| geneid | 2115 |
|---|---|
| ensemblid | ENSG00000006468.15 |
| hgncid | 3490 |
| symbol | ETV1 |
| name | ETS variant transcription factor 1 |
| refseq_nuc | NM_004956.5 |
| refseq_prot | NP_004947.2 |
| ensembl_nuc | ENST00000430479.6 |
| ensembl_prot | ENSP00000405327.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 13891229 |
| end | 13989666 |
| strand | - |
| ver | v1.2 |
| region | chr7:13891229-13989666 |
| region5000 | chr7:13886229-13994666 |
| regionname0 | ETV1_chr7_13891229_13989666 |
| regionname5000 | ETV1_chr7_13886229_13994666 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 477 | 219 | 63 | 41 | 79 | 12 | 22 | 59 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002 | 0/0 | 477 | 101 | 17 | 17 | 49 | 6 | 12 | 35 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1434 | 216 | 62 | 41 | 79 | 11 | 21 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| c0002 | 0/0 | 1434 | 101 | 17 | 17 | 49 | 6 | 12 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| c0003 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| c0004 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| c0005 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5026 | 39 | 1 | 7 | 15 | 4 | 12 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0002 | 0/0 | 5025 | 30 | 5 | 7 | 17 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0003 | 0/0 | 5025 | 29 | 0 | 1 | 24 | 2 | 2 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0004 | 0/0 | 5027 | 27 | 4 | 1 | 14 | 1 | 7 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0005 | 0/0 | 5026 | 22 | 0 | 3 | 14 | 0 | 5 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0006 | 0/0 | 5025 | 19 | 9 | 3 | 7 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0007 | 0/0 | 5026 | 17 | 3 | 4 | 8 | 1 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0008 | 0/0 | 5026 | 11 | 0 | 2 | 9 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0009 | 0/0 | 5026 | 11 | 2 | 6 | 0 | 0 | 3 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0010 | 0/0 | 5026 | 10 | 6 | 3 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0011 | 0/0 | 5025 | 10 | 0 | 9 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0012 | 0/0 | 5025 | 8 | 0 | 0 | 8 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0013 | 0/0 | 5025 | 7 | 4 | 2 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0014 | 0/0 | 5025 | 5 | 5 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0015 | 0/0 | 5026 | 5 | 5 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0016 | 0/0 | 5026 | 5 | 0 | 0 | 5 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0017 | 0/0 | 5026 | 4 | 4 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0018 | 0/0 | 5026 | 3 | 3 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0019 | 0/1 | 5026 | 3 | 0 | 0 | 0 | 1 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0020 | 0/0 | 5027 | 3 | 3 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0021 | 0/0 | 5027 | 3 | 2 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0022 | 0/0 | 5026 | 2 | 0 | 0 | 0 | 2 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0023 | 0/0 | 5026 | 2 | 1 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0024 | 0/0 | 5025 | 2 | 0 | 2 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0025 | 0/0 | 5026 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0026 | 0/0 | 5025 | 2 | 1 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0027 | 0/0 | 5027 | 2 | 1 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0028 | 0/0 | 5023 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0029 | 0/0 | 5026 | 2 | 0 | 1 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0030 | 0/0 | 5025 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0031 | 0/0 | 5026 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0032 | 0/0 | 5026 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0033 | 0/0 | 5025 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0034 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0035 | 0/0 | 5025 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0036 | 0/0 | 5025 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0037 | 0/0 | 5025 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0038 | 0/0 | 5025 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0039 | 0/0 | 5025 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0040 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0041 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0042 | 0/0 | 5025 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0043 | 0/0 | 5025 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0044 | 0/0 | 5025 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0045 | 0/0 | 5022 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0046 | 0/0 | 5025 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0047 | 0/0 | 5026 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0048 | 0/0 | 5027 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0049 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0050 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0051 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0052 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0053 | 0/0 | 5026 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0054 | 0/0 | 5026 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0055 | 0/0 | 5026 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0056 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0057 | 0/0 | 5027 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0058 | 0/0 | 5026 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0059 | 0/0 | 5026 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0060 | 1/0 | 5026 | 1 | 0 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0061 | 0/0 | 5026 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| t0062 | 0/0 | 5025 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1434 | 216 | 62 | 41 | 79 | 11 | 21 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0003 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0004 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0005 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002 | 0/0 | 1434 | 101 | 17 | 17 | 49 | 6 | 12 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6459 | 16 | 1 | 3 | 6 | 1 | 5 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0002 | 0/0 | 6458 | 26 | 5 | 6 | 15 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0003 | 0/0 | 6458 | 24 | 0 | 1 | 19 | 2 | 2 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0004 | 0/0 | 6460 | 15 | 3 | 0 | 6 | 0 | 6 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0005 | 0/0 | 6459 | 9 | 0 | 3 | 5 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0006 | 0/0 | 6458 | 17 | 8 | 2 | 7 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0007 | 0/0 | 6459 | 10 | 2 | 3 | 4 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0008 | 0/0 | 6459 | 4 | 0 | 1 | 3 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0009 | 0/0 | 6459 | 5 | 2 | 0 | 0 | 0 | 3 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0010 | 0/0 | 6459 | 8 | 4 | 3 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0011 | 0/0 | 6458 | 10 | 0 | 9 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0012 | 0/0 | 6458 | 5 | 0 | 0 | 5 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0013 | 0/0 | 6458 | 4 | 1 | 2 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0014 | 0/0 | 6458 | 4 | 4 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0015 | 0/0 | 6459 | 5 | 5 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0016 | 0/0 | 6459 | 4 | 0 | 0 | 4 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0017 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0018 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0019 | 0/1 | 6459 | 3 | 0 | 0 | 0 | 1 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0020 | 0/0 | 6460 | 3 | 3 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0021 | 0/0 | 6460 | 3 | 2 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0023 | 0/0 | 6459 | 2 | 1 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0024 | 0/0 | 6458 | 2 | 0 | 2 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0025 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0026 | 0/0 | 6458 | 2 | 1 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0027 | 0/0 | 6460 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0028 | 0/0 | 6456 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0029 | 0/0 | 6459 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0030 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0032 | 0/0 | 6459 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0035 | 0/0 | 6458 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0036 | 0/0 | 6458 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0038 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0039 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0040 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0041 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0042 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0043 | 0/0 | 6458 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0044 | 0/0 | 6458 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0045 | 0/0 | 6455 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0046 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0047 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0048 | 0/0 | 6460 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0050 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0051 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0053 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0054 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0055 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0056 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0057 | 0/0 | 6460 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0058 | 0/0 | 6459 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0059 | 0/0 | 6459 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0001t0060 | 1/0 | 6459 | 1 | 0 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0003t0002 | 0/0 | 6458 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0004t0001 | 0/0 | 6459 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0001c0005t0010 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0001 | 0/0 | 6459 | 22 | 0 | 4 | 9 | 3 | 6 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0002 | 0/0 | 6458 | 3 | 0 | 1 | 2 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0003 | 0/0 | 6458 | 5 | 0 | 0 | 5 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0004 | 0/0 | 6460 | 12 | 1 | 1 | 8 | 1 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0005 | 0/0 | 6459 | 13 | 0 | 0 | 9 | 0 | 4 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0006 | 0/0 | 6458 | 2 | 1 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0007 | 0/0 | 6459 | 7 | 1 | 1 | 4 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0008 | 0/0 | 6459 | 7 | 0 | 1 | 6 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0009 | 0/0 | 6459 | 6 | 0 | 6 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0010 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0012 | 0/0 | 6458 | 3 | 0 | 0 | 3 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0013 | 0/0 | 6458 | 3 | 3 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0014 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0016 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0017 | 0/0 | 6459 | 2 | 2 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0018 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0022 | 0/0 | 6459 | 2 | 0 | 0 | 0 | 2 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0027 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0029 | 0/0 | 6459 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0031 | 0/0 | 6459 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0033 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0034 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0037 | 0/0 | 6458 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0049 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0052 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0061 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| a0002c0002t0062 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | copy fasta | chr7 | 13886229 | 13994666 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0010g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0011g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0012g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0013g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0013g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0013g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0014g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0014g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0014g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0016g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0016g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0016g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0016g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0017g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0018g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0018g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0019g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0019g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0019g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0020g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0020g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0020g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0021g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0021g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0021g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0023g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0023g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0024g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0024g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0025g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0025g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0026g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0026g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0027g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0028g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0028g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0029g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0030g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0032g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0035g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0036g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0038g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0039g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0040g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0041g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0042g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0043g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0044g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0045g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0046g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0047g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0048g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0050g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0051g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0053g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0054g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0055g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0056g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0057g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0058g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0059g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0001t0060g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0001c0005t0010g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0006g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0007g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0008g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0012g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0012g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0013g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0013g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0013g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0014g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0016g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0017g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0018g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0022g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0022g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0027g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0029g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0031g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0033g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0034g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0037g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0049g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0052g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0061g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| a0002c0002t0062g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00099 | hp2 | a0001 | c0001 | t0035 | g0124 | EUR | GBR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00140 | hp1 | a0001 | c0001 | t0019 | g0153 | EUR | GBR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0068 | EUR | GBR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00280 | hp1 | a0001 | c0001 | t0029 | g0258 | EUR | FIN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0073 | EUR | FIN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0259 | EUR | FIN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00323 | hp2 | a0001 | c0001 | t0032 | g0006 | EUR | FIN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00408 | hp1 | a0002 | c0002 | t0007 | g0020 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0061 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0182 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00438 | hp1 | a0002 | c0002 | t0037 | g0062 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00438 | hp2 | a0001 | c0001 | t0054 | g0195 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00544 | hp1 | a0002 | c0002 | t0004 | g0243 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0168 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00597 | hp2 | a0001 | c0001 | t0012 | g0298 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00609 | hp1 | a0002 | c0002 | t0003 | g0051 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | CHS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0067 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00735 | hp1 | a0002 | c0002 | t0007 | g0049 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00738 | hp2 | a0001 | c0001 | t0023 | g0008 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00741 | hp1 | a0002 | c0002 | t0004 | g0202 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0074 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0250 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01070 | hp2 | a0002 | c0002 | t0009 | g0227 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01071 | hp1 | a0002 | c0002 | t0009 | g0228 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0069 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0101 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01074 | hp2 | a0002 | c0002 | t0006 | g0018 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01081 | hp2 | a0001 | c0001 | t0021 | g0140 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0247 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0066 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01109 | hp1 | a0001 | c0001 | t0058 | g0135 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01109 | hp2 | a0002 | c0002 | t0029 | g0163 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0085 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01167 | hp2 | a0001 | c0001 | t0011 | g0081 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0262 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0084 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0118 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01175 | hp2 | a0001 | c0001 | t0024 | g0028 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01192 | hp2 | a0001 | c0001 | t0024 | g0029 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0077 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0010 | AMR | PUR | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01255 | hp1 | a0001 | c0001 | t0026 | g0098 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01255 | hp2 | a0001 | c0001 | t0011 | g0064 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01258 | hp2 | a0002 | c0002 | t0008 | g0264 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01261 | hp1 | a0001 | c0001 | t0036 | g0095 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01261 | hp2 | a0002 | c0002 | t0031 | g0005 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0248 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01346 | hp2 | a0001 | c0001 | t0011 | g0110 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01361 | hp2 | a0001 | c0001 | t0013 | g0109 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0019 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01515 | hp2 | a0002 | c0002 | t0022 | g0003 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0217 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01516 | hp2 | a0001 | c0001 | t0044 | g0127 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0199 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01517 | hp2 | a0002 | c0002 | t0022 | g0004 | EUR | IBS | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0032 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0229 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01891 | hp1 | a0001 | c0001 | t0021 | g0265 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01891 | hp2 | a0002 | c0002 | t0049 | g0200 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01928 | hp1 | a0002 | c0002 | t0009 | g0196 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0088 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01981 | hp1 | a0002 | c0002 | t0009 | g0210 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01981 | hp2 | a0001 | c0001 | t0011 | g0089 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01993 | hp1 | a0002 | c0002 | t0009 | g0211 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01993 | hp2 | a0001 | c0001 | t0011 | g0129 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02015 | hp1 | a0001 | c0001 | t0057 | g0174 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0045 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02055 | hp2 | a0001 | c0001 | t0038 | g0306 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02071 | hp1 | a0002 | c0002 | t0005 | g0269 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02074 | hp1 | a0001 | c0001 | t0006 | g0130 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02074 | hp2 | a0001 | c0001 | t0016 | g0190 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02080 | hp2 | a0002 | c0002 | t0007 | g0286 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02129 | hp1 | a0002 | c0002 | t0008 | g0197 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02132 | hp1 | a0002 | c0002 | t0005 | g0176 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02135 | hp2 | a0002 | c0002 | t0004 | g0272 | EAS | KHV | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02145 | hp1 | a0001 | c0001 | t0020 | g0133 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02145 | hp2 | a0001 | c0001 | t0023 | g0007 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02155 | hp1 | a0002 | c0002 | t0008 | g0171 | EAS | CDX | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02155 | hp2 | a0002 | c0002 | t0005 | g0207 | EAS | CDX | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | CDX | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02165 | hp2 | a0001 | c0001 | t0012 | g0117 | EAS | CDX | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02257 | hp2 | a0001 | c0001 | t0040 | g0011 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02258 | hp1 | a0002 | c0002 | t0027 | g0242 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02258 | hp2 | a0002 | c0002 | t0004 | g0276 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02273 | hp1 | a0001 | c0001 | t0011 | g0093 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0111 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02280 | hp1 | a0002 | c0002 | t0033 | g0022 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0308 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02300 | hp1 | a0002 | c0002 | t0009 | g0206 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02300 | hp2 | a0001 | c0001 | t0043 | g0125 | AMR | PEL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02602 | hp2 | a0001 | c0001 | t0009 | g0180 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02622 | hp1 | a0001 | c0001 | t0020 | g0239 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02630 | hp1 | a0002 | c0002 | t0062 | g0319 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0307 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0025 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0134 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0080 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02723 | hp1 | a0001 | c0001 | t0051 | g0237 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02723 | hp2 | a0002 | c0002 | t0006 | g0078 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0181 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02738 | hp1 | a0002 | c0002 | t0005 | g0221 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0154 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02809 | hp1 | a0001 | c0001 | t0028 | g0241 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02809 | hp2 | a0001 | c0005 | t0010 | g0115 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0053 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02818 | hp2 | a0002 | c0002 | t0010 | g0116 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02886 | hp1 | a0002 | c0002 | t0052 | g0260 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02895 | hp1 | a0002 | c0002 | t0013 | g0304 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02895 | hp2 | a0001 | c0001 | t0018 | g0100 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02896 | hp2 | a0001 | c0001 | t0026 | g0041 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02897 | hp1 | a0002 | c0002 | t0013 | g0305 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02965 | hp2 | a0001 | c0001 | t0028 | g0240 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02970 | hp1 | a0001 | c0001 | t0021 | g0266 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0083 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02976 | hp2 | a0002 | c0002 | t0017 | g0039 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03017 | hp1 | a0001 | c0001 | t0009 | g0179 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0112 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0301 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0302 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0300 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03195 | hp1 | a0001 | c0001 | t0046 | g0072 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0044 | AFR | ESN | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0139 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03209 | hp2 | a0002 | c0002 | t0007 | g0310 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0042 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0252 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03453 | hp2 | a0002 | c0002 | t0013 | g0315 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0136 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0123 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0203 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0040 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03540 | hp2 | a0002 | c0002 | t0014 | g0314 | AFR | GWD | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03579 | hp1 | a0001 | c0001 | t0025 | g0043 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03669 | hp1 | a0002 | c0002 | t0004 | g0220 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0249 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0267 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0205 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0235 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0209 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03710 | hp2 | a0002 | c0002 | t0005 | g0151 | SAS | PJL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0219 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03831 | hp2 | a0001 | c0001 | t0059 | g0251 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03834 | hp2 | a0002 | c0002 | t0005 | g0150 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03927 | hp1 | a0001 | c0001 | t0027 | g0256 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0147 | SAS | BEB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04115 | hp1 | a0002 | c0002 | t0005 | g0236 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04115 | hp2 | a0001 | c0001 | t0019 | g0216 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04199 | hp2 | a0002 | c0002 | t0007 | g0114 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0099 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04228 | hp1 | a0001 | c0001 | t0013 | g0034 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0277 | SAS | STU | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18522 | hp1 | a0001 | c0001 | t0055 | g0257 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18522 | hp2 | a0001 | c0001 | t0042 | g0303 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0317 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0313 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18941 | hp2 | a0001 | c0001 | t0016 | g0192 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0280 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18944 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0188 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18946 | hp2 | a0002 | c0002 | t0012 | g0055 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18948 | hp2 | a0001 | c0001 | t0012 | g0108 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18953 | hp1 | a0002 | c0002 | t0004 | g0172 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18957 | hp1 | a0002 | c0002 | t0008 | g0169 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18960 | hp1 | a0002 | c0002 | t0016 | g0275 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18963 | hp1 | a0002 | c0002 | t0005 | g0162 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18964 | hp1 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18964 | hp2 | a0002 | c0002 | t0007 | g0120 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18967 | hp2 | a0001 | c0001 | t0008 | g0146 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18972 | hp2 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18977 | hp2 | a0002 | c0002 | t0004 | g0141 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18978 | hp1 | a0002 | c0002 | t0005 | g0144 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18978 | hp2 | a0002 | c0002 | t0007 | g0063 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18983 | hp2 | a0002 | c0002 | t0003 | g0122 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18988 | hp1 | a0001 | c0001 | t0006 | g0102 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18988 | hp2 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18991 | hp1 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18991 | hp2 | a0001 | c0001 | t0008 | g0173 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18992 | hp2 | a0002 | c0002 | t0012 | g0052 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18995 | hp2 | a0001 | c0001 | t0053 | g0226 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0297 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19004 | hp1 | a0002 | c0002 | t0005 | g0175 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19007 | hp1 | a0002 | c0002 | t0005 | g0204 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0296 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19009 | hp1 | a0002 | c0002 | t0004 | g0145 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19009 | hp2 | a0002 | c0002 | t0012 | g0033 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19011 | hp1 | a0002 | c0002 | t0004 | g0225 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19043 | hp1 | a0002 | c0002 | t0034 | g0311 | AFR | LWK | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19043 | hp2 | a0001 | c0001 | t0045 | g0113 | AFR | LWK | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19058 | hp1 | a0002 | c0002 | t0005 | g0274 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19058 | hp2 | a0001 | c0001 | t0016 | g0268 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19063 | hp1 | a0002 | c0002 | t0008 | g0159 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19065 | hp2 | a0002 | c0002 | t0008 | g0160 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19068 | hp1 | a0002 | c0002 | t0005 | g0271 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0046 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19072 | hp1 | a0001 | c0001 | t0016 | g0165 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19072 | hp2 | a0002 | c0002 | t0008 | g0161 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19078 | hp2 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0212 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0121 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19085 | hp2 | a0001 | c0001 | t0012 | g0285 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19087 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19087 | hp2 | a0001 | c0001 | t0048 | g0231 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19091 | hp1 | a0002 | c0002 | t0061 | g0318 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0316 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA19240 | hp2 | a0002 | c0002 | t0018 | g0299 | AFR | YRI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0126 | EUR | TSI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA20752 | hp2 | a0002 | c0002 | t0004 | g0246 | EUR | TSI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0030 | EUR | TSI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0076 | EUR | TSI | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01123 | hp1 | a0001 | c0001 | t0011 | g0128 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0198 | AMR | CLM | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02109 | hp1 | a0001 | c0001 | t0039 | g0086 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02109 | hp2 | a0001 | c0001 | t0025 | g0312 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02486 | hp2 | a0002 | c0002 | t0017 | g0037 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0138 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0132 | AFR | ACB | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03471 | hp1 | a0001 | c0001 | t0041 | g0309 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG03471 | hp2 | a0001 | c0001 | t0056 | g0261 | AFR | MSL | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG06807 | hp1 | a0001 | c0001 | t0030 | g0002 | AFR | USA | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0143 | AFR | USA | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA18955 | hp2 | a0001 | c0001 | t0047 | g0218 | EAS | JPT | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | LWK | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| NA21309 | hp2 | a0001 | c0001 | t0050 | g0142 | AFR | LWK | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0019 | g0152 | REF | REF | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0060 | g0208 | REF | REF | ETV1_chr7_13886229_13994666 | ETV1 | chr7 | 13886229 | 13994666 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:13939184
|
T | C | 1 | a0002 | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
missense_variant | MODERATE | c.298A>G | p.Ser100Gly | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/14 | 686/6459 | 298/1434 | 100/477 | chr7 | 13939184 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:13895917
|
C | T | 1 | a0001c0005 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1383G>A | p.Pro461Pro | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1771/6459 | 1383/1434 | 461/477 | chr7 | 13895917 | ||
| chr7:13906439
|
C | T | 1 | a0001c0004 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1101G>A | p.Glu367Glu | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/14 | 1489/6459 | 1101/1434 | 367/477 | chr7 | 13906439 | ||
| chr7:13977479
|
A | T | 1 | a0001c0003 | 1 | HG00280.hp2 | splice_region_variant&synonymous_variant | LOW | c.183T>A | p.Ala61Ala | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/14 | 571/6459 | 183/1434 | 61/477 | chr7 | 13977479 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:13891292
|
T | C | 1 | a0001c0001t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4574A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4574 | chr7 | 13891292 | |||||
| chr7:13891347
|
G | A | 2 | a0001c0001t0028a0001c0001t0045 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4519C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4519 | chr7 | 13891347 | |||||
| chr7:13891557
|
G | A | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(65): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*4309C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4309 | chr7 | 13891557 | |||||
| chr7:13891610
|
T | C | 5 | a0001c0001t0010a0001c0001t0020a0001c0001t0039others(2): Show | 14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4256A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4256 | chr7 | 13891610 | |||||
| chr7:13891611
|
A | G | 2 | a0001c0001t0028a0001c0001t0045 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4255T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4255 | chr7 | 13891611 | |||||
| chr7:13891678
|
T | C | 1 | a0002c0002t0033 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4188A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4188 | chr7 | 13891678 | |||||
| chr7:13891836
|
G | A | 1 | a0001c0001t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4030C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4030 | chr7 | 13891836 | |||||
| chr7:13891838
|
A | T | 1 | a0001c0001t0056 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4028T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 4028 | chr7 | 13891838 | |||||
| chr7:13891971
|
A | G | 1 | a0001c0001t0036 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3895T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3895 | chr7 | 13891971 | |||||
| chr7:13892043
|
T | C | 2 | a0001c0001t0028a0001c0001t0045 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3823A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3823 | chr7 | 13892043 | |||||
| chr7:13892045
|
C | T | 1 | a0001c0001t0055 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3821G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3821 | chr7 | 13892045 | |||||
| chr7:13892111
|
A | T | 1 | a0001c0001t0038 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3755T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3755 | chr7 | 13892111 | |||||
| chr7:13892142
|
T | A | 2 | a0001c0001t0053a0002c0002t0037 | 2 | HG00438.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3724A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3724 | chr7 | 13892142 | |||||
| chr7:13892151
|
A | G | 4 | a0001c0001t0012a0001c0001t0016a0002c0002t0012others(1): Show | 13 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3715T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3715 | chr7 | 13892151 | |||||
| chr7:13892273
|
T | C | 1 | a0001c0001t0054 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3593A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3593 | chr7 | 13892273 | |||||
| chr7:13892353
|
A | G | 2 | a0001c0001t0028a0001c0001t0045 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3513T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3513 | chr7 | 13892353 | |||||
| chr7:13892357
|
T | A | 70 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(67): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*3509A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3509 | chr7 | 13892357 | |||||
| chr7:13892431
|
G | A | 1 | a0001c0001t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3435C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3435 | chr7 | 13892431 | |||||
| chr7:13892532
|
G | A | 2 | a0001c0001t0026a0001c0001t0059 | 3 | HG01255.hp1 HG02896.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3334C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3334 | chr7 | 13892532 | |||||
| chr7:13892693
|
A | G | 1 | a0002c0002t0033 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3173T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3173 | chr7 | 13892693 | |||||
| chr7:13892790
|
C | G | 4 | a0001c0001t0029a0001c0001t0032a0002c0002t0029others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3076G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3076 | chr7 | 13892790 | |||||
| chr7:13892863
|
C | G | 1 | a0001c0001t0058 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3003G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 3003 | chr7 | 13892863 | |||||
| chr7:13892976
|
C | T | 44 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(41): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*2890G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2890 | chr7 | 13892976 | |||||
| chr7:13893000
|
G | A | 4 | a0001c0001t0012a0001c0001t0016a0002c0002t0012others(1): Show | 13 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2866C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2866 | chr7 | 13893000 | |||||
| chr7:13893064
|
T | C | 5 | a0001c0001t0009a0001c0001t0013a0002c0002t0009others(2): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2802A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2802 | chr7 | 13893064 | |||||
| chr7:13893068
|
G | A | 4 | a0001c0001t0029a0001c0001t0032a0002c0002t0029others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2798C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2798 | chr7 | 13893068 | |||||
| chr7:13893088
|
T | C | 1 | a0001c0001t0044 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2778A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2778 | chr7 | 13893088 | |||||
| chr7:13893281
|
A | G | 2 | a0001c0001t0019a0001c0001t0035 | 4 | HG00099.hp2 HG00140.hp1 HG04115.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2585T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2585 | chr7 | 13893281 | |||||
| chr7:13893341
|
A | C | 4 | a0001c0001t0012a0001c0001t0016a0002c0002t0012others(1): Show | 13 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2525T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2525 | chr7 | 13893341 | |||||
| chr7:13893466
|
C | T | 1 | a0001c0001t0042 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2400G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2400 | chr7 | 13893466 | |||||
| chr7:13893557
|
C | T | 1 | a0002c0002t0033 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2309G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2309 | chr7 | 13893557 | |||||
| chr7:13893613
|
