chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 34617082 34617083 T C 22 GENIC homozygous 581789929 4 34617847 34617848 T C 36 GENIC homozygous 584573257 4 34617899 34617900 T C 29 GENIC homozygous 584573258 4 34618085 34618086 C CAT 25 GENIC homozygous 719351441 4 34618279 34618280 G A 28 GENIC homozygous 584573259 4 34618317 34618318 T C 35 GENIC homozygous 581789930 4 34618717 34618718 T - 27 GENIC homozygous 719351442 4 34619204 34619205 C T 15 GENIC homozygous 584573260 4 34619215 34619216 A - 15 GENIC homozygous 719351443 4 34619379 34619380 T C 25 GENIC homozygous 584573261 4 34619476 34619477 G T 45 GENIC homozygous 581789931 4 34619754 34619755 G A 22 GENIC homozygous 584573262 4 34620301 34620302 A G 37 GENIC homozygous 581789932 4 34620345 34620346 G A 44 GENIC homozygous 584573263 4 34620551 34620552 T - 18 GENIC homozygous 719351444 4 34620737 34620738 C T 27 GENIC homozygous 581789933 4 34621519 34621520 G GA 26 GENIC homozygous 719351445 4 34621528 34621529 T G 28 GENIC homozygous 584573264 4 34621843 34621844 C CAT 6 GENIC homozygous 719351449 4 34622272 34622273 G A 22 GENIC homozygous 584573265 4 34622438 34622439 C T 34 GENIC homozygous 581789934 4 34622716 34622717 A AGTT 20 GENIC possibly homozygous 719351450 4 34622768 34622769 G A 28 GENIC homozygous 581789935 4 34622887 34622888 C T 33 GENIC homozygous 584573266 4 34622915 34622916 T C 38 GENIC homozygous 581789936 4 34623012 34623016 ACAC ---- 8 GENIC heterozygous 719351452 4 34623014 34623016 AC -- 8 GENIC heterozygous 719351453 4 34623082 34623083 A - 29 GENIC homozygous 719351454 4 34623090 34623091 G A 31 GENIC homozygous 584573267 4 34623287 34623288 G A 31 GENIC homozygous 584573268 4 34623565 34623566 A G 42 GENIC homozygous 581789937 4 34624035 34624036 G A 44 GENIC possibly homozygous 581789938 4 34624232 34624233 T C 25 GENIC homozygous 581789939