chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47952098	47952099	A	G	21	GENIC	homozygous	116588161
10	47952217	47952218	G	A	28	GENIC	homozygous	116588165
10	47952562	47952563	C	T	31	GENIC	homozygous	116878983
10	47952820	47952820		AAGGGCTGAGT	17	GENIC	homozygous	131092761
10	47953655	47953656	G	A	21	GENIC	homozygous	116878985
10	47956178	47956179	G	A	21	GENIC	homozygous	116878987
10	47959503	47959504	T	A	13	GENIC	homozygous	116588169
10	47959584	47959584		CAC	10	GENIC	heterozygous	135271625
10	47960091	47960094	AGG		23	GENIC	homozygous	131092762
10	47961974	47961975	C	G	21	GENIC	homozygous	116588171
10	47963329	47963330	T	C	23	GENIC	homozygous	116588177
10	47964581	47964582	A	G	22	GENIC	homozygous	116588179
10	47966076	47966077	A	G	25	GENIC	homozygous	116878989
10	47966642	47966643	G	A	17	GENIC	homozygous	117129099
10	47968473	47968474	T	G	18	GENIC	homozygous	116588183
10	47969212	47969212		TTG	14	GENIC	homozygous	131092763
10	47970923	47970924	T	C	23	GENIC	homozygous	116878991
10	47975362	47975362		C	14	GENIC	homozygous	128814999
10	47957935	47957940	ACTTA		20	GENIC	homozygous	128814996
10	47957942	47957942		GTC	20	GENIC	homozygous	128814997
10	47975475	47975476	A	G	14	GENIC	homozygous	116588187
10	47977112	47977113	T	C	23	GENIC	homozygous	116588189
10	47979709	47979710	G	C	27	GENIC	homozygous	116878995
10	47985967	47985968	T	C	21	GENIC	homozygous	116588191
10	47986418	47986419	A	G	25	GENIC	homozygous	116878997
10	47986857	47986858	T	C	33	GENIC	homozygous	116878999
10	47987256	47987257	A	G	19	GENIC	homozygous	116588193
10	47987300	47987301	C	T	18	GENIC	homozygous	116588195
10	47988383	47988383		TTTTTTTGT	1	GENIC	homozygous	128815001
10	47988532	47988533	C	T	7	GENIC	homozygous	117059163
10	47990409	47990410	C	T	22	GENIC	homozygous	116879001
10	47991994	47991995	G	A	27	GENIC	homozygous	116879003
10	47994206	47994207	G	A	13	GENIC	homozygous	116879005
10	47994389	47994389		C	2	GENIC	homozygous	128815002
10	47994389	47994390	G	T	2	GENIC	homozygous	116774451