chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	30036489	30036490	T	C	26	GENIC	homozygous	116542167
10	30037429	30037430	A	C	32	GENIC	homozygous	116751949
10	30037764	30037765	A	T	17	GENIC	homozygous	116542169
10	30038364	30038365	A	C	7	GENIC	homozygous	116542175
10	30038525	30038526	C	T	13	GENIC	homozygous	116751951
10	30039121	30039122	G	A	20	GENIC	homozygous	116751953
10	30039202	30039203	T	C	17	GENIC	homozygous	116542181
10	30039316	30039317	A	G	31	GENIC	possibly homozygous	116542183
10	30040104	30040105	G	A	11	GENIC	homozygous	116751955
10	30040648	30040649	C	T	17	GENIC	homozygous	116542189
10	30040707	30040708	C	T	15	GENIC	homozygous	116542193
10	30040712	30040713	A	G	15	GENIC	homozygous	116542195
10	30041592	30041593	C	T	3	GENIC	homozygous	116924227
10	30041710	30041711	T	A	15	GENIC	homozygous	116751957
10	30041941	30041942	A	G	27	GENIC	homozygous	116542203
10	30041978	30041979	A	T	25	GENIC	homozygous	116751959
10	30042312	30042313	C	T	27	GENIC	homozygous	116751963
10	30042780	30042781	G	A	19	GENIC	homozygous	116751967
10	30042808	30042809	T	G	19	GENIC	homozygous	116542211
10	30043152	30043153	T	C	21	GENIC	homozygous	116542213
10	30043170	30043171	C	T	18	GENIC	homozygous	116751969
10	30043429	30043430	A	G	20	GENIC	homozygous	116542215
10	30043437	30043438	G	A	20	GENIC	homozygous	116751971
10	30045238	30045239	C	T	28	GENIC	homozygous	116751979
10	30046149	30046150	G	A	27	GENIC	homozygous	116542221
10	30046402	30046403	G	T	19	GENIC	homozygous	116542223
10	30046951	30046952	A	G	20	GENIC	homozygous	116542225
10	30047356	30047357	C	T	18	GENIC	homozygous	116542227
10	30047436	30047437	T	C	14	GENIC	homozygous	116542229
10	30047860	30047861	G	A	18	GENIC	homozygous	116542231
10	30047895	30047896	G	C	12	GENIC	homozygous	116542233
10	30048145	30048146	A	G	12	GENIC	homozygous	116751981
10	30048429	30048430	A	G	16	GENIC	homozygous	116542235
10	30048690	30048691	G	A	14	GENIC	homozygous	116542237