Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3604 |
| ensemblid | ENSG00000049249.10 |
| hgncid | 11924 |
| symbol | TNFRSF9 |
| name | TNF receptor superfamily member 9 |
| refseq_nuc | NM_001561.6 |
| refseq_prot | NP_001552.2 |
| ensembl_nuc | ENST00000377507.8 |
| ensembl_prot | ENSP00000366729.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 7915871 |
| end | 7940839 |
| strand | - |
| ver | v1.2 |
| region | chr1:7915871-7940839 |
| region5000 | chr1:7910871-7945839 |
| regionname0 | TNFRSF9_chr1_7915871_7940839 |
| regionname5000 | TNFRSF9_chr1_7910871_7945839 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 255 | 378 | 88 | 70 | 170 | 18 | 30 | 138 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | MGNSC others(250): Show |
chr1 | 7910871 | 7945839 |
| a0002 | 0/0 | 255 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | MGNSC others(250): Show |
chr1 | 7910871 | 7945839 |
| a0003 | 0/0 | 255 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | MGNSC others(250): Show |
chr1 | 7910871 | 7945839 |
| a0004 | 0/0 | 255 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | MGNSC others(250): Show |
chr1 | 7910871 | 7945839 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 765 | 362 | 77 | 67 | 168 | 18 | 30 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | ATGGG others(760): Show |
chr1 | 7910871 | 7945839 | ||
| a0001c0002 | 0/0 | 765 | 6 | 5 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | ATGGG others(760): Show |
chr1 | 7910871 | 7945839 | ||
| a0001c0003 | 0/0 | 765 | 6 | 4 | 2 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | ATGGG others(760): Show |
chr1 | 7910871 | 7945839 | ||
| a0001c0005 | 0/0 | 765 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | ATGGG others(760): Show |
chr1 | 7910871 | 7945839 | ||
| a0001c0006 | 0/0 | 765 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | ATGGG others(760): Show |
chr1 | 7910871 | 7945839 | ||
| a0001c0007 | 0/0 | 765 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | ATGGG others(760): Show |
chr1 | 7910871 | 7945839 | ||
| a0002c0004 | 0/0 | 765 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | ATGGG others(760): Show |
chr1 | 7910871 | 7945839 | ||
| a0003c0008 | 0/0 | 765 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | ATGGG others(760): Show |
chr1 | 7910871 | 7945839 | ||
| a0004c0009 | 0/0 | 765 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | ATGGG others(760): Show |
chr1 | 7910871 | 7945839 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5872 | 80 | 9 | 22 | 34 | 7 | 7 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0002 | 0/0 | 5871 | 63 | 0 | 21 | 41 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5866): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0003 | 0/0 | 5873 | 45 | 14 | 8 | 13 | 7 | 3 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5868): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0004 | 0/0 | 5873 | 18 | 1 | 1 | 14 | 0 | 2 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5868): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0005 | 0/0 | 5875 | 15 | 0 | 0 | 13 | 1 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5870): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0006 | 0/0 | 5872 | 14 | 0 | 0 | 13 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0007 | 0/0 | 5877 | 8 | 8 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5872): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0008 | 0/0 | 5874 | 11 | 0 | 6 | 1 | 0 | 4 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5869): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0009 | 0/0 | 5872 | 9 | 0 | 0 | 9 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0010 | 0/0 | 5868 | 7 | 7 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5863): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0011 | 0/0 | 5879 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5874): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0012 | 0/0 | 5876 | 6 | 0 | 2 | 0 | 2 | 2 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5871): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0013 | 0/0 | 5889 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5884): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0014 | 0/0 | 5871 | 4 | 3 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5866): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0015 | 0/0 | 5878 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5873): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0016 | 0/0 | 5872 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0018 | 0/0 | 5871 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5866): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0019 | 0/0 | 5874 | 3 | 0 | 1 | 1 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5869): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0021 | 0/0 | 5875 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5870): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0022 | 0/0 | 5889 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5884): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0023 | 0/0 | 5874 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5869): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0024 | 0/0 | 5874 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5869): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0025 | 0/0 | 5875 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5870): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0026 | 0/0 | 5877 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5872): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0027 | 0/0 | 5875 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5870): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0028 | 0/0 | 5876 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5871): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0029 | 0/0 | 5874 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5869): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0030 | 0/0 | 5872 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0031 | 0/0 | 5876 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5871): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0032 | 0/0 | 5872 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0033 | 0/0 | 5872 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0034 | 0/0 | 5872 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0035 | 0/0 | 5873 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5868): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0036 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5872): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0037 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0039 | 0/0 | 5879 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5874): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0040 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5872): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0041 | 0/0 | 5878 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5873): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0042 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5872): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0043 | 0/0 | 5879 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5874): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0044 | 0/0 | 5873 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5868): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0045 | 0/0 | 5873 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5868): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0046 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5872): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0047 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5869): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0048 | 0/0 | 5878 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5873): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0049 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0050 | 0/0 | 5872 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0051 | 0/0 | 5872 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0052 | 0/0 | 5874 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5869): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0053 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0054 | 0/0 | 5872 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0055 | 0/0 | 5872 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0056 | 0/1 | 5876 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5871): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0057 | 0/0 | 5872 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0058 | 0/0 | 5871 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5866): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0059 | 0/0 | 5871 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5866): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0060 | 0/0 | 5871 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5866): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0061 | 0/0 | 5871 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5866): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0062 | 0/0 | 5871 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5866): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0063 | 0/0 | 5871 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5866): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0064 | 0/0 | 5870 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5865): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0065 | 0/0 | 5872 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0066 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5872): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0067 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5869): Show |
chr1 | 7910871 | 7945839 |
| a0001c0001t0068 | 0/0 | 5876 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5871): Show |
chr1 | 7910871 | 7945839 |
| a0001c0002t0007 | 0/0 | 5877 | 6 | 5 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5872): Show |
chr1 | 7910871 | 7945839 |
| a0001c0003t0001 | 0/0 | 5872 | 3 | 2 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0003t0017 | 0/0 | 5862 | 3 | 2 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5857): Show |
chr1 | 7910871 | 7945839 |
| a0001c0005t0011 | 0/0 | 5879 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5874): Show |
chr1 | 7910871 | 7945839 |
| a0001c0006t0001 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0001c0007t0006 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0002c0004t0001 | 0/0 | 5872 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0002c0004t0020 | 0/0 | 5869 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5864): Show |
chr1 | 7910871 | 7945839 |
| a0002c0004t0038 | 0/0 | 5869 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5864): Show |
chr1 | 7910871 | 7945839 |
| a0003c0008t0001 | 0/0 | 5872 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5867): Show |
chr1 | 7910871 | 7945839 |
| a0004c0009t0003 | 0/0 | 5873 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | GCAGA others(5868): Show |
