chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10861887	10861888	T	C	13	GENIC	homozygous	109994166
19	10861931	10861932	G	A	8	GENIC	homozygous	109994168
19	10863398	10863399	A	G	23	GENIC	homozygous	109635164
19	10864281	10864282	G	A	17	GENIC	homozygous	109635166
19	10865261	10865262	C	T	19	GENIC	homozygous	109635168
19	10865745	10865746	T	C	12	GENIC	homozygous	109635170
19	10865756	10865757	T	C	16	GENIC	homozygous	109635172
19	10865802	10865803	T	C	29	GENIC	homozygous	109635174
19	10866461	10866462	G	T	16	GENIC	homozygous	110131091
19	10867211	10867212	G	A	26	GENIC	homozygous	110131093
19	10868166	10868167	T	C	15	GENIC	homozygous	109635177
19	10868195	10868196	C	T	17	GENIC	homozygous	109635179
19	10869990	10869991	C	T	7	GENIC	heterozygous	125309985
19	10870788	10870789	C	T	29	GENIC	homozygous	119596423
19	10870978	10870979	T	C	23	GENIC	homozygous	109635183
19	10871069	10871070	T	C	14	GENIC	homozygous	110131096
19	10871073	10871074	C	T	12	GENIC	homozygous	110131098
19	10871335	10871336	C	G	31	GENIC	homozygous	110076587
19	10871615	10871616	G	A	10	GENIC	homozygous	110099039
19	10870403	10870404	C	G	23	GENIC	homozygous	125237243
19	10870614	10870615	A	G	26	GENIC	homozygous	125237244