chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	71394880	71394881	A	G	36	GENIC	homozygous	116630228
10	71394977	71394978	T	C	44	GENIC	homozygous	117083450
10	71395241	71395242	G	C	37	GENIC	homozygous	117083452
10	71400546	71400547	T	G	35	GENIC	homozygous	116630234
10	71401502	71401503	T	C	33	GENIC	homozygous	116630236
10	71402983	71402984	C	T	45	GENIC	homozygous	116630238
10	71403404	71403405	G	A	30	GENIC	homozygous	117083458
10	71404720	71404721	A	C	11	GENIC	homozygous	116630240
10	71406422	71406423	C	T	24	GENIC	homozygous	117083460
10	71408600	71408601	T	C	53	GENIC	homozygous	116630242
10	71413150	71413151	C	T	27	GENIC	homozygous	117197138
10	71417264	71417265	C	T	19	GENIC	homozygous	117083462
10	71421073	71421074	T	C	15	GENIC	homozygous	117083464
10	71423733	71423734	T	A	24	GENIC	homozygous	116630250
10	71427217	71427218	G	T	27	GENIC	homozygous	116630254
10	71427431	71427432	C	A	17	GENIC	homozygous	117083466
10	71428123	71428124	A	G	16	GENIC	homozygous	116630256
10	71428690	71428691	G	A	24	GENIC	homozygous	116630264
10	71429184	71429185	C	G	18	GENIC	homozygous	116630266
10	71430987	71430988	A	C	27	GENIC	homozygous	117083469
10	71431036	71431037	C	T	27	GENIC	homozygous	117083471
10	71432628	71432629	G	A	25	GENIC	homozygous	117083475
10	71433123	71433124	C	T	32	GENIC	homozygous	116630272
10	71433261	71433262	C	T	19	GENIC	homozygous	116630274
10	71434017	71434018	C	T	31	GENIC	homozygous	117083476
10	71434491	71434492	G	A	27	GENIC	homozygous	117083478
10	71435164	71435165	T	C	37	GENIC	homozygous	116630276
10	71436309	71436310	C	T	23	GENIC	homozygous	117083480
10	71436685	71436686	T	A	18	GENIC	homozygous	117083482
10	71436937	71436938	T	A	20	GENIC	homozygous	117083484
10	71440406	71440407	A	G	22	GENIC	homozygous	116630280
10	71430055	71430056	G	A	31	GENIC	homozygous	116800046
10	71430056	71430057	A	C	32	GENIC	homozygous	116800048