chr1 | 7910871 | 7945839 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 16 | 1 | 3 | 8 | 2 | 2 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0001 | 0/0 | 30 | 0 | 7 | 22 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0004 | 0/0 | 10 | 0 | 10 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0006 | 0/0 | 7 | 1 | 4 | 1 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0008 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0050 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0005g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0006g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0006g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0006g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0006g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0007g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0007g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0007g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0008g0025 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0008g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0008g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0008g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0008g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0009g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0009g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0009g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0009g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0010g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0011g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0011g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0012g0023 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0012g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0012g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0013g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0013g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0013g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0014g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0016g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0016g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0018g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0018g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0019g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0019g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0019g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0021g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0021g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0022g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0022g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0023g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0024g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0024g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0025g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0026g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0026g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0027g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0027g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0028g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0028g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0029g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0030g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0031g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0032g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0033g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0034g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0034g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0035g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0035g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0036g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0037g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0039g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0040g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0041g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0042g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0043g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0044g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0045g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0046g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0047g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0048g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0049g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0050g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0051g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0052g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0053g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0054g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0055g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0056g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0057g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0058g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0059g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0060g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0061g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0062g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0063g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0064g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0065g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0066g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0067g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0001t0068g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0002t0007g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0002t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0002t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0003t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0003t0017g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0003t0017g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0005t0011g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0005t0011g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0001c0007t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0002c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0002c0004t0020g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0002c0004t0038g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0003c0008t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| a0004c0009t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0012 | g0023 | EUR | GBR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0100 | EUR | GBR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00280 | hp1 | a0001 | c0001 | t0033 | g0043 | EUR | FIN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00323 | hp1 | a0001 | c0001 | t0012 | g0023 | EUR | FIN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00438 | hp1 | a0001 | c0001 | t0029 | g0049 | EAS | CHS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00544 | hp2 | a0001 | c0001 | t0049 | g0216 | EAS | CHS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0191 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00642 | hp1 | a0001 | c0001 | t0057 | g0186 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0183 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0044 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01069 | hp1 | a0001 | c0001 | t0033 | g0043 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01099 | hp2 | a0001 | c0001 | t0012 | g0023 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01106 | hp2 | a0001 | c0001 | t0026 | g0107 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01109 | hp2 | a0001 | c0002 | t0007 | g0013 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01167 | hp2 | a0001 | c0003 | t0017 | g0052 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0044 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01243 | hp1 | a0001 | c0001 | t0014 | g0015 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01243 | hp2 | a0001 | c0001 | t0055 | g0105 | AMR | PUR | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01257 | hp1 | a0001 | c0001 | t0019 | g0094 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01361 | hp2 | a0001 | c0001 | t0024 | g0181 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01496 | hp2 | a0001 | c0001 | t0012 | g0123 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0125 | EUR | IBS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0184 | EUR | IBS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0041 | EUR | IBS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0099 | EUR | IBS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0041 | EUR | IBS | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0200 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01891 | hp2 | a0001 | c0001 | t0066 | g0171 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0086 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01978 | hp1 | a0001 | c0001 | t0008 | g0085 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02071 | hp2 | a0001 | c0001 | t0068 | g0165 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02080 | hp2 | a0001 | c0001 | t0025 | g0048 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0018 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0025 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02135 | hp2 | a0001 | c0001 | t0045 | g0066 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02145 | hp1 | a0001 | c0001 | t0022 | g0141 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02145 | hp2 | a0001 | c0001 | t0028 | g0161 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02148 | hp1 | a0001 | c0001 | t0008 | g0084 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02155 | hp2 | a0001 | c0001 | t0060 | g0219 | EAS | CDX | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CDX | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02257 | hp1 | a0001 | c0001 | t0027 | g0075 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0199 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02280 | hp1 | a0001 | c0002 | t0007 | g0013 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0015 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02451 | hp1 | a0001 | c0001 | t0040 | g0198 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02451 | hp2 | a0001 | c0001 | t0064 | g0202 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02602 | hp1 | a0001 | c0001 | t0030 | g0036 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02602 | hp2 | a0001 | c0001 | t0008 | g0025 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02615 | hp1 | a0001 | c0001 | t0044 | g0153 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02622 | hp1 | a0001 | c0001 | t0039 | g0144 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02622 | hp2 | a0001 | c0001 | t0024 | g0072 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02630 | hp1 | a0001 | c0001 | t0047 | g0167 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0136 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0046 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02723 | hp1 | a0001 | c0001 | t0065 | g0178 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02809 | hp1 | a0001 | c0002 | t0007 | g0013 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02809 | hp2 | a0001 | c0005 | t0011 | g0158 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0143 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02818 | hp2 | a0001 | c0002 | t0007 | g0013 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0142 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02886 | hp2 | a0001 | c0001 | t0034 | g0060 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02895 | hp1 | a0002 | c0004 | t0020 | g0027 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02895 | hp2 | a0001 | c0001 | t0034 | g0061 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0024 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02897 | hp1 | a0002 | c0004 | t0020 | g0027 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0024 | AFR | GWD | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02922 | hp2 | a0001 | c0001 | t0046 | g0074 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02965 | hp1 | a0001 | c0001 | t0014 | g0015 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0138 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02970 | hp2 | a0001 | c0001 | t0043 | g0076 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02976 | hp2 | a0001 | c0002 | t0007 | g0197 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03098 | hp2 | a0001 | c0002 | t0007 | g0196 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03130 | hp2 | a0001 | c0003 | t0017 | g0026 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03139 | hp2 | a0001 | c0001 | t0023 | g0040 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03209 | hp2 | a0001 | c0001 | t0021 | g0155 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03225 | hp1 | a0002 | c0004 | t0038 | g0054 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0114 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03453 | hp2 | a0001 | c0001 | t0028 | g0162 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03490 | hp1 | a0001 | c0001 | t0054 | g0079 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03490 | hp2 | a0001 | c0001 | t0035 | g0122 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03492 | hp1 | a0001 | c0001 | t0051 | g0106 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03492 | hp2 | a0001 | c0001 | t0019 | g0121 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03516 | hp1 | a0001 | c0003 | t0017 | g0026 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03516 | hp2 | a0001 | c0001 | t0022 | g0140 | AFR | ESN | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03579 | hp1 | a0001 | c0005 | t0011 | g0157 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0039 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03669 | hp1 | a0001 | c0001 | t0012 | g0038 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03669 | hp2 | a0001 | c0001 | t0030 | g0036 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | STU | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03710 | hp1 | a0001 | c0001 | t0008 | g0025 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03834 | hp1 | a0001 | c0001 | t0012 | g0038 | SAS | BEB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0030 | SAS | BEB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG04115 | hp1 | a0001 | c0001 | t0035 | g0146 | SAS | STU | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG04115 | hp2 | a0001 | c0001 | t0041 | g0118 | SAS | STU | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0050 | SAS | BEB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG04228 | hp1 | a0001 | c0001 | t0008 | g0180 | SAS | STU | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG04228 | hp2 | a0001 | c0001 | t0050 | g0179 | SAS | STU | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0046 | AFR | YRI | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18522 | hp2 | a0001 | c0001 | t0011 | g0024 | AFR | YRI | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18612 | hp1 | a0001 | c0001 | t0048 | g0211 | EAS | CHB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | CHB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | CHB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18906 | hp1 | a0002 | c0004 | t0001 | g0055 | AFR | YRI | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | YRI | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0063 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18945 | hp2 | a0001 | c0001 | t0053 | g0108 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18946 | hp1 | a0001 | c0001 | t0061 | g0206 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18949 | hp2 | a0003 | c0008 | t0001 | g0195 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18950 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18952 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18954 | hp1 | a0001 | c0001 | t0032 | g0037 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18956 | hp1 | a0001 | c0001 | t0019 | g0149 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18956 | hp2 | a0001 | c0001 | t0016 | g0051 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18961 | hp1 | a0001 | c0001 | t0063 | g0220 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18964 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18970 | hp1 | a0001 | c0007 | t0006 | g0065 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18971 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18973 | hp2 | a0001 | c0001 | t0016 | g0051 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18974 | hp1 | a0001 | c0001 | t0058 | g0203 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18975 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18977 | hp1 | a0001 | c0001 | t0062 | g0215 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18980 | hp1 | a0001 | c0001 | t0059 | g0160 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18991 | hp1 | a0001 | c0001 | t0009 | g0090 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18997 | hp2 | a0001 | c0001 | t0009 | g0087 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18998 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19001 | hp1 | a0001 | c0001 | t0031 | g0034 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19001 | hp2 | a0001 | c0001 | t0032 | g0037 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19005 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19030 | hp1 | a0001 | c0001 | t0027 | g0068 | AFR | LWK | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19030 | hp2 | a0001 | c0001 | t0013 | g0137 | AFR | LWK | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | LWK | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19054 | hp1 | a0004 | c0009 | t0003 | g0190 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19058 | hp1 | a0001 | c0001 | t0025 | g0048 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19058 | hp2 | a0001 | c0001 | t0037 | g0128 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19062 | hp2 | a0001 | c0001 | t0018 | g0078 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19063 | hp2 | a0001 | c0006 | t0001 | g0159 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19064 | hp2 | a0001 | c0001 | t0036 | g0115 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19066 | hp1 | a0001 | c0001 | t0042 | g0103 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19070 | hp2 | a0001 | c0001 | t0018 | g0035 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19072 | hp2 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19077 | hp1 | a0001 | c0001 | t0029 | g0049 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19077 | hp2 | a0001 | c0001 | t0031 | g0034 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19078 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19078 | hp2 | a0001 | c0001 | t0016 | g0218 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19089 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19090 | hp2 | a0001 | c0001 | t0052 | g0117 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0039 | AFR | ASW | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0134 | EUR | TSI | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0187 | EUR | TSI | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0201 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG02559 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03471 | hp1 | a0001 | c0001 | t0067 | g0172 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG03471 | hp2 | a0001 | c0001 | t0015 | g0168 | AFR | MSL | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG06807 | hp1 | a0001 | c0001 | t0014 | g0015 | AFR | USA | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| HG06807 | hp2 | a0001 | c0001 | t0026 | g0073 | AFR | USA | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA18955 | hp2 | a0001 | c0001 | t0018 | g0035 | EAS | JPT | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA20300 | hp1 | a0001 | c0001 | t0023 | g0040 | AFR | USA | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA20300 | hp2 | a0001 | c0001 | t0015 | g0170 | AFR | USA | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA21309 | hp1 | a0001 | c0001 | t0021 | g0139 | AFR | LWK | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0169 | AFR | LWK | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0056 | g0150 | REF | REF | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0176 | REF | REF | TNFRSF9_chr1_7910871_7945839 | TNFRSF9 | chr1 | 7910871 | 7945839 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:7935030 | G | T | 1 | a0002 | 4 | HG02895.hp1 HG02897.hp1 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.527C>A | p.Ala176Asp | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/8 | 667/5872 | 527/768 | 176/255 | chr1 | 7935030 | |||
| chr1:7939935 | C | A | 1 | a0003 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.60G>T | p.Arg20Ser | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/8 | 200/5872 | 60/768 | 20/255 | chr1 | 7939935 | |||
| chr1:7939961 | G | C | 1 | a0004 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.34C>G | p.Leu12Val | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/8 | 174/5872 | 34/768 | 12/255 | chr1 | 7939961 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:7935062 | G | T | 1 | a0001c0006 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.495C>A | p.Leu165Leu | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/8 | 635/5872 | 495/768 | 165/255 | chr1 | 7935062 | |||
| chr1:7935092 | G | A | 1 | a0001c0007 | 1 | NA18970.hp1 | synonymous_variant | LOW | c.465C>T | p.Asp155Asp | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/8 | 605/5872 | 465/768 | 155/255 | chr1 | 7935092 | |||
| chr1:7938248 | T | C | 1 | a0001c0005 | 2 | HG02809.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.291A>G | p.Ala97Ala | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 4/8 | 431/5872 | 291/768 | 97/255 | chr1 | 7938248 | |||
| chr1:7939911 | A | G | 1 | a0001c0002 | 6 | HG01109.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
synonymous_variant | LOW | c.84T>C | p.Cys28Cys | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/8 | 224/5872 | 84/768 | 28/255 | chr1 | 7939911 | |||
| chr1:7939965 | G | A | 1 | a0001c0003 | 6 | HG00639.hp2 HG01167.hp2 HG02615.hp2 others(3): Show |
synonymous_variant | LOW | c.30C>T | p.Ala10Ala | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/8 | 170/5872 | 30/768 | 10/255 | chr1 | 7939965 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:7915907 | T | C | 1 | a0001c0001t0055 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4928A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 4928 | chr1 | 7915907 | ||||||
| chr1:7915946 | G | A | 1 | a0001c0001t0049 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4889C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 4889 | chr1 | 7915946 | ||||||
| chr1:7916272 | C | A | 8 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0015 others(5): Show |
26 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4563G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 4563 | chr1 | 7916272 | ||||||
| chr1:7916518 | C | T | 3 | a0001c0001t0060 a0001c0001t0066 a0001c0001t0067 |
3 | HG01891.hp2 HG02155.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4317G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 4317 | chr1 | 7916518 | ||||||
| chr1:7916610 | G | A | 1 | a0001c0001t0034 | 2 | HG02886.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4225C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 4225 | chr1 | 7916610 | ||||||
| chr1:7916633 | A | C | 1 | a0001c0001t0040 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4202T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 4202 | chr1 | 7916633 | ||||||
| chr1:7916695 | T | A | 1 | a0001c0001t0037 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4140A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 4140 | chr1 | 7916695 | ||||||
| chr1:7916699 | A | G | 2 | a0001c0001t0066 a0001c0001t0067 |
2 | HG01891.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4136T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 4136 | chr1 | 7916699 | ||||||
| chr1:7917177 | C | T | 1 | a0001c0001t0068 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3658G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 3658 | chr1 | 7917177 | ||||||
| chr1:7917180 | G | A | 1 | a0002c0004t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3655C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 3655 | chr1 | 7917180 | ||||||
| chr1:7917235 | T | G | 1 | a0001c0001t0037 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3600A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 3600 | chr1 | 7917235 | ||||||
| chr1:7917359 | G | A | 1 | a0001c0001t0061 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3476C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 3476 | chr1 | 7917359 | ||||||
| chr1:7917443 | A | G | 2 | a0001c0001t0066 a0001c0001t0067 |
2 | HG01891.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3392T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 3392 | chr1 | 7917443 | ||||||
| chr1:7917521 | A | T | 1 | a0001c0001t0058 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3314T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 3314 | chr1 | 7917521 | ||||||
| chr1:7917580 | A | C | 1 | a0001c0001t0033 | 2 | HG00280.hp1 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3255T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 3255 | chr1 | 7917580 | ||||||
| chr1:7917771 | C | T | 1 | a0002c0004t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3064G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 3064 | chr1 | 7917771 | ||||||
| chr1:7917819 | G | A | 1 | a0001c0001t0062 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3016C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 3016 | chr1 | 7917819 | ||||||
| chr1:7917955 | G | GAT | 11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0011 others(8): Show |
46 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2878_*2879dupAT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2879 | chr1 | 7917955 | ||||||
| chr1:7917955 | G | GATAT | 4 | a0001c0001t0031 a0001c0001t0036 a0001c0001t0041 others(1): Show |
5 | HG04115.hp2 NA19001.hp1 NA19064.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2876_*2879dupATAT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2879 | chr1 | 7917955 | ||||||
| chr1:7917967 | TATATATA others(3): Show |
T | 1 | a0001c0003t0017 | 3 | HG01167.hp2 HG03130.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2858_*2867delCTAT others(6): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2858 | chr1 | 7917967 | ||||||
| chr1:7917969 | T | G | 1 | a0001c0001t0002 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2866A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2866 | chr1 | 7917969 | ||||||
| chr1:7917969 | TATATATA others(7): Show |
T | 1 | a0002c0004t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2852_*2865delCTAT others(10): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2852 | chr1 | 7917969 | ||||||
| chr1:7917971 | T | G | 1 | a0001c0001t0001 | 2 | HG00099.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2864A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2864 | chr1 | 7917971 | ||||||
| chr1:7917973 | T | G | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(2): Show |
