Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2022 |
|---|---|
| ensemblid | ENSG00000106991.14 |
| hgncid | 3349 |
| symbol | ENG |
| name | endoglin |
| refseq_nuc | NM_001114753.3 |
| refseq_prot | NP_001108225.1 |
| ensembl_nuc | ENST00000373203.9 |
| ensembl_prot | ENSP00000362299.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 127815016 |
| end | 127854658 |
| strand | - |
| ver | v1.2 |
| region | chr9:127815016-127854658 |
| region5000 | chr9:127810016-127859658 |
| regionname0 | ENG_chr9_127815016_127854658 |
| regionname5000 | ENG_chr9_127810016_127859658 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 658 | 303 | 75 | 52 | 121 | 11 | 42 | 85 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0002 | 0/0 | 658 | 16 | 0 | 0 | 16 | 0 | 0 | 10 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0003 | 0/0 | 658 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0004 | 0/0 | 658 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0005 | 0/0 | 658 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0006 | 0/0 | 658 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0007 | 0/0 | 658 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0008 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0009 | 0/0 | 658 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0010 | 0/0 | 658 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0011 | 0/0 | 658 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0012 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0013 | 0/0 | 658 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1977 | 230 | 44 | 36 | 107 | 9 | 32 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0002 | 0/0 | 1977 | 35 | 21 | 7 | 5 | 1 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0003 | 0/0 | 1977 | 18 | 2 | 3 | 4 | 1 | 8 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0004 | 0/0 | 1977 | 15 | 0 | 0 | 15 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0005 | 0/0 | 1977 | 11 | 8 | 3 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0006 | 0/0 | 1977 | 5 | 3 | 1 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0007 | 0/0 | 1977 | 4 | 0 | 2 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0008 | 0/0 | 1977 | 2 | 1 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0009 | 0/0 | 1977 | 2 | 2 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0010 | 0/0 | 1977 | 2 | 0 | 0 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0011 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0012 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0013 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0014 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0015 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0016 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0017 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0018 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0019 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0020 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0021 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0022 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0023 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0024 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0025 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0026 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0027 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0028 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0029 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| c0030 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 970 | 310 | 82 | 55 | 126 | 11 | 34 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0002 | 0/0 | 966 | 17 | 2 | 3 | 3 | 1 | 8 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0003 | 0/0 | 970 | 4 | 0 | 0 | 4 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0004 | 0/0 | 970 | 4 | 0 | 0 | 4 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0005 | 0/0 | 970 | 2 | 2 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0006 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0007 | 0/0 | 970 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0008 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0009 | 0/0 | 970 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0010 | 0/0 | 970 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0011 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| t0012 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1977 | 230 | 44 | 36 | 107 | 9 | 32 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0002 | 0/0 | 1977 | 35 | 21 | 7 | 5 | 1 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0003 | 0/0 | 1977 | 18 | 2 | 3 | 4 | 1 | 8 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0006 | 0/0 | 1977 | 5 | 3 | 1 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0007 | 0/0 | 1977 | 4 | 0 | 2 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0008 | 0/0 | 1977 | 2 | 1 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0010 | 0/0 | 1977 | 2 | 0 | 0 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0013 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0014 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0016 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0021 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0022 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0024 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0025 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0002c0004 | 0/0 | 1977 | 15 | 0 | 0 | 15 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0002c0012 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0003c0005 | 0/0 | 1977 | 11 | 8 | 3 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0003c0029 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0003c0030 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0004c0009 | 0/0 | 1977 | 2 | 2 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0004c0015 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0005c0027 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0006c0026 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0007c0017 | 0/0 | 1977 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0008c0020 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0009c0019 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0010c0023 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0011c0011 | 0/0 | 1977 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0012c0018 | 0/0 | 1977 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0013c0028 | 0/0 | 1977 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2946 | 218 | 41 | 36 | 99 | 9 | 31 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0001t0003 | 0/0 | 2946 | 4 | 0 | 0 | 4 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0001t0004 | 0/0 | 2946 | 4 | 0 | 0 | 4 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0001t0008 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0001t0009 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0001t0011 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0001t0012 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0002t0001 | 0/0 | 2946 | 34 | 20 | 7 | 5 | 1 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0002t0006 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0003t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0003t0002 | 0/0 | 2942 | 17 | 2 | 3 | 3 | 1 | 8 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0006t0001 | 0/0 | 2946 | 4 | 3 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0006t0010 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0007t0001 | 0/0 | 2946 | 4 | 0 | 2 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0008t0001 | 0/0 | 2946 | 2 | 1 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0010t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0010t0007 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0013t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0014t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0016t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0021t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0022t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0024t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0001c0025t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0002c0004t0001 | 0/0 | 2946 | 15 | 0 | 0 | 15 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0002c0012t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0003c0005t0001 | 0/0 | 2946 | 11 | 8 | 3 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0003c0029t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0003c0030t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0004c0009t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0004c0009t0005 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0004c0015t0005 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0005c0027t0001 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0006c0026t0001 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0007c0017t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0008c0020t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0009c0019t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0010c0023t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0011c0011t0001 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0012c0018t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| a0013c0028t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | copy fasta | chr9 | 127810016 | 127859658 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0011g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0001t0012g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0002t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0003t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0006t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0006t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0006t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0006t0010g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0007t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0007t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0007t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0007t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0008t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0008t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0010t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0010t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0013t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0014t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0016t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0021t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0022t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0024t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0001c0025t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0002c0012t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0005t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0029t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0003c0030t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0004c0009t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0004c0009t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0004c0015t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0005c0027t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0006c0026t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0007c0017t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0008c0020t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0009c0019t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0010c0023t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0011c0011t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0012c0018t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| a0013c0028t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0261 | EUR | FIN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00323 | hp2 | a0011 | c0011 | t0001 | g0020 | EUR | FIN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00438 | hp1 | a0002 | c0004 | t0001 | g0093 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00544 | hp1 | a0002 | c0004 | t0001 | g0195 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00639 | hp2 | a0003 | c0005 | t0001 | g0334 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00642 | hp1 | a0001 | c0025 | t0001 | g0258 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00673 | hp1 | a0001 | c0007 | t0001 | g0203 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01069 | hp1 | a0003 | c0005 | t0001 | g0330 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0122 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01074 | hp1 | a0001 | c0013 | t0001 | g0041 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01081 | hp2 | a0001 | c0007 | t0001 | g0214 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01099 | hp1 | a0001 | c0008 | t0001 | g0016 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0086 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01109 | hp1 | a0003 | c0005 | t0001 | g0328 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01167 | hp1 | a0001 | c0006 | t0001 | g0003 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01255 | hp1 | a0013 | c0028 | t0001 | g0150 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0296 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01346 | hp2 | a0010 | c0023 | t0001 | g0149 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01433 | hp2 | a0009 | c0019 | t0001 | g0158 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | IBS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0030 | EUR | IBS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02040 | hp1 | a0002 | c0004 | t0001 | g0234 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02135 | hp1 | a0002 | c0004 | t0001 | g0083 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02135 | hp2 | a0001 | c0007 | t0001 | g0211 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02155 | hp1 | a0002 | c0004 | t0001 | g0286 | EAS | CDX | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02165 | hp1 | a0002 | c0004 | t0001 | g0090 | EAS | CDX | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02300 | hp1 | a0001 | c0007 | t0001 | g0218 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02451 | hp1 | a0003 | c0005 | t0001 | g0336 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02451 | hp2 | a0003 | c0005 | t0001 | g0329 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02615 | hp2 | a0003 | c0005 | t0001 | g0325 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02647 | hp1 | a0004 | c0015 | t0005 | g0032 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02683 | hp2 | a0006 | c0026 | t0001 | g0264 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0260 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02723 | hp1 | a0001 | c0006 | t0001 | g0059 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0123 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02738 | hp2 | a0001 | c0006 | t0010 | g0337 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02809 | hp1 | a0012 | c0018 | t0001 | g0267 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02818 | hp1 | a0004 | c0009 | t0001 | g0054 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02818 | hp2 | a0001 | c0014 | t0001 | g0028 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0139 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02895 | hp1 | a0003 | c0005 | t0001 | g0332 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02897 | hp1 | a0003 | c0005 | t0001 | g0331 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02922 | hp1 | a0001 | c0001 | t0011 | g0338 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02922 | hp2 | a0003 | c0029 | t0001 | g0335 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03017 | hp1 | a0005 | c0027 | t0001 | g0191 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03098 | hp2 | a0004 | c0009 | t0005 | g0055 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03130 | hp1 | a0001 | c0024 | t0001 | g0141 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03195 | hp1 | a0008 | c0020 | t0001 | g0061 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03209 | hp1 | a0003 | c0005 | t0001 | g0326 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03453 | hp1 | a0003 | c0005 | t0001 | g0327 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0130 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03516 | hp1 | a0003 | c0005 | t0001 | g0324 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03516 | hp2 | a0001 | c0006 | t0001 | g0058 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03540 | hp1 | a0001 | c0008 | t0001 | g0027 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0057 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0126 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03831 | hp2 | a0001 | c0003 | t0002 | g0134 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0136 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03942 | hp1 | a0001 | c0001 | t0009 | g0171 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0154 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0133 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18612 | hp1 | a0001 | c0010 | t0001 | g0199 | EAS | CHB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0003 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18944 | hp1 | a0001 | c0003 | t0002 | g0125 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18947 | hp1 | a0002 | c0004 | t0001 | g0075 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18950 | hp2 | a0002 | c0004 | t0001 | g0077 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18957 | hp2 | a0002 | c0004 | t0001 | g0164 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18959 | hp1 | a0001 | c0021 | t0001 | g0074 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18964 | hp2 | a0002 | c0004 | t0001 | g0067 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18966 | hp2 | a0001 | c0003 | t0002 | g0120 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18971 | hp2 | a0002 | c0004 | t0001 | g0206 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18977 | hp1 | a0002 | c0004 | t0001 | g0076 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18979 | hp2 | a0007 | c0017 | t0001 | g0121 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18988 | hp2 | a0002 | c0004 | t0001 | g0163 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18995 | hp2 | a0002 | c0004 | t0001 | g0167 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19012 | hp2 | a0001 | c0003 | t0002 | g0066 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0339 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19030 | hp2 | a0003 | c0030 | t0001 | g0333 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19043 | hp2 | a0001 | c0022 | t0001 | g0050 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19064 | hp2 | a0002 | c0004 | t0001 | g0232 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19070 | hp2 | a0002 | c0012 | t0001 | g0309 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19081 | hp1 | a0001 | c0010 | t0007 | g0198 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ASW | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ASW | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | TSI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | TSI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | GIH | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | GIH | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0087 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | USA | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0302 | AFR | USA | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20300 | hp1 | a0001 | c0016 | t0001 | g0060 | AFR | USA | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | USA | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0157 | REF | REF | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0062 | REF | REF | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127818169
