Item | Value |
---|---|
geneid | 84334 |
ensemblid | ENSG00000256053.9 |
hgncid | 20492 |
symbol | COA8 |
name | cytochrome c oxidase assembly factor 8 |
refseq_nuc | NM_001370595.2 |
refseq_prot | NP_001357524.1 |
ensembl_nuc | ENST00000409074.8 |
ensembl_prot | ENSP00000386485.3 |
mane_status | MANE Select |
chr | chr14 |
start | 103562960 |
end | 103590896 |
strand | + |
ver | v1.2 |
region | chr14:103562960-103590896 |
region5000 | chr14:103557960-103595896 |
regionname0 | COA8_chr14_103562960_103590896 |
regionname5000 | COA8_chr14_103557960_103595896 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 193 | 263 | 42 | 47 | 132 | 10 | 30 | 94 | COA8_chr14_103557960_103595896 | COA8 | MVVLR others(188): Show |
chr14 | 103557960 | 103595896 |
a0002 | 0/0 | 193 | 93 | 23 | 20 | 30 | 8 | 12 | 28 | COA8_chr14_103557960_103595896 | COA8 | MVVLR others(188): Show |
chr14 | 103557960 | 103595896 |
a0003 | 0/0 | 193 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | MVALR others(188): Show |
chr14 | 103557960 | 103595896 |
a0004 | 0/0 | 193 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | MVVLR others(188): Show |
chr14 | 103557960 | 103595896 |
a0005 | 0/0 | 193 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | MVVLR others(188): Show |
chr14 | 103557960 | 103595896 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 579 | 169 | 34 | 28 | 83 | 5 | 17 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 | ||
a0001c0003 | 0/0 | 579 | 88 | 7 | 16 | 48 | 5 | 12 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 | ||
a0001c0006 | 0/0 | 579 | 3 | 0 | 3 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 | ||
a0001c0008 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 | ||
a0001c0009 | 0/0 | 579 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 | ||
a0001c0010 | 0/0 | 579 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 | ||
a0002c0002 | 0/0 | 579 | 93 | 23 | 20 | 30 | 8 | 12 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 | ||
a0003c0004 | 0/0 | 579 | 12 | 12 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 | ||
a0004c0005 | 0/0 | 579 | 11 | 10 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 | ||
a0005c0007 | 0/0 | 579 | 3 | 1 | 2 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | ATGGT others(574): Show |
chr14 | 103557960 | 103595896 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1234 | 166 | 32 | 28 | 82 | 5 | 17 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0001c0001t0002 | 0/0 | 1234 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0001c0001t0003 | 0/0 | 1234 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0001c0001t0006 | 0/0 | 1234 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0001c0003t0001 | 0/0 | 1234 | 88 | 7 | 16 | 48 | 5 | 12 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0001c0006t0001 | 0/0 | 1234 | 3 | 0 | 3 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0001c0008t0001 | 0/0 | 1234 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0001c0009t0001 | 0/0 | 1234 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0001c0010t0001 | 0/0 | 1234 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0002c0002t0001 | 0/0 | 1234 | 90 | 20 | 20 | 30 | 8 | 12 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0002c0002t0004 | 0/0 | 1234 | 3 | 3 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0003c0004t0001 | 0/0 | 1234 | 4 | 4 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0003c0004t0002 | 0/0 | 1234 | 8 | 8 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0004c0005t0001 | 0/0 | 1234 | 10 | 9 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0004c0005t0005 | 0/0 | 1234 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
a0005c0007t0003 | 0/0 | 1234 | 3 | 1 | 2 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | GCAAT others(1229): Show |
chr14 | 103557960 | 103595896 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 2 | 7 | 1 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0287 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0004 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0006t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0006t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0006t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0008t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0009t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0001c0010t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0002c0002t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0003c0004t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0004c0005t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0005c0007t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0005c0007t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
a0005c0007t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0070 | EUR | GBR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0038 | EUR | GBR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0004 | EUR | GBR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0118 | EUR | GBR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0129 | EUR | FIN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0077 | EUR | FIN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0010 | EUR | FIN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00408 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00438 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00621 | hp2 | a0001 | c0003 | t0001 | g0082 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0086 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0067 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0071 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01099 | hp2 | a0004 | c0005 | t0001 | g0320 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01167 | hp2 | a0005 | c0007 | t0003 | g0189 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01168 | hp2 | a0001 | c0006 | t0001 | g0079 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01169 | hp1 | a0001 | c0006 | t0001 | g0076 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01169 | hp2 | a0005 | c0007 | t0003 | g0190 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0033 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01243 | hp2 | a0001 | c0006 | t0001 | g0078 | AMR | PUR | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0048 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0134 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0074 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0132 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0066 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0049 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | CLM | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0133 | EUR | IBS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | IBS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | IBS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0150 | EUR | IBS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0089 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01884 | hp2 | a0003 | c0004 | t0002 | g0101 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0030 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0075 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0041 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0042 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0059 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0091 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02056 | hp2 | a0001 | c0003 | t0001 | g0093 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02071 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0083 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0046 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CDX | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02280 | hp2 | a0004 | c0005 | t0001 | g0328 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0040 | AMR | PEL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0105 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02615 | hp2 | a0004 | c0005 | t0001 | g0327 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02630 | hp2 | a0004 | c0005 | t0001 | g0321 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02647 | hp1 | a0004 | c0005 | t0001 | g0323 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0331 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02717 | hp1 | a0003 | c0004 | t0002 | g0102 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02723 | hp2 | a0004 | c0005 | t0001 | g0322 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0087 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02818 | hp1 | a0003 | c0004 | t0002 | g0014 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02886 | hp2 | a0004 | c0005 | t0001 | g0319 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02896 | hp1 | a0003 | c0004 | t0001 | g0013 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02897 | hp1 | a0003 | c0004 | t0001 | g0013 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02922 | hp1 | a0003 | c0004 | t0002 | g0098 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02922 | hp2 | a0002 | c0002 | t0004 | g0158 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02965 | hp2 | a0004 | c0005 | t0001 | g0326 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02970 | hp2 | a0005 | c0007 | t0003 | g0191 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03017 | hp1 | a0001 | c0009 | t0001 | g0270 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0052 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03041 | hp2 | a0004 | c0005 | t0001 | g0324 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03139 | hp1 | a0004 | c0005 | t0005 | g0325 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0090 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03491 | hp1 | a0001 | c0003 | t0001 | g0069 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03492 | hp1 | a0001 | c0003 | t0001 | g0053 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03516 | hp1 | a0003 | c0004 | t0002 | g0099 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0058 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03704 | hp1 | a0001 | c0003 | t0001 | g0056 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0055 | SAS | BEB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0152 | SAS | BEB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0065 | SAS | STU | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0031 | SAS | STU | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0028 | SAS | STU | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | STU | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18522 | hp1 | a0003 | c0004 | t0002 | g0014 | AFR | YRI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18522 | hp2 | a0002 | c0002 | t0004 | g0171 | AFR | YRI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | CHB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | CHB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18906 | hp1 | a0004 | c0005 | t0001 | g0314 | AFR | YRI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18948 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18961 | hp2 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18963 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18972 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18981 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18985 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18990 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18994 | hp1 | a0001 | c0008 | t0001 | g0308 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18994 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18995 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19003 | hp2 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19010 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | LWK | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19030 | hp2 | a0003 | c0004 | t0002 | g0100 | AFR | LWK | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19054 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19056 | hp2 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19057 | hp1 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19064 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19077 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19080 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19089 | hp1 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | YRI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA19240 | hp2 | a0003 | c0004 | t0001 | g0097 | AFR | YRI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20129 | hp1 | a0002 | c0002 | t0004 | g0157 | AFR | ASW | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20129 | hp2 | a0003 | c0004 | t0002 | g0095 | AFR | ASW | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0162 | EUR | TSI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0151 | EUR | TSI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0120 | EUR | TSI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0127 | EUR | TSI | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0015 | SAS | GIH | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20905 | hp2 | a0001 | c0003 | t0001 | g0036 | SAS | GIH | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02109 | hp1 | a0003 | c0004 | t0001 | g0096 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | USA | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | USA | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA21309 | hp1 | a0001 | c0010 | t0001 | g0177 | AFR | LWK | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0215 | REF | REF | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0287 | REF | REF | COA8_chr14_103557960_103595896 | COA8 | chr14 | 103557960 | 103595896 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:103563009 | T | C | 1 | a0003 | 12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
