chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6974053	6974054	A	T	12	GENIC	homozygous	109297571
20	6974072	6974073	C	A	7	GENIC	homozygous	109297573
20	6974791	6974792	T	C	8	GENIC	homozygous	109235234
20	6974843	6974844	G	C	15	GENIC	homozygous	109082557
20	6975700	6975701	C	T	13	GENIC	homozygous	109235235
20	6976356	6976357	G	A	10	GENIC	possibly homozygous	109235236
20	6976866	6976867	C	T	11	GENIC	homozygous	109235237
20	6976916	6976917	C	G	10	GENIC	homozygous	109082570
20	6977547	6977548	T	C	13	GENIC	homozygous	109082574
20	6977765	6977766	G	A	10	GENIC	homozygous	109235238
20	6978465	6978466	G	T	17	GENIC	possibly homozygous	109235239
20	6979118	6979119	G	A	3	GENIC	homozygous	109082576
20	6980121	6980122	C	T	8	GENIC	homozygous	109235240
20	6983970	6983971	G	T	18	GENIC	homozygous	109082584
20	6984065	6984066	G	A	14	GENIC	homozygous	109235241
20	6984081	6984082	C	T	14	GENIC	homozygous	109082586
20	6984406	6984407	C	T	13	GENIC	homozygous	109235242
20	6984808	6984809	A	G	10	GENIC	homozygous	109082590
20	6985126	6985127	C	T	5	GENIC	homozygous	109082592
20	6985205	6985206	A	C	4	GENIC	homozygous	109082594
20	6985207	6985208	A	G	3	GENIC	homozygous	109082596
20	6985260	6985261	C	T	7	GENIC	homozygous	109082598
20	6985633	6985634	C	G	18	GENIC	homozygous	109082600
20	6986285	6986286	C	T	10	GENIC	homozygous	109082604
20	6986578	6986579	C	T	7	GENIC	homozygous	109082606
20	6986949	6986950	G	T	2	GENIC	homozygous	109297575
20	6987048	6987049	A	C	5	GENIC	homozygous	109082608
20	6988148	6988149	T	C	7	GENIC	homozygous	109082610
20	6988208	6988209	A	G	16	GENIC	homozygous	109082612
20	6989431	6989432	C	T	20	GENIC	homozygous	109235246
20	6989590	6989591	A	G	12	GENIC	homozygous	109082618
20	6989809	6989810	A	C	13	GENIC	homozygous	109082620
20	6989835	6989836	T	C	14	GENIC	homozygous	109082622