Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5601 |
|---|---|
| ensemblid | ENSG00000050748.18 |
| hgncid | 6886 |
| symbol | MAPK9 |
| name | mitogen-activated protein kinase 9 |
| refseq_nuc | NM_002752.5 |
| refseq_prot | NP_002743.3 |
| ensembl_nuc | ENST00000452135.7 |
| ensembl_prot | ENSP00000394560.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 180233143 |
| end | 180292083 |
| strand | - |
| ver | v1.2 |
| region | chr5:180233143-180292083 |
| region5000 | chr5:180228143-180297083 |
| regionname0 | MAPK9_chr5_180233143_180292083 |
| regionname5000 | MAPK9_chr5_180228143_180297083 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 424 | 371 | 90 | 68 | 151 | 16 | 44 | 109 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0002 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1275 | 369 | 88 | 68 | 151 | 16 | 44 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| c0002 | 0/0 | 1275 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| c0003 | 0/0 | 1275 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3522 | 109 | 18 | 13 | 66 | 5 | 7 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0002 | 1/0 | 3525 | 38 | 6 | 3 | 19 | 2 | 7 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0003 | 0/0 | 3525 | 30 | 5 | 11 | 8 | 3 | 3 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0004 | 0/0 | 3519 | 24 | 1 | 10 | 9 | 0 | 4 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0005 | 0/0 | 3519 | 21 | 1 | 0 | 20 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0006 | 0/0 | 3528 | 18 | 9 | 2 | 7 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0007 | 0/0 | 3522 | 18 | 0 | 1 | 13 | 1 | 3 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0008 | 0/0 | 3525 | 17 | 2 | 9 | 0 | 3 | 3 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0009 | 0/0 | 3522 | 13 | 2 | 9 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0010 | 0/0 | 3525 | 6 | 0 | 1 | 0 | 1 | 4 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0011 | 0/0 | 3522 | 5 | 2 | 1 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0012 | 0/0 | 3522 | 5 | 5 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0013 | 0/1 | 3522 | 5 | 1 | 0 | 1 | 1 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0014 | 0/0 | 3519 | 5 | 5 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0015 | 0/0 | 3528 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0016 | 0/0 | 3525 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0017 | 0/0 | 3522 | 4 | 1 | 1 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0018 | 0/0 | 3522 | 4 | 0 | 3 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0019 | 0/0 | 3522 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0020 | 0/0 | 3522 | 4 | 1 | 0 | 1 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0021 | 0/0 | 3522 | 3 | 2 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0022 | 0/0 | 3522 | 3 | 3 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0023 | 0/0 | 3525 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0024 | 0/0 | 3522 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0025 | 0/0 | 3522 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0026 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0027 | 0/0 | 3519 | 2 | 1 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0028 | 0/0 | 3528 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0029 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0030 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0031 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0032 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0033 | 0/0 | 3525 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0034 | 0/0 | 3522 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0035 | 0/0 | 3522 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0036 | 0/0 | 3522 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0037 | 0/0 | 3522 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0038 | 0/0 | 3522 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0039 | 0/0 | 3522 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0040 | 0/0 | 3522 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0041 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0042 | 0/0 | 3522 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0043 | 0/0 | 3522 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0044 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| t0045 | 0/0 | 3522 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1275 | 369 | 88 | 68 | 151 | 16 | 44 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0002 | 0/0 | 1275 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0002c0003 | 0/0 | 1275 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4796 | 109 | 18 | 13 | 66 | 5 | 7 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0002 | 1/0 | 4799 | 38 | 6 | 3 | 19 | 2 | 7 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0003 | 0/0 | 4799 | 29 | 5 | 11 | 7 | 3 | 3 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0004 | 0/0 | 4793 | 24 | 1 | 10 | 9 | 0 | 4 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0005 | 0/0 | 4793 | 21 | 1 | 0 | 20 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0006 | 0/0 | 4802 | 18 | 9 | 2 | 7 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0007 | 0/0 | 4796 | 18 | 0 | 1 | 13 | 1 | 3 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0008 | 0/0 | 4799 | 17 | 2 | 9 | 0 | 3 | 3 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0009 | 0/0 | 4796 | 13 | 2 | 9 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0010 | 0/0 | 4799 | 6 | 0 | 1 | 0 | 1 | 4 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0011 | 0/0 | 4796 | 5 | 2 | 1 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0012 | 0/0 | 4796 | 3 | 3 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0013 | 0/1 | 4796 | 5 | 1 | 0 | 1 | 1 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0014 | 0/0 | 4793 | 5 | 5 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0015 | 0/0 | 4802 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0016 | 0/0 | 4799 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0017 | 0/0 | 4796 | 4 | 1 | 1 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0018 | 0/0 | 4796 | 4 | 0 | 3 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0019 | 0/0 | 4796 | 4 | 4 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0020 | 0/0 | 4796 | 4 | 1 | 0 | 1 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0021 | 0/0 | 4796 | 3 | 2 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0022 | 0/0 | 4796 | 3 | 3 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0023 | 0/0 | 4799 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0024 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0025 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0026 | 0/0 | 4793 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0027 | 0/0 | 4793 | 2 | 1 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0028 | 0/0 | 4802 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0029 | 0/0 | 4799 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0030 | 0/0 | 4799 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0031 | 0/0 | 4799 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0032 | 0/0 | 4799 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0033 | 0/0 | 4799 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0034 | 0/0 | 4796 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0035 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0036 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0037 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0038 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0039 | 0/0 | 4796 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0040 | 0/0 | 4796 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0041 | 0/0 | 4793 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0042 | 0/0 | 4796 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0043 | 0/0 | 4796 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0044 | 0/0 | 4799 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0001t0045 | 0/0 | 4796 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0001c0002t0012 | 0/0 | 4796 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| a0002c0003t0003 | 0/0 | 4799 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | copy fasta | chr5 | 180228143 | 180297083 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0009g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0010g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0011g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0012g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0012g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0249 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0013g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0014g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0015g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0015g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0015g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0016g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0016g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0016g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0017g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0017g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0017g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0018g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0018g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0018g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0018g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0019g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0019g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0019g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0019g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0020g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0020g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0020g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0020g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0021g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0021g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0021g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0022g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0022g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0022g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0023g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0023g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0024g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0024g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0025g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0025g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0026g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0026g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0027g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0027g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0028g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0029g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0030g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0031g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0032g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0033g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0034g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0035g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0036g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0037g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0038g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0039g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0040g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0041g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0042g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0043g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0044g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0001t0045g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0002t0012g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0001c0002t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| a0002c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0049 | EUR | GBR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0136 | EUR | GBR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0089 | EUR | FIN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0332 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0309 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0295 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00621 | hp2 | a0001 | c0001 | t0035 | g0146 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0331 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0044 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0329 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00733 | hp2 | a0001 | c0001 | t0008 | g0008 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0073 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0004 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01099 | hp1 | a0001 | c0001 | t0018 | g0125 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0333 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0008 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0335 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0074 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0236 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01192 | hp1 | a0001 | c0001 | t0011 | g0195 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01243 | hp1 | a0001 | c0001 | t0017 | g0156 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0026 | AMR | PUR | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0330 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01256 | hp1 | a0001 | c0001 | t0034 | g0238 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0098 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0015 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01261 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0334 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01358 | hp1 | a0001 | c0001 | t0008 | g0052 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01358 | hp2 | a0001 | c0001 | t0009 | g0233 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0072 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0015 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0076 | AMR | CLM | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0094 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0078 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0080 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0079 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0085 | EUR | IBS | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0022 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0348 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01928 | hp2 | a0001 | c0001 | t0018 | g0126 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0318 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01934 | hp2 | a0001 | c0001 | t0033 | g0058 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01952 | hp2 | a0001 | c0001 | t0039 | g0247 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0336 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01978 | hp2 | a0001 | c0001 | t0009 | g0271 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01993 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02004 | hp2 | a0001 | c0001 | t0018 | g0215 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0020 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02055 | hp2 | a0001 | c0001 | t0028 | g0025 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0293 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0328 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02080 | hp1 | a0001 | c0001 | t0041 | g0307 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0208 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02145 | hp2 | a0001 | c0001 | t0045 | g0349 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02148 | hp1 | a0001 | c0001 | t0009 | g0239 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02155 | hp2 | a0001 | c0001 | t0007 | g0133 | EAS | CDX | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02165 | hp1 | a0001 | c0001 | t0030 | g0065 | EAS | CDX | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0083 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02258 | hp1 | a0001 | c0001 | t0032 | g0112 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02258 | hp2 | a0001 | c0001 | t0024 | g0266 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02280 | hp1 | a0001 | c0001 | t0025 | g0213 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0121 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02300 | hp1 | a0001 | c0001 | t0040 | g0210 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0004 | AMR | PEL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0312 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | KHV | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02572 | hp1 | a0001 | c0001 | t0020 | g0206 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02602 | hp2 | a0001 | c0001 | t0009 | g0237 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0023 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0021 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02622 | hp2 | a0001 | c0001 | t0022 | g0347 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02630 | hp2 | a0001 | c0002 | t0012 | g0250 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02647 | hp1 | a0001 | c0001 | t0026 | g0296 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02683 | hp1 | a0001 | c0001 | t0027 | g0339 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02683 | hp2 | a0001 | c0001 | t0009 | g0234 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02698 | hp1 | a0001 | c0001 | t0010 | g0101 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0071 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02717 | hp2 | a0001 | c0001 | t0019 | g0219 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0222 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02895 | hp1 | a0001 | c0001 | t0016 | g0042 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0245 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0246 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02922 | hp1 | a0001 | c0001 | t0016 | g0006 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02922 | hp2 | a0001 | c0001 | t0019 | g0217 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02965 | hp1 | a0001 | c0001 | t0023 | g0124 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0316 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0155 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0314 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03139 | hp1 | a0001 | c0001 | t0019 | g0216 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0019 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03195 | hp1 | a0001 | c0001 | t0013 | g0252 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03225 | hp1 | a0001 | c0001 | t0024 | g0265 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03239 | hp1 | a0001 | c0001 | t0013 | g0131 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0272 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03490 | hp1 | a0001 | c0001 | t0021 | g0258 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03490 | hp2 | a0001 | c0001 | t0017 | g0012 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0059 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03491 | hp2 | a0001 | c0001 | t0010 | g0010 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03492 | hp1 | a0001 | c0001 | t0017 | g0012 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03492 | hp2 | a0001 | c0001 | t0010 | g0010 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0218 | AFR | ESN | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0220 | AFR | GWD | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03579 | hp1 | a0001 | c0001 | t0023 | g0123 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0313 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0338 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0324 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03688 | hp2 | a0001 | c0001 | t0007 | g0221 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0317 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03710 | hp1 | a0001 | c0001 | t0042 | g0343 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03710 | hp2 | a0001 | c0001 | t0011 | g0196 | SAS | PJL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03927 | hp2 | a0001 | c0001 | t0008 | g0043 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03942 | hp1 | a0001 | c0001 | t0020 | g0230 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0104 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0323 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04184 | hp1 | a0001 | c0001 | t0020 | g0231 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04204 | hp2 | a0001 | c0001 | t0036 | g0139 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04228 | hp1 | a0001 | c0001 | t0011 | g0197 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0315 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18906 | hp2 | a0001 | c0001 | t0022 | g0346 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18944 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18949 | hp1 | a0001 | c0001 | t0043 | g0344 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18951 | hp1 | a0002 | c0003 | t0003 | g0109 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18951 | hp2 | a0001 | c0001 | t0037 | g0285 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18964 | hp1 | a0001 | c0001 | t0020 | g0232 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0341 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18977 | hp1 | a0001 | c0001 | t0018 | g0214 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18982 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0305 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18991 | hp2 | a0001 | c0001 | t0013 | g0270 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18992 | hp1 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0310 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | g0134 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0226 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0311 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19030 | hp1 | a0001 | c0001 | t0044 | g0345 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19030 | hp2 | a0001 | c0001 | t0031 | g0119 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19043 | hp2 | a0001 | c0001 | t0021 | g0268 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19057 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0342 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19078 | hp1 | a0001 | c0001 | t0007 | g0223 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19084 | hp2 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19086 | hp2 | a0001 | c0001 | t0038 | g0138 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19087 | hp1 | a0001 | c0001 | t0007 | g0228 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA19240 | hp2 | a0001 | c0002 | t0012 | g0251 | AFR | YRI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20129 | hp1 | a0001 | c0001 | t0026 | g0298 | AFR | ASW | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ASW | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0100 | EUR | TSI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | TSI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20805 | hp1 | a0001 | c0001 | t0013 | g0248 | EUR | TSI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | TSI | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | GIH | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | GIH | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0235 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02109 | hp2 | a0001 | c0001 | t0016 | g0006 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02486 | hp1 | a0001 | c0001 | t0027 | g0340 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0057 | AFR | ACB | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03471 | hp1 | a0001 | c0001 | t0025 | g0289 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | MSL | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | USA | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| HG06807 | hp2 | a0001 | c0001 | t0021 | g0267 | AFR | USA | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18955 | hp1 | a0001 | c0001 | t0029 | g0068 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0337 | AFR | USA | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0194 | AFR | USA | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0240 | AFR | LWK | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0013 | g0249 | REF | REF | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0045 | REF | REF | MAPK9_chr5_180228143_180297083 | MAPK9 | chr5 | 180228143 | 180297083 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180280528