13 | HG00544.hp1 HG00639.hp2 HG01074.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2862A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2862 | chr1 | 7917973 | ||||||
| chr1:7917975 | TAG | T | 1 | a0001c0001t0002 | 5 | HG01496.hp1 HG01943.hp2 HG01975.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2858_*2859delCT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2858 | chr1 | 7917975 | ||||||
| chr1:7917977 | G | T | 12 | a0001c0001t0013 a0001c0001t0015 a0001c0001t0021 others(9): Show |
20 | HG00544.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2858C>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2858 | chr1 | 7917977 | ||||||
| chr1:7917977 | GAT | G | 9 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0016 others(6): Show |
75 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2856_*2857delAT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2856 | chr1 | 7917977 | ||||||
| chr1:7917979 | T | G | 4 | a0001c0001t0044 a0001c0001t0049 a0001c0001t0051 others(1): Show |
4 | HG00544.hp2 HG02615.hp1 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2856A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2856 | chr1 | 7917979 | ||||||
| chr1:7917979 | T | TAG | 11 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(8): Show |
47 | HG00438.hp1 HG01109.hp2 HG01346.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2855_*2856insCT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2855 | chr1 | 7917979 | ||||||
| chr1:7917979 | T | TAGATAG | 2 | a0001c0001t0015 a0001c0001t0048 |
4 | HG03471.hp2 NA18612.hp1 NA20300.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2855_*2856insCTAT others(2): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2855 | chr1 | 7917979 | ||||||
| chr1:7917979 | T | TATAG | 4 | a0001c0001t0026 a0001c0001t0039 a0001c0001t0043 others(1): Show |
5 | HG01106.hp2 HG02622.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2852_*2855dupCTAT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2855 | chr1 | 7917979 | ||||||
| chr1:7917979 | T | TATATAGA others(7): Show |
1 | a0001c0001t0013 | 4 | HG02965.hp2 HG03579.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2855_*2856insCTAT others(10): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2855 | chr1 | 7917979 | ||||||
| chr1:7917979 | T | TATATATA others(7): Show |
1 | a0001c0001t0022 | 2 | HG02145.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2855_*2856insCTAT others(10): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2855 | chr1 | 7917979 | ||||||
| chr1:7917989 | T | G | 1 | a0002c0004t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2846A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2846 | chr1 | 7917989 | ||||||
| chr1:7917993 | T | G | 1 | a0002c0004t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2842A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2842 | chr1 | 7917993 | ||||||
| chr1:7917997 | T | G | 1 | a0002c0004t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2838A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2838 | chr1 | 7917997 | ||||||
| chr1:7918001 | T | G | 1 | a0002c0004t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2834A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2834 | chr1 | 7918001 | ||||||
| chr1:7918004 | G | A | 1 | a0002c0004t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2831C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2831 | chr1 | 7918004 | ||||||
| chr1:7918115 | C | G | 1 | a0001c0001t0032 | 2 | NA18954.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2720G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2720 | chr1 | 7918115 | ||||||
| chr1:7918130 | C | A | 1 | a0001c0001t0037 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2705G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2705 | chr1 | 7918130 | ||||||
| chr1:7918131 | C | T | 3 | a0001c0001t0009 a0001c0001t0031 a0001c0001t0042 |
12 | NA18950.hp1 NA18952.hp2 NA18971.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2704G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2704 | chr1 | 7918131 | ||||||
| chr1:7918150 | A | T | 1 | a0001c0001t0058 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2685T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2685 | chr1 | 7918150 | ||||||
| chr1:7918174 | T | C | 3 | a0001c0001t0006 a0001c0001t0045 a0001c0007t0006 |
16 | HG02071.hp1 HG02129.hp1 HG02135.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2661A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2661 | chr1 | 7918174 | ||||||
| chr1:7918175 | G | A | 1 | a0001c0001t0057 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2660C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2660 | chr1 | 7918175 | ||||||
| chr1:7918265 | T | C | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(16): Show |
114 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2570A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2570 | chr1 | 7918265 | ||||||
| chr1:7918306 | C | T | 1 | a0002c0004t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2529G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2529 | chr1 | 7918306 | ||||||
| chr1:7918327 | T | A | 1 | a0001c0001t0058 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2508A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2508 | chr1 | 7918327 | ||||||
| chr1:7918342 | A | G | 19 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(16): Show |
113 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2493T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2493 | chr1 | 7918342 | ||||||
| chr1:7918434 | A | G | 1 | a0001c0001t0053 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2401T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2401 | chr1 | 7918434 | ||||||
| chr1:7918586 | C | T | 1 | a0001c0001t0059 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2249G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2249 | chr1 | 7918586 | ||||||
| chr1:7918662 | C | T | 18 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(15): Show |
112 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2173G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2173 | chr1 | 7918662 | ||||||
| chr1:7918727 | C | T | 1 | a0001c0001t0052 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2108G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 2108 | chr1 | 7918727 | ||||||
| chr1:7918845 | T | C | 1 | a0001c0001t0046 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1990A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1990 | chr1 | 7918845 | ||||||
| chr1:7918853 | G | T | 1 | a0001c0001t0058 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982C>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1982 | chr1 | 7918853 | ||||||
| chr1:7918869 | T | C | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1966A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1966 | chr1 | 7918869 | ||||||
| chr1:7918916 | C | T | 1 | a0001c0001t0051 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1919G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1919 | chr1 | 7918916 | ||||||
| chr1:7918922 | A | G | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1913T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1913 | chr1 | 7918922 | ||||||
| chr1:7918977 | C | T | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1858G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1858 | chr1 | 7918977 | ||||||
| chr1:7918986 | A | C | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1849T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1849 | chr1 | 7918986 | ||||||
| chr1:7919001 | A | T | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1834T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1834 | chr1 | 7919001 | ||||||
| chr1:7919305 | T | C | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1530A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1530 | chr1 | 7919305 | ||||||
| chr1:7919353 | T | C | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1482A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1482 | chr1 | 7919353 | ||||||
| chr1:7919390 | C | G | 1 | a0001c0001t0030 | 2 | HG02602.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1445G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1445 | chr1 | 7919390 | ||||||
| chr1:7919514 | G | A | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(17): Show |
115 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1321C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1321 | chr1 | 7919514 | ||||||
| chr1:7919567 | G | A | 1 | a0001c0001t0065 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1268C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1268 | chr1 | 7919567 | ||||||
| chr1:7919793 | G | A | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1042C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 1042 | chr1 | 7919793 | ||||||
| chr1:7919874 | G | T | 1 | a0001c0001t0037 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*961C>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 961 | chr1 | 7919874 | ||||||
| chr1:7919875 | T | A | 1 | a0001c0001t0037 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*960A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 960 | chr1 | 7919875 | ||||||
| chr1:7919876 | A | T | 1 | a0001c0001t0037 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*959T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 959 | chr1 | 7919876 | ||||||
| chr1:7920075 | G | A | 2 | a0001c0001t0014 a0001c0001t0027 |
6 | HG01243.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*760C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 760 | chr1 | 7920075 | ||||||
| chr1:7920108 | C | T | 1 | a0001c0001t0050 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*727G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 727 | chr1 | 7920108 | ||||||
| chr1:7920122 | G | A | 1 | a0001c0001t0041 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*713C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 713 | chr1 | 7920122 | ||||||
| chr1:7920278 | A | G | 33 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(30): Show |
151 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*557T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 557 | chr1 | 7920278 | ||||||
| chr1:7920286 | AGTG | A | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546_*548delCAC | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 546 | chr1 | 7920286 | ||||||
| chr1:7920304 | C | CT | 16 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0012 others(13): Show |
84 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*530dupA | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 530 | chr1 | 7920304 | ||||||
| chr1:7920304 | C | CTT | 4 | a0001c0001t0023 a0001c0001t0024 a0001c0001t0041 others(1): Show |
6 | HG01361.hp2 HG01891.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*529_*530dupAA | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 530 | chr1 | 7920304 | ||||||
| chr1:7920304 | C | CTTT | 9 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0013 others(6): Show |
30 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*528_*530dupAAA | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 530 | chr1 | 7920304 | ||||||
| chr1:7920304 | CT | C | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0014 others(7): Show |
94 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*530delA | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 530 | chr1 | 7920304 | ||||||
| chr1:7920304 | CTTTT | C | 2 | a0001c0001t0010 a0001c0001t0064 |
8 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*527_*530delAAAA | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 527 | chr1 | 7920304 | ||||||
| chr1:7920412 | C | T | 2 | a0002c0004t0020 a0002c0004t0038 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*423G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 423 | chr1 | 7920412 | ||||||
| chr1:7920509 | G | A | 1 | a0001c0001t0065 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 326 | chr1 | 7920509 | ||||||
| chr1:7920565 | A | T | 1 | a0001c0001t0037 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*270T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 270 | chr1 | 7920565 | ||||||
| chr1:7920648 | C | CA | 6 | a0001c0001t0012 a0001c0001t0019 a0001c0001t0035 others(3): Show |
14 | HG00099.hp1 HG00323.hp1 HG01099.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*186dupT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 186 | chr1 | 7920648 | ||||||
| chr1:7920686 | C | T | 1 | a0001c0001t0036 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 8/8 | 149 | chr1 | 7920686 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:7921052 | T | C | 1 | a0001c0001t0003g0041 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.680-129A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921052 | |||||||
| chr1:7921061 | C | T | 1 | a0001c0001t0024g0181 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.680-138G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921061 | |||||||
