chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90398049	90398050	G	A	40	GENIC	homozygous	116904589
10	90398068	90398069	C	T	35	GENIC	homozygous	116904591
10	90398104	90398105	C	A	43	GENIC	homozygous	116904593
10	90398740	90398741	T	C	49	GENIC	homozygous	116904595
10	90398962	90398963	G	A	43	GENIC	homozygous	116904597
10	90399354	90399355	T	C	62	GENIC	homozygous	116904599
10	90399373	90399374	C	T	62	GENIC	homozygous	116904601
10	90399405	90399406	C	T	58	GENIC	homozygous	116904603
10	90400500	90400501	G	T	58	GENIC	homozygous	116904605
10	90400501	90400502	G	C	58	GENIC	homozygous	116676210
10	90400510	90400511	T	C	60	GENIC	homozygous	116676212
10	90401582	90401583	C	T	37	GENIC	homozygous	116904607
10	90402052	90402053	C	A	41	GENIC	homozygous	116904609
10	90405078	90405079	C	T	50	GENIC	homozygous	116904611
10	90405252	90405253	A	C	46	GENIC	homozygous	116904613
10	90405305	90405306	A	T	48	GENIC	homozygous	116904615
10	90406528	90406529	G	A	25	GENIC	homozygous	116904617
10	90407093	90407094	G	C	39	GENIC	homozygous	116676216
10	90407213	90407214	A	G	36	GENIC	homozygous	116904619
10	90407485	90407486	G	A	40	GENIC	homozygous	116676218
10	90408576	90408577	T	C	43	GENIC	homozygous	116904621
10	90409478	90409479	C	T	35	GENIC	homozygous	116904623
10	90409902	90409903	G	T	43	GENIC	homozygous	116676222
10	90410024	90410025	G	A	51	GENIC	homozygous	116904625
10	90414204	90414205	C	T	45	GENIC	homozygous	116904627
10	90414650	90414651	G	A	39	GENIC	homozygous	116904629
10	90414912	90414913	T	C	41	GENIC	homozygous	116904631
10	90415163	90415164	G	A	54	GENIC	homozygous	116676236
10	90415390	90415391	A	T	40	GENIC	homozygous	116676238
10	90401055	90401055		C	49	GENIC	possibly homozygous	131469397
10	90403753	90403754	A		17	GENIC	possibly homozygous	131469398
10	90415159	90415160	A		54	GENIC	homozygous	128844161
10	90415162	90415163	G		54	GENIC	homozygous	128844162
10	90409346	90409347	C	G	19	GENIC	homozygous	117227976
10	90409399	90409400	A	G	29	GENIC	homozygous	117413162