| geneid | 943 |
|---|---|
| ensemblid | ENSG00000120949.15 |
| hgncid | 11923 |
| symbol | TNFRSF8 |
| name | TNF receptor superfamily member 8 |
| refseq_nuc | NM_001243.5 |
| refseq_prot | NP_001234.3 |
| ensembl_nuc | ENST00000263932.7 |
| ensembl_prot | ENSP00000263932.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 12063303 |
| end | 12144207 |
| strand | + |
| ver | v1.2 |
| region | chr1:12063303-12144207 |
| region5000 | chr1:12058303-12149207 |
| regionname0 | TNFRSF8_chr1_12063303_12144207 |
| regionname5000 | TNFRSF8_chr1_12058303_12149207 |
| 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 | 595 | 316 | 77 | 63 | 121 | 14 | 39 | 95 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002 | 0/0 | 595 | 33 | 16 | 1 | 15 | 0 | 1 | 11 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0003 | 0/0 | 595 | 5 | 0 | 0 | 4 | 1 | 0 | 4 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0004 | 0/0 | 595 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0005 | 0/0 | 595 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0006 | 0/0 | 595 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0007 | 0/0 | 595 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0008 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0009 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0010 | 0/0 | 595 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| 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 | 1788 | 147 | 30 | 35 | 51 | 9 | 20 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0002 | 0/0 | 1788 | 70 | 3 | 21 | 25 | 4 | 17 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0003 | 0/0 | 1788 | 61 | 26 | 7 | 27 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0004 | 0/0 | 1788 | 24 | 10 | 0 | 13 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0005 | 0/0 | 1788 | 13 | 8 | 0 | 5 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0006 | 0/0 | 1788 | 11 | 3 | 1 | 6 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0007 | 0/0 | 1788 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0008 | 0/0 | 1788 | 3 | 0 | 0 | 2 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0009 | 0/0 | 1788 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0010 | 0/0 | 1788 | 3 | 1 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0011 | 0/0 | 1788 | 3 | 1 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0012 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0013 | 0/0 | 1788 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0014 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0015 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0016 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0017 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0018 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0019 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0020 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0021 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0022 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0023 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0024 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0025 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0026 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0027 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0028 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0029 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| c0030 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| 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 | 1/0 | 1973 | 289 | 42 | 61 | 132 | 14 | 39 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0002 | 0/0 | 1973 | 11 | 11 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0003 | 0/0 | 1975 | 7 | 7 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0004 | 0/0 | 1973 | 7 | 2 | 2 | 2 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0005 | 0/0 | 1973 | 6 | 6 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0006 | 0/0 | 1973 | 6 | 6 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0007 | 0/0 | 1973 | 5 | 5 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0008 | 0/0 | 1973 | 5 | 0 | 0 | 5 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0009 | 0/0 | 1973 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0010 | 0/0 | 1973 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0011 | 0/0 | 1973 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0012 | 0/0 | 1973 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0013 | 0/0 | 1973 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0014 | 0/0 | 1973 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0015 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0016 | 0/0 | 1973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0017 | 0/0 | 1973 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0018 | 0/0 | 1973 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0019 | 0/0 | 1973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0020 | 0/0 | 1973 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0021 | 0/0 | 1973 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0022 | 0/1 | 1973 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0023 | 0/0 | 1973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0024 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0025 | 0/0 | 1973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| t0026 | 0/0 | 1973 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| 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 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| 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 | 1788 | 147 | 30 | 35 | 51 | 9 | 20 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0002 | 0/0 | 1788 | 70 | 3 | 21 | 25 | 4 | 17 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003 | 0/0 | 1788 | 61 | 26 | 7 | 27 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0004 | 0/0 | 1788 | 24 | 10 | 0 | 13 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0007 | 0/0 | 1788 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0009 | 0/0 | 1788 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0013 | 0/0 | 1788 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0014 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0017 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0018 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0023 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0025 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0026 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0005 | 0/0 | 1788 | 13 | 8 | 0 | 5 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0006 | 0/0 | 1788 | 11 | 3 | 1 | 6 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0010 | 0/0 | 1788 | 3 | 1 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0011 | 0/0 | 1788 | 3 | 1 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0012 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0016 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0003c0008 | 0/0 | 1788 | 3 | 0 | 0 | 2 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0003c0019 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0003c0027 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0004c0022 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0004c0028 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0005c0015 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0006c0021 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0007c0020 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0008c0029 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0009c0030 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0010c0024 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3760 | 124 | 15 | 32 | 47 | 9 | 20 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0002 | 0/0 | 3760 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0004 | 0/0 | 3760 | 2 | 0 | 1 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0005 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0006 | 0/0 | 3760 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0007 | 0/0 | 3760 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0008 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0009 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0011 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0013 | 0/0 | 3760 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0016 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0001t0022 | 0/1 | 3760 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0002t0001 | 0/0 | 3760 | 64 | 2 | 20 | 22 | 4 | 16 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0002t0002 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0002t0004 | 0/0 | 3760 | 2 | 0 | 1 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0002t0008 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0002t0011 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0002t0018 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0001 | 0/0 | 3760 | 41 | 9 | 6 | 25 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0002 | 0/0 | 3760 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0003 | 0/0 | 3762 | 5 | 5 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0005 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0007 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0008 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0010 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0012 | 0/0 | 3760 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0019 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0020 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0003t0026 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0004t0001 | 0/0 | 3760 | 20 | 6 | 0 | 13 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0004t0002 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0004t0003 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0004t0010 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0004t0025 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0007t0001 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0007t0009 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0007t0015 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0009t0001 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0009t0006 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0013t0001 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0014t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0017t0014 | 0/0 | 3760 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0018t0009 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0023t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0025t0001 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0001c0026t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0005t0001 | 0/0 | 3760 | 7 | 2 | 0 | 5 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0005t0002 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0005t0005 | 0/0 | 3760 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0005t0006 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0006t0001 | 0/0 | 3760 | 9 | 2 | 1 | 5 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0006t0003 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0006t0008 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0010t0001 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0010t0024 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0011t0001 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0011t0004 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0012t0001 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0012t0023 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0002c0016t0004 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0003c0008t0001 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0003c0008t0017 | 0/0 | 3760 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0003c0019t0004 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0003c0027t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0004c0022t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0004c0028t0021 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0005c0015t0001 | 0/0 | 3760 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0006c0021t0001 | 0/0 | 3760 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0007c0020t0001 | 0/0 | 3760 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0008c0029t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0009c0030t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| a0010c0024t0001 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | copy fasta | chr1 | 12058303 | 12149207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0005g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0006g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0008g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0011g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0013g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0013g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0016g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0022g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0011g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0018g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0012g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0020g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0026g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0025g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0007t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0007t0009g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0007t0015g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0009t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0009t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0009t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0013t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0013t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0014t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0017t0014g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0018t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0023t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0025t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0026t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0010t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0010t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0010t0024g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0011t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0011t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0011t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0012t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0012t0023g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0016t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0008t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0008t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0008t0017g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0019t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0027t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0004c0022t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0004c0028t0021g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0005c0015t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0006c0021t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0007c0020t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0008c0029t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0009c0030t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0010c0024t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0017 | t0014 | g0264 | EUR | GBR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | GBR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0065 | EUR | FIN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0078 | EUR | FIN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00544 | hp1 | a0002 | c0005 | t0001 | g0051 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00544 | hp2 | a0002 | c0006 | t0008 | g0162 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00558 | hp2 | a0001 | c0014 | t0001 | g0101 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00597 | hp1 | a0002 | c0006 | t0001 | g0081 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00597 | hp2 | a0001 | c0002 | t0018 | g0097 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0266 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0139 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0076 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0077 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01069 | hp1 | a0001 | c0001 | t0013 | g0205 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01071 | hp1 | a0001 | c0001 | t0013 | g0182 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01106 | hp2 | a0005 | c0015 | t0001 | g0350 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0042 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01167 | hp2 | a0001 | c0003 | t0012 | g0199 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0314 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01175 | hp2 | a0006 | c0021 | t0001 | g0154 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01243 | hp1 | a0002 | c0006 | t0001 | g0222 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0102 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0316 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0334 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0309 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01515 | hp2 | a0007 | c0020 | t0001 | g0019 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0211 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0253 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01891 | hp1 | a0001 | c0003 | t0012 | g0236 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01891 | hp2 | a0002 | c0010 | t0024 | g0354 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0315 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0255 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0331 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0307 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0270 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0322 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0249 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02055 | hp1 | a0002 | c0005 | t0005 | g0210 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0234 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0135 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0341 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02145 | hp1 | a0001 | c0009 | t0001 | g0360 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | CDX | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0057 | EAS | CDX | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02257 | hp1 | a0001 | c0003 | t0007 | g0301 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0196 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02258 | hp2 | a0001 | c0004 | t0010 | g0202 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0217 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02523 | hp1 | a0002 | c0010 | t0001 | g0146 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02523 | hp2 | a0001 | c0004 | t0001 | g0320 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0165 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0193 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0355 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02622 | hp2 | a0001 | c0007 | t0001 | g0215 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0219 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02630 | hp2 | a0001 | c0003 | t0003 | g0208 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0198 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0169 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0192 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0147 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0252 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0088 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02818 | hp1 | a0001 | c0003 | t0005 | g0223 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0200 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02895 | hp2 | a0001 | c0003 | t0003 | g0225 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0168 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0226 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0091 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02965 | hp1 | a0001 | c0003 | t0026 | g0161 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0313 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02976 | hp1 | a0001 | c0009 | t0001 | g0358 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02976 | hp2 | a0002 | c0005 | t0002 | g0235 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0214 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0148 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03098 | hp2 | a0002 | c0006 | t0001 | g0155 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03130 | hp1 | a0002 | c0006 | t0003 | g0149 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03130 | hp2 | a0001 | c0007 | t0009 | g0357 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0089 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03139 | hp2 | a0001 | c0018 | t0009 | g0260 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03195 | hp1 | a0002 | c0006 | t0001 | g0170 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0227 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03225 | hp1 | a0001 | c0007 | t0015 | g0189 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03225 | hp2 | a0001 | c0003 | t0005 | g0092 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03453 | hp1 | a0001 | c0009 | t0006 | g0171 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03453 | hp2 | a0002 | c0005 | t0005 | g0230 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0352 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03486 | hp2 | a0001 | c0003 | t0019 | g0207 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03516 | hp2 | a0002 | c0005 | t0005 | g0232 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03540 | hp1 | a0001 | c0003 | t0003 | g0152 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0216 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03579 | hp1 | a0002 | c0005 | t0002 | g0206 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03579 | hp2 | a0001 | c0004 | t0003 | g0220 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03710 | hp2 | a0002 | c0006 | t0001 | g0347 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0339 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0132 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0348 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0269 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0082 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0340 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18612 | hp1 | a0001 | c0004 | t0001 | g0291 | EAS | CHB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | CHB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0213 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18906 | hp2 | a0001 | c0003 | t0010 | g0259 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18939 | hp1 | a0004 | c0022 | t0001 | g0002 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18941 | hp1 | a0001 | c0002 | t0011 | g0285 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18942 | hp1 | a0002 | c0005 | t0001 | g0094 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18942 | hp2 | a0001 | c0003 | t0020 | g0073 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18947 | hp1 | a0001 | c0004 | t0001 | g0131 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18947 | hp2 | a0001 | c0004 | t0001 | g0142 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0319 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18956 | hp1 | a0002 | c0005 | t0001 | g0349 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18956 | hp2 | a0001 | c0004 | t0001 | g0164 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18957 | hp2 | a0002 | c0006 | t0001 | g0090 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0310 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18960 | hp2 | a0001 | c0023 | t0001 | g0061 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18969 | hp1 | a0002 | c0011 | t0001 | g0303 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18969 | hp2 | a0003 | c0027 | t0001 | g0060 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18970 | hp1 | a0003 | c0008 | t0001 | g0105 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18972 | hp1 | a0001 | c0026 | t0001 | g0337 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18973 | hp1 | a0001 | c0004 | t0001 | g0069 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0321 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18980 | hp1 | a0001 | c0004 | t0001 | g0283 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18980 | hp2 | a0001 | c0001 | t0008 | g0362 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18983 | hp1 | a0002 | c0011 | t0001 | g0292 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0276 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18989 | hp2 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18990 | hp1 | a0001 | c0002 | t0008 | g0212 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18993 | hp1 | a0008 | c0029 | t0001 | g0240 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18994 | hp2 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18999 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19002 | hp1 | a0001 | c0004 | t0001 | g0070 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19007 | hp2 | a0001 | c0001 | t0011 | g0282 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19009 | hp2 | a0004 | c0028 | t0021 | g0113 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19010 | hp1 | a0003 | c0019 | t0004 | g0017 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19011 | hp1 | a0002 | c0005 | t0001 | g0121 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19030 | hp1 | a0001 | c0004 | t0025 | g0356 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0237 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19043 | hp2 | a0002 | c0016 | t0004 | g0228 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0052 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0281 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19064 | hp1 | a0002 | c0005 | t0001 | g0084 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19064 | hp2 | a0009 | c0030 | t0001 | g0120 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0324 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19066 | hp2 | a0003 | c0008 | t0001 | g0087 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19070 | hp1 | a0002 | c0006 | t0001 | g0056 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19070 | hp2 | a0001 | c0013 | t0001 | g0251 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19074 | hp1 | a0002 | c0006 | t0001 | g0361 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19082 | hp1 | a0001 | c0013 | t0001 | g0280 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19082 | hp2 | a0001 | c0003 | t0008 | g0204 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19083 | hp1 | a0001 | c0004 | t0001 | g0186 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19085 | hp2 | a0002 | c0010 | t0001 | g0345 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19089 | hp1 | a0001 | c0003 | t0001 | g0336 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19091 | hp2 | a0002 | c0006 | t0001 | g0021 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0248 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19240 | hp2 | a0010 | c0024 | t0001 | g0238 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20129 | hp2 | a0002 | c0011 | t0004 | g0221 | AFR | ASW | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20752 | hp1 | a0003 | c0008 | t0017 | g0009 | EUR | TSI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0067 | EUR | TSI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0130 | EUR | TSI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02109 | hp1 | a0002 | c0005 | t0006 | g0209 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0359 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0036 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02559 | hp1 | a0002 | c0005 | t0001 | g0059 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03471 | hp1 | a0002 | c0012 | t0023 | g0353 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03471 | hp2 | a0001 | c0003 | t0010 | g0195 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG06807 | hp1 | a0001 | c0001 | t0016 | g0194 | AFR | USA | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0197 | AFR | USA | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA21309 | hp1 | a0002 | c0012 | t0001 | g0178 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA21309 | hp2 | a0001 | c0025 | t0001 | g0231 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0022 | g0072 | REF | REF | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0071 | REF | REF | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:12104394
|
A | G | 1 | a0010 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.284A>G | p.Lys95Arg | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/15 | 580/3760 | 284/1788 | 95/595 | chr1 | 12104394 | ||
| chr1:12115610
|
A | G | 1 | a0009 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.827A>G | p.Asn276Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/15 | 1123/3760 | 827/1788 | 276/595 | chr1 | 12115610 | ||
| chr1:12115723
|
C | T | 1 | a0008 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.940C>T | p.Pro314Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/15 | 1236/3760 | 940/1788 | 314/595 | chr1 | 12115723 | ||
| chr1:12126001
|
A | G | 3 | a0002a0004a0005 | 36 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(33): Show |
missense_variant | MODERATE | c.1204A>G | p.Ser402Gly | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 11/15 | 1500/3760 | 1204/1788 | 402/595 | chr1 | 12126001 | ||
| chr1:12138248
|
C | T | 1 | a0006 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1355C>T | p.Ser452Leu | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1651/3760 | 1355/1788 | 452/595 | chr1 | 12138248 | ||
| chr1:12138290
|
A | G | 1 | a0005 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1397A>G | p.Gln466Arg | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1693/3760 | 1397/1788 | 466/595 | chr1 | 12138290 | ||
| chr1:12138305
|
C | A | 2 | a0003a0004 | 7 | NA18939.hp1 NA18969.hp2 NA18970.hp1 others(4): Show |
missense_variant | MODERATE | c.1412C>A | p.Thr471Asn | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1708/3760 | 1412/1788 | 471/595 | chr1 | 12138305 | ||
| chr1:12138370
|
G | A | 1 | a0007 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.1477G>A | p.Gly493Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1773/3760 | 1477/1788 | 493/595 | chr1 | 12138370 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:12097147
|
G | A | 1 | a0001c0014 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.198G>A | p.Arg66Arg | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/15 | 494/3760 | 198/1788 | 66/595 | chr1 | 12097147 | ||
| chr1:12104380
|
C | T | 11 | a0001c0002a0001c0004a0001c0009others(8): Show | 109 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
splice_region_variant&synonymous_variant | LOW | c.270C>T | p.Asp90Asp | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/15 | 566/3760 | 270/1788 | 90/595 | chr1 | 12104380 | ||
| chr1:12110155
|
G | A | 1 | a0001c0025 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.627G>A | p.Thr209Thr | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/15 | 923/3760 | 627/1788 | 209/595 | chr1 | 12110155 | ||
| chr1:12111992
|
G | A | 4 | a0001c0009a0002c0012a0002c0016others(1): Show | 7 | HG01106.hp2 HG02145.hp1 HG02976.hp1 others(4): Show |
synonymous_variant | LOW | c.771G>A | p.Thr257Thr | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/15 | 1067/3760 | 771/1788 | 257/595 | chr1 | 12111992 | ||
| chr1:12123315
|
G | A | 1 | a0001c0017 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.978G>A | p.Ala326Ala | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/15 | 1274/3760 | 978/1788 | 326/595 | chr1 | 12123315 | ||
| chr1:12123781
|
C | T | 2 | a0001c0013a0001c0023 | 3 | NA18960.hp2 NA19070.hp2 NA19082.hp1 |
synonymous_variant | LOW | c.1107C>T | p.Ser369Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/15 | 1403/3760 | 1107/1788 | 369/595 | chr1 | 12123781 | ||
| chr1:12135604
|
G | A | 2 | a0001c0007a0001c0018 | 4 | HG02622.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.1326G>A | p.Arg442Arg | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/15 | 1622/3760 | 1326/1788 | 442/595 | chr1 | 12135604 | ||
| chr1:12138240
|
T | C | 13 | a0001c0003a0001c0004a0001c0007others(10): Show | 111 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(108): Show |
synonymous_variant | LOW | c.1347T>C | p.Ser449Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1643/3760 | 1347/1788 | 449/595 | chr1 | 12138240 | ||
| chr1:12138315
|
C | T | 1 | a0001c0026 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.1422C>T | p.Ser474Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1718/3760 | 1422/1788 | 474/595 | chr1 | 12138315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:12063319
|
C | T | 1 | a0001c0003t0026 | 1 | HG02965.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-280C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/15 | chr1 | 12063319 | ||||||
| chr1:12063442
|
G | T | 4 | a0001c0001t0008a0001c0002t0008a0001c0003t0008others(1): Show | 5 | HG00544.hp2 NA18980.hp2 NA18990.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-157G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/15 | 157 | chr1 | 12063442 | |||||
| chr1:12063566
|
G | T | 2 | a0001c0004t0025a0002c0010t0024 | 2 | HG01891.hp2 NA19030.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/15 | chr1 | 12063566 | ||||||
| chr1:12142705
|
C | G | 1 | a0002c0012t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 174 | chr1 | 12142705 | |||||
| chr1:12142731
|
G | A | 1 | a0002c0012t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 200 | chr1 | 12142731 | |||||
| chr1:12142774
|
G | A | 2 | a0001c0001t0011a0001c0002t0011 | 2 | NA18941.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*243G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 243 | chr1 | 12142774 | |||||
| chr1:12142835
|
G | A | 1 | a0001c0017t0014 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 304 | chr1 | 12142835 | |||||
| chr1:12142897
|
C | T | 3 | a0001c0001t0006a0001c0009t0006a0002c0005t0006 | 6 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*366C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 366 | chr1 | 12142897 | |||||
| chr1:12142996
|
G | A | 1 | a0001c0007t0015 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 465 | chr1 | 12142996 | |||||
| chr1:12143101
|
G | A | 3 | a0001c0001t0009a0001c0007t0009a0001c0018t0009 | 4 | HG02055.hp2 HG03130.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 570 | chr1 | 12143101 | |||||
| chr1:12143138
|
A | G | 9 | a0001c0001t0004a0001c0001t0022a0001c0002t0004others(6): Show | 12 | HG01109.hp2 HG02004.hp1 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*607A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 607 | chr1 | 12143138 | |||||
| chr1:12143320
|
