chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 25929592 25929593 G C 14 GENIC homozygous 983204524 13 25930014 25930015 C G 34 GENIC homozygous 983204525 13 25932098 25932099 A G 20 GENIC homozygous 983204526 13 25933968 25933969 A G 18 GENIC homozygous 983204527 13 25934709 25934710 G T 23 GENIC homozygous 983204528 13 25935708 25935709 C T 20 GENIC homozygous 983204529 13 25935922 25935923 G A 16 GENIC homozygous 983204530 13 25939690 25939691 C T 26 GENIC homozygous 983204531 13 25939981 25939982 C G 15 GENIC homozygous 983204532 13 25940180 25940181 C A 9 GENIC homozygous 983204533 13 25940369 25940370 G A 19 GENIC homozygous 983204534 13 25941095 25941096 T C 18 GENIC homozygous 983204535 13 25941195 25941196 C A 30 GENIC homozygous 983204536 13 25941208 25941209 C T 28 GENIC possibly homozygous 983204537 13 25941736 25941737 A G 38 GENIC homozygous 983204538 13 25942084 25942085 C T 13 GENIC homozygous 983204539 13 25943081 25943082 G A 38 GENIC homozygous 983204540 13 25945548 25945549 C T 25 GENIC homozygous 983204541 13 25947683 25947684 C G 8 GENIC homozygous 983204542 13 25949824 25949825 T A 23 GENIC homozygous 983204543