missense_variant | MODERATE | c.8T>C | p.Val3Ala | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/5 | 50/1234 | 8/582 | 3/193 | chr14 | 103563009 | |||
chr14:103563024 | A | G | 1 | a0004 | 11 | HG01099.hp2 HG02280.hp2 HG02615.hp2 others(8): Show |
missense_variant | MODERATE | c.23A>G | p.Lys8Arg | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/5 | 65/1234 | 23/582 | 8/193 | chr14 | 103563024 | |||
chr14:103563041 | C | G | 1 | a0002 | 93 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(90): Show |
missense_variant | MODERATE | c.40C>G | p.Pro14Ala | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/5 | 82/1234 | 40/582 | 14/193 | chr14 | 103563041 | |||
chr14:103571723 | A | G | 1 | a0005 | 3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.224A>G | p.Asn75Ser | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/5 | 266/1234 | 224/582 | 75/193 | chr14 | 103571723 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:103563037 | C | T | 1 | a0001c0010 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.36C>T | p.Leu12Leu | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/5 | 78/1234 | 36/582 | 12/193 | chr14 | 103563037 | |||
chr14:103563112 | G | A | 2 | a0001c0003 a0001c0006 |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
synonymous_variant | LOW | c.111G>A | p.Thr37Thr | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/5 | 153/1234 | 111/582 | 37/193 | chr14 | 103563112 | |||
chr14:103571700 | T | C | 1 | a0001c0008 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.201T>C | p.Pro67Pro | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/5 | 243/1234 | 201/582 | 67/193 | chr14 | 103571700 | |||
chr14:103574136 | A | G | 1 | a0001c0006 | 3 | HG01168.hp2 HG01169.hp1 HG01243.hp2 |
synonymous_variant | LOW | c.351A>G | p.Leu117Leu | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/5 | 393/1234 | 351/582 | 117/193 | chr14 | 103574136 | |||
chr14:103590241 | G | A | 1 | a0001c0009 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.537G>A | p.Arg179Arg | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 5/5 | 579/1234 | 537/582 | 179/193 | chr14 | 103590241 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:103590408 | C | T | 2 | a0001c0001t0003 a0005c0007t0003 |
4 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*122C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 5/5 | 122 | chr14 | 103590408 | ||||||
chr14:103590409 | C | G | 2 | a0001c0001t0003 a0005c0007t0003 |
4 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*123C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 5/5 | 123 | chr14 | 103590409 | ||||||
chr14:103590625 | T | C | 2 | a0001c0001t0002 a0003c0004t0002 |
9 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*339T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 5/5 | 339 | chr14 | 103590625 | ||||||
chr14:103590634 | G | A | 1 | a0002c0002t0004 | 3 | HG02922.hp2 NA18522.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*348G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 5/5 | 348 | chr14 | 103590634 | ||||||
chr14:103590639 | G | A | 1 | a0004c0005t0005 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*353G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 5/5 | 353 | chr14 | 103590639 | ||||||
chr14:103590731 | G | A | 1 | a0001c0001t0006 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 5/5 | 445 | chr14 | 103590731 | ||||||
chr14:103590847 | G | C | 2 | a0001c0001t0002 a0003c0004t0002 |
9 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*561G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 5/5 | 561 | chr14 | 103590847 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:103563174 | AGACAAAC others(12): Show |
A | 1 | a0001c0003t0001g0331 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.123+52_123+70delAC others(17): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103563174 | ||||||
chr14:103563184 | G | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+60G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563184 | |||||||
chr14:103563201 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.123+77C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563201 | |||||||
chr14:103563276 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.123+152G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563276 | |||||||
chr14:103563455 | G | A | 164 | a0001c0001t0006g0103 a0001c0003t0001g0002 a0001c0003t0001g0004 others(161): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.123+331G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563455 | |||||||
chr14:103563455 | G | T | 1 | a0002c0002t0001g0329 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.123+331G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563455 | |||||||
chr14:103563482 | T | G | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.123+358T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563482 | |||||||
chr14:103563495 | C | A | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+371C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563495 | |||||||
chr14:103563516 | AAGCGGCG | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG02976.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+396_123+402del others(7): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103563516 | ||||||
chr14:103563535 | A | G | 15 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(12): Show |
15 | HG01099.hp2 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.123+411A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563535 | |||||||
chr14:103563559 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.123+435T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563559 | |||||||
chr14:103563590 | G | A | 1 | a0004c0005t0001g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123+466G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563590 | |||||||
chr14:103563657 | A | G | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+533A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563657 | |||||||
chr14:103563855 | A | T | 1 | a0001c0001t0001g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.123+731A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563855 | |||||||
chr14:103563856 | A | T | 1 | a0002c0002t0001g0173 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.123+732A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103563856 | |||||||
chr14:103564011 | G | T | 1 | a0001c0003t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.123+887G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564011 | |||||||
chr14:103564151 | CA | C | 79 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(76): Show |
93 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.123+1039delA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103564151 | ||||||
chr14:103564198 | A | T | 1 | a0001c0001t0001g0312 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.123+1074A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564198 | |||||||
chr14:103564237 | C | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.123+1113C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564237 | |||||||
chr14:103564421 | A | C | 1 | a0001c0001t0001g0311 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.123+1297A>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564421 | |||||||
chr14:103564481 | G | C | 1 | a0001c0001t0001g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.123+1357G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564481 | |||||||
chr14:103564564 | T | C | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.123+1440T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564564 | |||||||
chr14:103564571 | C | CT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0212 others(19): Show |
23 | HG00423.hp2 HG01106.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.123+1473dupT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103564571 | ||||||
chr14:103564571 | CT | C | 81 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0174 others(78): Show |
92 | HG00140.hp2 HG00544.hp2 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.123+1473delT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103564571 | ||||||
chr14:103564571 | CTTTT | C | 72 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(69): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.123+1470_123+1473d others(6): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103564571 | ||||||
chr14:103564571 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.123+1460_123+1473d others(16): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103564571 | ||||||
chr14:103564622 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.123+1498C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564622 | |||||||
chr14:103564673 | G | A | 3 | a0002c0002t0001g0106 a0002c0002t0001g0107 a0002c0002t0001g0108 |
3 | NA18945.hp2 NA18988.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.123+1549G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564673 | |||||||
chr14:103564687 | C | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.123+1563C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564687 | |||||||
chr14:103564970 | C | T | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+1846C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103564970 | |||||||
chr14:103565014 | C | T | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.123+1890C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103565014 | |||||||
chr14:103565055 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+1931G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103565055 | |||||||
chr14:103565124 | T | A | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+2000T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103565124 | |||||||
chr14:103565125 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.123+2001T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103565125 | |||||||
chr14:103565163 | C | G | 2 | a0001c0003t0001g0092 a0001c0003t0001g0093 |
2 | HG02056.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.123+2039C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103565163 | |||||||
chr14:103565503 | CT | C | 5 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG00558.hp2 HG00621.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+2388delT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103565503 | ||||||
chr14:103565705 | G | A | 5 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(2): Show |
7 | HG02109.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+2581G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103565705 | |||||||
