chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 23538304 23538305 A G 56 GENIC homozygous 139250251 13 23539501 23539502 T 35 GENIC homozygous 139164093 13 23540172 23540173 T C 46 GENIC homozygous 139250252 13 23540978 23540978 A 33 GENIC possibly homozygous 139164094 13 23541169 23541170 C T 27 GENIC homozygous 139250253 13 23541175 23541175 G 28 GENIC homozygous 139164095 13 23541918 23541919 T C 34 GENIC homozygous 139250254 13 23542383 23542384 G T 55 GENIC homozygous 139250255 13 23544505 23544506 C A 10 GENIC homozygous 139250256 13 23544590 23544591 T 28 GENIC homozygous 139164096 13 23545266 23545267 G C 44 GENIC homozygous 139250257 13 23545393 23545394 A C 44 GENIC homozygous 139250258 13 23545637 23545638 C A 48 GENIC homozygous 139250259 13 23546130 23546131 G T 33 GENIC homozygous 139250260 13 23546131 23546132 G A 32 GENIC homozygous 139250261 13 23546201 23546202 T A 29 GENIC homozygous 139250262 13 23547462 23547463 T C 50 GENIC homozygous 139250263 13 23547577 23547578 C T 48 GENIC homozygous 139250264 13 23548142 23548143 T C 44 GENIC homozygous 139250265 13 23548225 23548226 C 44 GENIC homozygous 139164097 13 23548520 23548521 C T 44 GENIC homozygous 139250266 13 23548682 23548683 C G 54 GENIC homozygous 139250267 13 23548720 23548721 A G 56 GENIC homozygous 139250268 13 23548786 23548787 A G 55 GENIC homozygous 139250269 13 23549045 23549046 T A 40 GENIC homozygous 139250270 13 23550594 23550595 A G 44 GENIC homozygous 139250271 13 23550646 23550647 C T 42 GENIC homozygous 139250272 13 23550753 23550754 C T 46 GENIC homozygous 139250273 13 23550789 23550790 T C 48 GENIC homozygous 139250274 13 23551636 23551637 G C 39 GENIC homozygous 139250275 13 23544458 23544458 TA 10 GENIC homozygous 142341526 13 23544470 23544470 TC 10 GENIC homozygous 142341527