chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	31267009	31267010	T	G	5	GENIC	homozygous	109339456
20	31267694	31267695	A	G	15	GENIC	homozygous	109339458
20	31268623	31268624	T	G	16	GENIC	homozygous	109339460
20	31268898	31268899	T	G	8	GENIC	homozygous	109572953
20	31269808	31269809	G	A	18	GENIC	homozygous	109339462
20	31270305	31270306	C	T	20	GENIC	homozygous	109339464
20	31272663	31272664	G	A	19	GENIC	homozygous	109339466
20	31273919	31273920	T	C	13	GENIC	homozygous	109339468
20	31274066	31274067	G	A	18	GENIC	homozygous	109164602
20	31275485	31275486	T	C	27	GENIC	homozygous	109339470
20	31275713	31275714	T	C	19	GENIC	homozygous	109339472
20	31275833	31275834	G	T	22	GENIC	homozygous	109339474
20	31276185	31276186	C	T	21	GENIC	homozygous	109339476
20	31277129	31277130	T	C	25	GENIC	homozygous	109339480
20	31277461	31277462	G	A	26	GENIC	homozygous	109339482
20	31281124	31281125	G	T	9	GENIC	homozygous	109572954
20	31281877	31281878	G	A	22	GENIC	homozygous	109339486
20	31282906	31282907	T	A	16	GENIC	homozygous	109339488
20	31283667	31283668	T	C	18	GENIC	homozygous	109339490
20	31284794	31284795	G	C	19	GENIC	homozygous	109339492
20	31286364	31286365	A	G	15	GENIC	homozygous	109435542
20	31273015	31273016	A	T	17	GENIC	homozygous	109253097
20	31287741	31287742	A	G	13	GENIC	homozygous	109572955
20	31288096	31288097	G	C	21	GENIC	homozygous	109339494
20	31289839	31289840	A	T	15	GENIC	homozygous	109339496
20	31290045	31290046	G	A	23	GENIC	homozygous	109164614