| chr1:7921065 | G | A | 7 | a0001c0001t0013g0039 a0001c0001t0013g0137 a0001c0001t0013g0138 others(4): Show |
8 | HG02145.hp1 HG02965.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-142C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921065 | |||||||
| chr1:7921143 | G | C | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-220C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921143 | |||||||
| chr1:7921192 | C | T | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-269G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921192 | |||||||
| chr1:7921193 | G | A | 2 | a0001c0001t0002g0217 a0001c0001t0021g0155 |
2 | HG03209.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.680-270C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921193 | |||||||
| chr1:7921324 | G | A | 2 | a0001c0001t0003g0070 a0001c0001t0003g0192 |
2 | HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.680-401C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921324 | |||||||
| chr1:7921338 | A | AAAAAC | 100 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0032 others(97): Show |
151 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.680-420_680-416dup others(5): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921338 | |||||||
| chr1:7921338 | A | AAAAACAA others(3): Show |
6 | a0001c0001t0001g0020 a0001c0001t0001g0088 a0001c0001t0005g0116 others(3): Show |
8 | HG00741.hp2 HG01069.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-425_680-416dup others(10): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921338 | |||||||
| chr1:7921338 | A | AAAAACAA others(8): Show |
2 | a0001c0001t0028g0161 a0001c0001t0028g0162 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.680-430_680-416dup others(15): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921338 | |||||||
| chr1:7921338 | AAAAAC | A | 9 | a0001c0001t0003g0192 a0001c0001t0007g0014 a0001c0001t0007g0046 others(6): Show |
18 | HG00099.hp1 HG00323.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.680-420_680-416del others(5): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921338 | |||||||
| chr1:7921338 | AAAAACAA others(3): Show |
A | 53 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(50): Show |
122 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.680-425_680-416del others(10): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921338 | |||||||
| chr1:7921389 | C | T | 2 | a0001c0001t0006g0028 a0001c0001t0006g0063 |
3 | NA18943.hp2 NA18945.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.680-466G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921389 | |||||||
| chr1:7921393 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(126): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.680-470G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921393 | |||||||
| chr1:7921476 | G | A | 1 | a0001c0001t0036g0115 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.680-553C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921476 | |||||||
| chr1:7921518 | A | G | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-595T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921518 | |||||||
| chr1:7921530 | G | C | 1 | a0001c0001t0003g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.680-607C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921530 | |||||||
| chr1:7921542 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.680-619C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921542 | |||||||
| chr1:7921571 | A | C | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-648T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921571 | |||||||
| chr1:7921582 | C | A | 9 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0047 others(6): Show |
30 | HG00438.hp2 HG00673.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.680-659G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921582 | |||||||
| chr1:7921592 | T | C | 79 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
158 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.680-669A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921592 | |||||||
| chr1:7921627 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.680-704G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921627 | |||||||
| chr1:7921629 | C | T | 1 | a0001c0001t0062g0215 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.680-706G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921629 | |||||||
| chr1:7921729 | C | A | 1 | a0001c0001t0001g0102 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.680-806G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921729 | |||||||
| chr1:7921805 | A | G | 1 | a0001c0001t0007g0199 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.680-882T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921805 | |||||||
| chr1:7921833 | A | G | 1 | a0001c0001t0034g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.680-910T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921833 | |||||||
| chr1:7921958 | G | A | 4 | a0001c0001t0001g0104 a0001c0001t0001g0133 a0001c0001t0001g0164 others(1): Show |
4 | HG01243.hp2 HG02055.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-1035C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921958 | |||||||
| chr1:7921974 | T | C | 52 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(49): Show |
119 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.680-1051A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7921974 | |||||||
| chr1:7922173 | A | G | 1 | a0001c0001t0008g0183 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.680-1250T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922173 | |||||||
| chr1:7922378 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.680-1455T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922378 | |||||||
| chr1:7922411 | C | T | 1 | a0002c0004t0038g0054 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.680-1488G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922411 | |||||||
| chr1:7922459 | A | T | 37 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(34): Show |
95 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.680-1536T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922459 | |||||||
| chr1:7922476 | C | T | 1 | a0001c0001t0048g0211 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.680-1553G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922476 | |||||||
| chr1:7922633 | G | A | 1 | a0001c0001t0016g0218 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.680-1710C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922633 | |||||||
| chr1:7922681 | G | A | 2 | a0001c0001t0066g0171 a0001c0001t0067g0172 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.680-1758C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922681 | |||||||
| chr1:7922700 | T | C | 2 | a0001c0001t0066g0171 a0001c0001t0067g0172 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.680-1777A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922700 | |||||||
| chr1:7922756 | G | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0145 others(13): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.680-1833C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922756 | |||||||
| chr1:7922798 | C | A | 2 | a0001c0001t0007g0014 a0001c0001t0040g0198 |
5 | HG01884.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-1875G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922798 | |||||||
| chr1:7922871 | G | A | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-1948C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922871 | |||||||
| chr1:7922896 | T | TC | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.680-1974dupG | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922896 | |||||||
| chr1:7922897 | C | CT | 6 | a0001c0001t0002g0214 a0001c0001t0004g0207 a0001c0001t0004g0210 others(3): Show |
7 | HG02895.hp1 HG02897.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-1975dupA | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922897 | |||||||
| chr1:7922907 | T | TTC | 39 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(36): Show |
102 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.680-1985_680-1984i others(4): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922907 | |||||||
| chr1:7922908 | C | T | 39 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(36): Show |
103 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.680-1985G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922908 | |||||||
| chr1:7922909 | T | C | 1 | a0001c0001t0003g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.680-1986A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7922909 | |||||||
| chr1:7923230 | T | G | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.680-2307A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923230 | |||||||
| chr1:7923311 | C | A | 3 | a0001c0001t0023g0040 a0001c0001t0028g0161 a0001c0001t0028g0162 |
4 | HG02145.hp2 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-2388G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923311 | |||||||
| chr1:7923340 | C | T | 1 | a0001c0001t0051g0106 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.680-2417G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923340 | |||||||
| chr1:7923392 | C | T | 7 | a0001c0001t0001g0185 a0001c0001t0003g0187 a0001c0001t0005g0184 others(4): Show |
10 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.680-2469G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923392 | |||||||
| chr1:7923528 | G | A | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-2605C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923528 | |||||||
| chr1:7923761 | C | G | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-2838G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923761 | |||||||
| chr1:7923765 | G | C | 5 | a0001c0001t0044g0153 a0001c0003t0001g0045 a0001c0003t0001g0191 others(2): Show |
7 | HG00639.hp2 HG01167.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-2842C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923765 | |||||||
| chr1:7923787 | G | A | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-2864C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923787 | |||||||
| chr1:7923787 | G | T | 3 | a0001c0001t0023g0040 a0001c0001t0028g0161 a0001c0001t0028g0162 |
4 | HG02145.hp2 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-2864C>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923787 | |||||||
| chr1:7923850 | T | A | 1 | a0002c0004t0038g0054 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.680-2927A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923850 | |||||||
| chr1:7923964 | G | A | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.680-3041C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7923964 | |||||||
| chr1:7924081 | G | A | 2 | a0001c0001t0027g0068 a0001c0001t0027g0075 |
2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.680-3158C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924081 | |||||||
| chr1:7924294 | C | CAT | 6 | a0001c0001t0011g0024 a0001c0001t0034g0061 a0001c0003t0001g0191 others(3): Show |
9 | HG00639.hp2 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.680-3373_680-3372d others(4): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | C | CATAT | 2 | a0001c0001t0007g0142 a0001c0003t0001g0045 |
3 | HG02615.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.680-3375_680-3372d others(6): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | C | CATATGTA others(5): Show |
1 | a0001c0001t0047g0167 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.680-3372_680-3371i others(14): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | C | CATATGTA others(9): Show |
1 | a0001c0001t0015g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.680-3372_680-3371i others(18): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | C | CATATGTA others(13): Show |
1 | a0001c0001t0015g0170 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.680-3372_680-3371i others(22): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CAT | C | 3 | a0001c0001t0003g0041 a0001c0001t0011g0143 a0001c0001t0050g0179 |
4 | HG01516.hp1 HG01517.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-3373_680-3372d others(4): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATAT | C | 8 | a0001c0001t0001g0042 a0001c0001t0001g0177 a0001c0001t0001g0188 others(5): Show |
9 | HG00642.hp1 HG00735.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.680-3375_680-3372d others(6): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATATAT | C | 5 | a0001c0001t0001g0182 a0001c0001t0003g0100 a0001c0001t0013g0138 others(2): Show |
5 | HG00140.hp2 HG00733.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-3377_680-3372d others(8): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATATATA others(1): Show |
C | 23 | a0001c0001t0001g0077 a0001c0001t0001g0101 a0001c0001t0001g0102 others(20): Show |
29 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.680-3379_680-3372d others(10): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATATATA others(3): Show |