|
T | C | 1 | a0002 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.34A>G | p.Ser12Gly | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/12 | 317/4799 | 34/1275 | 12/424 | chr5 | 180280528 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180280499
|
A | C | 1 | a0001c0002 | 2 | HG02630.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.63T>G | p.Thr21Thr | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/12 | 346/4799 | 63/1275 | 21/424 | chr5 | 180280499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180233336
|
T | A | 1 | a0001c0001t0029 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3048A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 3048 | chr5 | 180233336 | |||||
| chr5:180233703
|
T | A | 1 | a0001c0001t0037 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2681A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2681 | chr5 | 180233703 | |||||
| chr5:180233774
|
C | T | 5 | a0001c0001t0006a0001c0001t0016a0001c0001t0028others(2): Show | 25 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2610G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2610 | chr5 | 180233774 | |||||
| chr5:180233784
|
G | A | 1 | a0001c0001t0026 | 2 | HG02647.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2600C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2600 | chr5 | 180233784 | |||||
| chr5:180233786
|
T | A | 22 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(19): Show | 105 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2598A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2598 | chr5 | 180233786 | |||||
| chr5:180234265
|
C | G | 1 | a0001c0001t0036 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2119G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2119 | chr5 | 180234265 | |||||
| chr5:180234282
|
C | T | 1 | a0001c0001t0030 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2102G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2102 | chr5 | 180234282 | |||||
| chr5:180234342
|
G | A | 1 | a0001c0001t0045 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2042C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 2042 | chr5 | 180234342 | |||||
| chr5:180234388
|
T | C | 1 | a0001c0001t0026 | 2 | HG02647.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1996A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1996 | chr5 | 180234388 | |||||
| chr5:180234434
|
G | A | 1 | a0001c0001t0033 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1950C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1950 | chr5 | 180234434 | |||||
| chr5:180234528
|
C | T | 12 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(9): Show | 66 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1856G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1856 | chr5 | 180234528 | |||||
| chr5:180234610
|
A | C | 7 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(4): Show | 47 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1774T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1774 | chr5 | 180234610 | |||||
| chr5:180234616
|
G | A | 1 | a0001c0001t0034 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1768C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1768 | chr5 | 180234616 | |||||
| chr5:180234686
|
T | C | 1 | a0001c0001t0018 | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1698A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1698 | chr5 | 180234686 | |||||
| chr5:180234692
|
C | T | 12 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(9): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1692G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1692 | chr5 | 180234692 | |||||
| chr5:180234944
|
A | G | 1 | a0001c0001t0018 | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1440T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1440 | chr5 | 180234944 | |||||
| chr5:180235025
|
C | T | 3 | a0001c0001t0011a0001c0001t0023a0001c0001t0045 | 8 | HG01192.hp1 HG02145.hp2 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1359G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1359 | chr5 | 180235025 | |||||
| chr5:180235038
|
C | G | 1 | a0001c0001t0028 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1346 | chr5 | 180235038 | |||||
| chr5:180235057
|
T | C | 1 | a0001c0001t0007 | 18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1327A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1327 | chr5 | 180235057 | |||||
| chr5:180235172
|
G | A | 1 | a0001c0001t0019 | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1212C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1212 | chr5 | 180235172 | |||||
| chr5:180235358
|
G | A | 1 | a0001c0001t0040 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1026C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1026 | chr5 | 180235358 | |||||
| chr5:180235384
|
A | G | 28 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(25): Show | 148 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1000T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 1000 | chr5 | 180235384 | |||||
| chr5:180235579
|
A | G | 2 | a0001c0001t0031a0001c0001t0039 | 2 | HG01952.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*805T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 805 | chr5 | 180235579 | |||||
| chr5:180235722
|
C | A | 11 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(8): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*662G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 662 | chr5 | 180235722 | |||||
| chr5:180235870
|
A | G | 1 | a0001c0001t0024 | 2 | HG02258.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*514T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 514 | chr5 | 180235870 | |||||
| chr5:180236148
|
A | G | 1 | a0001c0001t0038 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 236 | chr5 | 180236148 | |||||
| chr5:180236180
|
C | T | 1 | a0001c0001t0017 | 4 | HG01243.hp1 HG03130.hp1 HG03490.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 204 | chr5 | 180236180 | |||||
| chr5:180236251
|
G | A | 23 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(20): Show | 122 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*133C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 12/12 | 133 | chr5 | 180236251 | |||||
| chr5:180280585
|
G | A | 1 | a0001c0001t0041 | 1 | HG02080.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/12 | chr5 | 180280585 | ||||||
| chr5:180291970
|
C | CCCG | 3 | a0001c0001t0006a0001c0001t0015a0001c0001t0028 | 23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-173_-171dupCGG | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | 11410 | chr5 | 180291970 | |||||
| chr5:180291970
|
CCCG | C | 25 | a0001c0001t0001a0001c0001t0007a0001c0001t0009others(22): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
5_prime_UTR_variant | MODIFIER | c.-173_-171delCGG | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | 11410 | chr5 | 180291970 | |||||
| chr5:180291970
|
CCCGCCG | C | 6 | a0001c0001t0004a0001c0001t0005a0001c0001t0014others(3): Show | 55 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-176_-171delCGGCGG | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | 11410 | chr5 | 180291970 | |||||
| chr5:180292000
|
G | A | 1 | a0001c0001t0042 | 1 | HG03710.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-200C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | chr5 | 180292000 | ||||||
| chr5:180292003
|
G | A | 1 | a0001c0001t0043 | 1 | NA18949.hp1 | 5_prime_UTR_variant | MODIFIER | c.-203C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | 11442 | chr5 | 180292003 | |||||
| chr5:180292057
|
C | A | 3 | a0001c0001t0022a0001c0001t0044a0001c0001t0045 | 5 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-257G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/12 | chr5 | 180292057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180236614
|
C | T | 116 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(113): Show | 122 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.1133-88G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180236614 | ||||||
| chr5:180236660
|
A | C | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1133-134T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180236660 | ||||||
| chr5:180236967
|
A | T | 8 | a0001c0001t0006g0032a0001c0001t0006g0033a0001c0001t0006g0034others(5): Show | 8 | HG02071.hp1 NA18949.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.1133-441T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180236967 | ||||||
| chr5:180236999
|
A | T | 18 | a0001c0001t0009g0004a0001c0001t0009g0015a0001c0001t0009g0233others(15): Show | 22 | HG00639.hp2 HG01074.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1133-473T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180236999 | ||||||
| chr5:180237550
|
C | T | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132+782G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237550 | ||||||
| chr5:180237693
|
A | G | 1 | a0001c0001t0005g0309 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1132+639T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237693 | ||||||
| chr5:180237814
|
T | G | 29 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(26): Show | 30 | HG00099.hp2 HG01192.hp1 HG01975.hp2 others(27): Show |
intron_variant | MODIFIER | c.1132+518A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237814 | ||||||
| chr5:180237909
|
C | T | 5 | a0001c0001t0011g0194a0001c0001t0011g0195a0001c0001t0011g0196others(2): Show | 5 | HG01192.hp1 HG02145.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132+423G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237909 | ||||||
| chr5:180237942
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1132+390C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237942 | ||||||
| chr5:180237966
|
G | A | 1 | a0001c0001t0008g0073 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1132+366C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180237966 | ||||||
| chr5:180238019
|
C | T | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132+313G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238019 | ||||||
| chr5:180238047
|
A | G | 138 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(135): Show | 148 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.1132+285T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238047 | ||||||
| chr5:180238131
|
A | G | 8 | a0001c0001t0011g0194a0001c0001t0011g0195a0001c0001t0011g0196others(5): Show | 8 | HG01192.hp1 HG02145.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1132+201T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238131 | ||||||
| chr5:180238183
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1132+149A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238183 | ||||||
| chr5:180238201
|
C | T | 165 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(162): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1132+131G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238201 | ||||||
| chr5:180238224
|
C | T | 16 | a0001c0001t0009g0004a0001c0001t0009g0015a0001c0001t0009g0233others(13): Show | 20 | HG00639.hp2 HG01074.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1132+108G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238224 | ||||||
| chr5:180238225
|
G | A | 5 | a0001c0001t0011g0194a0001c0001t0011g0195a0001c0001t0011g0196others(2): Show | 5 | HG01192.hp1 HG02145.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132+107C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238225 | ||||||
| chr5:180238226
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0075 | 2 | HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1132+106G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238226 | ||||||
| chr5:180238230
|
G | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132+102C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 11/11 | chr5 | 180238230 | ||||||
| chr5:180238572
|
A | G | 319 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(316): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1061-169T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238572 | ||||||
| chr5:180238596
|
TTTC | T | 41 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(38): Show | 42 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1061-196_1061-194d others(5): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238596 | ||||||
| chr5:180238605
|
CTTCT | C | 20 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(17): Show | 22 | HG01243.hp2 HG02055.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1061-206_1061-203d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238605 | ||||||
| chr5:180238608
|
C | CT | 50 | a0001c0001t0001g0127a0001c0001t0001g0159a0001c0001t0001g0183others(47): Show | 56 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1061-206dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238608 | ||||||
| chr5:180238608
|
CT | C | 21 | a0001c0001t0003g0110a0001c0001t0007g0011a0001c0001t0007g0132others(18): Show | 22 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.1061-206delA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238608 | ||||||
| chr5:180238611
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0186a0001c0001t0001g0188 | 3 | HG01175.hp1 HG01993.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1061-208A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238611 | ||||||
| chr5:180238687
|
A | C | 138 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(135): Show | 148 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.1061-284T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238687 | ||||||
| chr5:180238836
|
T | C | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1061-433A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180238836 | ||||||
| chr5:180239177
|
T | C | 1 | a0001c0001t0004g0319 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1060+747A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239177 | ||||||
| chr5:180239262
|
C | T | 2 | a0001c0001t0012g0245a0001c0001t0012g0246 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1060+662G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239262 | ||||||
| chr5:180239446
|
C | A | 3 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124 | 3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1060+478G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239446 | ||||||
| chr5:180239634
|
A | G | 2 | a0001c0002t0012g0250a0001c0002t0012g0251 | 2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1060+290T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239634 | ||||||
| chr5:180239641
|
T | G | 2 | a0001c0002t0012g0250a0001c0002t0012g0251 | 2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1060+283A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239641 | ||||||
| chr5:180239813
|
G | A | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1060+111C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239813 | ||||||
| chr5:180239827
|
C | T | 1 | a0001c0001t0010g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1060+97G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 10/11 | chr5 | 180239827 | ||||||
| chr5:180240000
|
T | C | 2 | a0001c0001t0031g0119a0001c0001t0039g0247 | 2 | HG01952.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.997-13A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240000 | ||||||
| chr5:180240101
|
T | C | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.997-114A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240101 | ||||||
| chr5:180240176
|
A | C | 1 | a0001c0001t0031g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.997-189T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240176 | ||||||
| chr5:180240231
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.997-244G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240231 | ||||||
| chr5:180240292
|
A | G | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.997-305T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240292 | ||||||
| chr5:180240327
|
G | A | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.997-340C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240327 | ||||||
| chr5:180240589
|
C | T | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.996+442G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240589 | ||||||
| chr5:180240708
|
T | G | 1 | a0001c0001t0004g0336 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.996+323A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240708 | ||||||
| chr5:180240733
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.996+298T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240733 | ||||||
| chr5:180240806
|
G | A | 53 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(50): Show | 56 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.996+225C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240806 | ||||||
| chr5:180240933
|
C | G | 80 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(77): Show | 87 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.996+98G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 9/11 | chr5 | 180240933 | ||||||
| chr5:180241304
|
A | ATT | 19 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(16): Show | 20 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.872-151_872-150dup others(2): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241304 | ||||||
| chr5:180241305
|
T | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0163a0001c0001t0001g0178others(7): Show | 10 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-150A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241305 | ||||||
| chr5:180241313
|
T | C | 1 | a0001c0001t0010g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.872-158A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241313 | ||||||
| chr5:180241327
|
C | T | 17 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(14): Show | 18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.872-172G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241327 | ||||||
| chr5:180241334
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.872-179A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241334 | ||||||
| chr5:180241344
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.872-189C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241344 | ||||||
| chr5:180241389
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.872-234G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241389 | ||||||
| chr5:180241391
|
G | A | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.872-236C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241391 | ||||||
| chr5:180241423
|
A | G | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.872-268T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241423 | ||||||
| chr5:180241494
|
T | A | 1 | a0001c0001t0021g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.872-339A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241494 | ||||||
| chr5:180241542
|
G | A | 2 | a0001c0001t0004g0317a0001c0001t0004g0318 | 2 | HG01934.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.872-387C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241542 | ||||||
| chr5:180241708
|
T | C | 138 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(135): Show | 148 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.872-553A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241708 | ||||||
| chr5:180241823
|
C | T | 2 | a0001c0001t0004g0323a0001c0001t0004g0324 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.872-668G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180241823 | ||||||
| chr5:180242066
|
C | T | 21 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(18): Show | 22 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.871+507G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180242066 | ||||||
| chr5:180242075
|
G | C | 9 | a0001c0001t0001g0153a0001c0001t0001g0185a0001c0001t0001g0186others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+498C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180242075 | ||||||
| chr5:180242330
|
A | G | 1 | a0001c0001t0005g0300 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.871+243T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180242330 | ||||||
| chr5:180242461
|
G | A | 2 | a0001c0001t0004g0323a0001c0001t0004g0324 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.871+112C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 8/11 | chr5 | 180242461 | ||||||
| chr5:180242798
|
T | C | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.689-43A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180242798 | ||||||
| chr5:180242833
|
T | G | 52 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(49): Show | 55 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.689-78A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180242833 | ||||||
| chr5:180242845
|
G | C | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.689-90C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180242845 | ||||||
| chr5:180242924
|
T | G | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.689-169A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180242924 | ||||||
| chr5:180243087
|
T | C | 9 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(6): Show | 9 | HG01952.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.689-332A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243087 | ||||||
| chr5:180243116
|
T | C | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-361A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243116 | ||||||
| chr5:180243119
|
T | G | 3 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0215 | 3 | HG01099.hp1 HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.689-364A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243119 | ||||||
| chr5:180243200
|
T | C | 1 | a0001c0001t0032g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.689-445A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243200 | ||||||
| chr5:180243271
|
T | C | 52 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(49): Show | 55 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.689-516A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243271 | ||||||
| chr5:180243516
|
A | G | 52 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(49): Show | 55 | HG00099.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.689-761T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243516 | ||||||
| chr5:180243528
|
C | T | 164 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(161): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.689-773G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243528 | ||||||
| chr5:180243531
|
G | A | 1 | a0001c0001t0007g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.689-776C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243531 | ||||||