C | T | 1 | a0001c0001t0013 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*789C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 789 | chr1 | 12143320 | |||||
| chr1:12143418
|
A | G | 1 | a0002c0012t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*887A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 887 | chr1 | 12143418 | |||||
| chr1:12143451
|
T | C | 1 | a0004c0028t0021 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*920T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 920 | chr1 | 12143451 | |||||
| chr1:12143542
|
A | ACG | 5 | a0001c0003t0003a0001c0004t0003a0001c0007t0015others(2): Show | 9 | HG01884.hp1 HG01891.hp2 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1013_*1014dupGC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1015 | INFO_REALIGN_3_PRIME | chr1 | 12143542 | ||||
| chr1:12143544
|
G | A | 1 | a0001c0001t0022 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1013G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1013 | chr1 | 12143544 | |||||
| chr1:12143544
|
G | C | 14 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(11): Show | 25 | HG01167.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1013G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1013 | chr1 | 12143544 | |||||
| chr1:12143598
|
A | C | 1 | a0001c0003t0020 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1067 | chr1 | 12143598 | |||||
| chr1:12143705
|
C | T | 1 | a0001c0003t0019 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1174C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1174 | chr1 | 12143705 | |||||
| chr1:12143718
|
G | C | 1 | a0001c0003t0012 | 2 | HG01167.hp2 HG01891.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1187G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1187 | chr1 | 12143718 | |||||
| chr1:12143815
|
C | T | 3 | a0001c0001t0005a0001c0003t0005a0002c0005t0005 | 6 | HG02055.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1284C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1284 | chr1 | 12143815 | |||||
| chr1:12143817
|
G | C | 1 | a0003c0008t0017 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1286G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1286 | chr1 | 12143817 | |||||
| chr1:12143821
|
G | A | 14 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(11): Show | 28 | HG01167.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1290G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1290 | chr1 | 12143821 | |||||
| chr1:12144010
|
G | A | 1 | a0001c0002t0018 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1479G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1479 | chr1 | 12144010 | |||||
| chr1:12144123
|
A | C | 2 | a0001c0003t0010a0001c0004t0010 | 3 | HG02258.hp2 HG03471.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1592A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1592 | chr1 | 12144123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:12063756
|
G | T | 1 | a0001c0001t0008g0362 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.63+95G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12063756 | ||||||
| chr1:12063968
|
G | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(15): Show | 18 | HG01074.hp2 HG01192.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+307G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12063968 | ||||||
| chr1:12064003
|
C | T | 1 | a0002c0006t0001g0361 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.63+342C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064003 | ||||||
| chr1:12064090
|
C | G | 8 | a0001c0001t0005g0355a0001c0001t0006g0359a0001c0004t0025g0356others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+429C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064090 | ||||||
| chr1:12064145
|
A | T | 3 | a0001c0001t0001g0351a0001c0004t0001g0352a0005c0015t0001g0350 | 3 | HG01106.hp2 HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.63+484A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064145 | ||||||
| chr1:12064157
|
G | A | 3 | a0001c0001t0001g0351a0001c0004t0001g0352a0005c0015t0001g0350 | 3 | HG01106.hp2 HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.63+496G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064157 | ||||||
| chr1:12064202
|
A | G | 115 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.63+541A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064202 | ||||||
| chr1:12064448
|
C | T | 1 | a0001c0001t0009g0234 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+787C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064448 | ||||||
| chr1:12064486
|
ACCATAGT others(5): Show |
A | 20 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0002g0218others(17): Show | 20 | HG01243.hp1 HG02055.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+827_63+838delCA others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12064486 | |||||
| chr1:12064544
|
G | A | 4 | a0001c0003t0001g0237a0001c0003t0012g0236a0002c0005t0002g0235others(1): Show | 4 | HG01891.hp1 HG02976.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+883G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064544 | ||||||
| chr1:12064778
|
C | G | 2 | a0001c0003t0002g0213a0001c0003t0002g0214 | 2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+1117C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064778 | ||||||
| chr1:12064949
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.63+1288G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064949 | ||||||
| chr1:12065064
|
C | T | 1 | a0001c0002t0008g0212 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.63+1403C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065064 | ||||||
| chr1:12065078
|
C | CT | 61 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(58): Show | 61 | HG00544.hp2 HG00738.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+1439dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | |||||
| chr1:12065078
|
C | CTT | 16 | a0001c0001t0001g0229a0001c0001t0001g0244a0001c0001t0001g0351others(13): Show | 16 | HG01069.hp1 HG01106.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+1438_63+1439dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | |||||
| chr1:12065078
|
C | CTTT | 95 | a0001c0001t0001g0233a0001c0001t0001g0245a0001c0001t0001g0246others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.63+1437_63+1439dup others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | |||||
| chr1:12065078
|
C | CTTTT | 16 | a0001c0001t0001g0335a0001c0001t0001g0338a0001c0001t0001g0342others(13): Show | 16 | HG02080.hp1 HG02280.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+1436_63+1439dup others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | |||||
| chr1:12065078
|
CT | C | 7 | a0001c0001t0001g0020a0001c0002t0001g0022a0001c0003t0001g0023others(4): Show | 7 | HG01515.hp2 HG03471.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+1439delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | |||||
| chr1:12065111
|
C | T | 4 | a0001c0001t0001g0203a0001c0003t0003g0208a0002c0005t0005g0210others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1450C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065111 | ||||||
| chr1:12065163
|
A | C | 7 | a0001c0001t0001g0201a0001c0001t0007g0198a0001c0003t0002g0197others(4): Show | 7 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+1502A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065163 | ||||||
| chr1:12065167
|
C | A | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+1506C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065167 | ||||||
| chr1:12065190
|
C | T | 158 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0173others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.63+1529C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065190 | ||||||
| chr1:12065303
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+1642G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065303 | ||||||
| chr1:12065352
|
G | A | 114 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244others(111): Show | 114 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.63+1691G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065352 | ||||||
| chr1:12065611
|
T | C | 3 | a0001c0001t0001g0351a0001c0004t0001g0352a0005c0015t0001g0350 | 3 | HG01106.hp2 HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.63+1950T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065611 | ||||||
| chr1:12065655
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.63+1994T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065655 | ||||||
| chr1:12065714
|
C | A | 5 | a0001c0001t0008g0163a0001c0001t0008g0362a0001c0002t0008g0212others(2): Show | 5 | HG00544.hp2 NA18980.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2053C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065714 | ||||||
| chr1:12065779
|
T | C | 7 | a0001c0001t0001g0203a0001c0001t0002g0218a0001c0001t0007g0216others(4): Show | 7 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2118T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065779 | ||||||
| chr1:12065857
|
C | G | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0007g0192others(5): Show | 8 | HG02257.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+2196C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065857 | ||||||
| chr1:12066084
|
A | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG01099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.63+2423A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066084 | ||||||
| chr1:12066142
|
G | A | 1 | a0002c0006t0001g0361 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.63+2481G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066142 | ||||||
| chr1:12066153
|
G | A | 3 | a0001c0001t0001g0229a0001c0003t0001g0219a0001c0004t0003g0220 | 3 | HG02630.hp1 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+2492G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066153 | ||||||
| chr1:12066308
|
T | A | 118 | a0001c0001t0001g0241a0001c0001t0001g0244a0001c0001t0001g0245others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.63+2647T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066308 | ||||||
| chr1:12066308
|
T | TA | 7 | a0001c0001t0001g0201a0001c0001t0007g0198a0001c0003t0002g0197others(4): Show | 7 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2657dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12066308 | |||||
| chr1:12066309
|
A | T | 2 | a0001c0002t0001g0018a0003c0019t0004g0017 | 2 | NA18985.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.63+2648A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066309 | ||||||
| chr1:12066350
|
T | A | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+2689T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066350 | ||||||
| chr1:12066350
|
T | TA | 3 | a0001c0001t0001g0159a0001c0003t0026g0161a0001c0009t0006g0171 | 3 | HG02965.hp1 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.63+2693dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12066350 | |||||
| chr1:12066354
|
A | AT | 41 | a0001c0001t0001g0160a0001c0001t0001g0173a0001c0001t0001g0174others(38): Show | 41 | HG00438.hp2 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.63+2710dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12066354 | |||||
| chr1:12066354
|
AT | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0203a0001c0001t0001g0247others(3): Show | 6 | HG02647.hp2 HG03491.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2710delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12066354 | |||||
| chr1:12066501
|
T | C | 1 | a0001c0003t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+2840T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066501 | ||||||
| chr1:12066505
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+2844C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066505 | ||||||
| chr1:12066593
|
T | C | 1 | a0001c0001t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.63+2932T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066593 | ||||||
| chr1:12066599
|
C | T | 5 | a0001c0001t0008g0163a0001c0001t0008g0362a0001c0002t0008g0212others(2): Show | 5 | HG00544.hp2 NA18980.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2938C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066599 | ||||||
| chr1:12066600
|
A | G | 189 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0160others(186): Show | 189 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.63+2939A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066600 | ||||||
| chr1:12066642
|
C | T | 7 | a0001c0001t0002g0224a0001c0003t0003g0225a0001c0003t0003g0226others(4): Show | 7 | HG02895.hp2 HG02897.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2981C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066642 | ||||||
| chr1:12066706
|
G | A | 1 | a0001c0003t0001g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+3045G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066706 | ||||||
| chr1:12066720
|
T | G | 3 | a0001c0001t0002g0224a0001c0003t0003g0225a0001c0003t0003g0226 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3059T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066720 | ||||||
| chr1:12066797
|
T | C | 118 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244others(115): Show | 118 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.63+3136T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066797 | ||||||
| chr1:12066823
|
T | C | 7 | a0001c0001t0002g0224a0001c0003t0003g0225a0001c0003t0003g0226others(4): Show | 7 | HG02895.hp2 HG02897.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+3162T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066823 | ||||||
| chr1:12066992
|
C | T | 3 | a0001c0001t0002g0224a0001c0003t0003g0225a0001c0003t0003g0226 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3331C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066992 | ||||||
| chr1:12066993
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.63+3332G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066993 | ||||||
| chr1:12067075
|
C | T | 1 | a0001c0007t0009g0357 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.63+3414C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067075 | ||||||
| chr1:12067092
|
C | T | 3 | a0001c0001t0002g0224a0001c0003t0003g0225a0001c0003t0003g0226 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3431C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067092 | ||||||
| chr1:12067205
|
G | C | 20 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0174others(17): Show | 20 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+3544G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067205 | ||||||
| chr1:12067209
|
C | T | 4 | a0001c0001t0008g0163a0001c0001t0008g0362a0001c0003t0008g0204others(1): Show | 4 | HG00544.hp2 NA18980.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3548C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067209 | ||||||
| chr1:12067236
|
C | T | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+3575C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067236 | ||||||
| chr1:12067255
|
C | G | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.63+3594C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067255 | ||||||
| chr1:12067414
|
C | T | 3 | a0001c0001t0006g0359a0001c0009t0001g0358a0001c0009t0001g0360 | 3 | HG02109.hp2 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.63+3753C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067414 | ||||||
| chr1:12067457
|
G | T | 4 | a0001c0001t0001g0144a0001c0003t0001g0143a0001c0003t0001g0145others(1): Show | 4 | HG02523.hp1 NA18966.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3796G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067457 | ||||||
| chr1:12067550
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.63+3889A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067550 | ||||||
| chr1:12067562
|
G | A | 4 | a0001c0001t0008g0163a0001c0001t0008g0362a0001c0003t0008g0204others(1): Show | 4 | HG00544.hp2 NA18980.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3901G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067562 | ||||||
| chr1:12067646
|
C | T | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+3985C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067646 | ||||||
| chr1:12067654
|
T | C | 1 | a0008c0029t0001g0240 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.63+3993T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067654 | ||||||
| chr1:12067713
|
C | T | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+4052C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067713 | ||||||
| chr1:12067760
|
C | T | 7 | a0001c0001t0002g0224a0001c0003t0003g0225a0001c0003t0003g0226others(4): Show | 7 | HG02895.hp2 HG02897.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+4099C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067760 | ||||||
| chr1:12067818
|
A | G | 1 | a0001c0004t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.63+4157A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067818 | ||||||
| chr1:12067875
|
C | T | 3 | a0001c0001t0001g0241a0001c0004t0001g0348a0002c0006t0001g0347 | 3 | HG03710.hp2 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.63+4214C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067875 | ||||||
| chr1:12067903
|
C | CG | 130 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0028others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.63+4251dupG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12067903 | |||||
| chr1:12067903
|
C | CGG | 48 | a0001c0001t0001g0159a0001c0001t0001g0173a0001c0001t0001g0183others(45): Show | 48 | HG00438.hp2 HG00738.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.63+4250_63+4251dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12067903 | |||||
| chr1:12067903
|
C | G | 15 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0002g0218others(12): Show | 15 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+4242C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067903 | ||||||
| chr1:12067912
|
G | GT | 3 | a0001c0001t0001g0241a0001c0004t0001g0348a0002c0006t0001g0347 | 3 | HG03710.hp2 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.63+4251_63+4252ins others(1): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067912 | ||||||
| chr1:12068101
|
G | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0124 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.63+4440G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068101 | ||||||
| chr1:12068183
|
A | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+4522A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068183 | ||||||
| chr1:12068222
|
G | A | 7 | a0001c0001t0001g0201a0001c0001t0007g0198a0001c0003t0002g0197others(4): Show | 7 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+4561G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068222 | ||||||
| chr1:12068235
|
A | G | 1 | a0001c0003t0001g0123 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.63+4574A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068235 | ||||||
| chr1:12068246
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+4585T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068246 | ||||||
| chr1:12068378
|
A | G | 59 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0098others(56): Show | 59 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.63+4717A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068378 | ||||||
| chr1:12068441
|
G | A | 117 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244others(114): Show | 117 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.63+4780G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068441 | ||||||
| chr1:12068876
|
C | CT | 46 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0099others(43): Show | 46 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.63+5228dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12068876 | |||||
| chr1:12068935
|
G | A | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+5274G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068935 | ||||||
| chr1:12068998
|
A | G | 1 | a0003c0008t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.63+5337A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068998 | ||||||
| chr1:12069117
|
C | T | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+5456C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069117 | ||||||
| chr1:12069167
|
G | T | 1 | a0001c0001t0009g0234 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+5506G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069167 | ||||||
| chr1:12069170
|
C | CT | 16 | a0001c0001t0001g0012a0001c0001t0001g0083a0001c0001t0001g0086others(13): Show | 16 | HG00438.hp1 HG00597.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+5536dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | |||||
| chr1:12069170
|
CT | C | 20 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0332others(17): Show | 20 | HG00438.hp2 HG00741.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+5536delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | |||||
| chr1:12069170
|
CTT | C | 134 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.63+5535_63+5536del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | |||||
| chr1:12069170
|
CTTT | C | 86 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0099others(83): Show | 86 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.63+5534_63+5536del others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | |||||
| chr1:12069170
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0002g0172a0002c0005t0002g0206 | 2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.63+5524_63+5536del others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | |||||
| chr1:12069170
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0002t0001g0166a0001c0004t0001g0165a0001c0004t0001g0168 | 3 | HG02572.hp1 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+5523_63+5536del others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | |||||
| chr1:12069248
|
A | G | 116 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0099others(113): Show | 116 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.63+5587A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069248 | ||||||
| chr1:12069367
|
C | T | 6 | a0001c0001t0001g0151a0001c0001t0006g0150a0001c0003t0001g0153others(3): Show | 6 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+5706C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069367 | ||||||
| chr1:12069424
|
C | A | 6 | a0001c0001t0001g0344a0001c0001t0006g0248a0001c0003t0001g0252others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+5763C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069424 | ||||||
| chr1:12069471
|
C | T | 1 | a0001c0004t0001g0164 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.63+5810C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069471 | ||||||
| chr1:12069509
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.63+5848C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069509 | ||||||
| chr1:12069593
|
T | C | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+5932T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069593 | ||||||
| chr1:12069717
|
C | T | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.63+6056C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069717 | ||||||
| chr1:12069718
|
G | A | 8 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0007g0192others(5): Show | 8 | HG02257.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+6057G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069718 | ||||||
| chr1:12069816
|
A | C | 1 | a0002c0006t0001g0347 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.63+6155A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069816 | ||||||
| chr1:12069875
|
T | C | 1 | a0001c0002t0001g0254 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.63+6214T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069875 | ||||||
| chr1:12069881
|
C | T | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+6220C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069881 | ||||||
| chr1:12069912
|
G | A | 16 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0175others(13): Show | 16 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+6251G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069912 | ||||||
| chr1:12069992
|
G | T | 1 | a0001c0001t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.63+6331G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069992 | ||||||
| chr1:12069994
|
C | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(129): Show | 132 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.63+6333C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069994 | ||||||
| chr1:12070013
|
T | C | 1 | a0002c0006t0001g0021 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.63+6352T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070013 | ||||||
| chr1:12070145
|
TG | T | 231 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(228): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.63+6490delG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12070145 | |||||
| chr1:12070159
|
A | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.63+6498A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070159 | ||||||
| chr1:12070161
|
TGGG | T | 181 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.63+6504_63+6506del others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12070161 | |||||
| chr1:12070205
|
T | C | 2 | a0001c0001t0007g0216a0001c0003t0001g0217 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.63+6544T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070205 | ||||||
| chr1:12070395
|
C | T | 2 | a0001c0001t0001g0300a0001c0001t0001g0330 | 2 | NA18962.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.63+6734C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070395 | ||||||
| chr1:12070460
|
C | T | 206 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(203): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.63+6799C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070460 | ||||||
| chr1:12070504
|
A | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG01099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.63+6843A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070504 | ||||||
| chr1:12070525
|
A | G | 5 | a0001c0001t0002g0172a0001c0002t0001g0166a0001c0004t0001g0165others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6864A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070525 | ||||||
| chr1:12070557
|
C | G | 1 | a0001c0003t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+6896C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070557 | ||||||
| chr1:12070641
|
T | C | 8 | a0001c0001t0002g0218a0001c0001t0007g0216a0001c0002t0001g0188others(5): Show | 8 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+6980T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070641 | ||||||
| chr1:12070712
|
C | T | 1 | a0001c0003t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+7051C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070712 | ||||||
| chr1:12070754
|
T | C | 1 | a0002c0005t0001g0349 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.63+7093T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070754 | ||||||
| chr1:12071152
|
C | T | 6 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+7491C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071152 | ||||||
| chr1:12071235
|
T | G | 12 | a0001c0001t0001g0203a0001c0001t0002g0218a0001c0001t0007g0216others(9): Show | 12 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+7574T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071235 | ||||||
| chr1:12071265
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+7604C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071265 | ||||||
| chr1:12071332
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.63+7671G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071332 | ||||||
| chr1:12071423
|
A | G | 1 | a0001c0001t0001g0300 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.63+7762A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071423 | ||||||
| chr1:12071447
|
A | T | 1 | a0001c0001t0001g0079 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.63+7786A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071447 | ||||||
| chr1:12071551
|
G | C | 1 | a0001c0001t0001g0300 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.63+7890G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071551 | ||||||
| chr1:12071624
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+7963C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071624 | ||||||
| chr1:12071632
|
C | T | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+7971C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071632 | ||||||
| chr1:12071651
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.63+7990C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071651 | ||||||
| chr1:12071684
|
C | T | 3 | a0001c0001t0002g0224a0001c0003t0003g0225a0001c0003t0003g0226 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+8023C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071684 | ||||||
| chr1:12071713
|
G | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0037others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.63+8052G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071713 | ||||||
| chr1:12071733
|
T | C | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.63+8072T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071733 | ||||||
| chr1:12072108
|
G | A | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+8447G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072108 | ||||||
| chr1:12072362
|
G | A | 3 | a0001c0001t0002g0224a0001c0003t0003g0225a0001c0003t0003g0226 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+8701G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072362 | ||||||
| chr1:12072521
|
G | C | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+8860G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072521 | ||||||
| chr1:12072575
|
G | A | 74 | a0001c0001t0001g0040a0001c0001t0001g0096a0001c0001t0001g0098others(71): Show | 74 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.63+8914G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072575 | ||||||
| chr1:12072663
|
T | C | 3 | a0002c0005t0001g0227a0002c0005t0005g0232a0002c0016t0004g0228 | 3 | HG03195.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.63+9002T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072663 | ||||||
| chr1:12072668
|
G | A | 1 | a0001c0002t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.63+9007G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072668 | ||||||
| chr1:12072736
|
T | C | 3 | a0001c0003t0005g0223a0002c0006t0001g0222a0002c0011t0004g0221 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+9075T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072736 | ||||||
| chr1:12072828
|
C | T | 8 | a0001c0002t0001g0166a0001c0002t0001g0188a0001c0003t0003g0225others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+9167C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072828 | ||||||
| chr1:12072876
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.63+9215G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072876 | ||||||
| chr1:12072877
|
G | A | 3 | a0001c0003t0005g0223a0002c0006t0001g0222a0002c0011t0004g0221 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+9216G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072877 | ||||||
| chr1:12072988
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.63+9327G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072988 | ||||||
| chr1:12073026
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.63+9365G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073026 | ||||||
| chr1:12073100
|
C | T | 8 | a0001c0001t0001g0151a0001c0001t0006g0148a0001c0001t0006g0150others(5): Show | 8 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+9439C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073100 | ||||||
| chr1:12073107
|
A | C | 1 | a0001c0002t0001g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.63+9446A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073107 | ||||||
| chr1:12073264
|
A | AAAACAAA others(5): Show |
6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9605_63+9616dup others(12): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073264 | |||||
| chr1:12073284
|
C | A | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.63+9623C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073284 | ||||||
| chr1:12073371
|
G | A | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9710G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073371 | ||||||
| chr1:12073417
|
A | G | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9756A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073417 | ||||||
| chr1:12073439
|
TTTTCTTC others(24): Show |
T | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9781_63+9811del others(31): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073439 | |||||
| chr1:12073476
|
C | T | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9815C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073476 | ||||||
| chr1:12073478
|
T | C | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9817T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073478 | ||||||
| chr1:12073483
|
T | TC | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9823dupC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073483 | |||||
| chr1:12073548
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+9887C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073548 | ||||||
| chr1:12073592
|
C | CT | 6 | a0001c0001t0002g0172a0001c0001t0002g0224a0001c0002t0001g0032others(3): Show | 6 | HG01256.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+9943dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073592 | |||||
| chr1:12073592
|
CT | C | 7 | a0001c0003t0001g0336a0001c0003t0005g0223a0002c0005t0001g0227others(4): Show | 7 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+9943delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073592 | |||||
| chr1:12073596
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.63+9935T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073596 | ||||||
| chr1:12073696
|
C | T | 5 | a0001c0001t0001g0293a0001c0001t0001g0342a0001c0003t0001g0341others(2): Show | 5 | HG02080.hp1 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+10035C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073696 | ||||||
| chr1:12073735
|
A | G | 19 | a0001c0001t0001g0233a0001c0001t0002g0218a0001c0001t0002g0224others(16): Show | 19 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.63+10074A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073735 | ||||||
| chr1:12073750
|
C | T | 2 | a0001c0001t0001g0342a0001c0003t0001g0341 | 2 | HG02080.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.63+10089C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073750 | ||||||
| chr1:12073757
|
C | A | 3 | a0001c0003t0003g0225a0001c0003t0003g0226a0001c0004t0001g0196 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.63+10096C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073757 | ||||||
| chr1:12073770
|
A | G | 3 | a0001c0003t0005g0223a0002c0006t0001g0222a0002c0011t0004g0221 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+10109A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073770 | ||||||
| chr1:12073801
|
G | A | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10140G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073801 | ||||||
| chr1:12073810
|
G | A | 4 | a0001c0001t0002g0172a0001c0003t0003g0225a0001c0003t0003g0226others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+10149G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073810 | ||||||