C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0104 others(23): Show |
39 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.680-3381_680-3372d others(12): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATATATA others(5): Show |
C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0022 others(73): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.680-3383_680-3372d others(14): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATATATA others(7): Show |
C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0110 others(11): Show |
27 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.680-3385_680-3372d others(16): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATATATA others(9): Show |
C | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0002c0004t0001g0055 |
3 | HG02258.hp2 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.680-3387_680-3372d others(18): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATATATA others(15): Show |
C | 1 | a0001c0001t0060g0219 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.680-3393_680-3372d others(24): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATATATA others(17): Show |
C | 44 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(41): Show |
110 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.680-3395_680-3372d others(26): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924294 | CATATATA others(19): Show |
C | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.680-3397_680-3372d others(28): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924294 | |||||||
| chr1:7924334 | T | A | 1 | a0001c0001t0060g0219 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.680-3411A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924334 | |||||||
| chr1:7924425 | G | C | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-3502C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924425 | |||||||
| chr1:7924575 | C | T | 2 | a0001c0001t0003g0031 a0001c0002t0007g0013 |
6 | HG01109.hp2 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.680-3652G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924575 | |||||||
| chr1:7924580 | C | A | 45 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(42): Show |
111 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.680-3657G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924580 | |||||||
| chr1:7924582 | G | A | 1 | a0001c0001t0004g0209 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.680-3659C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7924582 | |||||||
| chr1:7925041 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.680-4118G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925041 | |||||||
| chr1:7925080 | G | A | 1 | a0001c0001t0003g0111 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.680-4157C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925080 | |||||||
| chr1:7925096 | C | T | 2 | a0001c0003t0017g0026 a0001c0003t0017g0052 |
3 | HG01167.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.680-4173G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925096 | |||||||
| chr1:7925302 | C | CAA | 18 | a0001c0001t0002g0212 a0001c0001t0004g0008 a0001c0001t0004g0050 others(15): Show |
27 | HG00438.hp1 HG01346.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.680-4381_680-4380d others(4): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925302 | |||||||
| chr1:7925302 | C | CAAA | 26 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(23): Show |
83 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.680-4382_680-4380d others(5): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925302 | |||||||
| chr1:7925312 | A | T | 1 | a0001c0001t0003g0098 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.680-4389T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925312 | |||||||
| chr1:7925374 | G | T | 1 | a0001c0001t0034g0061 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.680-4451C>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925374 | |||||||
| chr1:7925454 | A | G | 2 | a0001c0001t0019g0121 a0001c0001t0035g0122 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.680-4531T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925454 | |||||||
| chr1:7925729 | G | A | 1 | a0001c0001t0004g0050 | 2 | HG02135.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.680-4806C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925729 | |||||||
| chr1:7925740 | C | G | 45 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(42): Show |
111 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.680-4817G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925740 | |||||||
| chr1:7925748 | C | T | 2 | a0001c0001t0015g0168 a0001c0001t0047g0167 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.680-4825G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925748 | |||||||
| chr1:7925797 | C | T | 1 | a0001c0001t0006g0063 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.680-4874G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925797 | |||||||
| chr1:7925798 | G | A | 3 | a0001c0001t0023g0040 a0001c0001t0028g0161 a0001c0001t0028g0162 |
4 | HG02145.hp2 HG03139.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.680-4875C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925798 | |||||||
| chr1:7925899 | C | T | 1 | a0002c0004t0001g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.680-4976G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7925899 | |||||||
| chr1:7926062 | G | A | 1 | a0001c0001t0008g0084 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.680-5139C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926062 | |||||||
| chr1:7926121 | G | A | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-5198C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926121 | |||||||
| chr1:7926272 | C | T | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.680-5349G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926272 | |||||||
| chr1:7926302 | T | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0047 a0001c0001t0002g0205 |
13 | HG01099.hp1 HG01192.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.680-5379A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926302 | |||||||
| chr1:7926546 | C | T | 5 | a0001c0001t0044g0153 a0001c0003t0001g0045 a0001c0003t0001g0191 others(2): Show |
7 | HG00639.hp2 HG01167.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-5623G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926546 | |||||||
| chr1:7926549 | G | C | 1 | a0001c0002t0007g0013 | 4 | HG01109.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-5626C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926549 | |||||||
| chr1:7926551 | C | T | 5 | a0001c0001t0044g0153 a0001c0003t0001g0045 a0001c0003t0001g0191 others(2): Show |
7 | HG00639.hp2 HG01167.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.680-5628G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926551 | |||||||
| chr1:7926612 | T | G | 1 | a0001c0001t0002g0204 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.680-5689A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926612 | |||||||
| chr1:7926699 | A | G | 1 | a0001c0001t0065g0178 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.680-5776T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926699 | |||||||
| chr1:7926703 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.680-5780T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7926703 | |||||||
| chr1:7927011 | G | T | 43 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(40): Show |
108 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.680-6088C>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927011 | |||||||
| chr1:7927062 | T | TA | 110 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0020 others(107): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.679+6099dupT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927062 | |||||||
| chr1:7927103 | G | A | 1 | a0002c0004t0020g0027 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.679+6059C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927103 | |||||||
| chr1:7927492 | T | C | 45 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(42): Show |
111 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.679+5670A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927492 | |||||||
| chr1:7927498 | C | A | 1 | a0001c0001t0044g0153 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.679+5664G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927498 | |||||||
| chr1:7927498 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.679+5664G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927498 | |||||||
| chr1:7927597 | G | A | 1 | a0001c0001t0032g0037 | 2 | NA18954.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.679+5565C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927597 | |||||||
| chr1:7927629 | T | A | 43 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(40): Show |
108 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.679+5533A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927629 | |||||||
| chr1:7927730 | G | GA | 33 | a0001c0001t0001g0177 a0001c0001t0003g0019 a0001c0001t0003g0031 others(30): Show |
45 | HG00099.hp1 HG00323.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.679+5431dupT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927730 | |||||||
| chr1:7927932 | C | G | 2 | a0001c0001t0028g0161 a0001c0001t0028g0162 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.679+5230G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7927932 | |||||||
| chr1:7928085 | G | A | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
159 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.679+5077C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7928085 | |||||||
| chr1:7928187 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.679+4975G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7928187 | |||||||
| chr1:7928251 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0096 a0001c0001t0001g0124 others(1): Show |
4 | NA19006.hp1 NA19011.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+4911G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7928251 | |||||||
| chr1:7928443 | A | C | 43 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(40): Show |
108 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.679+4719T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7928443 | |||||||
| chr1:7928621 | G | A | 1 | a0001c0001t0057g0186 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.679+4541C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7928621 | |||||||
| chr1:7928731 | T | A | 1 | a0001c0001t0003g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.679+4431A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7928731 | |||||||
| chr1:7928835 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.679+4327G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7928835 | |||||||
| chr1:7928951 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.679+4211G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7928951 | |||||||
| chr1:7928962 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0145 others(13): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.679+4200G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7928962 | |||||||
| chr1:7929079 | T | C | 43 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(40): Show |
108 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.679+4083A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929079 | |||||||
| chr1:7929132 | C | T | 1 | a0001c0001t0068g0165 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.679+4030G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929132 | |||||||
| chr1:7929142 | C | CT | 52 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(49): Show |
125 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.679+4019dupA | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929142 | |||||||
| chr1:7929156 | TC | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(108): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.679+4005delG | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929156 | |||||||
| chr1:7929157 | CCT | C | 28 | a0001c0001t0001g0174 a0001c0001t0003g0135 a0001c0001t0007g0142 others(25): Show |
33 | HG00639.hp2 HG01074.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.679+4003_679+4004d others(4): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929157 | |||||||
| chr1:7929157 | CCTT | C | 3 | a0001c0001t0004g0209 a0002c0004t0001g0055 a0002c0004t0020g0027 |
4 | HG02895.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+4002_679+4004d others(5): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929157 | |||||||
| chr1:7929157 | CCTTT | C | 41 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(38): Show |
106 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.679+4001_679+4004d others(6): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929157 | |||||||