chr14:103565805 | G | A | 1 | a0002c0002t0001g0109 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.123+2681G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103565805 | |||||||
chr14:103565848 | C | G | 1 | a0001c0003t0001g0012 | 2 | NA18969.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.123+2724C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103565848 | |||||||
chr14:103566158 | G | C | 1 | a0003c0004t0002g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.123+3034G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103566158 | |||||||
chr14:103566173 | G | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.123+3049G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103566173 | |||||||
chr14:103566440 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.123+3316G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103566440 | |||||||
chr14:103566530 | T | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.123+3406T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103566530 | |||||||
chr14:103566593 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.123+3469T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103566593 | |||||||
chr14:103566601 | T | C | 3 | a0005c0007t0003g0189 a0005c0007t0003g0190 a0005c0007t0003g0191 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.123+3477T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103566601 | |||||||
chr14:103566928 | C | G | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.123+3804C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103566928 | |||||||
chr14:103567233 | C | T | 1 | a0001c0001t0001g0309 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.123+4109C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567233 | |||||||
chr14:103567304 | C | T | 2 | a0001c0001t0001g0307 a0001c0008t0001g0308 |
2 | HG02165.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.123+4180C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567304 | |||||||
chr14:103567344 | G | T | 1 | a0001c0003t0001g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.123+4220G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567344 | |||||||
chr14:103567372 | C | CA | 33 | a0001c0001t0001g0019 a0001c0001t0001g0178 a0001c0001t0001g0179 others(30): Show |
37 | HG00544.hp2 HG00741.hp2 HG01358.hp1 others(34): Show |
intron_variant | MODIFIER | c.124-4230dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103567372 | ||||||
chr14:103567372 | CA | C | 93 | a0001c0001t0001g0188 a0001c0001t0001g0302 a0001c0001t0001g0303 others(90): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.124-4230delA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103567372 | ||||||
chr14:103567372 | CAA | C | 6 | a0001c0003t0001g0086 a0001c0003t0001g0087 a0001c0003t0001g0088 others(3): Show |
6 | HG00639.hp1 HG01884.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-4231_124-4230d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103567372 | ||||||
chr14:103567393 | A | T | 84 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(81): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.124-4230A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567393 | |||||||
chr14:103567394 | T | A | 13 | a0001c0001t0001g0019 a0001c0001t0001g0192 a0001c0001t0001g0193 others(10): Show |
14 | HG00544.hp2 HG02015.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.124-4229T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567394 | |||||||
chr14:103567417 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.124-4206C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567417 | |||||||
chr14:103567631 | C | A | 1 | a0002c0002t0001g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.124-3992C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567631 | |||||||
chr14:103567717 | A | T | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.124-3906A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567717 | |||||||
chr14:103567817 | A | G | 1 | a0002c0002t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124-3806A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567817 | |||||||
chr14:103567902 | A | G | 1 | a0001c0001t0001g0300 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.124-3721A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567902 | |||||||
chr14:103567986 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.124-3637G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103567986 | |||||||
chr14:103568048 | A | G | 10 | a0004c0005t0001g0319 a0004c0005t0001g0320 a0004c0005t0001g0321 others(7): Show |
10 | HG01099.hp2 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.124-3575A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568048 | |||||||
chr14:103568178 | A | G | 1 | a0001c0003t0001g0085 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.124-3445A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568178 | |||||||
chr14:103568232 | G | A | 79 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(76): Show |
93 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.124-3391G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568232 | |||||||
chr14:103568310 | C | G | 15 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(12): Show |
15 | HG01099.hp2 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.124-3313C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568310 | |||||||
chr14:103568409 | C | T | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.124-3214C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568409 | |||||||
chr14:103568431 | G | GTA | 5 | a0001c0001t0006g0103 a0002c0002t0001g0162 a0002c0002t0001g0163 others(2): Show |
5 | HG01175.hp2 HG02886.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-3179_124-3178d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568431 | ||||||
chr14:103568444 | T | C | 3 | a0001c0001t0001g0181 a0001c0003t0001g0029 a0001c0003t0001g0030 |
3 | HG01928.hp2 HG01978.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.124-3179T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568444 | |||||||
chr14:103568466 | TAC | T | 6 | a0001c0001t0001g0178 a0001c0001t0001g0299 a0004c0005t0001g0326 others(3): Show |
6 | HG01433.hp1 HG02074.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-3147_124-3146d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568466 | ||||||
chr14:103568488 | C | T | 2 | a0001c0001t0001g0307 a0001c0008t0001g0308 |
2 | HG02165.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.124-3135C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568488 | |||||||
chr14:103568490 | T | C | 8 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(5): Show |
8 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-3133T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568490 | |||||||
chr14:103568493 | A | G | 1 | a0004c0005t0001g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.124-3130A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568493 | |||||||
chr14:103568512 | T | C | 85 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(82): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.124-3111T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568512 | |||||||
chr14:103568526 | C | T | 86 | a0001c0001t0006g0103 a0001c0003t0001g0002 a0001c0003t0001g0004 others(83): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.124-3097C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568526 | |||||||
chr14:103568544 | CAT | C | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-3078_124-3077d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568544 | |||||||
chr14:103568553 | A | G | 3 | a0001c0001t0001g0212 a0001c0001t0001g0297 a0001c0001t0001g0298 |
3 | NA18974.hp2 NA19009.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.124-3070A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568553 | |||||||
chr14:103568570 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG00323.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.124-3053C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568570 | |||||||
chr14:103568579 | GTA | G | 171 | a0001c0001t0001g0024 a0001c0001t0001g0179 a0001c0001t0001g0200 others(168): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.124-3030_124-3029d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568579 | ||||||
chr14:103568579 | GTATA | G | 3 | a0002c0002t0001g0104 a0002c0002t0001g0105 a0002c0002t0004g0158 |
3 | HG02572.hp2 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.124-3032_124-3029d others(6): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568579 | ||||||
chr14:103568581 | A | G | 5 | a0001c0001t0001g0001 a0004c0005t0001g0326 a0004c0005t0001g0327 others(2): Show |
5 | HG01168.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-3042A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568581 | |||||||
chr14:103568583 | A | G | 6 | a0001c0001t0006g0103 a0002c0002t0001g0114 a0002c0002t0001g0159 others(3): Show |
6 | NA18612.hp1 NA18939.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-3040A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568583 | |||||||
chr14:103568611 | A | ATG | 3 | a0004c0005t0001g0326 a0004c0005t0001g0327 a0004c0005t0001g0328 |
3 | HG02280.hp2 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.124-3002_124-3001d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568611 | ||||||
chr14:103568621 | G | GTA | 6 | a0001c0001t0001g0294 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02027.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-2977_124-2976d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568621 | ||||||
chr14:103568621 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-2985_124-2976d others(12): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568621 | ||||||
chr14:103568621 | G | GTATATAT others(5): Show |
3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02055.hp1 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.124-2987_124-2976d others(14): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568621 | ||||||
chr14:103568621 | G | GTGTA | 4 | a0004c0005t0001g0321 a0004c0005t0001g0322 a0004c0005t0001g0323 others(1): Show |
4 | HG02630.hp2 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-3001_124-3000i others(6): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568621 | ||||||
chr14:103568621 | GTA | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0020 others(94): Show |
115 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.124-2977_124-2976d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568621 | ||||||
chr14:103568621 | GTATA | G | 9 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0003t0001g0028 others(6): Show |
9 | HG00621.hp2 HG00673.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-2979_124-2976d others(6): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568621 | ||||||
chr14:103568621 | GTATATA | G | 72 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(69): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.124-2981_124-2976d others(8): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568621 | ||||||
chr14:103568621 | GTATATAT others(1): Show |
G | 85 | a0001c0003t0001g0027 a0002c0002t0001g0003 a0002c0002t0001g0006 others(82): Show |
101 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.124-2983_124-2976d others(10): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568621 | ||||||
chr14:103568621 | GTATATAT others(3): Show |
G | 1 | a0001c0001t0006g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.124-2985_124-2976d others(12): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103568621 | ||||||
chr14:103568623 | A | G | 3 | a0005c0007t0003g0189 a0005c0007t0003g0190 a0005c0007t0003g0191 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.124-3000A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568623 | |||||||
chr14:103568625 | A | G | 4 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0307 others(1): Show |
4 | HG02165.hp2 NA18988.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-2998A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568625 | |||||||
chr14:103568627 | A | G | 1 | a0004c0005t0005g0325 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.124-2996A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568627 | |||||||
