chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47959445	47959446	G	A	37	GENIC	homozygous	117142077
10	47959503	47959504	T	A	27	GENIC	homozygous	116588169
10	47960608	47960609	G	A	20	GENIC	homozygous	117142079
10	47962200	47962201	C	T	22	GENIC	homozygous	117142081
10	47963155	47963156	G	A	29	GENIC	homozygous	117142083
10	47963329	47963330	T	C	27	GENIC	homozygous	116588177
10	47964581	47964582	A	G	35	GENIC	homozygous	116588179
10	47968473	47968474	T	G	37	GENIC	homozygous	116588183
10	47970099	47970100	T	C	29	GENIC	homozygous	117142085
10	47975475	47975476	A	G	40	GENIC	homozygous	116588187
10	47977112	47977113	T	C	30	GENIC	homozygous	116588189
10	47977187	47977188	G	A	32	GENIC	possibly homozygous	117142087
10	47982179	47982180	G	A	34	GENIC	homozygous	117142089
10	47985967	47985968	T	C	24	GENIC	homozygous	116588191
10	47987256	47987257	A	G	26	GENIC	homozygous	116588193
10	47987273	47987274	A	G	22	GENIC	homozygous	117142091
10	47987300	47987301	C	T	26	GENIC	homozygous	116588195
10	47988273	47988274	C	T	17	GENIC	homozygous	117142093
10	47989346	47989347	T	C	32	GENIC	possibly homozygous	117142095
10	47990143	47990144	T	C	30	GENIC	homozygous	117142097
10	47990543	47990544	T	C	31	GENIC	homozygous	117009016
10	47990574	47990575	G	T	29	GENIC	homozygous	117142099
10	47990639	47990640	T	G	31	GENIC	homozygous	117142101
10	47990877	47990878	C	A	29	GENIC	possibly homozygous	117142103
10	47990901	47990902	G	A	33	GENIC	homozygous	117142105
10	47991348	47991349	T	G	36	GENIC	homozygous	117142107
10	47991444	47991445	T	C	35	GENIC	homozygous	117142109
10	47991738	47991739	C	T	28	GENIC	homozygous	117142111
10	47992037	47992038	C	T	35	GENIC	homozygous	117142113
10	47992044	47992045	G	A	34	GENIC	homozygous	117142115
10	47993281	47993282	C	T	34	GENIC	homozygous	117142117
10	47993696	47993697	A	G	18	GENIC	homozygous	116588201
10	47996525	47996526	T	G	21	GENIC	homozygous	116588205