|
G | A | 1 | a0008 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1637C>T | p.Thr546Ile | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1940/2946 | 1637/1977 | 546/658 | chr9 | 127818169 | ||
| chr9:127818173
|
C | T | 1 | a0009 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1633G>A | p.Gly545Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1936/2946 | 1633/1977 | 545/658 | chr9 | 127818173 | ||
| chr9:127818296
|
C | T | 1 | a0004 | 3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.1510G>A | p.Val504Met | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1813/2946 | 1510/1977 | 504/658 | chr9 | 127818296 | ||
| chr9:127824338
|
G | C | 1 | a0010 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1100C>G | p.Ala367Gly | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/15 | 1403/2946 | 1100/1977 | 367/658 | chr9 | 127824338 | ||
| chr9:127824342
|
C | G | 1 | a0002 | 16 | HG00438.hp1 HG00544.hp1 HG02040.hp1 others(13): Show |
missense_variant | MODERATE | c.1096G>C | p.Asp366His | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/15 | 1399/2946 | 1096/1977 | 366/658 | chr9 | 127824342 | ||
| chr9:127824811
|
G | T | 1 | a0011 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.980C>A | p.Ala327Asp | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/15 | 1283/2946 | 980/1977 | 327/658 | chr9 | 127824811 | ||
| chr9:127825744
|
C | T | 1 | a0012 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.640G>A | p.Gly214Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/15 | 943/2946 | 640/1977 | 214/658 | chr9 | 127825744 | ||
| chr9:127825788
|
C | T | 1 | a0007 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.596G>A | p.Arg199His | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/15 | 899/2946 | 596/1977 | 199/658 | chr9 | 127825788 | ||
| chr9:127825810
|
G | C | 1 | a0006 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.574C>G | p.Arg192Gly | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/15 | 877/2946 | 574/1977 | 192/658 | chr9 | 127825810 | ||
| chr9:127826641
|
G | A | 1 | a0005 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.392C>T | p.Pro131Leu | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/15 | 695/2946 | 392/1977 | 131/658 | chr9 | 127826641 | ||
| chr9:127843143
|
G | C | 1 | a0013 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.170C>G | p.Ala57Gly | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/15 | 473/2946 | 170/1977 | 57/658 | chr9 | 127843143 | ||
| chr9:127854342
|
G | A | 1 | a0003 | 13 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(10): Show |
missense_variant | MODERATE | c.14C>T | p.Thr5Met | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | 317/2946 | 14/1977 | 5/658 | chr9 | 127854342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127815727
|
G | A | 1 | a0001c0007 | 4 | HG00673.hp1 HG01081.hp2 HG02135.hp2 others(1): Show |
synonymous_variant | LOW | c.1932C>T | p.Ile644Ile | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 2235/2946 | 1932/1977 | 644/658 | chr9 | 127815727 | ||
| chr9:127816001
|
A | G | 2 | a0001c0006a0001c0014 | 6 | HG01167.hp1 HG02723.hp1 HG02738.hp2 others(3): Show |
synonymous_variant | LOW | c.1794T>C | p.Gly598Gly | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 14/15 | 2097/2946 | 1794/1977 | 598/658 | chr9 | 127816001 | ||
| chr9:127818174
|
G | A | 1 | a0001c0021 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.1632C>T | p.Thr544Thr | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1935/2946 | 1632/1977 | 544/658 | chr9 | 127818174 | ||
| chr9:127818354
|
G | A | 2 | a0004c0009a0004c0015 | 3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1452C>T | p.Ser484Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1755/2946 | 1452/1977 | 484/658 | chr9 | 127818354 | ||
| chr9:127818360
|
G | A | 1 | a0003c0029 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1446C>T | p.Ser482Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1749/2946 | 1446/1977 | 482/658 | chr9 | 127818360 | ||
| chr9:127818737
|
C | T | 1 | a0001c0013 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.1407G>A | p.Pro469Pro | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 11/15 | 1710/2946 | 1407/1977 | 469/658 | chr9 | 127818737 | ||
| chr9:127818770
|
T | C | 1 | a0001c0025 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.1374A>G | p.Pro458Pro | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 11/15 | 1677/2946 | 1374/1977 | 458/658 | chr9 | 127818770 | ||
| chr9:127819939
|
G | A | 1 | a0001c0022 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1233C>T | p.Ser411Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 9/15 | 1536/2946 | 1233/1977 | 411/658 | chr9 | 127819939 | ||
| chr9:127824378
|
G | A | 4 | a0001c0008a0001c0024a0001c0025others(1): Show | 5 | HG00642.hp1 HG01099.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.1060C>T | p.Leu354Leu | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/15 | 1363/2946 | 1060/1977 | 354/658 | chr9 | 127824378 | ||
| chr9:127824409
|
G | A | 1 | a0001c0003 | 18 | HG00323.hp1 HG01070.hp1 HG01106.hp1 others(15): Show |
synonymous_variant | LOW | c.1029C>T | p.Thr343Thr | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/15 | 1332/2946 | 1029/1977 | 343/658 | chr9 | 127824409 | ||
| chr9:127829813
|
C | T | 1 | a0001c0016 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.234G>A | p.Leu78Leu | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/15 | 537/2946 | 234/1977 | 78/658 | chr9 | 127829813 | ||
| chr9:127829822
|
C | T | 1 | a0001c0016 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.225G>A | p.Pro75Pro | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/15 | 528/2946 | 225/1977 | 75/658 | chr9 | 127829822 | ||
| chr9:127843106
|
C | T | 7 | a0001c0002a0001c0008a0001c0013others(4): Show | 42 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(39): Show |
synonymous_variant | LOW | c.207G>A | p.Leu69Leu | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/15 | 510/2946 | 207/1977 | 69/658 | chr9 | 127843106 | ||
| chr9:127843154
|
G | A | 1 | a0001c0010 | 2 | NA18612.hp1 NA19081.hp1 |
synonymous_variant | LOW | c.159C>T | p.Cys53Cys | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/15 | 462/2946 | 159/1977 | 53/658 | chr9 | 127843154 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127815124
|
T | C | 1 | a0001c0010t0007 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 558 | chr9 | 127815124 | |||||
| chr9:127815190
|
C | T | 1 | a0001c0001t0004 | 4 | NA18943.hp1 NA18950.hp1 NA18984.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 492 | chr9 | 127815190 | |||||
| chr9:127815213
|
CAGTT | C | 1 | a0001c0003t0002 | 17 | HG00323.hp1 HG01070.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*465_*468delAACT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 465 | chr9 | 127815213 | |||||
| chr9:127815533
|
C | G | 2 | a0004c0009t0005a0004c0015t0005 | 2 | HG02647.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 149 | chr9 | 127815533 | |||||
| chr9:127815564
|
G | A | 1 | a0001c0001t0008 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*118C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 118 | chr9 | 127815564 | |||||
| chr9:127815573
|
G | A | 1 | a0001c0001t0009 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*109C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 109 | chr9 | 127815573 | |||||
| chr9:127815619
|
C | T | 1 | a0001c0002t0006 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*63G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 63 | chr9 | 127815619 | |||||
| chr9:127854409
|
G | T | 1 | a0001c0001t0003 | 4 | HG00609.hp1 HG02027.hp2 HG02129.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-54C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | 54 | chr9 | 127854409 | |||||
| chr9:127854425
|
G | A | 1 | a0001c0006t0010 | 1 | HG02738.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | chr9 | 127854425 | ||||||
| chr9:127854475
|
C | A | 1 | a0001c0001t0011 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | 120 | chr9 | 127854475 | |||||
| chr9:127854476
|
G | A | 1 | a0001c0001t0012 | 1 | NA19030.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-121C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | chr9 | 127854476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127815829
|
G | A | 1 | a0008c0020t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1853-23C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 14/14 | chr9 | 127815829 | ||||||
| chr9:127816068
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1742-15G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816068 | ||||||
| chr9:127816125
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(181): Show | 188 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1742-72T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816125 | ||||||
| chr9:127816188
|
C | T | 2 | a0001c0003t0002g0013a0001c0003t0002g0302 | 2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1742-135G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816188 | ||||||
| chr9:127816214
|
G | T | 1 | a0001c0003t0002g0120 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1742-161C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816214 | ||||||
| chr9:127816346
|
G | A | 20 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0138others(17): Show | 20 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.1742-293C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816346 | ||||||
| chr9:127816461
|
G | A | 1 | a0001c0025t0001g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1742-408C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816461 | ||||||
| chr9:127816539
|
A | G | 4 | a0001c0008t0001g0016a0001c0008t0001g0027a0001c0024t0001g0141others(1): Show | 4 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1742-486T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816539 | ||||||
| chr9:127816543
|
G | A | 7 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0259others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1742-490C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816543 | ||||||
| chr9:127816639
|
T | C | 1 | a0008c0020t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1741+510A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816639 | ||||||
| chr9:127816756
|
G | C | 1 | a0001c0025t0001g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1741+393C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816756 | ||||||
| chr9:127816770
|
C | T | 1 | a0001c0010t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1741+379G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816770 | ||||||
| chr9:127816921
|
C | G | 5 | a0001c0008t0001g0016a0001c0008t0001g0027a0001c0016t0001g0060others(2): Show | 5 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1741+228G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816921 | ||||||
| chr9:127816928
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1741+221G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816928 | ||||||
| chr9:127817320
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 121 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1687-117G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817320 | ||||||
| chr9:127817360
|
C | G | 5 | a0001c0002t0001g0002a0001c0002t0001g0042a0001c0002t0001g0043others(2): Show | 6 | HG01109.hp2 HG01891.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1687-157G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817360 | ||||||
| chr9:127817425
|
C | G | 2 | a0001c0002t0001g0312a0001c0002t0001g0314 | 2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1687-222G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817425 | ||||||
| chr9:127817531
|
C | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 196 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1687-328G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817531 | ||||||
| chr9:127817625
|
A | G | 25 | a0001c0001t0001g0051a0001c0001t0001g0300a0001c0002t0001g0052others(22): Show | 25 | HG00438.hp1 HG00544.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1687-422T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817625 | ||||||
| chr9:127817760
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1686+360A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817760 | ||||||
| chr9:127817781
|
A | G | 1 | a0001c0022t0001g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1686+339T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817781 | ||||||
| chr9:127817803
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1686+317A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817803 | ||||||
| chr9:127817808
|
G | A | 1 | a0001c0025t0001g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1686+312C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817808 | ||||||
| chr9:127817814
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 197 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1686+306A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817814 | ||||||
| chr9:127817996
|
C | A | 4 | a0001c0008t0001g0016a0001c0008t0001g0027a0001c0024t0001g0141others(1): Show | 4 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1686+124G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817996 | ||||||
| chr9:127817997
|
C | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00673.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1686+123G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817997 | ||||||
| chr9:127818660
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1428+56G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 11/14 | chr9 | 127818660 | ||||||
| chr9:127818690
|
C | T | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1428+26G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 11/14 | chr9 | 127818690 | ||||||
| chr9:127818870
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00673.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1312-38C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127818870 | ||||||
| chr9:127818940
|
C | CT | 46 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0053others(43): Show | 46 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1312-109dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127818940 | ||||||
| chr9:127818942
|
T | C | 1 | a0008c0020t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1312-110A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127818942 | ||||||
| chr9:127818968
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-136G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127818968 | ||||||
| chr9:127819021
|
T | G | 2 | a0001c0001t0001g0174a0001c0002t0001g0039 | 2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1312-189A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819021 | ||||||
| chr9:127819098
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1312-266G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819098 | ||||||
| chr9:127819099
|
G | A | 4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-267C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819099 | ||||||
| chr9:127819140
|