AAGG | A | 2 | a0001c0001t0028a0001c0001t0045 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2250_*2252delCCT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2250 | chr7 | 13893613 | |||||
| chr7:13893745
|
T | C | 18 | a0001c0001t0010a0001c0001t0014a0001c0001t0015others(15): Show | 37 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2121A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 2121 | chr7 | 13893745 | |||||
| chr7:13893926
|
C | T | 1 | a0001c0001t0057 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1940G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1940 | chr7 | 13893926 | |||||
| chr7:13894049
|
G | T | 1 | a0001c0001t0041 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1817C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1817 | chr7 | 13894049 | |||||
| chr7:13894147
|
G | T | 9 | a0001c0001t0017a0001c0001t0018a0001c0001t0027others(6): Show | 12 | HG02258.hp1 HG02486.hp2 HG02723.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1719C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1719 | chr7 | 13894147 | |||||
| chr7:13894154
|
A | AT | 25 | a0001c0001t0004a0001c0001t0007a0001c0001t0010others(22): Show | 80 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1711dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1711 | chr7 | 13894154 | |||||
| chr7:13894186
|
T | A | 4 | a0001c0001t0029a0001c0001t0032a0002c0002t0029others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1680A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1680 | chr7 | 13894186 | |||||
| chr7:13894261
|
C | T | 2 | a0001c0001t0021a0001c0001t0025 | 5 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1605G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1605 | chr7 | 13894261 | |||||
| chr7:13894536
|
A | C | 2 | a0001c0001t0040a0001c0001t0055 | 2 | HG02257.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1330T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1330 | chr7 | 13894536 | |||||
| chr7:13894613
|
T | C | 4 | a0001c0001t0012a0001c0001t0016a0002c0002t0012others(1): Show | 13 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1253A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1253 | chr7 | 13894613 | |||||
| chr7:13894733
|
A | T | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0019others(13): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1133T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 1133 | chr7 | 13894733 | |||||
| chr7:13895063
|
A | G | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(22): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*803T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 803 | chr7 | 13895063 | |||||
| chr7:13895087
|
C | T | 1 | a0001c0001t0024 | 2 | HG01175.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*779G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 779 | chr7 | 13895087 | |||||
| chr7:13895107
|
G | A | 1 | a0001c0001t0046 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*759C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 759 | chr7 | 13895107 | |||||
| chr7:13895382
|
A | G | 3 | a0001c0001t0017a0001c0001t0051a0002c0002t0017 | 5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*484T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 484 | chr7 | 13895382 | |||||
| chr7:13895446
|
A | G | 1 | a0001c0001t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*420T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 420 | chr7 | 13895446 | |||||
| chr7:13895511
|
C | T | 1 | a0001c0001t0047 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*355G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 355 | chr7 | 13895511 | |||||
| chr7:13895557
|
A | T | 1 | a0002c0002t0049 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 309 | chr7 | 13895557 | |||||
| chr7:13895682
|
C | T | 9 | a0001c0001t0003a0001c0001t0005a0001c0001t0024others(6): Show | 58 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*184G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 184 | chr7 | 13895682 | |||||
| chr7:13895683
|
C | G | 1 | a0002c0002t0033 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 14/14 | 183 | chr7 | 13895683 | |||||
| chr7:13989082
|
TA | T | 42 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(39): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
5_prime_UTR_variant | MODIFIER | c.-31delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/14 | 31 | chr7 | 13989082 | |||||
| chr7:13989340
|
C | T | 4 | a0001c0001t0023a0001c0001t0032a0002c0002t0022others(1): Show | 6 | HG00323.hp2 HG00738.hp2 HG01261.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-160G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/14 | 288 | chr7 | 13989340 | |||||
| chr7:13989351
|
T | A | 1 | a0002c0002t0061 | 1 | NA19091.hp1 | 5_prime_UTR_variant | MODIFIER | c.-171A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/14 | 299 | chr7 | 13989351 | |||||
| chr7:13989406
|
G | A | 1 | a0002c0002t0062 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-226C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/14 | 354 | chr7 | 13989406 | |||||
| chr7:13989624
|
A | C | 1 | a0001c0001t0030 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-346T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 1/14 | 572 | chr7 | 13989624 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:13896189
|
T | C | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1213-102A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896189 | ||||||
| chr7:13896236
|
T | TA | 116 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.1213-150dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896236 | ||||||
| chr7:13896362
|
C | T | 119 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.1213-275G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896362 | ||||||
| chr7:13896431
|
T | C | 1 | a0001c0001t0056g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1213-344A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896431 | ||||||
| chr7:13896437
|
G | C | 2 | a0001c0001t0040g0011a0001c0001t0055g0257 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1213-350C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896437 | ||||||
| chr7:13896438
|
C | T | 5 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0051g0237others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1213-351G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896438 | ||||||
| chr7:13896494
|
T | G | 81 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(78): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.1213-407A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896494 | ||||||
| chr7:13896523
|
G | A | 10 | a0001c0001t0004g0238a0001c0001t0004g0263a0001c0001t0007g0053others(7): Show | 10 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1213-436C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896523 | ||||||
| chr7:13896538
|
T | C | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1213-451A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896538 | ||||||
| chr7:13896552
|
G | T | 2 | a0001c0001t0040g0011a0001c0001t0055g0257 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1213-465C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896552 | ||||||
| chr7:13896605
|
G | A | 3 | a0001c0001t0018g0100a0001c0001t0027g0256a0001c0001t0056g0261 | 3 | HG02895.hp2 HG03471.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1213-518C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896605 | ||||||
| chr7:13896675
|
T | G | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1213-588A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896675 | ||||||
| chr7:13896681
|
A | AAGAC | 244 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(241): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1213-595_1213-594i others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896681 | ||||||
| chr7:13896693
|
A | AGAGAGAG others(12): Show |
85 | a0001c0001t0001g0157a0001c0001t0001g0184a0001c0001t0001g0185others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1213-625_1213-607d others(21): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896693 | ||||||
| chr7:13896700
|
G | GAAAGAAA others(12): Show |
1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1213-614_1213-613i others(21): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896700 | ||||||
| chr7:13896710
|
A | G | 1 | a0001c0001t0026g0041 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1213-623T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896710 | ||||||
| chr7:13896725
|
A | AAGAAAGG others(6): Show |
1 | a0001c0001t0056g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1213-639_1213-638i others(15): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896725 | ||||||
| chr7:13896725
|
A | AAGAAAGG others(22): Show |
30 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0002g0014others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1213-639_1213-638i others(31): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896725 | ||||||
| chr7:13896725
|
A | AAGAAAGG others(31): Show |
17 | a0001c0001t0001g0167a0001c0001t0001g0215a0001c0001t0001g0254others(14): Show | 17 | HG00438.hp1 HG01516.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.1213-639_1213-638i others(40): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896725 | ||||||
| chr7:13896725
|
A | AAGAAAGG others(35): Show |
2 | a0001c0001t0002g0104a0002c0002t0001g0230 | 2 | NA18956.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1213-639_1213-638i others(44): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896725 | ||||||
| chr7:13896731
|
A | AAG | 19 | a0001c0001t0001g0167a0001c0001t0001g0215a0001c0001t0001g0254others(16): Show | 19 | HG00438.hp1 HG01516.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.1213-645_1213-644i others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896731 | ||||||
| chr7:13896731
|
A | AAGG | 30 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0002g0014others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1213-645_1213-644i others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896731 | ||||||
| chr7:13896742
|
AG | A | 12 | a0001c0001t0001g0254a0001c0001t0002g0013a0001c0001t0014g0080others(9): Show | 12 | HG00438.hp1 HG01516.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.1213-656delC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896742 | ||||||
| chr7:13896743
|
G | GAAA | 37 | a0001c0001t0001g0167a0001c0001t0001g0215a0001c0001t0001g0222others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1213-657_1213-656i others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
G | GAAAGAAA others(16): Show |
1 | a0001c0001t0008g0173 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1213-657_1213-656i others(25): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
G | GGAAA | 39 | a0001c0001t0002g0107a0001c0001t0003g0054a0001c0001t0003g0290others(36): Show | 39 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1213-660_1213-657d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
G | GGAAAGAA others(1): Show |
83 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0244others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1213-664_1213-657d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
G | GGAAAGAA others(5): Show |
73 | a0001c0001t0001g0157a0001c0001t0001g0184a0001c0001t0001g0186others(70): Show | 74 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1213-668_1213-657d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
G | GGAAAGAA others(9): Show |
16 | a0001c0001t0003g0016a0001c0001t0003g0050a0001c0001t0003g0288others(13): Show | 16 | HG00423.hp2 HG01123.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.1213-672_1213-657d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
G | GGAAAGAA others(13): Show |
10 | a0001c0001t0003g0092a0001c0001t0003g0281a0001c0001t0006g0284others(7): Show | 10 | HG00738.hp1 HG02071.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1213-676_1213-657d others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
G | GGAAAGAA others(17): Show |
4 | a0001c0001t0004g0249a0001c0001t0006g0088a0001c0001t0006g0280others(1): Show | 4 | HG01192.hp2 HG01978.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-680_1213-657d others(26): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
G | GGAAGAAA others(4): Show |
1 | a0002c0002t0007g0286 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1213-657_1213-656i others(13): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
GGAAA | G | 7 | a0001c0001t0004g0181a0001c0001t0013g0010a0001c0001t0023g0007others(4): Show | 7 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1213-660_1213-657d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
GGAAAGAA others(1): Show |
G | 4 | a0001c0001t0004g0189a0002c0002t0004g0145a0002c0002t0007g0120others(1): Show | 4 | HG01891.hp2 NA18946.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-664_1213-657d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
GGAAAGAA others(5): Show |
G | 2 | a0001c0001t0029g0258a0001c0001t0032g0006 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.1213-668_1213-657d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896743
|
GGAAAGAA others(9): Show |
G | 3 | a0001c0001t0006g0302a0001c0001t0006g0307a0002c0002t0006g0078 | 3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1213-672_1213-657d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896743 | ||||||
| chr7:13896744
|
G | A | 1 | a0001c0001t0056g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1213-657C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896744 | ||||||
| chr7:13896747
|
A | G | 1 | a0001c0001t0056g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1213-660T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896747 | ||||||
| chr7:13896768
|
G | GAA | 5 | a0001c0001t0021g0140a0001c0001t0021g0265a0001c0001t0021g0266others(2): Show | 5 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213-683_1213-682d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896768 | ||||||
| chr7:13896789
|
A | AAAGAAAG others(12): Show |
1 | a0001c0001t0030g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1213-703_1213-702i others(21): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896789 | ||||||
| chr7:13896790
|
A | AAGAAAGA others(11): Show |
1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1213-704_1213-703i others(20): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896790 | ||||||
| chr7:13896792
|
G | GAAAGAAA others(8): Show |
1 | a0001c0001t0005g0262 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1213-706_1213-705i others(17): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896792 | ||||||
| chr7:13896802
|
C | G | 1 | a0001c0001t0042g0303 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1213-715G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896802 | ||||||
| chr7:13896887
|
T | A | 1 | a0002c0002t0001g0131 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1213-800A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896887 | ||||||
| chr7:13896921
|
G | A | 1 | a0002c0002t0004g0225 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1213-834C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896921 | ||||||
| chr7:13896941
|
G | T | 1 | a0001c0001t0003g0019 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1213-854C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896941 | ||||||
| chr7:13896995
|
T | C | 115 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.1213-908A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13896995 | ||||||
| chr7:13897015
|
C | T | 115 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.1213-928G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897015 | ||||||
| chr7:13897020
|
T | G | 1 | a0002c0002t0004g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1213-933A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897020 | ||||||
| chr7:13897038
|
C | A | 12 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0018g0100others(9): Show | 12 | HG02258.hp1 HG02486.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1213-951G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897038 | ||||||
| chr7:13897131
|
G | A | 3 | a0002c0002t0003g0122a0002c0002t0005g0269a0002c0002t0005g0271 | 3 | HG02071.hp1 NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1213-1044C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897131 | ||||||
| chr7:13897189
|
C | T | 1 | a0001c0001t0005g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1213-1102G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897189 | ||||||
| chr7:13897325
|
C | T | 1 | a0001c0001t0003g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1213-1238G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897325 | ||||||
| chr7:13897364
|
T | C | 5 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0051g0237others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1213-1277A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897364 | ||||||
| chr7:13897511
|
T | C | 1 | a0002c0002t0005g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1213-1424A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897511 | ||||||
| chr7:13897538
|
G | C | 1 | a0002c0002t0005g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1213-1451C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897538 | ||||||
| chr7:13897641
|
C | T | 1 | a0001c0001t0007g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1213-1554G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897641 | ||||||
| chr7:13897788
|
CT | C | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1213-1702delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897788 | ||||||
| chr7:13897887
|
G | A | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1213-1800C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897887 | ||||||
| chr7:13897904
|
T | G | 124 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.1213-1817A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13897904 | ||||||
| chr7:13898040
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1213-1953A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898040 | ||||||
| chr7:13898239
|
C | G | 1 | a0001c0001t0013g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1213-2152G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898239 | ||||||
| chr7:13898251
|
G | T | 15 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(12): Show | 15 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.1213-2164C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898251 | ||||||
| chr7:13898412
|
A | C | 1 | a0002c0002t0004g0141 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1213-2325T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898412 | ||||||
| chr7:13898431
|
T | G | 15 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(12): Show | 15 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212+2307A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898431 | ||||||
| chr7:13898440
|
T | C | 1 | a0001c0001t0019g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1212+2298A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898440 | ||||||
| chr7:13898442
|
A | G | 1 | a0001c0001t0056g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1212+2296T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898442 | ||||||
| chr7:13898454
|
A | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1212+2284T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898454 | ||||||
| chr7:13898476
|
G | T | 1 | a0001c0001t0003g0291 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1212+2262C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898476 | ||||||
| chr7:13898534
|
A | G | 138 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1212+2204T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898534 | ||||||
| chr7:13898560
|
C | T | 118 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1212+2178G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898560 | ||||||
| chr7:13898664
|
A | C | 2 | a0001c0001t0040g0011a0001c0001t0055g0257 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1212+2074T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898664 | ||||||
| chr7:13898708
|
A | G | 1 | a0001c0001t0011g0064 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1212+2030T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898708 | ||||||
| chr7:13898839
|
C | A | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1212+1899G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898839 | ||||||
| chr7:13898839
|
C | T | 54 | a0001c0001t0004g0001a0001c0001t0004g0137a0001c0001t0004g0177others(51): Show | 55 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1212+1899G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898839 | ||||||
| chr7:13898967
|
G | A | 1 | a0002c0002t0008g0264 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1212+1771C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13898967 | ||||||
| chr7:13899074
|
G | A | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1212+1664C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899074 | ||||||
| chr7:13899214
|
T | C | 3 | a0001c0001t0003g0295a0001c0001t0005g0168a0002c0002t0003g0051 | 3 | HG00544.hp2 HG00609.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1212+1524A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899214 | ||||||
| chr7:13899277
|
G | C | 1 | a0001c0001t0006g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1212+1461C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899277 | ||||||
| chr7:13899328
|
T | C | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1212+1410A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899328 | ||||||
| chr7:13899434
|
G | A | 1 | a0002c0002t0001g0259 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1212+1304C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899434 | ||||||
| chr7:13899555
|
T | G | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1212+1183A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899555 | ||||||
| chr7:13899591
|
A | G | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212+1147T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899591 | ||||||
| chr7:13899742
|
G | A | 3 | a0001c0001t0006g0302a0001c0001t0006g0307a0002c0002t0006g0078 | 3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1212+996C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899742 | ||||||
| chr7:13899818
|
T | C | 15 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(12): Show | 15 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212+920A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899818 | ||||||
| chr7:13899921
|
G | C | 7 | a0001c0001t0015g0132a0001c0001t0015g0139a0001c0001t0021g0140others(4): Show | 7 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212+817C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899921 | ||||||
| chr7:13899958
|
A | G | 102 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.1212+780T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899958 | ||||||
| chr7:13899969
|
G | T | 2 | a0001c0001t0002g0106a0002c0002t0001g0194 | 2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1212+769C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13899969 | ||||||
| chr7:13900037
|
G | A | 8 | a0001c0001t0004g0263a0001c0001t0014g0044a0001c0001t0018g0100others(5): Show | 8 | HG02258.hp1 HG02895.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1212+701C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900037 | ||||||
| chr7:13900129
|
AAAAC | A | 7 | a0001c0001t0014g0025a0001c0001t0014g0080a0001c0001t0014g0112others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212+605_1212+608d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900129 | ||||||
| chr7:13900147
|
A | C | 1 | a0001c0001t0026g0041 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1212+591T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900147 | ||||||
| chr7:13900207
|
A | C | 102 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.1212+531T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900207 | ||||||
| chr7:13900241
|
A | G | 15 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(12): Show | 15 | HG00597.hp2 HG02074.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212+497T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900241 | ||||||
| chr7:13900251
|
A | T | 3 | a0001c0001t0004g0189a0002c0002t0004g0145a0002c0002t0007g0120 | 3 | NA18946.hp1 NA18964.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1212+487T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900251 | ||||||
| chr7:13900333
|
T | A | 102 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.1212+405A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900333 | ||||||
| chr7:13900363
|
C | A | 2 | a0001c0001t0004g0238a0001c0001t0007g0317 | 2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1212+375G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900363 | ||||||
| chr7:13900493
|
T | C | 1 | a0002c0002t0005g0176 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1212+245A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900493 | ||||||
| chr7:13900666
|
G | A | 7 | a0001c0001t0012g0117a0001c0001t0012g0297a0001c0001t0012g0298others(4): Show | 7 | HG00597.hp2 HG02165.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1212+72C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900666 | ||||||
| chr7:13900669
|
G | A | 2 | a0001c0001t0040g0011a0001c0001t0055g0257 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1212+69C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 13/13 | chr7 | 13900669 | ||||||
| chr7:13900989
|
C | G | 1 | a0001c0001t0003g0290 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1111-150G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13900989 | ||||||
| chr7:13901005
|
CT | C | 239 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1111-167delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901005 | ||||||
| chr7:13901030
|
G | C | 16 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(13): Show | 16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1111-191C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901030 | ||||||
| chr7:13901106
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1111-267C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901106 | ||||||
| chr7:13901109
|
A | C | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111-270T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901109 | ||||||
| chr7:13901204
|
C | A | 7 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0018g0316others(4): Show | 7 | HG02280.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111-365G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901204 | ||||||
| chr7:13901215
|
G | C | 1 | a0001c0001t0005g0170 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1111-376C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901215 | ||||||
| chr7:13901296
|
C | T | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1111-457G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901296 | ||||||
| chr7:13901297
|
G | C | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-458C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901297 | ||||||
| chr7:13901325
|
G | T | 1 | a0001c0001t0005g0247 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1111-486C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901325 | ||||||
| chr7:13901428
|
A | G | 3 | a0001c0001t0003g0047a0001c0001t0003g0050a0001c0001t0003g0094 | 3 | HG02135.hp1 NA18971.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1111-589T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901428 | ||||||
| chr7:13901498
|
G | C | 85 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.1111-659C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901498 | ||||||
| chr7:13901577
|
C | G | 1 | a0002c0002t0008g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1111-738G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901577 | ||||||
| chr7:13901762
|
C | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0254others(1): Show | 4 | HG03540.hp2 HG03834.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111-923G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901762 | ||||||
| chr7:13901913
|
T | G | 14 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(11): Show | 14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111-1074A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901913 | ||||||
| chr7:13901929
|
T | C | 1 | a0001c0001t0054g0195 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1111-1090A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13901929 | ||||||
| chr7:13902083
|
T | C | 1 | a0002c0002t0012g0055 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1111-1244A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902083 | ||||||
| chr7:13902210
|
T | A | 101 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.1111-1371A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902210 | ||||||
| chr7:13902374
|
G | A | 1 | a0002c0002t0003g0122 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1111-1535C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902374 | ||||||
| chr7:13902420
|
T | C | 1 | a0001c0001t0003g0282 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1111-1581A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902420 | ||||||
| chr7:13902515
|
C | T | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111-1676G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902515 | ||||||
| chr7:13902521
|
T | TG | 14 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(11): Show | 14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111-1683dupC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902521 | ||||||
| chr7:13902562
|
C | G | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1111-1723G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902562 | ||||||
| chr7:13902716
|
G | T | 118 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0004g0001others(115): Show | 119 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1111-1877C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902716 | ||||||
| chr7:13902963
|
T | C | 1 | a0001c0001t0006g0061 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1111-2124A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13902963 | ||||||
| chr7:13903058
|
A | G | 1 | a0001c0001t0012g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1111-2219T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903058 | ||||||
| chr7:13903089
|
G | A | 85 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.1111-2250C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903089 | ||||||
| chr7:13903124
|
C | G | 1 | a0001c0001t0004g0001 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1111-2285G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903124 | ||||||
| chr7:13903256
|
C | A | 12 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0083others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1111-2417G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903256 | ||||||
| chr7:13903283
|
A | C | 1 | a0002c0002t0001g0259 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1111-2444T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903283 | ||||||
| chr7:13903365
|
C | T | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1111-2526G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903365 | ||||||
| chr7:13903460
|
C | G | 1 | a0002c0002t0031g0005 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1111-2621G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903460 | ||||||
| chr7:13903481
|
G | A | 1 | a0001c0001t0009g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1111-2642C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903481 | ||||||
| chr7:13903509
|
T | A | 1 | a0002c0002t0005g0274 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1111-2670A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903509 | ||||||
| chr7:13903554
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1111-2715C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903554 | ||||||
| chr7:13903613
|
A | G | 4 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0001t0019g0216others(1): Show | 4 | HG00099.hp2 HG00140.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-2774T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903613 | ||||||
| chr7:13903762
|
C | CA | 10 | a0001c0001t0002g0024a0001c0001t0002g0048a0001c0001t0002g0060others(7): Show | 10 | HG00597.hp1 HG01192.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1110+2667dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903762 | ||||||
| chr7:13903762
|
CA | C | 62 | a0001c0001t0001g0187a0001c0001t0002g0026a0001c0001t0002g0283others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1110+2667delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903762 | ||||||
| chr7:13903762
|
CAA | C | 92 | a0001c0001t0004g0001a0001c0001t0004g0137a0001c0001t0004g0177others(89): Show | 93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1110+2666_1110+266 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903762 | ||||||
| chr7:13903787
|
T | C | 1 | a0001c0001t0007g0103 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1110+2643A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903787 | ||||||
| chr7:13903829
|
T | C | 5 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0051g0237others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110+2601A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903829 | ||||||
| chr7:13903896
|
C | T | 3 | a0001c0001t0015g0139a0001c0001t0021g0140a0001c0001t0025g0312 | 3 | HG01081.hp2 HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1110+2534G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13903896 | ||||||
| chr7:13904069
|
T | C | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+2361A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904069 | ||||||
| chr7:13904154
|
G | T | 7 | a0001c0001t0015g0132a0001c0001t0015g0139a0001c0001t0021g0140others(4): Show | 7 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110+2276C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904154 | ||||||
| chr7:13904291
|
C | T | 1 | a0001c0001t0055g0257 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1110+2139G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904291 | ||||||
| chr7:13904496
|
G | T | 2 | a0001c0001t0053g0226a0002c0002t0037g0062 | 2 | HG00438.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1110+1934C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904496 | ||||||
| chr7:13904523
|
A | C | 2 | a0001c0001t0040g0011a0001c0001t0055g0257 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1110+1907T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904523 | ||||||
| chr7:13904668
|
T | C | 116 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0004g0001others(113): Show | 117 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1110+1762A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904668 | ||||||
| chr7:13904672
|
T | G | 17 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0010g0040others(14): Show | 17 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1110+1758A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904672 | ||||||
| chr7:13904697
|
G | A | 3 | a0001c0001t0006g0302a0001c0001t0006g0307a0002c0002t0006g0078 | 3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1110+1733C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904697 | ||||||
| chr7:13904771
|
C | A | 3 | a0001c0001t0006g0031a0001c0001t0006g0123a0001c0001t0006g0313 | 3 | HG02486.hp1 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1110+1659G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904771 | ||||||
| chr7:13904893
|
A | C | 2 | a0001c0001t0018g0100a0001c0001t0056g0261 | 2 | HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1110+1537T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904893 | ||||||
| chr7:13904919
|
T | G | 1 | a0001c0004t0001g0154 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1110+1511A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904919 | ||||||
| chr7:13904966
|
G | A | 13 | a0001c0001t0004g0263a0001c0001t0018g0100a0001c0001t0018g0316others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1110+1464C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13904966 | ||||||
| chr7:13905217
|
G | A | 17 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(14): Show | 17 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1110+1213C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905217 | ||||||
| chr7:13905226
|
G | A | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1110+1204C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905226 | ||||||
| chr7:13905271
|
C | T | 24 | a0001c0001t0004g0166a0001c0001t0004g0189a0001c0001t0004g0249others(21): Show | 24 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1110+1159G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905271 | ||||||
| chr7:13905288
|
A | C | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1110+1142T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905288 | ||||||
| chr7:13905379
|
T | C | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1110+1051A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905379 | ||||||
| chr7:13905433
|
T | A | 1 | a0001c0001t0004g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1110+997A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905433 | ||||||
| chr7:13905502
|
T | C | 110 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.1110+928A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905502 | ||||||
| chr7:13905693
|
C | T | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1110+737G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905693 | ||||||
| chr7:13905718
|
G | C | 13 | a0001c0001t0004g0263a0001c0001t0017g0023a0001c0001t0017g0042others(10): Show | 13 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1110+712C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905718 | ||||||
| chr7:13905787
|
C | A | 1 | a0001c0001t0046g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1110+643G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905787 | ||||||
| chr7:13905833
|
C | G | 142 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1110+597G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905833 | ||||||
| chr7:13905941
|
C | T | 1 | a0001c0001t0011g0081 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1110+489G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13905941 | ||||||
| chr7:13906050
|
A | G | 218 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(215): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1110+380T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906050 | ||||||
| chr7:13906081
|
G | A | 2 | a0001c0001t0002g0106a0002c0002t0001g0194 | 2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1110+349C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906081 | ||||||
| chr7:13906155
|
T | G | 14 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(11): Show | 14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110+275A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906155 | ||||||
| chr7:13906239
|
C | T | 24 | a0001c0001t0004g0166a0001c0001t0004g0189a0001c0001t0004g0249others(21): Show | 24 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1110+191G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906239 | ||||||
| chr7:13906250
|
C | T | 3 | a0001c0001t0006g0302a0001c0001t0006g0307a0002c0002t0006g0078 | 3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1110+180G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906250 | ||||||
| chr7:13906251
|
G | C | 1 | a0001c0001t0003g0016 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1110+179C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906251 | ||||||
| chr7:13906298
|
C | T | 1 | a0001c0001t0004g0238 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1110+132G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906298 | ||||||
| chr7:13906306
|
T | C | 3 | a0001c0001t0006g0302a0001c0001t0006g0307a0002c0002t0006g0078 | 3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1110+124A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906306 | ||||||
| chr7:13906364
|
C | G | 2 | a0001c0001t0010g0084a0001c0001t0010g0085 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1110+66G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 12/13 | chr7 | 13906364 | ||||||
| chr7:13906623
|
T | C | 1 | a0002c0002t0003g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.941-24A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906623 | ||||||
| chr7:13906658
|
A | G | 16 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(13): Show | 16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.941-59T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906658 | ||||||
| chr7:13906691
|
C | T | 55 | a0001c0001t0002g0013a0001c0001t0002g0057a0001c0001t0004g0001others(52): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.941-92G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906691 | ||||||
| chr7:13906790
|
C | T | 1 | a0002c0002t0005g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.941-191G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906790 | ||||||
| chr7:13906879
|
G | A | 2 | a0002c0002t0007g0020a0002c0002t0007g0049 | 2 | HG00408.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.941-280C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906879 | ||||||
| chr7:13906889
|
C | CT | 14 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(11): Show | 14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.941-291dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13906889 | ||||||
| chr7:13907014
|
G | A | 16 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(13): Show | 16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.941-415C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907014 | ||||||
| chr7:13907028
|
T | C | 5 | a0001c0001t0026g0041a0001c0001t0026g0098a0001c0001t0028g0240others(2): Show | 5 | HG01255.hp1 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.941-429A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907028 | ||||||
| chr7:13907062
|
T | C | 7 | a0001c0001t0007g0067a0001c0001t0007g0076a0001c0001t0007g0077others(4): Show | 7 | HG00642.hp1 HG00741.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.941-463A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907062 | ||||||
| chr7:13907069
|
T | A | 55 | a0001c0001t0002g0013a0001c0001t0002g0057a0001c0001t0004g0001others(52): Show | 56 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.941-470A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907069 | ||||||
| chr7:13907187
|
G | C | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-588C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907187 | ||||||
| chr7:13907306
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.941-707T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907306 | ||||||
| chr7:13907486
|
A | G | 1 | a0002c0002t0005g0176 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.941-887T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907486 | ||||||
| chr7:13907545
|
C | CA | 49 | a0001c0001t0001g0157a0001c0001t0002g0013a0001c0001t0002g0017others(46): Show | 50 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.941-947dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907545 | ||||||
| chr7:13907545
|
C | CAA | 11 | a0001c0001t0004g0238a0001c0001t0007g0053a0001c0001t0007g0317others(8): Show | 11 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.941-948_941-947dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907545 | ||||||
| chr7:13907664
|
G | A | 119 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(116): Show | 120 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.941-1065C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907664 | ||||||
| chr7:13907980
|