chr14:103568629 | A | G | 3 | a0002c0002t0004g0157 a0002c0002t0004g0158 a0002c0002t0004g0171 |
3 | HG02922.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.124-2994A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568629 | |||||||
chr14:103568631 | A | G | 3 | a0002c0002t0004g0157 a0002c0002t0004g0158 a0002c0002t0004g0171 |
3 | HG02922.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.124-2992A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568631 | |||||||
chr14:103568892 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.124-2731A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568892 | |||||||
chr14:103568911 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.124-2712C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568911 | |||||||
chr14:103568955 | G | A | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.124-2668G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103568955 | |||||||
chr14:103569101 | G | A | 1 | a0001c0003t0001g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.124-2522G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569101 | |||||||
chr14:103569148 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0293 |
2 | HG03834.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.124-2475C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569148 | |||||||
chr14:103569182 | A | G | 4 | a0001c0003t0001g0077 a0001c0006t0001g0076 a0001c0006t0001g0078 others(1): Show |
4 | HG00280.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-2441A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569182 | |||||||
chr14:103569243 | C | G | 1 | a0002c0002t0001g0156 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.124-2380C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569243 | |||||||
chr14:103569260 | G | A | 1 | a0002c0002t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.124-2363G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569260 | |||||||
chr14:103569410 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02004.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.124-2213G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569410 | |||||||
chr14:103569524 | T | A | 2 | a0002c0002t0001g0118 a0002c0002t0001g0119 |
2 | HG00140.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.124-2099T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569524 | |||||||
chr14:103569600 | G | A | 1 | a0001c0003t0001g0080 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.124-2023G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569600 | |||||||
chr14:103569687 | G | C | 209 | a0001c0001t0001g0019 a0001c0001t0001g0174 a0001c0001t0001g0175 others(206): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.124-1936G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569687 | |||||||
chr14:103569695 | G | T | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-1928G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569695 | |||||||
chr14:103569857 | G | C | 11 | a0004c0005t0001g0314 a0004c0005t0001g0319 a0004c0005t0001g0320 others(8): Show |
11 | HG01099.hp2 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-1766G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569857 | |||||||
chr14:103569865 | G | GT | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-1749dupT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr14 | 103569865 | ||||||
chr14:103569869 | T | G | 1 | a0001c0001t0001g0220 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.124-1754T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569869 | |||||||
chr14:103569926 | G | A | 1 | a0004c0005t0001g0314 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.124-1697G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103569926 | |||||||
chr14:103570002 | G | A | 79 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(76): Show |
93 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.124-1621G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103570002 | |||||||
chr14:103570365 | A | G | 5 | a0001c0001t0001g0212 a0001c0001t0001g0274 a0001c0001t0001g0275 others(2): Show |
5 | NA18747.hp2 NA18974.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-1258A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103570365 | |||||||
chr14:103570424 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0221 |
2 | HG01192.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.124-1199T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103570424 | |||||||
chr14:103570665 | G | A | 1 | a0001c0003t0001g0032 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.124-958G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103570665 | |||||||
chr14:103570793 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.124-830T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103570793 | |||||||
chr14:103570844 | T | A | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-779T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103570844 | |||||||
chr14:103570899 | G | T | 1 | a0003c0004t0002g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.124-724G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103570899 | |||||||
chr14:103570984 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.124-639G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103570984 | |||||||
chr14:103571048 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-575A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103571048 | |||||||
chr14:103571230 | G | T | 2 | a0001c0001t0001g0273 a0002c0002t0001g0108 |
2 | HG01192.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.124-393G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103571230 | |||||||
chr14:103571240 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124-383G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103571240 | |||||||
chr14:103571269 | T | C | 4 | a0002c0002t0001g0006 a0002c0002t0001g0015 a0002c0002t0001g0110 others(1): Show |
7 | HG00741.hp2 HG01358.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-354T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103571269 | |||||||
chr14:103571532 | G | A | 15 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(12): Show |
15 | HG01099.hp2 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.124-91G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 1/4 | chr14 | 103571532 | |||||||
chr14:103571862 | T | C | 1 | a0002c0002t0001g0156 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.321+42T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103571862 | |||||||
chr14:103571866 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.321+46G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103571866 | |||||||
chr14:103571988 | G | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG02055.hp1 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+168G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103571988 | |||||||
chr14:103572010 | C | G | 1 | a0001c0001t0001g0310 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.321+190C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572010 | |||||||
chr14:103572081 | T | G | 73 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(70): Show |
87 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.321+261T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572081 | |||||||
chr14:103572113 | C | A | 1 | a0001c0001t0006g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.321+293C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572113 | |||||||
chr14:103572125 | C | CA | 15 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(12): Show |
15 | HG01099.hp2 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.321+318dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 103572125 | ||||||
chr14:103572228 | C | T | 1 | a0001c0010t0001g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.321+408C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572228 | |||||||
chr14:103572229 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.321+409G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572229 | |||||||
chr14:103572249 | T | C | 2 | a0001c0003t0001g0033 a0001c0003t0001g0094 |
2 | HG01175.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.321+429T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572249 | |||||||
chr14:103572347 | A | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02055.hp1 HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.321+527A>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572347 | |||||||
chr14:103572522 | G | A | 1 | a0002c0002t0001g0016 | 2 | HG02559.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.321+702G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572522 | |||||||
chr14:103572661 | C | G | 1 | a0002c0002t0001g0155 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.321+841C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572661 | |||||||
chr14:103572662 | G | A | 1 | a0001c0003t0001g0034 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.321+842G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572662 | |||||||
chr14:103572787 | A | AT | 73 | a0001c0001t0001g0296 a0001c0003t0001g0002 a0001c0003t0001g0004 others(70): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.321+974dupT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 103572787 | ||||||
chr14:103572787 | A | T | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.321+967A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572787 | |||||||
chr14:103572794 | TC | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0206 a0002c0002t0001g0154 |
3 | HG02257.hp2 HG02965.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.321+975delC | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572794 | |||||||
chr14:103572795 | C | T | 206 | a0001c0001t0001g0019 a0001c0001t0001g0174 a0001c0001t0001g0175 others(203): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.321+975C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572795 | |||||||
chr14:103572861 | C | T | 1 | a0001c0003t0001g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.321+1041C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572861 | |||||||
chr14:103572907 | C | T | 5 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0073 others(2): Show |
5 | HG01261.hp2 HG01928.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.321+1087C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572907 | |||||||
chr14:103572926 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.321+1106G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103572926 | |||||||
chr14:103573041 | A | T | 1 | a0001c0003t0001g0072 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.322-1066A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103573041 | |||||||
chr14:103573315 | G | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.322-792G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103573315 | |||||||
chr14:103573318 | C | T | 2 | a0001c0003t0001g0070 a0001c0003t0001g0071 |
2 | HG00099.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.322-789C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103573318 | |||||||
chr14:103573413 | C | T | 1 | a0001c0003t0001g0012 | 2 | NA18969.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.322-694C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103573413 | |||||||
chr14:103573526 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.322-581T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103573526 | |||||||
chr14:103573550 | T | C | 1 | a0002c0002t0001g0120 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.322-557T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103573550 | |||||||
chr14:103573728 | T | C | 85 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(82): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.322-379T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103573728 | |||||||
chr14:103573847 | C | G | 1 | a0001c0003t0001g0012 | 2 | NA18969.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.322-260C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103573847 | |||||||
chr14:103573959 | C | T | 1 | a0002c0002t0001g0170 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.322-148C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103573959 | |||||||
