chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	39621955	39621956	G	A	57	GENIC	homozygous	114191238
5	39625630	39625631	A		31	GENIC	homozygous	128172130
5	39625636	39625636		T	32	GENIC	homozygous	128172131
5	39625649	39625649		G	33	GENIC	homozygous	128172132
5	39625694	39625695	T		33	GENIC	homozygous	128172133
5	39625699	39625699		A	34	GENIC	homozygous	128172134
5	39625710	39625710		C	36	GENIC	homozygous	128172135
5	39628444	39628445	C		32	GENIC	homozygous	128172136
5	39629715	39629715		T	6	GENIC	homozygous	128172137
5	39637737	39637737		A	33	GENIC	possibly homozygous	128172150
5	39647150	39647151	A		28	GENIC	heterozygous	128172152
5	39649018	39649019	G	A	46	GENIC	homozygous	113758379
5	39649080	39649081	G	A	45	GENIC	homozygous	113758381
5	39649121	39649122	C	A	40	GENIC	homozygous	114191239
5	39649325	39649326	A	G	32	GENIC	homozygous	113758383
5	39650429	39650431	AA		44	GENIC	homozygous	128172153
5	39650454	39650455	A	G	44	GENIC	homozygous	113758385
5	39650635	39650636	A	G	44	GENIC	homozygous	113758387
5	39650668	39650669	G	C	43	GENIC	homozygous	113758389
5	39650734	39650735	G	T	37	GENIC	homozygous	114191240
5	39649379	39649379		TATA	36	GENIC	homozygous	130952493
5	39638924	39638931	CAGGGAC		38	GENIC	homozygous	130952492