chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 20935703 20935704 C T 21 GENIC homozygous 939219270 14 20935965 20935966 G A 30 GENIC homozygous 939219271 14 20936350 20936351 G A 23 GENIC homozygous 939219272 14 20939394 20939395 A G 19 GENIC homozygous 939219273 14 20942229 20942230 T C 35 GENIC homozygous 939219274 14 20942232 20942233 C A 38 GENIC homozygous 939219275 14 20942614 20942615 G C 23 GENIC homozygous 939219276 14 20944684 20944685 A G 19 GENIC homozygous 939219277 14 20946014 20946015 A T 14 GENIC homozygous 939219278 14 20947570 20947571 A G 20 GENIC homozygous 939219279 14 20948218 20948219 G A 20 GENIC homozygous 939219280 14 20948383 20948384 G A 13 GENIC homozygous 939219281 14 20948435 20948436 A T 13 GENIC homozygous 939219282 14 20948985 20948986 G C 27 GENIC homozygous 939219283 14 20948989 20948990 T A 27 GENIC homozygous 939219284 14 20948992 20948993 G T 27 GENIC homozygous 939219285 14 20948998 20948999 T A 24 GENIC homozygous 939219286 14 20949006 20949007 A T 27 GENIC homozygous 939219287 14 20949008 20949009 G C 26 GENIC homozygous 939219288 14 20949562 20949563 A T 30 GENIC homozygous 939219289 14 20950421 20950422 C A 34 GENIC homozygous 939219290 14 20951075 20951076 C T 34 GENIC homozygous 939219291