chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 117255591 117255592 G A 38 GENIC homozygous 978833427 4 117257889 117257890 C A 35 GENIC homozygous 978833428 4 117258118 117258119 C T 48 GENIC homozygous 978833429 4 117260219 117260220 G A 24 GENIC homozygous 978833430 4 117261107 117261108 T C 48 GENIC homozygous 978833431 4 117263458 117263459 C T 79 GENIC homozygous 978833432 4 117264605 117264606 A T 63 GENIC homozygous 978833433 4 117264644 117264645 C G 63 GENIC homozygous 978833434 4 117265590 117265591 C A 37 GENIC homozygous 978833435 4 117266678 117266679 G A 27 GENIC homozygous 978833436 4 117268107 117268108 C T 57 GENIC homozygous 978833437 4 117268193 117268194 T C 41 GENIC homozygous 978833438 4 117271434 117271435 T C 55 GENIC homozygous 978833439 4 117272285 117272286 A G 33 GENIC homozygous 978833440 4 117274035 117274036 C G 31 GENIC homozygous 978833441 4 117275127 117275128 A C 39 GENIC homozygous 978833442 4 117277269 117277270 A G 36 GENIC homozygous 978833443 4 117277305 117277306 C T 46 GENIC homozygous 978833444 4 117277584 117277585 T C 29 GENIC homozygous 978833445 4 117277602 117277603 A C 22 GENIC homozygous 978833446 4 117278233 117278234 C T 22 GENIC homozygous 978833447 4 117279408 117279409 T C 45 GENIC homozygous 978833448 4 117281635 117281636 G T 25 GENIC homozygous 978833449 4 117282737 117282738 G A 41 GENIC homozygous 978833450 4 117283800 117283801 C T 27 GENIC homozygous 978833451