chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 170262372 170262373 A C 8 GENIC homozygous 108375500 1 170262418 170262419 A C 8 GENIC possibly homozygous 108375502 1 170262757 170262758 A G 11 GENIC homozygous 108375504 1 170262979 170262980 C T 26 GENIC homozygous 108375506 1 170263862 170263863 A G 29 GENIC homozygous 108375508 1 170264182 170264183 T C 25 GENIC homozygous 108375510 1 170264224 170264225 A G 24 GENIC homozygous 108375512 1 170264473 170264474 A G 20 GENIC homozygous 108375514 1 170264622 170264623 A G 17 GENIC homozygous 108375516 1 170265015 170265016 A G 20 GENIC homozygous 108375520 1 170265503 170265504 T C 35 GENIC homozygous 108375522 1 170265683 170265684 T C 37 GENIC homozygous 108375524 1 170266750 170266751 C T 51 GENIC homozygous 108375526 1 170267220 170267221 C T 13 GENIC homozygous 108375532 1 170267548 170267549 T A 4 GENIC homozygous 109523819 1 170267551 170267552 A T 4 GENIC homozygous 120474632 1 170267553 170267554 G A 4 GENIC homozygous 120474633 1 170267885 170267886 G A 23 GENIC homozygous 108375536 1 170267919 170267920 A G 25 GENIC homozygous 108375538 1 170269227 170269228 T C 24 GENIC homozygous 108375540 1 170269278 170269279 T G 28 GENIC homozygous 108375542 1 170269659 170269660 G A 19 GENIC homozygous 108375544 1 170270944 170270945 T C 25 GENIC homozygous 108375546 1 170271310 170271311 C G 21 GENIC homozygous 108375548 1 170271689 170271690 A G 22 GENIC homozygous 108375550