| chr5:180243647
|
C | T | 2 | a0001c0001t0012g0245a0001c0001t0012g0246 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.689-892G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243647 | ||||||
| chr5:180243727
|
A | G | 1 | a0001c0001t0010g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.689-972T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243727 | ||||||
| chr5:180243761
|
C | T | 7 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.689-1006G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243761 | ||||||
| chr5:180243850
|
T | C | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.689-1095A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243850 | ||||||
| chr5:180243856
|
T | C | 23 | a0001c0001t0001g0003a0001c0001t0007g0011a0001c0001t0007g0132others(20): Show | 26 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.689-1101A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180243856 | ||||||
| chr5:180244045
|
C | T | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-1290G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244045 | ||||||
| chr5:180244069
|
G | A | 1 | a0001c0001t0006g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.689-1314C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244069 | ||||||
| chr5:180244212
|
C | T | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.689-1457G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244212 | ||||||
| chr5:180244231
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.689-1476A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244231 | ||||||
| chr5:180244379
|
T | C | 1 | a0001c0001t0031g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.689-1624A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244379 | ||||||
| chr5:180244443
|
C | T | 1 | a0001c0001t0008g0078 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.689-1688G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244443 | ||||||
| chr5:180244444
|
G | A | 1 | a0001c0001t0007g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.689-1689C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244444 | ||||||
| chr5:180244482
|
T | A | 10 | a0001c0001t0002g0082a0001c0001t0002g0086a0001c0001t0002g0088others(7): Show | 10 | HG02258.hp2 HG02630.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.689-1727A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244482 | ||||||
| chr5:180244591
|
C | T | 1 | a0001c0001t0013g0248 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.689-1836G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244591 | ||||||
| chr5:180244595
|
G | A | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.689-1840C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244595 | ||||||
| chr5:180244607
|
CT | C | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-1853delA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244607 | ||||||
| chr5:180244722
|
T | C | 345 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(342): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.689-1967A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244722 | ||||||
| chr5:180244766
|
T | A | 1 | a0001c0001t0002g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.689-2011A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244766 | ||||||
| chr5:180244778
|
GA | G | 109 | a0001c0001t0001g0159a0001c0001t0001g0182a0001c0001t0001g0203others(106): Show | 117 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.689-2024delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244778 | ||||||
| chr5:180244778
|
GAA | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(155): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.689-2025_689-2024d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244778 | ||||||
| chr5:180244953
|
C | T | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-2198G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244953 | ||||||
| chr5:180244954
|
G | A | 2 | a0001c0001t0012g0245a0001c0001t0012g0246 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.689-2199C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180244954 | ||||||
| chr5:180245108
|
G | A | 137 | a0001c0001t0002g0089a0001c0001t0004g0018a0001c0001t0004g0291others(134): Show | 147 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(144): Show |
intron_variant | MODIFIER | c.688+2331C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245108 | ||||||
| chr5:180245305
|
G | A | 1 | a0001c0001t0027g0339 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.688+2134C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245305 | ||||||
| chr5:180245440
|
T | C | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.688+1999A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245440 | ||||||
| chr5:180245583
|
C | T | 17 | a0001c0001t0002g0089a0001c0001t0009g0004a0001c0001t0009g0015others(14): Show | 21 | HG00280.hp2 HG00639.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.688+1856G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245583 | ||||||
| chr5:180245588
|
G | A | 1 | a0001c0001t0025g0289 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.688+1851C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245588 | ||||||
| chr5:180245825
|
T | C | 139 | a0001c0001t0002g0089a0001c0001t0004g0018a0001c0001t0004g0291others(136): Show | 149 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.688+1614A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245825 | ||||||
| chr5:180245831
|
G | A | 1 | a0001c0001t0010g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.688+1608C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245831 | ||||||
| chr5:180245885
|
A | G | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+1554T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245885 | ||||||
| chr5:180245960
|
G | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0321a0001c0001t0004g0327others(1): Show | 4 | HG01934.hp2 NA18961.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+1479C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245960 | ||||||
| chr5:180245984
|
C | T | 6 | a0001c0001t0002g0082a0001c0001t0002g0088a0001c0001t0002g0102others(3): Show | 6 | HG03490.hp1 HG03669.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+1455G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180245984 | ||||||
| chr5:180246104
|
G | A | 2 | a0001c0001t0005g0341a0001c0001t0005g0342 | 2 | NA18972.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.688+1335C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246104 | ||||||
| chr5:180246128
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.688+1311C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246128 | ||||||
| chr5:180246306
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.688+1133C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246306 | ||||||
| chr5:180246506
|
C | G | 4 | a0001c0001t0012g0245a0001c0001t0012g0246a0001c0002t0012g0250others(1): Show | 4 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.688+933G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246506 | ||||||
| chr5:180246708
|
T | C | 124 | a0001c0001t0002g0089a0001c0001t0004g0018a0001c0001t0004g0291others(121): Show | 134 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.688+731A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246708 | ||||||
| chr5:180246763
|
TG | T | 17 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(14): Show | 18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.688+675delC | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246763 | ||||||
| chr5:180246809
|
T | C | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.688+630A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246809 | ||||||
| chr5:180246830
|
A | C | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.688+609T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246830 | ||||||
| chr5:180246914
|
A | G | 23 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0043others(20): Show | 25 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.688+525T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246914 | ||||||
| chr5:180246955
|
T | C | 1 | a0001c0001t0003g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.688+484A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180246955 | ||||||
| chr5:180247067
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.688+372G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180247067 | ||||||
| chr5:180247326
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.688+113T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180247326 | ||||||
| chr5:180247357
|
G | A | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+82C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 7/11 | chr5 | 180247357 | ||||||
| chr5:180247668
|
T | C | 1 | a0001c0001t0028g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.617-158A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180247668 | ||||||
| chr5:180248011
|
G | A | 1 | a0001c0001t0011g0194 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.617-501C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248011 | ||||||
| chr5:180248052
|
C | A | 28 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(25): Show | 29 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.617-542G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248052 | ||||||
| chr5:180248178
|
C | T | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.617-668G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248178 | ||||||
| chr5:180248256
|
A | C | 9 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(6): Show | 9 | HG01952.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.616+717T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248256 | ||||||
| chr5:180248442
|
T | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0253a0001c0001t0001g0254 | 4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.616+531A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248442 | ||||||
| chr5:180248488
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.616+485A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248488 | ||||||
| chr5:180248594
|
T | C | 1 | a0001c0001t0011g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.616+379A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248594 | ||||||
| chr5:180248726
|
T | C | 1 | a0001c0001t0032g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.616+247A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 6/11 | chr5 | 180248726 | ||||||
| chr5:180249367
|
T | C | 1 | a0001c0001t0002g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.451-229A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249367 | ||||||
| chr5:180249386
|
G | A | 2 | a0001c0001t0004g0335a0001c0001t0004g0337 | 2 | HG01109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.451-248C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249386 | ||||||
| chr5:180249432
|
C | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0130a0001c0001t0001g0141others(2): Show | 6 | HG00408.hp2 HG02155.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-294G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249432 | ||||||
| chr5:180249432
|
C | T | 43 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(40): Show | 49 | HG00639.hp2 HG01074.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.451-294G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249432 | ||||||
| chr5:180249473
|
C | T | 1 | a0001c0001t0021g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-335G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249473 | ||||||
| chr5:180249518
|
G | GCTCT | 138 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(135): Show | 148 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(145): Show |
intron_variant | MODIFIER | c.451-381_451-380ins others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249518 | ||||||
| chr5:180249649
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.451-511A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249649 | ||||||
| chr5:180249651
|
T | C | 4 | a0001c0001t0001g0143a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG00140.hp2 HG01516.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-513A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249651 | ||||||
| chr5:180249661
|
C | T | 43 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(40): Show | 49 | HG00639.hp2 HG01074.hp2 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.451-523G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249661 | ||||||
| chr5:180249758
|
C | T | 17 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(14): Show | 18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.451-620G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249758 | ||||||
| chr5:180249760
|
A | G | 6 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(3): Show | 6 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-622T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249760 | ||||||
| chr5:180249798
|
C | T | 23 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0043others(20): Show | 25 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.451-660G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249798 | ||||||
| chr5:180249875
|
G | A | 2 | a0001c0001t0004g0291a0001c0001t0004g0327 | 2 | NA19084.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.451-737C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249875 | ||||||
| chr5:180249937
|
A | G | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-799T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249937 | ||||||
| chr5:180249979
|
C | T | 52 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(49): Show | 58 | HG00639.hp2 HG01074.hp2 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.451-841G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180249979 | ||||||
| chr5:180250029
|
C | T | 21 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(18): Show | 22 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.451-891G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250029 | ||||||
| chr5:180250037
|
C | T | 1 | a0001c0001t0005g0303 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.451-899G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250037 | ||||||
| chr5:180250051
|
G | A | 2 | a0001c0001t0007g0226a0001c0001t0007g0227 | 2 | NA18966.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.451-913C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250051 | ||||||
| chr5:180250082
|
C | T | 1 | a0001c0001t0021g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.451-944G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250082 | ||||||
| chr5:180250119
|
C | T | 4 | a0001c0001t0004g0334a0001c0001t0004g0335a0001c0001t0004g0337others(1): Show | 4 | HG01109.hp2 HG01346.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-981G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250119 | ||||||
| chr5:180250285
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.451-1147G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250285 | ||||||
| chr5:180250494
|
C | A | 1 | a0001c0001t0013g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.451-1356G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250494 | ||||||
| chr5:180250517
|
G | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 84 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.451-1379C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250517 | ||||||
| chr5:180250545
|
C | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(283): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.451-1407G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250545 | ||||||
| chr5:180250555
|
T | C | 32 | a0001c0001t0001g0148a0001c0001t0003g0040a0001c0001t0004g0018others(29): Show | 33 | HG00558.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.451-1417A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250555 | ||||||
| chr5:180250778
|
C | G | 24 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0043others(21): Show | 26 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.451-1640G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250778 | ||||||
| chr5:180250821
|
G | A | 1 | a0001c0001t0039g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.451-1683C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250821 | ||||||
| chr5:180250842
|
G | A | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-1704C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250842 | ||||||
| chr5:180250866
|
C | T | 1 | a0001c0001t0014g0313 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.451-1728G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250866 | ||||||
| chr5:180250940
|
T | G | 20 | a0001c0001t0008g0008a0001c0001t0008g0009a0001c0001t0008g0043others(17): Show | 22 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.451-1802A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250940 | ||||||
| chr5:180250985
|
C | CA | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-1848dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250985 | ||||||
| chr5:180250989
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.451-1851C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180250989 | ||||||
| chr5:180251089
|
A | C | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-1951T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251089 | ||||||
| chr5:180251113
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.451-1975C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251113 | ||||||
| chr5:180251127
|
A | G | 1 | a0001c0001t0044g0345 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451-1989T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251127 | ||||||
| chr5:180251290
|
G | A | 1 | a0001c0001t0040g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.451-2152C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251290 | ||||||
| chr5:180251310
|
C | T | 3 | a0001c0001t0012g0208a0001c0001t0032g0112a0001c0001t0039g0247 | 3 | HG01952.hp2 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.451-2172G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251310 | ||||||
| chr5:180251405
|
C | T | 23 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(20): Show | 25 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.451-2267G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251405 | ||||||
| chr5:180251573
|
C | T | 1 | a0001c0001t0012g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.451-2435G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251573 | ||||||
| chr5:180251602
|
C | T | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-2464G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251602 | ||||||
| chr5:180251603
|
G | A | 28 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(25): Show | 29 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.451-2465C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251603 | ||||||
| chr5:180251617
|
G | A | 17 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(14): Show | 18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.451-2479C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251617 | ||||||
| chr5:180251665
|
C | T | 1 | a0001c0001t0013g0270 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.451-2527G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251665 | ||||||
| chr5:180251732
|
A | AGTGACGC others(12): Show |
1 | a0001c0001t0008g0059 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.451-2595_451-2594i others(21): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251732 | ||||||
| chr5:180251732
|
A | AGTGACGC others(12): Show |
83 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(80): Show | 88 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.451-2613_451-2595d others(21): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251732 | ||||||
| chr5:180251811
|
C | T | 3 | a0001c0001t0014g0314a0001c0001t0014g0315a0001c0001t0025g0289 | 3 | HG03130.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.451-2673G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251811 | ||||||
| chr5:180251927
|
C | T | 2 | a0001c0001t0001g0148a0001c0001t0003g0040 | 2 | HG00558.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.451-2789G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180251927 | ||||||
| chr5:180252021
|
C | T | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.451-2883G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252021 | ||||||
| chr5:180252071
|
C | T | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-2933G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252071 | ||||||
| chr5:180252085
|
C | T | 1 | a0001c0001t0009g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451-2947G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252085 | ||||||
| chr5:180252144
|
C | T | 48 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(45): Show | 52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-3006G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252144 | ||||||
| chr5:180252183
|
A | G | 7 | a0001c0001t0012g0208a0001c0001t0018g0125a0001c0001t0018g0126others(4): Show | 7 | HG01099.hp1 HG01928.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.451-3045T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252183 | ||||||
| chr5:180252237
|
T | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0284 | 2 | HG03927.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.451-3099A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252237 | ||||||
| chr5:180252315
|
C | T | 1 | a0001c0001t0039g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.451-3177G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252315 | ||||||
| chr5:180252350
|
C | T | 48 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(45): Show | 52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-3212G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252350 | ||||||
| chr5:180252504
|
C | T | 48 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(45): Show | 52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-3366G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252504 | ||||||
| chr5:180252652
|
C | T | 1 | a0001c0001t0020g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.451-3514G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252652 | ||||||
| chr5:180252726
|
G | A | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-3588C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252726 | ||||||
| chr5:180252744
|
G | A | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-3606C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252744 | ||||||
| chr5:180252760
|
C | A | 125 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0127others(122): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.451-3622G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252760 | ||||||
| chr5:180252763
|
G | A | 4 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3625C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252763 | ||||||
| chr5:180252833
|
T | C | 3 | a0001c0001t0012g0208a0001c0001t0032g0112a0001c0001t0039g0247 | 3 | HG01952.hp2 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.451-3695A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252833 | ||||||
| chr5:180252848
|
C | T | 4 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-3710G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252848 | ||||||
| chr5:180252980
|
G | T | 28 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(25): Show | 29 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.451-3842C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180252980 | ||||||
| chr5:180253039
|
G | A | 3 | a0001c0001t0005g0297a0001c0001t0015g0019a0001c0001t0015g0020 | 3 | HG02055.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.451-3901C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253039 | ||||||
| chr5:180253076
|
