20	14565505	14565506	A	G	20	GENIC	homozygous	109102748
20	14565782	14565783	C	T	32	GENIC	homozygous	109102753
20	14567029	14567030	C	T	20	GENIC	homozygous	109102761
20	14567995	14567996	T	C	40	GENIC	homozygous	109102767
20	14568598	14568599	T	C	40	GENIC	homozygous	109102777
20	14569890	14569891	G	A	27	GENIC	homozygous	109303548
20	14570220	14570221	T	G	25	GENIC	homozygous	109240951
20	14570305	14570306	T	G	11	GENIC	homozygous	109240953
20	14570780	14570781	G	A	11	GENIC	homozygous	109303550
20	14570873	14570874	T	C	19	GENIC	homozygous	109102793
20	14571072	14571073	A	C	35	GENIC	homozygous	109102799
20	14571503	14571504	A	C	19	GENIC	homozygous	109303552
20	14571649	14571650	A	G	26	GENIC	homozygous	109102807
20	14571817	14571818	C	G	33	GENIC	homozygous	109102811
20	14571854	14571855	A	G	38	GENIC	homozygous	109102815
20	14571921	14571922	T	C	40	GENIC	homozygous	109303554
20	14572263	14572264	A	G	20	GENIC	homozygous	109102819
20	14572963	14572964	A	C	28	GENIC	homozygous	109303556