chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 9443104 9443105 T C 9 GENIC homozygous 57142628 3 9443175 9443176 G - 19 GENIC homozygous 57142630 3 9444173 9444174 G GTCC 23 GENIC homozygous 57142632 3 9445349 9445350 C A 14 GENIC homozygous 59995104 3 9445539 9445540 G A 22 GENIC homozygous 59757586 3 9446709 9446710 A G 34 GENIC possibly homozygous 57142636 3 9446796 9446797 A G 16 GENIC homozygous 57142638 3 9447106 9447107 T A 20 GENIC homozygous 57142640 3 9447610 9447614 TGTG ---- 5 GENIC homozygous 59465249 3 9447731 9447732 T C 37 GENIC homozygous 57142644 3 9447915 9447916 T C 14 GENIC homozygous 59995105 3 9448037 9448038 C CT 7 GENIC possibly homozygous 58637462 3 9448149 9448150 C T 18 GENIC homozygous 59995106 3 9448262 9448263 A AC 1 GENIC homozygous 58412535 3 9448615 9448617 TT -- 29 GENIC possibly homozygous 59036644 3 9448616 9448617 T TAGGGA 29 GENIC possibly homozygous 59036646 3 9448618 9448619 G GGGC 29 GENIC possibly homozygous 57142650 3 9448918 9448919 C - 22 GENIC homozygous 59995107 3 9449411 9449412 C T 27 GENIC possibly homozygous 59995108 3 9449597 9449598 G T 34 GENIC possibly homozygous 59995109 3 9449957 9449958 C T 14 GENIC homozygous 57142652 3 9450623 9450624 C T 16 GENIC possibly homozygous 57142654 3 9449780 9449781 G A 24 GENIC homozygous 59826156