chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	78168841	78168842	G	C	14	GENIC	homozygous	116643339
10	78169805	78169806	T	C	15	GENIC	homozygous	116806147
10	78169917	78169918	A	G	14	GENIC	homozygous	117017250
10	78169947	78169948	C	T	21	GENIC	homozygous	116643343
10	78170040	78170041	T	A	23	GENIC	homozygous	116643347
10	78170397	78170398	C	T	14	GENIC	homozygous	116643351
10	78170992	78170993	T	C	21	GENIC	homozygous	116643367
10	78171474	78171475	T	C	20	GENIC	homozygous	116643377
10	78171512	78171513	T	C	15	GENIC	homozygous	116643379
10	78171515	78171516	C	G	16	GENIC	homozygous	116643381
10	78171661	78171662	G	A	10	GENIC	homozygous	116806149
10	78171864	78171865	T	C	19	GENIC	homozygous	116643393
10	78172186	78172187	A	G	15	GENIC	homozygous	117017251
10	78170272	78170272		T	18	GENIC	homozygous	128834098
10	78171381	78171381		AA	16	GENIC	homozygous	128834099
10	78171726	78171726		AAAAATAATTTACTGCGTGAAGCTGGCTAAGTAAAGAGTAAAGTTTTCAGTGATGTGAACTAATAAAACAAGTCTAGGTGCTTTAAAA	8	GENIC	homozygous	131096743
10	78172296	78172297	C	A	8	GENIC	homozygous	118002190