chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 23686098 23686099 T C 28 GENIC homozygous 48259325 15 23687012 23687013 A G 23 GENIC homozygous 48259326 15 23687431 23687432 T C 27 GENIC homozygous 48259327 15 23687788 23687789 C T 31 GENIC homozygous 48259328 15 23687854 23687855 G A 31 GENIC homozygous 48259329 15 23687889 23687890 C G 29 GENIC homozygous 48259330 15 23689047 23689048 A - 26 GENIC homozygous 48259331 15 23689548 23689549 T C 42 GENIC homozygous 48259332 15 23689779 23689780 T C 36 GENIC homozygous 48259333 15 23690472 23690473 A G 34 GENIC homozygous 48259334 15 23690787 23690788 A G 36 GENIC homozygous 48259335 15 23692294 23692295 A AT 27 GENIC homozygous 48259336 15 23692975 23692976 T TA 9 GENIC heterozygous 48259337 15 23692975 23692976 T TAA 9 GENIC heterozygous 48475251 15 23693065 23693066 A G 18 GENIC homozygous 48259338 15 23693080 23693081 G A 17 GENIC homozygous 48259339 15 23693318 23693319 G A 24 GENIC homozygous 48259340 15 23693322 23693323 G A 26 GENIC homozygous 48259341 15 23693667 23693668 T C 39 GENIC homozygous 48259342 15 23694153 23694154 A ACT 28 GENIC homozygous 48259343 15 23694805 23694806 T G 33 GENIC homozygous 48259344 15 23695475 23695476 C T 31 GENIC homozygous 48259345 15 23696004 23696005 C T 23 GENIC homozygous 48259346 15 23696134 23696135 A G 37 GENIC homozygous 48259347 15 23697080 23697081 A T 23 GENIC homozygous 48259348 15 23697347 23697348 T TC 8 GENIC possibly homozygous 48259349