chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	106759939	106759940	C	A	30	GENIC	homozygous	114438335
13	106769437	106769438	G	C	41	GENIC	homozygous	114438337
13	106769439	106769440	G	C	38	GENIC	homozygous	114438339
13	106769442	106769443	A	C	34	GENIC	homozygous	114438341
13	106785631	106785632	G	T	26	GENIC	homozygous	114438343
13	106798552	106798553	A	G	28	GENIC	homozygous	114438345
13	106803897	106803898	A	G	30	GENIC	homozygous	114438347
13	106803917	106803918	A	G	23	GENIC	homozygous	114438349
13	106845708	106845709	G	A	41	GENIC	homozygous	114438351
13	106919152	106919153	T	G	50	GENIC	homozygous	114438353
13	106923193	106923194	T	A	34	GENIC	homozygous	114438355
13	107009791	107009792	T	G	35	GENIC	heterozygous	114438357
13	107040378	107040379	T	G	3	GENIC	homozygous	114438359
13	107040381	107040382	T	G	2	GENIC	homozygous	114438361
13	107093167	107093168	G	A	20	GENIC	homozygous	114438363
13	107147090	107147091	T	C	38	GENIC	homozygous	114438365
13	107164028	107164029	A	C	43	GENIC	homozygous	114438367
13	107189327	107189328	T	A	7	GENIC	homozygous	114438369
13	107189565	107189566	G	T	27	GENIC	homozygous	114438371
13	107189576	107189577	A	C	28	GENIC	homozygous	114438373
13	107190380	107190381	A	T	61	GENIC	homozygous	114438375
13	107190381	107190382	T	C	61	GENIC	homozygous	114438377
13	107190426	107190427	G	C	56	GENIC	homozygous	114438379
13	107291266	107291267	A	G	35	GENIC	homozygous	114438381
13	107298140	107298141	A	G	32	GENIC	homozygous	114438382
13	107326801	107326802	A	T	27	GENIC	homozygous	114438384
13	107356603	107356604	G	T	25	GENIC	homozygous	114438386