chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 157100649 157100650 G A 28 GENIC homozygous 108354164 X 157109417 157109418 G A 27 GENIC heterozygous 132790727 X 157109375 157109376 T A 26 GENIC heterozygous 131979833 X 157109406 157109407 G C 26 GENIC heterozygous 132790725 X 157109414 157109415 A G 26 GENIC heterozygous 132790726 X 157109418 157109419 C T 27 GENIC heterozygous 132790728 X 157109422 157109423 C A 28 GENIC heterozygous 132790729 X 157109428 157109429 G A 25 GENIC heterozygous 132790730 X 157110105 157110106 A G 26 GENIC heterozygous 120771035 X 157110107 157110108 T A 26 GENIC heterozygous 120771036 X 157110153 157110154 G T 21 GENIC heterozygous 120771038 X 157110191 157110192 G A 21 GENIC heterozygous 120771040 X 157110217 157110218 A C 29 GENIC heterozygous 120771041 X 157109857 157109858 A G 29 GENIC heterozygous 129832317 X 157109878 157109879 A C 27 GENIC heterozygous 130204069 X 157109895 157109896 A G 31 GENIC heterozygous 130204070 X 157109919 157109920 G A 29 GENIC heterozygous 130516041 X 157110155 157110155 AAACTTTTA 20 GENIC heterozygous 133456593 X 157110212 157110213 T A 28 GENIC heterozygous 119965198 X 157110386 157110387 G A 34 GENIC heterozygous 120771051 X 157110406 157110407 T G 33 GENIC heterozygous 120038258 X 157110442 157110443 A G 34 GENIC heterozygous 131774997 X 157110448 157110449 T C 33 GENIC heterozygous 131774998