T | C | 1 | a0001c0003t0002g0125 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1312-308A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819140 | ||||||
| chr9:127819172
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1312-340G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819172 | ||||||
| chr9:127819237
|
CT | C | 6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0201others(3): Show | 6 | HG02572.hp1 NA18522.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311+384delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819237 | ||||||
| chr9:127819258
|
A | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0288 | 2 | HG00408.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1311+364T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819258 | ||||||
| chr9:127819444
|
A | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(278): Show | 286 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1311+178T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819444 | ||||||
| chr9:127819528
|
T | C | 6 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0259others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+94A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819528 | ||||||
| chr9:127819796
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1272+104G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 9/14 | chr9 | 127819796 | ||||||
| chr9:127820045
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02145.hp1 | splice_region_variant&intron_variant | LOW | c.1135-8C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820045 | ||||||
| chr9:127820293
|
A | C | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00673.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1135-256T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820293 | ||||||
| chr9:127820324
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0146 | 2 | HG01255.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1135-287C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820324 | ||||||
| chr9:127820506
|
T | G | 92 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0078others(89): Show | 93 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1135-469A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820506 | ||||||
| chr9:127820689
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1135-652G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820689 | ||||||
| chr9:127820690
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1135-653C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820690 | ||||||
| chr9:127820739
|
A | G | 41 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0047others(38): Show | 41 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1135-702T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820739 | ||||||
| chr9:127820746
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1135-709C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820746 | ||||||
| chr9:127820754
|
G | A | 9 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(6): Show | 9 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1135-717C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820754 | ||||||
| chr9:127820777
|
C | T | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-740G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820777 | ||||||
| chr9:127820791
|
T | G | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-754A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820791 | ||||||
| chr9:127820828
|
CA | C | 13 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0179others(10): Show | 13 | HG00544.hp1 HG01891.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1135-792delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820828 | ||||||
| chr9:127820837
|
A | T | 2 | a0002c0004t0001g0093a0008c0020t0001g0061 | 2 | HG00438.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1135-800T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820837 | ||||||
| chr9:127820839
|
A | AT | 31 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0070others(28): Show | 33 | HG00597.hp1 HG00738.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1135-803_1135-802i others(3): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820839 | ||||||
| chr9:127820839
|
A | T | 69 | a0001c0001t0001g0012a0001c0001t0001g0045a0001c0001t0001g0046others(66): Show | 70 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1135-802T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820839 | ||||||
| chr9:127820841
|
T | A | 16 | a0001c0001t0001g0014a0001c0001t0001g0162a0001c0001t0001g0176others(13): Show | 16 | HG00099.hp2 HG00423.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1135-804A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820841 | ||||||
| chr9:127820843
|
T | A | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-806A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820843 | ||||||
| chr9:127820895
|
A | G | 39 | a0001c0001t0001g0053a0001c0001t0001g0113a0001c0001t0001g0132others(36): Show | 39 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.1135-858T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820895 | ||||||
| chr9:127820948
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1135-911C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820948 | ||||||
| chr9:127820982
|
C | G | 3 | a0002c0004t0001g0195a0002c0004t0001g0206a0002c0004t0001g0234 | 3 | HG00544.hp1 HG02040.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1135-945G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820982 | ||||||
| chr9:127821009
|
G | A | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-972C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821009 | ||||||
| chr9:127821127
|
C | T | 2 | a0001c0006t0010g0337a0004c0015t0005g0032 | 2 | HG02647.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1135-1090G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821127 | ||||||
| chr9:127821146
|
C | CA | 3 | a0003c0005t0001g0327a0003c0005t0001g0329a0003c0005t0001g0330 | 3 | HG01069.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1135-1110dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821146 | ||||||
| chr9:127821170
|
G | T | 5 | a0001c0006t0001g0003a0001c0006t0001g0058a0001c0006t0001g0059others(2): Show | 6 | HG01167.hp1 HG02723.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-1133C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821170 | ||||||
| chr9:127821174
|
G | A | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0111others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135-1137C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821174 | ||||||
| chr9:127821242
|
G | A | 5 | a0001c0001t0001g0073a0001c0001t0001g0085a0001c0001t0001g0089others(2): Show | 5 | HG02027.hp2 NA18963.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135-1205C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821242 | ||||||
| chr9:127821378
|
C | A | 3 | a0004c0009t0001g0054a0004c0009t0005g0055a0004c0015t0005g0032 | 3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1135-1341G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821378 | ||||||
| chr9:127821493
|
G | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0246 | 2 | HG00408.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1135-1456C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821493 | ||||||
| chr9:127821525
|
T | A | 1 | a0001c0001t0009g0171 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1135-1488A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821525 | ||||||
| chr9:127821713
|
T | TA | 7 | a0001c0003t0002g0133a0001c0006t0001g0003a0001c0006t0001g0058others(4): Show | 8 | HG01167.hp1 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135-1677dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821713 | ||||||
| chr9:127821713
|
T | TAA | 129 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 132 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1135-1678_1135-167 others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821713 | ||||||
| chr9:127821723
|
A | G | 3 | a0002c0004t0001g0195a0002c0004t0001g0206a0002c0004t0001g0234 | 3 | HG00544.hp1 HG02040.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1135-1686T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821723 | ||||||
| chr9:127821751
|
T | C | 6 | a0001c0008t0001g0016a0001c0008t0001g0027a0001c0016t0001g0060others(3): Show | 6 | HG01099.hp1 HG02922.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-1714A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821751 | ||||||
| chr9:127821777
|
G | C | 3 | a0002c0004t0001g0195a0002c0004t0001g0206a0002c0004t0001g0234 | 3 | HG00544.hp1 HG02040.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1135-1740C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821777 | ||||||
| chr9:127821832
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1135-1795C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821832 | ||||||
| chr9:127821880
|
T | TA | 6 | a0001c0001t0001g0051a0001c0001t0001g0172a0001c0002t0001g0052others(3): Show | 6 | HG02055.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-1844dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821880 | ||||||
| chr9:127821880
|
TA | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 281 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1135-1844delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821880 | ||||||
| chr9:127821880
|
TAA | T | 12 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0118others(9): Show | 12 | HG00642.hp1 HG01081.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1135-1845_1135-184 others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821880 | ||||||
| chr9:127821880
|
TAAA | T | 20 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0138others(17): Show | 20 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.1135-1846_1135-184 others(7): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821880 | ||||||
| chr9:127821974
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1135-1937G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821974 | ||||||
| chr9:127821975
|
G | A | 2 | a0001c0001t0001g0051a0001c0002t0001g0052 | 2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1135-1938C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821975 | ||||||
| chr9:127822056
|
A | G | 1 | a0001c0001t0003g0006 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1135-2019T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822056 | ||||||
| chr9:127822315
|
G | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0080a0001c0001t0001g0293 | 3 | HG02071.hp2 NA18966.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1134+1989C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822315 | ||||||
| chr9:127822376
|
CAGT | C | 14 | a0002c0004t0001g0067a0002c0004t0001g0075a0002c0004t0001g0076others(11): Show | 14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.1134+1925_1134+192 others(7): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822376 | ||||||
| chr9:127822407
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1134+1897T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822407 | ||||||
| chr9:127822418
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0229 | 3 | HG01884.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1134+1886T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822418 | ||||||
| chr9:127822488
|
A | T | 1 | a0013c0028t0001g0150 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1134+1816T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822488 | ||||||
| chr9:127822535
|
T | G | 3 | a0004c0009t0001g0054a0004c0009t0005g0055a0004c0015t0005g0032 | 3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1134+1769A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822535 | ||||||
| chr9:127822557
|
A | G | 4 | a0001c0008t0001g0016a0001c0008t0001g0027a0001c0024t0001g0141others(1): Show | 4 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+1747T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822557 | ||||||
| chr9:127822640
|
T | C | 6 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0165others(3): Show | 6 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+1664A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822640 | ||||||
| chr9:127822713
|
T | C | 2 | a0001c0001t0001g0051a0001c0002t0001g0052 | 2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1134+1591A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822713 | ||||||
| chr9:127822752
|
T | C | 54 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0047others(51): Show | 54 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1134+1552A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822752 | ||||||
| chr9:127822954
|
C | T | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0152others(1): Show | 4 | HG01123.hp2 HG01346.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+1350G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822954 | ||||||
| chr9:127823001
|
C | T | 1 | a0001c0002t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1134+1303G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823001 | ||||||
| chr9:127823014
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1134+1290G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823014 | ||||||
| chr9:127823122
|
G | A | 1 | a0001c0002t0006g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1134+1182C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823122 | ||||||
| chr9:127823170
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1134+1134C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823170 | ||||||
| chr9:127823224
|
C | T | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1134+1080G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823224 | ||||||
| chr9:127823238
|
C | A | 1 | a0003c0029t0001g0335 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1134+1066G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823238 | ||||||
| chr9:127823390
|
C | CT | 18 | a0001c0001t0001g0051a0001c0002t0001g0052a0002c0004t0001g0067others(15): Show | 18 | HG00438.hp1 HG00544.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1134+913dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823390 | ||||||
| chr9:127823390
|
CT | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0132others(28): Show | 31 | HG01081.hp2 HG01433.hp1 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.1134+913delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823390 | ||||||
| chr9:127823505
|
C | T | 1 | a0001c0003t0002g0260 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1134+799G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823505 | ||||||
| chr9:127823514
|
G | A | 8 | a0002c0004t0001g0075a0002c0004t0001g0076a0002c0004t0001g0077others(5): Show | 8 | HG02155.hp1 NA18947.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.1134+790C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823514 | ||||||
| chr9:127823673
|
C | CT | 41 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0045others(38): Show | 42 | HG00323.hp1 HG01071.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.1134+630dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823673 | ||||||
| chr9:127823673
|
C | CTT | 29 | a0001c0001t0001g0012a0001c0001t0001g0051a0001c0001t0001g0138others(26): Show | 29 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1134+629_1134+630d others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823673 | ||||||
| chr9:127823673
|
C | CTTTT | 11 | a0002c0004t0001g0067a0002c0004t0001g0077a0002c0004t0001g0083others(8): Show | 11 | HG00544.hp1 HG02135.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1134+627_1134+630d others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823673 | ||||||
| chr9:127823673
|
CT | C | 10 | a0001c0001t0001g0160a0001c0001t0001g0170a0001c0001t0001g0183others(7): Show | 10 | HG00438.hp2 HG02132.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1134+630delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823673 | ||||||
| chr9:127823712
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1134+592G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823712 | ||||||
| chr9:127823816
|
G | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 121 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1134+488C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823816 | ||||||
| chr9:127824504
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.992-58C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824504 | ||||||
| chr9:127824512
|
C | CT | 143 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(140): Show | 145 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.992-67dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | ||||||
| chr9:127824512
|
C | CTT | 58 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0012others(55): Show | 59 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.992-68_992-67dupAA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | ||||||
| chr9:127824512
|
C | CTTT | 6 | a0001c0001t0001g0142a0001c0001t0001g0257a0001c0001t0001g0285others(3): Show | 6 | HG00741.hp1 HG01081.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-69_992-67dupAA others(1): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | ||||||
| chr9:127824512
|
CT | C | 7 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.992-67delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | ||||||
| chr9:127824512
|
CTTTTTTT | C | 7 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0111others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.992-73_992-67delAA others(5): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | ||||||
