chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 117255591 117255592 G A 39 GENIC homozygous 993510270 4 117257889 117257890 C A 25 GENIC homozygous 993510271 4 117258118 117258119 C T 15 GENIC possibly homozygous 993510272 4 117260219 117260220 G A 22 GENIC homozygous 993510273 4 117261107 117261108 T C 33 GENIC homozygous 993510274 4 117263458 117263459 C T 25 GENIC possibly homozygous 993510275 4 117264605 117264606 A T 12 GENIC homozygous 993510276 4 117264644 117264645 C G 18 GENIC homozygous 993510277 4 117264803 117264804 C A 20 GENIC possibly homozygous 993510278 4 117264818 117264819 C A 15 GENIC homozygous 993510279 4 117265590 117265591 C A 36 GENIC homozygous 993510280 4 117266678 117266679 G A 15 GENIC homozygous 993510281 4 117268107 117268108 C T 9 GENIC homozygous 993510282 4 117271434 117271435 T C 31 GENIC homozygous 993510283 4 117274035 117274036 C G 17 GENIC homozygous 993510284 4 117275127 117275128 A C 22 GENIC homozygous 993510285 4 117277269 117277270 A G 35 GENIC possibly homozygous 993510286 4 117277305 117277306 C T 31 GENIC possibly homozygous 993510287 4 117277584 117277585 T C 17 GENIC homozygous 993510288 4 117277602 117277603 A C 15 GENIC homozygous 993510289 4 117278233 117278234 C T 25 GENIC possibly homozygous 993510290 4 117279408 117279409 T C 36 GENIC homozygous 993510291 4 117281635 117281636 G T 32 GENIC homozygous 993510292 4 117282737 117282738 G A 37 GENIC possibly homozygous 993510293 4 117283800 117283801 C T 38 GENIC homozygous 993510294