| chr1:12073887
|
C | T | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10226C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073887 | ||||||
| chr1:12073888
|
A | G | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10227A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073888 | ||||||
| chr1:12073892
|
A | G | 173 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.63+10231A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073892 | ||||||
| chr1:12073929
|
G | A | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10268G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073929 | ||||||
| chr1:12073953
|
C | T | 1 | a0001c0007t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63+10292C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073953 | ||||||
| chr1:12073954
|
G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+10293G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073954 | ||||||
| chr1:12074156
|
G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-10308G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074156 | ||||||
| chr1:12074163
|
TGCTAAAA others(7): Show |
T | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-10297_64-10284d others(16): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12074163 | |||||
| chr1:12074171
|
C | T | 2 | a0001c0002t0001g0306a0001c0004t0001g0291 | 2 | NA18612.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.64-10293C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074171 | ||||||
| chr1:12074217
|
A | G | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-10247A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074217 | ||||||
| chr1:12074282
|
T | C | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-10182T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074282 | ||||||
| chr1:12074373
|
G | A | 1 | a0001c0003t0002g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-10091G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074373 | ||||||
| chr1:12074479
|
T | C | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9985T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074479 | ||||||
| chr1:12074526
|
C | T | 7 | a0001c0001t0001g0272a0001c0001t0001g0296a0001c0001t0001g0297others(4): Show | 7 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-9938C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074526 | ||||||
| chr1:12074527
|
G | T | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.64-9937G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074527 | ||||||
| chr1:12074565
|
C | G | 3 | a0001c0001t0001g0122a0001c0002t0001g0117a0001c0002t0001g0118 | 3 | NA18962.hp1 NA19063.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.64-9899C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074565 | ||||||
| chr1:12074633
|
A | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 8 | HG00741.hp1 HG01074.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-9831A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074633 | ||||||
| chr1:12074701
|
T | A | 8 | a0001c0001t0001g0201a0001c0001t0007g0198a0001c0003t0001g0091others(5): Show | 8 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-9763T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074701 | ||||||
| chr1:12074743
|
A | G | 5 | a0001c0001t0001g0293a0001c0001t0001g0342a0001c0003t0001g0341others(2): Show | 5 | HG02080.hp1 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-9721A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074743 | ||||||
| chr1:12074779
|
GTGTT | G | 6 | a0001c0001t0001g0173a0001c0003t0001g0237a0001c0003t0002g0200others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-9671_64-9668del others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12074779 | |||||
| chr1:12074874
|
G | A | 8 | a0001c0001t0001g0151a0001c0001t0006g0148a0001c0001t0006g0150others(5): Show | 8 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-9590G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074874 | ||||||
| chr1:12075093
|
G | A | 173 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.64-9371G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075093 | ||||||
| chr1:12075198
|
T | C | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9266T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075198 | ||||||
| chr1:12075241
|
C | CA | 9 | a0001c0001t0001g0151a0001c0001t0006g0148a0001c0001t0006g0150others(6): Show | 9 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-9213dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12075241 | |||||
| chr1:12075251
|
A | AT | 116 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.64-9198dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12075251 | |||||
| chr1:12075268
|
A | T | 85 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.64-9196A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075268 | ||||||
| chr1:12075291
|
G | A | 3 | a0001c0003t0003g0225a0001c0003t0003g0226a0001c0004t0001g0196 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64-9173G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075291 | ||||||
| chr1:12075300
|
G | A | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9164G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075300 | ||||||
| chr1:12075319
|
T | C | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9145T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075319 | ||||||
| chr1:12075341
|
T | C | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9123T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075341 | ||||||
| chr1:12075352
|
C | T | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9112C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075352 | ||||||
| chr1:12075354
|
G | T | 76 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.64-9110G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075354 | ||||||
| chr1:12075362
|
G | A | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9102G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075362 | ||||||
| chr1:12075383
|
T | G | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9081T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075383 | ||||||
| chr1:12075414
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-9050G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075414 | ||||||
| chr1:12075469
|
A | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.64-8995A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075469 | ||||||
| chr1:12075574
|
C | T | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8890C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075574 | ||||||
| chr1:12075647
|
A | T | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.64-8817A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075647 | ||||||
| chr1:12075680
|
C | T | 1 | a0001c0002t0001g0116 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.64-8784C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075680 | ||||||
| chr1:12075739
|
C | T | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8725C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075739 | ||||||
| chr1:12075761
|
C | T | 11 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0287others(8): Show | 11 | HG02040.hp2 NA18955.hp2 NA18971.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-8703C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075761 | ||||||
| chr1:12075835
|
G | C | 52 | a0001c0001t0001g0138a0001c0001t0001g0151a0001c0001t0001g0159others(49): Show | 52 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-8629G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075835 | ||||||
| chr1:12075859
|
A | T | 52 | a0001c0001t0001g0138a0001c0001t0001g0151a0001c0001t0001g0159others(49): Show | 52 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-8605A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075859 | ||||||
| chr1:12075913
|
T | C | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8551T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075913 | ||||||
| chr1:12075921
|
C | T | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8543C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075921 | ||||||
| chr1:12075992
|
C | T | 6 | a0001c0001t0001g0286a0001c0001t0001g0325a0001c0002t0001g0018others(3): Show | 6 | HG00438.hp2 HG02056.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8472C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075992 | ||||||
| chr1:12076086
|
C | CTCT | 77 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(74): Show | 77 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.64-8377_64-8376ins others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12076086 | |||||
| chr1:12076087
|
T | TC | 4 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(1): Show | 4 | HG02818.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-8377_64-8376ins others(1): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076087 | ||||||
| chr1:12076088
|
T | C | 2 | a0002c0006t0001g0222a0002c0011t0004g0221 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-8376T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076088 | ||||||
| chr1:12076097
|
C | CT | 69 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.64-8362dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12076097 | |||||
| chr1:12076097
|
C | T | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8367C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076097 | ||||||
| chr1:12076097
|
CTTTTTCT others(7): Show |
C | 86 | a0001c0001t0001g0138a0001c0001t0001g0151a0001c0001t0001g0159others(83): Show | 86 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(83): Show |
intron_variant | MODIFIER | c.64-8361_64-8348del others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12076097 | |||||
| chr1:12076099
|
T | C | 1 | a0001c0003t0005g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64-8365T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076099 | ||||||
| chr1:12076100
|
T | C | 5 | a0002c0005t0001g0227a0002c0005t0005g0232a0002c0006t0001g0222others(2): Show | 5 | HG01243.hp1 HG03195.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8364T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076100 | ||||||
| chr1:12076102
|
TC | T | 3 | a0001c0003t0003g0225a0001c0003t0003g0226a0001c0004t0001g0196 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64-8361delC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076102 | ||||||
| chr1:12076103
|
C | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.64-8361C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076103 | ||||||
| chr1:12076132
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.64-8332C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076132 | ||||||
| chr1:12076196
|
G | A | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8268G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076196 | ||||||
| chr1:12076203
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.64-8261C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076203 | ||||||
| chr1:12076336
|
G | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0037others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.64-8128G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076336 | ||||||
| chr1:12076442
|
T | G | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-8022T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076442 | ||||||
| chr1:12076670
|
T | C | 5 | a0001c0001t0001g0293a0001c0001t0001g0342a0001c0003t0001g0341others(2): Show | 5 | HG02080.hp1 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-7794T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076670 | ||||||
| chr1:12076732
|
T | C | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-7732T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076732 | ||||||
| chr1:12076865
|
G | T | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-7599G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076865 | ||||||
| chr1:12076895
|
G | T | 2 | a0001c0001t0001g0300a0001c0001t0001g0330 | 2 | NA18962.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.64-7569G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076895 | ||||||
| chr1:12076931
|
A | G | 6 | a0001c0003t0005g0223a0002c0005t0001g0227a0002c0005t0005g0232others(3): Show | 6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-7533A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076931 | ||||||
| chr1:12077008
|
C | A | 6 | a0001c0001t0002g0224a0001c0002t0001g0166a0001c0002t0001g0188others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-7456C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077008 | ||||||
| chr1:12077011
|
G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-7453G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077011 | ||||||
| chr1:12077022
|
T | C | 1 | a0002c0006t0003g0149 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.64-7442T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077022 | ||||||
| chr1:12077124
|
G | A | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-7340G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077124 | ||||||
| chr1:12077197
|
T | C | 1 | a0001c0004t0001g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-7267T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077197 | ||||||
| chr1:12077254
|
T | C | 7 | a0001c0003t0005g0223a0001c0007t0001g0215a0002c0005t0001g0227others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-7210T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077254 | ||||||
| chr1:12077261
|
A | G | 7 | a0001c0003t0005g0223a0001c0007t0001g0215a0002c0005t0001g0227others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-7203A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077261 | ||||||
| chr1:12077302
|
G | A | 3 | a0001c0003t0005g0223a0002c0006t0001g0222a0002c0011t0004g0221 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-7162G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077302 | ||||||
| chr1:12077303
|
G | C | 7 | a0001c0003t0005g0223a0001c0007t0001g0215a0002c0005t0001g0227others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-7161G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077303 | ||||||
| chr1:12077382
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-7082G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077382 | ||||||
| chr1:12077546
|
A | C | 76 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.64-6918A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077546 | ||||||
| chr1:12077625
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64-6839A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077625 | ||||||
| chr1:12077640
|
G | A | 3 | a0001c0003t0003g0225a0001c0003t0003g0226a0001c0004t0001g0196 | 3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64-6824G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077640 | ||||||
| chr1:12077736
|
C | A | 7 | a0001c0003t0005g0223a0001c0007t0001g0215a0002c0005t0001g0227others(4): Show | 7 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-6728C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077736 | ||||||
| chr1:12077822
|
G | A | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-6642G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077822 | ||||||
| chr1:12077868
|
GT | G | 164 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.64-6582delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12077868 | |||||
| chr1:12077883
|
A | T | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-6581A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077883 | ||||||
| chr1:12077892
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64-6572C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077892 | ||||||
| chr1:12077973
|
C | T | 19 | a0001c0001t0001g0233a0001c0001t0002g0218a0001c0001t0002g0224others(16): Show | 19 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-6491C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077973 | ||||||
| chr1:12078043
|
T | C | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6421T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078043 | ||||||
| chr1:12078110
|
G | A | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-6354G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078110 | ||||||
| chr1:12078137
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.64-6327C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078137 | ||||||
| chr1:12078140
|
G | A | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6324G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078140 | ||||||
| chr1:12078149
|
C | G | 1 | a0001c0003t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64-6315C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078149 | ||||||
| chr1:12078280
|
T | A | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6184T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078280 | ||||||
| chr1:12078294
|
T | A | 22 | a0001c0001t0001g0151a0001c0001t0001g0173a0001c0001t0006g0148others(19): Show | 22 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-6170T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078294 | ||||||
| chr1:12078359
|
T | C | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6105T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078359 | ||||||
| chr1:12078388
|
A | G | 6 | a0001c0001t0001g0173a0001c0003t0001g0237a0001c0003t0002g0200others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-6076A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078388 | ||||||
| chr1:12078409
|
T | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(154): Show | 157 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.64-6055T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078409 | ||||||
| chr1:12078437
|
G | A | 1 | a0005c0015t0001g0350 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.64-6027G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078437 | ||||||
| chr1:12078437
|
G | T | 1 | a0001c0002t0001g0015 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.64-6027G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078437 | ||||||
| chr1:12078438
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.64-6026C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078438 | ||||||
| chr1:12078512
|
C | T | 1 | a0001c0003t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64-5952C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078512 | ||||||
| chr1:12078539
|
G | C | 1 | a0001c0002t0001g0340 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64-5925G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078539 | ||||||
| chr1:12078545
|
C | T | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-5919C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078545 | ||||||
| chr1:12078572
|
A | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(72): Show | 75 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.64-5892A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078572 | ||||||
| chr1:12078626
|
C | T | 1 | a0001c0004t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.64-5838C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078626 | ||||||
| chr1:12078630
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.64-5834A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078630 | ||||||
| chr1:12078696
|
C | T | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-5768C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078696 | ||||||
| chr1:12078744
|
G | A | 23 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0201others(20): Show | 23 | HG01109.hp1 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-5720G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078744 | ||||||
| chr1:12078758
|
C | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-5706C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078758 | ||||||
| chr1:12078761
|
C | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5703C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078761 | ||||||
| chr1:12078761
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.64-5703C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078761 | ||||||
| chr1:12078763
|
G | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5701G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078763 | ||||||
| chr1:12078767
|
A | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5697A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078767 | ||||||
| chr1:12078769
|
T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5695T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078769 | ||||||
| chr1:12078770
|
G | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5694G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078770 | ||||||
| chr1:12078771
|
G | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5693G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078771 | ||||||
| chr1:12078772
|
G | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5692G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078772 | ||||||
| chr1:12078774
|
T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5690T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078774 | ||||||
| chr1:12078780
|
T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5684T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078780 | ||||||
| chr1:12078781
|
T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5683T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078781 | ||||||
| chr1:12078783
|
T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5681T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078783 | ||||||
| chr1:12078784
|
T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5680T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078784 | ||||||
| chr1:12078787
|
C | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5677C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078787 | ||||||
| chr1:12078788
|
T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5676T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078788 | ||||||
| chr1:12078790
|
T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5674T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078790 | ||||||
| chr1:12078791
|
T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5673T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078791 | ||||||
| chr1:12078795
|
A | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5669A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078795 | ||||||
| chr1:12078796
|
T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5668T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078796 | ||||||
| chr1:12078797
|
T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5667T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078797 | ||||||
| chr1:12078801
|
T | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5663T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078801 | ||||||
| chr1:12078804
|
G | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5660G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078804 | ||||||
| chr1:12078806
|
TATGGAAA others(6): Show |
T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5657_64-5645del others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078806 | ||||||
| chr1:12078821
|
G | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5643G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078821 | ||||||
| chr1:12078824
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5640C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078824 | ||||||
| chr1:12078826
|
A | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5638A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078826 | ||||||
| chr1:12078827
|
G | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5637G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078827 | ||||||
| chr1:12078829
|
A | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5635A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078829 | ||||||
| chr1:12078831
|
T | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5633T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078831 | ||||||
| chr1:12078832
|
T | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5632T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078832 | ||||||
| chr1:12078833
|
G | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5631G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078833 | ||||||
| chr1:12078835
|
A | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5629A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078835 | ||||||
| chr1:12078836
|
C | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5628C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078836 | ||||||
| chr1:12078839
|
C | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5625C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078839 | ||||||
| chr1:12078842
|
T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5622T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078842 | ||||||
| chr1:12078843
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5621C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078843 | ||||||
| chr1:12078846
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5618C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078846 | ||||||
| chr1:12078848
|
C | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5616C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078848 | ||||||
| chr1:12078899
|
T | C | 10 | a0001c0001t0001g0257a0001c0001t0008g0163a0001c0001t0008g0362others(7): Show | 10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-5565T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078899 | ||||||
| chr1:12078998
|
C | T | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-5466C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078998 | ||||||
| chr1:12079150
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.64-5314G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079150 | ||||||
| chr1:12079193
|
T | A | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.64-5271T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079193 | ||||||
| chr1:12079447
|
C | T | 2 | a0001c0001t0001g0159a0001c0009t0006g0171 | 2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.64-5017C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079447 | ||||||
| chr1:12079448
|
G | A | 2 | a0001c0004t0025g0356a0002c0010t0024g0354 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.64-5016G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079448 | ||||||
| chr1:12079729
|
T | C | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-4735T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079729 | ||||||
| chr1:12079898
|
A | G | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-4566A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079898 | ||||||
| chr1:12079949
|
A | ATT | 9 | a0001c0001t0001g0151a0001c0001t0006g0148a0001c0001t0006g0150others(6): Show | 9 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-4499_64-4498dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12079949 | |||||
| chr1:12079949
|
AT | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(137): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.64-4498delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12079949 | |||||
| chr1:12079949
|
ATT | A | 13 | a0001c0001t0001g0233a0001c0001t0001g0244a0001c0001t0002g0218others(10): Show | 13 | HG01168.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-4499_64-4498del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12079949 | |||||
| chr1:12079949
|
ATTT | A | 11 | a0001c0001t0001g0257a0001c0001t0008g0163a0001c0001t0008g0362others(8): Show | 11 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-4500_64-4498del others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12079949 | |||||
| chr1:12079952
|
T | A | 3 | a0001c0003t0005g0223a0002c0006t0001g0222a0002c0011t0004g0221 | 3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-4512T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079952 | ||||||
| chr1:12079974
|
G | C | 1 | a0002c0010t0001g0345 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.64-4490G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079974 | ||||||
| chr1:12080060
|
C | T | 6 | a0001c0001t0002g0224a0001c0002t0001g0166a0001c0004t0001g0165others(3): Show | 6 | HG02572.hp1 HG02896.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-4404C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080060 | ||||||
| chr1:12080239
|
G | A | 5 | a0001c0001t0002g0224a0001c0002t0001g0166a0001c0004t0001g0165others(2): Show | 5 | HG02572.hp1 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-4225G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080239 | ||||||
| chr1:12080276
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.64-4188T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080276 | ||||||
| chr1:12080379
|
T | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0124others(3): Show | 6 | HG01081.hp2 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-4085T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080379 | ||||||
| chr1:12080508
|
T | C | 5 | a0001c0003t0001g0237a0001c0003t0002g0200a0001c0003t0012g0236others(2): Show | 5 | HG01891.hp1 HG02895.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3956T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080508 | ||||||
| chr1:12080519
|
G | A | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3945G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080519 | ||||||
| chr1:12080531
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-3933C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080531 | ||||||
| chr1:12080614
|
A | G | 1 | a0001c0003t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64-3850A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080614 | ||||||
| chr1:12080667
|
C | T | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-3797C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080667 | ||||||
| chr1:12080681
|
C | T | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3783C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080681 | ||||||
| chr1:12080812
|
A | C | 11 | a0001c0001t0001g0151a0001c0001t0002g0172a0001c0001t0006g0148others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-3652A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080812 | ||||||
| chr1:12080839
|
C | T | 8 | a0001c0001t0001g0201a0001c0001t0007g0198a0001c0003t0001g0091others(5): Show | 8 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-3625C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080839 | ||||||
| chr1:12080924
|
C | T | 2 | a0001c0001t0008g0163a0001c0001t0008g0362 | 2 | NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.64-3540C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080924 | ||||||
| chr1:12081126
|
C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-3338C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081126 | ||||||
| chr1:12081264
|
G | A | 2 | a0001c0001t0007g0216a0001c0003t0001g0217 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.64-3200G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081264 | ||||||
| chr1:12081285
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64-3179A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081285 | ||||||
| chr1:12081332
|
A | C | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3132A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081332 | ||||||
| chr1:12081368
|
C | T | 1 | a0001c0002t0001g0317 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64-3096C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081368 | ||||||
| chr1:12081404
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.64-3060A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081404 | ||||||
| chr1:12081458
|
C | A | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-3006C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081458 | ||||||
| chr1:12081546
|
G | A | 10 | a0001c0001t0001g0257a0001c0001t0008g0163a0001c0001t0008g0362others(7): Show | 10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-2918G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081546 | ||||||
| chr1:12081657
|
C | CA | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(91): Show | 94 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.64-2795dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12081657 | |||||
| chr1:12081819
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(185): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.64-2645A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081819 | ||||||
| chr1:12081943
|
G | C | 2 | a0001c0001t0001g0342a0001c0003t0001g0341 | 2 | HG02080.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.64-2521G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081943 | ||||||
| chr1:12081944
|
CCTCTTGC others(19): Show |
C | 46 | a0001c0001t0001g0048a0001c0001t0001g0138a0001c0001t0001g0159others(43): Show | 46 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.64-2457_64-2432del others(26): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12081944 | |||||
| chr1:12081947
|
C | T | 2 | a0001c0001t0001g0342a0001c0003t0001g0341 | 2 | HG02080.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.64-2517C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081947 | ||||||
| chr1:12082060
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.64-2404T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082060 | ||||||
| chr1:12082064
|
C | G | 7 | a0001c0001t0001g0173a0001c0001t0002g0224a0001c0002t0001g0166others(4): Show | 7 | HG02145.hp2 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-2400C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082064 | ||||||
| chr1:12082168
|
A | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-2296A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082168 | ||||||
| chr1:12082186
|
T | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-2278T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082186 | ||||||
| chr1:12082195
|
A | G | 1 | a0002c0005t0005g0210 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64-2269A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082195 | ||||||
| chr1:12082247
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-2217A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082247 | ||||||
| chr1:12082268
|
G | A | 2 | a0001c0003t0001g0153a0001c0003t0001g0167 | 2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.64-2196G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082268 | ||||||
| chr1:12082451
|
C | T | 1 | a0003c0008t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64-2013C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082451 | ||||||
| chr1:12082549
|
C | CA | 157 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(154): Show | 157 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.64-1901dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12082549 | |||||
| chr1:12082549
|
C | CAA | 20 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0173others(17): Show | 20 | HG00642.hp1 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-1902_64-1901dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12082549 | |||||
| chr1:12082561
|
A | AC | 4 | a0001c0001t0001g0268a0001c0001t0001g0342a0001c0002t0001g0316others(1): Show | 4 | HG00140.hp2 HG01261.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-1903_64-1902ins others(1): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082561 | ||||||
| chr1:12082564
|
C | A | 9 | a0001c0002t0001g0306a0001c0003t0001g0237a0001c0003t0002g0200others(6): Show | 9 | HG01891.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1900C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082564 | ||||||