G | GT | 83 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.941-1382dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13907980 | ||||||
| chr7:13908043
|
A | G | 1 | a0002c0002t0003g0071 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.941-1444T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908043 | ||||||
| chr7:13908094
|
G | A | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.941-1495C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908094 | ||||||
| chr7:13908151
|
T | C | 6 | a0001c0001t0003g0019a0001c0001t0003g0099a0001c0001t0005g0248others(3): Show | 6 | HG00280.hp2 HG01168.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.940+1481A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908151 | ||||||
| chr7:13908221
|
T | C | 1 | a0001c0001t0003g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.940+1411A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908221 | ||||||
| chr7:13908401
|
C | G | 24 | a0001c0001t0004g0166a0001c0001t0004g0189a0001c0001t0004g0249others(21): Show | 24 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.940+1231G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908401 | ||||||
| chr7:13908503
|
C | T | 1 | a0002c0002t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.940+1129G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908503 | ||||||
| chr7:13908554
|
G | A | 211 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.940+1078C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908554 | ||||||
| chr7:13908604
|
T | C | 1 | a0001c0001t0013g0032 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.940+1028A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908604 | ||||||
| chr7:13908662
|
G | A | 2 | a0001c0001t0002g0106a0002c0002t0001g0194 | 2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.940+970C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908662 | ||||||
| chr7:13908879
|
T | C | 3 | a0001c0001t0006g0302a0001c0001t0006g0307a0002c0002t0006g0078 | 3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.940+753A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908879 | ||||||
| chr7:13908892
|
T | C | 100 | a0001c0001t0001g0157a0001c0001t0002g0013a0001c0001t0002g0017others(97): Show | 101 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.940+740A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13908892 | ||||||
| chr7:13909058
|
A | G | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.940+574T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909058 | ||||||
| chr7:13909094
|
T | C | 112 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.940+538A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909094 | ||||||
| chr7:13909136
|
TA | T | 182 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.940+495delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909136 | ||||||
| chr7:13909136
|
TAA | T | 21 | a0001c0001t0002g0119a0001c0001t0007g0076a0001c0001t0010g0040others(18): Show | 21 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.940+494_940+495del others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909136 | ||||||
| chr7:13909172
|
C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.940+460G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909172 | ||||||
| chr7:13909210
|
C | T | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.940+422G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909210 | ||||||
| chr7:13909300
|
A | T | 1 | a0002c0002t0003g0121 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.940+332T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909300 | ||||||
| chr7:13909587
|
C | G | 1 | a0001c0001t0002g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.940+45G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 11/13 | chr7 | 13909587 | ||||||
| chr7:13909810
|
C | G | 5 | a0001c0001t0014g0080a0001c0001t0014g0112a0001c0001t0015g0136others(2): Show | 5 | HG02055.hp2 HG02717.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.872-110G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13909810 | ||||||
| chr7:13910036
|
T | G | 5 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0051g0237others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.872-336A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910036 | ||||||
| chr7:13910040
|
A | T | 3 | a0001c0001t0003g0292a0002c0002t0003g0071a0002c0002t0005g0274 | 3 | NA18956.hp1 NA18972.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.872-340T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910040 | ||||||
| chr7:13910228
|
C | CT | 110 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.872-529dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | ||||||
| chr7:13910228
|
C | CTT | 16 | a0001c0001t0001g0254a0001c0001t0004g0137a0001c0001t0004g0263others(13): Show | 16 | HG00438.hp2 HG00597.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.872-530_872-529dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | ||||||
| chr7:13910228
|
C | CTTT | 52 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0057others(49): Show | 53 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.872-531_872-529dup others(3): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | ||||||
| chr7:13910228
|
C | CTTTT | 30 | a0001c0001t0002g0013a0001c0001t0002g0024a0001c0001t0004g0267others(27): Show | 30 | HG00280.hp1 HG00597.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.872-532_872-529dup others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | ||||||
| chr7:13910228
|
CTTTT | C | 12 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0083others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.872-532_872-529del others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910228 | ||||||
| chr7:13910339
|
T | G | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.872-639A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910339 | ||||||
| chr7:13910429
|
T | C | 1 | a0001c0001t0004g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.872-729A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910429 | ||||||
| chr7:13910578
|
T | C | 1 | a0001c0001t0057g0174 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.871+661A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910578 | ||||||
| chr7:13910579
|
G | A | 2 | a0001c0001t0006g0300a0001c0001t0042g0303 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.871+660C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910579 | ||||||
| chr7:13910613
|
T | G | 2 | a0001c0001t0006g0036a0001c0001t0006g0308 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.871+626A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910613 | ||||||
| chr7:13910673
|
C | T | 13 | a0001c0001t0009g0179a0001c0001t0009g0180a0001c0001t0009g0205others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.871+566G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910673 | ||||||
| chr7:13910735
|
C | G | 46 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(43): Show | 47 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.871+504G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910735 | ||||||
| chr7:13910738
|
G | A | 16 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(13): Show | 16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.871+501C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910738 | ||||||
| chr7:13910970
|
G | A | 16 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(13): Show | 16 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.871+269C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13910970 | ||||||
| chr7:13911034
|
T | G | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.871+205A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13911034 | ||||||
| chr7:13911213
|
C | T | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.871+26G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 10/13 | chr7 | 13911213 | ||||||
| chr7:13911359
|
G | A | 1 | a0001c0001t0012g0108 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.803-52C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911359 | ||||||
| chr7:13911457
|
G | C | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803-150C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911457 | ||||||
| chr7:13911566
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.803-259T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911566 | ||||||
| chr7:13911693
|
T | C | 2 | a0001c0001t0026g0041a0001c0001t0026g0098 | 2 | HG01255.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.803-386A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911693 | ||||||
| chr7:13911774
|
T | G | 60 | a0001c0001t0001g0157a0001c0001t0002g0013a0001c0001t0002g0017others(57): Show | 61 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.803-467A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911774 | ||||||
| chr7:13911775
|
T | C | 60 | a0001c0001t0001g0157a0001c0001t0002g0013a0001c0001t0002g0017others(57): Show | 61 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.803-468A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911775 | ||||||
| chr7:13911820
|
A | G | 3 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | HG03834.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.803-513T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911820 | ||||||
| chr7:13911850
|
G | T | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-543C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13911850 | ||||||
| chr7:13912048
|
C | T | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-741G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912048 | ||||||
| chr7:13912113
|
T | G | 1 | a0001c0001t0004g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.803-806A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912113 | ||||||
| chr7:13912172
|
G | A | 1 | a0001c0001t0026g0041 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.803-865C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912172 | ||||||
| chr7:13912181
|
T | C | 5 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0051g0237others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-874A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912181 | ||||||
| chr7:13912183
|
G | A | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-876C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912183 | ||||||
| chr7:13912223
|
T | C | 7 | a0001c0001t0013g0109a0002c0002t0009g0196a0002c0002t0009g0206others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-916A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912223 | ||||||
| chr7:13912286
|
C | T | 1 | a0001c0001t0016g0190 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.803-979G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912286 | ||||||
| chr7:13912370
|
T | A | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-1063A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912370 | ||||||
| chr7:13912442
|
ATTTAC | A | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1140_803-1136d others(7): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912442 | ||||||
| chr7:13912479
|
G | A | 3 | a0001c0001t0019g0153a0001c0001t0019g0216a0001c0001t0035g0124 | 3 | HG00099.hp2 HG00140.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.803-1172C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912479 | ||||||
| chr7:13912644
|
C | T | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803-1337G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912644 | ||||||
| chr7:13912758
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.803-1451T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912758 | ||||||
| chr7:13912813
|
G | C | 2 | a0001c0001t0040g0011a0001c0001t0055g0257 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.803-1506C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13912813 | ||||||
| chr7:13913169
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.803-1862A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913169 | ||||||
| chr7:13913218
|
C | T | 2 | a0001c0001t0002g0065a0002c0002t0001g0203 | 2 | HG01106.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.803-1911G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913218 | ||||||
| chr7:13913363
|
T | C | 7 | a0001c0001t0004g0263a0001c0001t0014g0044a0001c0001t0018g0100others(4): Show | 7 | HG02258.hp1 HG02895.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-2056A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913363 | ||||||
| chr7:13913484
|
C | T | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-2177G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913484 | ||||||
| chr7:13913510
|
C | T | 120 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(117): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-2203G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913510 | ||||||
| chr7:13913536
|
C | T | 120 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(117): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-2229G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913536 | ||||||
| chr7:13913579
|
A | T | 120 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(117): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-2272T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913579 | ||||||
| chr7:13913775
|
T | G | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-2468A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913775 | ||||||
| chr7:13913776
|
A | G | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-2469T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913776 | ||||||
| chr7:13913869
|
GGGGTACC others(5): Show |
G | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803-2574_803-2563d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913869 | ||||||
| chr7:13913872
|
G | T | 3 | a0001c0001t0051g0237a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.803-2565C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913872 | ||||||
| chr7:13913878
|
C | CT | 34 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0254others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.803-2572dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | ||||||
| chr7:13913878
|
C | CTT | 66 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.803-2573_803-2572d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | ||||||
| chr7:13913878
|
CT | C | 21 | a0001c0001t0004g0166a0001c0001t0006g0300a0001c0001t0006g0302others(18): Show | 21 | HG01071.hp1 HG01109.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.803-2572delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | ||||||
| chr7:13913878
|
CTT | C | 77 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(74): Show | 78 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.803-2573_803-2572d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | ||||||
| chr7:13913878
|
CTTT | C | 12 | a0001c0001t0004g0238a0001c0001t0007g0317a0001c0001t0010g0045others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.803-2574_803-2572d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | ||||||
| chr7:13913878
|
CTTTT | C | 14 | a0001c0001t0010g0040a0001c0001t0010g0069a0001c0001t0010g0083others(11): Show | 14 | HG01071.hp2 HG01081.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.803-2575_803-2572d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913878 | ||||||
| chr7:13913883
|
T | C | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803-2576A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913883 | ||||||
| chr7:13913915
|
C | T | 7 | a0001c0001t0013g0109a0002c0002t0009g0196a0002c0002t0009g0206others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-2608G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13913915 | ||||||
| chr7:13914008
|
T | C | 93 | a0001c0001t0001g0157a0001c0001t0002g0013a0001c0001t0002g0017others(90): Show | 94 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.803-2701A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914008 | ||||||
| chr7:13914033
|
G | A | 7 | a0001c0001t0013g0109a0002c0002t0009g0196a0002c0002t0009g0206others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-2726C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914033 | ||||||
| chr7:13914066
|
G | C | 1 | a0002c0002t0005g0162 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.803-2759C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914066 | ||||||
| chr7:13914203
|
C | T | 1 | a0001c0001t0044g0127 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.803-2896G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914203 | ||||||
| chr7:13914211
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.803-2904A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914211 | ||||||
| chr7:13914244
|
C | G | 120 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(117): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-2937G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914244 | ||||||
| chr7:13914251
|
G | A | 1 | a0001c0001t0013g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.803-2944C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914251 | ||||||
| chr7:13914440
|
T | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0187 | 3 | HG00099.hp1 HG01361.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.803-3133A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914440 | ||||||
| chr7:13914505
|
C | T | 2 | a0001c0001t0006g0300a0001c0001t0042g0303 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.803-3198G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914505 | ||||||
| chr7:13914614
|
A | G | 15 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(12): Show | 15 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-3307T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914614 | ||||||
| chr7:13914618
|
TA | T | 104 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(101): Show | 105 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.803-3312delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914618 | ||||||
| chr7:13914618
|
TAA | T | 23 | a0001c0001t0004g0181a0001c0001t0004g0267a0001c0001t0006g0058others(20): Show | 23 | HG00408.hp1 HG00735.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.803-3313_803-3312d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914618 | ||||||
| chr7:13914653
|
G | A | 1 | a0002c0002t0005g0274 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.803-3346C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914653 | ||||||
| chr7:13914740
|
A | T | 120 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(117): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-3433T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914740 | ||||||
| chr7:13914741
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.803-3434A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914741 | ||||||
| chr7:13914784
|
A | G | 1 | a0001c0001t0012g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.803-3477T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914784 | ||||||
| chr7:13914867
|
G | A | 15 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(12): Show | 15 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-3560C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914867 | ||||||
| chr7:13914895
|
C | T | 207 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(204): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.803-3588G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914895 | ||||||
| chr7:13914915
|
C | A | 120 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(117): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-3608G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914915 | ||||||
| chr7:13914937
|
C | G | 2 | a0001c0001t0026g0041a0001c0001t0026g0098 | 2 | HG01255.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.803-3630G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13914937 | ||||||
| chr7:13915006
|
C | T | 120 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(117): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-3699G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915006 | ||||||
| chr7:13915483
|
C | T | 120 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(117): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-4176G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915483 | ||||||
| chr7:13915485
|
T | A | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-4178A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915485 | ||||||
| chr7:13915508
|
C | A | 1 | a0001c0001t0012g0285 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.803-4201G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915508 | ||||||
| chr7:13915530
|
T | C | 77 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(74): Show | 78 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.803-4223A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915530 | ||||||
| chr7:13915591
|
G | A | 33 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0010g0040others(30): Show | 33 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.803-4284C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915591 | ||||||
| chr7:13915599
|
G | T | 1 | a0002c0002t0004g0212 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.803-4292C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915599 | ||||||
| chr7:13915693
|
T | G | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803-4386A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915693 | ||||||
| chr7:13915699
|
C | T | 23 | a0001c0001t0004g0166a0001c0001t0004g0189a0001c0001t0004g0249others(20): Show | 23 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.803-4392G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915699 | ||||||
| chr7:13915701
|
C | G | 120 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(117): Show | 121 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.803-4394G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915701 | ||||||
| chr7:13915743
|
T | C | 9 | a0001c0001t0014g0025a0001c0001t0014g0044a0001c0001t0014g0080others(6): Show | 9 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-4436A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915743 | ||||||
| chr7:13915744
|
G | C | 3 | a0001c0001t0051g0237a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.803-4437C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915744 | ||||||
| chr7:13915757
|
A | AT | 6 | a0001c0001t0003g0287a0001c0001t0003g0293a0001c0001t0005g0193others(3): Show | 6 | HG02965.hp1 HG03225.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-4451dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915757 | ||||||
| chr7:13915757
|
AT | A | 24 | a0001c0001t0002g0017a0001c0001t0003g0295a0001c0001t0004g0189others(21): Show | 24 | HG00544.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.803-4451delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915757 | ||||||
| chr7:13915780
|
A | G | 2 | a0001c0001t0010g0069a0001c0001t0010g0126 | 2 | HG01071.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.803-4473T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915780 | ||||||
| chr7:13915980
|
G | A | 1 | a0001c0004t0001g0154 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.803-4673C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13915980 | ||||||
| chr7:13916012
|
G | T | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-4705C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916012 | ||||||
| chr7:13916013
|
G | C | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-4706C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916013 | ||||||
| chr7:13916015
|
T | C | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-4708A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916015 | ||||||
| chr7:13916016
|
G | A | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-4709C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916016 | ||||||
| chr7:13916017
|
C | T | 215 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.803-4710G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916017 | ||||||
| chr7:13916037
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.803-4730G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916037 | ||||||
| chr7:13916093
|
C | T | 1 | a0001c0001t0006g0088 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.803-4786G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916093 | ||||||
| chr7:13916110
|
T | G | 1 | a0001c0001t0041g0309 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.803-4803A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916110 | ||||||
| chr7:13916152
|
A | G | 3 | a0001c0001t0003g0092a0002c0002t0022g0003a0002c0002t0022g0004 | 3 | HG00738.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.803-4845T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916152 | ||||||
| chr7:13916154
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.803-4847T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916154 | ||||||
| chr7:13916307
|
T | C | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803-5000A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916307 | ||||||
| chr7:13916364
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.803-5057C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916364 | ||||||
| chr7:13916475
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.803-5168A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916475 | ||||||
| chr7:13916552
|
C | T | 3 | a0001c0001t0006g0302a0001c0001t0006g0307a0002c0002t0006g0078 | 3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.803-5245G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916552 | ||||||
| chr7:13916569
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.803-5262G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916569 | ||||||
| chr7:13916586
|
C | T | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-5279G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916586 | ||||||
| chr7:13916672
|
T | C | 1 | a0001c0001t0006g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.803-5365A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916672 | ||||||
| chr7:13916729
|
G | T | 5 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0051g0237others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-5422C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916729 | ||||||
| chr7:13916819
|
C | A | 108 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(105): Show | 109 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.803-5512G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916819 | ||||||
| chr7:13916827
|
G | C | 5 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0051g0237others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-5520C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916827 | ||||||
| chr7:13916859
|
G | A | 1 | a0001c0001t0006g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.803-5552C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916859 | ||||||
| chr7:13916906
|
T | G | 1 | a0002c0002t0001g0131 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.803-5599A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916906 | ||||||
| chr7:13916930
|
CA | C | 122 | a0001c0001t0001g0157a0001c0001t0002g0024a0001c0001t0002g0026others(119): Show | 123 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.803-5624delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916930 | ||||||
| chr7:13916961
|
G | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.803-5654C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916961 | ||||||
| chr7:13916973
|
A | G | 1 | a0001c0001t0041g0309 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.803-5666T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916973 | ||||||
| chr7:13916980
|
G | A | 122 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(119): Show | 123 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.803-5673C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916980 | ||||||
| chr7:13916988
|
A | G | 14 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(11): Show | 14 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.803-5681T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13916988 | ||||||
| chr7:13917004
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0018g0316 | 3 | NA18949.hp2 NA18953.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.803-5697C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917004 | ||||||
| chr7:13917107
|
C | T | 1 | a0002c0002t0017g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.803-5800G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917107 | ||||||
| chr7:13917152
|
T | C | 1 | a0001c0005t0010g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.803-5845A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917152 | ||||||
| chr7:13917168
|
T | C | 2 | a0001c0001t0017g0023a0001c0001t0017g0042 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.803-5861A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917168 | ||||||
| chr7:13917175
|
A | C | 1 | a0001c0001t0038g0306 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.803-5868T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917175 | ||||||
| chr7:13917273
|
C | T | 1 | a0002c0002t0009g0210 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.803-5966G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917273 | ||||||
| chr7:13917288
|
G | GTATT | 35 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0003g0009others(32): Show | 35 | HG00099.hp1 HG00323.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.803-5985_803-5982d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | ||||||
| chr7:13917288
|
G | GTATTTAT others(1): Show |
6 | a0001c0001t0001g0184a0001c0001t0002g0038a0001c0001t0019g0216others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-5989_803-5982d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | ||||||
| chr7:13917288
|
G | GTATTTAT others(5): Show |
1 | a0002c0002t0001g0198 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.803-5993_803-5982d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | ||||||
| chr7:13917288
|
GTATT | G | 45 | a0001c0001t0001g0167a0001c0001t0003g0292a0001c0001t0004g0166others(42): Show | 45 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.803-5985_803-5982d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | ||||||
| chr7:13917288
|
GTATTTAT others(1): Show |
G | 8 | a0001c0001t0006g0300a0001c0001t0011g0081a0001c0001t0011g0101others(5): Show | 8 | HG01074.hp1 HG01167.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-5989_803-5982d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | ||||||
| chr7:13917288
|
GTATTTAT others(5): Show |
G | 3 | a0001c0001t0010g0069a0001c0001t0010g0126a0001c0001t0039g0086 | 3 | HG01071.hp2 HG02109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.803-5993_803-5982d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | ||||||
| chr7:13917288
|
GTATTTAT others(13): Show |
G | 1 | a0001c0001t0017g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.803-6001_803-5982d others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917288 | ||||||
| chr7:13917340
|
G | A | 82 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.803-6033C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917340 | ||||||
| chr7:13917411
|
G | A | 82 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.803-6104C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917411 | ||||||
| chr7:13917420
|
T | C | 75 | a0001c0001t0001g0157a0001c0001t0002g0017a0001c0001t0002g0024others(72): Show | 76 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.803-6113A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917420 | ||||||
| chr7:13917429
|
C | T | 1 | a0001c0001t0005g0193 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.803-6122G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917429 | ||||||
| chr7:13917563
|
C | T | 1 | a0001c0001t0004g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.803-6256G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917563 | ||||||
| chr7:13917693
|
G | A | 94 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.803-6386C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917693 | ||||||
| chr7:13917781
|
G | A | 1 | a0002c0002t0004g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.803-6474C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917781 | ||||||
| chr7:13917819
|
C | T | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-6512G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917819 | ||||||
| chr7:13917833
|
G | A | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-6526C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917833 | ||||||
| chr7:13917874
|
A | G | 2 | a0001c0001t0029g0258a0001c0001t0032g0006 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.803-6567T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13917874 | ||||||
| chr7:13918075
|
A | G | 3 | a0001c0001t0006g0302a0001c0001t0006g0307a0002c0002t0006g0078 | 3 | HG02630.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.803-6768T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918075 | ||||||
| chr7:13918181
|
CT | C | 13 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(10): Show | 13 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.803-6875delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918181 | ||||||
| chr7:13918183
|
T | A | 13 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(10): Show | 13 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.803-6876A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918183 | ||||||
| chr7:13918230
|
G | C | 1 | a0001c0001t0041g0309 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.803-6923C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918230 | ||||||
| chr7:13918388
|
G | C | 1 | a0001c0001t0004g0001 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.803-7081C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918388 | ||||||
| chr7:13918430
|
A | C | 51 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.803-7123T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918430 | ||||||
| chr7:13918470
|
G | C | 1 | a0001c0001t0006g0102 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.803-7163C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918470 | ||||||
| chr7:13918540
|
C | G | 10 | a0001c0001t0001g0255a0001c0001t0002g0065a0001c0001t0002g0107others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-7233G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918540 | ||||||
| chr7:13918544
|
G | GCAGC | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-7241_803-7238d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918544 | ||||||
| chr7:13918578
|
T | C | 1 | a0002c0002t0007g0020 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.803-7271A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918578 | ||||||
| chr7:13918600
|
AATC | A | 27 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.803-7296_803-7294d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918600 | ||||||
| chr7:13918688
|
C | T | 2 | a0002c0002t0002g0075a0002c0002t0008g0197 | 2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.803-7381G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918688 | ||||||
| chr7:13918729
|
T | TG | 18 | a0001c0001t0001g0167a0001c0001t0001g0185a0001c0001t0001g0201others(15): Show | 18 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.803-7423dupC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918729 | ||||||
| chr7:13918734
|
G | GA | 3 | a0001c0001t0011g0074a0001c0001t0017g0042a0002c0002t0017g0037 | 3 | HG00741.hp2 HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.803-7428_803-7427i others(3): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918734 | ||||||
| chr7:13918737
|
C | T | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-7430G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918737 | ||||||
| chr7:13918738
|
G | A | 1 | a0001c0001t0004g0001 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.803-7431C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918738 | ||||||
| chr7:13918741
|
G | A | 1 | a0001c0001t0027g0256 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.803-7434C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918741 | ||||||
| chr7:13918754
|
T | C | 27 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.803-7447A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918754 | ||||||
| chr7:13918765
|
C | G | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.803-7458G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918765 | ||||||
| chr7:13918776
|
A | C | 1 | a0001c0001t0047g0218 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.803-7469T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918776 | ||||||
| chr7:13918798
|
G | A | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.803-7491C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918798 | ||||||
| chr7:13918798
|
G | T | 1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.803-7491C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918798 | ||||||
| chr7:13918843
|
G | A | 27 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.803-7536C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918843 | ||||||
| chr7:13918847
|
A | T | 8 | a0001c0001t0014g0025a0001c0001t0014g0080a0001c0001t0014g0112others(5): Show | 8 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.803-7540T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918847 | ||||||
| chr7:13918853
|
AC | A | 19 | a0001c0001t0002g0119a0001c0001t0002g0283a0001c0001t0004g0183others(16): Show | 19 | HG00621.hp2 HG02074.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.803-7547delG | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918853 | ||||||
| chr7:13918874
|
T | TA | 94 | a0001c0001t0001g0157a0001c0001t0001g0186a0001c0001t0002g0017others(91): Show | 95 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.803-7568dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | ||||||
| chr7:13918874
|
T | TAA | 101 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.803-7569_803-7568d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | ||||||
| chr7:13918874
|
T | TAAA | 11 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0083others(8): Show | 11 | HG01070.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.803-7570_803-7568d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | ||||||
| chr7:13918874
|
T | TAAAA | 26 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(23): Show | 26 | HG00280.hp1 HG00323.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.803-7571_803-7568d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | ||||||
| chr7:13918874
|
T | TAAAAA | 6 | a0001c0001t0010g0069a0001c0001t0010g0126a0001c0001t0028g0240others(3): Show | 6 | HG01071.hp2 HG02109.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-7572_803-7568d others(7): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918874 | ||||||
| chr7:13918910
|
C | T | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803-7603G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918910 | ||||||
| chr7:13918949
|
T | C | 2 | a0001c0001t0017g0023a0001c0001t0017g0042 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.803-7642A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918949 | ||||||
| chr7:13918988
|
C | T | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.803-7681G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13918988 | ||||||
| chr7:13919037
|
G | T | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-7730C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919037 | ||||||
| chr7:13919145
|
A | C | 25 | a0001c0001t0003g0288a0001c0001t0006g0302a0001c0001t0006g0307others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-7838T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919145 | ||||||
| chr7:13919289
|
C | G | 49 | a0001c0001t0003g0288a0001c0001t0006g0302a0001c0001t0006g0307others(46): Show | 49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.803-7982G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919289 | ||||||
| chr7:13919310
|
G | A | 49 | a0001c0001t0003g0288a0001c0001t0006g0302a0001c0001t0006g0307others(46): Show | 49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.803-8003C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919310 | ||||||
| chr7:13919311
|
T | C | 216 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.803-8004A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919311 | ||||||
| chr7:13919316
|
T | C | 5 | a0001c0001t0017g0023a0001c0001t0017g0042a0001c0001t0051g0237others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-8009A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919316 | ||||||
| chr7:13919369
|
C | T | 2 | a0001c0001t0004g0183a0001c0001t0004g0191 | 2 | NA18972.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.803-8062G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919369 | ||||||
| chr7:13919398
|
C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.803-8091G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919398 | ||||||
| chr7:13919463
|
G | A | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.803-8156C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919463 | ||||||
| chr7:13919475
|
G | GT | 7 | a0001c0001t0026g0041a0001c0001t0026g0098a0001c0001t0028g0240others(4): Show | 7 | HG01255.hp1 HG02257.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-8169dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919475 | ||||||
| chr7:13919475
|
GT | G | 6 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0013g0032others(3): Show | 6 | HG01884.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-8169delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919475 | ||||||
| chr7:13919510
|
G | C | 12 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0083others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-8203C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919510 | ||||||
| chr7:13919548
|
CAACT | C | 24 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(21): Show | 24 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.803-8245_803-8242d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919548 | ||||||
| chr7:13919565
|
T | TAC | 17 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0060others(14): Show | 17 | HG00642.hp2 HG00741.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-8260_803-8259d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919565
|
T | TACAC | 9 | a0001c0001t0003g0050a0001c0001t0006g0300a0001c0001t0009g0143others(6): Show | 9 | HG01243.hp2 HG02135.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.803-8262_803-8259d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919565
|
T | TACACAC | 21 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0009g0179others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.803-8264_803-8259d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919565
|
T | TACACACA others(3): Show |
18 | a0001c0001t0003g0288a0001c0001t0012g0108a0001c0001t0012g0117others(15): Show | 18 | HG00597.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.803-8268_803-8259d others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919565
|
T | TACACACA others(5): Show |
2 | a0001c0001t0002g0026a0001c0001t0012g0285 | 2 | NA19060.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.803-8270_803-8259d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919565
|
T | TACACACA others(7): Show |
1 | a0002c0002t0009g0211 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.803-8272_803-8259d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919565
|
TAC | T | 111 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(108): Show | 112 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.803-8260_803-8259d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919565
|
TACAC | T | 6 | a0001c0001t0004g0238a0001c0001t0006g0313a0002c0002t0001g0155others(3): Show | 6 | HG02080.hp1 HG02886.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-8262_803-8259d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919565