T | C | 93 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(90): Show | 98 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.451-3938A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253076 | ||||||
| chr5:180253078
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.451-3940G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253078 | ||||||
| chr5:180253115
|
G | A | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.451-3977C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253115 | ||||||
| chr5:180253172
|
C | T | 93 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(90): Show | 98 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.451-4034G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253172 | ||||||
| chr5:180253228
|
G | A | 1 | a0001c0001t0009g0237 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.451-4090C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253228 | ||||||
| chr5:180253233
|
A | G | 304 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(301): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.451-4095T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253233 | ||||||
| chr5:180253310
|
C | T | 11 | a0001c0001t0002g0082a0001c0001t0002g0086a0001c0001t0002g0088others(8): Show | 11 | HG00280.hp2 HG02258.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.451-4172G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253310 | ||||||
| chr5:180253311
|
G | A | 18 | a0001c0001t0001g0275a0001c0001t0007g0011a0001c0001t0007g0132others(15): Show | 19 | HG00099.hp2 HG00642.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.451-4173C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253311 | ||||||
| chr5:180253343
|
G | A | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.451-4205C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253343 | ||||||
| chr5:180253361
|
G | A | 1 | a0001c0001t0041g0307 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.451-4223C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253361 | ||||||
| chr5:180253666
|
G | A | 1 | a0001c0001t0039g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.451-4528C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253666 | ||||||
| chr5:180253820
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.451-4682A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253820 | ||||||
| chr5:180253896
|
GAC | G | 167 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(164): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.451-4760_451-4759d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253896 | ||||||
| chr5:180253906
|
C | T | 48 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(45): Show | 52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-4768G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253906 | ||||||
| chr5:180253961
|
C | CT | 4 | a0001c0001t0011g0194a0001c0001t0011g0195a0001c0001t0011g0196others(1): Show | 4 | HG01192.hp1 HG03710.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-4824dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253961 | ||||||
| chr5:180253963
|
C | CT | 86 | a0001c0001t0002g0118a0001c0001t0002g0120a0001c0001t0004g0018others(83): Show | 91 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.451-4826dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | ||||||
| chr5:180253963
|
C | CTT | 27 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0181others(24): Show | 31 | HG00609.hp1 HG00639.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.451-4827_451-4826d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | ||||||
| chr5:180253963
|
C | CTTT | 150 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(147): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.451-4828_451-4826d others(5): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | ||||||
| chr5:180253963
|
C | CTTTT | 6 | a0001c0001t0001g0163a0001c0001t0001g0191a0001c0001t0001g0203others(3): Show | 6 | HG02148.hp2 HG03516.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.451-4829_451-4826d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | ||||||
| chr5:180253963
|
C | T | 4 | a0001c0001t0011g0194a0001c0001t0011g0195a0001c0001t0011g0196others(1): Show | 4 | HG01192.hp1 HG03710.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-4825G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180253963 | ||||||
| chr5:180254004
|
T | G | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-4866A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254004 | ||||||
| chr5:180254124
|
G | C | 1 | a0001c0001t0037g0285 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.451-4986C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254124 | ||||||
| chr5:180254216
|
C | T | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.451-5078G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254216 | ||||||
| chr5:180254351
|
G | A | 345 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(342): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.451-5213C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254351 | ||||||
| chr5:180254423
|
A | G | 1 | a0001c0001t0003g0110 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.451-5285T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254423 | ||||||
| chr5:180254497
|
G | A | 5 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-5359C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254497 | ||||||
| chr5:180254514
|
A | G | 48 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(45): Show | 52 | HG00733.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.451-5376T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254514 | ||||||
| chr5:180254801
|
G | A | 77 | a0001c0001t0002g0102a0001c0001t0004g0018a0001c0001t0004g0291others(74): Show | 82 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.451-5663C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254801 | ||||||
| chr5:180254890
|
T | G | 3 | a0001c0001t0012g0208a0001c0001t0032g0112a0001c0001t0039g0247 | 3 | HG01952.hp2 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.451-5752A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254890 | ||||||
| chr5:180254903
|
G | A | 5 | a0001c0001t0001g0184a0001c0001t0001g0204a0001c0001t0012g0208others(2): Show | 5 | HG01952.hp2 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-5765C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254903 | ||||||
| chr5:180254957
|
C | T | 1 | a0001c0001t0004g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.451-5819G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180254957 | ||||||
| chr5:180255063
|
C | T | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.451-5925G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255063 | ||||||
| chr5:180255174
|
C | T | 75 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(72): Show | 80 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.451-6036G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255174 | ||||||
| chr5:180255205
|
C | T | 1 | a0001c0001t0004g0328 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.451-6067G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255205 | ||||||
| chr5:180255266
|
G | A | 5 | a0001c0001t0003g0091a0001c0001t0011g0220a0001c0001t0023g0123others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-6128C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255266 | ||||||
| chr5:180255287
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0003g0091a0001c0001t0007g0011others(28): Show | 34 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.451-6149T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255287 | ||||||
| chr5:180255412
|
A | G | 304 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(301): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.450+6272T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255412 | ||||||
| chr5:180255444
|
C | T | 1 | a0001c0001t0008g0078 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.450+6240G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255444 | ||||||
| chr5:180255482
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0004g0018a0001c0001t0004g0291others(117): Show | 128 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.450+6202T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255482 | ||||||
| chr5:180255493
|
G | C | 75 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(72): Show | 80 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.450+6191C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255493 | ||||||
| chr5:180255508
|
C | T | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+6176G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255508 | ||||||
| chr5:180255599
|
G | T | 1 | a0001c0001t0004g0333 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.450+6085C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255599 | ||||||
| chr5:180255667
|
G | A | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+6017C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255667 | ||||||
| chr5:180255832
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0004g0018a0001c0001t0004g0291others(115): Show | 126 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.450+5852A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255832 | ||||||
| chr5:180255993
|
C | T | 5 | a0001c0001t0001g0169a0001c0001t0002g0062a0001c0001t0005g0292others(2): Show | 5 | HG00544.hp2 HG00609.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+5691G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180255993 | ||||||
| chr5:180256162
|
G | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+5522C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256162 | ||||||
| chr5:180256278
|
T | C | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+5406A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256278 | ||||||
| chr5:180256294
|
T | C | 1 | a0001c0001t0040g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.450+5390A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256294 | ||||||
| chr5:180256634
|
A | G | 345 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(342): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.450+5050T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256634 | ||||||
| chr5:180256673
|
G | A | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+5011C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256673 | ||||||
| chr5:180256717
|
G | A | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+4967C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256717 | ||||||
| chr5:180256868
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450+4816C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180256868 | ||||||
| chr5:180257148
|
C | T | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+4536G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257148 | ||||||
| chr5:180257233
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.450+4451G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257233 | ||||||
| chr5:180257248
|
C | G | 2 | a0001c0001t0024g0265a0001c0001t0024g0266 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.450+4436G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257248 | ||||||
| chr5:180257427
|
C | T | 83 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(80): Show | 88 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.450+4257G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257427 | ||||||
| chr5:180257433
|
C | T | 183 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(180): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.450+4251G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257433 | ||||||
| chr5:180257455
|
G | A | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+4229C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257455 | ||||||
| chr5:180257583
|
G | A | 1 | a0001c0001t0004g0326 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.450+4101C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257583 | ||||||
| chr5:180257627
|
T | A | 1 | a0001c0001t0005g0301 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.450+4057A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257627 | ||||||
| chr5:180257864
|
G | A | 1 | a0001c0001t0005g0301 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.450+3820C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257864 | ||||||
| chr5:180257868
|
A | T | 345 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(342): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.450+3816T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180257868 | ||||||
| chr5:180258139
|
T | A | 1 | a0001c0001t0002g0067 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.450+3545A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258139 | ||||||
| chr5:180258313
|
T | C | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+3371A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258313 | ||||||
| chr5:180258331
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.450+3353G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258331 | ||||||
| chr5:180258514
|
C | T | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+3170G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258514 | ||||||
| chr5:180258515
|
G | A | 1 | a0001c0001t0032g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.450+3169C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258515 | ||||||
| chr5:180258523
|
T | C | 2 | a0001c0001t0008g0043a0001c0001t0020g0230 | 2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.450+3161A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258523 | ||||||
| chr5:180258683
|
G | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0191a0001c0001t0001g0204 | 3 | NA18946.hp2 NA18965.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.450+3001C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258683 | ||||||
| chr5:180258697
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0003g0087 | 2 | HG02886.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.450+2987G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258697 | ||||||
| chr5:180258853
|
T | C | 345 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(342): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.450+2831A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258853 | ||||||
| chr5:180258862
|
T | TA | 101 | a0001c0001t0001g0003a0001c0001t0001g0128a0001c0001t0001g0129others(98): Show | 108 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.450+2821dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258862 | ||||||
| chr5:180258862
|
T | TAA | 13 | a0001c0001t0004g0330a0001c0001t0004g0331a0001c0001t0004g0333others(10): Show | 13 | HG00639.hp1 HG01106.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+2820_450+2821d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258862 | ||||||
| chr5:180258862
|
TA | T | 11 | a0001c0001t0001g0172a0001c0001t0001g0180a0001c0001t0001g0211others(8): Show | 11 | HG01256.hp2 HG02451.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.450+2821delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180258862 | ||||||
| chr5:180259033
|
CA | C | 115 | a0001c0001t0001g0003a0001c0001t0003g0095a0001c0001t0004g0018others(112): Show | 123 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.450+2650delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259033 | ||||||
| chr5:180259083
|
T | C | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+2601A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259083 | ||||||
| chr5:180259114
|
AACCCTTT others(77): Show |
A | 1 | a0001c0001t0006g0031 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.450+2486_450+2569d others(86): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259114 | ||||||
| chr5:180259138
|
G | C | 1 | a0001c0001t0028g0025 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.450+2546C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259138 | ||||||
| chr5:180259163
|
T | C | 1 | a0001c0001t0003g0122 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.450+2521A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259163 | ||||||
| chr5:180259168
|
G | C | 8 | a0001c0001t0003g0002a0001c0001t0003g0085a0001c0001t0003g0093others(5): Show | 10 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.450+2516C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259168 | ||||||
| chr5:180259251
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.450+2433A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259251 | ||||||
| chr5:180259264
|
G | A | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+2420C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259264 | ||||||
| chr5:180259266
|
A | T | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+2418T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259266 | ||||||
| chr5:180259335
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.450+2349G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259335 | ||||||
| chr5:180259352
|
T | G | 1 | a0001c0001t0003g0070 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.450+2332A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259352 | ||||||
| chr5:180259374
|
G | C | 2 | a0001c0001t0012g0245a0001c0001t0012g0246 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.450+2310C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259374 | ||||||
| chr5:180259378
|
G | A | 83 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(80): Show | 88 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.450+2306C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259378 | ||||||
| chr5:180259404
|
C | T | 3 | a0001c0001t0021g0267a0001c0001t0024g0265a0001c0001t0024g0266 | 3 | HG02258.hp2 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.450+2280G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259404 | ||||||
| chr5:180259525
|
C | T | 1 | a0001c0001t0015g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.450+2159G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259525 | ||||||
| chr5:180259560
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.450+2124G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259560 | ||||||
| chr5:180259779
|
A | G | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+1905T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259779 | ||||||
| chr5:180259796
|
C | A | 2 | a0001c0001t0001g0147a0001c0001t0035g0146 | 2 | HG00621.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.450+1888G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259796 | ||||||
| chr5:180259816
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.450+1868A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259816 | ||||||
| chr5:180259882
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.450+1802G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259882 | ||||||
| chr5:180259917
|
G | C | 1 | a0001c0001t0024g0266 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.450+1767C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259917 | ||||||
| chr5:180259983
|
G | A | 1 | a0001c0001t0009g0239 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.450+1701C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180259983 | ||||||
| chr5:180260013
|
T | C | 76 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(73): Show | 81 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.450+1671A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260013 | ||||||
| chr5:180260095
|
C | G | 17 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(14): Show | 18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.450+1589G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260095 | ||||||
| chr5:180260166
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.450+1518A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260166 | ||||||
| chr5:180260187
|
A | G | 2 | a0001c0001t0022g0346a0001c0001t0022g0348 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.450+1497T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260187 | ||||||
| chr5:180260223
|
G | A | 2 | a0001c0001t0012g0208a0001c0001t0032g0112 | 2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.450+1461C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260223 | ||||||
| chr5:180260247
|
G | C | 1 | a0001c0001t0007g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.450+1437C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260247 | ||||||
| chr5:180260257
|
A | G | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1427T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260257 | ||||||
| chr5:180260294
|
A | G | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1390T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260294 | ||||||
| chr5:180260564
|
G | A | 3 | a0001c0001t0005g0297a0001c0001t0015g0019a0001c0001t0015g0020 | 3 | HG02055.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.450+1120C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260564 | ||||||
| chr5:180260576
|
G | A | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+1108C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260576 | ||||||
| chr5:180260624
|
T | A | 1 | a0001c0001t0001g0286 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.450+1060A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260624 | ||||||
| chr5:180260685
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0004g0018a0001c0001t0004g0291others(110): Show | 121 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.450+999T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260685 | ||||||
| chr5:180260772
|
C | T | 182 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(179): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.450+912G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260772 | ||||||
| chr5:180260928
|
T | C | 1 | a0001c0001t0032g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.450+756A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260928 | ||||||
| chr5:180260943
|
GA | G | 115 | a0001c0001t0001g0003a0001c0001t0004g0018a0001c0001t0004g0291others(112): Show | 123 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.450+740delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180260943 | ||||||
| chr5:180261090
|
A | G | 2 | a0001c0001t0006g0029a0001c0001t0006g0039 | 2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.450+594T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261090 | ||||||
| chr5:180261140
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.450+544G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261140 | ||||||
| chr5:180261192
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.450+492G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261192 | ||||||
| chr5:180261316
|
C | A | 348 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(345): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.450+368G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261316 | ||||||
| chr5:180261356
|
T | C | 1 | a0001c0001t0010g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.450+328A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261356 | ||||||
| chr5:180261447
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.450+237G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261447 | ||||||
| chr5:180261478
|
C | T | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.450+206G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261478 | ||||||
| chr5:180261542
|
A | G | 3 | a0001c0001t0017g0012a0001c0001t0017g0155a0001c0001t0017g0156 | 4 | HG01243.hp1 HG03130.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+142T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261542 | ||||||
| chr5:180261556
|
C | T | 14 | a0001c0001t0009g0004a0001c0001t0009g0015a0001c0001t0009g0233others(11): Show | 17 | HG00639.hp2 HG01074.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.450+128G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261556 | ||||||
| chr5:180261559
|
T | C | 1 | a0001c0001t0039g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.450+125A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261559 | ||||||
| chr5:180261606
|