chr14:103574077 | C | A | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.322-30C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | chr14 | 103574077 | |||||||
chr14:103574078 | C | CT | 28 | a0001c0001t0001g0192 a0001c0001t0001g0198 a0001c0001t0001g0212 others(25): Show |
29 | HG00280.hp1 HG01071.hp1 HG01256.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.322-4dupT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 103574078 | ||||||
chr14:103574078 | C | CTT | 51 | a0001c0001t0006g0103 a0002c0002t0001g0003 a0002c0002t0001g0006 others(48): Show |
64 | HG00140.hp2 HG00423.hp2 HG00741.hp2 others(61): Show |
splice_region_variant&intron_variant | LOW | c.322-5_322-4dupTT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 103574078 | ||||||
chr14:103574078 | C | CTTT | 7 | a0002c0002t0001g0107 a0002c0002t0001g0113 a0002c0002t0001g0153 others(4): Show |
7 | HG01081.hp1 HG01175.hp2 NA18945.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.322-6_322-4dupTTT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 103574078 | ||||||
chr14:103574078 | CT | C | 95 | a0001c0001t0001g0020 a0001c0001t0001g0174 a0001c0001t0001g0175 others(92): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
splice_region_variant&intron_variant | LOW | c.322-4delT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 103574078 | ||||||
chr14:103574078 | CTT | C | 13 | a0001c0003t0001g0035 a0001c0003t0001g0036 a0001c0003t0001g0037 others(10): Show |
13 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.322-5_322-4delTT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | 103574078 | ||||||
chr14:103574222 | T | A | 1 | a0001c0003t0001g0012 | 2 | NA18969.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.385+52T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574222 | |||||||
chr14:103574246 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.385+76G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574246 | |||||||
chr14:103574295 | A | G | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+125A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574295 | |||||||
chr14:103574303 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0225 |
3 | HG00408.hp2 NA18954.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.385+133G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574303 | |||||||
chr14:103574303 | G | C | 1 | a0001c0003t0001g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.385+133G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574303 | |||||||
chr14:103574322 | C | T | 2 | a0001c0003t0001g0041 a0001c0003t0001g0042 |
2 | HG01993.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.385+152C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574322 | |||||||
chr14:103574381 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.385+211G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574381 | |||||||
chr14:103574640 | A | C | 1 | a0001c0003t0001g0042 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.385+470A>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574640 | |||||||
chr14:103574641 | A | C | 4 | a0001c0001t0003g0277 a0005c0007t0003g0189 a0005c0007t0003g0190 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+471A>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574641 | |||||||
chr14:103574964 | C | A | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.385+794C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574964 | |||||||
chr14:103574982 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.385+812A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103574982 | |||||||
chr14:103575037 | C | T | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.385+867C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575037 | |||||||
chr14:103575115 | C | T | 1 | a0003c0004t0002g0014 | 2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.385+945C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575115 | |||||||
chr14:103575116 | G | A | 1 | a0003c0004t0002g0098 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.385+946G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575116 | |||||||
chr14:103575133 | T | C | 164 | a0001c0001t0001g0316 a0001c0001t0006g0103 a0001c0003t0001g0002 others(161): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.385+963T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575133 | |||||||
chr14:103575313 | A | G | 2 | a0001c0003t0001g0086 a0001c0003t0001g0089 |
2 | HG00639.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.385+1143A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575313 | |||||||
chr14:103575431 | G | T | 2 | a0001c0003t0001g0070 a0001c0003t0001g0071 |
2 | HG00099.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.385+1261G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575431 | |||||||
chr14:103575441 | C | A | 11 | a0004c0005t0001g0314 a0004c0005t0001g0319 a0004c0005t0001g0320 others(8): Show |
11 | HG01099.hp2 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.385+1271C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575441 | |||||||
chr14:103575645 | G | A | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.385+1475G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575645 | |||||||
chr14:103575855 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.385+1685A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575855 | |||||||
chr14:103575891 | C | T | 1 | a0001c0003t0001g0029 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.385+1721C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103575891 | |||||||
chr14:103576036 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385+1866G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576036 | |||||||
chr14:103576122 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0330 |
2 | HG00544.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.385+1952A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576122 | |||||||
chr14:103576238 | G | A | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+2068G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576238 | |||||||
chr14:103576293 | G | C | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.385+2123G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576293 | |||||||
chr14:103576312 | AT | A | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+2143delT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576312 | |||||||
chr14:103576416 | A | G | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.385+2246A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576416 | |||||||
chr14:103576766 | C | G | 1 | a0001c0003t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.385+2596C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576766 | |||||||
chr14:103576839 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.385+2669C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576839 | |||||||
chr14:103576898 | G | A | 1 | a0002c0002t0001g0156 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.385+2728G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576898 | |||||||
chr14:103576909 | T | G | 1 | a0001c0001t0006g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.385+2739T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576909 | |||||||
chr14:103576983 | C | A | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.385+2813C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103576983 | |||||||
chr14:103577047 | G | A | 3 | a0002c0002t0004g0157 a0002c0002t0004g0158 a0002c0002t0004g0171 |
3 | HG02922.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.385+2877G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577047 | |||||||
chr14:103577238 | T | TTG | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+3084_385+3085d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103577238 | ||||||
chr14:103577377 | A | G | 5 | a0002c0002t0001g0133 a0002c0002t0001g0150 a0002c0002t0001g0151 others(2): Show |
5 | HG01358.hp2 HG01515.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+3207A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577377 | |||||||
chr14:103577513 | G | A | 1 | a0002c0002t0001g0165 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.385+3343G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577513 | |||||||
chr14:103577556 | G | A | 1 | a0002c0002t0001g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.385+3386G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577556 | |||||||
chr14:103577613 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385+3443T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577613 | |||||||
chr14:103577642 | G | C | 2 | a0003c0004t0001g0013 a0003c0004t0001g0096 |
3 | HG02109.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.385+3472G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577642 | |||||||
chr14:103577746 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.385+3576C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577746 | |||||||
chr14:103577800 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.385+3630G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577800 | |||||||
chr14:103577876 | T | G | 1 | a0001c0003t0001g0043 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.385+3706T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577876 | |||||||
chr14:103577878 | G | T | 77 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(74): Show |
91 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.385+3708G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577878 | |||||||
chr14:103577885 | G | A | 1 | a0001c0001t0003g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385+3715G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577885 | |||||||
chr14:103577956 | G | A | 2 | a0002c0002t0001g0162 a0002c0002t0001g0165 |
2 | HG01175.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.385+3786G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103577956 | |||||||
chr14:103578024 | C | CA | 23 | a0001c0001t0001g0178 a0001c0001t0001g0194 a0001c0001t0001g0195 others(20): Show |
23 | HG00544.hp2 HG01175.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.385+3877dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103578024 | ||||||
chr14:103578024 | CA | C | 93 | a0001c0001t0001g0026 a0001c0001t0001g0174 a0001c0001t0001g0175 others(90): Show |
109 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.385+3877delA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103578024 | ||||||
chr14:103578046 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | NA18962.hp2 NA18973.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+3876A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578046 | |||||||
chr14:103578047 | A | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0200 a0001c0001t0001g0201 others(1): Show |
4 | NA18962.hp2 NA18973.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+3877A>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578047 | |||||||
chr14:103578326 | T | C | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.385+4156T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578326 | |||||||
chr14:103578612 | G | A | 2 | a0001c0009t0001g0270 a0002c0002t0001g0104 |
2 | HG02615.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.385+4442G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578612 | |||||||
chr14:103578665 | T | C | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.385+4495T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578665 | |||||||
chr14:103578736 | G | C | 1 | a0002c0002t0001g0156 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.385+4566G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578736 | |||||||
chr14:103578885 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.385+4715G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578885 | |||||||
chr14:103578886 | C | T | 2 | a0001c0003t0001g0066 a0001c0003t0001g0067 |
2 | HG00733.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.385+4716C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578886 | |||||||
chr14:103578921 | T | G | 1 | a0002c0002t0001g0114 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.385+4751T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578921 | |||||||