|
TACACACA others(7): Show |
T | 4 | a0001c0001t0026g0098a0001c0001t0028g0240a0001c0001t0028g0241others(1): Show | 4 | HG01255.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-8272_803-8259d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919565
|
TACACACA others(9): Show |
T | 2 | a0001c0001t0018g0316a0001c0001t0026g0041 | 2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.803-8274_803-8259d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919565 | ||||||
| chr7:13919593
|
CACACACA others(3): Show |
C | 1 | a0001c0001t0002g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-8296_803-8287d others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919593 | ||||||
| chr7:13919602
|
A | AC | 3 | a0001c0001t0006g0061a0001c0001t0059g0251a0002c0002t0005g0221 | 3 | HG00423.hp1 HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.803-8296_803-8295i others(3): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919602 | ||||||
| chr7:13919632
|
T | C | 2 | a0001c0001t0006g0300a0001c0001t0042g0303 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.803-8325A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919632 | ||||||
| chr7:13919685
|
G | A | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.803-8378C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919685 | ||||||
| chr7:13919764
|
A | G | 1 | a0001c0001t0003g0290 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.803-8457T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919764 | ||||||
| chr7:13919781
|
G | A | 85 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.803-8474C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919781 | ||||||
| chr7:13919873
|
A | G | 1 | a0001c0001t0012g0117 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.803-8566T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919873 | ||||||
| chr7:13919880
|
G | GAC | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-8575_803-8574d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919880 | ||||||
| chr7:13919886
|
C | A | 5 | a0001c0001t0026g0041a0001c0001t0026g0098a0001c0001t0028g0240others(2): Show | 5 | HG01255.hp1 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-8579G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919886 | ||||||
| chr7:13919890
|
C | G | 1 | a0001c0001t0002g0090 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.803-8583G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919890 | ||||||
| chr7:13919892
|
G | C | 19 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(16): Show | 19 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-8585C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919892 | ||||||
| chr7:13919900
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.803-8593C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13919900 | ||||||
| chr7:13920093
|
C | G | 1 | a0001c0001t0005g0235 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.803-8786G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920093 | ||||||
| chr7:13920129
|
C | G | 25 | a0001c0001t0003g0288a0001c0001t0006g0302a0001c0001t0006g0307others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.803-8822G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920129 | ||||||
| chr7:13920209
|
T | C | 1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.803-8902A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920209 | ||||||
| chr7:13920300
|
G | C | 5 | a0001c0001t0026g0041a0001c0001t0026g0098a0001c0001t0028g0240others(2): Show | 5 | HG01255.hp1 HG02809.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-8993C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920300 | ||||||
| chr7:13920417
|
T | C | 6 | a0001c0001t0014g0044a0001c0001t0018g0100a0001c0001t0027g0256others(3): Show | 6 | HG02258.hp1 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-9110A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920417 | ||||||
| chr7:13920441
|
A | AGT | 64 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(61): Show | 64 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.803-9136_803-9135d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | ||||||
| chr7:13920441
|
A | AGTGT | 57 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0002g0017others(54): Show | 58 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.803-9138_803-9135d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | ||||||
| chr7:13920441
|
A | AGTGTGT | 28 | a0001c0001t0002g0026a0001c0001t0002g0119a0001c0001t0002g0283others(25): Show | 28 | HG00597.hp2 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.803-9140_803-9135d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | ||||||
| chr7:13920441
|
A | AGTGTGTG others(1): Show |
10 | a0001c0001t0004g0270a0001c0001t0006g0130a0001c0001t0006g0284others(7): Show | 10 | HG00544.hp1 HG00621.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.803-9142_803-9135d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | ||||||
| chr7:13920441
|
A | AGTGTGTG others(3): Show |
4 | a0001c0001t0007g0296a0001c0001t0029g0258a0001c0001t0032g0006others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-9144_803-9135d others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | ||||||
| chr7:13920441
|
A | AGTGTGTG others(5): Show |
1 | a0002c0002t0029g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.803-9146_803-9135d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | ||||||
| chr7:13920441
|
A | AGTGTGTG others(7): Show |
1 | a0001c0001t0051g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.803-9148_803-9135d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | ||||||
| chr7:13920441
|
A | AGTGTGTG others(9): Show |
2 | a0002c0002t0017g0037a0002c0002t0017g0039 | 2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.803-9150_803-9135d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920441 | ||||||
| chr7:13920511
|
A | C | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-9204T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920511 | ||||||
| chr7:13920628
|
T | C | 2 | a0001c0001t0006g0300a0001c0001t0042g0303 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.803-9321A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920628 | ||||||
| chr7:13920696
|
C | T | 57 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(54): Show | 57 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.803-9389G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920696 | ||||||
| chr7:13920776
|
C | G | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.803-9469G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920776 | ||||||
| chr7:13920782
|
T | C | 15 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(12): Show | 15 | HG00597.hp2 HG02074.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-9475A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920782 | ||||||
| chr7:13920808
|
G | T | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-9501C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920808 | ||||||
| chr7:13920894
|
A | G | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.803-9587T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920894 | ||||||
| chr7:13920955
|
A | G | 58 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-9648T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13920955 | ||||||
| chr7:13921050
|
A | C | 58 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-9743T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921050 | ||||||
| chr7:13921080
|
T | C | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-9773A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921080 | ||||||
| chr7:13921348
|
T | G | 58 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.803-10041A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921348 | ||||||
| chr7:13921419
|
G | A | 55 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.802+10083C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921419 | ||||||
| chr7:13921474
|
G | GA | 6 | a0001c0001t0007g0056a0001c0005t0010g0115a0002c0002t0001g0156others(3): Show | 6 | HG02080.hp1 HG02809.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+10027dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921474 | ||||||
| chr7:13921526
|
G | T | 23 | a0001c0001t0003g0288a0001c0001t0006g0302a0001c0001t0006g0307others(20): Show | 23 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.802+9976C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921526 | ||||||
| chr7:13921601
|
G | A | 3 | a0001c0001t0051g0237a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.802+9901C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921601 | ||||||
| chr7:13921645
|
G | A | 3 | a0002c0002t0003g0122a0002c0002t0005g0269a0002c0002t0005g0271 | 3 | HG02071.hp1 NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.802+9857C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921645 | ||||||
| chr7:13921660
|
G | A | 1 | a0001c0001t0004g0270 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.802+9842C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921660 | ||||||
| chr7:13921680
|
C | T | 3 | a0001c0001t0051g0237a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.802+9822G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921680 | ||||||
| chr7:13921681
|
C | T | 55 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.802+9821G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921681 | ||||||
| chr7:13921737
|
G | A | 53 | a0001c0001t0003g0288a0001c0001t0006g0302a0001c0001t0006g0307others(50): Show | 53 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.802+9765C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921737 | ||||||
| chr7:13921834
|
G | A | 1 | a0002c0002t0007g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.802+9668C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921834 | ||||||
| chr7:13921837
|
A | T | 30 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(27): Show | 30 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.802+9665T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921837 | ||||||
| chr7:13921839
|
C | T | 11 | a0001c0001t0014g0025a0001c0001t0014g0080a0001c0001t0014g0112others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+9663G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921839 | ||||||
| chr7:13921846
|
C | T | 55 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.802+9656G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921846 | ||||||
| chr7:13921863
|
G | C | 3 | a0001c0001t0051g0237a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.802+9639C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921863 | ||||||
| chr7:13921970
|
T | C | 13 | a0001c0001t0003g0290a0001c0001t0009g0179a0001c0001t0009g0180others(10): Show | 13 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+9532A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13921970 | ||||||
| chr7:13922072
|
A | C | 31 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(28): Show | 31 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.802+9430T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922072 | ||||||
| chr7:13922257
|
C | T | 19 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0012g0108others(16): Show | 19 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.802+9245G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922257 | ||||||
| chr7:13922337
|
C | A | 1 | a0002c0002t0005g0274 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.802+9165G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922337 | ||||||
| chr7:13922363
|
TG | T | 55 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.802+9138delC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922363 | ||||||
| chr7:13922390
|
C | T | 13 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0069others(10): Show | 13 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+9112G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922390 | ||||||
| chr7:13922618
|
A | G | 7 | a0001c0001t0004g0263a0001c0001t0014g0044a0001c0001t0018g0100others(4): Show | 7 | HG02258.hp1 HG02895.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+8884T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922618 | ||||||
| chr7:13922741
|
C | T | 1 | a0001c0001t0013g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.802+8761G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922741 | ||||||
| chr7:13922801
|
C | T | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+8701G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922801 | ||||||
| chr7:13922893
|
A | G | 1 | a0001c0001t0026g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.802+8609T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922893 | ||||||
| chr7:13922995
|
T | C | 70 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(67): Show | 70 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.802+8507A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13922995 | ||||||
| chr7:13923030
|
T | C | 1 | a0001c0001t0006g0280 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.802+8472A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923030 | ||||||
| chr7:13923048
|
T | C | 2 | a0002c0002t0005g0151a0002c0002t0005g0221 | 2 | HG02738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.802+8454A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923048 | ||||||
| chr7:13923079
|
T | C | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.802+8423A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923079 | ||||||
| chr7:13923191
|
T | C | 12 | a0001c0001t0014g0025a0001c0001t0014g0080a0001c0001t0014g0112others(9): Show | 12 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+8311A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923191 | ||||||
| chr7:13923217
|
C | A | 11 | a0001c0001t0014g0025a0001c0001t0014g0080a0001c0001t0014g0112others(8): Show | 11 | HG02055.hp2 HG02559.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+8285G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923217 | ||||||
| chr7:13923237
|
G | C | 118 | a0001c0001t0001g0157a0001c0001t0001g0245a0001c0001t0002g0017others(115): Show | 119 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.802+8265C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923237 | ||||||
| chr7:13923353
|
T | C | 19 | a0001c0001t0009g0143a0001c0001t0009g0179a0001c0001t0009g0180others(16): Show | 19 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.802+8149A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923353 | ||||||
| chr7:13923375
|
T | C | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+8127A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923375 | ||||||
| chr7:13923392
|
T | C | 25 | a0001c0001t0003g0278a0001c0001t0004g0166a0001c0001t0004g0189others(22): Show | 25 | HG00423.hp1 HG01074.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+8110A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923392 | ||||||
| chr7:13923534
|
G | A | 59 | a0001c0001t0002g0026a0001c0001t0002g0035a0001c0001t0003g0288others(56): Show | 59 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.802+7968C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923534 | ||||||
| chr7:13923560
|
T | C | 1 | a0002c0002t0005g0236 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.802+7942A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923560 | ||||||
| chr7:13923603
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.802+7899C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923603 | ||||||
| chr7:13923625
|
G | A | 25 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+7877C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923625 | ||||||
| chr7:13923804
|
G | A | 5 | a0001c0001t0018g0100a0001c0001t0027g0256a0001c0001t0056g0261others(2): Show | 5 | HG02258.hp1 HG02895.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+7698C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923804 | ||||||
| chr7:13923804
|
G | T | 4 | a0001c0001t0003g0287a0001c0001t0003g0293a0001c0001t0005g0193others(1): Show | 4 | NA18967.hp1 NA18978.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+7698C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923804 | ||||||
| chr7:13923808
|
G | A | 2 | a0001c0001t0003g0019a0001c0003t0002g0073 | 2 | HG00280.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.802+7694C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923808 | ||||||
| chr7:13923966
|
C | T | 200 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.802+7536G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923966 | ||||||
| chr7:13923990
|
G | A | 37 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(34): Show | 37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+7512C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13923990 | ||||||
| chr7:13924008
|
C | T | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.802+7494G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924008 | ||||||
| chr7:13924048
|
A | T | 2 | a0001c0001t0026g0041a0001c0001t0026g0098 | 2 | HG01255.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.802+7454T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924048 | ||||||
| chr7:13924178
|
A | G | 2 | a0002c0002t0034g0311a0002c0002t0052g0260 | 2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.802+7324T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924178 | ||||||
| chr7:13924336
|
C | G | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.802+7166G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924336 | ||||||
| chr7:13924447
|
T | A | 20 | a0001c0001t0002g0035a0001c0001t0009g0179a0001c0001t0009g0180others(17): Show | 20 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.802+7055A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924447 | ||||||
| chr7:13924491
|
C | G | 11 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0083others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+7011G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924491 | ||||||
| chr7:13924528
|
C | T | 38 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6974G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924528 | ||||||
| chr7:13924578
|
G | A | 37 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(34): Show | 37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+6924C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924578 | ||||||
| chr7:13924578
|
G | C | 2 | a0001c0001t0058g0135a0002c0002t0004g0225 | 2 | HG01109.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.802+6924C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924578 | ||||||
| chr7:13924665
|
T | C | 1 | a0001c0001t0028g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.802+6837A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924665 | ||||||
| chr7:13924724
|
G | A | 4 | a0001c0001t0029g0258a0001c0001t0032g0006a0002c0002t0029g0163others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+6778C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924724 | ||||||
| chr7:13924763
|
A | G | 38 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6739T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924763 | ||||||
| chr7:13924901
|
G | A | 38 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6601C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924901 | ||||||
| chr7:13924930
|
T | C | 38 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6572A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924930 | ||||||
| chr7:13924931
|
CAAAG | C | 38 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.802+6567_802+6570d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924931 | ||||||
| chr7:13924964
|
C | T | 16 | a0001c0001t0014g0025a0001c0001t0014g0044a0001c0001t0014g0080others(13): Show | 16 | HG00280.hp1 HG00323.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.802+6538G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13924964 | ||||||
| chr7:13925013
|
C | G | 2 | a0001c0001t0011g0081a0001c0001t0011g0101 | 2 | HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.802+6489G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925013 | ||||||
| chr7:13925219
|
A | G | 1 | a0001c0004t0001g0154 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.802+6283T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925219 | ||||||
| chr7:13925255
|
C | A | 37 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(34): Show | 37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+6247G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925255 | ||||||
| chr7:13925256
|
A | T | 1 | a0001c0001t0042g0303 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.802+6246T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925256 | ||||||
| chr7:13925306
|
A | G | 37 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(34): Show | 37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+6196T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925306 | ||||||
| chr7:13925327
|
G | A | 37 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0006g0302others(34): Show | 37 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.802+6175C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925327 | ||||||
| chr7:13925348
|
C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+6154G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925348 | ||||||
| chr7:13925362
|
T | C | 1 | a0001c0001t0004g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.802+6140A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925362 | ||||||
| chr7:13925375
|
G | A | 12 | a0001c0001t0014g0025a0001c0001t0014g0044a0001c0001t0014g0080others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+6127C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925375 | ||||||
| chr7:13925552
|
A | G | 1 | a0001c0001t0014g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.802+5950T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925552 | ||||||
| chr7:13925558
|
C | A | 25 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0003g0295others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.802+5944G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925558 | ||||||
| chr7:13925567
|
A | AT | 12 | a0001c0001t0004g0263a0001c0001t0006g0307a0001c0001t0007g0103others(9): Show | 12 | HG01243.hp2 HG01517.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+5934dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925567 | ||||||
| chr7:13925567
|
AT | A | 82 | a0001c0001t0001g0157a0001c0001t0001g0184a0001c0001t0001g0185others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.802+5934delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925567 | ||||||
| chr7:13925628
|
C | T | 1 | a0002c0002t0008g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.802+5874G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925628 | ||||||
| chr7:13925690
|
A | C | 51 | a0001c0001t0001g0255a0001c0001t0002g0021a0001c0001t0002g0026others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.802+5812T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925690 | ||||||
| chr7:13925716
|
C | T | 1 | a0002c0002t0005g0150 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.802+5786G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925716 | ||||||
| chr7:13925726
|
C | T | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.802+5776G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925726 | ||||||
| chr7:13925728
|
G | A | 18 | a0001c0001t0002g0026a0001c0001t0003g0288a0001c0001t0003g0295others(15): Show | 18 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.802+5774C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925728 | ||||||
| chr7:13925741
|
A | AT | 142 | a0001c0001t0001g0186a0001c0001t0001g0201a0001c0001t0001g0222others(139): Show | 143 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.802+5760dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925741 | ||||||
| chr7:13925750
|
A | T | 2 | a0001c0001t0003g0292a0002c0002t0005g0274 | 2 | NA18956.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.802+5752T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925750 | ||||||
| chr7:13925859
|
C | T | 11 | a0001c0001t0010g0040a0001c0001t0010g0045a0001c0001t0010g0083others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+5643G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925859 | ||||||
| chr7:13925862
|
A | ATTTTTTT others(6077): Show |
1 | a0001c0001t0014g0112 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.802+5639_802+5640i others(6086): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925862 | ||||||
| chr7:13925994
|
T | A | 1 | a0001c0001t0007g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.802+5508A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13925994 | ||||||
| chr7:13926000
|
T | C | 1 | a0002c0002t0001g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.802+5502A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926000 | ||||||
| chr7:13926390
|
T | A | 95 | a0001c0001t0001g0167a0001c0001t0002g0035a0001c0001t0003g0019others(92): Show | 95 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.802+5112A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926390 | ||||||
| chr7:13926549
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0002g0096 | 2 | HG01978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.802+4953G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926549 | ||||||
| chr7:13926552
|
A | T | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.802+4950T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926552 | ||||||
| chr7:13926578
|
C | G | 26 | a0001c0001t0004g0238a0001c0001t0006g0123a0001c0001t0006g0302others(23): Show | 26 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.802+4924G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926578 | ||||||
| chr7:13926743
|
T | C | 60 | a0001c0001t0001g0167a0001c0001t0003g0019a0001c0001t0003g0047others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.802+4759A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926743 | ||||||
| chr7:13926785
|
C | G | 1 | a0001c0001t0027g0256 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.802+4717G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13926785 | ||||||
| chr7:13927174
|
T | C | 26 | a0001c0001t0004g0238a0001c0001t0006g0123a0001c0001t0006g0302others(23): Show | 26 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.802+4328A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927174 | ||||||
| chr7:13927243
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.802+4259C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927243 | ||||||
| chr7:13927276
|
C | T | 26 | a0001c0001t0004g0238a0001c0001t0006g0123a0001c0001t0006g0302others(23): Show | 26 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.802+4226G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927276 | ||||||
| chr7:13927338
|
A | G | 2 | a0002c0002t0013g0304a0002c0002t0013g0305 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.802+4164T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927338 | ||||||
| chr7:13927466
|
A | G | 2 | a0001c0001t0007g0296a0002c0002t0007g0063 | 2 | NA18978.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.802+4036T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927466 | ||||||
| chr7:13927512
|
T | C | 27 | a0001c0001t0004g0238a0001c0001t0006g0123a0001c0001t0006g0302others(24): Show | 27 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+3990A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927512 | ||||||
| chr7:13927594
|
T | TCC | 27 | a0001c0001t0004g0238a0001c0001t0006g0123a0001c0001t0006g0302others(24): Show | 27 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+3906_802+3907d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927594 | ||||||
| chr7:13927752
|
C | T | 27 | a0001c0001t0004g0238a0001c0001t0006g0123a0001c0001t0006g0302others(24): Show | 27 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+3750G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927752 | ||||||
| chr7:13927899
|
G | A | 27 | a0001c0001t0004g0238a0001c0001t0006g0123a0001c0001t0006g0302others(24): Show | 27 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+3603C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927899 | ||||||
| chr7:13927922
|
T | A | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.802+3580A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13927922 | ||||||
| chr7:13928037
|
A | G | 1 | a0002c0002t0008g0197 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.802+3465T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928037 | ||||||
| chr7:13928152
|
T | G | 70 | a0001c0001t0001g0167a0001c0001t0002g0035a0001c0001t0003g0019others(67): Show | 70 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.802+3350A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928152 | ||||||
| chr7:13928154
|
A | G | 1 | a0002c0002t0006g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.802+3348T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928154 | ||||||
| chr7:13928243
|
C | G | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+3259G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928243 | ||||||
| chr7:13928388
|
A | G | 71 | a0001c0001t0001g0167a0001c0001t0002g0035a0001c0001t0003g0019others(68): Show | 71 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.802+3114T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928388 | ||||||
| chr7:13928399
|
G | T | 70 | a0001c0001t0001g0167a0001c0001t0002g0035a0001c0001t0003g0019others(67): Show | 70 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.802+3103C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928399 | ||||||
| chr7:13928430
|
C | T | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.802+3072G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928430 | ||||||
| chr7:13928482
|
C | T | 69 | a0001c0001t0001g0167a0001c0001t0002g0035a0001c0001t0003g0019others(66): Show | 69 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+3020G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928482 | ||||||
| chr7:13928508
|
G | A | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+2994C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928508 | ||||||
| chr7:13928528
|
C | T | 1 | a0002c0002t0001g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.802+2974G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928528 | ||||||
| chr7:13928555
|
G | A | 1 | a0001c0001t0004g0001 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.802+2947C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928555 | ||||||
| chr7:13928600
|
G | A | 12 | a0001c0001t0002g0090a0001c0001t0010g0040a0001c0001t0010g0045others(9): Show | 12 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.802+2902C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928600 | ||||||
| chr7:13928629
|
G | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.802+2873C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928629 | ||||||
| chr7:13928635
|
G | C | 1 | a0001c0001t0036g0095 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.802+2867C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928635 | ||||||
| chr7:13928819
|
G | A | 1 | a0001c0001t0007g0046 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.802+2683C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928819 | ||||||
| chr7:13928847
|
A | G | 4 | a0002c0002t0013g0304a0002c0002t0013g0305a0002c0002t0013g0315others(1): Show | 4 | HG02630.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+2655T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928847 | ||||||
| chr7:13928936
|
C | T | 1 | a0002c0002t0003g0079 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.802+2566G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13928936 | ||||||
| chr7:13929204
|
G | C | 1 | a0002c0002t0004g0182 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.802+2298C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929204 | ||||||
| chr7:13929241
|
G | A | 17 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0007g0317others(14): Show | 17 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.802+2261C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929241 | ||||||
| chr7:13929344
|
T | C | 68 | a0001c0001t0002g0119a0001c0001t0002g0283a0001c0001t0003g0092others(65): Show | 69 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+2158A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929344 | ||||||
| chr7:13929378
|
A | G | 16 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0007g0317others(13): Show | 16 | HG00323.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.802+2124T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929378 | ||||||
| chr7:13929460
|
A | C | 69 | a0001c0001t0001g0167a0001c0001t0002g0035a0001c0001t0003g0019others(66): Show | 69 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.802+2042T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929460 | ||||||
| chr7:13929521
|
A | G | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+1981T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929521 | ||||||
| chr7:13929522
|
C | T | 2 | a0001c0001t0024g0028a0001c0001t0024g0029 | 2 | HG01175.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.802+1980G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929522 | ||||||
| chr7:13929564
|
G | C | 9 | a0001c0001t0004g0238a0001c0001t0006g0123a0001c0001t0015g0132others(6): Show | 9 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+1938C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929564 | ||||||
| chr7:13929735
|
T | C | 1 | a0001c0001t0002g0021 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.802+1767A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929735 | ||||||
| chr7:13929894
|
C | G | 13 | a0001c0001t0002g0026a0001c0001t0003g0295a0001c0001t0005g0168others(10): Show | 13 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+1608G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13929894 | ||||||
| chr7:13930329
|
A | T | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.802+1173T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930329 | ||||||
| chr7:13930444
|
A | T | 3 | a0001c0001t0015g0138a0001c0001t0050g0142a0001c0001t0055g0257 | 3 | HG02559.hp1 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.802+1058T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930444 | ||||||
| chr7:13930507
|
C | G | 1 | a0002c0002t0029g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.802+995G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930507 | ||||||
| chr7:13930512
|
A | G | 1 | a0002c0002t0006g0018 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.802+990T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930512 | ||||||
| chr7:13930515
|
G | T | 12 | a0001c0001t0003g0295a0001c0001t0005g0168a0001c0001t0012g0117others(9): Show | 12 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.802+987C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930515 | ||||||
| chr7:13930564
|
G | A | 1 | a0001c0001t0059g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.802+938C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930564 | ||||||
| chr7:13930601
|
G | A | 3 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0001t0035g0124 | 3 | HG00099.hp2 HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.802+901C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930601 | ||||||
| chr7:13930606
|
C | T | 1 | a0001c0001t0003g0050 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.802+896G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930606 | ||||||
| chr7:13930608
|
A | G | 1 | a0002c0002t0001g0203 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.802+894T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930608 | ||||||
| chr7:13930641
|
T | C | 4 | a0001c0001t0004g0137a0001c0001t0006g0313a0001c0001t0039g0086others(1): Show | 4 | HG02109.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+861A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930641 | ||||||
| chr7:13930672
|
G | A | 4 | a0001c0001t0006g0123a0001c0001t0038g0306a0002c0002t0007g0310others(1): Show | 4 | HG02055.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+830C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930672 | ||||||
| chr7:13930693
|
G | A | 1 | a0002c0002t0013g0315 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.802+809C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930693 | ||||||
| chr7:13930705
|
A | G | 8 | a0001c0001t0007g0053a0001c0001t0009g0143a0001c0001t0014g0044others(5): Show | 8 | HG02559.hp1 HG02818.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+797T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930705 | ||||||
| chr7:13930789
|
A | AAT | 11 | a0001c0001t0002g0013a0001c0001t0002g0057a0001c0001t0003g0292others(8): Show | 11 | HG00544.hp1 HG00544.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+711_802+712dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930789 | ||||||
| chr7:13930797
|
T | TA | 123 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(120): Show | 124 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.802+704_802+705ins others(1): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930797 | ||||||
| chr7:13930798
|
T | A | 126 | a0001c0001t0001g0201a0001c0001t0002g0012a0001c0001t0002g0013others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.802+704A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930798 | ||||||
| chr7:13930799
|
T | A | 113 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(110): Show | 114 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.802+703A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930799 | ||||||
| chr7:13930800
|
T | A | 126 | a0001c0001t0001g0201a0001c0001t0002g0012a0001c0001t0002g0013others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.802+702A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930800 | ||||||
| chr7:13930801
|
T | A | 2 | a0001c0001t0005g0232a0001c0001t0007g0296 | 2 | HG00408.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.802+701A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930801 | ||||||
| chr7:13930802
|
T | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.802+700A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930802 | ||||||
| chr7:13930805
|
T | C | 9 | a0001c0001t0002g0035a0001c0001t0028g0240a0001c0001t0028g0241others(6): Show | 9 | HG01109.hp1 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+697A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930805 | ||||||
| chr7:13930823
|
C | T | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.802+679G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930823 | ||||||
| chr7:13930847
|
C | G | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.802+655G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930847 | ||||||
| chr7:13930870
|
G | A | 2 | a0001c0001t0053g0226a0002c0002t0001g0194 | 2 | NA18965.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.802+632C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930870 | ||||||
| chr7:13930927
|
A | T | 6 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0010g0301others(3): Show | 6 | HG02257.hp2 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.802+575T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930927 | ||||||
| chr7:13930975
|
T | C | 5 | a0001c0001t0008g0250a0001c0001t0019g0152a0001c0001t0019g0153others(2): Show | 5 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.802+527A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13930975 | ||||||
| chr7:13931040
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.802+462G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931040 | ||||||
| chr7:13931114
|
C | T | 301 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(298): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.802+388G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931114 | ||||||
| chr7:13931126
|
TTCAGAAG others(4): Show |
T | 2 | a0001c0001t0006g0280a0001c0001t0053g0226 | 2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.802+365_802+375del others(11): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931126 | ||||||
| chr7:13931174
|
A | G | 8 | a0001c0001t0003g0292a0001c0001t0003g0295a0001c0001t0005g0168others(5): Show | 8 | HG00544.hp2 HG00597.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+328T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931174 | ||||||
| chr7:13931201
|
A | G | 17 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0010g0301others(14): Show | 17 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+301T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931201 | ||||||
| chr7:13931211
|
G | GA | 13 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0010g0301others(10): Show | 13 | HG02257.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.802+290dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931211 | ||||||
| chr7:13931300
|
C | G | 1 | a0001c0001t0003g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.802+202G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931300 | ||||||
| chr7:13931492
|
G | A | 13 | a0001c0001t0006g0123a0001c0001t0015g0136a0002c0002t0006g0078others(10): Show | 13 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.802+10C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 9/13 | chr7 | 13931492 | ||||||
| chr7:13931798
|
T | C | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-49A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931798 | ||||||
| chr7:13931822
|
C | T | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-73G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931822 | ||||||
| chr7:13931886
|
G | A | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-137C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931886 | ||||||
| chr7:13931977
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.555-228A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931977 | ||||||
| chr7:13931982
|
G | A | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-233C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13931982 | ||||||
| chr7:13932037
|
T | TAC | 3 | a0001c0001t0004g0137a0001c0001t0039g0086a0001c0001t0042g0303 | 3 | HG02109.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.555-290_555-289dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932037 | ||||||
| chr7:13932042
|
ACC | A | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.555-295_555-294del others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932042 | ||||||
| chr7:13932044
|
C | A | 4 | a0001c0001t0004g0137a0001c0001t0020g0239a0001c0001t0039g0086others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-295G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | ||||||
| chr7:13932044
|
C | CCA | 99 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(96): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.555-297_555-296dup others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | ||||||
| chr7:13932044
|
C | CCACA | 51 | a0001c0001t0002g0012a0001c0001t0002g0021a0001c0001t0002g0027others(48): Show | 51 | HG00544.hp2 HG00597.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.555-299_555-296dup others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | ||||||
| chr7:13932044
|
C | CCACACA | 11 | a0001c0001t0004g0166a0001c0001t0015g0132a0001c0001t0015g0139others(8): Show | 11 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.555-301_555-296dup others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | ||||||
| chr7:13932044
|
C | CCACACAC others(3): Show |
5 | a0002c0002t0006g0078a0002c0002t0013g0315a0002c0002t0018g0299others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.555-305_555-296dup others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | ||||||
| chr7:13932044
|
CCACA | C | 4 | a0001c0001t0006g0130a0001c0001t0028g0240a0001c0001t0028g0241others(1): Show | 4 | HG02074.hp1 HG02809.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-299_555-296del others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932044 | ||||||
| chr7:13932115
|
