chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	77448861	77448862	A	G	26	GENIC	homozygous	50893275
11	77449548	77449549	T	C	25	GENIC	possibly homozygous	50893277
11	77450960	77450961	A	G	29	GENIC	homozygous	50893279
11	77451439	77451440	G	A	27	GENIC	homozygous	51020355
11	77451834	77451835	T	C	24	GENIC	homozygous	50893287
11	77452223	77452224	T	TG	36	GENIC	homozygous	51020356
11	77452409	77452410	T	TA	22	GENIC	homozygous	50893289
11	77452585	77452586	T	A	29	GENIC	homozygous	51020357
11	77452962	77452963	T	-	22	GENIC	homozygous	50893293
11	77452969	77452971	TG	--	22	GENIC	homozygous	51020358
11	77453309	77453310	G	C	21	GENIC	homozygous	50893299
11	77453902	77453903	A	-	10	GENIC	possibly homozygous	50966484
11	77453964	77453965	T	TAGCA	6	GENIC	homozygous	50893303
11	77453968	77453969	T	-	3	GENIC	homozygous	50893305
11	77455205	77455206	A	G	42	GENIC	homozygous	50893307
11	77455495	77455496	C	CTCT	26	GENIC	homozygous	50893311
11	77455534	77455535	T	-	24	GENIC	possibly homozygous	50893313
11	77455858	77455859	A	G	42	GENIC	homozygous	50893315
11	77455859	77455860	A	C	41	GENIC	homozygous	50893317
11	77456343	77456344	T	A	25	GENIC	homozygous	51020359
11	77456346	77456347	A	G	25	GENIC	homozygous	50893319
11	77456373	77456374	A	-	25	GENIC	homozygous	51020360
11	77456439	77456440	T	C	34	GENIC	homozygous	51020361
11	77456466	77456467	T	C	35	GENIC	possibly homozygous	51020362
11	77456541	77456542	G	A	44	GENIC	homozygous	50893321
11	77456921	77456922	A	ATTTT	5	GENIC	homozygous	51020363