chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 9579472 9579473 C T 25 GENIC homozygous 593945250 9 9582029 9582030 C CA 3 GENIC heterozygous 726185996 9 9585458 9585459 T TC 13 GENIC heterozygous 726185998 9 9588104 9588105 C T 19 GENIC homozygous 593945251 9 9588458 9588459 A C 26 GENIC homozygous 593945252 9 9589184 9589185 G - 16 GENIC homozygous 726185999 9 9594207 9594208 G GT 27 GENIC possibly homozygous 726186000 9 9600833 9600834 C - 20 GENIC homozygous 726186001 9 9603609 9603610 T C 19 GENIC possibly homozygous 593945253 9 9607624 9607625 G GA 13 GENIC heterozygous 726186003 9 9613557 9613558 T TC 10 GENIC homozygous 726186004 9 9614980 9614982 TT -- 14 GENIC possibly homozygous 726186006 9 9615005 9615006 C T 17 GENIC homozygous 593945254 9 9615386 9615387 A T 25 GENIC homozygous 593945255 9 9619579 9619580 C CCA 24 GENIC homozygous 726186008 9 9619582 9619583 G - 26 GENIC homozygous 726186009 9 9619584 9619585 T TCA 26 GENIC homozygous 726186010 9 9619585 9619586 G C 26 GENIC homozygous 593945256 9 9620520 9620521 A G 25 GENIC homozygous 593945257 9 9625193 9625194 T G 27 GENIC homozygous 593945258 9 9625202 9625203 C CT 22 GENIC homozygous 726186011 9 9625238 9625243 TTTTT ----- 8 GENIC homozygous 726186012 9 9626982 9626989 GCCCCGG ------- 3 GENIC homozygous 726186015 9 9627023 9627024 A AGTCTCG 13 GENIC homozygous 726186016 9 9630799 9630800 T TCA 8 GENIC heterozygous 726186018 9 9630799 9630800 T TCACACACA 8 GENIC possibly homozygous 726186019 9 9632720 9632721 A G 23 GENIC homozygous 593945259 9 9634070 9634071 C - 6 GENIC heterozygous 726186021 9 9634072 9634085 CACACACACACAC ------------- 6 GENIC heterozygous 726186022 9 9635655 9635657 GT -- 14 GENIC heterozygous 726186024 9 9637244 9637245 C A 26 GENIC homozygous 593945260