A | T | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.450+78T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 5/11 | chr5 | 180261606 | ||||||
| chr5:180261920
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.312-98C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180261920 | ||||||
| chr5:180262027
|
A | C | 13 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0329others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.312-205T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262027 | ||||||
| chr5:180262028
|
C | A | 1 | a0001c0001t0039g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.312-206G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262028 | ||||||
| chr5:180262144
|
A | G | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.312-322T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262144 | ||||||
| chr5:180262259
|
A | G | 2 | a0001c0001t0007g0226a0001c0001t0007g0227 | 2 | NA18966.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.312-437T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262259 | ||||||
| chr5:180262289
|
A | G | 21 | a0001c0001t0003g0002a0001c0001t0003g0048a0001c0001t0003g0049others(18): Show | 23 | HG00099.hp1 HG00423.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.312-467T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262289 | ||||||
| chr5:180262308
|
C | A | 1 | a0001c0001t0004g0329 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.312-486G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262308 | ||||||
| chr5:180262386
|
GA | G | 181 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(178): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.312-565delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262386 | ||||||
| chr5:180262521
|
G | A | 21 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0046others(18): Show | 25 | HG00544.hp1 HG00621.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.312-699C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262521 | ||||||
| chr5:180262570
|
T | TA | 120 | a0001c0001t0001g0003a0001c0001t0001g0243a0001c0001t0002g0082others(117): Show | 129 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.312-749dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262570 | ||||||
| chr5:180262627
|
G | C | 4 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(1): Show | 4 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.312-805C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262627 | ||||||
| chr5:180262662
|
C | A | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.312-840G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262662 | ||||||
| chr5:180262764
|
T | C | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.312-942A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262764 | ||||||
| chr5:180262866
|
C | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-1044G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262866 | ||||||
| chr5:180262867
|
G | A | 8 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(5): Show | 8 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.312-1045C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262867 | ||||||
| chr5:180262898
|
G | C | 23 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(20): Show | 25 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.312-1076C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180262898 | ||||||
| chr5:180263025
|
G | C | 1 | a0001c0001t0003g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.312-1203C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263025 | ||||||
| chr5:180263354
|
C | T | 59 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0329others(56): Show | 63 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.311+1427G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263354 | ||||||
| chr5:180263401
|
C | T | 59 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0329others(56): Show | 63 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.311+1380G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263401 | ||||||
| chr5:180263653
|
T | C | 1 | a0001c0001t0039g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.311+1128A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263653 | ||||||
| chr5:180263706
|
C | CT | 155 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0128others(152): Show | 166 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.311+1074dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263706 | ||||||
| chr5:180263706
|
C | CTT | 137 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0127others(134): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.311+1073_311+1074d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263706 | ||||||
| chr5:180263706
|
C | CTTT | 20 | a0001c0001t0001g0003a0001c0001t0001g0263a0001c0001t0001g0276others(17): Show | 23 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.311+1072_311+1074d others(5): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263706 | ||||||
| chr5:180263749
|
T | C | 3 | a0001c0001t0006g0026a0001c0001t0006g0027a0001c0001t0006g0028 | 3 | HG01167.hp2 HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.311+1032A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263749 | ||||||
| chr5:180263863
|
G | A | 17 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(14): Show | 18 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.311+918C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263863 | ||||||
| chr5:180263932
|
C | T | 1 | a0001c0001t0021g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.311+849G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180263932 | ||||||
| chr5:180264011
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.311+770T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180264011 | ||||||
| chr5:180264145
|
T | C | 3 | a0001c0001t0012g0208a0001c0001t0032g0112a0001c0001t0039g0247 | 3 | HG01952.hp2 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.311+636A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180264145 | ||||||
| chr5:180264468
|
C | T | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.311+313G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180264468 | ||||||
| chr5:180264715
|
T | C | 1 | a0001c0001t0007g0221 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.311+66A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 4/11 | chr5 | 180264715 | ||||||
| chr5:180264923
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253-84G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180264923 | ||||||
| chr5:180264951
|
ACTT | A | 100 | a0001c0001t0001g0003a0001c0001t0004g0018a0001c0001t0004g0291others(97): Show | 106 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.253-115_253-113del others(3): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180264951 | ||||||
| chr5:180265019
|
A | C | 1 | a0001c0001t0027g0339 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.253-180T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265019 | ||||||
| chr5:180265023
|
G | A | 3 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124 | 3 | HG02965.hp1 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.253-184C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265023 | ||||||
| chr5:180265024
|
C | T | 1 | a0001c0001t0024g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253-185G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265024 | ||||||
| chr5:180265039
|
C | T | 3 | a0001c0001t0013g0252a0001c0001t0026g0296a0001c0001t0026g0298 | 3 | HG02647.hp1 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.253-200G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265039 | ||||||
| chr5:180265078
|
T | G | 1 | a0001c0001t0039g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.253-239A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265078 | ||||||
| chr5:180265419
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.253-580C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265419 | ||||||
| chr5:180265566
|
C | T | 21 | a0001c0001t0002g0082a0001c0001t0002g0086a0001c0001t0002g0088others(18): Show | 22 | HG00280.hp2 HG02258.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.253-727G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265566 | ||||||
| chr5:180265587
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA18966.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.253-748C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265587 | ||||||
| chr5:180265682
|
C | T | 2 | a0001c0001t0012g0245a0001c0001t0012g0246 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.253-843G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265682 | ||||||
| chr5:180265698
|
C | A | 1 | a0001c0001t0003g0122 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.253-859G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265698 | ||||||
| chr5:180265799
|
G | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-960C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265799 | ||||||
| chr5:180265891
|
T | A | 1 | a0001c0001t0009g0015 | 2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.253-1052A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265891 | ||||||
| chr5:180265945
|
C | T | 345 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(342): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.253-1106G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180265945 | ||||||
| chr5:180266062
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.253-1223T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266062 | ||||||
| chr5:180266083
|
T | C | 13 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0329others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-1244A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266083 | ||||||
| chr5:180266113
|
T | C | 1 | a0001c0001t0011g0195 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.253-1274A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266113 | ||||||
| chr5:180266150
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.253-1311A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266150 | ||||||
| chr5:180266441
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.253-1602T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266441 | ||||||
| chr5:180266451
|
A | G | 3 | a0001c0001t0003g0085a0001c0001t0003g0093a0001c0001t0003g0094 | 3 | HG01515.hp1 HG01517.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.253-1612T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266451 | ||||||
| chr5:180266530
|
C | T | 13 | a0001c0001t0002g0082a0001c0001t0002g0086a0001c0001t0002g0088others(10): Show | 14 | HG00280.hp2 HG02258.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.253-1691G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266530 | ||||||
| chr5:180266542
|
C | T | 5 | a0001c0001t0001g0144a0001c0001t0001g0150a0001c0001t0001g0152others(2): Show | 5 | HG00558.hp1 HG02056.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-1703G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266542 | ||||||
| chr5:180266576
|
C | A | 1 | a0001c0001t0001g0287 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.253-1737G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266576 | ||||||
| chr5:180266613
|
C | T | 38 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0046others(35): Show | 44 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.253-1774G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266613 | ||||||
| chr5:180266641
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.253-1802A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266641 | ||||||
| chr5:180266658
|
G | T | 1 | a0001c0002t0012g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.253-1819C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266658 | ||||||
| chr5:180266820
|
C | T | 8 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0001g0160others(5): Show | 8 | HG02135.hp2 HG02165.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-1981G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266820 | ||||||
| chr5:180266959
|
C | T | 1 | a0001c0001t0005g0299 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.253-2120G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266959 | ||||||
| chr5:180266960
|
G | T | 8 | a0001c0001t0002g0082a0001c0001t0002g0088a0001c0001t0002g0089others(5): Show | 9 | HG00280.hp2 HG03490.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-2121C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180266960 | ||||||
| chr5:180267062
|
T | C | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.252+2218A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267062 | ||||||
| chr5:180267068
|
G | A | 86 | a0001c0001t0002g0082a0001c0001t0002g0086a0001c0001t0002g0088others(83): Show | 90 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.252+2212C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267068 | ||||||
| chr5:180267166
|
A | G | 14 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0319others(11): Show | 15 | HG00733.hp1 HG01074.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.252+2114T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267166 | ||||||
| chr5:180267178
|
C | T | 13 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0329others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.252+2102G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267178 | ||||||
| chr5:180267279
|
A | G | 6 | a0001c0001t0001g0149a0001c0001t0003g0105a0001c0001t0003g0106others(3): Show | 6 | HG00423.hp1 HG00673.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+2001T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267279 | ||||||
| chr5:180267283
|
C | T | 40 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0128others(37): Show | 43 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.252+1997G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267283 | ||||||
| chr5:180267289
|
C | T | 3 | a0001c0001t0015g0022a0001c0001t0032g0112a0001c0001t0039g0247 | 3 | HG01884.hp1 HG01952.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.252+1991G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267289 | ||||||
| chr5:180267324
|
C | G | 11 | a0001c0001t0004g0317a0001c0001t0004g0318a0001c0001t0004g0329others(8): Show | 11 | HG00642.hp2 HG01109.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+1956G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267324 | ||||||
| chr5:180267328
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.252+1952C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267328 | ||||||
| chr5:180267343
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.252+1937G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267343 | ||||||
| chr5:180267357
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.252+1923G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267357 | ||||||
| chr5:180267384
|
A | G | 3 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115 | 3 | HG02886.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.252+1896T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267384 | ||||||
| chr5:180267387
|
C | G | 5 | a0001c0001t0001g0142a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG00140.hp1 HG00280.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1893G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267387 | ||||||
| chr5:180267388
|
CT | C | 15 | a0001c0001t0003g0106a0001c0001t0007g0011a0001c0001t0007g0132others(12): Show | 16 | HG00099.hp2 HG00673.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.252+1891delA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267388 | ||||||
| chr5:180267389
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.252+1891A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267389 | ||||||
| chr5:180267392
|
C | G | 1 | a0001c0001t0003g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.252+1888G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267392 | ||||||
| chr5:180267418
|
T | C | 29 | a0001c0001t0001g0244a0001c0001t0003g0041a0001c0001t0004g0018others(26): Show | 30 | HG00733.hp1 HG01074.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.252+1862A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267418 | ||||||
| chr5:180267422
|
T | C | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1858A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267422 | ||||||
| chr5:180267430
|
C | T | 1 | a0001c0001t0007g0221 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.252+1850G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267430 | ||||||
| chr5:180267431
|
G | A | 245 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(242): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.252+1849C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267431 | ||||||
| chr5:180267435
|
A | G | 36 | a0001c0001t0001g0151a0001c0001t0001g0161a0001c0001t0001g0163others(33): Show | 38 | HG00099.hp2 HG00733.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+1845T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267435 | ||||||
| chr5:180267447
|
G | A | 5 | a0001c0001t0016g0042a0001c0001t0019g0217a0001c0001t0019g0218others(2): Show | 5 | HG01934.hp2 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1833C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267447 | ||||||
| chr5:180267454
|
C | T | 1 | a0001c0001t0002g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.252+1826G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267454 | ||||||
| chr5:180267455
|
G | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1825C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267455 | ||||||
| chr5:180267472
|
G | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1808C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267472 | ||||||
| chr5:180267474
|
A | G | 1 | a0001c0001t0041g0307 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.252+1806T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267474 | ||||||
| chr5:180267478
|
C | T | 6 | a0001c0001t0004g0322a0001c0001t0007g0225a0001c0001t0007g0228others(3): Show | 7 | HG03491.hp2 HG03492.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+1802G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267478 | ||||||
| chr5:180267486
|
T | C | 15 | a0001c0001t0001g0151a0001c0001t0001g0161a0001c0001t0001g0163others(12): Show | 15 | HG01884.hp1 HG02135.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.252+1794A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267486 | ||||||
| chr5:180267493
|
C | T | 1 | a0001c0001t0014g0314 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.252+1787G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267493 | ||||||
| chr5:180267503
|
A | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(85): Show | 95 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.252+1777T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267503 | ||||||
| chr5:180267510
|
T | C | 22 | a0001c0001t0001g0142a0001c0001t0001g0153a0001c0001t0003g0122others(19): Show | 26 | HG00280.hp1 HG00639.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.252+1770A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267510 | ||||||
| chr5:180267516
|
C | T | 3 | a0001c0001t0002g0046a0001c0001t0002g0055a0001c0001t0002g0084 | 3 | HG00741.hp1 HG01099.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.252+1764G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267516 | ||||||
| chr5:180267517
|
G | A | 1 | a0001c0001t0031g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+1763C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267517 | ||||||
| chr5:180267519
|
G | A | 3 | a0001c0001t0004g0319a0001c0001t0004g0320a0001c0001t0010g0044 | 3 | HG00639.hp2 NA19062.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.252+1761C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267519 | ||||||
| chr5:180267527
|
C | A | 3 | a0001c0001t0002g0060a0001c0001t0007g0134a0001c0001t0010g0044 | 3 | HG00639.hp2 HG03831.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.252+1753G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267527 | ||||||
| chr5:180267534
|
G | A | 1 | a0001c0001t0007g0134 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.252+1746C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267534 | ||||||
| chr5:180267534
|
G | C | 1 | a0001c0001t0010g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252+1746C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267534 | ||||||
| chr5:180267535
|
T | C | 2 | a0001c0001t0007g0134a0001c0001t0010g0044 | 2 | HG00639.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.252+1745A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267535 | ||||||
| chr5:180267540
|
C | A | 1 | a0001c0001t0010g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252+1740G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267540 | ||||||
| chr5:180267540
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0002g0120a0001c0001t0007g0134 | 3 | HG03486.hp1 NA19002.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.252+1740G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267540 | ||||||
| chr5:180267548
|
C | T | 1 | a0001c0001t0032g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.252+1732G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267548 | ||||||
| chr5:180267554
|
T | A | 1 | a0001c0001t0007g0134 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.252+1726A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267554 | ||||||
| chr5:180267556
|
C | T | 1 | a0001c0001t0005g0301 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.252+1724G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267556 | ||||||
| chr5:180267557
|
G | A | 2 | a0001c0001t0024g0265a0001c0001t0024g0266 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.252+1723C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267557 | ||||||
| chr5:180267561
|
C | CA | 8 | a0001c0001t0002g0054a0001c0001t0002g0056a0001c0001t0002g0114others(5): Show | 8 | HG00741.hp2 HG01109.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+1718dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267561 | ||||||
| chr5:180267561
|
CA | C | 191 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0127others(188): Show | 201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.252+1718delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267561 | ||||||
| chr5:180267561
|
CAA | C | 77 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 83 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.252+1717_252+1718d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267561 | ||||||
| chr5:180267599
|
CATGCATT others(17): Show |
C | 1 | a0001c0001t0007g0223 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.252+1657_252+1680d others(26): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267599 | ||||||
| chr5:180267680
|
G | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(212): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.252+1600C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267680 | ||||||
| chr5:180267690
|
C | G | 22 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0192others(19): Show | 24 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.252+1590G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267690 | ||||||
| chr5:180267691
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.252+1589G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267691 | ||||||
| chr5:180267717
|
C | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0128others(72): Show | 80 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.252+1563G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267717 | ||||||
| chr5:180267734
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.252+1546C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267734 | ||||||
| chr5:180267760
|
A | G | 140 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0153others(137): Show | 145 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.252+1520T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267760 | ||||||
| chr5:180267778
|