| chr1:12082584
|
C | A | 4 | a0001c0003t0005g0223a0002c0005t0001g0094a0002c0006t0001g0222others(1): Show | 4 | HG01243.hp1 HG02818.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-1880C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082584 | ||||||
| chr1:12082596
|
C | T | 9 | a0001c0001t0001g0351a0001c0001t0005g0355a0001c0001t0006g0248others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-1868C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082596 | ||||||
| chr1:12082615
|
G | A | 7 | a0001c0001t0001g0173a0001c0001t0002g0224a0001c0002t0001g0166others(4): Show | 7 | HG02145.hp2 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-1849G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082615 | ||||||
| chr1:12082623
|
G | A | 1 | a0001c0003t0001g0336 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.64-1841G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082623 | ||||||
| chr1:12082641
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(92): Show | 95 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.64-1823C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082641 | ||||||
| chr1:12082943
|
C | A | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-1521C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082943 | ||||||
| chr1:12083103
|
A | G | 1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.64-1361A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083103 | ||||||
| chr1:12083167
|
G | T | 8 | a0001c0001t0001g0201a0001c0001t0007g0198a0001c0003t0001g0091others(5): Show | 8 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-1297G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083167 | ||||||
| chr1:12083318
|
G | A | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-1146G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083318 | ||||||
| chr1:12083399
|
C | T | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-1065C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083399 | ||||||
| chr1:12083411
|
C | T | 7 | a0001c0001t0001g0286a0001c0001t0001g0325a0001c0002t0001g0018others(4): Show | 7 | HG00438.hp2 HG02056.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-1053C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083411 | ||||||
| chr1:12083623
|
G | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(92): Show | 95 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.64-841G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083623 | ||||||
| chr1:12083760
|
A | G | 1 | a0001c0003t0001g0179 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64-704A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083760 | ||||||
| chr1:12083855
|
C | T | 10 | a0001c0001t0001g0257a0001c0001t0008g0163a0001c0001t0008g0362others(7): Show | 10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-609C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083855 | ||||||
| chr1:12083884
|
G | A | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-580G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083884 | ||||||
| chr1:12083913
|
C | T | 1 | a0003c0019t0004g0017 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.64-551C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083913 | ||||||
| chr1:12083950
|
G | A | 2 | a0001c0003t0003g0225a0001c0003t0003g0226 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64-514G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083950 | ||||||
| chr1:12084064
|
C | T | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-400C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084064 | ||||||
| chr1:12084162
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.64-302A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084162 | ||||||
| chr1:12084355
|
C | A | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-109C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084355 | ||||||
| chr1:12084363
|
T | C | 2 | a0001c0001t0008g0163a0001c0001t0008g0362 | 2 | NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.64-101T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084363 | ||||||
| chr1:12084364
|
A | G | 1 | a0001c0002t0001g0118 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-100A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084364 | ||||||
| chr1:12084377
|
G | A | 46 | a0001c0001t0001g0048a0001c0001t0001g0138a0001c0001t0001g0159others(43): Show | 46 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.64-87G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084377 | ||||||
| chr1:12084377
|
G | T | 1 | a0001c0004t0001g0164 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.64-87G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084377 | ||||||
| chr1:12084563
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.151+12C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084563 | ||||||
| chr1:12084586
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0124a0001c0001t0001g0160others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+35G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084586 | ||||||
| chr1:12084605
|
T | A | 69 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.151+54T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084605 | ||||||
| chr1:12084610
|
C | T | 69 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.151+59C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084610 | ||||||
| chr1:12084729
|
G | T | 1 | a0002c0006t0001g0090 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.151+178G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084729 | ||||||
| chr1:12084744
|
CTG | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.151+197_151+198del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12084744 | |||||
| chr1:12085007
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.151+456C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085007 | ||||||
| chr1:12085044
|
T | A | 12 | a0001c0001t0001g0257a0001c0001t0001g0342a0001c0001t0008g0163others(9): Show | 12 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+493T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085044 | ||||||
| chr1:12085167
|
A | G | 1 | a0001c0004t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151+616A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085167 | ||||||
| chr1:12085256
|
A | G | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+705A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085256 | ||||||
| chr1:12085274
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.151+723C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085274 | ||||||
| chr1:12085307
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.151+756G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085307 | ||||||
| chr1:12085614
|
T | C | 8 | a0001c0003t0005g0223a0001c0003t0010g0259a0001c0007t0001g0215others(5): Show | 8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+1063T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085614 | ||||||
| chr1:12085729
|
G | T | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.151+1178G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085729 | ||||||
| chr1:12086040
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.151+1489G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086040 | ||||||
| chr1:12086146
|
C | T | 10 | a0001c0001t0001g0257a0001c0001t0008g0163a0001c0001t0008g0362others(7): Show | 10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+1595C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086146 | ||||||
| chr1:12086148
|
C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.151+1597C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086148 | ||||||
| chr1:12086198
|
G | A | 9 | a0001c0001t0001g0351a0001c0001t0005g0355a0001c0001t0006g0248others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+1647G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086198 | ||||||
| chr1:12086440
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.151+1889C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086440 | ||||||
| chr1:12086490
|
A | G | 1 | a0001c0002t0001g0309 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+1939A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086490 | ||||||
| chr1:12086538
|
A | G | 1 | a0001c0009t0001g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.151+1987A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086538 | ||||||
| chr1:12086672
|
A | C | 1 | a0001c0003t0001g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.151+2121A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086672 | ||||||
| chr1:12087022
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.151+2471G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087022 | ||||||
| chr1:12087074
|
T | TATCC | 11 | a0001c0001t0001g0074a0001c0001t0001g0246a0001c0001t0001g0289others(8): Show | 11 | NA18942.hp1 NA18942.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+2575_151+2578d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | |||||
| chr1:12087074
|
TATCC | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(156): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.151+2575_151+2578d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | |||||
| chr1:12087074
|
TATCCATC others(1): Show |
T | 97 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0040others(94): Show | 97 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.151+2571_151+2578d others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | |||||
| chr1:12087074
|
TATCCATC others(5): Show |
T | 16 | a0001c0001t0001g0257a0001c0001t0002g0172a0001c0001t0008g0163others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.151+2567_151+2578d others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | |||||
| chr1:12087074
|
TATCCATC others(13): Show |
T | 24 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(21): Show | 24 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.151+2559_151+2578d others(22): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | |||||
| chr1:12087165
|
C | CT | 67 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(64): Show | 67 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.151+2634dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087165 | |||||
| chr1:12087165
|
C | CTT | 41 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(38): Show | 41 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.151+2633_151+2634d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087165 | |||||
| chr1:12087165
|
CT | C | 21 | a0001c0001t0001g0047a0001c0001t0001g0124a0001c0001t0001g0125others(18): Show | 21 | HG00558.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.151+2634delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087165 | |||||
| chr1:12087165
|
CTTTTTT | C | 9 | a0001c0001t0001g0151a0001c0001t0006g0148a0001c0001t0006g0150others(6): Show | 9 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+2629_151+2634d others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087165 | |||||
| chr1:12087221
|
A | T | 1 | a0001c0003t0012g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.151+2670A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087221 | ||||||
| chr1:12087254
|
G | A | 34 | a0001c0001t0001g0048a0001c0001t0001g0138a0001c0001t0001g0159others(31): Show | 34 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.151+2703G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087254 | ||||||
| chr1:12087357
|
G | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(42): Show | 45 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.151+2806G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087357 | ||||||
| chr1:12087543
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.151+2992G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087543 | ||||||
| chr1:12087647
|
T | C | 1 | a0001c0002t0001g0053 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.151+3096T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087647 | ||||||
| chr1:12087696
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.151+3145G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087696 | ||||||
| chr1:12087867
|
C | T | 3 | a0001c0001t0001g0138a0001c0001t0009g0089a0001c0003t0005g0092 | 3 | HG03139.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.151+3316C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087867 | ||||||
| chr1:12087960
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.151+3409G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087960 | ||||||
| chr1:12088012
|
C | T | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.151+3461C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088012 | ||||||
| chr1:12088014
|
C | T | 2 | a0001c0001t0005g0355a0002c0006t0001g0170 | 2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.151+3463C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088014 | ||||||
| chr1:12088015
|
G | A | 1 | a0001c0004t0001g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.151+3464G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088015 | ||||||
| chr1:12088171
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0144a0001c0003t0001g0143others(2): Show | 5 | HG02071.hp1 HG02523.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+3620T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088171 | ||||||
| chr1:12088329
|
TA | T | 32 | a0001c0001t0001g0201a0001c0001t0001g0203a0001c0001t0001g0257others(29): Show | 32 | HG01109.hp1 HG01167.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.151+3780delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12088329 | |||||
| chr1:12088331
|
AG | A | 110 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0020others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.151+3781delG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088331 | ||||||
| chr1:12088410
|
C | T | 10 | a0001c0001t0001g0257a0001c0001t0008g0163a0001c0001t0008g0362others(7): Show | 10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+3859C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088410 | ||||||
| chr1:12088544
|
G | A | 10 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0001t0008g0362others(7): Show | 10 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+3993G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088544 | ||||||
| chr1:12088604
|
A | C | 9 | a0001c0001t0001g0201a0001c0001t0007g0198a0001c0003t0001g0091others(6): Show | 9 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+4053A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088604 | ||||||
| chr1:12088665
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0068 | 2 | HG00280.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.151+4114G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088665 | ||||||
| chr1:12088795
|
C | T | 1 | a0001c0003t0001g0336 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.151+4244C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088795 | ||||||
| chr1:12088842
|
C | T | 2 | a0001c0001t0001g0040a0007c0020t0001g0019 | 2 | HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.151+4291C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088842 | ||||||
| chr1:12088889
|
C | T | 3 | a0001c0002t0001g0112a0001c0002t0001g0140a0001c0002t0018g0097 | 3 | HG00597.hp2 HG03704.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.151+4338C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088889 | ||||||
| chr1:12088923
|
G | A | 11 | a0001c0001t0001g0151a0001c0001t0002g0218a0001c0001t0006g0148others(8): Show | 11 | HG02257.hp2 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+4372G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088923 | ||||||
| chr1:12088967
|
C | G | 1 | a0001c0002t0001g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.151+4416C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088967 | ||||||
| chr1:12089052
|
G | C | 2 | a0001c0003t0002g0213a0002c0005t0002g0206 | 2 | HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.151+4501G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089052 | ||||||
| chr1:12089146
|
C | T | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+4595C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089146 | ||||||
| chr1:12089234
|
A | G | 8 | a0001c0001t0001g0173a0001c0001t0002g0224a0001c0004t0001g0088others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+4683A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089234 | ||||||
| chr1:12089238
|
C | T | 1 | a0001c0001t0004g0177 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.151+4687C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089238 | ||||||
| chr1:12089245
|
A | G | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+4694A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089245 | ||||||
| chr1:12089533
|
A | T | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0007g0193others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+4982A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089533 | ||||||
| chr1:12089600
|
A | C | 2 | a0001c0004t0001g0165a0001c0004t0001g0168 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.151+5049A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089600 | ||||||
| chr1:12089684
|
G | A | 7 | a0001c0001t0001g0229a0001c0002t0001g0166a0001c0003t0002g0213others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+5133G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089684 | ||||||
| chr1:12089828
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.151+5277C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089828 | ||||||
| chr1:12089829
|
ACATCCAT others(102): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.151+5313_151+5421d others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12089829 | |||||
| chr1:12090025
|
C | G | 1 | a0001c0001t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151+5474C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090025 | ||||||
| chr1:12090030
|
C | G | 6 | a0001c0002t0001g0166a0001c0003t0002g0213a0001c0004t0001g0196others(3): Show | 6 | HG02257.hp2 HG03453.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+5479C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090030 | ||||||
| chr1:12090056
|
TACCCATC others(5): Show |
T | 10 | a0001c0001t0001g0201a0001c0001t0002g0224a0001c0001t0007g0198others(7): Show | 10 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+5507_151+5518d others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12090056 | |||||
| chr1:12090066
|
TCCATCTA others(90): Show |
T | 11 | a0001c0001t0001g0229a0001c0002t0001g0166a0001c0003t0001g0219others(8): Show | 11 | HG01891.hp1 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+5665_151+5761d others(99): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12090066 | |||||
| chr1:12090281
|
T | C | 1 | a0001c0002t0001g0263 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151+5730T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090281 | ||||||
| chr1:12090321
|
CCCAT | C | 38 | a0001c0001t0001g0096a0001c0001t0001g0103a0001c0001t0001g0229others(35): Show | 38 | HG00558.hp2 HG01243.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.151+5790_151+5793d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12090321 | |||||
| chr1:12090328
|
A | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0012others(21): Show | 24 | HG00280.hp2 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.151+5777A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090328 | ||||||
| chr1:12090352
|
G | A | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+5801G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090352 | ||||||
| chr1:12090361
|
TC | T | 3 | a0001c0001t0001g0229a0001c0003t0001g0219a0001c0003t0012g0236 | 3 | HG01891.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.151+5812delC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12090361 | |||||
| chr1:12090431
|
A | G | 3 | a0001c0001t0001g0103a0001c0014t0001g0101a0004c0028t0021g0113 | 3 | HG00558.hp2 NA18955.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.151+5880A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090431 | ||||||
| chr1:12090536
|
C | T | 1 | a0001c0002t0001g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.151+5985C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090536 | ||||||
| chr1:12090581
|
C | T | 2 | a0001c0002t0001g0239a0001c0002t0001g0243 | 2 | NA18999.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.151+6030C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090581 | ||||||
| chr1:12090633
|
C | A | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+6082C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090633 | ||||||
| chr1:12090685
|
A | G | 3 | a0001c0001t0001g0229a0001c0003t0001g0219a0001c0003t0012g0236 | 3 | HG01891.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.151+6134A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090685 | ||||||
| chr1:12090772
|
C | T | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+6221C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090772 | ||||||
| chr1:12090881
|
C | A | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-6220C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090881 | ||||||
| chr1:12090902
|
C | T | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.152-6199C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090902 | ||||||
| chr1:12090909
|
C | T | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-6192C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090909 | ||||||
| chr1:12091026
|
C | T | 1 | a0001c0001t0001g0328 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.152-6075C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091026 | ||||||
| chr1:12091041
|
A | T | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-6060A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091041 | ||||||
| chr1:12091146
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152-5955A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091146 | ||||||
| chr1:12091225
|
G | A | 18 | a0001c0001t0001g0103a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 18 | HG00558.hp2 HG02040.hp2 HG02895.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-5876G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091225 | ||||||
| chr1:12091352
|
G | A | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0007g0193others(4): Show | 7 | HG02257.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-5749G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091352 | ||||||
| chr1:12091361
|
C | T | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-5740C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091361 | ||||||
| chr1:12091374
|
T | C | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-5727T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091374 | ||||||
| chr1:12091457
|
C | G | 1 | a0001c0002t0001g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.152-5644C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091457 | ||||||
| chr1:12091611
|
G | C | 2 | a0001c0002t0001g0166a0002c0005t0002g0206 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.152-5490G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091611 | ||||||
| chr1:12091826
|
T | C | 1 | a0001c0002t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.152-5275T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091826 | ||||||
| chr1:12091828
|
A | G | 4 | a0001c0003t0002g0213a0001c0004t0001g0196a0002c0005t0005g0230others(1): Show | 4 | HG02257.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-5273A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091828 | ||||||
| chr1:12091869
|
A | G | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-5232A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091869 | ||||||
| chr1:12092350
|
A | G | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-4751A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092350 | ||||||
| chr1:12092418
|
C | T | 1 | a0001c0003t0001g0336 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.152-4683C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092418 | ||||||
| chr1:12092509
|
C | CT | 20 | a0001c0001t0001g0020a0001c0001t0001g0086a0001c0001t0001g0098others(17): Show | 20 | HG00544.hp2 HG01069.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.152-4576dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12092509 | |||||
| chr1:12092509
|
CT | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0012others(54): Show | 57 | HG00280.hp2 HG00438.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.152-4576delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12092509 | |||||
| chr1:12092577
|
T | C | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.152-4524T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092577 | ||||||
| chr1:12092757
|
C | G | 3 | a0001c0002t0001g0015a0001c0002t0001g0317a0002c0006t0008g0162 | 3 | HG00544.hp2 HG02040.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.152-4344C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092757 | ||||||
| chr1:12092798
|
G | A | 19 | a0001c0001t0001g0103a0001c0001t0001g0203a0001c0001t0001g0246others(16): Show | 19 | HG00558.hp2 HG02040.hp2 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-4303G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092798 | ||||||
| chr1:12092808
|
T | C | 1 | a0001c0003t0003g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.152-4293T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092808 | ||||||
| chr1:12092867
|
G | A | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-4234G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092867 | ||||||
| chr1:12092941
|
G | A | 2 | a0001c0002t0001g0166a0002c0005t0002g0206 | 2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.152-4160G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092941 | ||||||
| chr1:12093086
|
G | A | 4 | a0001c0001t0001g0201a0001c0003t0001g0091a0001c0003t0002g0197others(1): Show | 4 | HG01192.hp1 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-4015G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093086 | ||||||
| chr1:12093131
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(232): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.152-3970G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093131 | ||||||
| chr1:12093257
|
T | C | 18 | a0001c0001t0001g0103a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 18 | HG00558.hp2 HG02040.hp2 HG02895.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-3844T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093257 | ||||||
| chr1:12093341
|
T | C | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-3760T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093341 | ||||||
| chr1:12093356
|
G | T | 20 | a0001c0001t0001g0103a0001c0001t0001g0203a0001c0001t0001g0246others(17): Show | 20 | HG00558.hp2 HG02040.hp2 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.152-3745G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093356 | ||||||
| chr1:12093601
|
C | T | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-3500C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093601 | ||||||
| chr1:12093655
|
C | T | 3 | a0001c0001t0001g0229a0001c0003t0001g0219a0001c0003t0012g0236 | 3 | HG01891.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.152-3446C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093655 | ||||||
| chr1:12093658
|
A | G | 10 | a0001c0001t0001g0229a0001c0002t0001g0166a0001c0003t0001g0219others(7): Show | 10 | HG01891.hp1 HG02257.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-3443A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093658 | ||||||
| chr1:12093676
|
T | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 222 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.152-3425T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093676 | ||||||
| chr1:12093697
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.152-3404C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093697 | ||||||
| chr1:12093746
|
G | A | 22 | a0001c0001t0001g0159a0001c0001t0001g0173a0001c0001t0002g0172others(19): Show | 22 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.152-3355G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093746 | ||||||
| chr1:12093752
|
G | A | 3 | a0001c0003t0002g0213a0001c0004t0001g0196a0002c0012t0023g0353 | 3 | HG02257.hp2 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.152-3349G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093752 | ||||||
| chr1:12093809
|
G | A | 10 | a0001c0001t0001g0201a0001c0001t0002g0224a0001c0001t0007g0198others(7): Show | 10 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-3292G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093809 | ||||||
| chr1:12093812
|
T | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3289T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093812 | ||||||
| chr1:12093813
|
G | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3288G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093813 | ||||||
| chr1:12093814
|
T | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3287T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093814 | ||||||
| chr1:12093815
|
A | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3286A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093815 | ||||||
| chr1:12093817
|
T | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3284T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093817 | ||||||
| chr1:12093846
|
C | T | 1 | a0001c0004t0010g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.152-3255C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093846 | ||||||
| chr1:12093875
|
T | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3226T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093875 | ||||||
| chr1:12093882
|
T | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3219T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093882 | ||||||
| chr1:12093895
|
C | A | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.152-3206C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093895 | ||||||
| chr1:12093897
|
C | T | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3204C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093897 | ||||||
| chr1:12093899
|
G | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3202G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093899 | ||||||
| chr1:12093908
|
A | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3193A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093908 | ||||||
| chr1:12093925
|
A | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3176A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093925 | ||||||
| chr1:12093932
|
A | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3169A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093932 | ||||||
| chr1:12093944
|
G | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3157G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093944 | ||||||
| chr1:12093956
|
A | AGTACTGG others(3): Show |
1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3144_152-3143i others(12): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12093956 | |||||
| chr1:12093983
|
T | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3118T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093983 | ||||||
| chr1:12093991
|
G | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3110G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093991 | ||||||
| chr1:12094005
|
G | A | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-3096G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094005 | ||||||
| chr1:12094007
|
T | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3094T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094007 | ||||||
| chr1:12094013
|
C | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3088C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094013 | ||||||
| chr1:12094014
|
C | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3087C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094014 | ||||||
| chr1:12094015
|
T | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3086T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094015 | ||||||
| chr1:12094026
|
T | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3075T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094026 | ||||||
| chr1:12094027
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152-3074C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094027 | ||||||
| chr1:12094058
|
C | CA | 64 | a0001c0001t0001g0035a0001c0001t0001g0050a0001c0001t0001g0058others(61): Show | 64 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.152-3019dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | |||||
| chr1:12094058
|
C | CAA | 23 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(20): Show | 23 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.152-3020_152-3019d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | |||||
| chr1:12094058
|
C | CAAA | 11 | a0001c0001t0006g0248a0001c0002t0001g0053a0001c0002t0001g0314others(8): Show | 11 | HG00738.hp2 HG00741.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-3021_152-3019d others(5): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | |||||
| chr1:12094058
|
C | CAAAA | 11 | a0001c0001t0001g0012a0001c0001t0001g0096a0001c0001t0001g0229others(8): Show | 11 | HG01891.hp1 HG01928.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-3022_152-3019d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | |||||
| chr1:12094058
|
CA | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(102): Show | 105 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.152-3019delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | |||||
| chr1:12094058
|
CAA | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0160a0001c0001t0009g0089others(3): Show | 6 | HG01515.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-3020_152-3019d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | |||||
| chr1:12094229
|
G | T | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-2872G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094229 | ||||||
| chr1:12094342
|
G | A | 1 | a0001c0017t0014g0264 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.152-2759G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094342 | ||||||
| chr1:12094613
|
G | GT | 28 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0075others(25): Show | 28 | HG00140.hp2 HG00642.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.152-2471dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094613 | |||||
| chr1:12094613
|
G | GTT | 23 | a0001c0001t0001g0096a0001c0001t0001g0159a0001c0001t0002g0218others(20): Show | 23 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.152-2472_152-2471d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094613 | |||||
| chr1:12094620
|
TTTTTTTT others(5): Show |
T | 19 | a0001c0001t0001g0103a0001c0001t0001g0246a0001c0001t0001g0247others(16): Show | 19 | HG00558.hp2 HG02040.hp2 HG02895.hp1 others(16): Show |
intron_variant | MODIFIER | c.152-2470_152-2459d others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094620 | |||||
| chr1:12094689
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.152-2412G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094689 | ||||||
| chr1:12094776
|
C | T | 1 | a0009c0030t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.152-2325C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094776 | ||||||
| chr1:12094921
|
C | T | 11 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0001t0009g0234others(8): Show | 11 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-2180C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094921 | ||||||
| chr1:12095014
|
C | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0012others(21): Show | 24 | HG00280.hp2 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.152-2087C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095014 | ||||||
| chr1:12095200
|
T | C | 1 | a0001c0002t0001g0032 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.152-1901T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095200 | ||||||
| chr1:12095231
|
G | A | 9 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-1870G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095231 | ||||||
| chr1:12095289
|
CT | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0012others(22): Show | 25 | HG00280.hp2 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.152-1797delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12095289 | |||||
| chr1:12095433
|
G | A | 2 | a0001c0007t0001g0215a0001c0007t0009g0357 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1668G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095433 | ||||||
| chr1:12095436
|
T | C | 2 | a0001c0007t0001g0215a0001c0007t0009g0357 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1665T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095436 | ||||||
| chr1:12095437
|
G | A | 2 | a0001c0007t0001g0215a0001c0007t0009g0357 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1664G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095437 | ||||||
| chr1:12095442
|
G | C | 2 | a0001c0007t0001g0215a0001c0007t0009g0357 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1659G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095442 | ||||||
| chr1:12095445
|
A | T | 2 | a0001c0007t0001g0215a0001c0007t0009g0357 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1656A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095445 | ||||||
| chr1:12095588
|
T | C | 2 | a0001c0001t0009g0234a0001c0002t0001g0188 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.152-1513T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095588 | ||||||
| chr1:12095640
|
T | C | 1 | a0001c0001t0001g0330 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.152-1461T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095640 | ||||||
| chr1:12095650
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.152-1451C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095650 | ||||||
| chr1:12095654
|
A | G | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.152-1447A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095654 | ||||||
| chr1:12095784
|
A | G | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152-1317A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095784 | ||||||
| chr1:12096175
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.152-926G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096175 | ||||||
| chr1:12096179
|
A | G | 24 | a0001c0001t0001g0038a0001c0001t0001g0048a0001c0001t0001g0138others(21): Show | 24 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.152-922A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096179 | ||||||
| chr1:12096253
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152-848C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096253 | ||||||
| chr1:12096411
|
A | G | 111 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(108): Show | 111 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.152-690A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096411 | ||||||
| chr1:12096424
|
T | TA | 56 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(53): Show | 56 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.152-657dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096424 | |||||
| chr1:12096424
|
TA | T | 127 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.152-657delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096424 | |||||
| chr1:12096424
|
TAA | T | 45 | a0001c0001t0001g0103a0001c0001t0001g0159a0001c0001t0001g0246others(42): Show | 45 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.152-658_152-657del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096424 | |||||
| chr1:12096453
|
A | G | 1 | a0001c0003t0001g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.152-648A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096453 | ||||||
| chr1:12096622
|
A | G | 1 | a0002c0006t0001g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152-479A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096622 | ||||||
| chr1:12096651
|
G | C | 10 | a0001c0001t0001g0096a0001c0001t0008g0163a0001c0002t0001g0255others(7): Show | 10 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-450G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096651 | ||||||
| chr1:12096715
|
C | T | 16 | a0001c0001t0001g0159a0001c0001t0002g0218a0001c0001t0006g0248others(13): Show | 16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-386C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096715 | ||||||
| chr1:12096789
|
T | TCA | 17 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0203others(14): Show | 17 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.152-295_152-294dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096789 | |||||
| chr1:12096789
|
TCA | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0012others(48): Show | 51 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.152-295_152-294del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096789 | |||||
| chr1:12096810
|
T | C | 2 | a0001c0003t0002g0213a0001c0004t0001g0196 | 2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.152-291T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096810 | ||||||
| chr1:12096913
|
G | A | 1 | a0001c0002t0001g0334 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152-188G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096913 | ||||||
| chr1:12096980
|
C | T | 4 | a0001c0001t0006g0148a0001c0001t0006g0150a0001c0002t0002g0147others(1): Show | 4 | HG02622.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-121C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096980 | ||||||
| chr1:12097019
|
A | C | 19 | a0001c0001t0001g0048a0001c0001t0001g0151a0001c0001t0001g0175others(16): Show | 19 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-82A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12097019 | ||||||
| chr1:12097231
|
T | C | 22 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0014others(19): Show | 22 | HG00280.hp2 HG00738.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.268+14T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097231 | ||||||
| chr1:12097264
|
G | C | 12 | a0001c0001t0001g0047a0001c0001t0001g0096a0001c0001t0008g0163others(9): Show | 12 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.268+47G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097264 | ||||||
| chr1:12097683
|
C | T | 2 | a0001c0001t0008g0163a0001c0004t0001g0348 | 2 | HG03942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.268+466C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097683 | ||||||
| chr1:12097749
|
G | C | 1 | a0001c0003t0012g0236 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.268+532G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097749 | ||||||
| chr1:12097824
|
G | A | 9 | a0001c0001t0001g0058a0001c0002t0001g0043a0001c0002t0001g0078others(6): Show | 9 | HG00323.hp2 HG00741.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+607G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097824 | ||||||
| chr1:12097869
|
G | A | 1 | a0001c0002t0001g0265 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.268+652G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097869 | ||||||
| chr1:12097870
|
T | C | 2 | a0001c0003t0003g0225a0001c0003t0003g0226 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.268+653T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097870 | ||||||
| chr1:12098021
|
G | C | 10 | a0001c0001t0001g0201a0001c0001t0006g0359a0001c0001t0007g0198others(7): Show | 10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.268+804G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098021 | ||||||
| chr1:12098237
|
A | C | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.268+1020A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098237 | ||||||
| chr1:12098250
|
T | C | 36 | a0001c0002t0001g0027a0001c0002t0001g0031a0001c0002t0001g0043others(33): Show | 36 | HG00323.hp2 HG00741.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.268+1033T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098250 | ||||||
| chr1:12098255
|
A | G | 13 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0044others(10): Show | 13 | HG02258.hp1 NA18953.hp1 NA18961.hp2 others(10): Show |
intron_variant | MODIFIER | c.268+1038A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098255 | ||||||
| chr1:12098431
|
A | G | 1 | a0001c0001t0004g0177 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.268+1214A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098431 | ||||||
| chr1:12098510
|
C | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.268+1293C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098510 | ||||||
| chr1:12098546
|
T | C | 4 | a0001c0003t0001g0252a0001c0003t0001g0253a0001c0003t0003g0211others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+1329T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098546 | ||||||
| chr1:12098677
|
TA | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0233others(77): Show | 80 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.268+1471delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12098677 | |||||
| chr1:12099014
|
C | G | 3 | a0001c0001t0001g0346a0001c0003t0001g0276a0001c0013t0001g0251 | 3 | NA18967.hp2 NA18989.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.268+1797C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099014 | ||||||
| chr1:12099214
|
AAT | A | 4 | a0001c0001t0001g0233a0001c0009t0001g0358a0001c0009t0001g0360others(1): Show | 4 | HG02145.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+1998_268+1999d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099214 | ||||||
| chr1:12099301
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0233others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.268+2084C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099301 | ||||||
| chr1:12099375
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268+2158C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099375 | ||||||
| chr1:12099763
|
C | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.268+2546C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099763 | ||||||
| chr1:12099851
|
C | G | 5 | a0001c0001t0001g0151a0001c0001t0001g0351a0001c0003t0002g0197others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+2634C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099851 | ||||||
| chr1:12099891
|
G | A | 9 | a0001c0001t0001g0203a0001c0001t0001g0229a0001c0001t0016g0194others(6): Show | 9 | HG02630.hp2 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+2674G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099891 | ||||||
| chr1:12100028
|
G | A | 5 | a0001c0001t0001g0005a0001c0003t0001g0143a0001c0003t0001g0145others(2): Show | 5 | HG00544.hp1 HG02071.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+2811G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100028 | ||||||
| chr1:12100033
|
G | T | 1 | a0001c0007t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268+2816G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100033 | ||||||
| chr1:12100050
|
T | C | 6 | a0001c0001t0001g0233a0001c0002t0001g0166a0001c0004t0010g0202others(3): Show | 6 | HG02145.hp1 HG02258.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+2833T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100050 | ||||||
| chr1:12100124
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(107): Show | 110 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.268+2907A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100124 | ||||||
| chr1:12100388
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.268+3171A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100388 | ||||||
| chr1:12100449
|
TG | T | 32 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0190others(29): Show | 32 | HG01192.hp1 HG02109.hp2 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.268+3233delG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100449 | ||||||
| chr1:12100680
|
C | T | 24 | a0001c0001t0001g0159a0001c0001t0001g0201a0001c0001t0001g0203others(21): Show | 24 | HG01192.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.268+3463C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100680 | ||||||
| chr1:12100789
|
T | G | 1 | a0001c0002t0001g0004 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.268+3572T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100789 | ||||||
| chr1:12100849
|
C | T | 1 | a0001c0003t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.269-3530C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100849 | ||||||
| chr1:12100882
|
G | A | 1 | a0001c0002t0001g0033 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.269-3497G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100882 | ||||||
| chr1:12100889
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0233others(77): Show | 80 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.269-3490G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100889 | ||||||
| chr1:12100956
|
CA | C | 25 | a0001c0001t0001g0173a0001c0001t0002g0172a0001c0001t0002g0218others(22): Show | 25 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.269-3407delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12100956 | |||||
| chr1:12100956
|
CAA | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(134): Show | 137 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.269-3408_269-3407d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12100956 | |||||
| chr1:12101004
|
C | T | 1 | a0001c0002t0001g0095 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.269-3375C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101004 | ||||||
| chr1:12101186
|
A | C | 2 | a0001c0009t0001g0358a0001c0009t0001g0360 | 2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.269-3193A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101186 | ||||||
| chr1:12101416
|
G | C | 1 | a0001c0002t0001g0314 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.269-2963G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101416 | ||||||
| chr1:12101426
|
C | CA | 25 | a0001c0001t0001g0030a0001c0001t0001g0124a0001c0001t0001g0160others(22): Show | 25 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.269-2941dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12101426 | |||||
| chr1:12101426
|
C | CAA | 121 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(118): Show | 121 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.269-2942_269-2941d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12101426 | |||||
| chr1:12101426
|
C | CAAA | 8 | a0001c0001t0001g0203a0001c0001t0001g0229a0001c0001t0016g0194others(5): Show | 8 | HG02630.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-2943_269-2941d others(5): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12101426 | |||||
| chr1:12101561
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0009g0089 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.269-2818G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101561 | ||||||
| chr1:12101609
|
A | G | 1 | a0001c0003t0003g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.269-2770A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101609 | ||||||
| chr1:12101686
|
GT | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0138others(114): Show | 117 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.269-2685delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12101686 | |||||
| chr1:12101695
|
G | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-2684G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101695 | ||||||
| chr1:12101828
|
T | G | 77 | a0001c0001t0006g0150a0001c0002t0001g0004a0001c0002t0001g0010others(74): Show | 77 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.269-2551T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101828 | ||||||
| chr1:12101863
|
C | T | 7 | a0001c0001t0001g0093a0001c0001t0001g0261a0001c0001t0001g0271others(4): Show | 7 | HG01257.hp1 HG02280.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-2516C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101863 | ||||||
| chr1:12101964
|
C | T | 23 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(20): Show | 23 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.269-2415C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101964 | ||||||
| chr1:12102289
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.269-2090G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102289 | ||||||
| chr1:12102290
|
C | T | 1 | a0002c0016t0004g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.269-2089C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102290 | ||||||
| chr1:12102301
|
G | A | 4 | a0001c0001t0006g0150a0001c0009t0001g0358a0001c0009t0001g0360others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-2078G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102301 | ||||||
| chr1:12102349
|
T | C | 1 | a0002c0005t0005g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.269-2030T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102349 | ||||||
| chr1:12102422
|
C | T | 1 | a0001c0003t0002g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.269-1957C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102422 | ||||||
| chr1:12102512
|
CA | C | 6 | a0001c0001t0001g0201a0001c0001t0007g0198a0001c0003t0001g0091others(3): Show | 6 | HG01192.hp1 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-1866delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102512 | ||||||
| chr1:12102535
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0009g0089a0001c0003t0002g0214 | 3 | HG03041.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.269-1844G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102535 | ||||||
| chr1:12102610
|
C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.269-1769C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102610 | ||||||
| chr1:12102778
|
G | A | 101 | a0001c0002t0001g0004a0001c0002t0001g0010a0001c0002t0001g0015others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.269-1601G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102778 | ||||||
| chr1:12102977
|
C | T | 7 | a0001c0001t0001g0229a0001c0001t0016g0194a0001c0003t0003g0208others(4): Show | 7 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-1402C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102977 | ||||||
| chr1:12102999
|
G | T | 2 | a0001c0007t0001g0215a0001c0007t0009g0357 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.269-1380G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102999 | ||||||
| chr1:12103130
|
G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.269-1249G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103130 | ||||||
| chr1:12103224
|
C | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-1155C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103224 | ||||||
| chr1:12103231
|
G | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-1148G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103231 | ||||||
| chr1:12103303
|
C | T | 1 | a0001c0004t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.269-1076C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103303 | ||||||
| chr1:12103311
|
C | T | 1 | a0001c0001t0006g0150 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.269-1068C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103311 | ||||||
| chr1:12103354
|
TA | T | 32 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(29): Show | 32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.269-1012delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12103354 | |||||
| chr1:12103496
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0005g0355a0001c0003t0010g0259others(1): Show | 4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-883G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103496 | ||||||
| chr1:12103534
|
A | G | 123 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0190others(120): Show | 123 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.269-845A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103534 | ||||||
| chr1:12103582
|
G | A | 10 | a0001c0001t0001g0035a0001c0001t0001g0190a0001c0001t0001g0191others(7): Show | 10 | HG02080.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-797G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103582 | ||||||
| chr1:12103626
|
T | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-753T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103626 | ||||||
| chr1:12103644
|
AT | A | 23 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(20): Show | 23 | HG00642.hp2 HG01168.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.269-725delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12103644 | |||||
| chr1:12103662
|
C | T | 106 | a0001c0002t0001g0004a0001c0002t0001g0010a0001c0002t0001g0015others(103): Show | 106 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.269-717C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103662 | ||||||
| chr1:12103717
|
A | G | 1 | a0001c0003t0005g0092 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.269-662A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103717 | ||||||
| chr1:12103773
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0005g0355a0001c0003t0010g0259others(1): Show | 4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-606G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103773 | ||||||
| chr1:12103961
|
A | G | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.269-418A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103961 | ||||||
| chr1:12104014
|
T | C | 194 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(191): Show | 194 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.269-365T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104014 | ||||||
| chr1:12104021
|
C | T | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(140): Show | 143 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.269-358C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104021 | ||||||
| chr1:12104022
|
C | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-357C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104022 | ||||||
| chr1:12104033
|
C | G | 1 | a0001c0002t0001g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.269-346C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104033 | ||||||
| chr1:12104033
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0012others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.269-346C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104033 | ||||||
| chr1:12104080
|
A | G | 143 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(140): Show | 143 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.269-299A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104080 | ||||||
| chr1:12104153
|
A | G | 5 | a0001c0001t0002g0218a0001c0001t0007g0192a0001c0001t0007g0193others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.269-226A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104153 | ||||||
| chr1:12104285
|
G | A | 1 | a0001c0001t0007g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.269-94G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104285 | ||||||
| chr1:12104334
|
G | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-45G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104334 | ||||||
| chr1:12104575
|
T | C | 1 | a0001c0001t0008g0362 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.421+44T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104575 | ||||||
| chr1:12104617
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.421+86C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104617 | ||||||
| chr1:12104618
|
G | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+87G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104618 | ||||||
| chr1:12104633
|
G | T | 1 | a0001c0004t0025g0356 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.421+102G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104633 | ||||||
| chr1:12104714
|
C | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0006g0150others(2): Show | 5 | HG02257.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+183C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104714 | ||||||
| chr1:12104751
|
C | G | 1 | a0002c0016t0004g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.421+220C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104751 | ||||||
| chr1:12104818
|
C | A | 5 | a0001c0001t0002g0218a0001c0001t0007g0192a0001c0001t0007g0193others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+287C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104818 | ||||||
| chr1:12104921
|
G | A | 1 | a0001c0009t0001g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.421+390G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104921 | ||||||
| chr1:12104980
|
T | C | 129 | a0001c0001t0001g0138a0001c0001t0001g0201a0001c0001t0001g0203others(126): Show | 129 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.421+449T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104980 | ||||||
| chr1:12104981
|
C | T | 1 | a0001c0002t0001g0134 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.421+450C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104981 | ||||||
| chr1:12105007
|
C | T | 2 | a0002c0005t0001g0227a0002c0005t0005g0232 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.421+476C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105007 | ||||||
| chr1:12105034
|
A | AC | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0002g0172others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+504dupC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105034 | |||||
| chr1:12105073
|
G | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+542G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105073 | ||||||
| chr1:12105191
|
C | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+660C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105191 | ||||||
| chr1:12105308
|
G | A | 4 | a0001c0001t0001g0159a0001c0001t0005g0355a0001c0003t0010g0259others(1): Show | 4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+777G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105308 | ||||||
| chr1:12105316
|
C | G | 3 | a0001c0003t0002g0197a0001c0003t0005g0092a0002c0006t0003g0149 | 3 | HG03130.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.421+785C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105316 | ||||||
| chr1:12105426
|
C | T | 3 | a0001c0003t0001g0237a0001c0003t0002g0200a0002c0006t0001g0222 | 3 | HG01243.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.421+895C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105426 | ||||||
| chr1:12105527
|
C | CCT | 3 | a0001c0004t0002g0169a0001c0013t0001g0280a0002c0011t0004g0221 | 3 | HG02717.hp2 NA19082.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.421+1018_421+1019d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | |||||
| chr1:12105527
|
C | CCTCT | 21 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0044others(18): Show | 21 | HG00642.hp2 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.421+1016_421+1019d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | |||||
| chr1:12105527
|
C | CCTCTCT | 4 | a0001c0001t0001g0013a0001c0001t0001g0342a0002c0012t0001g0178others(1): Show | 4 | HG03471.hp1 NA18990.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+1014_421+1019d others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | |||||
| chr1:12105527
|
CCTCT | C | 7 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0065others(4): Show | 7 | HG00323.hp1 HG01261.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+1016_421+1019d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | |||||
| chr1:12105527
|
CCTCTCTC others(1): Show |
C | 9 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0233others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.421+1012_421+1019d others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | |||||
| chr1:12105547
|
T | A | 92 | a0001c0002t0001g0004a0001c0002t0001g0015a0001c0002t0001g0016others(89): Show | 92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1016T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105547 | ||||||
| chr1:12105558
|
C | G | 1 | a0001c0001t0008g0362 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.421+1027C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105558 | ||||||
| chr1:12105559
|
A | T | 92 | a0001c0002t0001g0004a0001c0002t0001g0015a0001c0002t0001g0016others(89): Show | 92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1028A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105559 | ||||||
| chr1:12105566
|
C | G | 92 | a0001c0002t0001g0004a0001c0002t0001g0015a0001c0002t0001g0016others(89): Show | 92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1035C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105566 | ||||||
| chr1:12105570
|
G | C | 92 | a0001c0002t0001g0004a0001c0002t0001g0015a0001c0002t0001g0016others(89): Show | 92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1039G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105570 | ||||||
| chr1:12105571
|
T | A | 92 | a0001c0002t0001g0004a0001c0002t0001g0015a0001c0002t0001g0016others(89): Show | 92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1040T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105571 | ||||||
| chr1:12105573
|
T | A | 92 | a0001c0002t0001g0004a0001c0002t0001g0015a0001c0002t0001g0016others(89): Show | 92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1042T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105573 | ||||||
| chr1:12105573
|
T | TCA | 6 | a0001c0001t0001g0151a0001c0001t0001g0351a0001c0001t0002g0218others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+1066_421+1067d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105573 | |||||
| chr1:12105573
|
T | TCACA | 178 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.421+1064_421+1067d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105573 | |||||
| chr1:12105573
|
T | TCACACA | 24 | a0001c0001t0001g0093a0001c0001t0001g0125a0001c0001t0001g0126others(21): Show | 24 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.421+1062_421+1067d others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105573 | |||||
| chr1:12105573
|
TCA | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+1066_421+1067d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105573 | |||||
| chr1:12105939
|
C | CA | 52 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0020others(49): Show | 52 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(49): Show |
intron_variant | MODIFIER | c.421+1427dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105939 | |||||
| chr1:12105939
|
CA | C | 8 | a0001c0002t0001g0078a0001c0003t0001g0249a0001c0003t0001g0252others(5): Show | 8 | HG00323.hp2 HG01515.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+1427delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105939 | |||||
| chr1:12105953
|
A | G | 1 | a0002c0010t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.421+1422A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105953 | ||||||
| chr1:12106040
|
G | A | 2 | a0001c0007t0001g0215a0001c0007t0009g0357 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.421+1509G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106040 | ||||||
| chr1:12106097
|
A | C | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.421+1566A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106097 | ||||||
| chr1:12106112
|
C | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+1581C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106112 | ||||||
| chr1:12106149
|
A | G | 8 | a0001c0002t0001g0166a0001c0004t0001g0036a0001c0004t0010g0202others(5): Show | 8 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+1618A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106149 | ||||||
| chr1:12106309
|
G | T | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0233others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.421+1778G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106309 | ||||||
| chr1:12106442
|
C | T | 6 | a0001c0001t0001g0096a0001c0001t0001g0250a0001c0001t0001g0272others(3): Show | 6 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+1911C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106442 | ||||||
| chr1:12106798
|
G | T | 129 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0201others(126): Show | 129 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.421+2267G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106798 | ||||||
| chr1:12106808
|
G | A | 2 | a0001c0007t0001g0215a0001c0007t0009g0357 | 2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.421+2277G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106808 | ||||||
| chr1:12106853
|
C | T | 3 | a0001c0004t0001g0088a0001c0004t0002g0169a0002c0011t0004g0221 | 3 | HG02717.hp2 HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.421+2322C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106853 | ||||||
| chr1:12107026
|
C | A | 12 | a0001c0001t0001g0159a0001c0001t0005g0355a0001c0002t0001g0166others(9): Show | 12 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.421+2495C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107026 | ||||||
| chr1:12107060
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.422-2506A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107060 | ||||||
| chr1:12107084
|
C | T | 12 | a0001c0001t0001g0159a0001c0001t0005g0355a0001c0002t0001g0166others(9): Show | 12 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-2482C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107084 | ||||||
| chr1:12107091
|
A | G | 1 | a0001c0002t0001g0016 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.422-2475A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107091 | ||||||
| chr1:12107109
|
TA | T | 3 | a0001c0002t0001g0166a0001c0004t0001g0036a0001c0004t0010g0202 | 3 | HG02258.hp2 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.422-2456delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107109 | ||||||
| chr1:12107122
|
C | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.422-2444C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107122 | ||||||
| chr1:12107169
|
C | T | 1 | a0001c0002t0001g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.422-2397C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107169 | ||||||
| chr1:12107179
|
G | A | 12 | a0001c0001t0001g0173a0001c0003t0001g0167a0001c0003t0001g0219others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-2387G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107179 | ||||||
| chr1:12107210
|
T | C | 33 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(30): Show | 33 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-2356T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107210 | ||||||
| chr1:12107322
|
G | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0124a0001c0001t0001g0160others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-2244G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107322 | ||||||
| chr1:12107335
|
T | C | 193 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(190): Show | 193 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.422-2231T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107335 | ||||||
| chr1:12107359
|
C | T | 12 | a0001c0001t0001g0173a0001c0003t0001g0167a0001c0003t0001g0219others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-2207C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107359 | ||||||
