Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57120 |
| ensemblid | ENSG00000047932.14 |
| hgncid | 17643 |
| symbol | GOPC |
| name | golgi associated PDZ and coiled-coil motif containing |
| refseq_nuc | NM_020399.4 |
| refseq_prot | NP_065132.1 |
| ensembl_nuc | ENST00000368498.7 |
| ensembl_prot | ENSP00000357484.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 117560269 |
| end | 117602511 |
| strand | - |
| ver | v1.2 |
| region | chr6:117560269-117602511 |
| region5000 | chr6:117555269-117607511 |
| regionname0 | GOPC_chr6_117560269_117602511 |
| regionname5000 | GOPC_chr6_117555269_117607511 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 462 | 373 | 82 | 64 | 177 | 16 | 32 | 139 | GOPC_chr6_117555269_117607511 | GOPC | MSAGG others(457): Show |
chr6 | 117555269 | 117607511 |
| a0002 | 0/0 | 461 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | MSAGG others(456): Show |
chr6 | 117555269 | 117607511 |
| a0003 | 0/0 | 462 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | MSAGG others(457): Show |
chr6 | 117555269 | 117607511 |
| a0004 | 0/0 | 462 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | MSAGG others(457): Show |
chr6 | 117555269 | 117607511 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1386 | 370 | 82 | 64 | 176 | 15 | 31 | GOPC_chr6_117555269_117607511 | GOPC | ATGTC others(1381): Show |
chr6 | 117555269 | 117607511 | ||
| a0001c0003 | 0/0 | 1386 | 2 | 0 | 0 | 0 | 1 | 1 | GOPC_chr6_117555269_117607511 | GOPC | ATGTC others(1381): Show |
chr6 | 117555269 | 117607511 | ||
| a0001c0006 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | ATGTC others(1381): Show |
chr6 | 117555269 | 117607511 | ||
| a0002c0002 | 0/0 | 1385 | 7 | 7 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | ATGTC others(1380): Show |
chr6 | 117555269 | 117607511 | ||
| a0003c0005 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | ATGTC others(1381): Show |
chr6 | 117555269 | 117607511 | ||
| a0004c0004 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | ATGTC others(1381): Show |
chr6 | 117555269 | 117607511 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4597 | 118 | 11 | 27 | 72 | 2 | 6 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0002 | 0/0 | 4597 | 95 | 17 | 16 | 56 | 4 | 2 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0003 | 0/1 | 4597 | 71 | 10 | 14 | 31 | 3 | 12 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0004 | 0/0 | 4597 | 28 | 13 | 3 | 4 | 3 | 5 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0005 | 0/0 | 4597 | 18 | 18 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0006 | 0/0 | 4597 | 11 | 0 | 1 | 5 | 2 | 3 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0007 | 0/0 | 4597 | 7 | 6 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0009 | 0/0 | 4597 | 4 | 0 | 0 | 4 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0010 | 0/0 | 4597 | 3 | 0 | 2 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0011 | 0/0 | 4597 | 2 | 1 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0012 | 0/0 | 4597 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0013 | 0/0 | 4597 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0014 | 0/0 | 4597 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0015 | 0/0 | 4597 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0016 | 1/0 | 4597 | 1 | 0 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0017 | 0/0 | 4597 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0018 | 0/0 | 4597 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0019 | 0/0 | 4597 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0020 | 0/0 | 4597 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0021 | 0/0 | 4597 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0022 | 0/0 | 4597 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0001t0023 | 0/0 | 4597 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0003t0002 | 0/0 | 4597 | 2 | 0 | 0 | 0 | 1 | 1 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0001c0006t0003 | 0/0 | 4597 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0002c0002t0008 | 0/0 | 4594 | 7 | 7 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4589): Show |
chr6 | 117555269 | 117607511 |
| a0003c0005t0001 | 0/0 | 4597 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| a0004c0004t0003 | 0/0 | 4597 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | GGGAC others(4592): Show |
chr6 | 117555269 | 117607511 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 0 | 4 | 17 | 0 | 2 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0003 | 0/0 | 19 | 0 | 7 | 12 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0002 | 0/0 | 20 | 0 | 3 | 16 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0004 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0005 | 0/0 | 6 | 1 | 3 | 0 | 0 | 2 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0006 | 0/0 | 6 | 0 | 3 | 1 | 2 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0006g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0006g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0007g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0009g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0010g0025 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0011g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0012g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0013g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0014g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0016g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0017g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0018g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0019g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0020g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0021g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0022g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0001t0023g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0003t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0001c0006t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0002c0002t0008g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0002c0002t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0002c0002t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0003c0005t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| a0004c0004t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | GBR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0040 | EUR | GBR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0038 | EUR | GBR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0031 | EUR | FIN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0025 | EUR | FIN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0152 | EUR | FIN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0070 | EUR | FIN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00438 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0053 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0025 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0025 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0139 | EUR | IBS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0113 | EUR | IBS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01891 | hp2 | a0002 | c0002 | t0008 | g0009 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0040 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0149 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02071 | hp2 | a0001 | c0001 | t0009 | g0126 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02132 | hp1 | a0001 | c0006 | t0003 | g0105 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02145 | hp2 | a0002 | c0002 | t0008 | g0186 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | CDX | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02165 | hp1 | a0001 | c0001 | t0009 | g0036 | EAS | CDX | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0153 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0220 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0103 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02723 | hp2 | a0001 | c0001 | t0020 | g0219 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0148 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02896 | hp1 | a0002 | c0002 | t0008 | g0170 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02897 | hp1 | a0002 | c0002 | t0008 | g0009 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0210 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03239 | hp1 | a0001 | c0001 | t0021 | g0121 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03239 | hp2 | a0001 | c0001 | t0023 | g0225 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0051 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03486 | hp2 | a0002 | c0002 | t0008 | g0009 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0072 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03704 | hp2 | a0001 | c0003 | t0002 | g0038 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | BEB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | BEB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | BEB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0085 | SAS | STU | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0030 | SAS | STU | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0091 | SAS | STU | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | STU | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0101 | AFR | YRI | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | YRI | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | YRI | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0213 | AFR | YRI | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18941 | hp1 | a0001 | c0001 | t0012 | g0116 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18964 | hp2 | a0004 | c0004 | t0003 | g0080 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18978 | hp2 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18988 | hp1 | a0001 | c0001 | t0009 | g0036 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19000 | hp1 | a0001 | c0001 | t0012 | g0122 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19003 | hp1 | a0001 | c0001 | t0009 | g0120 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19010 | hp2 | a0001 | c0001 | t0017 | g0063 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | LWK | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | LWK | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19091 | hp2 | a0001 | c0001 | t0018 | g0074 | EAS | JPT | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19240 | hp1 | a0002 | c0002 | t0008 | g0009 | AFR | YRI | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | YRI | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | ASW | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0086 | AFR | ASW | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0031 | EUR | TSI | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | TSI | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | GIH | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | GIH | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02109 | hp1 | a0001 | c0001 | t0015 | g0076 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02109 | hp2 | a0001 | c0001 | t0019 | g0157 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG02559 | hp2 | a0003 | c0005 | t0001 | g0180 | AFR | ACB | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | USA | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | USA | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0209 | AFR | USA | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | USA | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA21309 | hp1 | a0002 | c0002 | t0008 | g0009 | AFR | LWK | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | LWK | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0079 | REF | REF | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0016 | g0071 | REF | REF | GOPC_chr6_117555269_117607511 | GOPC | chr6 | 117555269 | 117607511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:117563254 | TTAA | T | 1 | a0002 | 7 | HG01891.hp2 HG02145.hp2 HG02896.hp1 others(4): Show |
disruptive_inframe_deletion | MODERATE | c.1386_1388delTTA | p.Tyr462del | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 1611/4597 | 1386/1389 | 462/462 | chr6 | 117563254 | |||
| chr6:117566937 | C | T | 1 | a0004 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.1175G>A | p.Arg392His | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/9 | 1398/4597 | 1175/1389 | 392/462 | chr6 | 117566937 | |||
| chr6:117578983 | G | C | 1 | a0003 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.367C>G | p.Leu123Val | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 2/9 | 590/4597 | 367/1389 | 123/462 | chr6 | 117578983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:117578909 | C | T | 1 | a0001c0003 | 2 | HG00140.hp2 HG03704.hp2 |
synonymous_variant | LOW | c.441G>A | p.Lys147Lys | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 2/9 | 664/4597 | 441/1389 | 147/462 | chr6 | 117578909 | |||
| chr6:117602055 | T | C | 1 | a0001c0006 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.234A>G | p.Ala78Ala | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/9 | 457/4597 | 234/1389 | 78/462 | chr6 | 117602055 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:117560274 | C | T | 1 | a0001c0001t0011 | 2 | HG04199.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2980G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 2980 | chr6 | 117560274 | ||||||
| chr6:117560275 | G | A | 1 | a0001c0001t0010 | 3 | HG00280.hp2 HG01071.hp2 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2979C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 2979 | chr6 | 117560275 | ||||||
| chr6:117560382 | A | G | 1 | a0001c0001t0017 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2872T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 2872 | chr6 | 117560382 | ||||||
| chr6:117560390 | C | T | 1 | a0001c0001t0012 | 2 | NA18941.hp1 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2864G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 2864 | chr6 | 117560390 | ||||||
| chr6:117560442 | A | T | 11 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(8): Show |
125 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*2812T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 2812 | chr6 | 117560442 | ||||||
| chr6:117560537 | A | G | 1 | a0001c0001t0019 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2717T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 2717 | chr6 | 117560537 | ||||||
| chr6:117560542 | T | C | 1 | a0001c0001t0017 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2712A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 2712 | chr6 | 117560542 | ||||||
| chr6:117561046 | G | A | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0015 others(2): Show |
33 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2208C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 2208 | chr6 | 117561046 | ||||||
| chr6:117561178 | C | G | 1 | a0001c0001t0015 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2076G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 2076 | chr6 | 117561178 | ||||||
| chr6:117561364 | G | A | 1 | a0001c0001t0007 | 7 | HG00741.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1890C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 1890 | chr6 | 117561364 | ||||||
| chr6:117561488 | T | C | 1 | a0001c0001t0018 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1766A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 1766 | chr6 | 117561488 | ||||||
| chr6:117561516 | T | C | 6 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(3): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1738A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 1738 | chr6 | 117561516 | ||||||
| chr6:117561721 | C | T | 1 | a0001c0001t0020 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1533G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 1533 | chr6 | 117561721 | ||||||
| chr6:117562065 | T | C | 1 | a0001c0001t0020 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1189A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 1189 | chr6 | 117562065 | ||||||
| chr6:117562126 | C | G | 1 | a0001c0001t0006 | 11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1128G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 1128 | chr6 | 117562126 | ||||||
| chr6:117562271 | G | C | 1 | a0001c0001t0021 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*983C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 983 | chr6 | 117562271 | ||||||
| chr6:117562290 | C | T | 1 | a0001c0001t0014 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*964G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 964 | chr6 | 117562290 | ||||||
| chr6:117562416 | A | G | 1 | a0001c0001t0009 | 4 | HG02071.hp2 HG02165.hp1 NA18988.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*838T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 838 | chr6 | 117562416 | ||||||
| chr6:117562870 | T | A | 1 | a0001c0001t0022 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*384A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 9/9 | 384 | chr6 | 117562870 | ||||||
| chr6:117602436 | T | C | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(13): Show |
273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
5_prime_UTR_variant | MODIFIER | c.-148A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/9 | 148 | chr6 | 117602436 | ||||||
| chr6:117602480 | G | T | 2 | a0001c0001t0007 a0001c0001t0013 |
8 | HG00741.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-192C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/9 | 192 | chr6 | 117602480 | ||||||
| chr6:117602493 | G | A | 1 | a0001c0001t0023 | 1 | HG03239.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-205C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/9 | chr6 | 117602493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:117563575 | C | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(165): Show |
288 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.1259-191G>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117563575 | |||||||
| chr6:117563683 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1259-299G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117563683 | |||||||
| chr6:117563734 | TA | T | 12 | a0001c0001t0001g0043 a0001c0001t0001g0164 a0001c0001t0001g0167 others(9): Show |
13 | HG01167.hp2 HG02965.hp2 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.1259-351delT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117563734 | |||||||
| chr6:117564213 | C | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0162 a0001c0001t0003g0090 |
3 | HG01515.hp1 HG01517.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1259-829G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117564213 | |||||||
| chr6:117564537 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(63): Show |
136 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.1259-1153G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117564537 | |||||||
| chr6:117564796 | C | T | 35 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0006 others(32): Show |
62 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.1259-1412G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117564796 | |||||||
| chr6:117564804 | A | C | 1 | a0001c0001t0003g0022 | 3 | HG02055.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1259-1420T>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117564804 | |||||||