| chr9:127824619
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.992-173T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824619 | ||||||
| chr9:127824742
|
T | A | 7 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0111others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.991+58A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824742 | ||||||
| chr9:127824773
|
A | AGGGAGG | 98 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0078others(95): Show | 99 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.991+21_991+26dupCC others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824773 | ||||||
| chr9:127824987
|
A | G | 1 | a0001c0003t0002g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.817-13T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 6/14 | chr9 | 127824987 | ||||||
| chr9:127825219
|
C | T | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.816+12G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 6/14 | chr9 | 127825219 | ||||||
| chr9:127825628
|
C | CG | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.689+66dupC | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/14 | chr9 | 127825628 | ||||||
| chr9:127825628
|
C | CGG | 132 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0001g0048others(129): Show | 133 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.689+65_689+66dupCC | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/14 | chr9 | 127825628 | ||||||
| chr9:127825875
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0186 | 3 | HG01928.hp2 HG01993.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.524-15C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127825875 | ||||||
| chr9:127825883
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.524-23C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127825883 | ||||||
| chr9:127825890
|
C | T | 5 | a0001c0006t0001g0003a0001c0006t0001g0058a0001c0006t0001g0059others(2): Show | 6 | HG01167.hp1 HG02723.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-30G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127825890 | ||||||
| chr9:127826051
|
C | T | 1 | a0013c0028t0001g0150 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.524-191G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826051 | ||||||
| chr9:127826124
|
A | G | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.524-264T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826124 | ||||||
| chr9:127826305
|
C | A | 1 | a0001c0006t0001g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.523+205G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826305 | ||||||
| chr9:127826353
|
C | T | 3 | a0001c0001t0001g0156a0001c0010t0001g0199a0001c0010t0007g0198 | 3 | NA18612.hp1 NA18994.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.523+157G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826353 | ||||||
| chr9:127826471
|
C | T | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.523+39G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826471 | ||||||
| chr9:127826832
|
C | G | 1 | a0001c0002t0001g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.361-160G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127826832 | ||||||
| chr9:127826953
|
C | T | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.361-281G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127826953 | ||||||
| chr9:127826962
|
C | T | 1 | a0003c0005t0001g0328 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.361-290G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127826962 | ||||||
| chr9:127826977
|
G | GTC | 5 | a0001c0008t0001g0016a0001c0008t0001g0027a0001c0016t0001g0060others(2): Show | 5 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-307_361-306dup others(2): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127826977 | ||||||
| chr9:127827031
|
G | C | 3 | a0003c0005t0001g0327a0003c0005t0001g0329a0003c0005t0001g0330 | 3 | HG01069.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.361-359C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827031 | ||||||
| chr9:127827066
|
C | T | 1 | a0001c0002t0001g0036 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.361-394G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827066 | ||||||
| chr9:127827149
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.361-477C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827149 | ||||||
| chr9:127827556
|
G | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00741.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.361-884C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827556 | ||||||
| chr9:127827574
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.361-902G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827574 | ||||||
| chr9:127827660
|
A | G | 26 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(23): Show | 26 | HG00438.hp1 HG00544.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.361-988T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827660 | ||||||
| chr9:127827787
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.361-1115C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827787 | ||||||
| chr9:127827933
|
T | A | 16 | a0002c0004t0001g0067a0002c0004t0001g0075a0002c0004t0001g0076others(13): Show | 16 | HG00438.hp1 HG00544.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.361-1261A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827933 | ||||||
| chr9:127827961
|
G | C | 1 | a0001c0003t0002g0087 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.361-1289C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827961 | ||||||
| chr9:127827988
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0229 | 3 | HG01884.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.361-1316G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827988 | ||||||
| chr9:127828019
|
C | CA | 42 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0085others(39): Show | 42 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.361-1348dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | ||||||
| chr9:127828019
|
C | CAA | 6 | a0001c0001t0001g0048a0001c0001t0001g0175a0001c0003t0002g0086others(3): Show | 6 | HG00642.hp1 HG01106.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-1349_361-1348d others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | ||||||
| chr9:127828019
|
C | CAAAAAA | 12 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0155others(9): Show | 12 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.361-1353_361-1348d others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | ||||||
| chr9:127828019
|
C | CAAAAAAA | 12 | a0001c0001t0001g0012a0001c0001t0001g0142a0001c0001t0001g0257others(9): Show | 12 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.361-1354_361-1348d others(9): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | ||||||
| chr9:127828019
|
CA | C | 16 | a0001c0001t0001g0072a0001c0001t0001g0082a0001c0001t0001g0098others(13): Show | 16 | HG01169.hp1 HG01496.hp1 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.361-1348delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | ||||||
| chr9:127828064
|
C | T | 1 | a0001c0025t0001g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.361-1392G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828064 | ||||||
| chr9:127828065
|
T | C | 10 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-1393A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828065 | ||||||
| chr9:127828157
|
C | T | 3 | a0004c0009t0001g0054a0004c0009t0005g0055a0004c0015t0005g0032 | 3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.361-1485G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828157 | ||||||
| chr9:127828186
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.360+1501T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828186 | ||||||
| chr9:127828231
|
T | C | 10 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0051others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+1456A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828231 | ||||||
| chr9:127828412
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0229 | 3 | HG01884.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.360+1275A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828412 | ||||||
| chr9:127828553
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0165others(3): Show | 6 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+1134C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828553 | ||||||
| chr9:127828610
|
C | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0128 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.360+1077G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828610 | ||||||
| chr9:127828667
|
C | A | 1 | a0001c0001t0001g0071 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.360+1020G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828667 | ||||||
| chr9:127828792
|
C | T | 9 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | HG01496.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+895G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828792 | ||||||
| chr9:127828824
|
G | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 185 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.360+863C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828824 | ||||||
| chr9:127828833
|
A | C | 1 | a0001c0010t0007g0198 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.360+854T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828833 | ||||||
| chr9:127828881
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.360+806C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828881 | ||||||
| chr9:127829082
|
G | C | 4 | a0001c0008t0001g0016a0001c0008t0001g0027a0001c0024t0001g0141others(1): Show | 4 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+605C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829082 | ||||||
| chr9:127829258
|
C | T | 2 | a0001c0001t0001g0226a0001c0002t0001g0030 | 2 | HG01517.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.360+429G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829258 | ||||||
| chr9:127829296
|
C | G | 1 | a0001c0002t0006g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.360+391G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829296 | ||||||
| chr9:127829333
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.360+354C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829333 | ||||||
| chr9:127829545
|
C | T | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.360+142G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829545 | ||||||
| chr9:127829666
|
G | A | 7 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0111others(4): Show | 7 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+21C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829666 | ||||||
| chr9:127830059
|
A | C | 1 | a0001c0001t0001g0156 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.220-232T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830059 | ||||||
| chr9:127830161
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.220-334C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830161 | ||||||
| chr9:127830340
|
T | TA | 34 | a0001c0001t0001g0010a0001c0001t0001g0051a0001c0001t0001g0071others(31): Show | 34 | HG00621.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.220-514dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830340 | ||||||
| chr9:127830340
|
TA | T | 10 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0111others(7): Show | 10 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-514delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830340 | ||||||
| chr9:127830437
|
G | T | 5 | a0001c0001t0001g0155a0001c0001t0001g0165a0001c0001t0001g0295others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-610C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830437 | ||||||
| chr9:127830440
|
C | G | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-613G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830440 | ||||||
| chr9:127830446
|
T | C | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-619A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830446 | ||||||
| chr9:127830449
|
T | C | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-622A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830449 | ||||||
| chr9:127830453
|
T | A | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-626A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830453 | ||||||
| chr9:127830460
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220-633A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830460 | ||||||
| chr9:127830603
|
C | T | 1 | a0008c0020t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.220-776G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830603 | ||||||
| chr9:127830637
|
C | T | 8 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0111others(5): Show | 8 | HG01891.hp1 HG02040.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-810G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830637 | ||||||
| chr9:127830647
|
CA | C | 9 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0111others(6): Show | 9 | HG01891.hp1 HG02040.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-821delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830647 | ||||||
| chr9:127830713
|
A | G | 4 | a0001c0006t0001g0003a0001c0006t0001g0058a0001c0006t0001g0059others(1): Show | 5 | HG01167.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-886T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830713 | ||||||
| chr9:127830889
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.220-1062C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830889 | ||||||
| chr9:127831068
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.220-1241C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831068 | ||||||
| chr9:127831074
|
A | T | 1 | a0002c0004t0001g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.220-1247T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831074 | ||||||
| chr9:127831119
|
A | G | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220-1292T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831119 | ||||||
| chr9:127831159
|
A | AT | 22 | a0001c0001t0001g0053a0001c0001t0001g0071a0001c0001t0001g0078others(19): Show | 22 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.220-1333dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831159 | ||||||
| chr9:127831159
|
A | ATT | 24 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0046others(21): Show | 24 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-1334_220-1333d others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831159 | ||||||
| chr9:127831159
|
AT | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0186a0001c0001t0001g0230others(2): Show | 6 | HG01928.hp2 HG01993.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-1333delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831159 | ||||||
| chr9:127831314
|
C | T | 1 | a0001c0025t0001g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.220-1487G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831314 | ||||||
| chr9:127831372
|
G | T | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-1545C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831372 | ||||||
| chr9:127831432
|
A | G | 30 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0053others(27): Show | 30 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.220-1605T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831432 | ||||||
| chr9:127831489
|
T | G | 30 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0053others(27): Show | 30 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.220-1662A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831489 | ||||||
| chr9:127831660
|
C | T | 7 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-1833G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831660 | ||||||
| chr9:127831684
|
C | CT | 30 | a0001c0001t0001g0053a0001c0001t0001g0099a0001c0001t0001g0100others(27): Show | 30 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.220-1858dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831684 | ||||||
| chr9:127831697
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0107 | 2 | HG03017.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.220-1870A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831697 | ||||||
| chr9:127831718
|
G | T | 6 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0165others(3): Show | 6 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-1891C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831718 | ||||||
| chr9:127831785
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0155a0001c0001t0001g0165others(3): Show | 6 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-1958C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831785 | ||||||
| chr9:127831893
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.220-2066T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831893 | ||||||
| chr9:127832003
|
T | C | 1 | a0001c0006t0010g0337 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.220-2176A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832003 | ||||||
| chr9:127832028
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.220-2201C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832028 | ||||||
| chr9:127832040
|
T | G | 14 | a0002c0004t0001g0067a0002c0004t0001g0075a0002c0004t0001g0076others(11): Show | 14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-2213A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832040 | ||||||
| chr9:127832069
|