chr14:103578926 | T | G | 1 | a0002c0002t0001g0114 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.385+4756T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578926 | |||||||
chr14:103578931 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.385+4761G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103578931 | |||||||
chr14:103579212 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.385+5042G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579212 | |||||||
chr14:103579254 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.385+5084C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579254 | |||||||
chr14:103579363 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.385+5193C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579363 | |||||||
chr14:103579680 | C | T | 1 | a0001c0003t0001g0012 | 2 | NA18969.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.385+5510C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579680 | |||||||
chr14:103579687 | G | T | 21 | a0001c0001t0001g0019 a0001c0001t0001g0179 a0001c0001t0001g0192 others(18): Show |
22 | HG00544.hp2 HG02015.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.385+5517G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579687 | |||||||
chr14:103579700 | C | T | 1 | a0001c0003t0001g0065 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.385+5530C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579700 | |||||||
chr14:103579757 | G | A | 77 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(74): Show |
91 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.385+5587G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579757 | |||||||
chr14:103579779 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0001g0291 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.385+5609A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579779 | |||||||
chr14:103579792 | G | A | 1 | a0002c0002t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.385+5622G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579792 | |||||||
chr14:103579829 | G | A | 2 | a0001c0003t0001g0086 a0001c0003t0001g0089 |
2 | HG00639.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.385+5659G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579829 | |||||||
chr14:103579918 | A | C | 16 | a0001c0001t0001g0026 a0001c0001t0001g0231 a0001c0001t0001g0232 others(13): Show |
16 | HG01074.hp2 HG01167.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.385+5748A>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579918 | |||||||
chr14:103579962 | C | CA | 289 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(286): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.385+5811dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103579962 | ||||||
chr14:103579962 | C | CAA | 8 | a0001c0001t0001g0226 a0001c0001t0001g0237 a0001c0001t0001g0281 others(5): Show |
8 | HG01106.hp2 HG01175.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+5810_385+5811d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103579962 | ||||||
chr14:103579962 | CA | C | 12 | a0001c0001t0001g0259 a0001c0001t0001g0289 a0003c0004t0001g0013 others(9): Show |
14 | HG01070.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.385+5811delA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103579962 | ||||||
chr14:103579995 | A | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0280 a0001c0001t0001g0291 |
3 | HG02040.hp2 HG02071.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.385+5825A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103579995 | |||||||
chr14:103580140 | G | A | 1 | a0003c0004t0002g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.385+5970G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103580140 | |||||||
chr14:103580144 | G | A | 1 | a0002c0002t0001g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.385+5974G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103580144 | |||||||
chr14:103580255 | A | T | 85 | a0001c0001t0006g0103 a0001c0003t0001g0002 a0001c0003t0001g0004 others(82): Show |
103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.385+6085A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103580255 | |||||||
chr14:103580497 | G | T | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.385+6327G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103580497 | |||||||
chr14:103580780 | A | G | 1 | a0001c0003t0001g0012 | 2 | NA18969.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.386-6494A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103580780 | |||||||
chr14:103580797 | G | GT | 14 | a0001c0001t0001g0255 a0001c0001t0001g0286 a0001c0001t0001g0313 others(11): Show |
14 | HG00408.hp1 HG02055.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.386-6461dupT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103580797 | ||||||
chr14:103580958 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.386-6316G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103580958 | |||||||
chr14:103581090 | G | A | 1 | a0003c0004t0001g0013 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.386-6184G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581090 | |||||||
chr14:103581091 | C | T | 84 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(81): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.386-6183C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581091 | |||||||
chr14:103581397 | A | G | 75 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.386-5877A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581397 | |||||||
chr14:103581413 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.386-5861G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581413 | |||||||
chr14:103581420 | C | T | 77 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(74): Show |
91 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.386-5854C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581420 | |||||||
chr14:103581480 | T | C | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.386-5794T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581480 | |||||||
chr14:103581583 | C | G | 1 | a0001c0003t0001g0060 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.386-5691C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581583 | |||||||
chr14:103581741 | G | A | 4 | a0001c0001t0003g0277 a0005c0007t0003g0189 a0005c0007t0003g0190 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-5533G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581741 | |||||||
chr14:103581828 | C | T | 1 | a0002c0002t0001g0132 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.386-5446C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581828 | |||||||
chr14:103581884 | CTG | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | NA18952.hp1 NA18990.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.386-5387_386-5386d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103581884 | ||||||
chr14:103581917 | C | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0254 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.386-5357C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581917 | |||||||
chr14:103581922 | C | T | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.386-5352C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103581922 | |||||||
chr14:103582101 | C | T | 3 | a0005c0007t0003g0189 a0005c0007t0003g0190 a0005c0007t0003g0191 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.386-5173C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582101 | |||||||
chr14:103582223 | A | G | 1 | a0001c0003t0001g0081 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.386-5051A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582223 | |||||||
chr14:103582234 | T | C | 73 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(70): Show |
87 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.386-5040T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582234 | |||||||
chr14:103582254 | GGT | G | 11 | a0004c0005t0001g0314 a0004c0005t0001g0319 a0004c0005t0001g0320 others(8): Show |
11 | HG01099.hp2 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.386-5019_386-5018d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582254 | |||||||
chr14:103582290 | C | T | 10 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0001g0097 others(7): Show |
12 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.386-4984C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582290 | |||||||
chr14:103582403 | G | A | 1 | a0001c0003t0001g0073 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.386-4871G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582403 | |||||||
chr14:103582497 | G | A | 49 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(46): Show |
57 | HG00140.hp2 HG00423.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.386-4777G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582497 | |||||||
chr14:103582499 | G | C | 3 | a0002c0002t0004g0157 a0002c0002t0004g0158 a0002c0002t0004g0171 |
3 | HG02922.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.386-4775G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582499 | |||||||
chr14:103582533 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.386-4741G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582533 | |||||||
chr14:103582631 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.386-4643C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582631 | |||||||
chr14:103582700 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0282 |
2 | HG00733.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.386-4574T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582700 | |||||||
chr14:103582737 | C | CTTTT | 69 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(66): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.386-4524_386-4521d others(6): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103582737 | ||||||
chr14:103582737 | C | CTTTTT | 12 | a0001c0001t0001g0200 a0001c0003t0001g0028 a0001c0003t0001g0033 others(9): Show |
12 | HG00140.hp2 HG01070.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.386-4525_386-4521d others(7): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103582737 | ||||||
chr14:103582737 | C | CTTTTTT | 82 | a0001c0001t0001g0019 a0001c0001t0001g0175 a0001c0001t0001g0176 others(79): Show |
97 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.386-4526_386-4521d others(8): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103582737 | ||||||
chr14:103582737 | C | CTTTTTTT | 36 | a0001c0001t0001g0174 a0001c0001t0001g0179 a0001c0001t0001g0199 others(33): Show |
36 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.386-4527_386-4521d others(9): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103582737 | ||||||
chr14:103582737 | C | CTTTTTTT others(1): Show |
8 | a0003c0004t0001g0013 a0003c0004t0001g0096 a0003c0004t0002g0014 others(5): Show |
10 | HG01884.hp2 HG02109.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.386-4528_386-4521d others(10): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103582737 | ||||||
chr14:103582971 | A | G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0290 a0001c0001t0001g0294 |
3 | HG02027.hp1 HG02056.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.386-4303A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103582971 | |||||||
chr14:103583230 | G | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.386-4044G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103583230 | |||||||
chr14:103583417 | T | C | 6 | a0001c0001t0001g0211 a0001c0001t0001g0240 a0001c0001t0001g0281 others(3): Show |
6 | HG01106.hp2 HG01928.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-3857T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103583417 | |||||||
chr14:103583456 | T | C | 165 | a0001c0001t0006g0103 a0001c0003t0001g0002 a0001c0003t0001g0004 others(162): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.386-3818T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103583456 | |||||||
chr14:103583517 | G | T | 1 | a0001c0001t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.386-3757G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103583517 | |||||||
chr14:103583541 | C | CA | 20 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0001g0234 others(17): Show |