| chr6:117564902 | G | C | 1 | a0001c0001t0005g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1259-1518C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117564902 | |||||||
| chr6:117565064 | T | C | 84 | a0001c0001t0001g0224 a0001c0001t0003g0004 a0001c0001t0003g0005 others(81): Show |
126 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1259-1680A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117565064 | |||||||
| chr6:117565413 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1258+1441C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117565413 | |||||||
| chr6:117565679 | G | A | 2 | a0001c0001t0005g0211 a0001c0001t0005g0212 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1258+1175C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117565679 | |||||||
| chr6:117565801 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1258+1053T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117565801 | |||||||
| chr6:117565808 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1258+1046C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117565808 | |||||||
| chr6:117566008 | T | A | 1 | a0001c0001t0003g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1258+846A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117566008 | |||||||
| chr6:117566052 | G | T | 1 | a0001c0001t0002g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1258+802C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117566052 | |||||||
| chr6:117566195 | C | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1258+659G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117566195 | |||||||
| chr6:117566334 | T | C | 1 | a0001c0001t0005g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1258+520A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117566334 | |||||||
| chr6:117566582 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0128 |
5 | NA18957.hp2 NA18966.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1258+272C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 8/8 | chr6 | 117566582 | |||||||
| chr6:117567204 | G | T | 1 | a0001c0001t0002g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1078-170C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117567204 | |||||||
| chr6:117567499 | A | T | 7 | a0001c0001t0005g0208 a0001c0001t0005g0209 a0001c0001t0005g0211 others(4): Show |
7 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-465T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117567499 | |||||||
| chr6:117568026 | C | CA | 32 | a0001c0001t0001g0161 a0001c0001t0001g0183 a0001c0001t0001g0193 others(29): Show |
35 | HG00408.hp2 HG01123.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1078-993dupT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117568026 | |||||||
| chr6:117568026 | C | CAA | 7 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(4): Show |
9 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(6): Show |
intron_variant | MODIFIER | c.1078-994_1078-993d others(4): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117568026 | |||||||
| chr6:117568026 | CA | C | 5 | a0001c0001t0001g0164 a0001c0001t0001g0198 a0001c0001t0002g0018 others(2): Show |
8 | HG00099.hp1 HG02717.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-993delT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117568026 | |||||||
| chr6:117568106 | G | A | 8 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0149 others(5): Show |
10 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(7): Show |
intron_variant | MODIFIER | c.1078-1072C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117568106 | |||||||
| chr6:117568200 | C | T | 5 | a0001c0001t0004g0073 a0001c0001t0004g0083 a0001c0001t0004g0084 others(2): Show |
5 | HG00408.hp1 HG00544.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1078-1166G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117568200 | |||||||
| chr6:117568330 | G | A | 1 | a0001c0001t0004g0072 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1077+1242C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117568330 | |||||||
| chr6:117568439 | G | C | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.1077+1133C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117568439 | |||||||
| chr6:117568631 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1077+941T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117568631 | |||||||
| chr6:117569031 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1077+541A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117569031 | |||||||
| chr6:117569086 | G | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(169): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1077+486C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117569086 | |||||||
| chr6:117569192 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1077+380C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117569192 | |||||||
| chr6:117569315 | A | G | 1 | a0001c0001t0005g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1077+257T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 7/8 | chr6 | 117569315 | |||||||
| chr6:117570035 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.913-299G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570035 | |||||||
| chr6:117570071 | T | G | 5 | a0001c0001t0005g0049 a0001c0001t0005g0204 a0001c0001t0005g0205 others(2): Show |
6 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.913-335A>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570071 | |||||||
| chr6:117570168 | T | A | 1 | a0001c0001t0003g0054 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.913-432A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570168 | |||||||
| chr6:117570234 | T | TA | 26 | a0001c0001t0003g0088 a0001c0001t0004g0020 a0001c0001t0004g0029 others(23): Show |
32 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(29): Show |
intron_variant | MODIFIER | c.913-499dupT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570234 | |||||||
| chr6:117570321 | A | G | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.912+539T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570321 | |||||||
| chr6:117570336 | G | T | 4 | a0001c0001t0004g0073 a0001c0001t0004g0083 a0001c0001t0004g0104 others(1): Show |
4 | HG00408.hp1 HG00544.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.912+524C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570336 | |||||||
| chr6:117570344 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.912+516G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570344 | |||||||
| chr6:117570511 | C | T | 1 | a0001c0001t0019g0157 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.912+349G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570511 | |||||||
| chr6:117570569 | C | T | 4 | a0001c0001t0005g0026 a0001c0001t0005g0214 a0001c0001t0005g0221 others(1): Show |
6 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.912+291G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570569 | |||||||
| chr6:117570607 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.912+253A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570607 | |||||||
| chr6:117570663 | G | T | 11 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(8): Show |
14 | HG00280.hp1 HG00323.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.912+197C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 6/8 | chr6 | 117570663 | |||||||
| chr6:117571021 | C | T | 1 | a0001c0001t0003g0034 | 2 | HG02080.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.817-66G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117571021 | |||||||
| chr6:117571246 | T | C | 1 | a0001c0001t0003g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.817-291A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117571246 | |||||||
| chr6:117571251 | G | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(51): Show |
112 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(109): Show |
intron_variant | MODIFIER | c.817-296C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117571251 | |||||||
| chr6:117571617 | T | C | 1 | a0001c0001t0003g0028 | 2 | NA18972.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.817-662A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117571617 | |||||||
| chr6:117571759 | C | T | 4 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-804G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117571759 | |||||||
| chr6:117571941 | A | G | 67 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0006 others(64): Show |
104 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.817-986T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117571941 | |||||||
| chr6:117572032 | G | A | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.817-1077C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117572032 | |||||||
| chr6:117572162 | T | G | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.817-1207A>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117572162 | |||||||
| chr6:117572221 | G | A | 1 | a0001c0001t0005g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.816+1246C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117572221 | |||||||
| chr6:117572367 | T | C | 4 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+1100A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117572367 | |||||||
| chr6:117572411 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.816+1056A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117572411 | |||||||
| chr6:117572517 | C | G | 1 | a0001c0001t0007g0052 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.816+950G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117572517 | |||||||
| chr6:117572648 | CT | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0159 a0001c0001t0001g0173 others(4): Show |
