chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 159590044 159590045 C T 21 GENIC homozygous 114072974 5 159590355 159590356 A C 8 GENIC homozygous 114072975 5 159590356 159590357 G C 6 GENIC homozygous 114072976 5 159590377 159590378 G A 10 GENIC homozygous 114072977 5 159590516 159590517 A G 16 GENIC homozygous 114072978 5 159590543 159590544 T C 21 GENIC homozygous 114072979 5 159590567 159590568 T C 13 GENIC homozygous 114072980 5 159591041 159591042 C T 29 GENIC homozygous 114072983 5 159591165 159591166 A G 26 GENIC homozygous 114072984 5 159591294 159591295 G A 19 GENIC homozygous 114072985 5 159591492 159591493 C T 18 GENIC homozygous 114072986 5 159591711 159591712 G A 19 GENIC homozygous 114072987 5 159591959 159591960 C T 21 GENIC homozygous 114072988 5 159592241 159592242 A G 17 GENIC homozygous 114072989 5 159592551 159592552 G A 30 GENIC homozygous 114072990 5 159592593 159592594 G A 25 GENIC homozygous 114072991 5 159592713 159592714 C T 13 GENIC homozygous 114072992 5 159593011 159593012 T A 11 GENIC homozygous 114072993 5 159593229 159593230 A G 17 GENIC homozygous 114072994 5 159593316 159593317 A C 17 GENIC homozygous 114072995 5 159594481 159594482 G A 19 GENIC homozygous 114072996 5 159595521 159595522 G A 17 GENIC homozygous 114072997 5 159598268 159598269 G A 20 GENIC homozygous 114072998 5 159599504 159599505 T C 28 GENIC homozygous 114072999 5 159600471 159600472 T C 20 GENIC homozygous 114073000 5 159601143 159601144 C T 29 GENIC homozygous 114073001 5 159601217 159601218 A G 15 GENIC homozygous 114073002 5 159601274 159601275 A G 26 GENIC homozygous 114073003 5 159602018 159602019 C T 12 GENIC homozygous 114073004