chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	61135921	61135922	T	C	22	GENIC	heterozygous	46181747
19	61136055	61136056	C	T	21	GENIC	heterozygous	46181748
19	61136272	61136273	A	G	25	GENIC	heterozygous	46181749
19	61136294	61136295	G	A	28	GENIC	heterozygous	46181750
19	61136423	61136424	G	A	14	GENIC	heterozygous	46181751
19	61136744	61136745	A	G	11	GENIC	heterozygous	46181752
19	61137191	61137192	C	T	15	GENIC	heterozygous	46181754
19	61138983	61138984	T	TGTG	12	GENIC	homozygous	46181763
19	61139284	61139285	C	CT	23	GENIC	heterozygous	46181766
19	61139440	61139441	C	A	16	GENIC	heterozygous	46181767
19	61139595	61139596	C	CCAAACA	11	GENIC	homozygous	46275122
19	61140138	61140139	G	A	20	GENIC	heterozygous	46181768
19	61140290	61140291	G	A	10	GENIC	heterozygous	46181769
19	61140493	61140494	C	T	12	GENIC	heterozygous	46181771
19	61140506	61140507	G	A	13	GENIC	heterozygous	46181772
19	61140629	61140630	A	T	14	GENIC	heterozygous	46181773
19	61140721	61140722	C	-	10	GENIC	heterozygous	46181774
19	61140728	61140729	C	A	10	GENIC	heterozygous	46892228
19	61141174	61141175	G	T	9	GENIC	heterozygous	46181780
19	61141433	61141434	G	A	13	GENIC	heterozygous	46181785
19	61142098	61142099	G	A	21	GENIC	heterozygous	46181788
19	61142099	61142100	C	T	21	GENIC	heterozygous	46181789
19	61142262	61142263	C	T	10	GENIC	heterozygous	46181790
19	61142278	61142279	T	C	9	GENIC	heterozygous	46181791
19	61142560	61142561	A	G	20	GENIC	heterozygous	46181792
19	61142787	61142788	G	GC	18	GENIC	heterozygous	46181793
19	61142795	61142796	C	T	17	GENIC	heterozygous	46181794
19	61142961	61142962	G	GCA	15	GENIC	heterozygous	46181795
19	61142963	61142964	G	A	15	GENIC	heterozygous	46181796
19	61143004	61143005	G	A	20	GENIC	heterozygous	46181797
19	61143300	61143301	G	A	12	GENIC	heterozygous	46181799
19	61143534	61143535	G	T	12	GENIC	heterozygous	46181802
19	61143583	61143584	T	C	13	GENIC	heterozygous	46181803