11 | HG01361.hp2 HG01928.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.816+818delA | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117572648 | |||||||
| chr6:117572721 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(219): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.816+746G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117572721 | |||||||
| chr6:117572944 | A | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0147 a0001c0001t0019g0157 |
6 | HG02109.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+523T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117572944 | |||||||
| chr6:117573038 | AC | A | 2 | a0001c0001t0004g0029 a0001c0001t0004g0070 |
3 | HG00323.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.816+428delG | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 5/8 | chr6 | 117573038 | |||||||
| chr6:117573636 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18991.hp2 | splice_region_variant&intron_variant | LOW | c.651-4G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117573636 | |||||||
| chr6:117573830 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0135 |
3 | HG01192.hp2 HG01943.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.651-198T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117573830 | |||||||
| chr6:117574116 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.651-484C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574116 | |||||||
| chr6:117574232 | C | T | 2 | a0001c0001t0006g0149 a0001c0001t0006g0151 |
2 | HG02071.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.651-600G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574232 | |||||||
| chr6:117574241 | A | AC | 4 | a0001c0001t0003g0014 a0001c0001t0003g0096 a0001c0001t0003g0098 others(1): Show |
7 | HG01243.hp2 HG02132.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.651-610dupG | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574241 | |||||||
| chr6:117574259 | T | A | 1 | a0001c0001t0001g0046 | 2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.651-627A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574259 | |||||||
| chr6:117574260 | A | T | 1 | a0001c0001t0002g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.651-628T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574260 | |||||||
| chr6:117574346 | A | G | 1 | a0001c0001t0007g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.651-714T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574346 | |||||||
| chr6:117574651 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0147 a0001c0001t0019g0157 |
6 | HG02109.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.650+526C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574651 | |||||||
| chr6:117574674 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.650+503A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574674 | |||||||
| chr6:117574907 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.650+270G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574907 | |||||||
| chr6:117574940 | G | A | 1 | a0001c0001t0004g0077 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.650+237C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574940 | |||||||
| chr6:117574963 | C | T | 7 | a0001c0001t0003g0012 a0001c0001t0003g0027 a0001c0001t0003g0054 others(4): Show |
11 | NA18942.hp1 NA18944.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.650+214G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117574963 | |||||||
| chr6:117575054 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.650+123C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117575054 | |||||||
| chr6:117575076 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.650+101G>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 4/8 | chr6 | 117575076 | |||||||
| chr6:117575371 | C | G | 1 | a0001c0001t0003g0022 | 3 | HG02055.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.475-19G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117575371 | |||||||
| chr6:117575548 | C | T | 1 | a0001c0001t0002g0142 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.475-196G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117575548 | |||||||
| chr6:117575565 | A | C | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-213T>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117575565 | |||||||
| chr6:117575623 | A | G | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-271T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117575623 | |||||||
| chr6:117575677 | GA | G | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.475-326delT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117575677 | |||||||
| chr6:117575699 | G | T | 6 | a0001c0001t0005g0208 a0001c0001t0005g0209 a0001c0001t0005g0211 others(3): Show |
6 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.475-347C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117575699 | |||||||
| chr6:117575736 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(50): Show |
110 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(107): Show |
intron_variant | MODIFIER | c.475-384C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117575736 | |||||||
| chr6:117575954 | G | A | 1 | a0001c0001t0002g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.475-602C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117575954 | |||||||
| chr6:117576202 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.475-850G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117576202 | |||||||
| chr6:117576238 | T | TAA | 11 | a0001c0001t0001g0003 a0001c0001t0001g0146 a0001c0001t0001g0160 others(8): Show |
29 | HG00673.hp2 HG00735.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.475-888_475-887dup others(2): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117576238 | |||||||
| chr6:117576238 | T | TAAA | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0191 others(2): Show |
7 | HG01074.hp2 HG01123.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.475-889_475-887dup others(3): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117576238 | |||||||
| chr6:117576759 | A | G | 5 | a0001c0001t0007g0011 a0001c0001t0007g0050 a0001c0001t0007g0052 others(2): Show |
8 | HG00741.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.474+689T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117576759 | |||||||
| chr6:117577029 | C | CACAT | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(207): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.474+418_474+419ins others(4): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117577029 | |||||||
| chr6:117577048 | A | G | 84 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0006 others(81): Show |
126 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.474+400T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 3/8 | chr6 | 117577048 | |||||||
| chr6:117578274 | A | C | 1 | a0001c0001t0002g0138 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.450+626T>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 2/8 | chr6 | 117578274 | |||||||
| chr6:117578279 | T | C | 2 | a0001c0001t0002g0119 a0001c0001t0002g0141 |
2 | HG02074.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.450+621A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 2/8 | chr6 | 117578279 | |||||||
| chr6:117578326 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.450+574C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 2/8 | chr6 | 117578326 | |||||||
| chr6:117578489 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.450+411C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 2/8 | chr6 | 117578489 | |||||||
| chr6:117578508 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(50): Show |
110 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(107): Show |
intron_variant | MODIFIER | c.450+392C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 2/8 | chr6 | 117578508 | |||||||
| chr6:117579492 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.286-428T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117579492 | |||||||
| chr6:117579534 | T | TG | 5 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
10 | HG00544.hp1 HG02083.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.286-471_286-470ins others(1): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117579534 | |||||||
| chr6:117579536 | A | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
10 | HG00544.hp1 HG02083.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.286-472T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117579536 | |||||||
| chr6:117579538 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
10 | HG00544.hp1 HG02083.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.286-474C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117579538 | |||||||
| chr6:117579540 | T | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
10 | HG00544.hp1 HG02083.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.286-476A>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117579540 | |||||||
| chr6:117579781 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.286-717G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117579781 | |||||||
| chr6:117579885 | T | C | 35 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0006 others(32): Show |
62 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.286-821A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117579885 | |||||||
| chr6:117580013 | G | C | 1 | a0001c0001t0004g0020 | 3 | HG02257.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.286-949C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117580013 | |||||||
| chr6:117580120 | T | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(169): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.286-1056A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117580120 | |||||||
