chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 20935703 20935704 C T 16 GENIC homozygous 962105538 14 20935965 20935966 G A 13 GENIC homozygous 962105539 14 20936350 20936351 G A 21 GENIC homozygous 962105540 14 20939038 20939039 A T 28 GENIC homozygous 962105541 14 20939394 20939395 A G 23 GENIC homozygous 962105542 14 20942229 20942230 T C 19 GENIC homozygous 962105543 14 20942232 20942233 C A 18 GENIC homozygous 962105544 14 20942614 20942615 G C 23 GENIC homozygous 962105545 14 20944684 20944685 A G 18 GENIC homozygous 962105546 14 20946014 20946015 A T 14 GENIC homozygous 962105547 14 20947570 20947571 A G 27 GENIC homozygous 962105548 14 20948218 20948219 G A 18 GENIC homozygous 962105549 14 20948383 20948384 G A 16 GENIC homozygous 962105550 14 20948435 20948436 A T 12 GENIC homozygous 962105551 14 20948985 20948986 G C 23 GENIC homozygous 962105552 14 20948989 20948990 T A 24 GENIC homozygous 962105553 14 20948992 20948993 G T 24 GENIC homozygous 962105554 14 20948998 20948999 T A 22 GENIC homozygous 962105555 14 20949006 20949007 A T 25 GENIC homozygous 962105556 14 20949008 20949009 G C 27 GENIC homozygous 962105557 14 20949540 20949541 T G 23 GENIC homozygous 962105558 14 20949562 20949563 A T 27 GENIC homozygous 962105559 14 20950421 20950422 C A 39 GENIC homozygous 962105560 14 20951075 20951076 C T 21 GENIC homozygous 962105561 14 20952226 20952227 C T 14 GENIC homozygous 962105562