| chr1:7929157 | CCTTTT | C | 8 | a0001c0001t0004g0208 a0001c0001t0007g0014 a0001c0001t0007g0046 others(5): Show |
15 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.679+4000_679+4004d others(7): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929157 | |||||||
| chr1:7929157 | CCTTTTTT others(5): Show |
C | 4 | a0001c0001t0005g0136 a0001c0001t0012g0123 a0001c0001t0019g0121 others(1): Show |
4 | HG01496.hp2 HG02698.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+3993_679+4004d others(14): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929157 | |||||||
| chr1:7929158 | C | T | 31 | a0001c0001t0001g0042 a0001c0001t0001g0088 a0001c0001t0001g0175 others(28): Show |
37 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.679+4004G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929158 | |||||||
| chr1:7929163 | T | C | 1 | a0001c0001t0013g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.679+3999A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929163 | |||||||
| chr1:7929164 | T | C | 4 | a0001c0001t0013g0039 a0001c0001t0022g0141 a0001c0001t0066g0171 others(1): Show |
5 | HG01891.hp2 HG02145.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+3998A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929164 | |||||||
| chr1:7929165 | T | C | 6 | a0001c0001t0003g0187 a0001c0001t0008g0044 a0001c0001t0013g0138 others(3): Show |
7 | HG00741.hp1 HG01175.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.679+3997A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929165 | |||||||
| chr1:7929226 | T | C | 52 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(49): Show |
125 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.679+3936A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929226 | |||||||
| chr1:7929228 | C | T | 1 | a0002c0004t0020g0027 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.679+3934G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929228 | |||||||
| chr1:7929233 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.679+3929A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929233 | |||||||
| chr1:7929295 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.679+3867T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929295 | |||||||
| chr1:7929351 | G | A | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.679+3811C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929351 | |||||||
| chr1:7929395 | G | C | 2 | a0002c0004t0020g0027 a0002c0004t0038g0054 |
3 | HG02895.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.679+3767C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929395 | |||||||
| chr1:7929402 | G | A | 1 | a0001c0001t0022g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.679+3760C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929402 | |||||||
| chr1:7929491 | G | A | 2 | a0001c0001t0027g0068 a0001c0001t0027g0075 |
2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.679+3671C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929491 | |||||||
| chr1:7929506 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0020 others(75): Show |
124 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.679+3656G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929506 | |||||||
| chr1:7929572 | G | C | 9 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(6): Show |
17 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.679+3590C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929572 | |||||||
| chr1:7929577 | CTCTA | C | 3 | a0001c0001t0010g0200 a0001c0001t0010g0201 a0002c0004t0001g0055 |
3 | HG01884.hp2 HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.679+3581_679+3584d others(6): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929577 | |||||||
| chr1:7929638 | T | C | 43 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(40): Show |
108 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.679+3524A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929638 | |||||||
| chr1:7929695 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.679+3467C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929695 | |||||||
| chr1:7929696 | G | A | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.679+3466C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929696 | |||||||
| chr1:7929710 | T | C | 5 | a0001c0001t0044g0153 a0001c0003t0001g0045 a0001c0003t0001g0191 others(2): Show |
7 | HG00639.hp2 HG01167.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.679+3452A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929710 | |||||||
| chr1:7929967 | C | CT | 145 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(142): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.679+3194dupA | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929967 | |||||||
| chr1:7929967 | C | CTT | 17 | a0001c0001t0001g0081 a0001c0001t0001g0088 a0001c0001t0001g0089 others(14): Show |
17 | HG01123.hp1 HG01192.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.679+3193_679+3194d others(4): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929967 | |||||||
| chr1:7929967 | C | CTTT | 39 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(36): Show |
99 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.679+3192_679+3194d others(5): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929967 | |||||||
| chr1:7929967 | C | CTTTT | 15 | a0001c0001t0002g0047 a0001c0001t0004g0207 a0001c0001t0004g0208 others(12): Show |
23 | HG01192.hp1 HG01884.hp2 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.679+3191_679+3194d others(6): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7929967 | |||||||
| chr1:7930033 | G | C | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.679+3129C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7930033 | |||||||
| chr1:7930126 | C | T | 45 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(42): Show |
111 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.679+3036G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7930126 | |||||||
| chr1:7930178 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.679+2984C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7930178 | |||||||
| chr1:7930231 | A | G | 80 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
159 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.679+2931T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7930231 | |||||||
| chr1:7930278 | C | T | 7 | a0001c0001t0013g0039 a0001c0001t0013g0137 a0001c0001t0013g0138 others(4): Show |
8 | HG02145.hp1 HG02965.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.679+2884G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7930278 | |||||||
| chr1:7930307 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0020 others(109): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.679+2855C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7930307 | |||||||
| chr1:7930316 | A | C | 10 | a0001c0001t0007g0142 a0001c0001t0011g0024 a0001c0001t0011g0143 others(7): Show |
12 | HG02622.hp1 HG02630.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.679+2846T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7930316 | |||||||
| chr1:7930319 | G | A | 1 | a0001c0001t0002g0221 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.679+2843C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7930319 | |||||||
| chr1:7930398 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.679+2764A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7930398 | |||||||
| chr1:7931069 | C | T | 1 | a0001c0001t0061g0206 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.679+2093G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931069 | |||||||
| chr1:7931076 | A | G | 3 | a0001c0001t0008g0084 a0001c0001t0008g0085 a0001c0001t0008g0086 |
3 | HG01975.hp2 HG01978.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.679+2086T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931076 | |||||||
| chr1:7931143 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0020 others(109): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.679+2019C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931143 | |||||||
| chr1:7931290 | A | C | 1 | a0002c0004t0001g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.679+1872T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931290 | |||||||
| chr1:7931362 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.679+1800G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931362 | |||||||
| chr1:7931489 | C | T | 1 | a0002c0004t0020g0027 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.679+1673G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931489 | |||||||
| chr1:7931561 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.679+1601T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931561 | |||||||
| chr1:7931664 | G | A | 1 | a0001c0001t0059g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.679+1498C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931664 | |||||||
| chr1:7931765 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.679+1397C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931765 | |||||||
| chr1:7931918 | C | T | 2 | a0001c0001t0066g0171 a0001c0001t0067g0172 |
2 | HG01891.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.679+1244G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7931918 | |||||||
| chr1:7932006 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.679+1156C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932006 | |||||||
| chr1:7932035 | C | G | 1 | a0001c0001t0002g0228 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.679+1127G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932035 | |||||||
| chr1:7932237 | A | G | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.679+925T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932237 | |||||||
| chr1:7932313 | A | C | 3 | a0001c0001t0006g0028 a0001c0001t0006g0029 a0001c0001t0006g0063 |
5 | NA18747.hp2 NA18943.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+849T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932313 | |||||||
| chr1:7932393 | A | T | 2 | a0001c0001t0028g0161 a0001c0001t0028g0162 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.679+769T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932393 | |||||||
| chr1:7932498 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.679+664C>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932498 | |||||||
| chr1:7932555 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0020 others(111): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.679+607G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932555 | |||||||
| chr1:7932685 | G | A | 13 | a0001c0001t0007g0142 a0001c0001t0011g0024 a0001c0001t0011g0143 others(10): Show |
16 | HG02145.hp2 HG02622.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.679+477C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932685 | |||||||
| chr1:7932690 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.679+472G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932690 | |||||||
| chr1:7932691 | G | A | 1 | a0001c0001t0037g0128 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.679+471C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932691 | |||||||
| chr1:7932691 | G | GCA | 5 | a0001c0001t0044g0153 a0001c0003t0001g0045 a0001c0003t0001g0191 others(2): Show |
7 | HG00639.hp2 HG01167.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.679+469_679+470dup others(2): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932691 | |||||||
| chr1:7932703 | G | A | 2 | a0001c0001t0028g0161 a0001c0001t0028g0162 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.679+459C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932703 | |||||||
| chr1:7932706 | C | G | 2 | a0001c0001t0028g0161 a0001c0001t0028g0162 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.679+456G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932706 | |||||||
| chr1:7932734 | T | TAC | 52 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0002g0001 others(49): Show |
118 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.679+426_679+427dup others(2): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932734 | |||||||
| chr1:7932734 | TACAC | T | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.679+424_679+427del others(4): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932734 | |||||||
| chr1:7932858 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.679+304A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7932858 | |||||||
| chr1:7933062 | A | G | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.679+100T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 7/7 | chr1 | 7933062 | |||||||
| chr1:7933841 | A | T | 2 | a0001c0001t0001g0081 a0001c0001t0003g0080 |
2 | HG01123.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.545-545T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7933841 | |||||||