C | CT | 57 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0014others(54): Show | 57 | HG00597.hp2 HG00741.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.220-2243dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832069 | ||||||
| chr9:127832069
|
C | CTTTTTT | 11 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0155others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.220-2248_220-2243d others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832069 | ||||||
| chr9:127832069
|
CT | C | 7 | a0001c0001t0001g0096a0001c0001t0001g0103a0001c0001t0001g0137others(4): Show | 7 | HG00323.hp1 HG01496.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-2243delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832069 | ||||||
| chr9:127832069
|
CTTTTTTT others(4): Show |
C | 14 | a0002c0004t0001g0067a0002c0004t0001g0075a0002c0004t0001g0076others(11): Show | 14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-2253_220-2243d others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832069 | ||||||
| chr9:127832202
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.220-2375C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832202 | ||||||
| chr9:127832223
|
T | G | 1 | a0008c0020t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.220-2396A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832223 | ||||||
| chr9:127832473
|
C | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.220-2646G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832473 | ||||||
| chr9:127832518
|
CT | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.220-2692delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832518 | ||||||
| chr9:127832530
|
T | G | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220-2703A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832530 | ||||||
| chr9:127832572
|
G | A | 1 | a0001c0007t0001g0214 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.220-2745C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832572 | ||||||
| chr9:127832583
|
C | G | 21 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0259others(18): Show | 21 | HG00438.hp1 HG00642.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.220-2756G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832583 | ||||||
| chr9:127832607
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.220-2780C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832607 | ||||||
| chr9:127832610
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.220-2783G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832610 | ||||||
| chr9:127832837
|
A | G | 24 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0111others(21): Show | 24 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-3010T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832837 | ||||||
| chr9:127832972
|
G | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.220-3145C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832972 | ||||||
| chr9:127833248
|
G | A | 14 | a0002c0004t0001g0067a0002c0004t0001g0075a0002c0004t0001g0076others(11): Show | 14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-3421C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833248 | ||||||
| chr9:127833350
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.220-3523G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833350 | ||||||
| chr9:127833488
|
C | G | 14 | a0002c0004t0001g0067a0002c0004t0001g0075a0002c0004t0001g0076others(11): Show | 14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-3661G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833488 | ||||||
| chr9:127833522
|
C | CA | 27 | a0001c0001t0001g0101a0001c0001t0001g0113a0001c0001t0001g0119others(24): Show | 27 | HG00423.hp2 HG01071.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.220-3696dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833522 | ||||||
| chr9:127833522
|
CA | C | 29 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0064others(26): Show | 30 | HG01081.hp2 HG01167.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.220-3696delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833522 | ||||||
| chr9:127833522
|
CAA | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 140 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.220-3697_220-3696d others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833522 | ||||||
| chr9:127833522
|
CAAAA | C | 19 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0259others(16): Show | 19 | HG00438.hp1 HG00642.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.220-3699_220-3696d others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833522 | ||||||
| chr9:127833632
|
C | G | 1 | a0012c0018t0001g0267 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.220-3805G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833632 | ||||||
| chr9:127833819
|
C | T | 17 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0138others(14): Show | 17 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-3992G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833819 | ||||||
| chr9:127833865
|
T | C | 1 | a0001c0024t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.220-4038A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833865 | ||||||
| chr9:127833907
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.220-4080A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833907 | ||||||
| chr9:127833909
|
A | G | 336 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(333): Show | 341 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.220-4082T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833909 | ||||||
| chr9:127834098
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.220-4271C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834098 | ||||||
| chr9:127834141
|
C | T | 3 | a0001c0002t0001g0015a0001c0008t0001g0016a0003c0030t0001g0333 | 3 | HG01099.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.220-4314G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834141 | ||||||
| chr9:127834173
|
A | G | 5 | a0001c0001t0001g0155a0001c0001t0001g0165a0001c0001t0001g0295others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-4346T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834173 | ||||||
| chr9:127834198
|
A | G | 1 | a0001c0002t0006g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-4371T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834198 | ||||||
| chr9:127834265
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.220-4438A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834265 | ||||||
| chr9:127834269
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.220-4442C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834269 | ||||||
| chr9:127834301
|
G | A | 1 | a0001c0006t0010g0337 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.220-4474C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834301 | ||||||
| chr9:127834387
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.220-4560C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834387 | ||||||
| chr9:127834395
|
G | ACCCAACT others(160): Show |
1 | a0001c0001t0001g0094 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.220-4568_220-4567i others(169): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834395 | ||||||
| chr9:127834395
|
G | ACCCAACT others(160): Show |
4 | a0001c0001t0001g0106a0001c0001t0003g0007a0001c0001t0003g0008others(1): Show | 4 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-4568_220-4567i others(169): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834395 | ||||||
| chr9:127834498
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.220-4671C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834498 | ||||||
| chr9:127834537
|
T | G | 24 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(21): Show | 24 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-4710A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834537 | ||||||
| chr9:127834695
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.220-4868C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834695 | ||||||
| chr9:127834827
|
C | T | 1 | a0001c0022t0001g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220-5000G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834827 | ||||||
| chr9:127834835
|
T | TAGGTTGG others(291): Show |
1 | a0001c0001t0001g0263 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.220-5009_220-5008i others(300): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | ||||||
| chr9:127834835
|
T | TAGGTTGG others(289): Show |
1 | a0001c0001t0001g0266 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.220-5009_220-5008i others(298): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | ||||||
| chr9:127834835
|
T | TAGGTTGG others(291): Show |
9 | a0001c0001t0001g0138a0001c0001t0001g0142a0001c0001t0001g0215others(6): Show | 9 | HG02602.hp2 HG02683.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.220-5009_220-5008i others(300): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | ||||||
| chr9:127834835
|
T | TAGGTTGG others(292): Show |
1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220-5009_220-5008i others(301): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | ||||||
| chr9:127834835
|
T | TAGGTTGG others(292): Show |
4 | a0001c0001t0001g0281a0001c0001t0001g0318a0001c0001t0001g0321others(1): Show | 4 | HG03139.hp1 HG03239.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-5009_220-5008i others(301): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | ||||||
| chr9:127834835
|
T | TAGGTTGG others(293): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0317a0001c0001t0001g0319others(5): Show | 8 | HG02280.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-5009_220-5008i others(302): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | ||||||
| chr9:127834835
|
T | TAGGTTGG others(294): Show |
1 | a0001c0001t0001g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.220-5009_220-5008i others(303): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | ||||||
| chr9:127834895
|
A | G | 1 | a0001c0002t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.220-5068T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834895 | ||||||
| chr9:127834944
|
T | C | 53 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0116others(50): Show | 54 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.220-5117A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834944 | ||||||
| chr9:127835325
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.220-5498C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835325 | ||||||
| chr9:127835680
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG01496.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.220-5853G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835680 | ||||||
| chr9:127835696
|
C | T | 1 | a0001c0002t0001g0314 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.220-5869G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835696 | ||||||
| chr9:127835718
|
T | G | 1 | a0001c0001t0001g0127 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-5891A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835718 | ||||||
| chr9:127835774
|
G | GA | 7 | a0001c0001t0001g0230a0001c0001t0001g0240a0001c0001t0001g0241others(4): Show | 7 | HG02129.hp2 NA18960.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-5948dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835774 | ||||||
| chr9:127835784
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0304 | 2 | HG03834.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.220-5957C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835784 | ||||||
| chr9:127835846
|
G | A | 33 | a0001c0001t0001g0115a0001c0001t0001g0138a0001c0001t0001g0143others(30): Show | 33 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.220-6019C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835846 | ||||||
| chr9:127835934
|
T | A | 8 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(5): Show | 8 | HG02622.hp2 HG02922.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-6107A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835934 | ||||||
| chr9:127835982
|
G | A | 8 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(5): Show | 8 | HG02622.hp2 HG02922.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-6155C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835982 | ||||||
| chr9:127836021
|
A | G | 8 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(5): Show | 8 | HG02622.hp2 HG02922.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-6194T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836021 | ||||||
| chr9:127836109
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.220-6282G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836109 | ||||||
| chr9:127836155
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.220-6328G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836155 | ||||||
| chr9:127836177
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.220-6350T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836177 | ||||||
| chr9:127836267
|
C | T | 11 | a0001c0001t0001g0294a0001c0001t0001g0306a0003c0005t0001g0327others(8): Show | 11 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.220-6440G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836267 | ||||||
| chr9:127836645
|
G | A | 62 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0051others(59): Show | 64 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.219+6449C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836645 | ||||||
| chr9:127836880
|
T | C | 1 | a0002c0004t0001g0093 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.219+6214A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836880 | ||||||
| chr9:127837216
|
C | T | 1 | a0001c0003t0002g0086 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.219+5878G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837216 | ||||||
| chr9:127837384
|
A | T | 1 | a0001c0001t0008g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219+5710T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837384 | ||||||
| chr9:127837401
|
T | G | 2 | a0001c0002t0001g0052a0001c0002t0001g0056 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.219+5693A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837401 | ||||||
| chr9:127837476
|
C | A | 1 | a0001c0022t0001g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219+5618G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837476 | ||||||
| chr9:127837679
|
C | T | 6 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(3): Show | 6 | HG00099.hp2 HG00738.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+5415G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837679 | ||||||
| chr9:127837774
|
G | GCATC | 36 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0064others(33): Show | 36 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.219+5316_219+5319d others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837774 | ||||||
| chr9:127837774
|
G | GCATCCAT others(1): Show |
3 | a0001c0001t0001g0166a0001c0001t0001g0226a0001c0001t0001g0263 | 3 | HG01169.hp1 HG04228.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.219+5312_219+5319d others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837774 | ||||||
| chr9:127837774
|
G | GCATCCAT others(5): Show |
1 | a0001c0001t0001g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.219+5308_219+5319d others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837774 | ||||||
| chr9:127837810
|
C | CCACATCC others(7): Show |
1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.219+5283_219+5284i others(16): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | ||||||
| chr9:127837810
|
C | CCATCCAT others(15): Show |
18 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(15): Show | 19 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.219+5283_219+5284i others(24): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | ||||||
| chr9:127837810
|
C | CCATCCAT others(19): Show |
25 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0103others(22): Show | 26 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.219+5283_219+5284i others(28): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | ||||||
| chr9:127837810
|
C | CCATCCAT others(23): Show |
20 | a0001c0001t0001g0046a0001c0001t0001g0053a0001c0001t0001g0155others(17): Show | 20 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.219+5283_219+5284i others(32): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | ||||||
| chr9:127837810
|
C | CCATCCAT others(27): Show |
11 | a0001c0001t0001g0045a0001c0001t0001g0178a0001c0001t0001g0292others(8): Show | 11 | HG00738.hp2 HG01106.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.219+5283_219+5284i others(36): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | ||||||
| chr9:127837880
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.219+5214C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837880 | ||||||
| chr9:127838042
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.219+5052C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838042 | ||||||
| chr9:127838147
|
C | T | 7 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+4947G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838147 | ||||||
| chr9:127838150
|
AC | A | 8 | a0001c0001t0001g0161a0001c0001t0001g0200a0001c0001t0001g0243others(5): Show | 8 | HG02056.hp1 HG02083.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.219+4943delG | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838150 | ||||||
| chr9:127838183
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.219+4911T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838183 | ||||||
| chr9:127838269
|
