chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	7113416	7113417	C	A	25	GENIC	homozygous	45409011
20	7113803	7113805	GG	--	31	GENIC	homozygous	45409012
20	7114024	7114025	T	C	18	GENIC	homozygous	45409013
20	7114315	7114316	A	C	24	GENIC	homozygous	45409014
20	7114362	7114363	C	T	33	GENIC	homozygous	45409015
20	7114446	7114447	G	C	43	GENIC	homozygous	45409016
20	7114735	7114736	A	C	41	GENIC	homozygous	45409017
20	7115351	7115352	C	T	36	GENIC	homozygous	45409018
20	7115496	7115497	A	ACC	39	GENIC	possibly homozygous	45409019
20	7115496	7115497	A	AC	39	GENIC	heterozygous	45756067
20	7116092	7116093	A	G	25	GENIC	homozygous	45409020
20	7116159	7116160	A	G	22	GENIC	homozygous	45409021
20	7116634	7116635	T	C	38	GENIC	homozygous	45409023
20	7117198	7117199	A	-	47	GENIC	homozygous	45409024
20	7117997	7117998	A	-	38	GENIC	homozygous	45409025
20	7118426	7118427	G	A	2	GENIC	heterozygous	45756071
20	7118610	7118611	C	T	63	GENIC	homozygous	45409026
20	7119072	7119073	G	A	56	GENIC	homozygous	45409031
20	7119665	7119666	G	-	50	GENIC	homozygous	45409032
20	7119877	7119878	C	CAAACA	28	GENIC	homozygous	45409033
20	7119972	7119974	CC	--	18	GENIC	possibly homozygous	45818911
20	7116176	7116178	TT	--	8	GENIC	homozygous	45900016
20	7116180	7116182	TT	--	8	GENIC	homozygous	45900017
20	7116810	7116842	ATATATATATATATATATATATATATATATAT	--------------------------------	20	GENIC	homozygous	45900018
20	7118899	7118900	G	GTGTGTA	13	GENIC	heterozygous	45900019
20	7117997	7117998	A	T	38	GENIC	homozygous	45897415
20	7120878	7120880	TT	--	24	GENIC	homozygous	45409036
20	7120900	7120901	C	CTTTTTTT	9	GENIC	heterozygous	45900020
20	7121030	7121031	G	A	30	GENIC	homozygous	45409040
20	7121166	7121167	C	CT	18	GENIC	possibly homozygous	45840820
20	7121305	7121307	TT	--	37	GENIC	homozygous	45409042
20	7121399	7121400	A	G	44	GENIC	homozygous	45409043
20	7121415	7121416	T	-	42	GENIC	homozygous	45409044
20	7120900	7120901	C	CTTTTTTTTTTTTTTTT	9	GENIC	heterozygous	45859098