chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 90225271 90225272 A G 12 GENIC heterozygous 66374527 13 90225286 90225287 G A 10 GENIC homozygous 66374529 13 90225422 90225423 G A 5 GENIC heterozygous 66374531 13 90225683 90225684 T A 14 GENIC possibly homozygous 66374533 13 90225765 90225766 T C 6 GENIC homozygous 66374535 13 90225768 90225769 C T 6 GENIC homozygous 66374537 13 90226146 90226147 G A 20 GENIC homozygous 66374539 13 90226402 90226403 T C 18 GENIC homozygous 66374541 13 90226952 90226953 T G 11 GENIC homozygous 66374543 13 90227500 90227501 G A 30 GENIC homozygous 66374545 13 90227721 90227722 G A 20 GENIC homozygous 66374547 13 90228499 90228500 C T 28 GENIC possibly homozygous 66374549 13 90229613 90229614 C A 16 GENIC possibly homozygous 66374551 13 90230679 90230680 C T 13 GENIC homozygous 66374553 13 90234292 90234293 T G 11 GENIC homozygous 66374555 13 90235223 90235224 C T 26 GENIC possibly homozygous 66374557 13 90235442 90235443 G T 17 GENIC homozygous 66374559 13 90236528 90236529 A T 25 GENIC homozygous 66374561 13 90236671 90236672 G A 22 GENIC homozygous 66374563 13 90237704 90237705 A G 15 GENIC homozygous 66374565 13 90238329 90238330 C A 19 GENIC homozygous 66374567 13 90239184 90239185 C T 26 GENIC homozygous 66374569