chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 140107794 140107795 C A 16 GENIC homozygous 111752222 3 140108166 140108167 T C 20 GENIC homozygous 111752224 3 140108369 140108370 C T 27 GENIC homozygous 111752228 3 140108405 140108406 T G 23 GENIC homozygous 112166913 3 140108992 140108993 C T 16 GENIC homozygous 112166915 3 140109707 140109708 C T 22 GENIC homozygous 112166919 3 140112195 140112196 A T 19 GENIC homozygous 112166921 3 140112918 140112919 A G 22 GENIC homozygous 111752236 3 140113216 140113217 G A 20 GENIC homozygous 112166923 3 140113544 140113545 G A 21 GENIC homozygous 111752239 3 140114039 140114040 A G 32 GENIC homozygous 111752243 3 140114246 140114247 T C 28 GENIC homozygous 111752244 3 140114744 140114745 T C 13 GENIC homozygous 111752246 3 140117248 140117249 G T 11 GENIC homozygous 111752250 3 140119408 140119409 A G 14 GENIC homozygous 111752256 3 140119679 140119680 G A 15 GENIC homozygous 111752258 3 140119896 140119897 T C 14 GENIC homozygous 111752262 3 140120418 140120419 C T 12 GENIC homozygous 112166925 3 140120856 140120857 C T 34 GENIC homozygous 112166927 3 140121166 140121167 A G 29 GENIC homozygous 111752264 3 140123197 140123198 G C 12 GENIC homozygous 112166929 3 140123851 140123852 C T 26 GENIC homozygous 111752266