G | T | 11 | a0002c0002t0006g0078a0002c0002t0007g0310a0002c0002t0010g0116others(8): Show | 11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.555-366C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932115 | ||||||
| chr7:13932246
|
A | G | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-497T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932246 | ||||||
| chr7:13932367
|
C | T | 11 | a0002c0002t0006g0078a0002c0002t0007g0310a0002c0002t0010g0116others(8): Show | 11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.555-618G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932367 | ||||||
| chr7:13932573
|
G | C | 1 | a0001c0001t0006g0091 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.555-824C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932573 | ||||||
| chr7:13932584
|
G | T | 1 | a0002c0002t0016g0275 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.555-835C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932584 | ||||||
| chr7:13932682
|
C | T | 122 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(119): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.555-933G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932682 | ||||||
| chr7:13932730
|
C | A | 1 | a0001c0001t0002g0096 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.555-981G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932730 | ||||||
| chr7:13932785
|
A | T | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1036T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932785 | ||||||
| chr7:13932833
|
G | C | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1084C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932833 | ||||||
| chr7:13932836
|
T | A | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1087A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932836 | ||||||
| chr7:13932845
|
G | A | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.555-1096C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932845 | ||||||
| chr7:13932858
|
A | G | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1109T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13932858 | ||||||
| chr7:13933281
|
T | C | 12 | a0001c0001t0015g0136a0002c0002t0006g0078a0002c0002t0007g0310others(9): Show | 12 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.555-1532A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933281 | ||||||
| chr7:13933460
|
T | C | 1 | a0001c0001t0003g0278 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.555-1711A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933460 | ||||||
| chr7:13933512
|
G | C | 1 | a0002c0002t0004g0276 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.555-1763C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933512 | ||||||
| chr7:13933759
|
T | C | 1 | a0001c0001t0011g0068 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.554+1949A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933759 | ||||||
| chr7:13933826
|
G | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.554+1882C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933826 | ||||||
| chr7:13933847
|
T | C | 1 | a0001c0005t0010g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.554+1861A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933847 | ||||||
| chr7:13933848
|
C | T | 11 | a0002c0002t0006g0078a0002c0002t0007g0310a0002c0002t0010g0116others(8): Show | 11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+1860G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933848 | ||||||
| chr7:13933852
|
C | T | 8 | a0002c0002t0006g0078a0002c0002t0007g0310a0002c0002t0013g0304others(5): Show | 8 | HG02630.hp1 HG02723.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+1856G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933852 | ||||||
| chr7:13933936
|
G | T | 11 | a0002c0002t0006g0078a0002c0002t0007g0310a0002c0002t0010g0116others(8): Show | 11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+1772C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13933936 | ||||||
| chr7:13934138
|
A | C | 1 | a0002c0002t0002g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.554+1570T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934138 | ||||||
| chr7:13934298
|
A | G | 1 | a0001c0001t0004g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.554+1410T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934298 | ||||||
| chr7:13934509
|
C | T | 2 | a0001c0001t0006g0036a0001c0001t0006g0308 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.554+1199G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934509 | ||||||
| chr7:13934522
|
C | A | 1 | a0001c0001t0007g0046 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.554+1186G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934522 | ||||||
| chr7:13934756
|
C | G | 19 | a0001c0001t0002g0035a0001c0001t0006g0123a0001c0001t0006g0302others(16): Show | 19 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.554+952G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934756 | ||||||
| chr7:13934756
|
C | T | 2 | a0001c0001t0015g0134a0001c0001t0058g0135 | 2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.554+952G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934756 | ||||||
| chr7:13934824
|
A | G | 2 | a0001c0001t0015g0134a0001c0001t0058g0135 | 2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.554+884T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934824 | ||||||
| chr7:13934836
|
C | T | 92 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.554+872G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934836 | ||||||
| chr7:13934937
|
A | G | 13 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(10): Show | 13 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(10): Show |
intron_variant | MODIFIER | c.554+771T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934937 | ||||||
| chr7:13934938
|
G | A | 92 | a0002c0002t0001g0131a0002c0002t0001g0148a0002c0002t0001g0149others(89): Show | 92 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.554+770C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934938 | ||||||
| chr7:13934969
|
T | C | 2 | a0002c0002t0013g0304a0002c0002t0013g0305 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.554+739A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934969 | ||||||
| chr7:13934991
|
G | A | 2 | a0002c0002t0007g0063a0002c0002t0016g0275 | 2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.554+717C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13934991 | ||||||
| chr7:13935161
|
T | C | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.554+547A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935161 | ||||||
| chr7:13935251
|
T | C | 19 | a0001c0001t0002g0035a0001c0001t0006g0123a0001c0001t0006g0302others(16): Show | 19 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.554+457A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935251 | ||||||
| chr7:13935441
|
C | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.554+267G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935441 | ||||||
| chr7:13935454
|
C | T | 2 | a0001c0001t0039g0086a0001c0001t0042g0303 | 2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.554+254G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935454 | ||||||
| chr7:13935603
|
T | C | 1 | a0001c0001t0002g0119 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.554+105A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935603 | ||||||
| chr7:13935675
|
A | G | 11 | a0002c0002t0006g0078a0002c0002t0007g0310a0002c0002t0010g0116others(8): Show | 11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.554+33T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 8/13 | chr7 | 13935675 | ||||||
| chr7:13935949
|
T | A | 20 | a0001c0001t0002g0035a0001c0001t0006g0123a0001c0001t0006g0302others(17): Show | 20 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.366-53A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13935949 | ||||||
| chr7:13935950
|
A | T | 11 | a0002c0002t0006g0078a0002c0002t0007g0310a0002c0002t0010g0116others(8): Show | 11 | HG02486.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.366-54T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13935950 | ||||||
| chr7:13935968
|
A | G | 8 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(5): Show | 8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.366-72T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13935968 | ||||||
| chr7:13936070
|
C | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.366-174G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936070 | ||||||
| chr7:13936144
|
A | G | 100 | a0002c0002t0001g0131a0002c0002t0001g0148a0002c0002t0001g0149others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.366-248T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936144 | ||||||
| chr7:13936287
|
A | G | 1 | a0002c0002t0007g0114 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.366-391T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936287 | ||||||
| chr7:13936294
|
G | A | 1 | a0001c0001t0003g0287 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.366-398C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936294 | ||||||
| chr7:13936407
|
T | G | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.366-511A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936407 | ||||||
| chr7:13936633
|
G | T | 97 | a0002c0002t0001g0131a0002c0002t0001g0148a0002c0002t0001g0149others(94): Show | 97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.366-737C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936633 | ||||||
| chr7:13936766
|
C | T | 3 | a0002c0002t0003g0122a0002c0002t0005g0269a0002c0002t0005g0271 | 3 | HG02071.hp1 NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.366-870G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936766 | ||||||
| chr7:13936939
|
G | T | 2 | a0002c0002t0007g0063a0002c0002t0016g0275 | 2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.366-1043C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936939 | ||||||
| chr7:13936966
|
C | T | 1 | a0001c0001t0041g0309 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.366-1070G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13936966 | ||||||
| chr7:13937041
|
CA | C | 97 | a0002c0002t0001g0131a0002c0002t0001g0148a0002c0002t0001g0149others(94): Show | 97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.366-1146delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937041 | ||||||
| chr7:13937139
|
A | C | 1 | a0001c0001t0003g0094 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.366-1243T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937139 | ||||||
| chr7:13937200
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.366-1304A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937200 | ||||||
| chr7:13937208
|
T | G | 90 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(87): Show | 90 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.366-1312A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937208 | ||||||
| chr7:13937234
|
T | C | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.366-1338A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937234 | ||||||
| chr7:13937276
|
T | C | 1 | a0001c0001t0002g0026 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.366-1380A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937276 | ||||||
| chr7:13937370
|
C | A | 97 | a0002c0002t0001g0131a0002c0002t0001g0148a0002c0002t0001g0149others(94): Show | 97 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.366-1474G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937370 | ||||||
| chr7:13937390
|
T | A | 3 | a0001c0001t0015g0134a0001c0001t0017g0023a0001c0001t0017g0042 | 3 | HG02717.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.366-1494A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937390 | ||||||
| chr7:13937442
|
TTATTGCA others(7): Show |
T | 3 | a0001c0001t0004g0137a0001c0001t0039g0086a0001c0001t0042g0303 | 3 | HG02109.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.366-1560_366-1547d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937442 | ||||||
| chr7:13937461
|
T | G | 1 | a0002c0002t0001g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.366-1565A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937461 | ||||||
| chr7:13937484
|
C | T | 1 | a0001c0001t0010g0126 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.366-1588G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937484 | ||||||
| chr7:13937678
|
C | G | 1 | a0002c0002t0016g0275 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.365+1439G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937678 | ||||||
| chr7:13937688
|
G | A | 1 | a0001c0001t0003g0291 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.365+1429C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937688 | ||||||
| chr7:13937767
|
A | C | 8 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(5): Show | 8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+1350T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13937767 | ||||||
| chr7:13938008
|
C | T | 7 | a0002c0002t0001g0148a0002c0002t0001g0149a0002c0002t0001g0155others(4): Show | 7 | HG02080.hp1 NA18973.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+1109G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938008 | ||||||
| chr7:13938069
|
T | C | 6 | a0001c0001t0002g0021a0001c0001t0004g0263a0001c0001t0007g0317others(3): Show | 6 | HG02257.hp2 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+1048A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938069 | ||||||
| chr7:13938236
|
C | A | 1 | a0002c0002t0001g0198 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.365+881G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938236 | ||||||
| chr7:13938264
|
A | G | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.365+853T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938264 | ||||||
| chr7:13938280
|
C | T | 2 | a0002c0002t0022g0003a0002c0002t0022g0004 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.365+837G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938280 | ||||||
| chr7:13938381
|
A | C | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.365+736T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938381 | ||||||
| chr7:13938470
|
GAC | G | 22 | a0001c0001t0002g0035a0001c0001t0006g0123a0001c0001t0006g0302others(19): Show | 22 | HG01081.hp2 HG01109.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.365+645_365+646del others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938470 | ||||||
| chr7:13938488
|
T | G | 1 | a0001c0001t0028g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.365+629A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938488 | ||||||
| chr7:13938520
|
T | C | 6 | a0001c0001t0009g0143a0001c0001t0014g0044a0001c0001t0015g0138others(3): Show | 6 | HG02559.hp1 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.365+597A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938520 | ||||||
| chr7:13938632
|
C | A | 5 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0006g0091others(2): Show | 5 | NA18988.hp1 NA18991.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+485G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938632 | ||||||
| chr7:13938663
|
G | T | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.365+454C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938663 | ||||||
| chr7:13938682
|
T | A | 1 | a0002c0002t0027g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.365+435A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13938682 | ||||||
| chr7:13939020
|
C | T | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.365+97G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13939020 | ||||||
| chr7:13939023
|
T | A | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.365+94A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13939023 | ||||||
| chr7:13939058
|
C | G | 4 | a0002c0002t0001g0199a0002c0002t0001g0217a0002c0002t0001g0219others(1): Show | 4 | HG01074.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+59G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 7/13 | chr7 | 13939058 | ||||||
| chr7:13939419
|
T | C | 8 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(5): Show | 8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-173A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939419 | ||||||
| chr7:13939539
|
A | G | 19 | a0001c0001t0002g0035a0001c0001t0006g0123a0001c0001t0006g0302others(16): Show | 19 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.236-293T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939539 | ||||||
| chr7:13939600
|
G | A | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-354C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939600 | ||||||
| chr7:13939601
|
A | C | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-355T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939601 | ||||||
| chr7:13939645
|
C | A | 1 | a0001c0001t0009g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.236-399G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939645 | ||||||
| chr7:13939669
|
A | G | 1 | a0002c0002t0005g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.236-423T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939669 | ||||||
| chr7:13939730
|
C | T | 1 | a0001c0001t0004g0177 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.236-484G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939730 | ||||||
| chr7:13939760
|
G | C | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.236-514C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939760 | ||||||
| chr7:13939842
|
T | C | 1 | a0001c0001t0010g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.236-596A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939842 | ||||||
| chr7:13939953
|
C | T | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-707G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939953 | ||||||
| chr7:13939985
|
C | T | 8 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(5): Show | 8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-739G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939985 | ||||||
| chr7:13939986
|
G | A | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-740C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13939986 | ||||||
| chr7:13940104
|
G | A | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-858C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940104 | ||||||
| chr7:13940245
|
C | G | 3 | a0001c0001t0004g0137a0001c0001t0039g0086a0001c0001t0042g0303 | 3 | HG02109.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.236-999G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940245 | ||||||
| chr7:13940278
|
C | T | 1 | a0002c0002t0018g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.236-1032G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940278 | ||||||
| chr7:13940351
|
G | A | 2 | a0001c0001t0002g0021a0001c0001t0020g0239 | 2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.236-1105C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940351 | ||||||
| chr7:13940363
|
AAAAAAAA others(2): Show |
A | 102 | a0001c0001t0001g0255a0002c0002t0001g0131a0002c0002t0001g0147others(99): Show | 102 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.236-1126_236-1118d others(11): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940363 | ||||||
| chr7:13940441
|
C | A | 2 | a0001c0001t0007g0076a0001c0001t0007g0077 | 2 | HG01243.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.236-1195G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940441 | ||||||
| chr7:13940530
|
C | T | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-1284G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940530 | ||||||
| chr7:13940574
|
T | A | 8 | a0001c0001t0007g0067a0001c0001t0010g0069a0001c0001t0010g0126others(5): Show | 8 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.236-1328A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940574 | ||||||
| chr7:13940793
|
T | C | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG00099.hp1 HG01361.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-1547A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940793 | ||||||
| chr7:13940814
|
G | C | 1 | a0002c0002t0027g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.236-1568C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940814 | ||||||
| chr7:13940924
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.236-1678G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13940924 | ||||||
| chr7:13941037
|
G | C | 2 | a0002c0002t0007g0063a0002c0002t0016g0275 | 2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.236-1791C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941037 | ||||||
| chr7:13941045
|
C | T | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-1799G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941045 | ||||||
| chr7:13941193
|
G | T | 1 | a0001c0001t0042g0303 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.236-1947C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941193 | ||||||
| chr7:13941223
|
T | G | 2 | a0002c0002t0007g0063a0002c0002t0016g0275 | 2 | NA18960.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.236-1977A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941223 | ||||||
| chr7:13941638
|
A | G | 109 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(106): Show | 109 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.236-2392T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941638 | ||||||
| chr7:13941863
|
G | GAATA | 3 | a0001c0001t0001g0222a0001c0001t0002g0090a0001c0001t0011g0128 | 3 | HG00735.hp2 HG01123.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.236-2621_236-2618d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | ||||||
| chr7:13941863
|
GAATA | G | 77 | a0001c0001t0001g0157a0001c0001t0001g0184a0001c0001t0001g0185others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.236-2621_236-2618d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | ||||||
| chr7:13941863
|
GAATAAAT others(1): Show |
G | 64 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0254others(61): Show | 64 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.236-2625_236-2618d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | ||||||
| chr7:13941863
|
GAATAAAT others(5): Show |
G | 21 | a0001c0001t0003g0054a0001c0001t0004g0001a0001c0001t0004g0137others(18): Show | 22 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.236-2629_236-2618d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | ||||||
| chr7:13941863
|
GAATAAAT others(9): Show |
G | 1 | a0001c0001t0012g0297 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.236-2633_236-2618d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | ||||||
| chr7:13941863
|
GAATAAAT others(17): Show |
G | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-2641_236-2618d others(26): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941863 | ||||||
| chr7:13941948
|
C | G | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-2702G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941948 | ||||||
| chr7:13941957
|
G | C | 101 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(98): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.236-2711C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13941957 | ||||||
| chr7:13942020
|
CT | C | 155 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0185others(152): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.236-2775delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942020 | ||||||
| chr7:13942020
|
CTTTTT | C | 95 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(92): Show | 95 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.236-2779_236-2775d others(7): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942020 | ||||||
| chr7:13942060
|
T | G | 7 | a0002c0002t0006g0078a0002c0002t0007g0310a0002c0002t0013g0304others(4): Show | 7 | HG02630.hp1 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-2814A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942060 | ||||||
| chr7:13942061
|
T | C | 5 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(2): Show | 5 | HG00099.hp1 HG01361.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-2815A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942061 | ||||||
| chr7:13942062
|
C | T | 8 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(5): Show | 8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-2816G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942062 | ||||||
| chr7:13942115
|
C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-2869G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942115 | ||||||
| chr7:13942123
|
A | G | 100 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.236-2877T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942123 | ||||||
| chr7:13942140
|
C | T | 7 | a0001c0001t0003g0278a0001c0001t0003g0292a0001c0001t0003g0295others(4): Show | 7 | HG00544.hp2 HG00597.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-2894G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942140 | ||||||
| chr7:13942176
|
A | G | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-2930T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942176 | ||||||
| chr7:13942180
|
C | T | 8 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(5): Show | 8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-2934G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942180 | ||||||
| chr7:13942248
|
C | G | 1 | a0002c0002t0003g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.236-3002G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942248 | ||||||
| chr7:13942262
|
A | G | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-3016T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942262 | ||||||
| chr7:13942317
|
C | T | 2 | a0001c0001t0015g0134a0001c0001t0058g0135 | 2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.236-3071G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942317 | ||||||
| chr7:13942357
|
TA | T | 98 | a0002c0002t0001g0131a0002c0002t0001g0147a0002c0002t0001g0148others(95): Show | 98 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.236-3112delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942357 | ||||||
| chr7:13942410
|
T | C | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-3164A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942410 | ||||||
| chr7:13942421
|
C | T | 107 | a0001c0001t0003g0047a0001c0001t0003g0050a0001c0001t0003g0278others(104): Show | 107 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.236-3175G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942421 | ||||||
| chr7:13942435
|
A | G | 100 | a0001c0001t0003g0047a0001c0001t0003g0050a0002c0002t0001g0131others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.236-3189T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942435 | ||||||
| chr7:13942613
|
C | G | 1 | a0002c0002t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.236-3367G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942613 | ||||||
| chr7:13942628
|
C | G | 2 | a0001c0001t0028g0241a0001c0001t0039g0086 | 2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.236-3382G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942628 | ||||||
| chr7:13942795
|
A | C | 121 | a0001c0001t0003g0016a0001c0001t0003g0047a0001c0001t0003g0050others(118): Show | 121 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-3549T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942795 | ||||||
| chr7:13942991
|
A | G | 2 | a0001c0001t0029g0258a0001c0001t0032g0006 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.236-3745T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13942991 | ||||||
| chr7:13943108
|
A | G | 2 | a0001c0001t0004g0183a0001c0001t0004g0191 | 2 | NA18972.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.236-3862T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943108 | ||||||
| chr7:13943163
|
G | C | 1 | a0001c0001t0003g0287 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.236-3917C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943163 | ||||||
| chr7:13943420
|
G | A | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-4174C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943420 | ||||||
| chr7:13943549
|
T | C | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-4303A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943549 | ||||||
| chr7:13943587
|
T | A | 1 | a0001c0001t0001g0215 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.236-4341A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943587 | ||||||
| chr7:13943662
|
A | G | 1 | a0002c0002t0004g0182 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.236-4416T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943662 | ||||||
| chr7:13943737
|
G | A | 2 | a0001c0001t0028g0240a0001c0001t0045g0113 | 2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-4491C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943737 | ||||||
| chr7:13943744
|
T | A | 255 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(252): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.236-4498A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943744 | ||||||
| chr7:13943783
|
T | G | 14 | a0002c0002t0001g0148a0002c0002t0001g0149a0002c0002t0001g0155others(11): Show | 14 | HG02027.hp1 HG02080.hp1 NA18960.hp1 others(11): Show |
intron_variant | MODIFIER | c.236-4537A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943783 | ||||||
| chr7:13943791
|
T | C | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-4545A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943791 | ||||||
| chr7:13943826
|
C | T | 2 | a0001c0001t0028g0240a0001c0001t0045g0113 | 2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-4580G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943826 | ||||||
| chr7:13943862
|
A | G | 7 | a0001c0001t0003g0278a0001c0001t0003g0292a0001c0001t0003g0295others(4): Show | 7 | HG00544.hp2 HG00597.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-4616T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13943862 | ||||||
| chr7:13944075
|
C | T | 7 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(4): Show | 7 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-4829G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944075 | ||||||
| chr7:13944100
|
C | T | 7 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(4): Show | 7 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-4854G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944100 | ||||||
| chr7:13944110
|
A | G | 4 | a0002c0002t0001g0158a0002c0002t0005g0162a0002c0002t0008g0159others(1): Show | 4 | NA18963.hp1 NA19063.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-4864T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944110 | ||||||
| chr7:13944217
|
T | A | 15 | a0001c0001t0002g0048a0001c0001t0003g0094a0001c0001t0007g0067others(12): Show | 15 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-4971A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944217 | ||||||
| chr7:13944250
|
C | T | 294 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(291): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.236-5004G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944250 | ||||||
| chr7:13944420
|
C | A | 1 | a0001c0001t0001g0254 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.236-5174G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944420 | ||||||
| chr7:13944420
|
C | G | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-5174G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944420 | ||||||
| chr7:13944445
|
G | A | 1 | a0001c0001t0025g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.236-5199C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944445 | ||||||
| chr7:13944564
|
A | G | 9 | a0001c0001t0002g0012a0001c0001t0002g0027a0001c0001t0007g0053others(6): Show | 9 | HG02055.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.236-5318T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944564 | ||||||
| chr7:13944567
|
C | T | 1 | a0001c0001t0025g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.236-5321G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944567 | ||||||
| chr7:13944634
|
ATCCCTGA others(18): Show |
A | 4 | a0001c0001t0004g0137a0001c0001t0006g0313a0001c0001t0014g0080others(1): Show | 4 | HG02717.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-5413_236-5389d others(27): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944634 | ||||||
| chr7:13944771
|
A | C | 1 | a0001c0001t0055g0257 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.236-5525T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944771 | ||||||
| chr7:13944787
|
T | C | 4 | a0001c0001t0006g0031a0001c0001t0013g0032a0001c0001t0024g0028others(1): Show | 4 | HG01175.hp2 HG01192.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-5541A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944787 | ||||||
| chr7:13944944
|
G | C | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-5698C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944944 | ||||||
| chr7:13944973
|
A | G | 1 | a0001c0001t0004g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.236-5727T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13944973 | ||||||
| chr7:13945069
|
A | AAAC | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-5826_236-5824d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945069 | ||||||
| chr7:13945270
|
C | T | 3 | a0002c0002t0004g0182a0002c0002t0012g0033a0002c0002t0012g0055 | 3 | HG00423.hp2 NA18946.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.236-6024G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945270 | ||||||
| chr7:13945293
|
T | A | 139 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.236-6047A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945293 | ||||||
| chr7:13945294
|
A | T | 15 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(12): Show | 15 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-6048T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945294 | ||||||
| chr7:13945392
|
A | C | 2 | a0001c0001t0014g0080a0001c0001t0042g0303 | 2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.236-6146T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945392 | ||||||
| chr7:13945443
|
A | AT | 7 | a0001c0001t0003g0289a0001c0001t0009g0143a0001c0001t0010g0045others(4): Show | 7 | HG02055.hp1 HG02559.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-6198dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945443 | ||||||
| chr7:13945443
|
AT | A | 109 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(106): Show | 109 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.236-6198delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945443 | ||||||
| chr7:13945506
|
A | C | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-6260T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945506 | ||||||
| chr7:13945506
|
A | T | 5 | a0001c0001t0008g0250a0001c0001t0019g0152a0001c0001t0019g0153others(2): Show | 5 | HG00099.hp2 HG00140.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-6260T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945506 | ||||||
| chr7:13945507
|
T | A | 3 | a0001c0001t0014g0080a0001c0001t0015g0134a0001c0001t0058g0135 | 3 | HG01109.hp1 HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.236-6261A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945507 | ||||||
| chr7:13945543
|
G | C | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-6297C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945543 | ||||||
| chr7:13945841
|
A | T | 11 | a0001c0001t0002g0090a0001c0001t0005g0247a0001c0001t0005g0248others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.236-6595T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13945841 | ||||||
| chr7:13946265
|
G | A | 7 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(4): Show | 7 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-7019C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946265 | ||||||
| chr7:13946415
|
C | T | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.236-7169G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946415 | ||||||
| chr7:13946617
|
A | C | 1 | a0002c0002t0008g0264 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.236-7371T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946617 | ||||||
| chr7:13946623
|
A | C | 8 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(5): Show | 8 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-7377T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946623 | ||||||
| chr7:13946670
|
G | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-7424C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946670 | ||||||
| chr7:13946725
|
T | C | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-7479A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946725 | ||||||
| chr7:13946881
|
C | T | 28 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0002g0090others(25): Show | 28 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.236-7635G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13946881 | ||||||
| chr7:13947008
|
C | T | 1 | a0001c0001t0020g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.236-7762G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947008 | ||||||
| chr7:13947023
|
G | A | 15 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(12): Show | 15 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-7777C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947023 | ||||||
| chr7:13947031
|
C | G | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-7785G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947031 | ||||||
| chr7:13947100
|
C | T | 2 | a0001c0001t0002g0090a0001c0001t0026g0098 | 2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.236-7854G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947100 | ||||||
| chr7:13947294
|
AAAGAT | A | 7 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(4): Show | 7 | HG00423.hp1 HG02165.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-8053_236-8049d others(7): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947294 | ||||||
| chr7:13947392
|
C | CA | 100 | a0001c0001t0001g0201a0001c0001t0001g0223a0001c0001t0002g0013others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.236-8147dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947392 | ||||||
| chr7:13947392
|
CA | C | 26 | a0001c0001t0001g0222a0001c0001t0003g0016a0001c0001t0003g0278others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.236-8147delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947392 | ||||||
| chr7:13947402
|
A | C | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0001c0001t0045g0113 | 3 | HG02809.hp1 HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.236-8156T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947402 | ||||||
| chr7:13947405
|
A | C | 1 | a0001c0001t0006g0088 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.236-8159T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947405 | ||||||
| chr7:13947408
|
AC | A | 11 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0010g0040others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.236-8163delG | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947408 | ||||||
| chr7:13947409
|
C | A | 7 | a0001c0001t0006g0123a0001c0001t0015g0132a0001c0001t0015g0139others(4): Show | 7 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-8163G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947409 | ||||||
| chr7:13947497
|
T | C | 1 | a0002c0002t0001g0219 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.236-8251A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947497 | ||||||
| chr7:13947601
|
C | T | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-8355G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947601 | ||||||
| chr7:13947864
|
A | G | 1 | a0002c0002t0003g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.236-8618T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13947864 | ||||||
| chr7:13948019
|
C | T | 11 | a0001c0001t0002g0090a0001c0001t0005g0247a0001c0001t0005g0248others(8): Show | 11 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.236-8773G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948019 | ||||||
| chr7:13948153
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236-8907C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948153 | ||||||
| chr7:13948238
|
G | A | 16 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(13): Show | 16 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.236-8992C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948238 | ||||||
| chr7:13948320
|
G | A | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-9074C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948320 | ||||||
| chr7:13948356
|
T | C | 15 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(12): Show | 15 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-9110A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948356 | ||||||
| chr7:13948484
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236-9238A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948484 | ||||||
| chr7:13948501
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.236-9255G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948501 | ||||||
| chr7:13948545
|
G | A | 15 | a0001c0001t0002g0048a0001c0001t0003g0094a0001c0001t0007g0067others(12): Show | 15 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.236-9299C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948545 | ||||||
| chr7:13948622
|
G | C | 286 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0184others(283): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.236-9376C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948622 | ||||||
| chr7:13948697
|
A | C | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-9451T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948697 | ||||||
| chr7:13948888
|
T | A | 42 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0002g0090others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.236-9642A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948888 | ||||||
| chr7:13948898
|
C | A | 87 | a0001c0001t0002g0283a0001c0001t0004g0267a0001c0001t0004g0270others(84): Show | 87 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.236-9652G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948898 | ||||||
| chr7:13948943
|
C | G | 22 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0003g0278others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.236-9697G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13948943 | ||||||
| chr7:13949075
|
A | G | 1 | a0002c0002t0008g0197 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.236-9829T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949075 | ||||||
| chr7:13949097
|
A | C | 1 | a0001c0001t0003g0279 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.236-9851T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949097 | ||||||
| chr7:13949108
|
T | C | 3 | a0002c0002t0010g0116a0002c0002t0017g0037a0002c0002t0017g0039 | 3 | HG02486.hp2 HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.236-9862A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949108 | ||||||
| chr7:13949110
|
G | T | 4 | a0002c0002t0001g0158a0002c0002t0005g0162a0002c0002t0008g0159others(1): Show | 4 | NA18963.hp1 NA19063.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-9864C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949110 | ||||||
| chr7:13949117
|
T | C | 12 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0003g0019others(9): Show | 12 | HG00140.hp2 HG00280.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.236-9871A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949117 | ||||||
| chr7:13949165
|
T | A | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236-9919A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949165 | ||||||
| chr7:13949165
|