20 | HG00741.hp2 HG01361.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-3708dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103583541 | ||||||
chr14:103583541 | CA | C | 101 | a0001c0001t0001g0023 a0001c0001t0001g0197 a0001c0001t0001g0203 others(98): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.386-3708delA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103583541 | ||||||
chr14:103583541 | CAA | C | 6 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0003t0001g0074 others(3): Show |
6 | HG01261.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-3709_386-3708d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103583541 | ||||||
chr14:103583718 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.386-3556C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103583718 | |||||||
chr14:103583954 | A | T | 1 | a0001c0001t0001g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.386-3320A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103583954 | |||||||
chr14:103584020 | A | G | 72 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(69): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.386-3254A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584020 | |||||||
chr14:103584054 | T | G | 2 | a0001c0001t0001g0183 a0002c0002t0001g0156 |
2 | HG00621.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.386-3220T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584054 | |||||||
chr14:103584098 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.386-3176A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584098 | |||||||
chr14:103584162 | G | A | 1 | a0001c0001t0006g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.386-3112G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584162 | |||||||
chr14:103584206 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.386-3068A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584206 | |||||||
chr14:103584401 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.386-2873C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584401 | |||||||
chr14:103584409 | T | C | 1 | a0001c0003t0001g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.386-2865T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584409 | |||||||
chr14:103584455 | A | G | 1 | a0001c0001t0003g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-2819A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584455 | |||||||
chr14:103584510 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.386-2764A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584510 | |||||||
chr14:103584546 | G | A | 76 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0003t0001g0002 others(73): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.386-2728G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584546 | |||||||
chr14:103584548 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.386-2726G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584548 | |||||||
chr14:103584862 | A | G | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.386-2412A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584862 | |||||||
chr14:103584911 | G | A | 2 | a0001c0003t0001g0048 a0001c0003t0001g0049 |
2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.386-2363G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584911 | |||||||
chr14:103584915 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.386-2359G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584915 | |||||||
chr14:103584993 | C | T | 3 | a0005c0007t0003g0189 a0005c0007t0003g0190 a0005c0007t0003g0191 |
3 | HG01167.hp2 HG01169.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.386-2281C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584993 | |||||||
chr14:103584999 | A | G | 3 | a0002c0002t0004g0157 a0002c0002t0004g0158 a0002c0002t0004g0171 |
3 | HG02922.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.386-2275A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103584999 | |||||||
chr14:103585095 | G | A | 5 | a0001c0001t0001g0212 a0001c0001t0001g0274 a0001c0001t0001g0275 others(2): Show |
5 | NA18747.hp2 NA18974.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.386-2179G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585095 | |||||||
chr14:103585105 | T | G | 1 | a0001c0001t0006g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.386-2169T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585105 | |||||||
chr14:103585137 | C | CTAAA | 8 | a0001c0001t0002g0202 a0003c0004t0002g0014 a0003c0004t0002g0095 others(5): Show |
9 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.386-2122_386-2119d others(6): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103585137 | ||||||
chr14:103585194 | C | T | 1 | a0001c0003t0001g0057 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.386-2080C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585194 | |||||||
chr14:103585250 | G | A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG02486.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.386-2024G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585250 | |||||||
chr14:103585304 | C | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.386-1970C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585304 | |||||||
chr14:103585306 | C | T | 76 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(73): Show |
90 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.386-1968C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585306 | |||||||
chr14:103585340 | G | A | 1 | a0001c0003t0001g0081 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.386-1934G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585340 | |||||||
chr14:103585348 | A | G | 154 | a0001c0003t0001g0002 a0001c0003t0001g0004 a0001c0003t0001g0005 others(151): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.386-1926A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585348 | |||||||
chr14:103585374 | G | A | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-1900G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585374 | |||||||
chr14:103585446 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.386-1828T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585446 | |||||||
chr14:103585479 | CA | C | 98 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(95): Show |
113 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.386-1780delA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103585479 | ||||||
chr14:103585479 | CAA | C | 79 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0286 others(76): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.386-1781_386-1780d others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103585479 | ||||||
chr14:103585512 | G | C | 1 | a0001c0010t0001g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.386-1762G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585512 | |||||||
chr14:103585529 | AGATG | A | 11 | a0004c0005t0001g0314 a0004c0005t0001g0319 a0004c0005t0001g0320 others(8): Show |
11 | HG01099.hp2 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.386-1740_386-1737d others(6): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103585529 | ||||||
chr14:103585577 | C | CT | 9 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0204 others(6): Show |
9 | HG01361.hp2 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.386-1680dupT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103585577 | ||||||
chr14:103585577 | C | CTTT | 73 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0286 others(70): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.386-1682_386-1680d others(5): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103585577 | ||||||
chr14:103585608 | G | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0192 a0001c0001t0001g0193 others(12): Show |
16 | HG00544.hp2 HG01175.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.386-1666G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585608 | |||||||
chr14:103585616 | G | A | 1 | a0004c0005t0001g0321 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.386-1658G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585616 | |||||||
chr14:103585720 | C | T | 79 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0286 others(76): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.386-1554C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103585720 | |||||||
chr14:103585879 | CTTTTTTG others(3): Show |
C | 1 | a0001c0003t0001g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.386-1385_386-1376d others(12): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103585879 | ||||||
chr14:103586005 | A | G | 1 | a0001c0010t0001g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.386-1269A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103586005 | |||||||
chr14:103586121 | G | A | 8 | a0001c0001t0002g0202 a0003c0004t0002g0014 a0003c0004t0002g0095 others(5): Show |
9 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.386-1153G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103586121 | |||||||
chr14:103586200 | C | CT | 47 | a0001c0001t0001g0022 a0001c0001t0001g0174 a0001c0001t0001g0176 others(44): Show |
48 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.386-1052dupT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103586200 | ||||||
chr14:103586200 | C | CTTTTTTT | 35 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0306 others(32): Show |
47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.386-1058_386-1052d others(9): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103586200 | ||||||
chr14:103586200 | C | CTTTTTTT others(1): Show |
41 | a0001c0001t0001g0284 a0001c0003t0001g0005 a0001c0003t0001g0011 others(38): Show |
46 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.386-1059_386-1052d others(10): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103586200 | ||||||
chr14:103586200 | CTTTTT | C | 7 | a0001c0001t0002g0202 a0003c0004t0002g0014 a0003c0004t0002g0095 others(4): Show |
8 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-1056_386-1052d others(7): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103586200 | ||||||
chr14:103586325 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.386-949G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103586325 | |||||||
chr14:103586373 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.386-901A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103586373 | |||||||
chr14:103586583 | G | A | 2 | a0002c0002t0001g0127 a0002c0002t0001g0143 |
2 | HG01255.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.386-691G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103586583 | |||||||
chr14:103586616 | C | T | 15 | a0001c0001t0001g0019 a0001c0001t0001g0192 a0001c0001t0001g0193 others(12): Show |
16 | HG00544.hp2 HG01175.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.386-658C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103586616 | |||||||
chr14:103586640 | C | CT | 328 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(325): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.386-622dupT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr14 | 103586640 | ||||||
chr14:103586716 | C | G | 4 | a0002c0002t0001g0122 a0002c0002t0001g0123 a0002c0002t0001g0131 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-558C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103586716 | |||||||
chr14:103586833 | T | C | 2 | a0001c0003t0001g0036 a0001c0003t0001g0065 |
2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.386-441T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103586833 | |||||||
chr14:103587037 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.386-237G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103587037 | |||||||
chr14:103587071 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0282 |
2 | HG00733.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.386-203A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 3/4 | chr14 | 103587071 | |||||||
chr14:103587383 | C | T | 1 | a0002c0002t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.476+19C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587383 | |||||||
chr14:103587427 | C | T | 79 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0286 others(76): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.476+63C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587427 | |||||||
