chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 104808431 104808432 G A 13 GENIC homozygous 654362630 14 104808450 104808451 G T 16 GENIC homozygous 654362631 14 104808457 104808458 A T 16 GENIC homozygous 654362632 14 104808463 104808464 T C 15 GENIC homozygous 654362633 14 104808464 104808465 G C 15 GENIC homozygous 654362634 14 104808506 104808507 G T 21 GENIC homozygous 654362635 14 104809686 104809687 A - 31 GENIC homozygous 759676550 14 104810828 104810829 C T 28 GENIC homozygous 654362636 14 104810999 104811000 C T 21 GENIC homozygous 654362637 14 104811010 104811011 G T 24 GENIC homozygous 654362638 14 104811161 104811162 A AGT 16 GENIC homozygous 759676553 14 104811854 104811862 CCTTCAAA -------- 15 GENIC homozygous 759676555 14 104811969 104811970 T TTA 11 GENIC homozygous 759676556 14 104812136 104812137 G A 16 GENIC homozygous 654362639 14 104812395 104812396 A AC 13 GENIC homozygous 759676557 14 104813080 104813097 GGTGGCTAAAACTCTGT ----------------- 37 GENIC homozygous 759676558 14 104813102 104813103 C - 32 GENIC homozygous 759676559 14 104813107 104813108 G GT 33 GENIC homozygous 759676560 14 104813114 104813115 T G 35 GENIC homozygous 654362640 14 104813115 104813116 G T 35 GENIC homozygous 654362641 14 104813125 104813126 T C 36 GENIC homozygous 654362642 14 104813178 104813179 T G 39 GENIC homozygous 654362643 14 104813411 104813412 G A 25 GENIC homozygous 654362644 14 104813852 104813853 C T 32 GENIC possibly homozygous 654362645 14 104814048 104814049 A C 16 GENIC homozygous 654362646