chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4536254	4536255	G	C	21	GENIC	homozygous	109329524
20	4536432	4536433	G	A	19	GENIC	homozygous	109329526
20	4536769	4536770	G	A	11	GENIC	homozygous	109329528
20	4537191	4537192	C	T	25	GENIC	homozygous	109329530
20	4537428	4537429	T	C	29	GENIC	homozygous	109329532
20	4537650	4537651	C	A	23	GENIC	possibly homozygous	109329534
20	4538517	4538518	C	A	20	GENIC	homozygous	109329536
20	4538566	4538567	T	C	26	GENIC	homozygous	109329538
20	4538582	4538583	A	G	25	GENIC	homozygous	109329540
20	4538916	4538917	C	G	24	GENIC	homozygous	109329542
20	4539682	4539683	G	A	34	GENIC	homozygous	109329544
20	4539962	4539963	A	G	22	GENIC	homozygous	109074677
20	4540301	4540302	T	C	23	GENIC	homozygous	109074679
20	4540422	4540423	G	A	22	GENIC	homozygous	109329546
20	4540599	4540600	A	G	15	GENIC	homozygous	109074681
20	4540730	4540731	C	G	24	GENIC	homozygous	109074683
20	4540868	4540869	A	G	23	GENIC	homozygous	109074686
20	4541193	4541194	G	C	15	GENIC	homozygous	109074688
20	4541199	4541200	T	A	17	GENIC	homozygous	109074690
20	4541369	4541370	A	C	10	GENIC	homozygous	109074692