G | A | 1 | a0001c0001t0001g0242 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219+4825C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838269 | ||||||
| chr9:127838374
|
A | G | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.219+4720T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838374 | ||||||
| chr9:127838513
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0212 | 2 | NA18960.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.219+4581G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838513 | ||||||
| chr9:127838800
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.219+4294C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838800 | ||||||
| chr9:127838890
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG00408.hp1 HG00673.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.219+4204G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838890 | ||||||
| chr9:127838998
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 138 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.219+4096G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838998 | ||||||
| chr9:127839020
|
A | C | 1 | a0001c0001t0001g0270 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.219+4074T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839020 | ||||||
| chr9:127839115
|
C | T | 8 | a0001c0001t0001g0161a0001c0001t0001g0200a0001c0001t0001g0243others(5): Show | 8 | HG02056.hp1 HG02083.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.219+3979G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839115 | ||||||
| chr9:127839178
|
C | T | 8 | a0003c0005t0001g0327a0003c0005t0001g0328a0003c0005t0001g0329others(5): Show | 8 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+3916G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839178 | ||||||
| chr9:127839205
|
C | T | 3 | a0001c0006t0001g0003a0001c0006t0001g0058a0001c0006t0001g0059 | 4 | HG01167.hp1 HG02723.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+3889G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839205 | ||||||
| chr9:127839297
|
C | T | 65 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0065others(62): Show | 67 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.219+3797G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839297 | ||||||
| chr9:127839317
|
A | G | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+3777T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839317 | ||||||
| chr9:127839326
|
A | G | 335 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(332): Show | 340 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.219+3768T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839326 | ||||||
| chr9:127839462
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0140a0001c0001t0001g0142others(3): Show | 6 | HG02145.hp2 HG02280.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+3632C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839462 | ||||||
| chr9:127839562
|
T | C | 1 | a0008c0020t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.219+3532A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839562 | ||||||
| chr9:127839595
|
G | A | 1 | a0001c0002t0001g0034 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219+3499C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839595 | ||||||
| chr9:127839672
|
CAGCCTCT others(5): Show |
C | 1 | a0001c0001t0001g0299 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219+3410_219+3421d others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839672 | ||||||
| chr9:127839746
|
C | T | 12 | a0001c0001t0001g0071a0001c0001t0001g0078a0001c0001t0001g0080others(9): Show | 12 | NA18941.hp1 NA18943.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+3348G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839746 | ||||||
| chr9:127839845
|
T | C | 90 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0051others(87): Show | 92 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.219+3249A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839845 | ||||||
| chr9:127839854
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.219+3240G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839854 | ||||||
| chr9:127839951
|
G | A | 53 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0051others(50): Show | 55 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.219+3143C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839951 | ||||||
| chr9:127839971
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.219+3123C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839971 | ||||||
| chr9:127840017
|
G | A | 10 | a0001c0001t0001g0306a0003c0005t0001g0327a0003c0005t0001g0328others(7): Show | 10 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.219+3077C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840017 | ||||||
| chr9:127840129
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(218): Show | 224 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.219+2965C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840129 | ||||||
| chr9:127840147
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.219+2947C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840147 | ||||||
| chr9:127840281
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.219+2813C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840281 | ||||||
| chr9:127840504
|
A | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+2590T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840504 | ||||||
| chr9:127840606
|
T | C | 1 | a0002c0004t0001g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.219+2488A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840606 | ||||||
| chr9:127840872
|
A | C | 32 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0071others(29): Show | 32 | HG00438.hp1 HG01099.hp2 HG01975.hp1 others(29): Show |
intron_variant | MODIFIER | c.219+2222T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840872 | ||||||
| chr9:127841174
|
C | T | 12 | a0001c0001t0001g0306a0003c0005t0001g0325a0003c0005t0001g0326others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+1920G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841174 | ||||||
| chr9:127841215
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.219+1879C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841215 | ||||||
| chr9:127841367
|
C | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0016t0001g0060 | 3 | HG02572.hp1 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.219+1727G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841367 | ||||||
| chr9:127841491
|
G | GA | 12 | a0001c0001t0001g0306a0003c0005t0001g0325a0003c0005t0001g0326others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+1602dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841491 | ||||||
| chr9:127841655
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.219+1439C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841655 | ||||||
| chr9:127841717
|
G | A | 1 | a0003c0005t0001g0324 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+1377C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841717 | ||||||
| chr9:127841861
|
G | A | 3 | a0003c0005t0001g0327a0003c0005t0001g0329a0003c0005t0001g0330 | 3 | HG01069.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.219+1233C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841861 | ||||||
| chr9:127841873
|
G | A | 5 | a0001c0001t0001g0297a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG02622.hp2 NA18522.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.219+1221C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841873 | ||||||
| chr9:127842025
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG01884.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.219+1069G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842025 | ||||||
| chr9:127842037
|
G | T | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | NA18941.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.219+1057C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842037 | ||||||
| chr9:127842095
|
GGTCTCCT others(10): Show |
G | 1 | a0003c0005t0001g0336 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.219+982_219+998del others(17): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842095 | ||||||
| chr9:127842220
|
CTTTTCTT others(6): Show |
C | 1 | a0001c0002t0001g0315 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.219+861_219+873del others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842220 | ||||||
| chr9:127842225
|
CT | C | 49 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0065others(46): Show | 50 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+868delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842225 | ||||||
| chr9:127842225
|
CTT | C | 87 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0064others(84): Show | 88 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.219+867_219+868del others(2): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842225 | ||||||
| chr9:127842225
|
CTTT | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.219+866_219+868del others(3): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842225 | ||||||
| chr9:127842231
|
T | C | 8 | a0001c0001t0001g0065a0001c0001t0001g0281a0001c0001t0001g0317others(5): Show | 8 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+863A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842231 | ||||||
| chr9:127842232
|
T | C | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.219+862A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842232 | ||||||
| chr9:127842285
|
G | A | 3 | a0001c0002t0001g0052a0001c0002t0001g0056a0001c0002t0006g0057 | 3 | HG03041.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.219+809C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842285 | ||||||
| chr9:127842371
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG01884.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.219+723C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842371 | ||||||
| chr9:127842427
|
T | A | 7 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+667A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842427 | ||||||
| chr9:127842492
|
C | G | 1 | a0001c0001t0001g0049 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.219+602G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842492 | ||||||
| chr9:127842553
|
T | G | 12 | a0001c0001t0001g0306a0003c0005t0001g0325a0003c0005t0001g0326others(9): Show | 12 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+541A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842553 | ||||||
| chr9:127842587
|
A | G | 334 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(331): Show | 339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.219+507T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842587 | ||||||
| chr9:127842600
|
T | A | 1 | a0008c0020t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.219+494A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842600 | ||||||
| chr9:127842834
|
C | CA | 41 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0017others(38): Show | 42 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.219+259dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842834 | ||||||
| chr9:127843069
|
C | A | 20 | a0001c0001t0001g0115a0001c0001t0001g0138a0001c0001t0001g0262others(17): Show | 20 | HG00741.hp1 HG01516.hp1 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.219+25G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127843069 | ||||||
| chr9:127843398
|
C | G | 4 | a0001c0001t0001g0276a0001c0002t0001g0023a0001c0002t0001g0025others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-153G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843398 | ||||||
| chr9:127843460
|
A | G | 13 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0065others(10): Show | 13 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-215T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843460 | ||||||
| chr9:127843501
|
T | C | 5 | a0001c0006t0001g0003a0001c0006t0001g0058a0001c0006t0001g0059others(2): Show | 6 | HG01167.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-256A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843501 | ||||||
| chr9:127843623
|
ATGTATAT others(9): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68-394_68-379delCA others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843623 | ||||||
| chr9:127843658
|
C | T | 3 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0316 | 3 | HG04184.hp2 NA18941.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.68-413G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843658 | ||||||
| chr9:127843688
|
C | CAT | 290 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(287): Show | 294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.68-445_68-444dupAT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843688 | ||||||
| chr9:127843699
|
A | C | 1 | a0013c0028t0001g0150 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.68-454T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843699 | ||||||
| chr9:127843715
|
A | C | 1 | a0013c0028t0001g0150 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.68-470T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843715 | ||||||
| chr9:127843732
|
C | CACATATA others(5): Show |
1 | a0001c0001t0001g0321 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.68-488_68-487insAT others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | CACATATA others(7): Show |
2 | a0001c0001t0001g0281a0001c0001t0001g0320 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.68-488_68-487insAT others(12): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | CAT | 5 | a0001c0001t0001g0115a0001c0001t0001g0143a0001c0001t0001g0222others(2): Show | 5 | HG00639.hp2 HG00642.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-489_68-488dupAT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | CATAT | 6 | a0001c0001t0001g0094a0001c0001t0001g0221a0001c0001t0001g0225others(3): Show | 6 | HG00609.hp2 HG01192.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-488_68-487insAT others(2): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | CATATAT | 12 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(9): Show | 12 | HG00438.hp1 HG01081.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-488_68-487insAT others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | CATATATA others(1): Show |
8 | a0001c0001t0001g0070a0001c0001t0001g0310a0001c0001t0001g0316others(5): Show | 9 | HG01891.hp2 HG01975.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-488_68-487insAT others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | CATATATA others(3): Show |
2 | a0001c0013t0001g0041a0004c0015t0005g0032 | 2 | HG01074.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.68-488_68-487insAT others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | CATATATA others(5): Show |
4 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0006t0001g0003others(1): Show | 5 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-488_68-487insAT others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | CATATATA others(7): Show |
1 | a0001c0002t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-488_68-487insAT others(12): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | CATATATA others(9): Show |
1 | a0004c0009t0001g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.68-488_68-487insAT others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG01884.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.68-487G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843732
|
CATACATA others(3): Show |
C | 4 | a0001c0002t0001g0069a0001c0002t0001g0312a0001c0002t0001g0313others(1): Show | 4 | NA18981.hp1 NA19002.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-497_68-488delAT others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | ||||||
| chr9:127843734
|
T | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0065others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-489A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843734 | ||||||
| chr9:127843736
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(321): Show | 329 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.68-491G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843736 | ||||||
| chr9:127843745
|
ATATATAT others(4): Show |
A | 1 | a0002c0012t0001g0309 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.68-511_68-501delAT others(9): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843745 | ||||||
| chr9:127843747
|
ATATATAT others(5): Show |
A | 1 | a0001c0002t0001g0034 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.68-514_68-503delAA others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843747 | ||||||
| chr9:127843749
|
ATATATAT others(3): Show |
A | 2 | a0001c0002t0001g0052a0001c0002t0001g0315 | 2 | HG03041.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.68-514_68-505delAA others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843749 | ||||||
| chr9:127843751
|
ATATATTT others(3): Show |
A | 2 | a0001c0001t0001g0049a0001c0001t0001g0064 | 2 | HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.68-516_68-507delAA others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843751 | ||||||
| chr9:127843753
|
ATATTTTT others(3): Show |
A | 5 | a0001c0001t0001g0116a0001c0001t0001g0230a0001c0001t0001g0231others(2): Show | 5 | NA18960.hp2 NA18998.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-518_68-509delAA others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843753 | ||||||
| chr9:127843753
|
ATATTTTT others(9): Show |