| chr6:117580159 | A | G | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-1095T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117580159 | |||||||
| chr6:117580192 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.286-1128C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117580192 | |||||||
| chr6:117580543 | A | C | 2 | a0001c0001t0006g0041 a0001c0001t0006g0150 |
3 | HG00438.hp1 NA18944.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.286-1479T>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117580543 | |||||||
| chr6:117581122 | TA | T | 3 | a0001c0001t0009g0036 a0001c0001t0009g0120 a0001c0001t0009g0126 |
4 | HG02071.hp2 HG02165.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2059delT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581122 | |||||||
| chr6:117581266 | T | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.286-2202A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581266 | |||||||
| chr6:117581372 | T | A | 1 | a0001c0001t0019g0157 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-2308A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581372 | |||||||
| chr6:117581464 | GA | G | 38 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0147 others(35): Show |
51 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.286-2401delT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581464 | |||||||
| chr6:117581464 | GAA | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(130): Show |
240 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.286-2402_286-2401d others(4): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581464 | |||||||
| chr6:117581515 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | NA18981.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.286-2451C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581515 | |||||||
| chr6:117581619 | G | C | 1 | a0001c0001t0003g0022 | 3 | HG02055.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.286-2555C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581619 | |||||||
| chr6:117581685 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.286-2621G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581685 | |||||||
| chr6:117581882 | A | G | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286-2818T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581882 | |||||||
| chr6:117581943 | G | C | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-2879C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117581943 | |||||||
| chr6:117582061 | T | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
34 | HG00673.hp2 HG00735.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.286-2997A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582061 | |||||||
| chr6:117582109 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.286-3045G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582109 | |||||||
| chr6:117582131 | A | G | 27 | a0001c0001t0003g0088 a0001c0001t0004g0020 a0001c0001t0004g0029 others(24): Show |
34 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(31): Show |
intron_variant | MODIFIER | c.286-3067T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582131 | |||||||
| chr6:117582269 | C | T | 1 | a0001c0001t0014g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.286-3205G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582269 | |||||||
| chr6:117582273 | T | TAC | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(43): Show |
97 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.286-3211_286-3210d others(4): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582273 | T | TACAC | 52 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0146 others(49): Show |
77 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.286-3213_286-3210d others(6): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582273 | T | TACACAC | 28 | a0001c0001t0001g0047 a0001c0001t0001g0184 a0001c0001t0002g0019 others(25): Show |
51 | HG00099.hp1 HG00738.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.286-3215_286-3210d others(8): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582273 | T | TACACACA others(1): Show |
16 | a0001c0001t0001g0224 a0001c0001t0002g0024 a0001c0001t0003g0061 others(13): Show |
21 | HG01074.hp1 HG01168.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.286-3217_286-3210d others(10): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582273 | T | TACACACA others(3): Show |
3 | a0001c0001t0004g0092 a0001c0001t0005g0205 a0001c0001t0011g0091 |
3 | HG01891.hp1 HG04199.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.286-3219_286-3210d others(12): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582273 | T | TACACACA others(5): Show |
1 | a0001c0001t0005g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.286-3221_286-3210d others(14): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582273 | T | TACACACA others(9): Show |
1 | a0001c0001t0005g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286-3225_286-3210d others(18): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582273 | TAC | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(15): Show |
31 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.286-3211_286-3210d others(4): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582273 | TACAC | T | 12 | a0001c0001t0001g0158 a0001c0001t0001g0162 a0001c0001t0002g0119 others(9): Show |
14 | HG00140.hp1 HG00438.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.286-3213_286-3210d others(6): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582273 | TACACAC | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0147 a0001c0001t0019g0157 |
6 | HG02109.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-3215_286-3210d others(8): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582273 | |||||||
| chr6:117582519 | A | G | 3 | a0001c0001t0002g0115 a0001c0001t0002g0118 a0001c0001t0002g0131 |
3 | NA18959.hp2 NA18989.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.286-3455T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582519 | |||||||
| chr6:117582520 | T | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0147 a0001c0001t0019g0157 |
6 | HG02109.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-3456A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582520 | |||||||
| chr6:117582528 | C | CA | 3 | a0001c0001t0003g0021 a0001c0001t0003g0093 a0001c0001t0003g0099 |
5 | HG02818.hp1 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-3465dupT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582528 | |||||||
| chr6:117582554 | A | T | 6 | a0001c0001t0005g0208 a0001c0001t0005g0209 a0001c0001t0005g0211 others(3): Show |
6 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-3490T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582554 | |||||||
| chr6:117582674 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(49): Show |
109 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(106): Show |
intron_variant | MODIFIER | c.286-3610G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582674 | |||||||
| chr6:117582761 | C | G | 1 | a0001c0001t0003g0069 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.286-3697G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582761 | |||||||
| chr6:117582829 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0147 a0001c0001t0019g0157 |
6 | HG02109.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-3765C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582829 | |||||||
| chr6:117582849 | C | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0216 a0001c0001t0002g0217 others(1): Show |
7 | HG01243.hp1 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-3785G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117582849 | |||||||
| chr6:117583102 | ACCTGCTT others(13): Show |
A | 1 | a0001c0001t0001g0166 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.286-4058_286-4039d others(22): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117583102 | |||||||
| chr6:117583152 | C | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.286-4088G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117583152 | |||||||
| chr6:117583217 | G | A | 1 | a0001c0001t0003g0094 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.286-4153C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117583217 | |||||||
| chr6:117583277 | G | A | 4 | a0001c0001t0005g0026 a0001c0001t0005g0214 a0001c0001t0005g0221 others(1): Show |
6 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-4213C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117583277 | |||||||
| chr6:117583476 | G | C | 1 | a0001c0001t0001g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286-4412C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117583476 | |||||||
| chr6:117583528 | C | T | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01516.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.286-4464G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117583528 | |||||||
| chr6:117583631 | C | T | 1 | a0001c0001t0006g0148 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.286-4567G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117583631 | |||||||
| chr6:117583850 | T | C | 1 | a0001c0001t0003g0094 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.286-4786A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117583850 | |||||||
| chr6:117584038 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.286-4974G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117584038 | |||||||
| chr6:117584137 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0162 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.286-5073G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117584137 | |||||||
| chr6:117584597 | A | G | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286-5533T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117584597 | |||||||