| chr1:12107374
|
G | A | 6 | a0001c0002t0001g0043a0001c0002t0001g0078a0001c0002t0001g0128others(3): Show | 6 | HG00323.hp2 HG00741.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-2192G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107374 | ||||||
| chr1:12107394
|
C | CA | 25 | a0001c0001t0001g0173a0001c0001t0001g0190a0001c0001t0001g0191others(22): Show | 25 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.422-2162dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12107394 | |||||
| chr1:12107456
|
G | A | 1 | a0001c0001t0006g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.422-2110G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107456 | ||||||
| chr1:12107569
|
A | AAATATAC others(1): Show |
187 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(184): Show | 187 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.422-1996_422-1995i others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12107569 | |||||
| chr1:12107702
|
AC | A | 128 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0201others(125): Show | 128 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.422-1861delC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12107702 | |||||
| chr1:12107802
|
C | T | 2 | a0001c0002t0001g0166a0001c0004t0001g0036 | 2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.422-1764C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107802 | ||||||
| chr1:12107804
|
C | G | 1 | a0001c0003t0001g0064 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.422-1762C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107804 | ||||||
| chr1:12107822
|
C | A | 1 | a0001c0001t0006g0150 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.422-1744C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107822 | ||||||
| chr1:12107942
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.422-1624C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107942 | ||||||
| chr1:12108020
|
C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422-1546C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108020 | ||||||
| chr1:12108026
|
C | A | 1 | a0001c0001t0001g0338 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.422-1540C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108026 | ||||||
| chr1:12108034
|
C | T | 33 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(30): Show | 33 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-1532C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108034 | ||||||
| chr1:12108074
|
A | ATT | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0233others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-1486_422-1485d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | |||||
| chr1:12108074
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0244 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.422-1485_422-1484i others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | |||||
| chr1:12108074
|
A | ATTTTTTT others(5): Show |
9 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0106others(6): Show | 9 | HG02258.hp1 HG02683.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-1485_422-1484i others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | |||||
| chr1:12108074
|
A | ATTTTTTT others(6): Show |
11 | a0001c0001t0001g0044a0001c0001t0001g0136a0001c0001t0001g0273others(8): Show | 11 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-1485_422-1484i others(15): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | |||||
| chr1:12108074
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0013 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.422-1485_422-1484i others(16): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | |||||
| chr1:12108074
|
A | ATTTTTTT others(15): Show |
1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422-1485_422-1484i others(24): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | |||||
| chr1:12108078
|
T | A | 8 | a0001c0001t0001g0114a0001c0001t0006g0148a0001c0001t0006g0248others(5): Show | 8 | HG00280.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-1488T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108078 | ||||||
| chr1:12108081
|
T | A | 1 | a0001c0001t0001g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.422-1485T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108081 | ||||||
| chr1:12108082
|
A | T | 33 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(30): Show | 33 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-1484A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108082 | ||||||
| chr1:12108088
|
T | A | 13 | a0001c0001t0001g0068a0001c0001t0001g0138a0001c0001t0001g0201others(10): Show | 13 | HG01192.hp1 HG01934.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-1478T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108088 | ||||||
| chr1:12108089
|
T | A | 9 | a0001c0001t0001g0173a0001c0001t0001g0180a0001c0001t0001g0242others(6): Show | 9 | HG02145.hp2 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-1477T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108089 | ||||||
| chr1:12108269
|
G | T | 33 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(30): Show | 33 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-1297G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108269 | ||||||
| chr1:12108272
|
GT | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.422-1291delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108272 | |||||
| chr1:12108301
|
A | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422-1265A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108301 | ||||||
| chr1:12108341
|
G | C | 2 | a0001c0001t0001g0250a0001c0001t0001g0296 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.422-1225G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108341 | ||||||
| chr1:12108376
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.422-1190C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108376 | ||||||
| chr1:12108401
|
T | A | 173 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(170): Show | 173 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.422-1165T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108401 | ||||||
| chr1:12108466
|
C | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.422-1100C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108466 | ||||||
| chr1:12108527
|
G | A | 173 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(170): Show | 173 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.422-1039G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108527 | ||||||
| chr1:12108532
|
T | C | 1 | a0001c0003t0005g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-1034T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108532 | ||||||
| chr1:12108669
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.422-897C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108669 | ||||||
| chr1:12108670
|
G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422-896G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108670 | ||||||
| chr1:12108799
|
T | C | 32 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(29): Show | 32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.422-767T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108799 | ||||||
| chr1:12108873
|
G | A | 1 | a0001c0003t0005g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-693G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108873 | ||||||
| chr1:12108897
|
C | T | 10 | a0001c0001t0001g0138a0001c0001t0001g0203a0001c0001t0001g0229others(7): Show | 10 | HG02647.hp2 HG02818.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.422-669C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108897 | ||||||
| chr1:12108903
|
G | C | 1 | a0002c0006t0001g0347 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.422-663G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108903 | ||||||
| chr1:12108957
|
T | C | 4 | a0001c0001t0001g0159a0001c0001t0005g0355a0001c0003t0010g0259others(1): Show | 4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-609T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108957 | ||||||
| chr1:12109037
|
C | T | 3 | a0001c0001t0001g0005a0002c0005t0001g0051a0002c0005t0001g0084 | 3 | HG00544.hp1 HG02071.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.422-529C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109037 | ||||||
| chr1:12109196
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.422-370A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109196 | ||||||
| chr1:12109238
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.422-328G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109238 | ||||||
| chr1:12109280
|
G | A | 1 | a0001c0001t0002g0224 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.422-286G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109280 | ||||||
| chr1:12109333
|
G | A | 9 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0233others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-233G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109333 | ||||||
| chr1:12109343
|
C | T | 129 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0201others(126): Show | 129 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.422-223C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109343 | ||||||
| chr1:12109559
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | splice_region_variant&intron_variant | LOW | c.422-7C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109559 | ||||||
| chr1:12109920
|
C | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.513-121C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 5/14 | chr1 | 12109920 | ||||||
| chr1:12109931
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0124a0001c0001t0001g0160others(1): Show | 4 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-110G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 5/14 | chr1 | 12109931 | ||||||
| chr1:12109938
|
A | G | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0233others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-103A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 5/14 | chr1 | 12109938 | ||||||
| chr1:12109951
|
C | T | 1 | a0001c0001t0007g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.513-90C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 5/14 | chr1 | 12109951 | ||||||
| chr1:12110230
|
C | T | 19 | a0001c0001t0001g0138a0001c0001t0001g0201a0001c0001t0001g0203others(16): Show | 19 | HG01192.hp1 HG02451.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.676+26C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110230 | ||||||
| chr1:12110231
|
G | A | 32 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(29): Show | 32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+27G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110231 | ||||||
| chr1:12110368
|
G | A | 8 | a0001c0002t0001g0166a0001c0004t0001g0036a0001c0004t0010g0202others(5): Show | 8 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.676+164G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110368 | ||||||
| chr1:12110368
|
G | T | 32 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(29): Show | 32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+164G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110368 | ||||||
| chr1:12110437
|
C | G | 32 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(29): Show | 32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+233C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110437 | ||||||
| chr1:12110519
|
G | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.676+315G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110519 | ||||||
| chr1:12110629
|
G | A | 1 | a0001c0004t0001g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.676+425G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110629 | ||||||
| chr1:12110678
|
C | A | 32 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(29): Show | 32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+474C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110678 | ||||||
| chr1:12110826
|
G | A | 2 | a0002c0005t0002g0235a0002c0006t0001g0222 | 2 | HG01243.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.676+622G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110826 | ||||||
| chr1:12110866
|
GGGA | G | 161 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(158): Show | 161 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.676+666_676+668del others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 12110866 | |||||
| chr1:12110917
|
C | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.676+713C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110917 | ||||||
| chr1:12110935
|
C | T | 7 | a0001c0001t0001g0151a0001c0001t0001g0351a0001c0001t0002g0218others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.676+731C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110935 | ||||||
| chr1:12110955
|
T | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.676+751T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110955 | ||||||
| chr1:12111028
|
G | A | 7 | a0001c0001t0001g0151a0001c0001t0001g0351a0001c0001t0002g0218others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.676+824G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111028 | ||||||
| chr1:12111135
|
C | T | 2 | a0002c0012t0001g0178a0002c0012t0023g0353 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.677-763C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111135 | ||||||
| chr1:12111136
|
G | T | 1 | a0001c0004t0010g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.677-762G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111136 | ||||||
| chr1:12111154
|
T | A | 1 | a0001c0001t0004g0177 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.677-744T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111154 | ||||||
| chr1:12111277
|
G | A | 31 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(28): Show | 31 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.677-621G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111277 | ||||||
| chr1:12111300
|
G | A | 1 | a0002c0006t0001g0021 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.677-598G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111300 | ||||||
| chr1:12111328
|
C | T | 5 | a0001c0003t0012g0236a0001c0007t0015g0189a0002c0005t0001g0059others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-570C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111328 | ||||||
| chr1:12111383
|
T | C | 20 | a0001c0001t0001g0138a0001c0001t0001g0201a0001c0001t0001g0203others(17): Show | 20 | HG01192.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.677-515T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111383 | ||||||
| chr1:12111461
|
C | T | 24 | a0001c0002t0001g0016a0001c0002t0001g0022a0001c0002t0001g0027others(21): Show | 24 | HG00438.hp2 HG00597.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.677-437C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111461 | ||||||
| chr1:12111487
|
C | G | 1 | a0001c0001t0001g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.677-411C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111487 | ||||||
| chr1:12111519
|
A | C | 1 | a0001c0002t0001g0095 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.677-379A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111519 | ||||||
| chr1:12111621
|
A | G | 141 | a0001c0001t0001g0039a0001c0001t0001g0151a0001c0001t0001g0159others(138): Show | 141 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.677-277A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111621 | ||||||
| chr1:12111673
|
G | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.677-225G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111673 | ||||||
| chr1:12111724
|
C | T | 1 | a0001c0003t0001g0123 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.677-174C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111724 | ||||||
| chr1:12112026
|
G | A | 1 | a0003c0008t0017g0009 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.793+12G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112026 | ||||||
| chr1:12112068
|
C | T | 4 | a0001c0001t0001g0138a0001c0001t0007g0198a0001c0001t0009g0089others(1): Show | 4 | HG02717.hp1 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+54C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112068 | ||||||
| chr1:12112091
|
C | T | 3 | a0001c0002t0001g0166a0001c0004t0001g0036a0001c0004t0010g0202 | 3 | HG02258.hp2 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.793+77C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112091 | ||||||
| chr1:12112337
|
C | T | 8 | a0001c0001t0001g0203a0001c0001t0001g0229a0001c0001t0016g0194others(5): Show | 8 | HG02647.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.793+323C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112337 | ||||||
| chr1:12112566
|
A | T | 1 | a0001c0002t0001g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.793+552A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112566 | ||||||
| chr1:12112567
|
T | A | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.793+553T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112567 | ||||||
| chr1:12112742
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0144 | 2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.793+728G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112742 | ||||||
| chr1:12112790
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.793+776C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112790 | ||||||
| chr1:12112810
|
G | T | 32 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(29): Show | 32 | HG00642.hp2 HG01168.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.793+796G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112810 | ||||||
| chr1:12112990
|
T | C | 1 | a0001c0004t0001g0186 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.793+976T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112990 | ||||||
| chr1:12113040
|
A | C | 1 | a0001c0003t0005g0092 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.793+1026A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113040 | ||||||
| chr1:12113267
|
C | T | 1 | a0001c0003t0001g0064 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.793+1253C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113267 | ||||||
| chr1:12113304
|
A | G | 63 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(60): Show | 63 | HG00642.hp2 HG01255.hp2 HG01884.hp1 others(60): Show |
intron_variant | MODIFIER | c.793+1290A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113304 | ||||||
| chr1:12113316
|
C | T | 10 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0201others(7): Show | 10 | HG01192.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+1302C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113316 | ||||||
| chr1:12113389
|
G | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(17): Show | 20 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.793+1375G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113389 | ||||||
| chr1:12113484
|
T | TGA | 24 | a0001c0001t0001g0159a0001c0001t0001g0173a0001c0001t0001g0233others(21): Show | 24 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.793+1481_793+1482d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12113484 | |||||
| chr1:12113599
|
G | GAC | 361 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(358): Show | 361 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.793+1586_793+1587i others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12113599 | |||||
| chr1:12113604
|
T | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.793+1590T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113604 | ||||||
| chr1:12113652
|
A | G | 1 | a0001c0003t0001g0024 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.793+1638A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113652 | ||||||
| chr1:12113663
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0351 | 2 | HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.793+1649G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113663 | ||||||
| chr1:12113685
|
CAGAA | C | 149 | a0001c0001t0001g0005a0001c0001t0001g0074a0001c0001t0001g0079others(146): Show | 149 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.793+1675_793+1678d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12113685 | |||||
| chr1:12113731
|
C | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(19): Show | 22 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.793+1717C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113731 | ||||||
| chr1:12113781
|
GAGAC | G | 20 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(17): Show | 20 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.793+1775_793+1778d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12113781 | |||||
| chr1:12113807
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.794-1770C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113807 | ||||||
| chr1:12113981
|
A | C | 3 | a0001c0001t0001g0138a0001c0001t0006g0150a0001c0001t0009g0089 | 3 | HG02622.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.794-1596A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113981 | ||||||
| chr1:12114043
|
G | A | 23 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(20): Show | 23 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.794-1534G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114043 | ||||||
| chr1:12114081
|
C | G | 3 | a0001c0001t0006g0359a0001c0002t0001g0188a0002c0005t0001g0094 | 3 | HG02109.hp2 HG02559.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.794-1496C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114081 | ||||||
| chr1:12114133
|
C | T | 2 | a0001c0001t0006g0359a0001c0002t0001g0188 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.794-1444C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114133 | ||||||
| chr1:12114173
|
C | T | 1 | a0001c0002t0018g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.794-1404C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114173 | ||||||
| chr1:12114296
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.794-1281G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114296 | ||||||
| chr1:12114336
|
G | A | 2 | a0001c0001t0006g0359a0001c0002t0001g0188 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.794-1241G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114336 | ||||||
| chr1:12114569
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.794-1008C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114569 | ||||||
| chr1:12114588
|
A | G | 1 | a0001c0001t0001g0329 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.794-989A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114588 | ||||||
| chr1:12114612
|
G | A | 6 | a0001c0001t0001g0122a0001c0001t0001g0187a0001c0001t0001g0275others(3): Show | 6 | NA18939.hp2 NA18953.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-965G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114612 | ||||||
| chr1:12114636
|
A | G | 5 | a0001c0002t0001g0010a0001c0002t0001g0065a0001c0002t0001g0130others(2): Show | 5 | HG00323.hp1 HG01358.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-941A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114636 | ||||||
| chr1:12114694
|
C | CT | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(102): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.794-854dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | |||||
| chr1:12114694
|
C | CTT | 33 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0086others(30): Show | 33 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.794-855_794-854dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | |||||
| chr1:12114694
|
CT | C | 12 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0001g0233others(9): Show | 12 | HG01192.hp1 HG01884.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.794-854delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | |||||
| chr1:12114694
|
CTT | C | 19 | a0001c0001t0001g0159a0001c0001t0001g0173a0001c0001t0005g0355others(16): Show | 19 | HG02145.hp2 HG02257.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.794-855_794-854del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | |||||
| chr1:12114694
|
CTTTTTTT | C | 18 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0245others(15): Show | 18 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.794-860_794-854del others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | |||||
| chr1:12114694
|
CTTTTTTT others(1): Show |
C | 109 | a0001c0001t0001g0005a0001c0001t0001g0074a0001c0001t0001g0079others(106): Show | 109 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.794-861_794-854del others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | |||||
| chr1:12114694
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0006g0359a0001c0002t0001g0188 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.794-863_794-854del others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | |||||
| chr1:12114694
|
CTTTTTTT others(4): Show |
C | 23 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(20): Show | 23 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.794-864_794-854del others(11): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | |||||
| chr1:12114694
|
CTTTTTTT others(7): Show |
C | 6 | a0001c0003t0002g0197a0001c0009t0001g0358a0001c0009t0001g0360others(3): Show | 6 | HG01106.hp2 HG02145.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-867_794-854del others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | |||||
| chr1:12114795
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.794-782G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114795 | ||||||
| chr1:12114850
|
A | C | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.794-727A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114850 | ||||||
| chr1:12114982
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.794-595C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114982 | ||||||
| chr1:12115077
|
T | TATCACCC others(2903): Show |
1 | a0001c0001t0001g0258 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.794-487_794-486ins others(2910): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12115077 | |||||
| chr1:12115094
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.794-483C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115094 | ||||||
| chr1:12115348
|
C | T | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.794-229C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115348 | ||||||
| chr1:12115400
|
C | A | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-177C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115400 | ||||||
| chr1:12115403
|
G | A | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-174G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115403 | ||||||
| chr1:12115404
|
C | G | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-173C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115404 | ||||||
| chr1:12115406
|
G | T | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-171G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115406 | ||||||
| chr1:12115407
|
A | C | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-170A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115407 | ||||||
| chr1:12115408
|
A | G | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-169A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115408 | ||||||
| chr1:12115409
|
T | C | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-168T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115409 | ||||||
| chr1:12115410
|
T | G | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-167T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115410 | ||||||
| chr1:12115411
|
A | T | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-166A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115411 | ||||||
| chr1:12115412
|
T | G | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-165T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115412 | ||||||
| chr1:12115761
|
A | G | 160 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(157): Show | 160 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.946+32A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12115761 | ||||||
| chr1:12115828
|
C | CTA | 8 | a0001c0001t0001g0159a0001c0001t0001g0203a0001c0001t0005g0355others(5): Show | 8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.946+100_946+101dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 12115828 | |||||
| chr1:12115974
|
G | A | 5 | a0001c0002t0001g0015a0001c0002t0001g0033a0001c0002t0001g0045others(2): Show | 5 | HG02040.hp1 HG02071.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.946+245G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12115974 | ||||||
| chr1:12116017
|
T | C | 1 | a0001c0014t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.946+288T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116017 | ||||||
| chr1:12116131
|
G | A | 1 | a0001c0001t0007g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.946+402G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116131 | ||||||
| chr1:12116142
|
C | T | 5 | a0001c0001t0001g0229a0001c0001t0016g0194a0001c0003t0003g0225others(2): Show | 5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.946+413C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116142 | ||||||
| chr1:12116181
|
A | G | 22 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0044others(19): Show | 22 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.946+452A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116181 | ||||||
| chr1:12116200
|
C | T | 22 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0044others(19): Show | 22 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.946+471C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116200 | ||||||
| chr1:12116224
|
A | G | 4 | a0001c0001t0001g0159a0001c0001t0005g0355a0001c0003t0010g0259others(1): Show | 4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+495A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116224 | ||||||
| chr1:12116263
|
G | A | 7 | a0001c0001t0001g0028a0001c0001t0001g0050a0001c0001t0001g0286others(4): Show | 7 | HG02056.hp2 NA18970.hp2 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.946+534G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116263 | ||||||
| chr1:12116282
|
C | T | 2 | a0001c0004t0001g0135a0002c0010t0001g0146 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.946+553C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116282 | ||||||
| chr1:12116372
|
G | A | 2 | a0001c0001t0007g0192a0001c0001t0007g0216 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.946+643G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116372 | ||||||
| chr1:12116491
|
G | C | 1 | a0002c0006t0001g0347 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.946+762G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116491 | ||||||
| chr1:12116539
|
G | A | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.946+810G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116539 | ||||||
| chr1:12116591
|
A | G | 1 | a0001c0003t0001g0023 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.946+862A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116591 | ||||||
| chr1:12116594
|
A | T | 1 | a0001c0004t0002g0169 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.946+865A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116594 | ||||||
| chr1:12116613
|
C | G | 2 | a0001c0025t0001g0231a0002c0005t0005g0230 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.946+884C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116613 | ||||||
| chr1:12116718
|
T | G | 2 | a0001c0004t0001g0088a0002c0011t0004g0221 | 2 | HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.946+989T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116718 | ||||||
| chr1:12116759
|
C | A | 1 | a0001c0003t0001g0185 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.946+1030C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116759 | ||||||
| chr1:12116814
|
C | A | 1 | a0001c0003t0001g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.946+1085C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116814 | ||||||
| chr1:12116857
|
C | T | 1 | a0001c0003t0012g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.946+1128C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116857 | ||||||
| chr1:12116999
|
C | T | 4 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0001g0166others(1): Show | 4 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+1270C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116999 | ||||||
| chr1:12117038
|
T | C | 11 | a0001c0001t0001g0151a0001c0001t0001g0351a0001c0001t0002g0218others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.946+1309T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117038 | ||||||
| chr1:12117232
|
G | A | 1 | a0001c0003t0001g0288 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.946+1503G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117232 | ||||||
| chr1:12117277
|
T | C | 2 | a0001c0001t0001g0100a0001c0002t0001g0055 | 2 | HG01069.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.946+1548T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117277 | ||||||
| chr1:12117324
|
C | T | 1 | a0001c0003t0005g0092 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.946+1595C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117324 | ||||||
| chr1:12117423
|
G | A | 1 | a0001c0004t0001g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.946+1694G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117423 | ||||||
| chr1:12117442
|
A | G | 1 | a0001c0003t0001g0252 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.946+1713A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117442 | ||||||
| chr1:12117475
|
C | A | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.946+1746C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117475 | ||||||
| chr1:12117693
|
T | C | 10 | a0001c0001t0002g0224a0001c0007t0015g0189a0001c0009t0001g0358others(7): Show | 10 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.946+1964T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117693 | ||||||
| chr1:12117713
|
G | A | 2 | a0001c0001t0011g0282a0001c0004t0001g0266 | 2 | HG00609.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.946+1984G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117713 | ||||||
| chr1:12117744
|
C | T | 1 | a0001c0007t0009g0357 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.946+2015C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117744 | ||||||
| chr1:12117777
|
G | A | 9 | a0001c0001t0001g0058a0001c0001t0001g0106a0001c0003t0001g0102others(6): Show | 9 | HG01071.hp2 HG01255.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.946+2048G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117777 | ||||||
| chr1:12117843
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.946+2114C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117843 | ||||||
| chr1:12118106
|
T | TC | 47 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0001g0103others(44): Show | 47 | HG00438.hp2 HG00609.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.946+2385dupC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 12118106 | |||||
| chr1:12118111
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.946+2382C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118111 | ||||||
| chr1:12118112
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.946+2383C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118112 | ||||||
| chr1:12118113
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.946+2384C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118113 | ||||||
