chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	40511009	40511011	GT	--	19	GENIC	heterozygous	54869577
6	40511599	40511600	A	G	35	GENIC	homozygous	54869578
6	40512225	40512226	G	A	31	GENIC	homozygous	54869579
6	40512751	40512752	C	T	28	GENIC	homozygous	54869580
6	40512796	40512797	T	C	36	GENIC	homozygous	54869581
6	40512982	40512983	G	T	26	GENIC	homozygous	54869582
6	40513774	40513775	T	C	31	GENIC	homozygous	54869583
6	40513956	40513957	A	G	40	GENIC	homozygous	54869584
6	40513962	40513963	C	T	46	GENIC	homozygous	54869585
6	40514140	40514141	T	C	43	GENIC	homozygous	54869586
6	40514211	40514212	T	C	32	GENIC	homozygous	54869587
6	40515210	40515211	C	G	15	GENIC	homozygous	54869588
6	40515245	40515246	G	GTT	10	GENIC	homozygous	54869589
6	40515411	40515412	T	C	26	GENIC	homozygous	54869590
6	40515423	40515424	A	G	30	GENIC	homozygous	54869591
6	40516632	40516634	GT	--	14	GENIC	homozygous	54362298
6	40518439	40518440	T	-	8	GENIC	heterozygous	54362300
6	40520325	40520326	C	T	28	GENIC	homozygous	54869592
6	40520597	40520598	T	C	29	GENIC	homozygous	54869593
6	40521203	40521204	T	C	48	GENIC	homozygous	54869594
6	40522890	40522891	G	T	26	GENIC	homozygous	54869595
6	40524021	40524022	C	T	26	GENIC	homozygous	54869596
6	40524289	40524290	T	C	22	GENIC	heterozygous	54869597
6	40524351	40524352	A	G	22	GENIC	heterozygous	54869598
6	40524430	40524431	A	C	20	GENIC	homozygous	54869599
6	40524709	40524710	G	T	45	GENIC	homozygous	54869600
6	40525223	40525224	A	G	25	GENIC	homozygous	54869601
6	40525296	40525297	G	A	28	GENIC	homozygous	54869602
6	40525351	40525352	C	T	31	GENIC	homozygous	54869603
6	40525436	40525437	A	C	24	GENIC	homozygous	54869604
6	40525879	40525880	C	T	35	GENIC	possibly homozygous	54869605
6	40524327	40524328	T	TGA	1	GENIC	homozygous	54834174