| chr6:117584633 | C | T | 84 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0006 others(81): Show |
126 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.286-5569G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117584633 | |||||||
| chr6:117584848 | G | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0095 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.286-5784C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117584848 | |||||||
| chr6:117585126 | A | G | 7 | a0001c0001t0003g0012 a0001c0001t0003g0027 a0001c0001t0003g0054 others(4): Show |
11 | NA18942.hp1 NA18944.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-6062T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117585126 | |||||||
| chr6:117585280 | T | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0147 a0001c0001t0019g0157 |
6 | HG02109.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-6216A>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117585280 | |||||||
| chr6:117585921 | G | C | 1 | a0001c0001t0005g0207 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.286-6857C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117585921 | |||||||
| chr6:117586131 | G | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(169): Show |
292 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.286-7067C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586131 | |||||||
| chr6:117586205 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.286-7141C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586205 | |||||||
| chr6:117586436 | CCTGGAA | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0203 |
3 | HG02630.hp2 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.286-7378_286-7373d others(8): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586436 | |||||||
| chr6:117586440 | G | A | 1 | a0001c0001t0002g0106 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.286-7376C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586440 | |||||||
| chr6:117586448 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.286-7384G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586448 | |||||||
| chr6:117586475 | C | CT | 35 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(32): Show |
54 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.286-7412dupA | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586475 | |||||||
| chr6:117586475 | CT | C | 63 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0002g0134 others(60): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.286-7412delA | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586475 | |||||||
| chr6:117586475 | CTTTTTTT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(46): Show |
105 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(102): Show |
intron_variant | MODIFIER | c.286-7418_286-7412d others(9): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586475 | |||||||
| chr6:117586475 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.286-7422_286-7412d others(13): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586475 | |||||||
| chr6:117586475 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0003g0014 a0001c0001t0003g0096 a0001c0006t0003g0105 |
6 | HG01243.hp2 HG02132.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-7423_286-7412d others(14): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586475 | |||||||
| chr6:117586723 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.286-7659G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586723 | |||||||
| chr6:117586728 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.286-7664C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586728 | |||||||
| chr6:117586959 | T | C | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-7895A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117586959 | |||||||
| chr6:117587257 | T | C | 1 | a0001c0001t0003g0005 | 6 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-8193A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117587257 | |||||||
| chr6:117587315 | A | G | 1 | a0001c0001t0013g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.286-8251T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117587315 | |||||||
| chr6:117587529 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.286-8465T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117587529 | |||||||
| chr6:117587784 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0054 |
3 | NA18944.hp2 NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.286-8720G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117587784 | |||||||
| chr6:117587799 | G | C | 11 | a0001c0001t0005g0026 a0001c0001t0005g0208 a0001c0001t0005g0209 others(8): Show |
13 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.286-8735C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117587799 | |||||||
| chr6:117587839 | A | G | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-8775T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117587839 | |||||||
| chr6:117588035 | T | A | 1 | a0001c0001t0005g0206 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.286-8971A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588035 | |||||||
| chr6:117588038 | A | T | 2 | a0001c0001t0002g0018 a0001c0001t0002g0147 |
5 | HG02717.hp1 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-8974T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588038 | |||||||
| chr6:117588158 | A | G | 1 | a0001c0001t0003g0005 | 6 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-9094T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588158 | |||||||
| chr6:117588255 | T | A | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286-9191A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588255 | |||||||
| chr6:117588347 | C | A | 55 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(52): Show |
92 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.286-9283G>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588347 | |||||||
| chr6:117588435 | C | T | 1 | a0001c0001t0002g0015 | 4 | NA18957.hp2 NA18966.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-9371G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588435 | |||||||
| chr6:117588462 | G | T | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286-9398C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588462 | |||||||
| chr6:117588477 | T | G | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-9413A>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588477 | |||||||
| chr6:117588615 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.286-9551T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588615 | |||||||
| chr6:117588713 | AATG | A | 1 | a0001c0001t0002g0017 | 4 | NA18942.hp2 NA18957.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-9652_286-9650d others(5): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588713 | |||||||
| chr6:117588746 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.286-9682A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117588746 | |||||||
| chr6:117589192 | G | C | 51 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(48): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.286-10128C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589192 | |||||||
| chr6:117589290 | C | A | 1 | a0001c0001t0003g0060 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.286-10226G>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589290 | |||||||
| chr6:117589291 | A | C | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286-10227T>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589291 | |||||||
| chr6:117589305 | T | C | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.286-10241A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589305 | |||||||
| chr6:117589350 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(136): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.286-10286T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589350 | |||||||
| chr6:117589411 | C | A | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.286-10347G>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589411 | |||||||
| chr6:117589445 | C | G | 1 | a0001c0001t0006g0150 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.286-10381G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589445 | |||||||
| chr6:117589598 | G | A | 3 | a0001c0001t0006g0040 a0001c0001t0006g0153 a0001c0001t0006g0220 |
4 | HG00140.hp1 HG01981.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-10534C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589598 | |||||||
| chr6:117589599 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0203 |
3 | HG02630.hp2 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.286-10535G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589599 | |||||||
| chr6:117589625 | G | GT | 7 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0147 others(4): Show |
13 | HG01243.hp1 HG02109.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.286-10562dupA | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117589625 | |||||||
| chr6:117590431 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.286-11367C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590431 | |||||||
| chr6:117590505 | G | A | 1 | a0001c0001t0003g0097 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.286-11441C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590505 | |||||||
| chr6:117590571 | C | CA | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(69): Show |
146 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.285+11432dupT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590571 | |||||||
| chr6:117590571 | C | CAA | 8 | a0001c0001t0001g0146 a0001c0001t0001g0161 a0001c0001t0001g0185 others(5): Show |