A | 1 | a0001c0001t0001g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.68-524_68-509delAA others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843753 | ||||||
| chr9:127843755
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-511_68-510insAT others(27): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0318 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.68-511_68-510insAA others(15): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.68-511_68-510insAA others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0317 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.68-511_68-510insAA others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
A | T | 1 | a0001c0001t0001g0320 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.68-510T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
ATTTT | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG01255.hp2 HG02273.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-514_68-511delAA others(2): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
ATTTTT | A | 7 | a0001c0001t0001g0147a0001c0001t0001g0274a0001c0001t0001g0295others(4): Show | 7 | HG01123.hp2 HG02622.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-515_68-511delAA others(3): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
ATTTTTT | A | 13 | a0001c0001t0001g0113a0001c0001t0001g0124a0001c0001t0001g0137others(10): Show | 13 | HG01346.hp2 HG01952.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-516_68-511delAA others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
ATTTTTTT others(1): Show |
A | 34 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0107others(31): Show | 35 | HG00597.hp2 HG01070.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.68-518_68-511delAA others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
ATTTTTTT others(3): Show |
A | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0047others(94): Show | 99 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.68-520_68-511delAA others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
ATTTTTTT others(4): Show |
A | 11 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0210others(8): Show | 11 | HG00099.hp2 HG02135.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-521_68-511delAA others(9): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
ATTTTTTT others(5): Show |
A | 14 | a0001c0001t0001g0114a0001c0001t0001g0159a0001c0001t0001g0160others(11): Show | 14 | HG00438.hp2 HG00673.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-522_68-511delAA others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843755
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0212 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.68-523_68-511delAA others(11): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | ||||||
| chr9:127843756
|
T | TA | 4 | a0001c0001t0001g0223a0001c0003t0002g0013a0003c0005t0001g0331others(1): Show | 4 | HG01516.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-512_68-511insT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | ||||||
| chr9:127843756
|
T | TATA | 8 | a0001c0001t0001g0138a0001c0001t0001g0262a0001c0001t0001g0263others(5): Show | 8 | HG01993.hp1 HG02683.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-512_68-511insTA others(1): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | ||||||
| chr9:127843756
|
T | TATATA | 12 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0096others(9): Show | 12 | HG01069.hp1 HG02055.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-512_68-511insTA others(3): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | ||||||
| chr9:127843756
|
T | TATATATA | 9 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 9 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-512_68-511insTA others(5): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | ||||||
| chr9:127843756
|
T | TATATATA others(2): Show |
9 | a0001c0001t0001g0046a0001c0001t0001g0065a0001c0001t0001g0095others(6): Show | 9 | HG01099.hp2 HG01192.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-512_68-511insTA others(7): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | ||||||
| chr9:127843756
|
T | TATATATA others(4): Show |
1 | a0006c0026t0001g0264 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.68-512_68-511insTA others(9): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | ||||||
| chr9:127843756
|
T | TATATATA others(6): Show |
2 | a0001c0002t0001g0035a0001c0002t0001g0296 | 2 | HG01346.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.68-512_68-511insTA others(11): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | ||||||
| chr9:127843756
|
T | TATATATA others(8): Show |
2 | a0001c0001t0001g0322a0001c0008t0001g0016 | 2 | HG01099.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.68-512_68-511insTA others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | ||||||
| chr9:127843756
|
T | TATATATA others(10): Show |
3 | a0001c0002t0001g0029a0001c0006t0001g0058a0001c0006t0001g0059 | 3 | HG02723.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.68-512_68-511insTA others(15): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | ||||||
| chr9:127843757
|
T | A | 41 | a0001c0001t0001g0012a0001c0001t0001g0051a0001c0001t0001g0068others(38): Show | 43 | HG00438.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.68-512A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843757 | ||||||
| chr9:127843758
|
T | A | 39 | a0001c0001t0001g0065a0001c0001t0001g0095a0001c0001t0001g0096others(36): Show | 39 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-513A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843758 | ||||||
| chr9:127843759
|
T | A | 26 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0051others(23): Show | 27 | HG00639.hp2 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.68-514A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843759 | ||||||
| chr9:127843760
|
T | A | 19 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0226others(16): Show | 19 | HG00738.hp1 HG01496.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.68-515A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843760 | ||||||
| chr9:127843761
|
T | A | 21 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0051others(18): Show | 21 | HG00642.hp2 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.68-516A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843761 | ||||||
| chr9:127843762
|
T | A | 15 | a0001c0001t0001g0147a0001c0001t0001g0223a0001c0001t0001g0226others(12): Show | 15 | HG00738.hp1 HG01123.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-517A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843762 | ||||||
| chr9:127843763
|
T | A | 28 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0068others(25): Show | 28 | HG00642.hp2 HG01255.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.68-518A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843763 | ||||||
| chr9:127843764
|
T | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0147a0001c0001t0001g0162others(12): Show | 15 | HG00738.hp1 HG01123.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-519A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843764 | ||||||
| chr9:127843765
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(52): Show | 56 | HG00597.hp2 HG01070.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.68-520A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843765 | ||||||
| chr9:127843766
|
T | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0109a0001c0001t0001g0147others(12): Show | 15 | HG00738.hp1 HG01123.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-521A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843766 | ||||||
| chr9:127843767
|
T | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 124 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.68-522A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843767 | ||||||
| chr9:127843768
|
T | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0053a0001c0001t0001g0101others(15): Show | 18 | HG00099.hp2 HG01243.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-523A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843768 | ||||||
| chr9:127843769
|
T | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 126 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.68-524A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843769 | ||||||
| chr9:127843770
|
T | A | 15 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0109others(12): Show | 15 | HG00099.hp2 HG01243.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-525A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843770 | ||||||
| chr9:127843771
|
T | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0098others(78): Show | 83 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.68-526A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843771 | ||||||
| chr9:127843772
|
T | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0101a0001c0001t0001g0208others(6): Show | 9 | HG00099.hp2 HG02135.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-527A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843772 | ||||||
| chr9:127843773
|
T | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0113a0001c0001t0001g0213others(10): Show | 14 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-528A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843773 | ||||||
| chr9:127843775
|
T | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0283 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.68-530A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843775 | ||||||
| chr9:127843998
|
T | C | 337 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.68-753A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843998 | ||||||
| chr9:127844409
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0219others(1): Show | 4 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1164C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844409 | ||||||
| chr9:127844469
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG01884.hp1 HG02895.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1224C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844469 | ||||||
| chr9:127844501
|
G | GCAGCCT | 256 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.68-1262_68-1257dup others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844501 | ||||||
| chr9:127844709
|
A | G | 1 | a0008c0020t0001g0061 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.68-1464T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844709 | ||||||
| chr9:127844718
|
C | T | 10 | a0001c0001t0001g0143a0001c0001t0001g0220a0001c0001t0001g0221others(7): Show | 10 | HG00642.hp2 HG00738.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-1473G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844718 | ||||||
| chr9:127844727
|
C | G | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-1482G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844727 | ||||||
| chr9:127844927
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-1682G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844927 | ||||||
| chr9:127845031
|
G | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146 | 3 | HG01255.hp2 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.68-1786C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845031 | ||||||
| chr9:127845080
|
G | A | 115 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0103others(112): Show | 115 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.68-1835C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845080 | ||||||
| chr9:127845176
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.68-1931G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845176 | ||||||
| chr9:127845209
|
C | T | 3 | a0001c0001t0001g0303a0001c0003t0002g0302a0001c0016t0001g0060 | 3 | HG02970.hp1 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-1964G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845209 | ||||||
| chr9:127845239
|
T | G | 252 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(249): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.68-1994A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845239 | ||||||
| chr9:127845359
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0008g0139others(3): Show | 6 | HG02145.hp2 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-2114G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845359 | ||||||
| chr9:127845433
|
T | C | 40 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0017others(37): Show | 41 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.68-2188A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845433 | ||||||
| chr9:127845599
|
T | C | 1 | a0001c0003t0002g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.68-2354A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845599 | ||||||
| chr9:127845832
|
A | G | 337 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.68-2587T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845832 | ||||||
| chr9:127845853
|
T | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(256): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.68-2608A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845853 | ||||||
| chr9:127845968
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.68-2723T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845968 | ||||||
| chr9:127846017
|
T | G | 46 | a0001c0001t0001g0065a0001c0001t0001g0281a0001c0001t0001g0317others(43): Show | 47 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.68-2772A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846017 | ||||||
| chr9:127846073
|
T | G | 9 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0297others(6): Show | 9 | HG02280.hp2 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-2828A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846073 | ||||||
| chr9:127846128
|
G | A | 6 | a0001c0002t0001g0069a0001c0002t0001g0312a0001c0002t0001g0313others(3): Show | 6 | NA18963.hp2 NA18981.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-2883C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846128 | ||||||
| chr9:127846160
|
C | A | 3 | a0001c0002t0001g0052a0001c0002t0001g0056a0001c0002t0006g0057 | 3 | HG03041.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.68-2915G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846160 | ||||||
| chr9:127846259
|
G | A | 38 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0017others(35): Show | 39 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-3014C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846259 | ||||||
| chr9:127846549
|
G | T | 1 | a0001c0002t0001g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68-3304C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846549 | ||||||
| chr9:127846620
|
G | C | 2 | a0001c0001t0001g0303a0001c0003t0002g0302 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.68-3375C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846620 | ||||||
| chr9:127846667
|
G | A | 19 | a0001c0001t0001g0138a0001c0001t0001g0262a0001c0001t0001g0263others(16): Show | 19 | HG00741.hp1 HG01993.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-3422C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846667 | ||||||
| chr9:127846818
|
G | A | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-3573C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846818 | ||||||
| chr9:127847043
|
CCTCT | C | 6 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-3802_68-3799del others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847043 | ||||||
| chr9:127847050
|
GAGCCTCA others(5): Show |
G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.68-3817_68-3806del others(12): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847050 | ||||||
| chr9:127847096
|
G | T | 3 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0316 | 3 | HG04184.hp2 NA18941.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.68-3851C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847096 | ||||||
| chr9:127847237
|
T | C | 1 | a0001c0001t0012g0339 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-3992A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847237 | ||||||
| chr9:127847278
|
C | T | 2 | a0001c0001t0001g0303a0001c0003t0002g0302 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.68-4033G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847278 | ||||||
| chr9:127847450
|
C | T | 3 | a0001c0002t0001g0052a0001c0002t0001g0056a0001c0002t0006g0057 | 3 | HG03041.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.68-4205G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847450 | ||||||
| chr9:127847469
|
C | T | 301 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(298): Show | 305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.68-4224G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847469 | ||||||
| chr9:127847560
|
C | A | 1 | a0001c0003t0002g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.68-4315G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847560 | ||||||
| chr9:127847560
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0295 | 2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.68-4315G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847560 | ||||||
| chr9:127847638
|
C | T | 2 | a0001c0001t0001g0303a0001c0003t0002g0302 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.68-4393G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847638 | ||||||
| chr9:127847669
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.68-4424G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847669 | ||||||
| chr9:127847720
|
C | G | 2 | a0001c0016t0001g0060a0008c0020t0001g0061 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4475G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847720 | ||||||
