chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 34176228 34176229 A C 39 GENIC homozygous 972872708 7 34176544 34176545 C T 18 GENIC homozygous 972872709 7 34176548 34176549 T C 18 GENIC homozygous 972872710 7 34177464 34177465 A G 25 GENIC homozygous 972872711 7 34177530 34177531 A G 21 GENIC homozygous 972872712 7 34178391 34178392 A G 20 GENIC homozygous 972872713 7 34178460 34178461 A G 18 GENIC homozygous 972872714 7 34178514 34178515 A G 28 GENIC homozygous 972872715 7 34178829 34178830 A G 18 GENIC homozygous 972872716 7 34178895 34178896 C T 17 GENIC homozygous 972872717 7 34179664 34179665 G A 18 GENIC homozygous 972872718 7 34180873 34180874 G C 29 GENIC homozygous 972872719 7 34181587 34181588 T C 26 GENIC homozygous 972872720 7 34181700 34181701 A C 20 GENIC homozygous 972872721 7 34181704 34181705 A C 19 GENIC homozygous 972872722 7 34181919 34181920 G A 9 GENIC heterozygous 972872723 7 34181944 34181945 G T 12 GENIC homozygous 972872724 7 34184744 34184745 A G 26 GENIC homozygous 972872725