chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	40695638	40695639	A	T	3	GENIC	homozygous	114767357
6	40695725	40695726	C	T	3	GENIC	homozygous	114767359
6	40700910	40700911	G	C	2	GENIC	homozygous	114767361
6	40701109	40701110	G	C	3	GENIC	homozygous	114767363
6	40701612	40701613	T	C	5	GENIC	homozygous	114767365
6	40701672	40701673	G	A	4	GENIC	homozygous	114767367
6	40701778	40701779	A	G	2	GENIC	homozygous	114767369
6	40702020	40702021	G	T	7	GENIC	homozygous	114767371
6	40702277	40702278	G	C	3	GENIC	homozygous	114767377
6	40702298	40702299	A	T	3	GENIC	homozygous	114767379
6	40702577	40702578	G	A	2	GENIC	homozygous	114767381
6	40702680	40702681	C	T	9	GENIC	homozygous	114767383
6	40703109	40703110	A	G	3	GENIC	homozygous	114767385
6	40703137	40703138	T	C	3	GENIC	homozygous	114767387
6	40706180	40706181	C	A	6	GENIC	homozygous	114767391
6	40706410	40706411	G	T	4	GENIC	homozygous	114767393
6	40706494	40706495	C	A	4	GENIC	homozygous	114767395
6	40707475	40707476	G	T	3	GENIC	homozygous	114767397
6	40707995	40707996	G	A	8	GENIC	homozygous	114767405
6	40708002	40708003	A	G	6	GENIC	homozygous	114767407
6	40708701	40708702	C	T	3	GENIC	homozygous	114767409
6	40708791	40708792	A	G	4	GENIC	homozygous	114767411
6	40709143	40709144	T	A	3	GENIC	homozygous	114767413
6	40709153	40709154	T	G	5	GENIC	homozygous	114767415
6	40709432	40709433	T	C	2	GENIC	homozygous	114767417
6	40709471	40709472	T	A	5	GENIC	homozygous	114767419
6	40709853	40709854	T	A	5	GENIC	homozygous	114767421
6	40709854	40709855	G	C	5	GENIC	homozygous	114767423
6	40709880	40709881	G	A	4	GENIC	homozygous	114767425
6	40710413	40710414	T	C	6	GENIC	homozygous	114767427
6	40710667	40710668	G	A	3	GENIC	homozygous	114767429
6	40710680	40710681	G	A	4	GENIC	homozygous	114767431
6	40710767	40710768	C	T	3	GENIC	homozygous	114767433
6	40710799	40710800	A	G	2	GENIC	homozygous	114767435
6	40712500	40712501	T	A	11	GENIC	homozygous	114767437
6	40713315	40713316	T	C	7	GENIC	homozygous	114767439
6	40713338	40713339	G	A	8	GENIC	homozygous	114767441