chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	31933151	31933152	A	G	10	GENIC	homozygous	45521142
20	31969769	31969770	A	C	14	GENIC	homozygous	45521359
20	31969781	31969782	A	C	7	GENIC	homozygous	45521361
20	31969787	31969788	T	C	7	GENIC	homozygous	45521363
20	31969791	31969792	T	C	7	GENIC	homozygous	45521365
20	31969793	31969794	A	C	6	GENIC	homozygous	45521367
20	31969794	31969795	G	C	7	GENIC	homozygous	45521369
20	31969801	31969802	T	A	6	GENIC	homozygous	45846876
20	31969802	31969803	A	C	6	GENIC	homozygous	45846877
20	31969803	31969804	T	G	6	GENIC	homozygous	45846878
20	31969811	31969812	G	C	6	GENIC	homozygous	45521371
20	31969815	31969816	A	AGT	6	GENIC	homozygous	45846879
20	31969818	31969820	AA	--	6	GENIC	homozygous	45846880
20	31969822	31969823	C	-	8	GENIC	homozygous	45521373
20	31969855	31969857	CA	--	6	GENIC	homozygous	45846881
20	31969857	31969858	A	ACT	6	GENIC	homozygous	45846882
20	31969874	31969875	C	G	8	GENIC	homozygous	45846883
20	31969875	31969876	T	C	8	GENIC	homozygous	45846884
20	31969887	31969888	A	C	9	GENIC	homozygous	45521383
20	31969891	31969892	A	T	12	GENIC	homozygous	45521385
20	31969892	31969893	G	T	12	GENIC	homozygous	45521387
20	31969900	31969901	C	T	13	GENIC	homozygous	45521389
20	31969904	31969907	TGG	---	13	GENIC	homozygous	45846885
20	31969907	31969908	T	TCC	12	GENIC	homozygous	45846886
20	31969911	31969912	C	G	10	GENIC	homozygous	45521393
20	31969915	31969916	C	T	11	GENIC	homozygous	45521395
20	31969928	31969929	A	T	13	GENIC	homozygous	45521397
20	31969959	31969960	G	C	19	GENIC	homozygous	45521399
20	31969962	31969963	G	C	18	GENIC	homozygous	45521401
20	31956095	31956096	G	A	16	GENIC	homozygous	45703345