TA | T | 27 | a0001c0001t0002g0013a0001c0001t0002g0021a0001c0001t0002g0035others(24): Show | 27 | HG00544.hp2 HG00597.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.236-9920delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949165 | ||||||
| chr7:13949261
|
C | T | 7 | a0001c0001t0003g0278a0001c0001t0003g0292a0001c0001t0003g0295others(4): Show | 7 | HG00544.hp2 HG00597.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-10015G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949261 | ||||||
| chr7:13949550
|
C | T | 2 | a0002c0002t0001g0199a0002c0002t0001g0217 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.236-10304G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949550 | ||||||
| chr7:13949615
|
G | C | 1 | a0001c0001t0013g0109 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.236-10369C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949615 | ||||||
| chr7:13949696
|
G | T | 1 | a0002c0002t0006g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.236-10450C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949696 | ||||||
| chr7:13949720
|
C | A | 2 | a0002c0002t0022g0003a0002c0002t0022g0004 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.236-10474G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949720 | ||||||
| chr7:13949839
|
A | G | 8 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(5): Show | 8 | HG00140.hp2 HG01099.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.236-10593T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949839 | ||||||
| chr7:13949885
|
T | A | 1 | a0001c0001t0016g0190 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.236-10639A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949885 | ||||||
| chr7:13949902
|
T | A | 10 | a0001c0001t0004g0137a0001c0001t0009g0143a0001c0001t0010g0045others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-10656A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949902 | ||||||
| chr7:13949918
|
G | A | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0002c0002t0004g0246others(5): Show | 8 | HG00140.hp1 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-10672C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13949918 | ||||||
| chr7:13950049
|
T | A | 19 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0003g0054others(16): Show | 19 | HG01070.hp1 HG02015.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.236-10803A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950049 | ||||||
| chr7:13950065
|
G | C | 12 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(9): Show | 12 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.236-10819C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950065 | ||||||
| chr7:13950066
|
G | A | 1 | a0001c0001t0004g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.236-10820C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950066 | ||||||
| chr7:13950102
|
G | T | 12 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(9): Show | 12 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.236-10856C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950102 | ||||||
| chr7:13950124
|
T | C | 8 | a0001c0001t0003g0278a0001c0001t0003g0290a0001c0001t0003g0291others(5): Show | 8 | HG00597.hp2 HG00609.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-10878A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950124 | ||||||
| chr7:13950317
|
G | A | 1 | a0001c0001t0014g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.236-11071C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950317 | ||||||
| chr7:13950408
|
C | T | 5 | a0001c0001t0007g0053a0001c0001t0038g0306a0001c0001t0041g0309others(2): Show | 5 | HG02055.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-11162G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950408 | ||||||
| chr7:13950645
|
T | G | 1 | a0002c0002t0007g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.236-11399A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950645 | ||||||
| chr7:13950713
|
G | C | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-11467C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950713 | ||||||
| chr7:13950789
|
C | T | 1 | a0001c0001t0007g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.236-11543G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950789 | ||||||
| chr7:13950899
|
A | AAC | 26 | a0001c0001t0002g0026a0001c0001t0004g0214a0001c0001t0004g0270others(23): Show | 26 | HG00621.hp2 HG01099.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.236-11655_236-1165 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
A | AACAC | 21 | a0001c0001t0003g0278a0001c0001t0003g0290a0001c0001t0003g0291others(18): Show | 21 | HG00597.hp2 HG00609.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.236-11657_236-1165 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
A | AACACAC | 23 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0254others(20): Show | 23 | HG01106.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.236-11659_236-1165 others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
A | AACACACA others(1): Show |
7 | a0001c0001t0003g0009a0001c0001t0007g0076a0001c0001t0046g0072others(4): Show | 7 | HG02258.hp1 HG03195.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-11661_236-1165 others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
A | AACACACA others(3): Show |
10 | a0001c0001t0002g0096a0001c0001t0007g0077a0001c0001t0019g0152others(7): Show | 10 | HG00140.hp1 HG01175.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.236-11663_236-1165 others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
A | AACACACA others(5): Show |
2 | a0001c0001t0002g0012a0002c0002t0017g0037 | 2 | HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.236-11665_236-1165 others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
A | AACACACA others(7): Show |
1 | a0002c0002t0017g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.236-11667_236-1165 others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
A | AACACACA others(9): Show |
1 | a0001c0001t0024g0029 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.236-11669_236-1165 others(20): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
A | AACACACA others(11): Show |
1 | a0002c0002t0010g0116 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.236-11671_236-1165 others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
AAC | A | 5 | a0001c0001t0006g0123a0001c0001t0015g0132a0001c0001t0021g0265others(2): Show | 5 | HG01891.hp1 HG02559.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-11655_236-1165 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
AACAC | A | 5 | a0001c0001t0004g0137a0001c0001t0013g0109a0001c0001t0014g0080others(2): Show | 5 | HG01361.hp2 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-11657_236-1165 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
AACACACA others(1): Show |
A | 23 | a0001c0001t0002g0283a0001c0001t0003g0047a0001c0001t0003g0050others(20): Show | 23 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.236-11661_236-1165 others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
AACACACA others(3): Show |
A | 78 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(75): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.236-11663_236-1165 others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0023g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.236-11665_236-1165 others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950899
|
AACACACA others(11): Show |
A | 9 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(6): Show | 9 | HG00140.hp2 HG00544.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-11671_236-1165 others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950899 | ||||||
| chr7:13950941
|
C | A | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-11695G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950941 | ||||||
| chr7:13950941
|
C | CACAA | 8 | a0001c0001t0002g0038a0001c0001t0008g0250a0001c0001t0009g0179others(5): Show | 8 | HG01070.hp1 HG02602.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-11696_236-1169 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950941 | ||||||
| chr7:13950941
|
C | CACACAA | 7 | a0001c0001t0002g0035a0001c0001t0004g0263a0001c0001t0007g0317others(4): Show | 7 | HG02257.hp2 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-11696_236-1169 others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950941 | ||||||
| chr7:13950941
|
C | CACACACA others(3): Show |
2 | a0001c0001t0002g0021a0001c0001t0014g0025 | 2 | HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.236-11696_236-1169 others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13950941 | ||||||
| chr7:13951129
|
C | A | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-11883G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951129 | ||||||
| chr7:13951132
|
C | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.236-11886G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951132 | ||||||
| chr7:13951255
|
T | C | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-12009A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951255 | ||||||
| chr7:13951294
|
G | A | 9 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(6): Show | 9 | HG00140.hp2 HG00544.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-12048C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951294 | ||||||
| chr7:13951318
|
C | T | 149 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.236-12072G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951318 | ||||||
| chr7:13951367
|
A | G | 128 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.236-12121T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951367 | ||||||
| chr7:13951560
|
G | A | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0042g0303others(1): Show | 4 | HG02717.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-12314C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951560 | ||||||
| chr7:13951596
|
T | C | 150 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.236-12350A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951596 | ||||||
| chr7:13951730
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.236-12484A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951730 | ||||||
| chr7:13951753
|
T | A | 8 | a0001c0001t0003g0278a0001c0001t0003g0290a0001c0001t0003g0291others(5): Show | 8 | HG00597.hp2 HG00609.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.236-12507A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951753 | ||||||
| chr7:13951839
|
G | A | 45 | a0001c0001t0003g0016a0001c0001t0003g0278a0001c0001t0003g0279others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.236-12593C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951839 | ||||||
| chr7:13951972
|
C | A | 1 | a0002c0002t0052g0260 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.236-12726G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13951972 | ||||||
| chr7:13952046
|
AAAAT | A | 45 | a0001c0001t0003g0016a0001c0001t0003g0278a0001c0001t0003g0279others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.236-12804_236-1280 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952046 | ||||||
| chr7:13952069
|
A | G | 12 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(9): Show | 12 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.236-12823T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952069 | ||||||
| chr7:13952080
|
G | A | 1 | a0001c0001t0051g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.236-12834C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952080 | ||||||
| chr7:13952117
|
C | T | 3 | a0001c0001t0005g0248a0001c0001t0005g0262a0002c0002t0008g0264 | 3 | HG01168.hp1 HG01258.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.236-12871G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952117 | ||||||
| chr7:13952139
|
A | G | 1 | a0001c0001t0006g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.236-12893T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952139 | ||||||
| chr7:13952203
|
T | G | 128 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.236-12957A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952203 | ||||||
| chr7:13952204
|
G | A | 20 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0002g0038others(17): Show | 20 | HG01070.hp1 HG02015.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.236-12958C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952204 | ||||||
| chr7:13952228
|
C | G | 174 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.236-12982G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952228 | ||||||
| chr7:13952303
|
C | T | 1 | a0001c0001t0004g0166 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.236-13057G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952303 | ||||||
| chr7:13952608
|
T | A | 185 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(182): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.236-13362A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952608 | ||||||
| chr7:13952641
|
G | A | 1 | a0002c0002t0007g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.236-13395C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952641 | ||||||
| chr7:13952732
|
G | T | 1 | a0001c0001t0002g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.236-13486C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952732 | ||||||
| chr7:13952804
|
C | T | 1 | a0002c0002t0001g0230 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.236-13558G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952804 | ||||||
| chr7:13952835
|
A | G | 183 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(180): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.236-13589T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952835 | ||||||
| chr7:13952986
|
A | G | 4 | a0001c0001t0002g0035a0001c0001t0010g0083a0001c0001t0020g0133others(1): Show | 4 | HG02145.hp1 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-13740T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13952986 | ||||||
| chr7:13953065
|
A | G | 1 | a0001c0001t0051g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.236-13819T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953065 | ||||||
| chr7:13953085
|
A | G | 3 | a0001c0001t0003g0019a0001c0001t0009g0229a0001c0003t0002g0073 | 3 | HG00280.hp2 HG01515.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.236-13839T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953085 | ||||||
| chr7:13953111
|
C | T | 6 | a0002c0002t0001g0209a0002c0002t0001g0219a0002c0002t0009g0211others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-13865G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953111 | ||||||
| chr7:13953246
|
C | T | 13 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-14000G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953246 | ||||||
| chr7:13953357
|
C | T | 13 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-14111G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953357 | ||||||
| chr7:13953389
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.236-14143G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953389 | ||||||
| chr7:13953400
|
C | T | 2 | a0002c0002t0004g0145a0002c0002t0005g0144 | 2 | NA18978.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.236-14154G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953400 | ||||||
| chr7:13953439
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0059g0251 | 2 | HG03831.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.236-14193C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953439 | ||||||
| chr7:13953445
|
T | G | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.236-14199A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953445 | ||||||
| chr7:13953464
|
A | T | 1 | a0002c0002t0004g0172 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.236-14218T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953464 | ||||||
| chr7:13953501
|
G | A | 1 | a0001c0001t0006g0091 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.236-14255C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953501 | ||||||
| chr7:13953623
|
C | G | 13 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-14377G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953623 | ||||||
| chr7:13953669
|
G | T | 9 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0001g0154others(6): Show | 9 | HG00140.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.236-14423C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953669 | ||||||
| chr7:13953672
|
A | T | 9 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0001g0154others(6): Show | 9 | HG00140.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.236-14426T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953672 | ||||||
| chr7:13953684
|
A | G | 13 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-14438T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953684 | ||||||
| chr7:13953770
|
T | A | 1 | a0001c0001t0056g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.236-14524A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13953770 | ||||||
| chr7:13954144
|
C | T | 1 | a0001c0001t0006g0088 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.236-14898G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954144 | ||||||
| chr7:13954145
|
A | T | 7 | a0001c0001t0010g0040a0001c0001t0010g0084a0001c0001t0010g0085others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-14899T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954145 | ||||||
| chr7:13954162
|
C | A | 2 | a0001c0001t0039g0086a0001c0001t0046g0072 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.236-14916G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954162 | ||||||
| chr7:13954163
|
A | T | 2 | a0001c0001t0039g0086a0001c0001t0046g0072 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.236-14917T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954163 | ||||||
| chr7:13954288
|
C | T | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-15042G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954288 | ||||||
| chr7:13954332
|
A | G | 1 | a0001c0001t0006g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.236-15086T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954332 | ||||||
| chr7:13954475
|
G | A | 1 | a0001c0001t0058g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.236-15229C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954475 | ||||||
| chr7:13954640
|
C | T | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0001g0154others(5): Show | 8 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.236-15394G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954640 | ||||||
| chr7:13954758
|
C | T | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0001g0154others(5): Show | 8 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.236-15512G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13954758 | ||||||
| chr7:13955033
|
C | T | 19 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0003g0054others(16): Show | 19 | HG01070.hp1 HG02015.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.236-15787G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955033 | ||||||
| chr7:13955264
|
G | A | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-16018C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955264 | ||||||
| chr7:13955368
|
G | C | 2 | a0001c0001t0039g0086a0001c0001t0046g0072 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.236-16122C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955368 | ||||||
| chr7:13955519
|
G | C | 1 | a0002c0002t0005g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.236-16273C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955519 | ||||||
| chr7:13955584
|
G | T | 71 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0002g0038others(68): Show | 71 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.236-16338C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955584 | ||||||
| chr7:13955835
|
AT | A | 13 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-16590delA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955835 | ||||||
| chr7:13955899
|
A | T | 23 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0003g0054others(20): Show | 23 | HG01070.hp1 HG01243.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.236-16653T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955899 | ||||||
| chr7:13955944
|
A | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | NA18960.hp2 NA19006.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.236-16698T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13955944 | ||||||
| chr7:13956048
|
G | A | 13 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0004g0263others(10): Show | 13 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.236-16802C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956048 | ||||||
| chr7:13956162
|
T | G | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.236-16916A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956162 | ||||||
| chr7:13956193
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.236-16947A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956193 | ||||||
| chr7:13956257
|
T | G | 3 | a0001c0001t0006g0280a0001c0001t0012g0117a0001c0001t0053g0226 | 3 | HG02165.hp2 NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.236-17011A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956257 | ||||||
| chr7:13956258
|
C | T | 2 | a0001c0001t0014g0080a0001c0001t0042g0303 | 2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.236-17012G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956258 | ||||||
| chr7:13956305
|
G | T | 1 | a0002c0002t0005g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.236-17059C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956305 | ||||||
| chr7:13956321
|
A | AT | 32 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0003g0016others(29): Show | 32 | HG00140.hp2 HG00544.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.236-17076dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956321 | ||||||
| chr7:13956373
|
T | G | 1 | a0002c0002t0027g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.236-17127A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956373 | ||||||
| chr7:13956386
|
A | G | 2 | a0001c0001t0028g0240a0001c0001t0028g0241 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.236-17140T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956386 | ||||||
| chr7:13956399
|
G | C | 13 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-17153C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956399 | ||||||
| chr7:13956538
|
G | A | 13 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(10): Show | 13 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.236-17292C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956538 | ||||||
| chr7:13956787
|
A | G | 1 | a0001c0001t0004g0001 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.236-17541T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956787 | ||||||
| chr7:13956795
|
G | A | 1 | a0002c0002t0007g0020 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.236-17549C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956795 | ||||||
| chr7:13956927
|
CA | C | 15 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(12): Show | 15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-17682delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13956927 | ||||||
| chr7:13957156
|
G | A | 1 | a0002c0002t0001g0155 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.236-17910C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957156 | ||||||
| chr7:13957171
|
C | T | 12 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0019g0152others(9): Show | 12 | HG00140.hp1 HG02258.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.236-17925G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957171 | ||||||
| chr7:13957175
|
T | G | 15 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(12): Show | 15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-17929A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957175 | ||||||
| chr7:13957179
|
A | C | 1 | a0001c0001t0028g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.236-17933T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957179 | ||||||
| chr7:13957203
|
A | C | 15 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(12): Show | 15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-17957T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957203 | ||||||
| chr7:13957234
|
C | T | 4 | a0001c0001t0007g0076a0001c0001t0007g0077a0001c0001t0039g0086others(1): Show | 4 | HG01243.hp1 HG02109.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-17988G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957234 | ||||||
| chr7:13957277
|
G | A | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0001g0154others(5): Show | 8 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.236-18031C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957277 | ||||||
| chr7:13957322
|
G | A | 9 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(6): Show | 9 | HG00140.hp2 HG00544.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-18076C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957322 | ||||||
| chr7:13957526
|
A | G | 15 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(12): Show | 15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-18280T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957526 | ||||||
| chr7:13957534
|
T | C | 40 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0002g0038others(37): Show | 40 | HG01070.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.236-18288A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957534 | ||||||
| chr7:13957539
|
T | C | 3 | a0001c0001t0041g0309a0001c0001t0045g0113a0001c0001t0051g0237 | 3 | HG02723.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.236-18293A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957539 | ||||||
| chr7:13957917
|
G | A | 1 | a0001c0001t0012g0298 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.236-18671C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957917 | ||||||
| chr7:13957919
|
T | C | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0001g0154others(5): Show | 8 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.236-18673A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957919 | ||||||
| chr7:13957948
|
C | T | 2 | a0001c0001t0003g0099a0001c0001t0007g0118 | 2 | HG01175.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.236-18702G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13957948 | ||||||
| chr7:13958020
|
C | A | 14 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0006g0307others(11): Show | 14 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.236-18774G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958020 | ||||||
| chr7:13958154
|
G | C | 1 | a0002c0002t0009g0196 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.236-18908C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958154 | ||||||
| chr7:13958272
|
C | G | 1 | a0002c0002t0006g0018 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.236-19026G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958272 | ||||||
| chr7:13958306
|
C | T | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0001g0154others(5): Show | 8 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.236-19060G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958306 | ||||||
| chr7:13958415
|
T | C | 1 | a0001c0001t0004g0249 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235+19012A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958415 | ||||||
| chr7:13958416
|
G | T | 7 | a0001c0001t0003g0278a0001c0001t0003g0290a0001c0001t0003g0291others(4): Show | 7 | HG00597.hp2 HG00609.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+19011C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958416 | ||||||
| chr7:13958612
|
C | T | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0001g0154others(5): Show | 8 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+18815G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958612 | ||||||
| chr7:13958657
|
G | C | 1 | a0001c0001t0002g0065 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.235+18770C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958657 | ||||||
| chr7:13958913
|
T | G | 2 | a0001c0001t0028g0240a0001c0001t0028g0241 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.235+18514A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958913 | ||||||
| chr7:13958947
|
A | G | 8 | a0001c0001t0019g0152a0001c0001t0019g0153a0001c0004t0001g0154others(5): Show | 8 | HG00140.hp1 HG02258.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+18480T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13958947 | ||||||
| chr7:13959043
|
T | TA | 18 | a0001c0001t0003g0016a0001c0001t0003g0279a0001c0001t0003g0281others(15): Show | 18 | HG00140.hp2 HG00544.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+18383dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959043 | ||||||
| chr7:13959043
|
TA | T | 29 | a0001c0001t0003g0054a0001c0001t0004g0181a0001c0001t0006g0123others(26): Show | 29 | HG01070.hp1 HG01074.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.235+18383delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959043 | ||||||
| chr7:13959152
|
T | C | 3 | a0001c0001t0007g0076a0001c0001t0007g0077a0001c0001t0056g0261 | 3 | HG01243.hp1 HG03471.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.235+18275A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959152 | ||||||
| chr7:13959169
|
T | C | 6 | a0001c0001t0004g0183a0001c0001t0004g0191a0001c0001t0005g0193others(3): Show | 6 | NA18941.hp2 NA18965.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+18258A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959169 | ||||||
| chr7:13959203
|
T | G | 23 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0002g0038others(20): Show | 23 | HG01070.hp1 HG01243.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.235+18224A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959203 | ||||||
| chr7:13959415
|
A | C | 1 | a0002c0002t0006g0018 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.235+18012T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959415 | ||||||
| chr7:13959638
|
C | G | 8 | a0001c0001t0003g0278a0001c0001t0003g0290a0001c0001t0003g0291others(5): Show | 8 | HG00597.hp2 HG00609.hp2 NA18956.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+17789G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959638 | ||||||
| chr7:13959846
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.235+17581C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959846 | ||||||
| chr7:13959882
|
C | CA | 70 | a0001c0001t0001g0157a0001c0001t0001g0215a0001c0001t0001g0245others(67): Show | 70 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.235+17544dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959882 | ||||||
| chr7:13959882
|
CA | C | 25 | a0001c0001t0002g0027a0001c0001t0003g0016a0001c0001t0003g0278others(22): Show | 25 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.235+17544delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959882 | ||||||
| chr7:13959882
|
CAAAAAAA others(6): Show |
C | 21 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0002g0038others(18): Show | 21 | HG01070.hp1 HG02015.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.235+17532_235+1754 others(17): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959882 | ||||||
| chr7:13959882
|
CAAAAAAA others(7): Show |
C | 15 | a0001c0001t0006g0123a0001c0001t0006g0302a0001c0001t0010g0045others(12): Show | 15 | HG01074.hp1 HG01081.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.235+17531_235+1754 others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13959882 | ||||||
| chr7:13960033
|
C | T | 1 | a0002c0002t0033g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.235+17394G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960033 | ||||||
| chr7:13960069
|
CTAAAG | C | 3 | a0001c0001t0007g0076a0001c0001t0007g0077a0001c0001t0056g0261 | 3 | HG01243.hp1 HG03471.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.235+17353_235+1735 others(9): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960069 | ||||||
| chr7:13960102
|
A | G | 1 | a0001c0001t0005g0247 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.235+17325T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960102 | ||||||
| chr7:13960134
|
T | C | 24 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0254others(21): Show | 24 | HG00438.hp1 HG01106.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.235+17293A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960134 | ||||||
| chr7:13960137
|
G | C | 3 | a0001c0001t0007g0076a0001c0001t0007g0077a0001c0001t0056g0261 | 3 | HG01243.hp1 HG03471.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.235+17290C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960137 | ||||||
| chr7:13960182
|
G | A | 1 | a0001c0001t0007g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+17245C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960182 | ||||||
| chr7:13960229
|
A | G | 32 | a0001c0001t0002g0021a0001c0001t0002g0035a0001c0001t0002g0038others(29): Show | 32 | HG00140.hp2 HG00544.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.235+17198T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960229 | ||||||
| chr7:13960477
|
C | G | 11 | a0001c0001t0004g0137a0001c0001t0019g0152a0001c0001t0019g0153others(8): Show | 11 | HG00140.hp1 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.235+16950G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960477 | ||||||
| chr7:13960557
|
C | T | 58 | a0001c0001t0002g0035a0001c0001t0002g0038a0001c0001t0003g0278others(55): Show | 58 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.235+16870G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960557 | ||||||
| chr7:13960614
|
G | A | 16 | a0001c0001t0006g0036a0001c0001t0006g0123a0001c0001t0006g0302others(13): Show | 16 | HG01081.hp2 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.235+16813C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960614 | ||||||
| chr7:13960786
|
T | C | 1 | a0001c0001t0028g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.235+16641A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960786 | ||||||
| chr7:13960796
|
T | G | 21 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0254others(18): Show | 21 | HG00544.hp1 HG01070.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.235+16631A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13960796 | ||||||
| chr7:13961010
|
T | C | 7 | a0001c0001t0003g0278a0001c0001t0003g0291a0001c0001t0003g0292others(4): Show | 7 | HG00597.hp2 HG00609.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+16417A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961010 | ||||||
| chr7:13961016
|
C | T | 1 | a0001c0001t0006g0280 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.235+16411G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961016 | ||||||
| chr7:13961084
|
T | TG | 104 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(101): Show | 105 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.235+16342dupC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961084 | ||||||
| chr7:13961108
|
T | C | 14 | a0001c0001t0003g0278a0001c0001t0003g0282a0001c0001t0003g0287others(11): Show | 14 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+16319A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961108 | ||||||
| chr7:13961110
|
C | T | 14 | a0001c0001t0003g0278a0001c0001t0003g0282a0001c0001t0003g0287others(11): Show | 14 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+16317G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961110 | ||||||
| chr7:13961145
|
C | CA | 6 | a0001c0001t0002g0017a0001c0001t0002g0024a0001c0001t0002g0119others(3): Show | 6 | HG00597.hp1 HG02074.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+16281dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961145 | ||||||
| chr7:13961145
|
CA | C | 36 | a0001c0001t0001g0244a0001c0001t0001g0253a0001c0001t0001g0254others(33): Show | 36 | HG00140.hp2 HG00544.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.235+16281delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961145 | ||||||
| chr7:13961146
|
AAAAAAAA others(3): Show |
A | 24 | a0001c0001t0001g0157a0001c0001t0015g0136a0001c0001t0019g0152others(21): Show | 24 | HG00140.hp1 HG02080.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.235+16271_235+1628 others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961146 | ||||||
| chr7:13961191
|
A | G | 62 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0253others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.235+16236T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961191 | ||||||
| chr7:13961210
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.235+16217A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961210 | ||||||
| chr7:13961224
|
G | C | 1 | a0001c0001t0028g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+16203C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961224 | ||||||
| chr7:13961278
|
A | C | 1 | a0002c0002t0006g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.235+16149T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961278 | ||||||
| chr7:13961441
|
T | A | 9 | a0001c0001t0003g0278a0001c0001t0003g0290a0001c0001t0003g0291others(6): Show | 9 | HG00597.hp2 HG00609.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+15986A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961441 | ||||||
| chr7:13961504
|
G | C | 48 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(45): Show | 48 | HG00140.hp1 HG00544.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.235+15923C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961504 | ||||||
| chr7:13961549
|
T | C | 1 | a0002c0002t0013g0315 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235+15878A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961549 | ||||||
| chr7:13961553
|
T | C | 1 | a0001c0001t0003g0054 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.235+15874A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961553 | ||||||
| chr7:13961720
|
C | A | 6 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0018g0316others(3): Show | 6 | HG02280.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+15707G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961720 | ||||||
| chr7:13961783
|
G | A | 1 | a0002c0002t0009g0196 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.235+15644C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961783 | ||||||
| chr7:13961854
|
A | G | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+15573T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961854 | ||||||
| chr7:13961859
|
T | C | 2 | a0001c0001t0004g0137a0001c0001t0014g0080 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+15568A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961859 | ||||||
| chr7:13961944
|
A | G | 16 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0282others(13): Show | 16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+15483T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13961944 | ||||||
| chr7:13962038
|
G | A | 1 | a0001c0001t0007g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+15389C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962038 | ||||||
| chr7:13962070
|
A | G | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+15357T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962070 | ||||||
| chr7:13962113
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.235+15314A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962113 | ||||||
| chr7:13962180
|
T | TAC | 20 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0282others(17): Show | 20 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.235+15245_235+1524 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962180 | ||||||
| chr7:13962202
|
C | CACGT | 9 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0006g0313others(6): Show | 9 | HG01109.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.235+15224_235+1522 others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962202 | ||||||
| chr7:13962202
|
C | CGT | 13 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0010g0301others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+15223_235+1522 others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962202 | ||||||
| chr7:13962215
|
A | G | 88 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.235+15212T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962215 | ||||||
| chr7:13962218
|
T | C | 17 | a0001c0001t0001g0157a0001c0001t0019g0152a0001c0001t0019g0153others(14): Show | 17 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+15209A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962218 | ||||||
| chr7:13962248
|
G | A | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+15179C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962248 | ||||||
| chr7:13962418
|
C | T | 58 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(55): Show | 58 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.235+15009G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962418 | ||||||
| chr7:13962432
|
C | A | 8 | a0001c0001t0003g0279a0001c0001t0003g0281a0001c0001t0006g0066others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+14995G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962432 | ||||||
| chr7:13962507
|
C | T | 88 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.235+14920G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962507 | ||||||
| chr7:13962538
|
C | A | 10 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0018g0316others(7): Show | 10 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+14889G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962538 | ||||||
| chr7:13962604
|
C | G | 1 | a0001c0003t0002g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.235+14823G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962604 | ||||||
| chr7:13962664
|
A | G | 1 | a0001c0001t0011g0093 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.235+14763T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962664 | ||||||
| chr7:13962923
|
T | C | 1 | a0001c0001t0007g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+14504A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13962923 | ||||||
| chr7:13963115
|
C | G | 1 | a0002c0002t0018g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.235+14312G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963115 | ||||||
| chr7:13963181
|
G | A | 8 | a0001c0001t0003g0279a0001c0001t0003g0281a0001c0001t0006g0066others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+14246C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963181 | ||||||
| chr7:13963310
|
G | A | 1 | a0001c0001t0028g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+14117C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963310 | ||||||
| chr7:13963480
|
C | T | 84 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(81): Show | 84 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.235+13947G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963480 | ||||||
| chr7:13963522
|
C | T | 10 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0018g0316others(7): Show | 10 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+13905G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963522 | ||||||
| chr7:13963531
|
CA | C | 86 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(83): Show | 86 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.235+13895delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963531 | ||||||
| chr7:13963578
|
G | T | 18 | a0001c0001t0001g0157a0001c0001t0002g0096a0001c0001t0019g0152others(15): Show | 18 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+13849C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963578 | ||||||
| chr7:13963593
|
