chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 20935703 20935704 C T 24 GENIC homozygous 950804152 14 20935965 20935966 G A 24 GENIC homozygous 950804153 14 20936350 20936351 G A 17 GENIC homozygous 950804154 14 20939038 20939039 A T 30 GENIC homozygous 950804155 14 20939394 20939395 A G 22 GENIC homozygous 950804156 14 20942614 20942615 G C 9 GENIC homozygous 950804157 14 20944684 20944685 A G 34 GENIC homozygous 950804158 14 20946014 20946015 A T 28 GENIC homozygous 950804159 14 20947570 20947571 A G 12 GENIC homozygous 950804160 14 20948218 20948219 G A 19 GENIC homozygous 950804161 14 20948383 20948384 G A 28 GENIC homozygous 950804162 14 20948435 20948436 A T 20 GENIC homozygous 950804163 14 20948985 20948986 G C 21 GENIC homozygous 950804164 14 20948989 20948990 T A 22 GENIC homozygous 950804165 14 20948992 20948993 G T 22 GENIC homozygous 950804166 14 20948998 20948999 T A 25 GENIC homozygous 950804167 14 20949006 20949007 A T 22 GENIC homozygous 950804168 14 20949008 20949009 G C 22 GENIC homozygous 950804169 14 20949540 20949541 T G 19 GENIC homozygous 950804170 14 20949562 20949563 A T 18 GENIC homozygous 950804171 14 20950421 20950422 C A 27 GENIC homozygous 950804172 14 20951075 20951076 C T 22 GENIC homozygous 950804173 14 20952226 20952227 C T 8 GENIC homozygous 950804174