| chr1:12118117
|
C | A | 30 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0114others(27): Show | 30 | HG00280.hp2 HG01106.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.946+2388C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118117 | ||||||
| chr1:12118220
|
T | TA | 31 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0114others(28): Show | 31 | HG00280.hp2 HG01106.hp2 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.946+2491_946+2492i others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118220 | ||||||
| chr1:12118221
|
G | A | 31 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0114others(28): Show | 31 | HG00280.hp2 HG01106.hp2 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.946+2492G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118221 | ||||||
| chr1:12118391
|
G | A | 7 | a0001c0007t0015g0189a0002c0005t0001g0059a0002c0005t0002g0235others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.946+2662G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118391 | ||||||
| chr1:12118591
|
G | C | 16 | a0001c0001t0001g0159a0002c0005t0001g0059a0002c0005t0001g0227others(13): Show | 16 | HG01106.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.946+2862G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118591 | ||||||
| chr1:12118597
|
A | G | 16 | a0001c0001t0001g0159a0002c0005t0001g0059a0002c0005t0001g0227others(13): Show | 16 | HG01106.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.946+2868A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118597 | ||||||
| chr1:12118778
|
A | C | 2 | a0001c0001t0006g0150a0001c0003t0010g0195 | 2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.946+3049A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118778 | ||||||
| chr1:12118802
|
G | A | 2 | a0001c0001t0001g0159a0002c0006t0001g0222 | 2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.946+3073G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118802 | ||||||
| chr1:12118850
|
T | G | 17 | a0001c0001t0001g0159a0002c0005t0001g0059a0002c0005t0001g0227others(14): Show | 17 | HG01106.hp2 HG01243.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.946+3121T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118850 | ||||||
| chr1:12118870
|
C | G | 1 | a0001c0004t0025g0356 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.946+3141C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118870 | ||||||
| chr1:12118876
|
T | C | 1 | a0001c0002t0001g0018 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.946+3147T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118876 | ||||||
| chr1:12119115
|
G | A | 2 | a0002c0005t0002g0235a0002c0006t0001g0155 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.946+3386G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119115 | ||||||
| chr1:12119335
|
G | A | 4 | a0002c0006t0003g0149a0002c0012t0001g0178a0002c0012t0023g0353others(1): Show | 4 | HG01106.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.946+3606G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119335 | ||||||
| chr1:12119346
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.946+3617C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119346 | ||||||
| chr1:12119513
|
T | G | 12 | a0002c0005t0001g0059a0002c0005t0002g0206a0002c0005t0002g0235others(9): Show | 12 | HG01106.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.947-3771T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119513 | ||||||
| chr1:12119555
|
C | CT | 67 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0047others(64): Show | 67 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.947-3716dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 12119555 | |||||
| chr1:12119555
|
C | CTT | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.947-3717_947-3716d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 12119555 | |||||
| chr1:12119739
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.947-3545T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119739 | ||||||
| chr1:12120041
|
C | T | 2 | a0001c0003t0001g0091a0001c0003t0001g0253 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.947-3243C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120041 | ||||||
| chr1:12120061
|
A | T | 47 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0079others(44): Show | 47 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.947-3223A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120061 | ||||||
| chr1:12120067
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(231): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.947-3217G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120067 | ||||||
| chr1:12120181
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0009g0089 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.947-3103G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120181 | ||||||
| chr1:12120320
|
A | G | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0002g0172others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.947-2964A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120320 | ||||||
| chr1:12120475
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.947-2809C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120475 | ||||||
| chr1:12120748
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(229): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.947-2536C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120748 | ||||||
| chr1:12120905
|
C | A | 1 | a0002c0005t0006g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.947-2379C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120905 | ||||||
| chr1:12120906
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0351 | 2 | HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.947-2378C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120906 | ||||||
| chr1:12121344
|
C | T | 43 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0079others(40): Show | 43 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.947-1940C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121344 | ||||||
| chr1:12121395
|
C | A | 1 | a0001c0002t0001g0243 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.947-1889C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121395 | ||||||
| chr1:12121442
|
T | G | 2 | a0001c0003t0001g0091a0001c0003t0001g0253 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.947-1842T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121442 | ||||||
| chr1:12121615
|
C | T | 5 | a0001c0001t0002g0218a0001c0001t0006g0359a0001c0001t0007g0192others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.947-1669C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121615 | ||||||
| chr1:12121695
|
G | A | 1 | a0001c0001t0002g0224 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.947-1589G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121695 | ||||||
| chr1:12121774
|
A | G | 10 | a0001c0001t0001g0250a0001c0001t0001g0272a0001c0001t0001g0296others(7): Show | 10 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.947-1510A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121774 | ||||||
| chr1:12121801
|
G | A | 1 | a0001c0004t0001g0052 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.947-1483G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121801 | ||||||
| chr1:12121934
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.947-1350A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121934 | ||||||
| chr1:12121957
|
C | T | 1 | a0002c0012t0023g0353 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.947-1327C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121957 | ||||||
| chr1:12122048
|
C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.947-1236C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122048 | ||||||
| chr1:12122384
|
C | T | 1 | a0001c0002t0011g0285 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.947-900C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122384 | ||||||
| chr1:12122830
|
C | T | 3 | a0002c0005t0001g0227a0002c0005t0005g0230a0002c0005t0005g0232 | 3 | HG03195.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.947-454C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122830 | ||||||
| chr1:12122890
|
A | G | 1 | a0001c0001t0005g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.947-394A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122890 | ||||||
| chr1:12122921
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.947-363C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122921 | ||||||
| chr1:12123117
|
A | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(258): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.947-167A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12123117 | ||||||
| chr1:12123181
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.947-103C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12123181 | ||||||
| chr1:12123188
|
G | T | 46 | a0001c0001t0001g0058a0001c0001t0001g0098a0001c0001t0001g0099others(43): Show | 46 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.947-96G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12123188 | ||||||
| chr1:12123495
|
C | T | 4 | a0001c0002t0002g0147a0001c0003t0003g0211a0001c0004t0001g0352others(1): Show | 4 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1040+118C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123495 | ||||||
| chr1:12123498
|
T | C | 1 | a0001c0002t0001g0095 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1040+121T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123498 | ||||||
| chr1:12123666
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1041-49C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123666 | ||||||
| chr1:12123669
|
C | G | 1 | a0001c0002t0001g0032 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1041-46C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123669 | ||||||
| chr1:12123688
|
A | G | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1041-27A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123688 | ||||||
| chr1:12123949
|
G | A | 1 | a0001c0002t0001g0034 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1153+122G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12123949 | ||||||
| chr1:12124150
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1153+323G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124150 | ||||||
| chr1:12124174
|
T | C | 46 | a0001c0001t0001g0058a0001c0001t0001g0098a0001c0001t0001g0099others(43): Show | 46 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.1153+347T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124174 | ||||||
| chr1:12124318
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 215 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.1153+491T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124318 | ||||||
| chr1:12124333
|
G | A | 1 | a0001c0003t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1153+506G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124333 | ||||||
| chr1:12124365
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1153+538C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124365 | ||||||
| chr1:12124366
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(116): Show | 119 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1153+539G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124366 | ||||||
| chr1:12124462
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.1153+635A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124462 | ||||||
| chr1:12124489
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.1153+662A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124489 | ||||||
| chr1:12124606
|
G | A | 41 | a0001c0001t0001g0058a0001c0001t0001g0098a0001c0001t0001g0099others(38): Show | 41 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.1153+779G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124606 | ||||||
| chr1:12124616
|
G | A | 5 | a0001c0003t0003g0208a0001c0007t0001g0215a0001c0007t0009g0357others(2): Show | 5 | HG02622.hp2 HG02630.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+789G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124616 | ||||||
| chr1:12124653
|
C | T | 1 | a0002c0006t0001g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1153+826C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124653 | ||||||
| chr1:12124657
|
A | G | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1153+830A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124657 | ||||||
| chr1:12124667
|
C | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1153+840C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124667 | ||||||
| chr1:12124682
|
C | G | 29 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0127others(26): Show | 29 | HG00323.hp2 HG01358.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1153+855C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124682 | ||||||
| chr1:12124690
|
C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1153+863C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124690 | ||||||
| chr1:12124691
|
G | A | 12 | a0002c0005t0001g0059a0002c0005t0002g0206a0002c0005t0002g0235others(9): Show | 12 | HG01106.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153+864G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124691 | ||||||
| chr1:12124693
|
G | A | 46 | a0001c0001t0001g0058a0001c0001t0001g0098a0001c0001t0001g0099others(43): Show | 46 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.1153+866G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124693 | ||||||
| chr1:12124694
|
C | T | 36 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0114others(33): Show | 36 | HG00280.hp2 HG01516.hp2 HG01517.hp2 others(33): Show |
intron_variant | MODIFIER | c.1153+867C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124694 | ||||||
| chr1:12124695
|
G | A | 19 | a0002c0005t0001g0051a0002c0005t0001g0084a0002c0005t0001g0094others(16): Show | 19 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1153+868G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124695 | ||||||
| chr1:12124829
|
C | CAAACA | 40 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0104others(37): Show | 40 | HG00438.hp1 HG01074.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1153+1050_1153+105 others(9): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | |||||
| chr1:12124829
|
C | CAAACAAA others(3): Show |
11 | a0001c0001t0001g0114a0001c0001t0001g0137a0001c0001t0001g0151others(8): Show | 11 | HG00280.hp2 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1153+1045_1153+105 others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | |||||
| chr1:12124829
|
C | CAAACAAA others(15): Show |
1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1153+1015_1153+101 others(26): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | |||||
| chr1:12124829
|
C | CAAACAAA others(8): Show |
5 | a0001c0001t0001g0058a0001c0003t0001g0102a0001c0003t0001g0288others(2): Show | 5 | HG01071.hp2 HG01255.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+1040_1153+105 others(19): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | |||||
| chr1:12124829
|
C | CAAACAAA others(13): Show |
3 | a0001c0001t0001g0098a0001c0001t0001g0099a0003c0008t0001g0105 | 3 | HG01516.hp2 HG01517.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1153+1035_1153+105 others(24): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | |||||
| chr1:12124829
|
C | CAAACAAA others(18): Show |
2 | a0003c0008t0001g0087a0003c0008t0017g0009 | 2 | NA19066.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1153+1030_1153+105 others(29): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | |||||
| chr1:12124829
|
CAAACA | C | 26 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0030others(23): Show | 26 | HG01168.hp1 HG01169.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.1153+1050_1153+105 others(9): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | |||||
| chr1:12124829
|
CAAACAAA others(3): Show |
C | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 112 | HG00140.hp2 HG00558.hp1 HG00738.hp2 others(109): Show |
intron_variant | MODIFIER | c.1153+1045_1153+105 others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | |||||
| chr1:12124829
|
CAAACAAA others(8): Show |
C | 3 | a0001c0003t0002g0213a0001c0003t0010g0195a0001c0017t0014g0264 | 3 | HG00140.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1153+1040_1153+105 others(19): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | |||||
| chr1:12124874
|
AAAAC | A | 16 | a0002c0005t0001g0051a0002c0005t0001g0084a0002c0005t0001g0094others(13): Show | 16 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1153+1055_1153+105 others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124874 | |||||
| chr1:12124878
|
C | CA | 3 | a0002c0006t0001g0347a0002c0016t0004g0228a0004c0028t0021g0113 | 3 | HG03710.hp2 NA19009.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1153+1054dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124878 | |||||
| chr1:12124882
|
C | A | 1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1153+1055C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124882 | ||||||
| chr1:12124883
|
A | C | 1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1153+1056A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124883 | ||||||
| chr1:12124892
|
A | G | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0002g0172others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-1059A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124892 | ||||||
| chr1:12124894
|
G | A | 20 | a0002c0005t0001g0051a0002c0005t0001g0084a0002c0005t0001g0094others(17): Show | 20 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.1154-1057G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124894 | ||||||
| chr1:12124958
|
A | T | 2 | a0002c0005t0001g0051a0002c0005t0001g0084 | 2 | HG00544.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1154-993A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124958 | ||||||
| chr1:12124979
|
G | A | 31 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0114others(28): Show | 31 | HG00280.hp2 HG01516.hp2 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.1154-972G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124979 | ||||||
| chr1:12125149
|
G | A | 4 | a0002c0005t0001g0059a0002c0005t0002g0235a0002c0006t0001g0155others(1): Show | 4 | HG01891.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-802G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125149 | ||||||
| chr1:12125278
|
T | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(256): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1154-673T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125278 | ||||||
| chr1:12125309
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1154-642C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125309 | ||||||
| chr1:12125323
|
C | T | 2 | a0001c0004t0001g0135a0002c0010t0001g0146 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1154-628C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125323 | ||||||
| chr1:12125470
|
C | T | 7 | a0001c0001t0001g0159a0001c0003t0003g0208a0001c0004t0001g0052others(4): Show | 7 | HG02622.hp2 HG02630.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1154-481C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125470 | ||||||
| chr1:12125476
|
T | C | 61 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0079others(58): Show | 61 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1154-475T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125476 | ||||||
| chr1:12125717
|
A | G | 77 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0079others(74): Show | 77 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1154-234A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125717 | ||||||
| chr1:12125726
|
T | C | 77 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0079others(74): Show | 77 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1154-225T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125726 | ||||||
| chr1:12125898
|
TG | T | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158 | 3 | HG01099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1154-52delG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125898 | ||||||
| chr1:12126148
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1256-35C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 11/14 | chr1 | 12126148 | ||||||
| chr1:12126251
|
G | A | 5 | a0002c0005t0006g0209a0002c0006t0003g0149a0002c0012t0001g0178others(2): Show | 5 | HG01106.hp2 HG02109.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309+15G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126251 | ||||||
| chr1:12126299
|
C | T | 30 | a0001c0002t0001g0053a0001c0003t0001g0145a0002c0005t0001g0051others(27): Show | 30 | HG00544.hp1 HG00597.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1309+63C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126299 | ||||||
| chr1:12126335
|
G | A | 33 | a0001c0001t0002g0224a0001c0002t0001g0053a0001c0003t0001g0145others(30): Show | 33 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1309+99G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126335 | ||||||
| chr1:12126570
|
G | T | 41 | a0001c0001t0001g0020a0001c0001t0001g0050a0001c0001t0001g0063others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1309+334G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126570 | ||||||
| chr1:12126725
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1309+489C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126725 | ||||||
| chr1:12126737
|
C | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0002g0172others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309+501C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126737 | ||||||
| chr1:12126740
|
T | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1309+504T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126740 | ||||||
| chr1:12126857
|
C | T | 8 | a0001c0001t0005g0355a0001c0003t0001g0091a0001c0003t0001g0167others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309+621C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126857 | ||||||
| chr1:12126876
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(274): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1309+640A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126876 | ||||||
| chr1:12126879
|
G | A | 4 | a0001c0001t0005g0355a0001c0003t0001g0167a0001c0003t0010g0259others(1): Show | 4 | HG02572.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309+643G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126879 | ||||||
| chr1:12126994
|
G | C | 48 | a0001c0001t0001g0020a0001c0001t0001g0050a0001c0001t0001g0063others(45): Show | 48 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1309+758G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126994 | ||||||
| chr1:12127073
|
C | T | 87 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0050others(84): Show | 87 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1309+837C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127073 | ||||||
| chr1:12127084
|
C | T | 1 | a0001c0017t0014g0264 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1309+848C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127084 | ||||||
| chr1:12127107
|
G | A | 2 | a0001c0003t0001g0091a0001c0003t0001g0253 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1309+871G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127107 | ||||||
| chr1:12127175
|
G | A | 35 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0096others(32): Show | 35 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1309+939G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127175 | ||||||
| chr1:12127214
|
G | T | 1 | a0001c0001t0001g0342 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1309+978G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127214 | ||||||
| chr1:12127358
|
G | A | 1 | a0002c0006t0001g0056 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1309+1122G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127358 | ||||||
| chr1:12127365
|
C | T | 1 | a0002c0010t0001g0345 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1309+1129C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127365 | ||||||
| chr1:12127484
|
T | C | 133 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0038others(130): Show | 133 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1309+1248T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127484 | ||||||
| chr1:12127536
|
C | T | 11 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0233others(8): Show | 11 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309+1300C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127536 | ||||||
| chr1:12127537
|
G | A | 6 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(3): Show | 6 | HG02145.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309+1301G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127537 | ||||||
| chr1:12127655
|
A | G | 161 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0038others(158): Show | 161 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.1309+1419A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127655 | ||||||
| chr1:12127724
|
GCTGAGTG others(3): Show |
G | 7 | a0001c0001t0001g0229a0001c0003t0001g0219a0001c0003t0003g0225others(4): Show | 7 | HG01167.hp2 HG01891.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1309+1490_1309+149 others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12127724 | |||||
| chr1:12127748
|
G | A | 3 | a0001c0003t0010g0195a0002c0005t0001g0227a0002c0005t0005g0232 | 3 | HG03195.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1309+1512G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127748 | ||||||
| chr1:12127971
|
C | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1309+1735C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127971 | ||||||
| chr1:12128037
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(264): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1309+1801A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128037 | ||||||
| chr1:12128066
|
C | T | 2 | a0001c0001t0001g0037a0001c0004t0001g0052 | 2 | HG01074.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1309+1830C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128066 | ||||||
| chr1:12128288
|
G | A | 21 | a0001c0001t0001g0038a0001c0001t0001g0093a0001c0001t0001g0098others(18): Show | 21 | HG01358.hp2 HG01516.hp2 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.1309+2052G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128288 | ||||||
| chr1:12128332
|
G | A | 1 | a0001c0002t0004g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1309+2096G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128332 | ||||||
| chr1:12128370
|
T | C | 34 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0096others(31): Show | 34 | HG00323.hp2 HG00597.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1309+2134T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128370 | ||||||
| chr1:12128413
|
C | A | 11 | a0001c0004t0001g0196a0001c0004t0003g0220a0002c0005t0001g0059others(8): Show | 11 | HG01106.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309+2177C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128413 | ||||||
| chr1:12128425
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(238): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1309+2189G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128425 | ||||||
| chr1:12128433
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0351 | 2 | HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1309+2197C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128433 | ||||||
| chr1:12128490
|
T | G | 3 | a0003c0008t0001g0087a0003c0008t0001g0105a0003c0027t0001g0060 | 3 | NA18969.hp2 NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1309+2254T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128490 | ||||||
| chr1:12128556
|
G | A | 32 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0096others(29): Show | 32 | HG00323.hp2 HG00597.hp1 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.1309+2320G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128556 | ||||||
| chr1:12128557
|
G | A | 7 | a0001c0001t0001g0058a0001c0003t0001g0288a0001c0003t0001g0315others(4): Show | 7 | HG01071.hp2 HG01928.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309+2321G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128557 | ||||||
| chr1:12128569
|
G | A | 1 | a0001c0004t0001g0320 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1309+2333G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128569 | ||||||
| chr1:12128594
|
C | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(239): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1309+2358C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128594 | ||||||
| chr1:12128715
|
G | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(239): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1309+2479G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128715 | ||||||
| chr1:12128783
|
A | G | 6 | a0001c0001t0001g0159a0001c0003t0003g0208a0001c0007t0001g0215others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309+2547A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128783 | ||||||
| chr1:12128803
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1309+2567C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128803 | ||||||
| chr1:12128823
|
G | A | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1309+2587G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128823 | ||||||
| chr1:12128829
|
A | C | 2 | a0001c0003t0002g0197a0001c0003t0002g0213 | 2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1309+2593A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128829 | ||||||
| chr1:12128833
|
C | CT | 25 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0086others(22): Show | 25 | HG00558.hp1 HG02074.hp1 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.1309+2616dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | |||||
| chr1:12128833
|
C | CTTT | 112 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 112 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1309+2614_1309+261 others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | |||||
| chr1:12128833
|
C | CTTTT | 104 | a0001c0001t0001g0020a0001c0001t0001g0039a0001c0001t0001g0046others(101): Show | 104 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1309+2613_1309+261 others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | |||||
| chr1:12128833
|
C | CTTTTT | 21 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0047others(18): Show | 21 | HG00323.hp2 HG00597.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1309+2612_1309+261 others(9): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | |||||
| chr1:12128833
|
CT | C | 8 | a0001c0001t0001g0058a0001c0001t0001g0258a0001c0003t0001g0288others(5): Show | 8 | HG01071.hp2 HG01928.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309+2616delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | |||||
| chr1:12128928
|
G | A | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1309+2692G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128928 | ||||||
| chr1:12129176
|
T | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(238): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1309+2940T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129176 | ||||||
| chr1:12129204
|
T | A | 9 | a0001c0001t0001g0229a0001c0003t0001g0219a0001c0003t0002g0197others(6): Show | 9 | HG01167.hp2 HG01891.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1309+2968T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129204 | ||||||
| chr1:12129238
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1309+3002C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129238 | ||||||
| chr1:12129432
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(105): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1309+3196C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129432 | ||||||
| chr1:12129504
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1309+3268G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129504 | ||||||
| chr1:12129552
|
C | T | 1 | a0001c0004t0001g0168 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1309+3316C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129552 | ||||||
| chr1:12129634
|
G | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0086others(20): Show | 23 | HG00558.hp1 HG02165.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.1309+3398G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129634 | ||||||
| chr1:12129790
|
C | T | 1 | a0002c0005t0002g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1309+3554C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129790 | ||||||
| chr1:12129961
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1309+3725G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129961 | ||||||
| chr1:12130078
|
T | C | 6 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(3): Show | 6 | HG02145.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309+3842T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130078 | ||||||
| chr1:12130155
|
G | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0002g0172others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309+3919G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130155 | ||||||
| chr1:12130345
|
A | T | 1 | a0001c0004t0010g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1309+4109A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130345 | ||||||
| chr1:12130498
|
C | T | 1 | a0003c0019t0004g0017 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1309+4262C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130498 | ||||||
| chr1:12130624
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1309+4388C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130624 | ||||||
| chr1:12130638
|
A | T | 1 | a0002c0011t0004g0221 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1309+4402A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130638 | ||||||
| chr1:12130641
|
G | A | 1 | a0001c0002t0001g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1309+4405G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130641 | ||||||
| chr1:12130651
|
C | T | 9 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(6): Show | 9 | HG02145.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1309+4415C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130651 | ||||||
| chr1:12130670
|
C | T | 1 | a0001c0004t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1309+4434C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130670 | ||||||
| chr1:12130671
|
G | A | 2 | a0001c0003t0001g0091a0001c0003t0001g0253 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1309+4435G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130671 | ||||||
| chr1:12130684
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1309+4448G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130684 | ||||||
| chr1:12130710
|
C | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(3): Show | 6 | HG02145.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309+4474C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130710 | ||||||
| chr1:12131040
|
C | T | 15 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0173others(12): Show | 15 | HG01243.hp1 HG02145.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1310-4548C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131040 | ||||||
| chr1:12131143
|
G | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1310-4445G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131143 | ||||||
