chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47952098	47952099	A	G	34	GENIC	homozygous	116588161
10	47952217	47952218	G	A	36	GENIC	homozygous	116588165
10	47952562	47952563	C	T	34	GENIC	homozygous	116878983
10	47952820	47952820		AAGGGCTGAGT	23	GENIC	homozygous	131092761
10	47953655	47953656	G	A	29	GENIC	homozygous	116878985
10	47956178	47956179	G	A	18	GENIC	homozygous	116878987
10	47959503	47959504	T	A	20	GENIC	homozygous	116588169
10	47961974	47961975	C	G	25	GENIC	homozygous	116588171
10	47963329	47963330	T	C	22	GENIC	homozygous	116588177
10	47964581	47964582	A	G	20	GENIC	homozygous	116588179
10	47966076	47966077	A	G	20	GENIC	possibly homozygous	116878989
10	47968473	47968474	T	G	31	GENIC	homozygous	116588183
10	47957935	47957940	ACTTA		25	GENIC	homozygous	128814996
10	47960091	47960094	AGG		26	GENIC	homozygous	131092762
10	47969212	47969212		TTG	22	GENIC	homozygous	131092763
10	47957942	47957942		GTC	26	GENIC	homozygous	128814997
10	47966642	47966643	G	A	10	GENIC	homozygous	117129099
10	47970923	47970924	T	C	14	GENIC	homozygous	116878991
10	47971412	47971413	G	A	28	GENIC	homozygous	116878993
10	47975362	47975362		C	16	GENIC	homozygous	128814999
10	47975475	47975476	A	G	18	GENIC	homozygous	116588187
10	47977112	47977113	T	C	25	GENIC	homozygous	116588189
10	47979709	47979710	G	C	31	GENIC	homozygous	116878995
10	47985967	47985968	T	C	19	GENIC	homozygous	116588191
10	47986418	47986419	A	G	23	GENIC	homozygous	116878997
10	47986857	47986858	T	C	21	GENIC	homozygous	116878999
10	47987256	47987257	A	G	26	GENIC	homozygous	116588193
10	47987300	47987301	C	T	23	GENIC	homozygous	116588195
10	47988409	47988409		TTG	1	GENIC	homozygous	132331214
10	47988532	47988533	C	T	10	GENIC	homozygous	117059163
10	47990409	47990410	C	T	20	GENIC	homozygous	116879001
10	47991994	47991995	G	A	24	GENIC	homozygous	116879003
10	47994206	47994207	G	A	20	GENIC	homozygous	116879005
10	47994389	47994389		C	6	GENIC	homozygous	128815002
10	47994389	47994390	G	T	6	GENIC	homozygous	116774451