8 | HG01123.hp1 HG01928.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+11431_285+1143 others(6): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590571 | |||||||
| chr6:117590593 | AG | A | 2 | a0001c0001t0006g0041 a0001c0001t0006g0150 |
3 | HG00438.hp1 NA18944.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.285+11410delC | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590593 | |||||||
| chr6:117590715 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.285+11289A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590715 | |||||||
| chr6:117590832 | A | C | 3 | a0001c0001t0002g0023 a0001c0001t0002g0111 a0001c0001t0002g0112 |
5 | HG00423.hp2 HG00673.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+11172T>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590832 | |||||||
| chr6:117590834 | A | ATTTTG | 54 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(51): Show |
97 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.285+11165_285+1116 others(9): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590834 | |||||||
| chr6:117590834 | A | ATTTTGTT others(3): Show |
1 | a0001c0001t0002g0110 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.285+11160_285+1116 others(14): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590834 | |||||||
| chr6:117590864 | G | T | 7 | a0001c0001t0003g0022 a0001c0001t0005g0049 a0001c0001t0005g0204 others(4): Show |
10 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+11140C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590864 | |||||||
| chr6:117590889 | G | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(11): Show |
27 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.285+11115C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590889 | |||||||
| chr6:117590928 | A | G | 4 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+11076T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590928 | |||||||
| chr6:117590955 | C | A | 1 | a0001c0001t0003g0099 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.285+11049G>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590955 | |||||||
| chr6:117590977 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.285+11027G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117590977 | |||||||
| chr6:117591257 | G | A | 4 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+10747C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117591257 | |||||||
| chr6:117591267 | AAAG | A | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+10734_285+1073 others(7): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117591267 | |||||||
| chr6:117591329 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0001g0046 others(22): Show |
49 | HG00673.hp2 HG00735.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.285+10675C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117591329 | |||||||
| chr6:117591545 | C | G | 1 | a0001c0001t0002g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.285+10459G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117591545 | |||||||
| chr6:117591562 | C | T | 1 | a0001c0001t0004g0030 | 2 | HG02735.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.285+10442G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117591562 | |||||||
| chr6:117591684 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+10320G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117591684 | |||||||
| chr6:117591857 | G | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(153): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.285+10147C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117591857 | |||||||
| chr6:117592038 | A | G | 55 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(52): Show |
92 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.285+9966T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592038 | |||||||
| chr6:117592045 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0147 a0001c0001t0019g0157 |
6 | HG02109.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+9959A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592045 | |||||||
| chr6:117592095 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
10 | HG00544.hp1 HG02083.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+9909C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592095 | |||||||
| chr6:117592105 | G | A | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.285+9899C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592105 | |||||||
| chr6:117592237 | G | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(11): Show |
27 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.285+9767C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592237 | |||||||
| chr6:117592393 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.285+9611C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592393 | |||||||
| chr6:117592574 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.285+9430T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592574 | |||||||
| chr6:117592610 | T | A | 1 | a0001c0001t0002g0135 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.285+9394A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592610 | |||||||
| chr6:117592624 | T | C | 1 | a0001c0001t0002g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+9380A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592624 | |||||||
| chr6:117592744 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.285+9260C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592744 | |||||||
| chr6:117592931 | A | C | 4 | a0001c0001t0002g0019 a0001c0001t0002g0216 a0001c0001t0002g0217 others(1): Show |
7 | HG01243.hp1 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+9073T>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117592931 | |||||||
| chr6:117593302 | C | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(76): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.285+8702G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593302 | |||||||
| chr6:117593339 | A | G | 5 | a0001c0001t0005g0049 a0001c0001t0005g0204 a0001c0001t0005g0205 others(2): Show |
6 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+8665T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593339 | |||||||
| chr6:117593352 | T | C | 1 | a0001c0001t0003g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.285+8652A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593352 | |||||||
| chr6:117593365 | C | A | 1 | a0001c0001t0002g0137 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.285+8639G>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593365 | |||||||
| chr6:117593472 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(11): Show |
27 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.285+8532G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593472 | |||||||
| chr6:117593481 | T | C | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+8523A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593481 | |||||||
| chr6:117593560 | G | A | 3 | a0001c0001t0003g0028 a0001c0001t0003g0062 a0001c0001t0017g0063 |
4 | NA18972.hp1 NA19007.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+8444C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593560 | |||||||
| chr6:117593713 | T | C | 1 | a0001c0001t0002g0037 | 2 | NA18986.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.285+8291A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593713 | |||||||
| chr6:117593746 | T | C | 3 | a0001c0001t0005g0026 a0001c0001t0005g0221 a0001c0001t0005g0222 |
5 | HG02622.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+8258A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593746 | |||||||
| chr6:117593940 | A | G | 4 | a0001c0001t0002g0019 a0001c0001t0002g0216 a0001c0001t0002g0217 others(1): Show |
7 | HG01243.hp1 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+8064T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117593940 | |||||||
| chr6:117594239 | T | C | 5 | a0001c0001t0005g0049 a0001c0001t0005g0204 a0001c0001t0005g0205 others(2): Show |
6 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+7765A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117594239 | |||||||
| chr6:117594443 | A | G | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.285+7561T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117594443 | |||||||
| chr6:117594563 | A | G | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+7441T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117594563 | |||||||
| chr6:117594697 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0147 a0001c0001t0019g0157 |
6 | HG02109.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+7307C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117594697 | |||||||
| chr6:117594978 | A | G | 1 | a0001c0001t0003g0066 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.285+7026T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117594978 | |||||||
| chr6:117594983 | C | CCTCA | 4 | a0001c0001t0002g0019 a0001c0001t0002g0216 a0001c0001t0002g0217 others(1): Show |
7 | HG01243.hp1 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+7020_285+7021i others(6): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117594983 | |||||||
| chr6:117595092 | T | C | 1 | a0001c0001t0002g0138 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.285+6912A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117595092 | |||||||
| chr6:117595311 | C | T | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+6693G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117595311 | |||||||
| chr6:117595320 | C | T | 4 | a0001c0001t0005g0049 a0001c0001t0005g0204 a0001c0001t0005g0205 others(1): Show |
5 | HG01891.hp1 HG02055.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+6684G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117595320 | |||||||