T | C | 20 | a0001c0001t0001g0193a0001c0001t0001g0212a0001c0001t0001g0257others(17): Show | 20 | HG01884.hp1 HG01952.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.252+1502A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267778 | ||||||
| chr5:180267805
|
C | CTG | 3 | a0001c0001t0001g0186a0001c0001t0001g0259a0001c0001t0001g0261 | 3 | HG00673.hp2 HG02132.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.252+1473_252+1474d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267805 | ||||||
| chr5:180267808
|
T | C | 1 | a0001c0001t0004g0336 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.252+1472A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267808 | ||||||
| chr5:180267809
|
C | G | 3 | a0001c0001t0002g0046a0001c0001t0004g0322a0001c0001t0030g0065 | 3 | HG01099.hp2 HG02165.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.252+1471G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267809 | ||||||
| chr5:180267811
|
CA | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0016others(114): Show | 123 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.252+1468delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267811 | ||||||
| chr5:180267812
|
A | C | 2 | a0001c0001t0004g0322a0001c0001t0030g0065 | 2 | HG02165.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.252+1468T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267812 | ||||||
| chr5:180267824
|
C | CA | 7 | a0001c0001t0001g0168a0001c0001t0007g0136a0001c0001t0007g0228others(4): Show | 7 | HG00099.hp2 HG01884.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+1455dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267824 | ||||||
| chr5:180267824
|
CA | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0253a0001c0001t0001g0254others(7): Show | 11 | HG01515.hp2 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+1455delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267824 | ||||||
| chr5:180267833
|
C | A | 2 | a0001c0001t0006g0029a0001c0001t0044g0345 | 2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.252+1447G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267833 | ||||||
| chr5:180267852
|
TTTTA | T | 4 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0006g0026others(1): Show | 4 | HG01243.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1424_252+1427d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267852 | ||||||
| chr5:180267932
|
A | G | 12 | a0001c0001t0001g0173a0001c0001t0002g0116a0001c0001t0002g0117others(9): Show | 12 | HG01952.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.252+1348T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267932 | ||||||
| chr5:180267948
|
T | C | 4 | a0001c0001t0002g0053a0001c0001t0002g0081a0001c0001t0022g0348others(1): Show | 4 | HG01884.hp2 HG02015.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+1332A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267948 | ||||||
| chr5:180267949
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.252+1331C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267949 | ||||||
| chr5:180267963
|
T | C | 6 | a0001c0001t0001g0140a0001c0001t0021g0268a0001c0001t0022g0346others(3): Show | 6 | HG02258.hp1 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+1317A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267963 | ||||||
| chr5:180267964
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.252+1316C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267964 | ||||||
| chr5:180267975
|
A | G | 14 | a0001c0001t0005g0311a0001c0001t0007g0011a0001c0001t0007g0132others(11): Show | 15 | HG01975.hp2 HG02155.hp2 HG03239.hp2 others(12): Show |
intron_variant | MODIFIER | c.252+1305T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180267975 | ||||||
| chr5:180268000
|
C | T | 5 | a0001c0001t0001g0170a0001c0001t0021g0267a0001c0001t0021g0268others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1280G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268000 | ||||||
| chr5:180268014
|
T | C | 1 | a0001c0001t0031g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+1266A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268014 | ||||||
| chr5:180268021
|
T | G | 4 | a0001c0001t0007g0132a0001c0001t0007g0133a0001c0001t0007g0134others(1): Show | 4 | HG02155.hp2 NA19002.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1259A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268021 | ||||||
| chr5:180268026
|
A | G | 4 | a0001c0001t0007g0132a0001c0001t0007g0133a0001c0001t0007g0134others(1): Show | 4 | HG02155.hp2 NA19002.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1254T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268026 | ||||||
| chr5:180268046
|
T | G | 41 | a0001c0001t0001g0148a0001c0001t0002g0001a0001c0001t0002g0007others(38): Show | 46 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.252+1234A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268046 | ||||||
| chr5:180268054
|
G | A | 1 | a0001c0002t0012g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.252+1226C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268054 | ||||||
| chr5:180268057
|
G | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 45 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.252+1223C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268057 | ||||||
| chr5:180268069
|
C | G | 1 | a0001c0001t0006g0037 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.252+1211G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268069 | ||||||
| chr5:180268076
|
G | A | 42 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0001t0001g0147others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.252+1204C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268076 | ||||||
| chr5:180268083
|
T | C | 23 | a0001c0001t0001g0274a0001c0001t0002g0001a0001c0001t0002g0047others(20): Show | 27 | HG00099.hp2 HG01192.hp2 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.252+1197A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268083 | ||||||
| chr5:180268113
|
T | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0128others(111): Show | 127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.252+1167A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268113 | ||||||
| chr5:180268116
|
A | G | 43 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0128others(40): Show | 47 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.252+1164T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268116 | ||||||
| chr5:180268352
|
C | G | 253 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(250): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.252+928G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268352 | ||||||
| chr5:180268368
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.252+912G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268368 | ||||||
| chr5:180268430
|
T | C | 92 | a0001c0001t0001g0016a0001c0001t0001g0158a0001c0001t0001g0241others(89): Show | 96 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.252+850A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268430 | ||||||
| chr5:180268436
|
C | T | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+844G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268436 | ||||||
| chr5:180268447
|
T | C | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.252+833A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268447 | ||||||
| chr5:180268485
|
T | A | 19 | a0001c0001t0001g0017a0001c0001t0001g0211a0001c0001t0001g0244others(16): Show | 20 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.252+795A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268485 | ||||||
| chr5:180268550
|
G | A | 6 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+730C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268550 | ||||||
| chr5:180268566
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.252+714C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268566 | ||||||
| chr5:180268603
|
G | A | 1 | a0001c0001t0012g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.252+677C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268603 | ||||||
| chr5:180268610
|
G | A | 2 | a0001c0001t0011g0196a0001c0001t0011g0197 | 2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.252+670C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268610 | ||||||
| chr5:180268617
|
G | A | 1 | a0001c0001t0005g0309 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.252+663C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268617 | ||||||
| chr5:180268642
|
G | A | 4 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115others(1): Show | 4 | HG02258.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+638C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268642 | ||||||
| chr5:180268643
|
C | T | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.252+637G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268643 | ||||||
| chr5:180268688
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.252+592C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268688 | ||||||
| chr5:180268814
|
G | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 50 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.252+466C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268814 | ||||||
| chr5:180268949
|
C | G | 1 | a0001c0001t0002g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.252+331G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180268949 | ||||||
| chr5:180269088
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.252+192C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180269088 | ||||||
| chr5:180269095
|
C | T | 1 | a0001c0001t0018g0125 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.252+185G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180269095 | ||||||
| chr5:180269128
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.252+152G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 3/11 | chr5 | 180269128 | ||||||
| chr5:180269446
|
C | T | 1 | a0001c0001t0004g0330 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.123-37G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269446 | ||||||
| chr5:180269583
|
C | A | 1 | a0001c0001t0013g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.123-174G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269583 | ||||||
| chr5:180269821
|
A | T | 1 | a0001c0001t0001g0273 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.123-412T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269821 | ||||||
| chr5:180269872
|
T | C | 1 | a0001c0001t0025g0213 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.123-463A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269872 | ||||||
| chr5:180269976
|
C | A | 15 | a0001c0001t0002g0082a0001c0001t0003g0070a0001c0001t0008g0008others(12): Show | 17 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.123-567G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269976 | ||||||
| chr5:180269997
|
A | C | 11 | a0001c0001t0008g0043a0001c0001t0020g0206a0001c0001t0020g0230others(8): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.123-588T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269997 | ||||||
| chr5:180269997
|
A | G | 86 | a0001c0001t0001g0016a0001c0001t0001g0209a0001c0001t0001g0212others(83): Show | 90 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.123-588T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180269997 | ||||||
| chr5:180270230
|
C | A | 5 | a0001c0001t0004g0329a0001c0001t0004g0334a0001c0001t0004g0335others(2): Show | 5 | HG00642.hp2 HG01109.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-821G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270230 | ||||||
| chr5:180270502
|
T | C | 94 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0127others(91): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.123-1093A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270502 | ||||||
| chr5:180270516
|
G | A | 2 | a0001c0001t0017g0155a0001c0001t0017g0156 | 2 | HG01243.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.123-1107C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270516 | ||||||
| chr5:180270535
|
C | T | 158 | a0001c0001t0001g0016a0001c0001t0001g0209a0001c0001t0001g0212others(155): Show | 169 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.123-1126G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270535 | ||||||
| chr5:180270542
|
C | G | 2 | a0001c0001t0004g0317a0001c0001t0004g0318 | 2 | HG01934.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.123-1133G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270542 | ||||||
| chr5:180270543
|
T | G | 1 | a0001c0001t0005g0308 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.123-1134A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270543 | ||||||
| chr5:180270827
|
T | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0075 | 2 | HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.123-1418A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270827 | ||||||
| chr5:180270858
|
C | CA | 36 | a0001c0001t0001g0169a0001c0001t0001g0183a0001c0001t0001g0199others(33): Show | 37 | HG00423.hp1 HG00544.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.123-1450dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270858 | ||||||
| chr5:180270858
|
C | CAA | 15 | a0001c0001t0001g0184a0001c0001t0001g0191a0001c0001t0001g0204others(12): Show | 15 | HG01884.hp2 HG01978.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.123-1451_123-1450d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270858 | ||||||
| chr5:180270861
|
AAAAAAAA others(12): Show |
A | 6 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0021g0267others(3): Show | 6 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-1471_123-1453d others(21): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270861 | ||||||
| chr5:180270868
|
A | AAAAAAAG | 8 | a0001c0001t0006g0005a0001c0001t0006g0026a0001c0001t0006g0027others(5): Show | 9 | HG01167.hp2 HG01243.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-1460_123-1459i others(9): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270868 | ||||||
| chr5:180270868
|
A | AAAAAAG | 11 | a0001c0001t0006g0024a0001c0001t0006g0032a0001c0001t0006g0033others(8): Show | 12 | HG02055.hp2 HG02071.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-1465_123-1460d others(8): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270868 | ||||||
| chr5:180270873
|
A | G | 1 | a0001c0001t0016g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.123-1464T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270873 | ||||||
| chr5:180270873
|
AG | A | 43 | a0001c0001t0001g0016a0001c0001t0001g0253a0001c0001t0001g0254others(40): Show | 50 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.123-1465delC | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270873 | ||||||
| chr5:180270874
|
G | A | 113 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(110): Show | 117 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.123-1465C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270874 | ||||||
| chr5:180270880
|
G | A | 1 | a0001c0001t0004g0328 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.123-1471C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270880 | ||||||
| chr5:180270881
|
A | C | 1 | a0001c0001t0007g0223 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.123-1472T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270881 | ||||||
| chr5:180270907
|
G | C | 1 | a0001c0001t0003g0110 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.123-1498C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180270907 | ||||||
| chr5:180271036
|
TGA | T | 5 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-1629_123-1628d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271036 | ||||||
| chr5:180271187
|
TA | T | 5 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-1779delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271187 | ||||||
| chr5:180271391
|
C | A | 1 | a0001c0001t0012g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.123-1982G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271391 | ||||||
| chr5:180271442
|
C | T | 5 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(2): Show | 5 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-2033G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271442 | ||||||
| chr5:180271554
|
C | T | 156 | a0001c0001t0001g0016a0001c0001t0001g0209a0001c0001t0001g0212others(153): Show | 167 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.123-2145G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271554 | ||||||
| chr5:180271611
|
G | A | 1 | a0001c0001t0012g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.123-2202C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271611 | ||||||
| chr5:180271619
|
T | C | 5 | a0001c0001t0005g0303a0001c0001t0005g0304a0001c0001t0005g0305others(2): Show | 5 | HG00438.hp1 NA18969.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-2210A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271619 | ||||||
| chr5:180271848
|
T | G | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-2439A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271848 | ||||||
| chr5:180271890
|
T | C | 43 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0145others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.123-2481A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180271890 | ||||||
| chr5:180272012
|
A | ACTCCACA others(71): Show |
1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.123-2681_123-2604d others(80): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272012 | ||||||
| chr5:180272112
|
T | A | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.123-2703A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272112 | ||||||
| chr5:180272125
|
T | C | 43 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0046others(40): Show | 49 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.123-2716A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272125 | ||||||
| chr5:180272198
|
CTT | C | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-2791_123-2790d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272198 | ||||||
| chr5:180272267
|
T | C | 1 | a0001c0001t0020g0232 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.123-2858A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272267 | ||||||
| chr5:180272420
|
C | T | 1 | a0001c0001t0013g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.123-3011G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272420 | ||||||
| chr5:180272504
|
G | C | 209 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0209others(206): Show | 223 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.123-3095C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272504 | ||||||
| chr5:180272686
|
A | G | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-3277T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272686 | ||||||
| chr5:180272911
|
G | A | 336 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(333): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.123-3502C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180272911 | ||||||
| chr5:180273153
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.123-3744A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273153 | ||||||
| chr5:180273215
|
ATCTT | A | 43 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0046others(40): Show | 49 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.123-3810_123-3807d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273215 | ||||||
| chr5:180273464
|
C | T | 2 | a0001c0001t0012g0245a0001c0001t0012g0246 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.123-4055G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273464 | ||||||
| chr5:180273503
|
A | G | 1 | a0001c0001t0002g0054 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.123-4094T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273503 | ||||||
| chr5:180273603
|
T | C | 130 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0209others(127): Show | 137 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.123-4194A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273603 | ||||||
| chr5:180273621
|
G | A | 9 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0012g0245others(6): Show | 9 | HG01952.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-4212C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273621 | ||||||
| chr5:180273673
|
A | G | 1 | a0001c0001t0039g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.123-4264T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273673 | ||||||
| chr5:180273777
|
A | G | 43 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0046others(40): Show | 49 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.123-4368T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273777 | ||||||
| chr5:180273983
|
C | CT | 58 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(55): Show | 63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.123-4575dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180273983 | ||||||
| chr5:180274001
|
C | T | 1 | a0001c0001t0006g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.123-4592G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274001 | ||||||
| chr5:180274341
|
C | T | 3 | a0001c0001t0012g0208a0001c0002t0012g0250a0001c0002t0012g0251 | 3 | HG02145.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123-4932G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274341 | ||||||
| chr5:180274397
|
C | T | 5 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-4988G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274397 | ||||||
| chr5:180274502
|
C | T | 28 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(25): Show | 29 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.123-5093G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274502 | ||||||
| chr5:180274516
|
G | A | 1 | a0001c0001t0011g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.123-5107C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274516 | ||||||
| chr5:180274641
|
C | CA | 3 | a0001c0001t0012g0208a0001c0002t0012g0250a0001c0002t0012g0251 | 3 | HG02145.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123-5233dupT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274641 | ||||||
| chr5:180274753
|
A | G | 29 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(26): Show | 30 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.123-5344T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274753 | ||||||
| chr5:180274762
|
T | C | 5 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-5353A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180274762 | ||||||
| chr5:180275122
|
T | C | 5 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+5318A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275122 | ||||||
| chr5:180275198
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0261 | 2 | HG00673.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.122+5242G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275198 | ||||||
| chr5:180275332
|
C | T | 1 | a0001c0001t0017g0012 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.122+5108G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275332 | ||||||
| chr5:180275631
|
C | A | 3 | a0001c0001t0005g0297a0001c0001t0015g0019a0001c0001t0015g0020 | 3 | HG02055.hp1 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.122+4809G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275631 | ||||||
| chr5:180275749
|
C | T | 1 | a0001c0001t0032g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.122+4691G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275749 | ||||||
| chr5:180275797
|
T | C | 9 | a0001c0001t0001g0153a0001c0001t0001g0185a0001c0001t0001g0186others(6): Show | 9 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+4643A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275797 | ||||||
| chr5:180275890
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.122+4550G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275890 | ||||||
| chr5:180275980
|
CTTAAATG others(7): Show |
