chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 20935703 20935704 C T 21 GENIC homozygous 804597752 14 20935965 20935966 G A 18 GENIC homozygous 804597753 14 20936350 20936351 G A 19 GENIC homozygous 804597754 14 20937835 20937836 T G 15 GENIC possibly homozygous 804597755 14 20938336 20938337 T G 25 GENIC possibly homozygous 804597756 14 20939038 20939039 A T 19 GENIC homozygous 804597757 14 20939394 20939395 A G 12 GENIC homozygous 804597758 14 20941643 20941644 A G 15 GENIC homozygous 804597759 14 20941663 20941664 G C 17 GENIC homozygous 804597760 14 20941702 20941703 C A 10 GENIC homozygous 804597761 14 20941705 20941706 G A 9 GENIC homozygous 804597762 14 20942085 20942086 C A 11 GENIC homozygous 804597763 14 20942140 20942141 C G 11 GENIC homozygous 804597764 14 20942229 20942230 T C 19 GENIC homozygous 804597765 14 20942232 20942233 C A 18 GENIC homozygous 804597766 14 20942614 20942615 G C 14 GENIC homozygous 804597767 14 20944684 20944685 A G 18 GENIC homozygous 804597768 14 20944912 20944913 A G 25 GENIC homozygous 804597769 14 20946014 20946015 A T 14 GENIC homozygous 804597770 14 20947570 20947571 A G 16 GENIC homozygous 804597771 14 20948218 20948219 G A 17 GENIC homozygous 804597772 14 20948383 20948384 G A 24 GENIC homozygous 804597773 14 20948435 20948436 A T 20 GENIC homozygous 804597774 14 20948985 20948986 G C 17 GENIC homozygous 804597775 14 20948998 20948999 T A 19 GENIC homozygous 804597776 14 20949006 20949007 A T 18 GENIC homozygous 804597777 14 20949008 20949009 G C 18 GENIC homozygous 804597778 14 20949540 20949541 T G 17 GENIC homozygous 804597779 14 20949562 20949563 A T 18 GENIC homozygous 804597780 14 20950421 20950422 C A 17 GENIC homozygous 804597781 14 20951075 20951076 C T 15 GENIC homozygous 804597782 14 20952226 20952227 C T 36 GENIC homozygous 804597783