chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	11106179	11106180	T	C	63	GENIC	heterozygous	119676976
19	11106641	11106642	G	C	22	GENIC	homozygous	130483367
19	11106643	11106643		A	22	GENIC	homozygous	130478498
19	11106645	11106646	T	C	21	GENIC	homozygous	130483368
19	11106646	11106647	A	T	20	GENIC	homozygous	130483369
19	11106650	11106650		C	20	GENIC	homozygous	130478499
19	11106655	11106655		A	19	GENIC	homozygous	130478500
19	11106657	11106657		A	19	GENIC	homozygous	130478501
19	11106660	11106660		TC	19	GENIC	homozygous	130478502
19	11106663	11106664	T		16	GENIC	homozygous	130478503
19	11106669	11106669		C	15	GENIC	homozygous	130478504
19	11106673	11106673		A	14	GENIC	homozygous	130478505
19	11106678	11106679	A	T	13	GENIC	homozygous	110143502
19	11106679	11106680	T	A	14	GENIC	homozygous	109887079
19	11106682	11106682		A	12	GENIC	homozygous	130478506
19	11106700	11106701	A	G	4	GENIC	homozygous	130483370
19	11106701	11106702	A	G	4	GENIC	homozygous	130483371
19	11106918	11106919	A	T	12	GENIC	homozygous	109635648
19	11106919	11106920	T	C	12	GENIC	homozygous	109850057
19	11106933	11106933		C	13	GENIC	homozygous	129584254
19	11106902	11106902		AC	10	GENIC	homozygous	129584251
19	11106904	11106906	TT		10	GENIC	homozygous	129584252
19	11106924	11106924		AA	12	GENIC	homozygous	129584253
19	11113132	11113133	C	T	1	GENIC	homozygous	130181374