C | 3 | a0001c0001t0006g0032a0001c0001t0006g0036a0001c0001t0006g0037 | 3 | NA18956.hp1 NA18972.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.122+4446_122+4459d others(16): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275980 | ||||||
| chr5:180275986
|
T | C | 1 | a0001c0001t0006g0029 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.122+4454A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180275986 | ||||||
| chr5:180276098
|
C | T | 18 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(15): Show | 19 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+4342G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276098 | ||||||
| chr5:180276219
|
A | G | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.122+4221T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276219 | ||||||
| chr5:180276221
|
G | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+4219C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276221 | ||||||
| chr5:180276257
|
G | A | 1 | a0001c0001t0009g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.122+4183C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276257 | ||||||
| chr5:180276413
|
C | T | 5 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+4027G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276413 | ||||||
| chr5:180276458
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.122+3982T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276458 | ||||||
| chr5:180276709
|
C | A | 5 | a0001c0001t0008g0009a0001c0001t0008g0076a0001c0001t0008g0079others(2): Show | 6 | HG01071.hp1 HG01261.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+3731G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276709 | ||||||
| chr5:180276724
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.122+3716G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276724 | ||||||
| chr5:180276847
|
G | A | 2 | a0001c0001t0014g0314a0001c0001t0014g0315 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.122+3593C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276847 | ||||||
| chr5:180276926
|
A | G | 2 | a0001c0001t0017g0155a0001c0001t0017g0156 | 2 | HG01243.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.122+3514T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276926 | ||||||
| chr5:180276930
|
CAAAT | C | 18 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(15): Show | 19 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+3506_122+3509d others(6): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276930 | ||||||
| chr5:180276972
|
T | G | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+3468A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180276972 | ||||||
| chr5:180277020
|
G | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+3420C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277020 | ||||||
| chr5:180277032
|
G | A | 18 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(15): Show | 19 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+3408C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277032 | ||||||
| chr5:180277214
|
G | T | 1 | a0001c0001t0013g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.122+3226C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277214 | ||||||
| chr5:180277230
|
A | G | 3 | a0001c0001t0007g0132a0001c0001t0007g0133a0001c0001t0007g0137 | 3 | HG02155.hp2 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.122+3210T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277230 | ||||||
| chr5:180277255
|
G | A | 8 | a0001c0001t0008g0043a0001c0001t0020g0206a0001c0001t0020g0230others(5): Show | 8 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+3185C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277255 | ||||||
| chr5:180277523
|
G | A | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.122+2917C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277523 | ||||||
| chr5:180277542
|
T | C | 1 | a0001c0001t0045g0349 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.122+2898A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277542 | ||||||
| chr5:180277576
|
G | A | 3 | a0001c0001t0003g0002a0001c0001t0003g0099a0001c0001t0012g0208 | 5 | HG01928.hp1 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+2864C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277576 | ||||||
| chr5:180277627
|
T | C | 59 | a0001c0001t0001g0016a0001c0001t0001g0241a0001c0001t0001g0242others(56): Show | 63 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.122+2813A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277627 | ||||||
| chr5:180277651
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.122+2789G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277651 | ||||||
| chr5:180277712
|
C | T | 19 | a0001c0001t0001g0003a0001c0001t0007g0011a0001c0001t0007g0132others(16): Show | 22 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.122+2728G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277712 | ||||||
| chr5:180277740
|
T | C | 19 | a0001c0001t0001g0017a0001c0001t0001g0211a0001c0001t0001g0244others(16): Show | 20 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.122+2700A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277740 | ||||||
| chr5:180277758
|
C | A | 1 | a0001c0001t0006g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+2682G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277758 | ||||||
| chr5:180277761
|
C | T | 1 | a0001c0001t0008g0078 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.122+2679G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277761 | ||||||
| chr5:180277809
|
C | T | 11 | a0001c0001t0008g0043a0001c0001t0020g0206a0001c0001t0020g0230others(8): Show | 11 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.122+2631G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277809 | ||||||
| chr5:180277903
|
C | T | 34 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(31): Show | 35 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.122+2537G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180277903 | ||||||
| chr5:180278182
|
C | A | 1 | a0001c0001t0001g0260 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.122+2258G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278182 | ||||||
| chr5:180278265
|
T | G | 1 | a0001c0001t0012g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122+2175A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278265 | ||||||
| chr5:180278312
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.122+2128A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278312 | ||||||
| chr5:180278398
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.122+2042C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278398 | ||||||
| chr5:180278424
|
G | A | 1 | a0001c0001t0012g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122+2016C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278424 | ||||||
| chr5:180278646
|
C | A | 29 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(26): Show | 30 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.122+1794G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278646 | ||||||
| chr5:180278653
|
C | T | 18 | a0001c0001t0007g0011a0001c0001t0007g0132a0001c0001t0007g0133others(15): Show | 19 | HG00099.hp2 HG01975.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.122+1787G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278653 | ||||||
| chr5:180278655
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.122+1785G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278655 | ||||||
| chr5:180278785
|
CCT | C | 30 | a0001c0001t0001g0212a0001c0001t0004g0018a0001c0001t0004g0291others(27): Show | 31 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.122+1653_122+1654d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278785 | ||||||
| chr5:180278812
|
G | A | 1 | a0001c0001t0006g0031 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122+1628C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278812 | ||||||
| chr5:180278955
|
A | C | 5 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(2): Show | 5 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+1485T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278955 | ||||||
| chr5:180278957
|
C | CT | 27 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0153others(24): Show | 27 | HG01175.hp1 HG01952.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.122+1482dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278957 | ||||||
| chr5:180278970
|
T | C | 48 | a0001c0001t0001g0017a0001c0001t0001g0211a0001c0001t0001g0244others(45): Show | 51 | HG00609.hp2 HG00642.hp1 HG01167.hp2 others(48): Show |
intron_variant | MODIFIER | c.122+1470A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180278970 | ||||||
| chr5:180279019
|
G | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+1421C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279019 | ||||||
| chr5:180279025
|
T | C | 5 | a0001c0001t0011g0220a0001c0001t0023g0123a0001c0001t0023g0124others(2): Show | 5 | HG02145.hp2 HG02965.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+1415A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279025 | ||||||
| chr5:180279099
|
G | A | 20 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(17): Show | 22 | HG01167.hp2 HG01243.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.122+1341C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279099 | ||||||
| chr5:180279156
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.122+1284G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279156 | ||||||
| chr5:180279247
|
T | C | 209 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0209others(206): Show | 223 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.122+1193A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279247 | ||||||
| chr5:180279367
|
G | C | 1 | a0001c0001t0008g0078 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.122+1073C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279367 | ||||||
| chr5:180279395
|
A | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0147a0001c0001t0001g0148others(3): Show | 6 | HG00558.hp2 HG00621.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+1045T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279395 | ||||||
| chr5:180279705
|
GA | G | 29 | a0001c0001t0004g0018a0001c0001t0004g0291a0001c0001t0004g0317others(26): Show | 30 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.122+734delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279705 | ||||||
| chr5:180279829
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.122+611G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279829 | ||||||
| chr5:180279846
|
G | C | 1 | a0001c0001t0025g0289 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122+594C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279846 | ||||||
| chr5:180279892
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.122+548T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180279892 | ||||||
| chr5:180280194
|
G | A | 206 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0209others(203): Show | 220 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.122+246C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180280194 | ||||||
| chr5:180280254
|
G | A | 1 | a0001c0001t0014g0316 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122+186C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180280254 | ||||||
| chr5:180280339
|
T | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+101A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180280339 | ||||||
| chr5:180280394
|
T | C | 21 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(18): Show | 23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+46A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 2/11 | chr5 | 180280394 | ||||||
| chr5:180280657
|
G | A | 1 | a0001c0001t0032g0112 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-47-49C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180280657 | ||||||
| chr5:180280920
|
C | T | 2 | a0001c0001t0007g0221a0001c0001t0007g0222 | 2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-47-312G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180280920 | ||||||
| chr5:180280991
|
G | A | 1 | a0001c0001t0007g0137 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-47-383C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180280991 | ||||||
| chr5:180281065
|
T | A | 21 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(18): Show | 23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47-457A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281065 | ||||||
| chr5:180281186
|
A | T | 1 | a0001c0001t0001g0200 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-47-578T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281186 | ||||||
| chr5:180281372
|
T | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0130a0001c0001t0001g0192others(1): Show | 5 | HG02155.hp1 NA18747.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-764A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281372 | ||||||
| chr5:180281442
|
T | C | 1 | a0001c0001t0010g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-47-834A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281442 | ||||||
| chr5:180281506
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-47-898A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281506 | ||||||
| chr5:180281564
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0008g0043a0001c0001t0020g0206others(3): Show | 6 | HG02572.hp1 HG03927.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-956C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281564 | ||||||
| chr5:180281896
|
C | T | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-1288G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281896 | ||||||
| chr5:180281897
|
G | A | 1 | a0001c0001t0004g0018 | 2 | HG00733.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-47-1289C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180281897 | ||||||
| chr5:180282049
|
C | A | 2 | a0001c0001t0008g0079a0001c0001t0008g0080 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-47-1441G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282049 | ||||||
| chr5:180282154
|
T | C | 243 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-47-1546A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282154 | ||||||
| chr5:180282194
|
A | G | 2 | a0001c0001t0010g0010a0001c0001t0010g0104 | 3 | HG03491.hp2 HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-47-1586T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282194 | ||||||
| chr5:180282235
|
C | T | 3 | a0001c0001t0005g0297a0001c0001t0026g0296a0001c0001t0026g0298 | 3 | HG02647.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-47-1627G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282235 | ||||||
| chr5:180282267
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-1659C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282267 | ||||||
| chr5:180282268
|
C | G | 1 | a0001c0001t0002g0053 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-47-1660G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282268 | ||||||
| chr5:180282282
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-47-1674G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282282 | ||||||
| chr5:180282295
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0008g0043a0001c0001t0020g0206others(3): Show | 6 | HG02572.hp1 HG03927.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1687C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282295 | ||||||
| chr5:180282318
|
G | T | 1 | a0001c0001t0015g0022 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47-1710C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282318 | ||||||
| chr5:180282400
|
C | T | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-1792G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282400 | ||||||
| chr5:180282481
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-47-1873T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282481 | ||||||
| chr5:180282528
|
A | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(194): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.-47-1920T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282528 | ||||||
| chr5:180282528
|
A | T | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-1920T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282528 | ||||||
| chr5:180282544
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-47-1936G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282544 | ||||||
| chr5:180282560
|
T | C | 1 | a0001c0001t0006g0038 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-47-1952A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282560 | ||||||
| chr5:180282589
|
C | A | 91 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0211others(88): Show | 96 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-1981G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282589 | ||||||
| chr5:180282731
|
C | T | 15 | a0001c0001t0002g0046a0001c0001t0004g0018a0001c0001t0004g0291others(12): Show | 16 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47-2123G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282731 | ||||||
| chr5:180282922
|
G | A | 4 | a0001c0001t0011g0194a0001c0001t0011g0195a0001c0001t0011g0196others(1): Show | 4 | HG01192.hp1 HG03710.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-2314C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282922 | ||||||
| chr5:180282923
|
G | C | 5 | a0001c0001t0018g0125a0001c0001t0018g0126a0001c0001t0018g0214others(2): Show | 5 | HG01099.hp1 HG01928.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-2315C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282923 | ||||||
| chr5:180282926
|
G | A | 91 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0211others(88): Show | 96 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-2318C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282926 | ||||||
| chr5:180282968
|
G | A | 3 | a0001c0001t0012g0208a0001c0002t0012g0250a0001c0002t0012g0251 | 3 | HG02145.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47-2360C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180282968 | ||||||
| chr5:180283039
|
C | T | 2 | a0001c0001t0004g0317a0001c0001t0004g0318 | 2 | HG01934.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-47-2431G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283039 | ||||||
| chr5:180283087
|
C | T | 1 | a0001c0001t0045g0349 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-47-2479G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283087 | ||||||
| chr5:180283194
|
G | A | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-2586C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283194 | ||||||
| chr5:180283502
|
C | T | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-2894G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283502 | ||||||
| chr5:180283663
|
T | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-3055A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283663 | ||||||
| chr5:180283675
|
C | T | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-3067G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283675 | ||||||
| chr5:180283889
|
C | A | 7 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-3281G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283889 | ||||||
| chr5:180283897
|
T | G | 1 | a0001c0001t0001g0198 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-47-3289A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283897 | ||||||
| chr5:180283915
|
G | A | 73 | a0001c0001t0001g0016a0001c0001t0001g0241a0001c0001t0001g0242others(70): Show | 77 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-47-3307C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283915 | ||||||
| chr5:180283922
|
C | T | 29 | a0001c0001t0002g0046a0001c0001t0004g0018a0001c0001t0004g0291others(26): Show | 30 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-47-3314G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180283922 | ||||||
| chr5:180284032
|
C | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0253a0001c0001t0001g0254 | 4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-3424G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284032 | ||||||
| chr5:180284184
|
C | T | 121 | a0001c0001t0001g0016a0001c0001t0001g0209a0001c0001t0001g0212others(118): Show | 126 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.-47-3576G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284184 | ||||||
| chr5:180284186
|
A | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0253a0001c0001t0001g0254 | 4 | HG02896.hp1 HG02897.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-3578T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284186 | ||||||
| chr5:180284289
|
C | A | 65 | a0001c0001t0001g0016a0001c0001t0001g0241a0001c0001t0001g0242others(62): Show | 69 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.-47-3681G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284289 | ||||||
| chr5:180284502
|
G | A | 1 | a0001c0001t0010g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-47-3894C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284502 | ||||||
| chr5:180284561
|
A | C | 1 | a0001c0001t0002g0115 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-47-3953T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284561 | ||||||
| chr5:180284663
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-47-4055A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284663 | ||||||
| chr5:180284692
|
AT | A | 6 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-4085delA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284692 | ||||||
| chr5:180284695
|
T | G | 6 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-4087A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284695 | ||||||
| chr5:180284862
|
C | T | 1 | a0001c0001t0038g0138 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-47-4254G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284862 | ||||||
| chr5:180284898
|
G | A | 93 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0127others(90): Show | 96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-47-4290C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284898 | ||||||
| chr5:180284913
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-47-4305G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284913 | ||||||
| chr5:180284914
|
G | A | 21 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(18): Show | 23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47-4306C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284914 | ||||||
| chr5:180284954
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-47-4346A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180284954 | ||||||
| chr5:180285060
|
A | G | 49 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0002g0046others(46): Show | 50 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.-47-4452T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285060 | ||||||
| chr5:180285192
|
T | G | 7 | a0001c0001t0014g0312a0001c0001t0014g0313a0001c0001t0014g0314others(4): Show | 7 | HG02280.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-4584A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285192 | ||||||
| chr5:180285194
|
C | T | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-47-4586G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285194 | ||||||
| chr5:180285451
|
C | T | 19 | a0001c0001t0001g0209a0001c0001t0001g0212a0001c0001t0011g0220others(16): Show | 19 | HG01099.hp1 HG01928.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.-47-4843G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285451 | ||||||
| chr5:180285458
|
G | A | 4 | a0001c0001t0019g0216a0001c0001t0019g0217a0001c0001t0019g0218others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47-4850C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285458 | ||||||
| chr5:180285650
|
A | G | 1 | a0001c0001t0012g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-5042T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285650 | ||||||
