chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39688826	39688827	G	A	28	GENIC	homozygous	52963101
8	39690555	39690556	G	A	24	GENIC	homozygous	52591421
8	39690560	39690561	C	G	25	GENIC	homozygous	53501754
8	39690934	39690935	A	G	27	GENIC	homozygous	52591422
8	39690952	39690953	A	ATGTGTG	30	GENIC	homozygous	53501756
8	39691253	39691254	A	ATGTATGTGTGTGTG	4	GENIC	homozygous	53378061
8	39691382	39691383	G	-	19	GENIC	homozygous	52963103
8	39691385	39691393	TTGTTTTG	--------	20	GENIC	homozygous	52963104
8	39691393	39691394	T	A	16	GENIC	homozygous	53378063
8	39691742	39691743	C	T	29	GENIC	homozygous	52963106
8	39692640	39692641	A	G	28	GENIC	homozygous	52591430
8	39693527	39693528	C	CT	7	GENIC	heterozygous	53378065
8	39694463	39694464	A	ATAGACTGAC	52	GENIC	homozygous	52591439
8	39694656	39694657	T	TC	46	GENIC	homozygous	53501758
8	39695029	39695030	C	CTTTTT	14	GENIC	heterozygous	53378069
8	39695107	39695108	T	C	28	GENIC	homozygous	52591447
8	39695400	39695401	G	A	19	GENIC	homozygous	52963111
8	39695767	39695768	T	C	34	GENIC	homozygous	52591450
8	39696400	39696401	G	GT	12	GENIC	homozygous	52591452
8	39696568	39696569	A	G	42	GENIC	homozygous	52591453
8	39696961	39696962	C	T	45	GENIC	homozygous	52591454
8	39697481	39697482	A	G	41	GENIC	homozygous	52591455
8	39698748	39698749	C	T	49	GENIC	homozygous	53501760
8	39698790	39698791	G	A	45	GENIC	homozygous	53501761
8	39699902	39699903	A	C	30	GENIC	homozygous	53501763
8	39699967	39699968	C	T	41	GENIC	homozygous	52591460
8	39700512	39700513	C	-	20	GENIC	homozygous	52591462
8	39702186	39702187	G	A	35	GENIC	homozygous	53268804
8	39702312	39702315	TCC	---	17	GENIC	homozygous	52591465
8	39702345	39702346	A	AC	19	GENIC	possibly homozygous	53501765
8	39702415	39702416	G	GAA	22	GENIC	homozygous	52591466
8	39703327	39703328	G	A	37	GENIC	homozygous	53268805
8	39703866	39703869	CCC	---	26	GENIC	homozygous	53268806