| chr1:12131310
|
C | A | 9 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(6): Show | 9 | HG02145.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1310-4278C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131310 | ||||||
| chr1:12131342
|
C | T | 5 | a0001c0001t0001g0159a0001c0007t0001g0215a0001c0007t0009g0357others(2): Show | 5 | HG02622.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1310-4246C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131342 | ||||||
| chr1:12131445
|
G | A | 64 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0050others(61): Show | 64 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1310-4143G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131445 | ||||||
| chr1:12131474
|
A | C | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1310-4114A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131474 | ||||||
| chr1:12131502
|
AGTTTTTT | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(269): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1310-4066_1310-406 others(11): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12131502 | |||||
| chr1:12131684
|
A | G | 15 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0173others(12): Show | 15 | HG01243.hp1 HG02145.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1310-3904A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131684 | ||||||
| chr1:12131714
|
T | G | 15 | a0001c0001t0001g0138a0001c0001t0001g0159a0001c0001t0001g0173others(12): Show | 15 | HG01243.hp1 HG02145.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1310-3874T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131714 | ||||||
| chr1:12131940
|
C | T | 6 | a0001c0004t0001g0069a0001c0004t0001g0070a0001c0004t0001g0135others(3): Show | 6 | HG02074.hp2 HG02523.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-3648C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131940 | ||||||
| chr1:12131943
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1310-3645G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131943 | ||||||
| chr1:12132196
|
A | G | 64 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0050others(61): Show | 64 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1310-3392A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132196 | ||||||
| chr1:12132213
|
A | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(270): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1310-3375A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132213 | ||||||
| chr1:12132240
|
G | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(3): Show | 6 | HG02145.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-3348G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132240 | ||||||
| chr1:12132249
|
C | T | 64 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0050others(61): Show | 64 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1310-3339C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132249 | ||||||
| chr1:12132269
|
A | C | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1310-3319A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132269 | ||||||
| chr1:12132392
|
A | G | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1310-3196A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132392 | ||||||
| chr1:12132446
|
C | T | 1 | a0001c0002t0004g0269 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1310-3142C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132446 | ||||||
| chr1:12132569
|
A | G | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(291): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1310-3019A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132569 | ||||||
| chr1:12132837
|
C | CA | 64 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0014others(61): Show | 64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1310-2726dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | |||||
| chr1:12132837
|
C | CAA | 8 | a0001c0001t0001g0136a0001c0002t0001g0034a0001c0002t0001g0043others(5): Show | 8 | HG00741.hp1 HG00741.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1310-2727_1310-272 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | |||||
| chr1:12132837
|
CA | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0020others(66): Show | 69 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1310-2726delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | |||||
| chr1:12132837
|
CAA | C | 68 | a0001c0001t0001g0038a0001c0001t0001g0046a0001c0001t0001g0047others(65): Show | 68 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1310-2727_1310-272 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | |||||
| chr1:12132837
|
CAAA | C | 6 | a0001c0001t0005g0355a0001c0002t0001g0027a0001c0003t0010g0195others(3): Show | 6 | HG02615.hp2 HG03195.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-2728_1310-272 others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | |||||
| chr1:12132837
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0006g0359 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1310-2737_1310-272 others(16): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | |||||
| chr1:12132837
|
CAAAAAAA others(6): Show |
C | 9 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(6): Show | 9 | HG02145.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1310-2738_1310-272 others(17): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | |||||
| chr1:12132975
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(98): Show | 101 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1310-2613C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132975 | ||||||
| chr1:12132976
|
G | A | 2 | a0001c0001t0001g0286a0002c0005t0001g0094 | 2 | NA18942.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1310-2612G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132976 | ||||||
| chr1:12133043
|
G | A | 2 | a0001c0001t0002g0172a0001c0004t0003g0220 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1310-2545G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133043 | ||||||
| chr1:12133239
|
G | A | 2 | a0001c0003t0002g0214a0002c0005t0002g0235 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1310-2349G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133239 | ||||||
| chr1:12133269
|
C | T | 1 | a0001c0002t0001g0323 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1310-2319C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133269 | ||||||
| chr1:12133326
|
C | CT | 253 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1310-2250dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12133326 | |||||
| chr1:12133470
|
C | G | 253 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1310-2118C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133470 | ||||||
| chr1:12133523
|
C | T | 1 | a0002c0005t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1310-2065C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133523 | ||||||
| chr1:12133534
|
G | T | 2 | a0001c0003t0002g0214a0002c0005t0002g0235 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1310-2054G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133534 | ||||||
| chr1:12133570
|
T | C | 1 | a0002c0005t0005g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1310-2018T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133570 | ||||||
| chr1:12133672
|
G | A | 3 | a0001c0003t0002g0214a0002c0005t0002g0235a0002c0011t0004g0221 | 3 | HG02976.hp2 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1310-1916G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133672 | ||||||
| chr1:12133688
|
C | T | 1 | a0001c0004t0001g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1310-1900C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133688 | ||||||
| chr1:12133697
|
G | A | 1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1310-1891G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133697 | ||||||
| chr1:12133738
|
C | CA | 6 | a0001c0001t0001g0115a0001c0001t0001g0159a0001c0002t0001g0055others(3): Show | 6 | HG01243.hp1 HG02080.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-1826dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12133738 | |||||
| chr1:12133738
|
CAA | C | 10 | a0001c0001t0001g0304a0001c0001t0001g0329a0001c0002t0001g0176others(7): Show | 10 | HG01884.hp2 HG02922.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1310-1827_1310-182 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12133738 | |||||
| chr1:12133738
|
CAAA | C | 237 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(234): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1310-1828_1310-182 others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12133738 | |||||
| chr1:12133806
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1310-1782A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133806 | ||||||
| chr1:12133868
|
C | T | 34 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0096others(31): Show | 34 | HG00323.hp2 HG00597.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.1310-1720C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133868 | ||||||
| chr1:12133898
|
C | T | 1 | a0001c0003t0001g0276 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1310-1690C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133898 | ||||||
| chr1:12133913
|
C | T | 14 | a0001c0001t0002g0218a0001c0001t0007g0192a0001c0001t0007g0216others(11): Show | 14 | HG02280.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1310-1675C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133913 | ||||||
| chr1:12133922
|
A | G | 2 | a0001c0003t0001g0091a0001c0003t0001g0253 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1310-1666A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133922 | ||||||
| chr1:12134359
|
G | T | 27 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0190others(24): Show | 27 | HG01106.hp2 HG01243.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1310-1229G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134359 | ||||||
| chr1:12134394
|
T | C | 287 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(284): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1310-1194T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134394 | ||||||
| chr1:12134409
|
C | A | 7 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1310-1179C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134409 | ||||||
| chr1:12134470
|
T | C | 1 | a0001c0001t0016g0194 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1310-1118T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134470 | ||||||
| chr1:12134555
|
G | A | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0014others(143): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1310-1033G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134555 | ||||||
| chr1:12134688
|
G | A | 32 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0096others(29): Show | 32 | HG00323.hp2 HG00597.hp1 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.1310-900G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134688 | ||||||
| chr1:12134732
|
G | C | 34 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0096others(31): Show | 34 | HG00323.hp2 HG00597.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.1310-856G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134732 | ||||||
| chr1:12134945
|
G | A | 1 | a0001c0001t0008g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1310-643G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134945 | ||||||
| chr1:12134952
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1310-636A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134952 | ||||||
| chr1:12134969
|
G | A | 11 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(8): Show | 11 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1310-619G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134969 | ||||||
| chr1:12134996
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1310-592G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134996 | ||||||
| chr1:12135023
|
A | T | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1310-565A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135023 | ||||||
| chr1:12135054
|
G | A | 6 | a0001c0001t0001g0229a0001c0003t0001g0219a0001c0003t0003g0225others(3): Show | 6 | HG01167.hp2 HG01891.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1310-534G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135054 | ||||||
| chr1:12135119
|
G | C | 1 | a0001c0001t0011g0282 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1310-469G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135119 | ||||||
| chr1:12135124
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1310-464G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135124 | ||||||
| chr1:12135156
|
A | G | 14 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0001g0166others(11): Show | 14 | HG01106.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1310-432A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135156 | ||||||
| chr1:12135167
|
T | A | 252 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(249): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1310-421T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135167 | ||||||
| chr1:12135177
|
T | A | 11 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(8): Show | 11 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1310-411T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135177 | ||||||
| chr1:12135294
|
T | C | 251 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(248): Show | 251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1310-294T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135294 | ||||||
| chr1:12135315
|
C | CA | 52 | a0001c0001t0001g0035a0001c0001t0001g0096a0001c0001t0001g0106others(49): Show | 52 | HG01106.hp2 HG01358.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.1310-255dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12135315 | |||||
| chr1:12135315
|
C | CAA | 67 | a0001c0001t0001g0020a0001c0001t0001g0044a0001c0001t0001g0046others(64): Show | 67 | HG00558.hp2 HG00597.hp1 HG01884.hp2 others(64): Show |
intron_variant | MODIFIER | c.1310-256_1310-255d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12135315 | |||||
| chr1:12135315
|
C | CAAA | 141 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.1310-257_1310-255d others(5): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12135315 | |||||
| chr1:12135315
|
C | CAAAA | 14 | a0001c0001t0001g0005a0001c0001t0001g0086a0001c0001t0001g0136others(11): Show | 14 | HG00597.hp2 HG01433.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1310-258_1310-255d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12135315 | |||||
| chr1:12135446
|
G | T | 1 | a0002c0010t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1310-142G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135446 | ||||||
| chr1:12135537
|
G | T | 1 | a0001c0002t0001g0254 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1310-51G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135537 | ||||||
| chr1:12135672
|
C | T | 11 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(8): Show | 11 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1335+59C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12135672 | ||||||
| chr1:12135737
|
C | G | 1 | a0002c0005t0005g0232 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1335+124C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12135737 | ||||||
| chr1:12135931
|
C | T | 1 | a0001c0001t0007g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1335+318C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12135931 | ||||||
| chr1:12136082
|
T | C | 1 | a0001c0003t0003g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1335+469T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136082 | ||||||
| chr1:12136091
|
G | A | 254 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1335+478G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136091 | ||||||
| chr1:12136110
|
TC | T | 59 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0044others(56): Show | 59 | HG00438.hp2 HG00558.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.1335+498delC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136110 | ||||||
| chr1:12136208
|
G | A | 1 | a0001c0003t0005g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1335+595G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136208 | ||||||
| chr1:12136265
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1335+652A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136265 | ||||||
| chr1:12136284
|
C | G | 50 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0050others(47): Show | 50 | HG00438.hp2 HG00558.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1335+671C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136284 | ||||||
| chr1:12136447
|
G | A | 1 | a0001c0004t0003g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1335+834G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136447 | ||||||
| chr1:12136469
|
T | A | 223 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(220): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1335+856T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136469 | ||||||
| chr1:12136474
|
C | G | 2 | a0001c0004t0025g0356a0001c0025t0001g0231 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1335+861C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136474 | ||||||
| chr1:12136478
|
G | A | 6 | a0001c0004t0001g0069a0001c0004t0001g0070a0001c0004t0001g0135others(3): Show | 6 | HG02074.hp2 HG02523.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1335+865G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136478 | ||||||
| chr1:12136530
|
T | G | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+917T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136530 | ||||||
| chr1:12136531
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+918C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136531 | ||||||
| chr1:12136563
|
C | T | 1 | a0002c0005t0001g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1335+950C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136563 | ||||||
| chr1:12136619
|
C | A | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1006C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136619 | ||||||
| chr1:12136620
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1007A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136620 | ||||||
| chr1:12136622
|
C | T | 30 | a0001c0001t0001g0035a0001c0001t0001g0096a0001c0001t0001g0106others(27): Show | 30 | HG00544.hp2 HG00597.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.1335+1009C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136622 | ||||||
| chr1:12136649
|
G | GA | 8 | a0001c0001t0001g0115a0001c0001t0001g0159a0001c0001t0001g0258others(5): Show | 8 | HG02622.hp2 HG02965.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1335+1054dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | |||||
| chr1:12136649
|
G | GAA | 9 | a0001c0001t0001g0058a0001c0002t0001g0055a0001c0003t0001g0288others(6): Show | 9 | HG01071.hp2 HG01928.hp1 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.1335+1053_1335+105 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | |||||
| chr1:12136649
|
GAA | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0014others(151): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1335+1053_1335+105 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | |||||
| chr1:12136649
|
GAAA | G | 69 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0044others(66): Show | 69 | HG00438.hp2 HG00558.hp2 HG01106.hp2 others(66): Show |
intron_variant | MODIFIER | c.1335+1052_1335+105 others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | |||||
| chr1:12136649
|
GAAAA | G | 29 | a0001c0001t0001g0035a0001c0001t0001g0096a0001c0001t0001g0106others(26): Show | 29 | HG00544.hp2 HG00597.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.1335+1051_1335+105 others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | |||||
| chr1:12136673
|
T | C | 6 | a0001c0004t0001g0069a0001c0004t0001g0070a0001c0004t0001g0135others(3): Show | 6 | HG02074.hp2 HG02523.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1335+1060T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136673 | ||||||
| chr1:12136704
|
A | G | 1 | a0001c0003t0001g0324 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1335+1091A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136704 | ||||||
| chr1:12136712
|
G | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1335+1099G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136712 | ||||||
| chr1:12136733
|
A | G | 1 | a0001c0003t0001g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1335+1120A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136733 | ||||||
| chr1:12136779
|
G | A | 4 | a0001c0001t0001g0233a0001c0001t0007g0193a0001c0001t0016g0194others(1): Show | 4 | HG02258.hp2 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335+1166G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136779 | ||||||
| chr1:12136870
|
CT | C | 13 | a0001c0001t0001g0159a0001c0001t0001g0180a0001c0001t0001g0262others(10): Show | 13 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1335+1282delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | |||||
| chr1:12136870
|
CTT | C | 21 | a0001c0001t0001g0058a0001c0001t0001g0190a0001c0001t0001g0191others(18): Show | 21 | HG01071.hp2 HG01928.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1335+1281_1335+128 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | |||||
| chr1:12136870
|
CTTTTTTT | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0014others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1335+1276_1335+128 others(11): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | |||||
| chr1:12136870
|
CTTTTTTT others(1): Show |
C | 45 | a0001c0001t0001g0035a0001c0001t0001g0048a0001c0001t0001g0096others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1335+1275_1335+128 others(12): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | |||||
| chr1:12136870
|
CTTTTTTT others(2): Show |
C | 64 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0044others(61): Show | 64 | HG00438.hp2 HG00558.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1335+1274_1335+128 others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | |||||
| chr1:12136870
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0119a0001c0001t0001g0286a0001c0001t0001g0290others(1): Show | 4 | HG02523.hp2 NA19012.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335+1273_1335+128 others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | |||||
| chr1:12136877
|
T | A | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1264T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136877 | ||||||
| chr1:12136880
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1267T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136880 | ||||||
| chr1:12136898
|
T | A | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1335+1285T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136898 | ||||||
| chr1:12136921
|
T | G | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1308T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136921 | ||||||
| chr1:12136922
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1336-1307C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136922 | ||||||
| chr1:12136923
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1336-1306T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136923 | ||||||
| chr1:12137038
|
C | T | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1336-1191C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137038 | ||||||
| chr1:12137045
|
C | T | 261 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0013others(258): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1336-1184C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137045 | ||||||
| chr1:12137283
|
G | C | 1 | a0001c0003t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1336-946G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137283 | ||||||
| chr1:12137316
|
A | G | 1 | a0001c0002t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1336-913A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137316 | ||||||
| chr1:12137327
|
A | AATC | 162 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0014others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1336-900_1336-899i others(5): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137327 | |||||
| chr1:12137327
|
A | C | 2 | a0001c0009t0001g0358a0002c0011t0004g0221 | 2 | HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1336-902A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137327 | ||||||
| chr1:12137504
|
C | A | 1 | a0001c0004t0003g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1336-725C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137504 | ||||||
| chr1:12137540
|
GTTTTTTT others(3): Show |
G | 7 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0203others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-671_1336-662d others(12): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137540 | |||||
| chr1:12137548
|
GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0022g0072a0001c0004t0001g0164a0002c0005t0001g0059others(3): Show | 6 | HG02055.hp1 HG02559.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1336-660_1336-650d others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137548 | |||||
| chr1:12137558
|
G | T | 33 | a0001c0001t0001g0035a0001c0001t0001g0063a0001c0001t0001g0096others(30): Show | 33 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1336-671G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137558 | ||||||
| chr1:12137558
|
GT | G | 160 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(157): Show | 160 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1336-661delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137558 | |||||
| chr1:12137559
|
T | G | 3 | a0001c0001t0001g0063a0001c0002t0001g0323a0001c0003t0010g0195 | 3 | HG03471.hp2 NA18941.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1336-670T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137559 | ||||||
| chr1:12137559
|
T | TG | 28 | a0001c0001t0001g0035a0001c0001t0001g0106a0001c0001t0001g0127others(25): Show | 28 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1336-670_1336-669i others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137559 | ||||||
| chr1:12137567
|
TTG | T | 61 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0044others(58): Show | 61 | HG00438.hp2 HG00558.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1336-660_1336-659d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137567 | |||||
| chr1:12137568
|
T | G | 1 | a0002c0006t0001g0056 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1336-661T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137568 | ||||||
| chr1:12137569
|
G | T | 4 | a0001c0003t0001g0091a0001c0003t0001g0253a0002c0006t0001g0056others(1): Show | 4 | HG01106.hp2 HG01884.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-660G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137569 | ||||||
| chr1:12137570
|
T | G | 64 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0044others(61): Show | 64 | HG00438.hp2 HG00558.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1336-659T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137570 | ||||||
| chr1:12137878
|
C | T | 1 | a0001c0002t0001g0302 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1336-351C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137878 | ||||||
| chr1:12137879
|
G | A | 4 | a0001c0001t0005g0355a0002c0005t0001g0227a0002c0005t0005g0230others(1): Show | 4 | HG02615.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-350G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137879 | ||||||
| chr1:12138089
|
G | A | 4 | a0001c0001t0001g0229a0001c0001t0005g0355a0002c0005t0001g0227others(1): Show | 4 | HG02615.hp2 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-140G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12138089 | ||||||
| chr1:12138122
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(254): Show | 257 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(254): Show |
intron_variant | MODIFIER | c.1336-107G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12138122 | ||||||
| chr1:12138146
|
G | GA | 9 | a0001c0001t0007g0193a0001c0002t0001g0340a0001c0002t0004g0269others(6): Show | 9 | HG01106.hp2 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1336-73dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12138146 | |||||
| chr1:12138535
|
T | C | 10 | a0001c0001t0001g0233a0001c0003t0001g0091a0001c0003t0001g0253others(7): Show | 10 | HG01106.hp2 HG01884.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1543+99T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138535 | ||||||
| chr1:12138554
|
A | G | 7 | a0001c0003t0001g0167a0001c0003t0010g0259a0001c0003t0026g0161others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543+118A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138554 | ||||||
| chr1:12138578
|
T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(253): Show | 256 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.1543+142T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138578 | ||||||
| chr1:12138586
|
T | C | 2 | a0001c0001t0005g0355a0002c0005t0005g0232 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1543+150T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138586 | ||||||
| chr1:12138631
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0009g0089 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1543+195G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138631 | ||||||
| chr1:12138948
|
G | GCCTTGAA others(59): Show |
44 | a0001c0001t0001g0020a0001c0001t0001g0046a0001c0001t0001g0074others(41): Show | 44 | HG00438.hp2 HG00558.hp2 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1543+515_1543+580d others(68): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 12138948 | |||||
| chr1:12139002
|
G | A | 1 | a0001c0002t0001g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1543+566G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139002 | ||||||
| chr1:12139019
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1543+583A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139019 | ||||||
| chr1:12139120
|
G | C | 2 | a0002c0006t0003g0149a0002c0010t0024g0354 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1543+684G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139120 | ||||||
| chr1:12139138
|
A | G | 5 | a0001c0001t0007g0198a0001c0001t0009g0089a0001c0001t0009g0234others(2): Show | 5 | HG02055.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1543+702A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139138 | ||||||
| chr1:12139429
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1543+993G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139429 | ||||||
| chr1:12139483
|
T | G | 1 | a0001c0001t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1543+1047T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139483 | ||||||
| chr1:12139505
|
G | A | 3 | a0001c0001t0001g0233a0001c0003t0010g0195a0005c0015t0001g0350 | 3 | HG01106.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1543+1069G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139505 | ||||||
| chr1:12139694
|
T | C | 3 | a0001c0001t0007g0193a0001c0003t0007g0301a0010c0024t0001g0238 | 3 | HG02257.hp1 HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1543+1258T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139694 | ||||||
| chr1:12140093
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1543+1657C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140093 | ||||||
| chr1:12140234
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0007g0192a0001c0001t0007g0216 | 3 | HG01192.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1543+1798C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140234 | ||||||
| chr1:12140289
|
C | T | 3 | a0001c0001t0001g0233a0001c0003t0010g0195a0005c0015t0001g0350 | 3 | HG01106.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1543+1853C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140289 | ||||||
| chr1:12140380
|
A | G | 1 | a0001c0002t0001g0316 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1544-1907A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140380 | ||||||
| chr1:12140442
|
C | T | 1 | a0001c0009t0001g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1544-1845C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140442 | ||||||
| chr1:12140572
|
C | T | 4 | a0001c0001t0002g0172a0001c0003t0002g0197a0001c0004t0002g0169others(1): Show | 4 | HG02451.hp1 HG02717.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1544-1715C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140572 | ||||||
| chr1:12140656
|
C | T | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1544-1631C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140656 | ||||||
| chr1:12140824
|
C | T | 1 | a0001c0002t0001g0239 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1544-1463C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140824 | ||||||
| chr1:12140973
|
G | C | 1 | a0001c0002t0001g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1544-1314G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140973 | ||||||
| chr1:12140984
|
C | G | 2 | a0001c0003t0001g0336a0001c0003t0020g0073 | 2 | NA18942.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1544-1303C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140984 | ||||||
| chr1:12141026
|
T | C | 26 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0190others(23): Show | 26 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1544-1261T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141026 | ||||||
| chr1:12141183
|
T | C | 42 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0190others(39): Show | 42 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1544-1104T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141183 | ||||||
| chr1:12141191
|
C | T | 10 | a0001c0002t0001g0015a0001c0003t0001g0025a0001c0003t0001g0057others(7): Show | 10 | HG00558.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1544-1096C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141191 | ||||||
| chr1:12141416
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1544-871C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141416 | ||||||
| chr1:12141519
|
G | A | 1 | a0001c0003t0002g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1544-768G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141519 | ||||||
| chr1:12141779
|
G | T | 1 | a0001c0023t0001g0061 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1544-508G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141779 | ||||||
| chr1:12141788
|
T | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0030others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1544-499T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141788 | ||||||
| chr1:12142018
|
C | G | 3 | a0001c0003t0003g0225a0001c0003t0003g0226a0001c0007t0015g0189 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1544-269C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12142018 | ||||||
| chr1:12142038
|
G | C | 156 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0037others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1544-249G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12142038 | ||||||
| chr1:12142063
|
A | T | 3 | a0001c0003t0003g0225a0001c0003t0003g0226a0001c0007t0015g0189 | 3 | HG02895.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1544-224A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12142063 |