| chr5:180285689
|
G | A | 2 | a0001c0001t0002g0103a0001c0001t0021g0258 | 2 | HG03490.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-47-5081C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285689 | ||||||
| chr5:180285719
|
T | C | 3 | a0001c0001t0022g0346a0001c0001t0022g0347a0001c0001t0022g0348 | 3 | HG01884.hp2 HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-47-5111A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285719 | ||||||
| chr5:180285740
|
A | G | 21 | a0001c0001t0006g0005a0001c0001t0006g0023a0001c0001t0006g0024others(18): Show | 23 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-47-5132T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285740 | ||||||
| chr5:180285754
|
A | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-47-5146T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285754 | ||||||
| chr5:180285767
|
CAAT | C | 182 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0209others(179): Show | 194 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.-47-5162_-47-5160d others(5): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285767 | ||||||
| chr5:180285817
|
A | G | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5209T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285817 | ||||||
| chr5:180285846
|
T | A | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5238A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285846 | ||||||
| chr5:180285848
|
G | C | 1 | a0001c0001t0045g0349 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-47-5240C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285848 | ||||||
| chr5:180285850
|
G | A | 30 | a0001c0001t0002g0046a0001c0001t0004g0018a0001c0001t0004g0291others(27): Show | 31 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-47-5242C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285850 | ||||||
| chr5:180285851
|
T | G | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5243A>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285851 | ||||||
| chr5:180285853
|
T | C | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5245A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285853 | ||||||
| chr5:180285860
|
C | T | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5252G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285860 | ||||||
| chr5:180285861
|
G | A | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5253C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285861 | ||||||
| chr5:180285873
|
C | T | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5265G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285873 | ||||||
| chr5:180285874
|
G | C | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5266C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285874 | ||||||
| chr5:180285894
|
T | C | 3 | a0001c0001t0026g0298a0001c0002t0012g0250a0001c0002t0012g0251 | 3 | HG02630.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-47-5286A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285894 | ||||||
| chr5:180285895
|
G | A | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5287C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285895 | ||||||
| chr5:180285903
|
T | C | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5295A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285903 | ||||||
| chr5:180285906
|
G | A | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5298C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285906 | ||||||
| chr5:180285936
|
C | T | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5328G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285936 | ||||||
| chr5:180285944
|
G | C | 1 | a0001c0001t0026g0298 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-47-5336C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180285944 | ||||||
| chr5:180286075
|
G | A | 1 | a0001c0001t0010g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-47-5467C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286075 | ||||||
| chr5:180286079
|
CA | C | 181 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0209others(178): Show | 193 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.-47-5472delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286079 | ||||||
| chr5:180286112
|
T | C | 10 | a0001c0001t0001g0207a0001c0001t0008g0043a0001c0001t0020g0206others(7): Show | 10 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47-5504A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286112 | ||||||
| chr5:180286145
|
TTTCTTTT others(571): Show |
T | 18 | a0001c0001t0001g0017a0001c0001t0001g0211a0001c0001t0001g0244others(15): Show | 19 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-48+5125_-47-5538d others(2): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286145 | ||||||
| chr5:180286148
|
C | CT | 126 | a0001c0001t0001g0016a0001c0001t0001g0209a0001c0001t0001g0212others(123): Show | 133 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-47-5541dupA | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286148 | ||||||
| chr5:180286177
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | HG01516.hp2 NA20129.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-47-5569C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286177 | ||||||
| chr5:180286304
|
C | T | 3 | a0001c0001t0012g0208a0001c0002t0012g0250a0001c0002t0012g0251 | 3 | HG02145.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-48+5544G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286304 | ||||||
| chr5:180286366
|
G | A | 6 | a0001c0001t0003g0105a0001c0001t0003g0106a0001c0001t0003g0107others(3): Show | 6 | HG00438.hp2 HG00673.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+5482C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286366 | ||||||
| chr5:180286374
|
G | A | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+5474C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286374 | ||||||
| chr5:180286493
|
T | C | 30 | a0001c0001t0002g0046a0001c0001t0004g0018a0001c0001t0004g0291others(27): Show | 31 | HG00423.hp1 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-48+5355A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286493 | ||||||
| chr5:180286635
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-48+5213C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286635 | ||||||
| chr5:180286654
|
G | A | 1 | a0001c0001t0045g0349 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-48+5194C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286654 | ||||||
| chr5:180286719
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-48+5129C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286719 | ||||||
| chr5:180286779
|
G | A | 1 | a0001c0001t0002g0082 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-48+5069C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286779 | ||||||
| chr5:180286822
|
C | T | 92 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0127others(89): Show | 95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-48+5026G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286822 | ||||||
| chr5:180286877
|
T | A | 1 | a0001c0001t0004g0338 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-48+4971A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180286877 | ||||||
| chr5:180287085
|
T | C | 1 | a0001c0001t0003g0110 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-48+4763A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287085 | ||||||
| chr5:180287155
|
A | G | 161 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0209others(158): Show | 169 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.-48+4693T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287155 | ||||||
| chr5:180287235
|
C | G | 1 | a0001c0001t0040g0210 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-48+4613G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287235 | ||||||
| chr5:180287388
|
G | A | 1 | a0001c0001t0008g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-48+4460C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287388 | ||||||
| chr5:180287413
|
T | C | 1 | a0001c0001t0005g0311 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-48+4435A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287413 | ||||||
| chr5:180287453
|
T | C | 2 | a0001c0001t0026g0296a0001c0001t0026g0298 | 2 | HG02647.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-48+4395A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287453 | ||||||
| chr5:180287659
|
T | C | 1 | a0001c0001t0005g0309 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-48+4189A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287659 | ||||||
| chr5:180287699
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-48+4149T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287699 | ||||||
| chr5:180287733
|
T | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+4115A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287733 | ||||||
| chr5:180287803
|
G | A | 1 | a0001c0001t0044g0345 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+4045C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287803 | ||||||
| chr5:180287876
|
A | C | 3 | a0001c0001t0022g0346a0001c0001t0022g0347a0001c0001t0022g0348 | 3 | HG01884.hp2 HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-48+3972T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287876 | ||||||
| chr5:180287981
|
G | A | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+3867C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180287981 | ||||||
| chr5:180288059
|
C | T | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+3789G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288059 | ||||||
| chr5:180288061
|
C | T | 1 | a0001c0001t0008g0052 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-48+3787G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288061 | ||||||
| chr5:180288082
|
G | T | 3 | a0001c0001t0005g0297a0001c0001t0026g0296a0001c0001t0026g0298 | 3 | HG02647.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-48+3766C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288082 | ||||||
| chr5:180288086
|
C | A | 10 | a0001c0001t0001g0207a0001c0001t0008g0043a0001c0001t0020g0206others(7): Show | 10 | HG01884.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48+3762G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288086 | ||||||
| chr5:180288162
|
C | T | 1 | a0001c0001t0006g0032 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-48+3686G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288162 | ||||||
| chr5:180288270
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-48+3578G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288270 | ||||||
| chr5:180288317
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3531C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288317 | ||||||
| chr5:180288318
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3530C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288318 | ||||||
| chr5:180288319
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3529C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288319 | ||||||
| chr5:180288323
|
T | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3525A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288323 | ||||||
| chr5:180288325
|
T | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3523A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288325 | ||||||
| chr5:180288326
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3522C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288326 | ||||||
| chr5:180288327
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3521C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288327 | ||||||
| chr5:180288330
|
T | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3518A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288330 | ||||||
| chr5:180288332
|
A | T | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3516T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288332 | ||||||
| chr5:180288335
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3513C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288335 | ||||||
| chr5:180288340
|
T | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3508A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288340 | ||||||
| chr5:180288346
|
G | T | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3502C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288346 | ||||||
| chr5:180288349
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3499C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288349 | ||||||
| chr5:180288355
|
T | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+3493A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288355 | ||||||
| chr5:180288356
|
C | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3492G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288356 | ||||||
| chr5:180288357
|
C | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3491G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288357 | ||||||
| chr5:180288358
|
A | G | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+3490T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288358 | ||||||
| chr5:180288359
|
A | T | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3489T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288359 | ||||||
| chr5:180288360
|
T | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3488A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288360 | ||||||
| chr5:180288362
|
A | T | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3486T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288362 | ||||||
| chr5:180288366
|
A | T | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3482T>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288366 | ||||||
| chr5:180288368
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3480C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288368 | ||||||
| chr5:180288369
|
T | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3479A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288369 | ||||||
| chr5:180288372
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3476C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288372 | ||||||
| chr5:180288373
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3475C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288373 | ||||||
| chr5:180288374
|
C | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3474G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288374 | ||||||
| chr5:180288376
|
T | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3472A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288376 | ||||||
| chr5:180288377
|
T | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3471A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288377 | ||||||
| chr5:180288380
|
C | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3468G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288380 | ||||||
| chr5:180288385
|
T | C | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3463A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288385 | ||||||
| chr5:180288404
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3444C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288404 | ||||||
| chr5:180288405
|
G | T | 1 | a0001c0001t0003g0085 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-48+3443C>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288405 | ||||||
| chr5:180288426
|
A | C | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+3422T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288426 | ||||||
| chr5:180288519
|
C | CGAAGTGT others(35): Show |
1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-48+3287_-48+3328d others(44): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288519 | ||||||
| chr5:180288598
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-48+3250C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288598 | ||||||
| chr5:180288622
|
C | G | 1 | a0001c0001t0045g0349 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-48+3226G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288622 | ||||||
| chr5:180288803
|
A | G | 113 | a0001c0001t0001g0016a0001c0001t0001g0241a0001c0001t0001g0242others(110): Show | 123 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-48+3045T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288803 | ||||||
| chr5:180288828
|
A | C | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+3020T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288828 | ||||||
| chr5:180288836
|
C | A | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+3012G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288836 | ||||||
| chr5:180288869
|
A | C | 146 | a0001c0001t0001g0017a0001c0001t0001g0207a0001c0001t0001g0209others(143): Show | 156 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(153): Show |
intron_variant | MODIFIER | c.-48+2979T>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288869 | ||||||
| chr5:180288982
|
CA | C | 4 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(1): Show | 4 | NA18954.hp2 NA18955.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+2865delT | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180288982 | ||||||
| chr5:180289070
|
T | C | 11 | a0001c0001t0001g0207a0001c0001t0008g0043a0001c0001t0020g0206others(8): Show | 11 | HG01884.hp2 HG02145.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-48+2778A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289070 | ||||||
| chr5:180289076
|
C | A | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-48+2772G>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289076 | ||||||
| chr5:180289137
|
G | A | 1 | a0001c0001t0021g0268 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-48+2711C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289137 | ||||||
| chr5:180289240
|
C | T | 1 | a0001c0001t0012g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-48+2608G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289240 | ||||||
| chr5:180289265
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-48+2583T>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289265 | ||||||
| chr5:180289336
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0207others(169): Show | 185 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.-48+2512C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289336 | ||||||
| chr5:180289396
|
C | G | 1 | a0001c0001t0026g0296 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-48+2452G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289396 | ||||||
| chr5:180289477
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-48+2371A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289477 | ||||||
| chr5:180289533
|
G | A | 3 | a0001c0001t0005g0297a0001c0001t0026g0296a0001c0001t0026g0298 | 3 | HG02647.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-48+2315C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289533 | ||||||
| chr5:180289751
|
G | A | 42 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(39): Show | 48 | HG00544.hp1 HG00621.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.-48+2097C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289751 | ||||||
| chr5:180289932
|
T | C | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG02896.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-48+1916A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180289932 | ||||||
| chr5:180290046
|
C | CAG | 336 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(333): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.-48+1800_-48+1801d others(4): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290046 | ||||||
| chr5:180290446
|
C | T | 66 | a0001c0001t0001g0016a0001c0001t0001g0128a0001c0001t0001g0241others(63): Show | 73 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-48+1402G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290446 | ||||||
| chr5:180290460
|
T | C | 2 | a0001c0001t0005g0341a0001c0001t0005g0342 | 2 | NA18972.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-48+1388A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290460 | ||||||
| chr5:180290498
|
T | C | 7 | a0001c0001t0022g0346a0001c0001t0022g0347a0001c0001t0022g0348others(4): Show | 7 | HG01884.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+1350A>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290498 | ||||||
| chr5:180290643
|
T | A | 127 | a0001c0001t0001g0017a0001c0001t0001g0241a0001c0001t0001g0242others(124): Show | 136 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-48+1205A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290643 | ||||||
| chr5:180290720
|
C | T | 1 | a0001c0001t0036g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-48+1128G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290720 | ||||||
| chr5:180290849
|
G | A | 1 | a0001c0001t0013g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-48+999C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290849 | ||||||
| chr5:180290943
|
T | A | 2 | a0001c0001t0003g0122a0001c0001t0016g0121 | 2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-48+905A>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290943 | ||||||
| chr5:180290979
|
TTTAAATA others(3): Show |
T | 1 | a0001c0001t0038g0138 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-48+859_-48+868del others(10): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180290979 | ||||||
| chr5:180291131
|
C | T | 13 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(10): Show | 14 | HG00099.hp2 HG01258.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.-48+717G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291131 | ||||||
| chr5:180291134
|
AGG | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0274a0001c0001t0001g0275others(13): Show | 17 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+712_-48+713del others(2): Show |
MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291134 | ||||||
| chr5:180291189
|
G | C | 68 | a0001c0001t0001g0016a0001c0001t0001g0253a0001c0001t0001g0254others(65): Show | 72 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.-48+659C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291189 | ||||||
| chr5:180291330
|
G | C | 3 | a0001c0001t0023g0123a0001c0001t0023g0124a0001c0001t0025g0289 | 3 | HG02965.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-48+518C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291330 | ||||||
| chr5:180291478
|
G | A | 1 | a0001c0001t0009g0271 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-48+370C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291478 | ||||||
| chr5:180291486
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-48+362G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291486 | ||||||
| chr5:180291501
|
G | A | 1 | a0001c0001t0007g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-48+347C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291501 | ||||||
| chr5:180291699
|
C | T | 1 | a0001c0001t0044g0345 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-48+149G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291699 | ||||||
| chr5:180291762
|
C | T | 1 | a0001c0001t0005g0290 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-48+86G>A | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291762 | ||||||
| chr5:180291763
|
C | G | 2 | a0001c0001t0018g0125a0001c0001t0018g0126 | 2 | HG01099.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.-48+85G>C | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291763 | ||||||
| chr5:180291765
|
G | C | 1 | a0001c0001t0001g0273 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-48+83C>G | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291765 | ||||||
| chr5:180291804
|
G | A | 24 | a0001c0001t0001g0017a0001c0001t0001g0274a0001c0001t0001g0275others(21): Show | 25 | HG00609.hp2 HG00642.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.-48+44C>T | MAPK9 | ENSG00000050748.18 | transcript | ENST00000452135.7 | protein_coding | 1/11 | chr5 | 180291804 |