chr14:103587500 | CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0001g0162 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.476+144_476+157del others(14): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103587500 | ||||||
chr14:103587508 | C | CT | 16 | a0001c0001t0001g0181 a0001c0001t0001g0250 a0001c0001t0001g0261 others(13): Show |
17 | HG01099.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.476+161dupT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103587508 | ||||||
chr14:103587508 | CT | C | 8 | a0001c0001t0001g0217 a0001c0001t0001g0228 a0002c0002t0001g0147 others(5): Show |
8 | HG01074.hp1 HG01081.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.476+161delT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103587508 | ||||||
chr14:103587513 | T | C | 79 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0286 others(76): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.476+149T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587513 | |||||||
chr14:103587526 | G | C | 77 | a0001c0003t0001g0066 a0002c0002t0001g0003 a0002c0002t0001g0006 others(74): Show |
91 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.476+162G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587526 | |||||||
chr14:103587647 | A | G | 10 | a0001c0001t0001g0009 a0001c0001t0001g0214 a0001c0001t0001g0237 others(7): Show |
12 | NA18941.hp1 NA18947.hp2 NA18962.hp1 others(9): Show |
intron_variant | MODIFIER | c.476+283A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587647 | |||||||
chr14:103587650 | G | C | 8 | a0001c0001t0001g0211 a0001c0001t0001g0240 a0001c0001t0001g0250 others(5): Show |
8 | HG01106.hp2 HG01243.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.476+286G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587650 | |||||||
chr14:103587656 | C | G | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.476+292C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587656 | |||||||
chr14:103587680 | T | G | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.476+316T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587680 | |||||||
chr14:103587796 | T | G | 1 | a0001c0003t0001g0039 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.476+432T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587796 | |||||||
chr14:103587866 | C | T | 2 | a0001c0003t0001g0053 a0001c0003t0001g0069 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.476+502C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587866 | |||||||
chr14:103587867 | G | T | 7 | a0002c0002t0001g0003 a0002c0002t0001g0018 a0002c0002t0001g0116 others(4): Show |
12 | HG01074.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.476+503G>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587867 | |||||||
chr14:103587923 | T | A | 1 | a0002c0002t0001g0151 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.476+559T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103587923 | |||||||
chr14:103588017 | C | G | 183 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(180): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.476+653C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588017 | |||||||
chr14:103588032 | C | T | 1 | a0001c0001t0006g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.476+668C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588032 | |||||||
chr14:103588070 | C | T | 1 | a0001c0001t0006g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.476+706C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588070 | |||||||
chr14:103588071 | G | A | 11 | a0004c0005t0001g0314 a0004c0005t0001g0319 a0004c0005t0001g0320 others(8): Show |
11 | HG01099.hp2 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.476+707G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588071 | |||||||
chr14:103588088 | T | C | 218 | a0001c0001t0001g0019 a0001c0001t0001g0174 a0001c0001t0001g0175 others(215): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.476+724T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588088 | |||||||
chr14:103588116 | C | CA | 115 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0022 others(112): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.476+776dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103588116 | ||||||
chr14:103588116 | C | CAA | 26 | a0001c0001t0001g0186 a0001c0001t0001g0203 a0001c0001t0001g0205 others(23): Show |
26 | HG00423.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.476+775_476+776dup others(2): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103588116 | ||||||
chr14:103588116 | CA | C | 10 | a0001c0001t0001g0290 a0001c0001t0006g0103 a0002c0002t0001g0008 others(7): Show |
12 | HG02056.hp1 HG02280.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.476+776delA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103588116 | ||||||
chr14:103588116 | CAAAA | C | 6 | a0001c0001t0002g0202 a0003c0004t0002g0014 a0003c0004t0002g0095 others(3): Show |
7 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.476+773_476+776del others(4): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103588116 | ||||||
chr14:103588131 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.476+767A>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588131 | |||||||
chr14:103588235 | C | T | 167 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0286 others(164): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.476+871C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588235 | |||||||
chr14:103588296 | C | G | 4 | a0002c0002t0001g0156 a0002c0002t0004g0157 a0002c0002t0004g0158 others(1): Show |
4 | HG01081.hp1 HG02922.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.476+932C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588296 | |||||||
chr14:103588461 | ATAAG | A | 8 | a0001c0001t0002g0202 a0003c0004t0002g0014 a0003c0004t0002g0095 others(5): Show |
9 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.476+1105_476+1108d others(6): Show |
COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103588461 | ||||||
chr14:103588474 | T | TA | 5 | a0001c0001t0001g0239 a0001c0001t0001g0282 a0002c0002t0001g0122 others(2): Show |
5 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.476+1117dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103588474 | ||||||
chr14:103588480 | A | T | 2 | a0001c0003t0001g0090 a0001c0003t0001g0091 |
2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.476+1116A>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588480 | |||||||
chr14:103588481 | AT | A | 48 | a0001c0003t0001g0066 a0002c0002t0001g0006 a0002c0002t0001g0007 others(45): Show |
56 | HG00140.hp2 HG00423.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.476+1118delT | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588481 | |||||||
chr14:103588482 | T | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(145): Show |
170 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.476+1118T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588482 | |||||||
chr14:103588484 | T | A | 24 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0249 others(21): Show |
24 | HG01074.hp2 HG01361.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.476+1120T>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588484 | |||||||
chr14:103588626 | T | G | 1 | a0002c0002t0001g0105 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.476+1262T>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588626 | |||||||
chr14:103588703 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.476+1339G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103588703 | |||||||
chr14:103589002 | G | C | 1 | a0001c0001t0001g0292 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.477-1179G>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589002 | |||||||
chr14:103589073 | G | A | 8 | a0001c0001t0002g0202 a0003c0004t0002g0014 a0003c0004t0002g0095 others(5): Show |
9 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.477-1108G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589073 | |||||||
chr14:103589221 | T | C | 3 | a0004c0005t0001g0319 a0004c0005t0001g0320 a0004c0005t0001g0324 |
3 | HG01099.hp2 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.477-960T>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589221 | |||||||
chr14:103589265 | C | G | 1 | a0002c0002t0001g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.477-916C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589265 | |||||||
chr14:103589393 | C | G | 1 | a0002c0002t0001g0138 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.477-788C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589393 | |||||||
chr14:103589419 | A | G | 1 | a0001c0003t0001g0055 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.477-762A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589419 | |||||||
chr14:103589601 | G | GA | 4 | a0001c0001t0003g0277 a0005c0007t0003g0189 a0005c0007t0003g0190 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-574dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103589601 | ||||||
chr14:103589613 | C | CA | 14 | a0001c0001t0001g0019 a0001c0001t0001g0192 a0001c0001t0001g0193 others(11): Show |
15 | HG00544.hp2 HG01175.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.477-560dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103589613 | ||||||
chr14:103589637 | C | T | 3 | a0002c0002t0004g0157 a0002c0002t0004g0158 a0002c0002t0004g0171 |
3 | HG02922.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.477-544C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589637 | |||||||
chr14:103589649 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.477-532C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589649 | |||||||
chr14:103589703 | C | A | 1 | a0001c0003t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.477-478C>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589703 | |||||||
chr14:103589733 | C | G | 6 | a0001c0001t0001g0211 a0001c0001t0001g0240 a0001c0001t0001g0281 others(3): Show |
6 | HG01106.hp2 HG01928.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.477-448C>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589733 | |||||||
chr14:103589783 | G | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0248 a0001c0001t0001g0254 |
3 | HG01081.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.477-398G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589783 | |||||||
chr14:103589787 | G | A | 1 | a0001c0001t0006g0103 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.477-394G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589787 | |||||||
chr14:103589832 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.477-349C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589832 | |||||||
chr14:103589863 | G | A | 15 | a0001c0001t0001g0019 a0001c0001t0001g0192 a0001c0001t0001g0193 others(12): Show |
16 | HG00544.hp2 HG01175.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.477-318G>A | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589863 | |||||||
chr14:103589898 | A | C | 8 | a0001c0001t0001g0211 a0001c0001t0001g0240 a0001c0001t0001g0250 others(5): Show |
8 | HG01106.hp2 HG01243.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.477-283A>C | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589898 | |||||||
chr14:103589913 | C | CA | 6 | a0001c0001t0001g0210 a0001c0001t0001g0214 a0001c0001t0001g0228 others(3): Show |
6 | HG03834.hp2 NA18947.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.477-256dupA | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr14 | 103589913 | ||||||
chr14:103589949 | C | T | 2 | a0001c0003t0001g0038 a0001c0003t0001g0067 |
2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.477-232C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103589949 | |||||||
chr14:103590125 | C | T | 2 | a0002c0002t0001g0104 a0002c0002t0001g0105 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.477-56C>T | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103590125 | |||||||
chr14:103590146 | A | G | 4 | a0001c0003t0001g0028 a0001c0003t0001g0046 a0001c0003t0001g0052 others(1): Show |
4 | HG02145.hp2 HG02735.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.477-35A>G | COA8 | ENSG00000256053.9 | transcript | ENST00000409074.8 | protein_coding | 4/4 | chr14 | 103590146 |