chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
X	78160906	78160907	T	G	41	GENIC	heterozygous	119929390
X	78160994	78160995	C	T	44	GENIC	heterozygous	119929391
X	78161012	78161013	A	C	41	GENIC	heterozygous	119929392
X	78161030	78161031	T	A	39	GENIC	heterozygous	119929393
X	78161035	78161036	G	A	37	GENIC	heterozygous	120003768
X	78175909	78175910	G	A	37	GENIC	heterozygous	119929405
X	78175986	78175987	C	T	54	GENIC	heterozygous	119929406
X	78176077	78176078	C	A	34	GENIC	heterozygous	120003769
X	78176106	78176107	C	A	31	GENIC	heterozygous	120003770
X	78177331	78177332	A	T	25	GENIC	heterozygous	120054910
X	78177356	78177357	T	C	26	GENIC	heterozygous	119929412
X	78178092	78178093	A	G	23	GENIC	heterozygous	119929414
X	78178175	78178176	G	A	46	GENIC	heterozygous	119929416
X	78178424	78178425	G	C	54	GENIC	heterozygous	120030767
X	78180458	78180459	G	C	86	GENIC	heterozygous	120070161
X	78191187	78191188	C	T	31	GENIC	heterozygous	120030770
X	78173011	78173012	G	A	12	GENIC	heterozygous	120085741
X	78178554	78178555	G	C	22	GENIC	heterozygous	120085743
X	78191929	78191930	A	G	43	GENIC	heterozygous	120085745