T | C | 2 | a0001c0001t0018g0316a0002c0002t0007g0310 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.235+13834A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963593 | ||||||
| chr7:13963634
|
G | A | 15 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(12): Show | 15 | HG00544.hp1 HG01070.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.235+13793C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963634 | ||||||
| chr7:13963692
|
A | G | 1 | a0001c0001t0005g0248 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.235+13735T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963692 | ||||||
| chr7:13963702
|
C | T | 4 | a0001c0001t0001g0224a0001c0001t0002g0048a0002c0002t0002g0111others(1): Show | 4 | HG00735.hp1 HG01192.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+13725G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963702 | ||||||
| chr7:13963725
|
A | T | 1 | a0001c0001t0005g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.235+13702T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963725 | ||||||
| chr7:13963750
|
G | C | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+13677C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963750 | ||||||
| chr7:13963818
|
G | A | 8 | a0001c0001t0003g0279a0001c0001t0003g0281a0001c0001t0006g0066others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+13609C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963818 | ||||||
| chr7:13963874
|
C | T | 1 | a0001c0001t0010g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.235+13553G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963874 | ||||||
| chr7:13963899
|
C | T | 17 | a0001c0001t0001g0157a0001c0001t0019g0152a0001c0001t0019g0153others(14): Show | 17 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+13528G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13963899 | ||||||
| chr7:13964104
|
T | A | 1 | a0001c0001t0005g0235 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.235+13323A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964104 | ||||||
| chr7:13964167
|
A | T | 16 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0282others(13): Show | 16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+13260T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964167 | ||||||
| chr7:13964181
|
A | C | 1 | a0001c0001t0007g0056 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.235+13246T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964181 | ||||||
| chr7:13964273
|
T | C | 16 | a0001c0001t0004g0238a0001c0001t0006g0302a0001c0001t0006g0307others(13): Show | 16 | HG02055.hp2 HG02280.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.235+13154A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964273 | ||||||
| chr7:13964287
|
T | G | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+13140A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964287 | ||||||
| chr7:13964316
|
C | T | 1 | a0002c0002t0012g0055 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.235+13111G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964316 | ||||||
| chr7:13964341
|
C | G | 70 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(67): Show | 70 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.235+13086G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964341 | ||||||
| chr7:13964361
|
G | A | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+13066C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964361 | ||||||
| chr7:13964389
|
T | C | 1 | a0001c0001t0003g0279 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.235+13038A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964389 | ||||||
| chr7:13964454
|
C | T | 88 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.235+12973G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964454 | ||||||
| chr7:13964485
|
G | T | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12942C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964485 | ||||||
| chr7:13964528
|
G | A | 2 | a0001c0001t0002g0090a0001c0001t0006g0091 | 2 | HG00735.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.235+12899C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964528 | ||||||
| chr7:13964537
|
C | A | 16 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0282others(13): Show | 16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+12890G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964537 | ||||||
| chr7:13964613
|
G | T | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12814C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964613 | ||||||
| chr7:13964678
|
C | T | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12749G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964678 | ||||||
| chr7:13964705
|
A | G | 10 | a0001c0001t0002g0038a0001c0001t0009g0143a0001c0001t0010g0045others(7): Show | 10 | HG02055.hp1 HG02559.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+12722T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964705 | ||||||
| chr7:13964716
|
C | T | 1 | a0002c0002t0007g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.235+12711G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964716 | ||||||
| chr7:13964720
|
A | T | 1 | a0001c0001t0021g0265 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.235+12707T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964720 | ||||||
| chr7:13964722
|
CTGGAATA others(17): Show |
C | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12681_235+1270 others(28): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964722 | ||||||
| chr7:13964747
|
T | A | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12680A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964747 | ||||||
| chr7:13964749
|
T | A | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12678A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964749 | ||||||
| chr7:13964750
|
T | A | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12677A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964750 | ||||||
| chr7:13964768
|
G | T | 1 | a0001c0001t0027g0256 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.235+12659C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964768 | ||||||
| chr7:13964833
|
C | A | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+12594G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964833 | ||||||
| chr7:13964847
|
T | C | 79 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.235+12580A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13964847 | ||||||
| chr7:13965014
|
G | A | 2 | a0002c0002t0001g0164a0002c0002t0005g0274 | 2 | NA18977.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.235+12413C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965014 | ||||||
| chr7:13965019
|
A | G | 2 | a0001c0001t0017g0023a0002c0002t0033g0022 | 2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.235+12408T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965019 | ||||||
| chr7:13965045
|
C | T | 160 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.235+12382G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965045 | ||||||
| chr7:13965085
|
C | T | 159 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.235+12342G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965085 | ||||||
| chr7:13965183
|
A | G | 2 | a0001c0001t0004g0137a0001c0001t0014g0080 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+12244T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965183 | ||||||
| chr7:13965238
|
A | C | 1 | a0001c0001t0030g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.235+12189T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965238 | ||||||
| chr7:13965264
|
A | G | 1 | a0002c0002t0010g0116 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.235+12163T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965264 | ||||||
| chr7:13965312
|
C | T | 1 | a0001c0001t0008g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.235+12115G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965312 | ||||||
| chr7:13965459
|
T | A | 1 | a0001c0001t0042g0303 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.235+11968A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965459 | ||||||
| chr7:13965497
|
T | C | 1 | a0001c0001t0007g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+11930A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965497 | ||||||
| chr7:13965597
|
C | T | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+11830G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965597 | ||||||
| chr7:13965662
|
A | G | 14 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0006g0313others(11): Show | 14 | HG02055.hp2 HG02280.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.235+11765T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965662 | ||||||
| chr7:13965701
|
G | C | 18 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(15): Show | 18 | HG00544.hp1 HG01070.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+11726C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965701 | ||||||
| chr7:13965980
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.235+11447G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13965980 | ||||||
| chr7:13966002
|
A | C | 1 | a0001c0001t0002g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.235+11425T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966002 | ||||||
| chr7:13966069
|
T | A | 1 | a0001c0001t0003g0278 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.235+11358A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966069 | ||||||
| chr7:13966163
|
T | C | 4 | a0001c0001t0010g0040a0001c0001t0010g0084a0001c0001t0010g0085others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+11264A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966163 | ||||||
| chr7:13966285
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.235+11142G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966285 | ||||||
| chr7:13966392
|
G | C | 8 | a0001c0001t0003g0279a0001c0001t0003g0281a0001c0001t0006g0066others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+11035C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966392 | ||||||
| chr7:13966504
|
C | T | 1 | a0001c0001t0004g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.235+10923G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966504 | ||||||
| chr7:13966548
|
A | G | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+10879T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966548 | ||||||
| chr7:13966604
|
G | T | 158 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(155): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.235+10823C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966604 | ||||||
| chr7:13966630
|
G | C | 8 | a0001c0001t0003g0279a0001c0001t0003g0281a0001c0001t0006g0066others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+10797C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966630 | ||||||
| chr7:13966685
|
T | C | 2 | a0001c0001t0018g0316a0002c0002t0007g0310 | 2 | HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.235+10742A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966685 | ||||||
| chr7:13966689
|
A | C | 12 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0015g0134others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+10738T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13966689 | ||||||
| chr7:13967008
|
A | G | 3 | a0001c0001t0020g0252a0001c0001t0028g0241a0002c0002t0027g0242 | 3 | HG02258.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.235+10419T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967008 | ||||||
| chr7:13967012
|
G | A | 5 | a0001c0001t0005g0247a0001c0001t0005g0248a0001c0001t0005g0262others(2): Show | 5 | HG01099.hp1 HG01168.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+10415C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967012 | ||||||
| chr7:13967119
|
T | C | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+10308A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967119 | ||||||
| chr7:13967235
|
T | C | 1 | a0001c0001t0002g0024 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.235+10192A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967235 | ||||||
| chr7:13967270
|
T | C | 69 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(66): Show | 69 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.235+10157A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967270 | ||||||
| chr7:13967636
|
A | G | 1 | a0001c0001t0016g0268 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.235+9791T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967636 | ||||||
| chr7:13967677
|
C | G | 234 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+9750G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967677 | ||||||
| chr7:13967694
|
A | T | 2 | a0002c0002t0004g0172a0002c0002t0007g0310 | 2 | HG03209.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.235+9733T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967694 | ||||||
| chr7:13967758
|
T | TG | 12 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0015g0134others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+9668dupC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13967758 | ||||||
| chr7:13968004
|
T | C | 1 | a0001c0001t0019g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.235+9423A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968004 | ||||||
| chr7:13968040
|
T | C | 166 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.235+9387A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968040 | ||||||
| chr7:13968045
|
C | T | 12 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0015g0134others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+9382G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968045 | ||||||
| chr7:13968494
|
T | G | 12 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0015g0134others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+8933A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968494 | ||||||
| chr7:13968621
|
T | A | 1 | a0002c0002t0013g0315 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235+8806A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968621 | ||||||
| chr7:13968799
|
A | C | 4 | a0001c0001t0010g0040a0001c0001t0010g0084a0001c0001t0010g0085others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+8628T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968799 | ||||||
| chr7:13968841
|
T | C | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+8586A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968841 | ||||||
| chr7:13968954
|
T | C | 161 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.235+8473A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13968954 | ||||||
| chr7:13969001
|
C | T | 160 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.235+8426G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969001 | ||||||
| chr7:13969031
|
G | T | 2 | a0001c0001t0004g0137a0001c0001t0014g0080 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+8396C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969031 | ||||||
| chr7:13969034
|
C | G | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+8393G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969034 | ||||||
| chr7:13969206
|
A | C | 234 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+8221T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969206 | ||||||
| chr7:13969214
|
T | C | 1 | a0001c0001t0030g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.235+8213A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969214 | ||||||
| chr7:13969231
|
T | G | 1 | a0001c0001t0004g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235+8196A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969231 | ||||||
| chr7:13969303
|
A | G | 3 | a0001c0001t0020g0252a0001c0001t0028g0241a0002c0002t0027g0242 | 3 | HG02258.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.235+8124T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969303 | ||||||
| chr7:13969305
|
GAATA | G | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+8118_235+8121d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969305 | ||||||
| chr7:13969377
|
A | T | 41 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(38): Show | 41 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.235+8050T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969377 | ||||||
| chr7:13969391
|
A | T | 1 | a0001c0001t0014g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.235+8036T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969391 | ||||||
| chr7:13969447
|
A | G | 12 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0015g0134others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+7980T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969447 | ||||||
| chr7:13969512
|
A | G | 12 | a0001c0001t0006g0300a0001c0001t0006g0308a0001c0001t0015g0134others(9): Show | 12 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+7915T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969512 | ||||||
| chr7:13969557
|
C | A | 2 | a0001c0001t0004g0137a0001c0001t0014g0080 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+7870G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969557 | ||||||
| chr7:13969801
|
A | C | 1 | a0001c0001t0007g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+7626T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969801 | ||||||
| chr7:13969825
|
G | A | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.235+7602C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969825 | ||||||
| chr7:13969956
|
T | C | 18 | a0001c0001t0004g0238a0001c0001t0006g0302a0001c0001t0006g0307others(15): Show | 18 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+7471A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969956 | ||||||
| chr7:13969968
|
T | C | 2 | a0001c0001t0015g0136a0001c0001t0020g0133 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.235+7459A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13969968 | ||||||
| chr7:13970023
|
G | A | 17 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(14): Show | 17 | HG00544.hp1 HG01978.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+7404C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970023 | ||||||
| chr7:13970100
|
C | CA | 17 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(14): Show | 17 | HG00544.hp1 HG01978.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+7326dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970100 | ||||||
| chr7:13970116
|
C | T | 1 | a0002c0002t0005g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.235+7311G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970116 | ||||||
| chr7:13970122
|
G | A | 1 | a0001c0001t0013g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.235+7305C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970122 | ||||||
| chr7:13970153
|
C | T | 17 | a0001c0001t0001g0157a0001c0001t0019g0152a0001c0001t0019g0153others(14): Show | 17 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+7274G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970153 | ||||||
| chr7:13970244
|
G | A | 215 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.235+7183C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970244 | ||||||
| chr7:13970244
|
G | C | 16 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0282others(13): Show | 16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+7183C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970244 | ||||||
| chr7:13970257
|
T | A | 1 | a0001c0001t0014g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.235+7170A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970257 | ||||||
| chr7:13970262
|
AAACACAC others(6): Show |
A | 1 | a0002c0002t0027g0242 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.235+7152_235+7164d others(15): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970262 | ||||||
| chr7:13970262
|
AAACACAC others(14): Show |
A | 1 | a0001c0001t0008g0188 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.235+7144_235+7164d others(23): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970262 | ||||||
| chr7:13970263
|
A | AAC | 19 | a0001c0001t0001g0201a0001c0001t0001g0244a0001c0001t0001g0253others(16): Show | 19 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.235+7162_235+7163d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
A | AACAC | 3 | a0001c0001t0002g0283a0001c0001t0012g0117a0002c0002t0004g0141 | 3 | HG02165.hp1 HG02165.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.235+7160_235+7163d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
A | AACACAC | 6 | a0001c0001t0005g0168a0001c0001t0040g0011a0002c0002t0001g0198others(3): Show | 6 | HG00544.hp2 HG01123.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+7158_235+7163d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
A | AACACACA others(1): Show |
3 | a0001c0001t0003g0278a0001c0001t0012g0297a0002c0002t0005g0150 | 3 | HG03834.hp2 NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.235+7156_235+7163d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
A | AACACACA others(5): Show |
1 | a0002c0002t0008g0197 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.235+7152_235+7163d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
A | C | 2 | a0002c0002t0001g0199a0002c0002t0022g0004 | 2 | HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.235+7164T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AAC | A | 20 | a0001c0001t0001g0157a0001c0001t0001g0255a0001c0001t0003g0288others(17): Show | 20 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.235+7162_235+7163d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACAC | A | 25 | a0001c0001t0001g0215a0001c0001t0002g0024a0001c0001t0003g0282others(22): Show | 25 | HG00597.hp1 HG01993.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.235+7160_235+7163d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACAC | A | 16 | a0001c0001t0002g0026a0001c0001t0003g0289a0001c0001t0004g0263others(13): Show | 16 | HG00544.hp1 HG01516.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.235+7158_235+7163d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(1): Show |
A | 10 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0006g0302others(7): Show | 10 | HG01070.hp1 HG02080.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+7156_235+7163d others(10): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(3): Show |
A | 3 | a0001c0001t0004g0238a0001c0001t0017g0023a0002c0002t0034g0311 | 3 | HG02886.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.235+7154_235+7163d others(12): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(5): Show |
A | 5 | a0001c0001t0006g0308a0001c0001t0015g0134a0001c0001t0015g0136others(2): Show | 5 | HG01109.hp1 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+7152_235+7163d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(7): Show |
A | 2 | a0001c0001t0006g0300a0001c0001t0007g0067 | 2 | HG00642.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.235+7150_235+7163d others(16): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(9): Show |
A | 6 | a0001c0001t0003g0279a0001c0001t0003g0281a0001c0001t0010g0069others(3): Show | 6 | HG00140.hp2 HG01071.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+7148_235+7163d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(11): Show |
A | 6 | a0001c0001t0002g0038a0001c0001t0003g0047a0001c0001t0004g0001others(3): Show | 7 | HG02109.hp1 HG02976.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+7146_235+7163d others(20): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(13): Show |
A | 40 | a0001c0001t0001g0224a0001c0001t0002g0048a0001c0001t0003g0050others(37): Show | 40 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.235+7144_235+7163d others(22): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(15): Show |
A | 85 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(82): Show | 85 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.235+7142_235+7163d others(24): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(17): Show |
A | 23 | a0001c0001t0004g0166a0001c0001t0004g0183a0001c0001t0004g0191others(20): Show | 23 | HG00423.hp2 HG00621.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.235+7140_235+7163d others(26): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(19): Show |
A | 5 | a0001c0001t0011g0110a0001c0001t0013g0109a0001c0001t0054g0195others(2): Show | 5 | HG00438.hp2 HG01346.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+7138_235+7163d others(28): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970263
|
AACACACA others(23): Show |
A | 1 | a0001c0001t0046g0072 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.235+7134_235+7163d others(32): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970263 | ||||||
| chr7:13970265
|
C | A | 1 | a0001c0001t0050g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.235+7162G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970265 | ||||||
| chr7:13970267
|
C | A | 2 | a0001c0001t0050g0142a0002c0002t0013g0315 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.235+7160G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970267 | ||||||
| chr7:13970269
|
C | A | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+7158G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970269 | ||||||
| chr7:13970271
|
C | A | 3 | a0001c0001t0004g0137a0001c0001t0014g0080a0002c0002t0013g0315 | 3 | HG02717.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.235+7156G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970271 | ||||||
| chr7:13970273
|
C | A | 3 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142 | 3 | HG02717.hp2 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+7154G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970273 | ||||||
| chr7:13970275
|
C | A | 1 | a0002c0002t0013g0315 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235+7152G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970275 | ||||||
| chr7:13970277
|
C | A | 2 | a0001c0001t0004g0137a0001c0001t0014g0080 | 2 | HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235+7150G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970277 | ||||||
| chr7:13970305
|
C | G | 3 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142 | 3 | HG02717.hp2 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.235+7122G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970305 | ||||||
| chr7:13970305
|
CACACACA others(14): Show |
C | 1 | a0001c0001t0003g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.235+7101_235+7121d others(23): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970305 | ||||||
| chr7:13970307
|
C | G | 1 | a0002c0002t0013g0315 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.235+7120G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970307 | ||||||
| chr7:13970311
|
CACACACA others(8): Show |
C | 1 | a0001c0001t0006g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.235+7101_235+7115d others(17): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970311 | ||||||
| chr7:13970315
|
CACACACA others(4): Show |
C | 1 | a0002c0002t0007g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.235+7101_235+7111d others(13): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970315 | ||||||
| chr7:13970327
|
A | C | 4 | a0001c0001t0004g0137a0001c0001t0014g0080a0001c0001t0050g0142others(1): Show | 4 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+7100T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970327 | ||||||
| chr7:13970366
|
A | G | 8 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0010g0301others(5): Show | 8 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+7061T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970366 | ||||||
| chr7:13970812
|
C | T | 1 | a0002c0002t0009g0196 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.235+6615G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970812 | ||||||
| chr7:13970821
|
G | A | 2 | a0001c0001t0004g0238a0001c0001t0051g0237 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.235+6606C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970821 | ||||||
| chr7:13970879
|
G | A | 158 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(155): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.235+6548C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13970879 | ||||||
| chr7:13971026
|
C | T | 2 | a0001c0001t0017g0023a0002c0002t0033g0022 | 2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.235+6401G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971026 | ||||||
| chr7:13971045
|
C | T | 2 | a0001c0001t0004g0238a0001c0001t0051g0237 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.235+6382G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971045 | ||||||
| chr7:13971048
|
G | A | 1 | a0001c0001t0007g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+6379C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971048 | ||||||
| chr7:13971057
|
T | C | 2 | a0001c0001t0010g0083a0001c0001t0045g0113 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.235+6370A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971057 | ||||||
| chr7:13971076
|
A | G | 2 | a0001c0001t0017g0023a0002c0002t0033g0022 | 2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.235+6351T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971076 | ||||||
| chr7:13971120
|
C | T | 211 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.235+6307G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971120 | ||||||
| chr7:13971160
|
G | A | 40 | a0001c0001t0001g0224a0001c0001t0002g0012a0001c0001t0002g0013others(37): Show | 41 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.235+6267C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971160 | ||||||
| chr7:13971167
|
C | T | 4 | a0001c0001t0038g0306a0002c0002t0013g0304a0002c0002t0013g0305others(1): Show | 4 | HG02055.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+6260G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971167 | ||||||
| chr7:13971183
|
C | A | 1 | a0001c0001t0014g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.235+6244G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971183 | ||||||
| chr7:13971251
|
G | A | 1 | a0002c0002t0001g0277 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235+6176C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971251 | ||||||
| chr7:13971264
|
C | A | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.235+6163G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971264 | ||||||
| chr7:13971413
|
T | G | 16 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0282others(13): Show | 16 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.235+6014A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971413 | ||||||
| chr7:13971423
|
T | G | 235 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.235+6004A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971423 | ||||||
| chr7:13971503
|
T | C | 15 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(12): Show | 15 | HG00544.hp1 HG01070.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.235+5924A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971503 | ||||||
| chr7:13971642
|
C | T | 1 | a0001c0001t0007g0317 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.235+5785G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971642 | ||||||
| chr7:13971780
|
C | T | 1 | a0001c0001t0006g0091 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.235+5647G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971780 | ||||||
| chr7:13971825
|
T | C | 17 | a0001c0001t0004g0238a0001c0001t0006g0302a0001c0001t0006g0307others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.235+5602A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971825 | ||||||
| chr7:13971870
|
G | A | 13 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0006g0313others(10): Show | 13 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+5557C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13971870 | ||||||
| chr7:13972046
|
G | T | 234 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+5381C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972046 | ||||||
| chr7:13972064
|
C | T | 17 | a0001c0001t0004g0238a0001c0001t0006g0302a0001c0001t0006g0307others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.235+5363G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972064 | ||||||
| chr7:13972085
|
G | A | 234 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+5342C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972085 | ||||||
| chr7:13972186
|
T | A | 1 | a0002c0002t0004g0225 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.235+5241A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972186 | ||||||
| chr7:13972189
|
T | C | 1 | a0001c0001t0010g0083 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.235+5238A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972189 | ||||||
| chr7:13972208
|
C | T | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(1): Show | 4 | HG00099.hp1 HG01361.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+5219G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972208 | ||||||
| chr7:13972288
|
C | T | 1 | a0001c0001t0018g0316 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.235+5139G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972288 | ||||||
| chr7:13972469
|
T | C | 6 | a0001c0001t0015g0132a0001c0001t0015g0139a0001c0001t0021g0140others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+4958A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972469 | ||||||
| chr7:13972534
|
A | T | 11 | a0001c0001t0002g0035a0001c0001t0006g0300a0001c0001t0006g0308others(8): Show | 11 | HG01109.hp1 HG02280.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.235+4893T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972534 | ||||||
| chr7:13972551
|
C | A | 223 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.235+4876G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972551 | ||||||
| chr7:13972635
|
A | G | 2 | a0001c0001t0012g0297a0001c0001t0012g0298 | 2 | HG00597.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.235+4792T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972635 | ||||||
| chr7:13972738
|
T | C | 1 | a0002c0002t0029g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.235+4689A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972738 | ||||||
| chr7:13972867
|
C | T | 1 | a0002c0002t0004g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.235+4560G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13972867 | ||||||
| chr7:13973015
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.235+4412T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973015 | ||||||
| chr7:13973129
|
A | C | 1 | a0001c0001t0028g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+4298T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973129 | ||||||
| chr7:13973261
|
T | C | 8 | a0001c0001t0003g0279a0001c0001t0003g0281a0001c0001t0006g0066others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+4166A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973261 | ||||||
| chr7:13973300
|
T | A | 2 | a0001c0001t0015g0136a0001c0001t0020g0133 | 2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.235+4127A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973300 | ||||||
| chr7:13973374
|
T | C | 1 | a0001c0001t0004g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.235+4053A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973374 | ||||||
| chr7:13973404
|
G | A | 32 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(29): Show | 32 | HG00544.hp1 HG01070.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.235+4023C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973404 | ||||||
| chr7:13973436
|
T | C | 10 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0010g0301others(7): Show | 10 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+3991A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973436 | ||||||
| chr7:13973560
|
G | C | 21 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(18): Show | 21 | HG00544.hp1 HG01070.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.235+3867C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973560 | ||||||
| chr7:13973594
|
A | G | 233 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.235+3833T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973594 | ||||||
| chr7:13973644
|
C | CT | 28 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(25): Show | 28 | HG00544.hp1 HG01070.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.235+3782dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973644 | ||||||
| chr7:13973703
|
A | T | 223 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.235+3724T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973703 | ||||||
| chr7:13973827
|
G | A | 234 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.235+3600C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973827 | ||||||
| chr7:13973855
|
G | A | 3 | a0002c0002t0009g0227a0002c0002t0009g0228a0002c0002t0012g0033 | 3 | HG01070.hp2 HG01071.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.235+3572C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973855 | ||||||
| chr7:13973873
|
T | A | 2 | a0001c0001t0003g0019a0001c0001t0009g0229 | 2 | HG01515.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.235+3554A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973873 | ||||||
| chr7:13973895
|
G | A | 1 | a0001c0001t0002g0087 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.235+3532C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973895 | ||||||
| chr7:13973979
|
C | T | 232 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0185others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.235+3448G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13973979 | ||||||
| chr7:13974009
|
C | T | 1 | a0001c0001t0003g0278 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.235+3418G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974009 | ||||||
| chr7:13974074
|
T | C | 1 | a0001c0001t0023g0008 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.235+3353A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974074 | ||||||
| chr7:13974186
|
C | T | 2 | a0001c0001t0004g0263a0002c0002t0018g0299 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.235+3241G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974186 | ||||||
| chr7:13974366
|
G | A | 1 | a0001c0001t0006g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235+3061C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974366 | ||||||
| chr7:13974381
|
G | C | 26 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(23): Show | 26 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.235+3046C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974381 | ||||||
| chr7:13974428
|
T | C | 1 | a0001c0001t0004g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.235+2999A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974428 | ||||||
| chr7:13974474
|
G | C | 2 | a0001c0001t0028g0241a0002c0002t0027g0242 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.235+2953C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974474 | ||||||
| chr7:13974729
|
G | C | 7 | a0001c0001t0004g0238a0001c0001t0009g0143a0001c0001t0015g0136others(4): Show | 7 | HG02145.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+2698C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974729 | ||||||
| chr7:13974735
|
G | A | 4 | a0001c0001t0003g0279a0001c0001t0003g0281a0001c0001t0006g0280others(1): Show | 4 | NA18944.hp1 NA18949.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+2692C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974735 | ||||||
| chr7:13974738
|
G | A | 5 | a0001c0001t0002g0035a0001c0001t0006g0036a0001c0001t0020g0239others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+2689C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974738 | ||||||
| chr7:13974809
|
G | A | 1 | a0002c0002t0034g0311 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.235+2618C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974809 | ||||||
| chr7:13974843
|
C | T | 1 | a0001c0001t0028g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.235+2584G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974843 | ||||||
| chr7:13974964
|
G | C | 2 | a0001c0001t0004g0137a0001c0001t0015g0138 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.235+2463C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13974964 | ||||||
| chr7:13975135
|
C | T | 4 | a0001c0001t0015g0136a0001c0001t0017g0023a0001c0001t0020g0133others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+2292G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975135 | ||||||
| chr7:13975145
|
A | G | 2 | a0001c0001t0028g0241a0002c0002t0027g0242 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.235+2282T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975145 | ||||||
| chr7:13975155
|
C | T | 7 | a0001c0001t0006g0308a0001c0001t0007g0317a0001c0001t0018g0316others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+2272G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975155 | ||||||
| chr7:13975197
|
G | T | 1 | a0001c0001t0020g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.235+2230C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975197 | ||||||
| chr7:13975223
|
A | C | 1 | a0001c0001t0007g0296 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.235+2204T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975223 | ||||||
| chr7:13975240
|
A | T | 1 | a0001c0001t0013g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.235+2187T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975240 | ||||||
| chr7:13975252
|
T | C | 3 | a0001c0001t0004g0263a0001c0001t0046g0072a0002c0002t0018g0299 | 3 | HG03195.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.235+2175A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975252 | ||||||
| chr7:13975291
|
G | A | 17 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(14): Show | 17 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.235+2136C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975291 | ||||||
| chr7:13975328
|
C | T | 1 | a0001c0001t0006g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235+2099G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975328 | ||||||
| chr7:13975343
|
G | A | 1 | a0002c0002t0001g0230 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.235+2084C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975343 | ||||||
| chr7:13975357
|
C | T | 1 | a0001c0001t0020g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.235+2070G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975357 | ||||||
| chr7:13975386
|
A | G | 1 | a0002c0002t0018g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.235+2041T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975386 | ||||||
| chr7:13975442
|
A | AGGCTGAG others(10): Show |
17 | a0001c0001t0001g0157a0001c0001t0004g0183a0001c0001t0019g0152others(14): Show | 17 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.235+1968_235+1984d others(19): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975442 | ||||||
| chr7:13975442
|
AGGCTGAG others(10): Show |
A | 1 | a0001c0001t0025g0312 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.235+1968_235+1984d others(19): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975442 | ||||||
| chr7:13975521
|
C | G | 1 | a0002c0002t0004g0182 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.235+1906G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975521 | ||||||
| chr7:13975562
|
C | CA | 8 | a0001c0001t0004g0238a0001c0001t0006g0300a0001c0001t0009g0229others(5): Show | 8 | HG01884.hp2 HG02080.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+1864dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975562 | ||||||
| chr7:13975562
|
C | CAAAA | 12 | a0001c0001t0002g0024a0001c0001t0003g0282a0001c0001t0003g0290others(9): Show | 12 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.235+1861_235+1864d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975562 | ||||||
| chr7:13975580
