chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 32615951 32615952 T TA 6 GENIC homozygous 49707496 13 32616012 32616013 C T 5 GENIC homozygous 49707497 13 32616101 32616102 G A 12 GENIC homozygous 49707498 13 32617386 32617387 T C 11 GENIC homozygous 49707499 13 32617656 32617657 C G 15 GENIC homozygous 49707500 13 32618379 32618380 C T 19 GENIC homozygous 49707501 13 32618657 32618658 C T 16 GENIC homozygous 49707502 13 32619437 32619439 AA -- 11 GENIC homozygous 49707503 13 32621832 32621833 C A 20 GENIC homozygous 49707504 13 32621869 32621870 C T 15 GENIC homozygous 49707505 13 32622672 32622673 A T 20 GENIC homozygous 49707506 13 32622843 32622844 A C 17 GENIC homozygous 49707507 13 32624808 32624809 G A 16 GENIC heterozygous 49707511 13 32624335 32624336 G A 12 GENIC homozygous 49707508 13 32624794 32624797 TGG --- 16 GENIC homozygous 49707509 13 32624805 32624806 G A 16 GENIC heterozygous 49707510 13 32625182 32625183 T TG 13 GENIC homozygous 49707512 13 32625639 32625640 A G 13 GENIC homozygous 49707513 13 32626305 32626306 T C 11 GENIC homozygous 49707514 13 32626437 32626438 T TG 6 GENIC homozygous 49707515 13 32626682 32626685 AGA --- 7 GENIC heterozygous 49707516 13 32626687 32626688 T - 8 GENIC homozygous 49707517 13 32627178 32627179 C T 14 GENIC homozygous 49707518 13 32627365 32627366 G GT 21 GENIC homozygous 49707519 13 32627566 32627567 G A 16 GENIC homozygous 49707520 13 32627701 32627702 A T 16 GENIC homozygous 49707521 13 32627954 32627955 T C 19 GENIC homozygous 49707522 13 32628695 32628696 C T 14 GENIC homozygous 49707523 13 32630274 32630275 T A 16 GENIC homozygous 49707524 13 32630331 32630332 C A 15 GENIC homozygous 49707525 13 32630937 32630938 G A 17 GENIC homozygous 49707526 13 32631967 32631968 G A 16 GENIC homozygous 49707527 13 32632238 32632239 T - 20 GENIC homozygous 49707528 13 32633268 32633269 T C 11 GENIC homozygous 49707529