| chr6:117595445 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(136): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.285+6559A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117595445 | |||||||
| chr6:117595462 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.285+6542C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117595462 | |||||||
| chr6:117595779 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(76): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.285+6225G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117595779 | |||||||
| chr6:117595867 | G | C | 1 | a0001c0001t0014g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.285+6137C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117595867 | |||||||
| chr6:117596056 | A | T | 1 | a0001c0001t0002g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+5948T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117596056 | |||||||
| chr6:117596060 | A | AT | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(10): Show |
26 | HG00280.hp2 HG00544.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.285+5943dupA | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117596060 | |||||||
| chr6:117596111 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0147 a0001c0001t0019g0157 |
6 | HG02109.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5893A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117596111 | |||||||
| chr6:117596288 | G | A | 1 | a0001c0001t0004g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.285+5716C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117596288 | |||||||
| chr6:117596463 | G | C | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+5541C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117596463 | |||||||
| chr6:117596473 | A | G | 11 | a0001c0001t0005g0026 a0001c0001t0005g0208 a0001c0001t0005g0209 others(8): Show |
13 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.285+5531T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117596473 | |||||||
| chr6:117596484 | G | C | 2 | a0001c0001t0002g0139 a0001c0003t0002g0038 |
3 | HG00140.hp2 HG01515.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.285+5520C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117596484 | |||||||
| chr6:117596635 | T | C | 3 | a0001c0001t0005g0026 a0001c0001t0005g0221 a0001c0001t0005g0222 |
5 | HG02622.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5369A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117596635 | |||||||
| chr6:117596921 | A | T | 4 | a0001c0001t0002g0019 a0001c0001t0002g0216 a0001c0001t0002g0217 others(1): Show |
7 | HG01243.hp1 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+5083T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117596921 | |||||||
| chr6:117597024 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.285+4980C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117597024 | |||||||
| chr6:117597057 | T | G | 1 | a0001c0001t0006g0151 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.285+4947A>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117597057 | |||||||
| chr6:117597077 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.285+4927T>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117597077 | |||||||
| chr6:117597080 | T | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | NA18981.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.285+4924A>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117597080 | |||||||
| chr6:117597510 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.285+4494C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117597510 | |||||||
| chr6:117597653 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG02723.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.285+4351C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117597653 | |||||||
| chr6:117597801 | A | T | 1 | a0001c0001t0002g0108 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.285+4203T>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117597801 | |||||||
| chr6:117597861 | C | T | 1 | a0001c0001t0004g0029 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.285+4143G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117597861 | |||||||
| chr6:117598196 | T | TA | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0048 others(18): Show |
34 | HG00280.hp2 HG00544.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.285+3807dupT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117598196 | |||||||
| chr6:117598196 | T | TAA | 46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(43): Show |
103 | HG00423.hp1 HG00597.hp2 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.285+3806_285+3807d others(4): Show |
GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117598196 | |||||||
| chr6:117598196 | TA | T | 20 | a0001c0001t0003g0004 a0001c0001t0003g0012 a0001c0001t0003g0013 others(17): Show |
35 | HG00099.hp1 HG00597.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.285+3807delT | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117598196 | |||||||
| chr6:117598211 | AT | A | 5 | a0001c0001t0002g0039 a0001c0001t0002g0145 a0001c0001t0002g0218 others(2): Show |
6 | HG00323.hp1 HG02155.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+3792delA | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117598211 | |||||||
| chr6:117598212 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.285+3792A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117598212 | |||||||
| chr6:117598320 | C | T | 9 | a0001c0001t0006g0040 a0001c0001t0006g0041 a0001c0001t0006g0148 others(6): Show |
11 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+3684G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117598320 | |||||||
| chr6:117598365 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.285+3639G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117598365 | |||||||
| chr6:117598540 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(64): Show |
137 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.285+3464C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117598540 | |||||||
| chr6:117599081 | T | A | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.285+2923A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117599081 | |||||||
| chr6:117599487 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0203 |
3 | HG02630.hp2 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.285+2517A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117599487 | |||||||
| chr6:117599618 | C | T | 2 | a0001c0001t0002g0018 a0001c0001t0002g0147 |
5 | HG02717.hp1 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+2386G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117599618 | |||||||
| chr6:117599847 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(136): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.285+2157C>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117599847 | |||||||
| chr6:117599942 | T | C | 1 | a0001c0001t0004g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.285+2062A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117599942 | |||||||
| chr6:117600123 | C | T | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | NA18945.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.285+1881G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117600123 | |||||||
| chr6:117600219 | T | C | 1 | a0001c0001t0004g0104 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.285+1785A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117600219 | |||||||
| chr6:117600267 | C | T | 1 | a0001c0001t0003g0005 | 6 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+1737G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117600267 | |||||||
| chr6:117600387 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.285+1617C>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117600387 | |||||||
| chr6:117600388 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.285+1616G>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117600388 | |||||||
| chr6:117600440 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.285+1564G>A | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117600440 | |||||||
| chr6:117600723 | T | A | 1 | a0001c0001t0003g0022 | 3 | HG02055.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+1281A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117600723 | |||||||
| chr6:117601120 | G | A | 1 | a0001c0001t0006g0220 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.285+884C>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117601120 | |||||||
| chr6:117601138 | T | C | 3 | a0001c0001t0005g0026 a0001c0001t0005g0221 a0001c0001t0005g0222 |
5 | HG02622.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+866A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117601138 | |||||||
| chr6:117601174 | A | G | 17 | a0001c0001t0003g0004 a0001c0001t0003g0012 a0001c0001t0003g0013 others(14): Show |
31 | HG00099.hp1 HG00597.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.285+830T>C | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117601174 | |||||||
| chr6:117601204 | T | A | 51 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(48): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.285+800A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117601204 | |||||||
| chr6:117601398 | T | A | 1 | a0001c0001t0002g0223 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.285+606A>T | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117601398 | |||||||
| chr6:117601418 | A | C | 51 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(48): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.285+586T>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117601418 | |||||||
| chr6:117601965 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.285+39A>G | GOPC | ENSG00000047932.14 | transcript | ENST00000368498.7 | protein_coding | 1/8 | chr6 | 117601965 |