| chr1:7933971 | T | C | 75 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(72): Show |
152 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.545-675A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7933971 | |||||||
| chr1:7934295 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.544+718A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934295 | |||||||
| chr1:7934306 | G | A | 1 | a0001c0001t0064g0202 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.544+707C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934306 | |||||||
| chr1:7934360 | A | G | 95 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0145 others(92): Show |
187 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.544+653T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934360 | |||||||
| chr1:7934364 | G | C | 1 | a0001c0001t0043g0076 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.544+649C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934364 | |||||||
| chr1:7934432 | C | T | 1 | a0001c0001t0023g0040 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.544+581G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934432 | |||||||
| chr1:7934465 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.544+548G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934465 | |||||||
| chr1:7934486 | G | A | 2 | a0001c0003t0001g0045 a0001c0003t0001g0191 |
3 | HG00639.hp2 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.544+527C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934486 | |||||||
| chr1:7934494 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.544+519G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934494 | |||||||
| chr1:7934684 | G | A | 42 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(39): Show |
107 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.544+329C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934684 | |||||||
| chr1:7934712 | C | CA | 35 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(32): Show |
93 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.544+300dupT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934712 | |||||||
| chr1:7934898 | G | A | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.544+115C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934898 | |||||||
| chr1:7934909 | G | A | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.544+104C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934909 | |||||||
| chr1:7934982 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.544+31C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 6/7 | chr1 | 7934982 | |||||||
| chr1:7935423 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.414-280C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7935423 | |||||||
| chr1:7935760 | T | C | 2 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.414-617A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7935760 | |||||||
| chr1:7935946 | G | A | 1 | a0001c0001t0045g0066 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.414-803C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7935946 | |||||||
| chr1:7936278 | C | T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(33): Show |
94 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.414-1135G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936278 | |||||||
| chr1:7936365 | C | T | 1 | a0001c0001t0054g0079 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.414-1222G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936365 | |||||||
| chr1:7936418 | A | AAAAC | 74 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0145 others(71): Show |
159 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.413+1268_413+1271d others(6): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936418 | |||||||
| chr1:7936418 | A | AAAACAAA others(1): Show |
3 | a0001c0001t0001g0077 a0001c0001t0002g0204 a0001c0001t0018g0078 |
3 | HG02165.hp1 NA19062.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.413+1264_413+1271d others(10): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936418 | |||||||
| chr1:7936437 | A | ACAAG | 7 | a0001c0001t0013g0039 a0001c0001t0013g0137 a0001c0001t0013g0138 others(4): Show |
8 | HG02145.hp1 HG02965.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+1252_413+1253i others(6): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936437 | |||||||
| chr1:7936574 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.413+1116T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936574 | |||||||
| chr1:7936764 | A | G | 12 | a0001c0001t0003g0019 a0001c0001t0003g0031 a0001c0001t0003g0069 others(9): Show |
15 | HG01891.hp1 HG02257.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.413+926T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936764 | |||||||
| chr1:7936778 | T | C | 1 | a0001c0001t0005g0136 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.413+912A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936778 | |||||||
| chr1:7936834 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0020 others(110): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.413+856T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936834 | |||||||
| chr1:7936982 | T | C | 2 | a0002c0004t0001g0055 a0002c0004t0020g0027 |
3 | HG02895.hp1 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.413+708A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936982 | |||||||
| chr1:7936994 | G | C | 1 | a0001c0001t0023g0040 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.413+696C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7936994 | |||||||
| chr1:7937123 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0145 others(18): Show |
36 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.413+567C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7937123 | |||||||
| chr1:7937190 | T | A | 9 | a0001c0001t0006g0017 a0001c0001t0006g0018 a0001c0001t0006g0028 others(6): Show |
16 | HG02071.hp1 HG02129.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.413+500A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7937190 | |||||||
| chr1:7937453 | G | A | 1 | a0001c0001t0004g0223 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.413+237C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7937453 | |||||||
| chr1:7937500 | T | A | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.413+190A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7937500 | |||||||
| chr1:7937530 | G | A | 1 | a0001c0001t0021g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.413+160C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 5/7 | chr1 | 7937530 | |||||||
| chr1:7937886 | C | G | 1 | a0001c0001t0003g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.347-130G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 4/7 | chr1 | 7937886 | |||||||
| chr1:7938021 | C | T | 1 | a0001c0001t0004g0057 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.346+172G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 4/7 | chr1 | 7938021 | |||||||
| chr1:7938041 | A | C | 9 | a0001c0001t0006g0017 a0001c0001t0006g0018 a0001c0001t0006g0028 others(6): Show |
16 | HG02071.hp1 HG02129.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.346+152T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 4/7 | chr1 | 7938041 | |||||||
| chr1:7938189 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG00323.hp2 | splice_region_variant&intron_variant | LOW | c.346+4C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 4/7 | chr1 | 7938189 | |||||||
| chr1:7938399 | C | T | 1 | a0001c0001t0058g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.209-69G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 3/7 | chr1 | 7938399 | |||||||
| chr1:7938857 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.101-29C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7938857 | |||||||
| chr1:7938903 | T | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(222): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.101-75A>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7938903 | |||||||
| chr1:7938957 | T | C | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.101-129A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7938957 | |||||||
| chr1:7938976 | A | T | 1 | a0001c0001t0003g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.101-148T>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7938976 | |||||||
| chr1:7939046 | G | A | 1 | a0001c0006t0001g0159 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.101-218C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939046 | |||||||
| chr1:7939047 | C | T | 2 | a0001c0001t0028g0161 a0001c0001t0028g0162 |
2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.101-219G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939047 | |||||||
| chr1:7939125 | G | C | 42 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(39): Show |
107 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.101-297C>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939125 | |||||||
| chr1:7939252 | C | A | 1 | a0001c0001t0059g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.101-424G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939252 | |||||||
| chr1:7939275 | G | A | 2 | a0001c0002t0007g0196 a0001c0002t0007g0197 |
2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.101-447C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939275 | |||||||
| chr1:7939319 | CA | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(178): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.101-492delT | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939319 | |||||||
| chr1:7939319 | CAA | C | 7 | a0001c0001t0001g0059 a0001c0001t0010g0010 a0001c0001t0010g0200 others(4): Show |
11 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-493_101-492del others(2): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939319 | |||||||
| chr1:7939364 | C | A | 8 | a0001c0001t0004g0227 a0001c0001t0007g0014 a0001c0001t0007g0046 others(5): Show |
15 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+531G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939364 | |||||||
| chr1:7939388 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(205): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.100+507T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939388 | |||||||
| chr1:7939542 | C | T | 42 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(39): Show |
107 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.100+353G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939542 | |||||||
| chr1:7939656 | C | G | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+239G>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939656 | |||||||
| chr1:7939804 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.100+91A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 2/7 | chr1 | 7939804 | |||||||
| chr1:7940147 | A | G | 2 | a0001c0001t0003g0016 a0001c0001t0003g0056 |
4 | NA18948.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84-69T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940147 | |||||||
| chr1:7940148 | CTTA | C | 3 | a0002c0004t0001g0055 a0002c0004t0020g0027 a0002c0004t0038g0054 |
4 | HG02895.hp1 HG02897.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84-73_-84-71delTA others(1): Show |
TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940148 | |||||||
| chr1:7940152 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-84-74A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940152 | |||||||
| chr1:7940358 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-84-280C>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940358 | |||||||
| chr1:7940366 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-84-288A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940366 | |||||||
| chr1:7940437 | A | C | 1 | a0001c0001t0001g0053 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-85+347T>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940437 | |||||||
| chr1:7940437 | A | G | 2 | a0001c0003t0017g0026 a0001c0003t0017g0052 |
3 | HG01167.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-85+347T>C | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940437 | |||||||
| chr1:7940459 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-85+325G>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940459 | |||||||
| chr1:7940502 | C | T | 7 | a0001c0001t0007g0014 a0001c0001t0007g0046 a0001c0001t0007g0199 others(4): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-85+282G>A | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940502 | |||||||
| chr1:7940531 | T | A | 1 | a0003c0008t0001g0195 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-85+253A>T | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940531 | |||||||
| chr1:7940737 | T | C | 47 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(44): Show |
119 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.-85+47A>G | TNFRSF9 | ENSG00000049249.10 | transcript | ENST00000377507.8 | protein_coding | 1/7 | chr1 | 7940737 |