|
G | A | 3 | a0001c0001t0003g0287a0001c0001t0003g0288a0001c0001t0003g0289 | 3 | NA18965.hp2 NA18967.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.235+1847C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975580 | ||||||
| chr7:13975590
|
G | GA | 146 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(143): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.235+1836dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975590 | ||||||
| chr7:13975601
|
A | G | 4 | a0001c0001t0038g0306a0002c0002t0013g0304a0002c0002t0013g0305others(1): Show | 4 | HG02055.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+1826T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975601 | ||||||
| chr7:13975613
|
G | C | 1 | a0001c0005t0010g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.235+1814C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975613 | ||||||
| chr7:13975634
|
A | G | 21 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0279others(18): Show | 21 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.235+1793T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975634 | ||||||
| chr7:13975688
|
A | G | 3 | a0001c0001t0015g0132a0001c0001t0021g0265a0001c0001t0021g0266 | 3 | HG01891.hp1 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.235+1739T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975688 | ||||||
| chr7:13975693
|
T | A | 205 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(202): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.235+1734A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975693 | ||||||
| chr7:13975910
|
T | A | 1 | a0001c0001t0028g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.235+1517A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975910 | ||||||
| chr7:13975968
|
A | G | 2 | a0001c0001t0009g0143a0001c0001t0020g0239 | 2 | HG02622.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.235+1459T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975968 | ||||||
| chr7:13975982
|
C | A | 20 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0279others(17): Show | 20 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.235+1445G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13975982 | ||||||
| chr7:13976150
|
A | G | 3 | a0001c0001t0004g0181a0001c0001t0009g0179a0001c0001t0009g0180 | 3 | HG02602.hp2 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.235+1277T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976150 | ||||||
| chr7:13976419
|
A | G | 1 | a0001c0001t0005g0178 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.235+1008T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976419 | ||||||
| chr7:13976468
|
C | T | 1 | a0001c0001t0013g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.235+959G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976468 | ||||||
| chr7:13976485
|
A | G | 1 | a0001c0001t0004g0177 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.235+942T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976485 | ||||||
| chr7:13976548
|
C | T | 24 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(21): Show | 24 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.235+879G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976548 | ||||||
| chr7:13976554
|
T | C | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.235+873A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13976554 | ||||||
| chr7:13977039
|
A | G | 35 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0279others(32): Show | 35 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.235+388T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977039 | ||||||
| chr7:13977045
|
C | T | 35 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0279others(32): Show | 35 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.235+382G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977045 | ||||||
| chr7:13977124
|
T | A | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.235+303A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977124 | ||||||
| chr7:13977223
|
T | C | 1 | a0002c0002t0010g0116 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.235+204A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977223 | ||||||
| chr7:13977314
|
T | C | 167 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.235+113A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977314 | ||||||
| chr7:13977382
|
C | T | 166 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.235+45G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977382 | ||||||
| chr7:13977383
|
C | G | 166 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.235+44G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 6/13 | chr7 | 13977383 | ||||||
| chr7:13977501
|
T | TA | 166 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.182-22dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977501 | ||||||
| chr7:13977612
|
C | A | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.182-132G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977612 | ||||||
| chr7:13977671
|
T | C | 1 | a0001c0001t0005g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.182-191A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977671 | ||||||
| chr7:13977728
|
C | T | 16 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0281others(13): Show | 16 | HG00544.hp2 HG02015.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.182-248G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977728 | ||||||
| chr7:13977780
|
T | C | 16 | a0001c0001t0001g0157a0001c0001t0019g0152a0001c0001t0019g0153others(13): Show | 16 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.182-300A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13977780 | ||||||
| chr7:13978047
|
T | G | 9 | a0001c0001t0004g0238a0001c0001t0004g0263a0001c0001t0009g0143others(6): Show | 9 | HG01891.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.182-567A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978047 | ||||||
| chr7:13978177
|
A | C | 1 | a0001c0001t0015g0136 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.182-697T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978177 | ||||||
| chr7:13978202
|
T | G | 1 | a0001c0001t0007g0296 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.182-722A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978202 | ||||||
| chr7:13978331
|
A | G | 1 | a0001c0001t0011g0089 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.182-851T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978331 | ||||||
| chr7:13978334
|
G | A | 5 | a0001c0001t0004g0238a0001c0001t0004g0263a0001c0001t0009g0143others(2): Show | 5 | HG02723.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-854C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978334 | ||||||
| chr7:13978385
|
A | G | 1 | a0001c0001t0020g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.182-905T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978385 | ||||||
| chr7:13978398
|
AAC | A | 223 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(220): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.182-920_182-919del others(2): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978398 | ||||||
| chr7:13978418
|
C | T | 1 | a0001c0001t0012g0285 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.182-938G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978418 | ||||||
| chr7:13978519
|
C | T | 175 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(172): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.182-1039G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978519 | ||||||
| chr7:13978531
|
G | A | 131 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.182-1051C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978531 | ||||||
| chr7:13978576
|
C | T | 199 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(196): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.182-1096G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978576 | ||||||
| chr7:13978625
|
T | A | 16 | a0001c0001t0001g0157a0001c0001t0019g0152a0001c0001t0019g0153others(13): Show | 16 | HG00140.hp1 HG02080.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.182-1145A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978625 | ||||||
| chr7:13978735
|
G | T | 171 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.182-1255C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978735 | ||||||
| chr7:13978807
|
A | G | 2 | a0001c0001t0028g0241a0002c0002t0027g0242 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.182-1327T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978807 | ||||||
| chr7:13978840
|
G | T | 1 | a0001c0001t0006g0088 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.182-1360C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978840 | ||||||
| chr7:13978869
|
C | T | 199 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(196): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.182-1389G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978869 | ||||||
| chr7:13978918
|
C | T | 1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.182-1438G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978918 | ||||||
| chr7:13978951
|
C | A | 3 | a0001c0001t0004g0238a0001c0001t0051g0237a0002c0002t0018g0299 | 3 | HG02723.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.182-1471G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978951 | ||||||
| chr7:13978974
|
C | G | 1 | a0001c0001t0002g0087 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.182-1494G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13978974 | ||||||
| chr7:13979014
|
G | T | 7 | a0001c0001t0006g0308a0001c0001t0007g0317a0001c0001t0018g0316others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-1534C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979014 | ||||||
| chr7:13979018
|
A | T | 20 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0279others(17): Show | 20 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.182-1538T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979018 | ||||||
| chr7:13979032
|
G | A | 5 | a0001c0001t0004g0238a0001c0001t0004g0263a0001c0001t0009g0143others(2): Show | 5 | HG02723.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-1552C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979032 | ||||||
| chr7:13979051
|
A | C | 1 | a0001c0001t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.182-1571T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979051 | ||||||
| chr7:13979098
|
A | C | 4 | a0001c0001t0015g0132a0001c0001t0021g0265a0001c0001t0021g0266others(1): Show | 4 | HG01891.hp1 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1618T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979098 | ||||||
| chr7:13979120
|
G | A | 2 | a0001c0001t0004g0263a0001c0001t0009g0143 | 2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.182-1640C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979120 | ||||||
| chr7:13979237
|
C | T | 7 | a0001c0001t0006g0308a0001c0001t0007g0317a0001c0001t0018g0316others(4): Show | 7 | HG02109.hp2 HG02280.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-1757G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979237 | ||||||
| chr7:13979276
|
C | A | 24 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(21): Show | 24 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.182-1796G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979276 | ||||||
| chr7:13979317
|
T | C | 3 | a0002c0002t0001g0233a0002c0002t0001g0234a0002c0002t0029g0163 | 3 | HG01109.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.182-1837A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979317 | ||||||
| chr7:13979498
|
G | A | 1 | a0002c0002t0001g0147 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.182-2018C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979498 | ||||||
| chr7:13979500
|
AG | A | 20 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0279others(17): Show | 20 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.182-2021delC | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979500 | ||||||
| chr7:13979617
|
A | G | 211 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(208): Show | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.182-2137T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979617 | ||||||
| chr7:13979649
|
A | T | 3 | a0001c0001t0004g0238a0001c0001t0051g0237a0002c0002t0018g0299 | 3 | HG02723.hp1 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.182-2169T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979649 | ||||||
| chr7:13979785
|
A | C | 2 | a0002c0002t0003g0121a0002c0002t0003g0122 | 2 | NA18983.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.182-2305T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979785 | ||||||
| chr7:13979823
|
T | C | 165 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.182-2343A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979823 | ||||||
| chr7:13979915
|
G | T | 158 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(155): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.182-2435C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13979915 | ||||||
| chr7:13980052
|
T | G | 2 | a0001c0001t0015g0139a0001c0001t0021g0140 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.182-2572A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980052 | ||||||
| chr7:13980110
|
A | T | 1 | a0001c0001t0020g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.182-2630T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980110 | ||||||
| chr7:13980190
|
C | G | 8 | a0001c0001t0004g0137a0001c0001t0015g0134a0001c0001t0015g0136others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.182-2710G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980190 | ||||||
| chr7:13980415
|
A | C | 2 | a0001c0001t0004g0166a0001c0001t0016g0165 | 2 | NA18948.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.182-2935T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980415 | ||||||
| chr7:13980557
|
G | A | 1 | a0001c0001t0007g0118 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.182-3077C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980557 | ||||||
| chr7:13980658
|
C | T | 1 | a0001c0001t0039g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.182-3178G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980658 | ||||||
| chr7:13980679
|
C | T | 23 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(20): Show | 23 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.182-3199G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980679 | ||||||
| chr7:13980695
|
G | T | 1 | a0001c0001t0020g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.182-3215C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980695 | ||||||
| chr7:13980804
|
C | T | 10 | a0001c0001t0006g0308a0001c0001t0006g0313a0001c0001t0007g0317others(7): Show | 10 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.182-3324G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980804 | ||||||
| chr7:13980907
|
T | G | 1 | a0001c0001t0051g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.182-3427A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980907 | ||||||
| chr7:13980951
|
GC | G | 23 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(20): Show | 23 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.182-3472delG | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13980951 | ||||||
| chr7:13981018
|
G | A | 3 | a0001c0001t0002g0119a0001c0001t0006g0130a0002c0002t0007g0120 | 3 | HG02074.hp1 NA18964.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.182-3538C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981018 | ||||||
| chr7:13981061
|
T | C | 160 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(157): Show | 160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.182-3581A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981061 | ||||||
| chr7:13981137
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.182-3657G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981137 | ||||||
| chr7:13981138
|
A | T | 1 | a0001c0001t0001g0245 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.182-3658T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981138 | ||||||
| chr7:13981182
|
C | T | 1 | a0001c0001t0016g0268 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.182-3702G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981182 | ||||||
| chr7:13981225
|
T | C | 3 | a0002c0002t0003g0079a0002c0002t0003g0121a0002c0002t0003g0122 | 3 | NA18983.hp2 NA19078.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.182-3745A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981225 | ||||||
| chr7:13981470
|
G | A | 130 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(127): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.182-3990C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981470 | ||||||
| chr7:13981496
|
C | G | 169 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.182-4016G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981496 | ||||||
| chr7:13981501
|
TTACA | T | 29 | a0001c0001t0001g0244a0001c0001t0004g0137a0001c0001t0004g0238others(26): Show | 29 | HG01081.hp2 HG01109.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.182-4025_182-4022d others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981501 | ||||||
| chr7:13981501
|
TTACATAC others(5): Show |
T | 4 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0281others(1): Show | 4 | NA18944.hp1 NA18949.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-4033_182-4022d others(14): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981501 | ||||||
| chr7:13981532
|
C | CATACAT | 16 | a0001c0001t0003g0282a0001c0001t0003g0287a0001c0001t0003g0288others(13): Show | 16 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.182-4053_182-4052i others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981532 | ||||||
| chr7:13981532
|
C | T | 16 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0281others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.182-4052G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981532 | ||||||
| chr7:13981536
|
T | C | 1 | a0001c0001t0006g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.182-4056A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981536 | ||||||
| chr7:13981544
|
T | C | 25 | a0001c0001t0002g0024a0001c0001t0003g0278a0001c0001t0003g0279others(22): Show | 25 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.182-4064A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981544 | ||||||
| chr7:13981544
|
T | TAC | 5 | a0001c0001t0038g0306a0001c0003t0002g0073a0002c0002t0013g0304others(2): Show | 5 | HG00280.hp2 HG02055.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.182-4066_182-4065d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981544 | ||||||
| chr7:13981544
|
T | TATAC | 128 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.182-4065_182-4064i others(6): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981544 | ||||||
| chr7:13981708
|
T | G | 169 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.182-4228A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981708 | ||||||
| chr7:13981709
|
T | C | 169 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.182-4229A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981709 | ||||||
| chr7:13981732
|
A | G | 6 | a0001c0001t0006g0308a0001c0001t0007g0317a0001c0001t0018g0316others(3): Show | 6 | HG02280.hp2 HG03209.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-4252T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981732 | ||||||
| chr7:13981926
|
G | A | 4 | a0001c0001t0006g0313a0001c0001t0025g0312a0002c0002t0006g0078others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-4446C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13981926 | ||||||
| chr7:13982061
|
C | A | 1 | a0001c0001t0035g0124 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.181+4577G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982061 | ||||||
| chr7:13982061
|
C | T | 158 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(155): Show | 158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.181+4577G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982061 | ||||||
| chr7:13982236
|
CTCTAATG others(9): Show |
C | 1 | a0001c0001t0011g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.181+4386_181+4401d others(18): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982236 | ||||||
| chr7:13982318
|
C | T | 2 | a0001c0001t0020g0239a0001c0001t0050g0142 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.181+4320G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982318 | ||||||
| chr7:13982438
|
T | A | 1 | a0001c0001t0004g0238 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.181+4200A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982438 | ||||||
| chr7:13982439
|
A | T | 7 | a0001c0001t0010g0083a0001c0001t0015g0132a0001c0001t0021g0265others(4): Show | 7 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.181+4199T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982439 | ||||||
| chr7:13982590
|
C | A | 8 | a0001c0001t0004g0137a0001c0001t0015g0134a0001c0001t0015g0136others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+4048G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982590 | ||||||
| chr7:13982667
|
G | C | 2 | a0001c0001t0020g0239a0001c0001t0050g0142 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.181+3971C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982667 | ||||||
| chr7:13982736
|
T | C | 1 | a0001c0001t0043g0125 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.181+3902A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982736 | ||||||
| chr7:13982740
|
G | A | 151 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(148): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.181+3898C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982740 | ||||||
| chr7:13982749
|
G | A | 2 | a0001c0001t0020g0239a0001c0001t0050g0142 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.181+3889C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982749 | ||||||
| chr7:13982819
|
A | G | 169 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.181+3819T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982819 | ||||||
| chr7:13982886
|
T | C | 1 | a0001c0001t0056g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.181+3752A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982886 | ||||||
| chr7:13982893
|
T | C | 1 | a0001c0001t0007g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.181+3745A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982893 | ||||||
| chr7:13982897
|
A | G | 169 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.181+3741T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13982897 | ||||||
| chr7:13983081
|
GGTTGTT | G | 4 | a0001c0001t0004g0238a0001c0001t0004g0263a0001c0001t0009g0143others(1): Show | 4 | HG02723.hp1 HG02886.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+3551_181+3556d others(8): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983081 | ||||||
| chr7:13983231
|
A | G | 1 | a0002c0002t0029g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.181+3407T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983231 | ||||||
| chr7:13983267
|
A | C | 1 | a0001c0001t0004g0267 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.181+3371T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983267 | ||||||
| chr7:13983297
|
A | C | 8 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0010g0301others(5): Show | 8 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+3341T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983297 | ||||||
| chr7:13983305
|
T | G | 1 | a0001c0001t0003g0281 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.181+3333A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983305 | ||||||
| chr7:13983398
|
T | G | 1 | a0001c0001t0004g0263 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.181+3240A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983398 | ||||||
| chr7:13983435
|
G | A | 1 | a0001c0001t0024g0029 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.181+3203C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983435 | ||||||
| chr7:13983617
|
C | T | 2 | a0001c0001t0004g0238a0001c0001t0051g0237 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.181+3021G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983617 | ||||||
| chr7:13983618
|
T | C | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+3020A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983618 | ||||||
| chr7:13983621
|
C | CT | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+3016dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983621 | ||||||
| chr7:13983666
|
G | T | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2972C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983666 | ||||||
| chr7:13983681
|
A | G | 3 | a0001c0001t0002g0082a0001c0001t0011g0081a0001c0001t0030g0002 | 3 | HG01167.hp2 HG01258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.181+2957T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983681 | ||||||
| chr7:13983714
|
T | TA | 169 | a0001c0001t0002g0012a0001c0001t0002g0014a0001c0001t0002g0015others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.181+2923dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983714 | ||||||
| chr7:13983823
|
G | T | 1 | a0002c0002t0004g0243 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.181+2815C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983823 | ||||||
| chr7:13983833
|
A | C | 3 | a0001c0001t0028g0240a0001c0001t0028g0241a0002c0002t0027g0242 | 3 | HG02258.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.181+2805T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983833 | ||||||
| chr7:13983837
|
A | G | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2801T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983837 | ||||||
| chr7:13983863
|
C | G | 8 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0010g0301others(5): Show | 8 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+2775G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983863 | ||||||
| chr7:13983881
|
T | C | 1 | a0002c0002t0002g0075 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.181+2757A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983881 | ||||||
| chr7:13983899
|
C | T | 10 | a0001c0001t0006g0308a0001c0001t0006g0313a0001c0001t0007g0317others(7): Show | 10 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+2739G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983899 | ||||||
| chr7:13983924
|
C | G | 8 | a0001c0001t0006g0302a0001c0001t0006g0307a0001c0001t0010g0301others(5): Show | 8 | HG02055.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.181+2714G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983924 | ||||||
| chr7:13983987
|
T | C | 10 | a0001c0001t0006g0308a0001c0001t0006g0313a0001c0001t0007g0317others(7): Show | 10 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+2651A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13983987 | ||||||
| chr7:13984024
|
A | C | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2614T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984024 | ||||||
| chr7:13984182
|
C | G | 229 | a0001c0001t0001g0157a0001c0001t0001g0244a0001c0001t0001g0245others(226): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.181+2456G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984182 | ||||||
| chr7:13984197
|
A | G | 1 | a0002c0002t0003g0079 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.181+2441T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984197 | ||||||
| chr7:13984290
|
C | T | 1 | a0001c0001t0008g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.181+2348G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984290 | ||||||
| chr7:13984378
|
G | C | 2 | a0001c0001t0015g0134a0001c0001t0058g0135 | 2 | HG01109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.181+2260C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984378 | ||||||
| chr7:13984487
|
G | A | 23 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(20): Show | 23 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.181+2151C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984487 | ||||||
| chr7:13984523
|
C | G | 2 | a0001c0001t0020g0239a0001c0001t0050g0142 | 2 | HG02622.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.181+2115G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984523 | ||||||
| chr7:13984548
|
G | A | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2090C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984548 | ||||||
| chr7:13984606
|
C | T | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+2032G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984606 | ||||||
| chr7:13984755
|
C | T | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+1883G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984755 | ||||||
| chr7:13984771
|
A | T | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+1867T>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984771 | ||||||
| chr7:13984917
|
T | TCAA | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+1720_181+1721i others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984917 | ||||||
| chr7:13984921
|
T | TTA | 3 | a0001c0001t0006g0313a0002c0002t0006g0078a0002c0002t0014g0314 | 3 | HG02723.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.181+1716_181+1717i others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984921 | ||||||
| chr7:13984922
|
C | A | 4 | a0001c0001t0006g0313a0001c0001t0025g0312a0002c0002t0006g0078others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+1716G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984922 | ||||||
| chr7:13984922
|
C | T | 164 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(161): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.181+1716G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984922 | ||||||
| chr7:13984926
|
AGT | A | 157 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.181+1710_181+1711d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984926 | ||||||
| chr7:13984926
|
AGTT | A | 7 | a0001c0001t0006g0308a0001c0001t0007g0317a0001c0001t0010g0126others(4): Show | 7 | HG02280.hp2 HG03209.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+1709_181+1711d others(5): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984926 | ||||||
| chr7:13984927
|
G | A | 4 | a0001c0001t0006g0313a0001c0001t0025g0312a0002c0002t0006g0078others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+1711C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984927 | ||||||
| chr7:13984928
|
T | A | 4 | a0001c0001t0006g0313a0001c0001t0025g0312a0002c0002t0006g0078others(1): Show | 4 | HG02109.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+1710A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984928 | ||||||
| chr7:13984929
|
T | A | 161 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(158): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.181+1709A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984929 | ||||||
| chr7:13984964
|
AAG | A | 5 | a0001c0001t0004g0137a0001c0001t0015g0136a0001c0001t0015g0138others(2): Show | 5 | HG01081.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+1672_181+1673d others(4): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984964 | ||||||
| chr7:13984999
|
A | G | 1 | a0002c0002t0012g0033 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.181+1639T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13984999 | ||||||
| chr7:13985242
|
G | A | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+1396C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985242 | ||||||
| chr7:13985252
|
A | G | 1 | a0002c0002t0018g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.181+1386T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985252 | ||||||
| chr7:13985260
|
T | A | 2 | a0001c0001t0004g0238a0001c0001t0051g0237 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.181+1378A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985260 | ||||||
| chr7:13985455
|
A | G | 1 | a0001c0001t0009g0143 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.181+1183T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985455 | ||||||
| chr7:13985528
|
A | AT | 4 | a0001c0001t0002g0012a0001c0001t0002g0027a0001c0001t0024g0028others(1): Show | 4 | HG01175.hp2 HG01192.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.181+1109dupA | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985528 | ||||||
| chr7:13985536
|
C | T | 10 | a0001c0001t0006g0308a0001c0001t0006g0313a0001c0001t0007g0317others(7): Show | 10 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.181+1102G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985536 | ||||||
| chr7:13985597
|
C | T | 2 | a0001c0001t0012g0297a0001c0001t0012g0298 | 2 | HG00597.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.181+1041G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985597 | ||||||
| chr7:13985599
|
C | A | 2 | a0001c0001t0012g0297a0001c0001t0012g0298 | 2 | HG00597.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.181+1039G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985599 | ||||||
| chr7:13985692
|
A | G | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+946T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985692 | ||||||
| chr7:13985721
|
C | G | 2 | a0001c0001t0017g0023a0002c0002t0033g0022 | 2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.181+917G>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985721 | ||||||
| chr7:13985744
|
T | C | 139 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(136): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.181+894A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985744 | ||||||
| chr7:13985786
|
T | G | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+852A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985786 | ||||||
| chr7:13985819
|
G | T | 7 | a0001c0001t0002g0012a0001c0001t0002g0027a0001c0001t0003g0030others(4): Show | 7 | HG01175.hp2 HG01192.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.181+819C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985819 | ||||||
| chr7:13985849
|
A | G | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+789T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985849 | ||||||
| chr7:13985857
|
C | T | 6 | a0001c0001t0015g0132a0001c0001t0021g0265a0001c0001t0021g0266others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+781G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985857 | ||||||
| chr7:13985892
|
A | G | 2 | a0001c0001t0007g0076a0001c0001t0007g0077 | 2 | HG01243.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.181+746T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985892 | ||||||
| chr7:13985903
|
C | A | 22 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(19): Show | 22 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.181+735G>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13985903 | ||||||
| chr7:13986015
|
G | A | 170 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.181+623C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986015 | ||||||
| chr7:13986054
|
T | A | 3 | a0001c0001t0015g0132a0001c0001t0021g0265a0001c0001t0021g0266 | 3 | HG01891.hp1 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.181+584A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986054 | ||||||
| chr7:13986065
|
T | C | 1 | a0002c0002t0008g0264 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.181+573A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986065 | ||||||
| chr7:13986094
|
T | A | 8 | a0001c0001t0004g0137a0001c0001t0015g0134a0001c0001t0015g0136others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+544A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986094 | ||||||
| chr7:13986102
|
C | T | 167 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(164): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.181+536G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986102 | ||||||
| chr7:13986141
|
T | A | 168 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.181+497A>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986141 | ||||||
| chr7:13986282
|
C | T | 2 | a0002c0002t0004g0145a0002c0002t0005g0144 | 2 | NA18978.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.181+356G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986282 | ||||||
| chr7:13986583
|
T | C | 1 | a0002c0002t0005g0236 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.181+55A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 5/13 | chr7 | 13986583 | ||||||
| chr7:13986732
|
A | G | 213 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(210): Show | 213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.134-47T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13986732 | ||||||
| chr7:13986738
|
A | G | 1 | a0001c0001t0028g0240 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.134-53T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13986738 | ||||||
| chr7:13986775
|
T | C | 1 | a0001c0001t0006g0307 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.134-90A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13986775 | ||||||
| chr7:13986813
|
TA | T | 170 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-129delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13986813 | ||||||
| chr7:13987059
|
G | C | 2 | a0001c0001t0004g0238a0001c0001t0051g0237 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.134-374C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987059 | ||||||
| chr7:13987112
|
A | G | 163 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.134-427T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987112 | ||||||
| chr7:13987148
|
GTAT | G | 9 | a0001c0001t0006g0308a0001c0001t0006g0313a0001c0001t0007g0317others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-466_134-464del others(3): Show |
ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987148 | ||||||
| chr7:13987177
|
A | C | 55 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0026others(52): Show | 55 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.134-492T>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987177 | ||||||
| chr7:13987190
|
C | T | 1 | a0001c0001t0014g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.134-505G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987190 | ||||||
| chr7:13987204
|
G | C | 170 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-519C>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987204 | ||||||
| chr7:13987248
|
G | A | 4 | a0001c0001t0010g0126a0001c0001t0011g0128a0001c0001t0011g0129others(1): Show | 4 | HG01123.hp1 HG01516.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-563C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987248 | ||||||
| chr7:13987302
|
G | A | 170 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-617C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987302 | ||||||
| chr7:13987315
|
A | G | 170 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-630T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987315 | ||||||
| chr7:13987333
|
G | A | 170 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-648C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987333 | ||||||
| chr7:13987413
|
T | C | 170 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.133+673A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987413 | ||||||
| chr7:13987418
|
T | G | 170 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.133+668A>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987418 | ||||||
| chr7:13987458
|
G | A | 131 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.133+628C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987458 | ||||||
| chr7:13987494
|
G | T | 1 | a0001c0001t0006g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.133+592C>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987494 | ||||||
| chr7:13987553
|
T | C | 131 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.133+533A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987553 | ||||||
| chr7:13987734
|
A | G | 2 | a0001c0001t0017g0023a0002c0002t0033g0022 | 2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.133+352T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987734 | ||||||
| chr7:13987852
|
G | A | 171 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.133+234C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987852 | ||||||
| chr7:13987932
|
G | A | 213 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(210): Show | 213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.133+154C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 4/13 | chr7 | 13987932 | ||||||
| chr7:13988242
|
G | A | 1 | a0001c0001t0006g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.46-69C>T | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988242 | ||||||
| chr7:13988242
|
G | GCA | 159 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(156): Show | 159 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.46-71_46-70dupTG | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988242 | ||||||
| chr7:13988366
|
T | C | 172 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.46-193A>G | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988366 | ||||||
| chr7:13988422
|
C | T | 1 | a0001c0001t0003g0282 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.46-249G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988422 | ||||||
| chr7:13988431
|
A | G | 2 | a0001c0001t0004g0238a0001c0001t0051g0237 | 2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.46-258T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988431 | ||||||
| chr7:13988564
|
CA | C | 171 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.46-392delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988564 | ||||||
| chr7:13988595
|
G | GA | 145 | a0001c0001t0002g0021a0001c0001t0002g0024a0001c0001t0002g0026others(142): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.45+412dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988595 | ||||||
| chr7:13988595
|
G | GAA | 22 | a0001c0001t0002g0283a0001c0001t0003g0282a0001c0001t0003g0287others(19): Show | 22 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.45+411_45+412dupTT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988595 | ||||||
| chr7:13988595
|
GA | G | 39 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(36): Show | 39 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.45+412delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988595 | ||||||
| chr7:13988620
|
G | GA | 186 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0253others(183): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.45+387dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988620 | ||||||
| chr7:13988729
|
A | G | 1 | a0001c0001t0013g0010 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.45+279T>C | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988729 | ||||||
| chr7:13988745
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.45+263G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988745 | ||||||
| chr7:13988919
|
C | T | 1 | a0001c0001t0020g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45+89G>A | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 3/13 | chr7 | 13988919 | ||||||
| chr7:13989169
|
T | TA | 41 | a0001c0001t0002g0283a0001c0001t0003g0278a0001c0001t0003g0279others(38): Show | 41 | HG00597.hp2 HG00609.hp2 HG02027.hp2 others(38): Show |
intron_variant | MODIFIER | c.-87-31dupT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/13 | chr7 | 13989169 | ||||||
| chr7:13989169
|
T | TAA | 125 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-87-32_-87-31dupTT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/13 | chr7 | 13989169 | ||||||
| chr7:13989235
|
CA | C | 125 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-88+32delT | ETV1 | ENSG00000006468.15 | transcript | ENST00000430479.6 | protein_coding | 2/13 | chr7 | 13989235 |