| chr9:127847736
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.68-4491G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847736 | ||||||
| chr9:127847797
|
C | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00741.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.68-4552G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847797 | ||||||
| chr9:127847944
|
T | C | 1 | a0001c0001t0001g0316 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.68-4699A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847944 | ||||||
| chr9:127847992
|
T | C | 1 | a0002c0004t0001g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.68-4747A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847992 | ||||||
| chr9:127848062
|
C | A | 1 | a0001c0001t0001g0287 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.68-4817G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848062 | ||||||
| chr9:127848083
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0002c0012t0001g0309 | 3 | HG02572.hp1 NA18522.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.68-4838G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848083 | ||||||
| chr9:127848084
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.68-4839C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848084 | ||||||
| chr9:127848116
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0003t0002g0013 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.68-4871G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848116 | ||||||
| chr9:127848166
|
T | C | 335 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(332): Show | 340 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.68-4921A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848166 | ||||||
| chr9:127848262
|
A | G | 335 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(332): Show | 340 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.68-5017T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848262 | ||||||
| chr9:127848288
|
C | CT | 32 | a0001c0001t0001g0098a0001c0001t0001g0103a0001c0001t0001g0104others(29): Show | 32 | HG01070.hp1 HG01433.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.68-5044dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848288 | ||||||
| chr9:127848329
|
T | G | 335 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(332): Show | 340 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.68-5084A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848329 | ||||||
| chr9:127848446
|
C | G | 13 | a0001c0001t0001g0306a0003c0005t0001g0325a0003c0005t0001g0326others(10): Show | 13 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-5201G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848446 | ||||||
| chr9:127848471
|
A | G | 2 | a0001c0016t0001g0060a0008c0020t0001g0061 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.68-5226T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848471 | ||||||
| chr9:127848507
|
T | C | 335 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(332): Show | 340 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.68-5262A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848507 | ||||||
| chr9:127848549
|
G | A | 338 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 343 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.68-5304C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848549 | ||||||
| chr9:127848590
|
A | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.68-5345T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848590 | ||||||
| chr9:127848817
|
G | A | 3 | a0001c0006t0001g0003a0001c0006t0001g0058a0001c0006t0001g0059 | 4 | HG01167.hp1 HG02723.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+5472C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848817 | ||||||
| chr9:127848881
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.67+5408G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848881 | ||||||
| chr9:127849100
|
G | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.67+5189C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849100 | ||||||
| chr9:127849125
|
G | A | 2 | a0001c0001t0001g0051a0001c0022t0001g0050 | 2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67+5164C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849125 | ||||||
| chr9:127849179
|
C | A | 1 | a0001c0006t0001g0059 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.67+5110G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849179 | ||||||
| chr9:127849244
|
C | G | 44 | a0001c0001t0001g0306a0001c0002t0001g0002a0001c0002t0001g0015others(41): Show | 45 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.67+5045G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849244 | ||||||
| chr9:127849512
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0288 | 2 | HG02056.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.67+4777C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849512 | ||||||
| chr9:127849523
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.67+4766G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849523 | ||||||
| chr9:127849614
|
G | A | 3 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009 | 3 | HG00609.hp1 HG02129.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.67+4675C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849614 | ||||||
| chr9:127849626
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.67+4663C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849626 | ||||||
| chr9:127849712
|
C | T | 2 | a0003c0005t0001g0325a0003c0005t0001g0326 | 2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.67+4577G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849712 | ||||||
| chr9:127849732
|
A | C | 1 | a0001c0001t0001g0112 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.67+4557T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849732 | ||||||
| chr9:127849748
|
T | C | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+4541A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849748 | ||||||
| chr9:127849939
|
A | C | 31 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0017others(28): Show | 32 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+4350T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849939 | ||||||
| chr9:127850104
|
C | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.67+4185G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850104 | ||||||
| chr9:127850180
|
A | G | 13 | a0001c0001t0001g0306a0003c0005t0001g0325a0003c0005t0001g0326others(10): Show | 13 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+4109T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850180 | ||||||
| chr9:127850344
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.67+3945G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850344 | ||||||
| chr9:127850386
|
A | C | 31 | a0001c0002t0001g0002a0001c0002t0001g0015a0001c0002t0001g0017others(28): Show | 32 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+3903T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850386 | ||||||
| chr9:127850390
|
T | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA19006.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.67+3899A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850390 | ||||||
| chr9:127850510
|
G | C | 1 | a0001c0001t0001g0291 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.67+3779C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850510 | ||||||
| chr9:127850748
|
A | C | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67+3541T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850748 | ||||||
| chr9:127850781
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0107others(9): Show | 12 | HG02280.hp2 HG02615.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+3508G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850781 | ||||||
| chr9:127850840
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.67+3449C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850840 | ||||||
| chr9:127850977
|
T | C | 1 | a0001c0006t0010g0337 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.67+3312A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850977 | ||||||
| chr9:127850987
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.67+3302C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850987 | ||||||
| chr9:127851003
|
C | T | 2 | a0001c0002t0001g0017a0001c0008t0001g0016 | 2 | HG01099.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.67+3286G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851003 | ||||||
| chr9:127851052
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.67+3237T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851052 | ||||||
| chr9:127851105
|
T | C | 39 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0297others(36): Show | 40 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.67+3184A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851105 | ||||||
| chr9:127851312
|
C | T | 1 | a0001c0016t0001g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67+2977G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851312 | ||||||
| chr9:127851364
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG01496.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.67+2925G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851364 | ||||||
| chr9:127851450
|
C | A | 4 | a0001c0002t0001g0002a0001c0002t0001g0042a0001c0002t0001g0043others(1): Show | 5 | HG01109.hp2 HG01891.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+2839G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851450 | ||||||
| chr9:127851582
|
G | T | 336 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(333): Show | 341 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.67+2707C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851582 | ||||||
| chr9:127851706
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.67+2583G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851706 | ||||||
| chr9:127851735
|
C | T | 8 | a0001c0002t0001g0052a0001c0002t0001g0056a0001c0002t0006g0057others(5): Show | 9 | HG01167.hp1 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+2554G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851735 | ||||||
| chr9:127851747
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG00621.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.67+2542G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851747 | ||||||
| chr9:127852030
|
T | C | 39 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0071others(36): Show | 39 | HG00438.hp1 HG00609.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.67+2259A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852030 | ||||||
| chr9:127852077
|
G | A | 3 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0002t0001g0296 | 3 | HG01346.hp1 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67+2212C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852077 | ||||||
| chr9:127852359
|
G | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG00597.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.67+1930C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852359 | ||||||
| chr9:127852385
|
G | A | 5 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | HG02622.hp2 HG03486.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+1904C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852385 | ||||||
| chr9:127852457
|
G | A | 2 | a0001c0001t0001g0303a0001c0003t0002g0302 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.67+1832C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852457 | ||||||
| chr9:127852626
|
T | C | 38 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(35): Show | 39 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.67+1663A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852626 | ||||||
| chr9:127852633
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(225): Show | 231 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.67+1656C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852633 | ||||||
| chr9:127852719
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.67+1570C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852719 | ||||||
| chr9:127852909
|
C | T | 1 | a0001c0003t0002g0066 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.67+1380G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852909 | ||||||
| chr9:127852939
|
G | A | 6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+1350C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852939 | ||||||
| chr9:127852993
|
A | C | 1 | a0001c0001t0001g0065 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.67+1296T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852993 | ||||||
| chr9:127853303
|
C | T | 1 | a0001c0002t0001g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+986G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853303 | ||||||
| chr9:127853381
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.67+908C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853381 | ||||||
| chr9:127853472
|
G | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 269 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.67+817C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853472 | ||||||
| chr9:127853474
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.67+815G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853474 | ||||||
| chr9:127853543
|
C | G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+746G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853543 | ||||||
| chr9:127853544
|
C | A | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+745G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853544 | ||||||
| chr9:127853545
|
C | A | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+744G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853545 | ||||||
| chr9:127853546
|
C | A | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+743G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853546 | ||||||
| chr9:127853547
|
A | AGACGAAA others(6): Show |
1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+741_67+742insAA others(11): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853547 | ||||||
| chr9:127853548
|
C | G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+741G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853548 | ||||||
| chr9:127853551
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+738T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853551 | ||||||
| chr9:127853553
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+736G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853553 | ||||||
| chr9:127853554
|
C | G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+735G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853554 | ||||||
| chr9:127853555
|
C | G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+734G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853555 | ||||||
| chr9:127853556
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+733G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853556 | ||||||
| chr9:127853558
|
A | G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+731T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853558 | ||||||
| chr9:127853583
|
C | G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+706G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853583 | ||||||
| chr9:127853596
|
T | G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+693A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853596 | ||||||
| chr9:127853597
|
C | G | 1 | a0001c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+692G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853597 | ||||||
| chr9:127853674
|
C | T | 2 | a0001c0001t0001g0051a0001c0022t0001g0050 | 2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67+615G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853674 | ||||||
| chr9:127853813
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0003t0002g0013 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.67+476G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853813 | ||||||
| chr9:127853820
|
G | A | 14 | a0001c0001t0001g0306a0003c0005t0001g0324a0003c0005t0001g0325others(11): Show | 14 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+469C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853820 | ||||||
| chr9:127853860
|
A | G | 46 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0045others(43): Show | 47 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.67+429T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853860 | ||||||
| chr9:127853984
|
G | A | 10 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0310others(7): Show | 10 | HG04184.hp2 NA18941.hp2 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+305C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853984 | ||||||
| chr9:127854035
|
T | C | 6 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(3): Show | 6 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+254A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127854035 | ||||||
| chr9:127854091
|
C | T | 1 | a0001c0003t0001g0011 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67+198G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127854091 | ||||||
| chr9:127854114
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0010 | 3 | NA18952.hp2 NA19000.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.67+175T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127854114 | ||||||
| chr9:127854259
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.67+30A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127854259 |