chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	59833948	59833949	T	C	38	GENIC	homozygous	110366344
18	59838155	59838156	T	C	29	GENIC	homozygous	110366346
18	59843895	59843896	A	G	20	GENIC	homozygous	110366350
18	59844228	59844229	A	C	17	GENIC	homozygous	110366352
18	59844329	59844330	T	C	20	GENIC	homozygous	110366354
18	59844410	59844411	C	T	23	GENIC	homozygous	110366356
18	59844494	59844495	C	T	43	GENIC	homozygous	110366358
18	59845071	59845072	C	T	42	GENIC	homozygous	110366360
18	59845170	59845171	A	G	52	GENIC	homozygous	110366362
18	59845801	59845802	G	A	33	GENIC	homozygous	110480654
18	59845870	59845871	T	C	31	GENIC	homozygous	110366364
18	59853824	59853825	A	G	29	GENIC	homozygous	110366400
18	59859632	59859633	C	T	21	GENIC	homozygous	110815038
18	59862723	59862724	A	G	36	GENIC	homozygous	110815040
18	59864318	59864319	A	G	35	GENIC	homozygous	110480676
18	59864464	59864465	G	A	47	GENIC	homozygous	110864130
18	59865123	59865124	T	C	33	GENIC	homozygous	110815042
18	59869250	59869251	C	T	34	GENIC	homozygous	110815044
18	59869255	59869256	G	A	34	GENIC	homozygous	110815046
18	59869258	59869259	A	G	34	GENIC	homozygous	110366444
18	59869698	59869699	A	C	38	GENIC	homozygous	110815048
18	59870051	59870052	T	A	75	GENIC	homozygous	110864132
18	59870887	59870888	G	A	50	GENIC	homozygous	110815050
18	59873237	59873238	G	A	22	GENIC	homozygous	110815052
18	59875106	59875107	C	T	42	GENIC	homozygous	110864134
18	59875354	59875355	G	T	22	GENIC	homozygous	110366450
18	59875630	59875631	T	A	19	GENIC	homozygous	110366452
18	59877952	59877953	T	A	42	GENIC	homozygous	110366454
18	59880531	59880532	G	A	8	GENIC	homozygous	110815054