chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 145361099 145361100 A G 49 GENIC homozygous 522125548 5 145361900 145361901 G C 45 GENIC homozygous 522125549 5 145363123 145363126 CCA --- 13 GENIC heterozygous 690726205 5 145363124 145363126 CA -- 16 GENIC homozygous 690726206 5 145363320 145363321 A C 44 GENIC homozygous 522125550 5 145364001 145364002 C T 35 GENIC homozygous 519983359 5 145364976 145364977 A G 47 GENIC homozygous 522125551 5 145365273 145365274 C CAGTT 42 GENIC homozygous 690726207 5 145365654 145365655 A T 45 GENIC possibly homozygous 522125552 5 145365891 145365892 C T 55 GENIC homozygous 519983360 5 145366834 145366835 G A 40 GENIC homozygous 519983361 5 145367301 145367302 T G 46 GENIC homozygous 519983362 5 145368243 145368244 G GA 48 GENIC homozygous 690726208 5 145369071 145369072 A G 41 GENIC homozygous 522125553 5 145369147 145369148 T C 36 GENIC homozygous 522125554 5 145370295 145370296 A - 14 GENIC heterozygous 690726209 5 145370988 145370989 T C 24 GENIC possibly homozygous 522125555 5 145371450 145371456 GTGTGT ------ 11 GENIC possibly homozygous 690726210 5 145373159 145373160 T C 25 GENIC homozygous 519983363 5 145373253 145373254 T G 37 GENIC homozygous 519983364 5 145373669 145373670 C T 40 GENIC homozygous 519983365 5 145373689 145373695 TGTGTG ------ 19 GENIC heterozygous 690726212 5 145373691 145373695 TGTG ---- 19 GENIC possibly homozygous 690726213 5 145374274 145374275 C G 41 GENIC homozygous 522125556 5 145375208 145375209 C CT 21 GENIC homozygous 690726215 5 145375693 145375694 G A 9 GENIC possibly homozygous 522125557 5 145376435 145376436 G A 26 GENIC homozygous 519983366 5 145376586 145376587 G A 28 GENIC homozygous 519983367 5 145377734 145377735 T G 41 GENIC possibly homozygous 522125558 5 145377759 145377760 A G 44 GENIC homozygous 522125559 5 145377938 145377939 T C 47 GENIC homozygous 522125560 5 145378460 145378461 A G 41 GENIC possibly homozygous 519983368 5 145378986 145378987 G A 46 GENIC possibly homozygous 519983369