Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 944 |
| ensemblid | ENSG00000106952.8 |
| hgncid | 11938 |
| symbol | TNFSF8 |
| name | TNF superfamily member 8 |
| refseq_nuc | NM_001244.4 |
| refseq_prot | NP_001235.1 |
| ensembl_nuc | ENST00000223795.3 |
| ensembl_prot | ENSP00000223795.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 114901145 |
| end | 114930591 |
| strand | - |
| ver | v1.2 |
| region | chr9:114901145-114930591 |
| region5000 | chr9:114896145-114935591 |
| regionname0 | TNFSF8_chr9_114901145_114930591 |
| regionname5000 | TNFSF8_chr9_114896145_114935591 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 234 | 403 | 92 | 80 | 173 | 12 | 44 | 133 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | MDPGL others(229): Show |
chr9 | 114896145 | 114935591 |
| a0002 | 0/0 | 234 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | MDPGL others(229): Show |
chr9 | 114896145 | 114935591 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 702 | 278 | 78 | 41 | 123 | 7 | 28 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | ATGGA others(697): Show |
chr9 | 114896145 | 114935591 | ||
| a0001c0002 | 0/1 | 702 | 125 | 14 | 39 | 50 | 5 | 16 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | ATGGA others(697): Show |
chr9 | 114896145 | 114935591 | ||
| a0002c0003 | 0/0 | 702 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | ATGGA others(697): Show |
chr9 | 114896145 | 114935591 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3779 | 141 | 17 | 19 | 72 | 7 | 25 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0003 | 0/0 | 3779 | 53 | 42 | 9 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0004 | 0/0 | 3779 | 34 | 0 | 8 | 26 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0005 | 0/0 | 3779 | 12 | 11 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0006 | 0/0 | 3779 | 9 | 0 | 0 | 9 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0007 | 0/0 | 3779 | 7 | 0 | 0 | 7 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0009 | 0/0 | 3779 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0013 | 0/0 | 3779 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0015 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0018 | 0/0 | 3779 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0021 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0022 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0023 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0024 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0025 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0026 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0027 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0028 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0029 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0030 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0031 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0032 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0001t0033 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0002 | 0/0 | 3779 | 103 | 13 | 31 | 40 | 4 | 15 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0008 | 0/0 | 3777 | 5 | 0 | 1 | 3 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3772): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0010 | 0/0 | 3779 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0011 | 0/0 | 3777 | 4 | 0 | 4 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3772): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0012 | 0/0 | 3777 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3772): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0014 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0016 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0017 | 0/0 | 3779 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0019 | 0/0 | 3779 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0020 | 0/0 | 3779 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| a0001c0002t0034 | 0/1 | 3777 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3772): Show |
chr9 | 114896145 | 114935591 |
| a0002c0003t0007 | 0/0 | 3779 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | GTCAT others(3774): Show |
chr9 | 114896145 | 114935591 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0011 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0030 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0008 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0001 | 0/0 | 19 | 0 | 7 | 12 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0005g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0006g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0007g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0007g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0009g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0013g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0015g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0018g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0021g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0022g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0023g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0024g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0025g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0026g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0027g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0028g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0029g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0030g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0031g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0032g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0001t0033g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0003 | 0/0 | 10 | 0 | 7 | 1 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0004 | 0/0 | 9 | 0 | 1 | 0 | 2 | 6 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0007 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0022 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0008g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0008g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0010g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0010g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0010g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0011g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0011g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0012g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0014g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0016g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0017g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0019g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0020g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0001c0002t0034g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| a0002c0003t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0181 | EUR | GBR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | FIN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0209 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00673 | hp2 | a0001 | c0001 | t0029 | g0082 | EAS | CHS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00733 | hp1 | a0001 | c0002 | t0011 | g0024 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0210 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0132 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01081 | hp2 | a0001 | c0001 | t0027 | g0068 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0207 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01167 | hp1 | a0001 | c0002 | t0014 | g0059 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01192 | hp2 | a0001 | c0001 | t0031 | g0226 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0202 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01255 | hp2 | a0001 | c0002 | t0016 | g0164 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01261 | hp2 | a0001 | c0001 | t0028 | g0113 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0161 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01358 | hp2 | a0001 | c0002 | t0008 | g0042 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0129 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01515 | hp1 | a0001 | c0002 | t0008 | g0131 | EUR | IBS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0203 | EUR | IBS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0235 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0127 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01928 | hp2 | a0001 | c0002 | t0020 | g0206 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0166 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0249 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0205 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0128 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0180 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02004 | hp2 | a0001 | c0002 | t0011 | g0185 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02027 | hp1 | a0001 | c0002 | t0008 | g0168 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0255 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02074 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02148 | hp2 | a0001 | c0002 | t0011 | g0024 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02257 | hp2 | a0001 | c0001 | t0015 | g0222 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02293 | hp1 | a0001 | c0001 | t0032 | g0247 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02293 | hp2 | a0001 | c0002 | t0011 | g0024 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0195 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02723 | hp1 | a0001 | c0001 | t0013 | g0231 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02886 | hp1 | a0001 | c0001 | t0022 | g0220 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0160 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0197 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03130 | hp2 | a0001 | c0001 | t0024 | g0212 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03139 | hp2 | a0001 | c0001 | t0023 | g0213 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0194 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0227 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0175 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0153 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03704 | hp1 | a0001 | c0001 | t0018 | g0199 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0177 | SAS | PJL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0179 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG04184 | hp1 | a0001 | c0002 | t0019 | g0162 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | BEB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | CHB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | CHB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18747 | hp1 | a0001 | c0001 | t0030 | g0080 | EAS | CHB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | CHB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18945 | hp2 | a0001 | c0002 | t0012 | g0044 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18949 | hp2 | a0001 | c0001 | t0007 | g0257 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18950 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18957 | hp1 | a0001 | c0002 | t0010 | g0057 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18960 | hp1 | a0001 | c0001 | t0025 | g0134 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18965 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18966 | hp1 | a0001 | c0002 | t0010 | g0057 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18967 | hp1 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18969 | hp1 | a0001 | c0002 | t0010 | g0256 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18974 | hp1 | a0001 | c0002 | t0010 | g0056 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18982 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18985 | hp2 | a0001 | c0002 | t0008 | g0200 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18987 | hp2 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18991 | hp1 | a0001 | c0002 | t0012 | g0044 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18994 | hp2 | a0001 | c0002 | t0008 | g0042 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19000 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19001 | hp1 | a0002 | c0003 | t0007 | g0260 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0258 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19003 | hp1 | a0001 | c0001 | t0033 | g0248 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19004 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0261 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0163 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19030 | hp2 | a0001 | c0001 | t0021 | g0238 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0253 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19059 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19062 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19064 | hp1 | a0001 | c0001 | t0006 | g0088 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19070 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19090 | hp1 | a0001 | c0002 | t0010 | g0056 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA19240 | hp2 | a0001 | c0001 | t0026 | g0094 | AFR | YRI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ASW | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | ASW | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | TSI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | GIH | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | GIH | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | MSL | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | USA | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| HG06807 | hp2 | a0001 | c0002 | t0017 | g0191 | AFR | USA | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0034 | g0178 | REF | REF | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0030 | REF | REF | TNFSF8_chr9_114896145_114935591 | TNFSF8 | chr9 | 114896145 | 114935591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:114904017 | T | G | 1 | a0002 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.619A>C | p.Asn207His | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 907/3779 | 619/705 | 207/234 | chr9 | 114904017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:114905862 | C | T | 1 | a0001c0002 | 124 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
synonymous_variant | LOW | c.276G>A | p.Arg92Arg | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/4 | 564/3779 | 276/705 | 92/234 | chr9 | 114905862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:114901270 | T | C | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(14): Show |
226 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*2661A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2661 | chr9 | 114901270 | ||||||
| chr9:114901328 | T | G | 2 | a0001c0001t0013 a0001c0001t0023 |
3 | HG02723.hp1 HG03139.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2603A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2603 | chr9 | 114901328 | ||||||
| chr9:114901349 | T | C | 2 | a0001c0001t0013 a0001c0001t0023 |
3 | HG02723.hp1 HG03139.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2582A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2582 | chr9 | 114901349 | ||||||
| chr9:114901384 | G | T | 1 | a0001c0001t0027 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2547C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2547 | chr9 | 114901384 | ||||||
| chr9:114901414 | G | A | 1 | a0001c0002t0017 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2517C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2517 | chr9 | 114901414 | ||||||
| chr9:114901520 | G | C | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(15): Show |
228 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*2411C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2411 | chr9 | 114901520 | ||||||
| chr9:114901604 | G | T | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(15): Show |
228 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*2327C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2327 | chr9 | 114901604 | ||||||
| chr9:114901700 | T | C | 1 | a0001c0001t0022 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2231A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2231 | chr9 | 114901700 | ||||||
| chr9:114901877 | T | C | 1 | a0001c0001t0028 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2054A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2054 | chr9 | 114901877 | ||||||
| chr9:114901892 | T | C | 19 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(16): Show |
229 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2039A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2039 | chr9 | 114901892 | ||||||
| chr9:114901931 | T | C | 19 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(16): Show |
229 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2000A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 2000 | chr9 | 114901931 | ||||||
| chr9:114901961 | G | A | 1 | a0001c0001t0029 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1970C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1970 | chr9 | 114901961 | ||||||
| chr9:114902100 | C | T | 1 | a0001c0001t0009 | 5 | HG02074.hp2 NA18950.hp2 NA19000.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1831G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1831 | chr9 | 114902100 | ||||||
| chr9:114902164 | G | A | 1 | a0001c0001t0006 | 9 | NA18747.hp2 NA18957.hp2 NA18965.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1767C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1767 | chr9 | 114902164 | ||||||
| chr9:114902293 | C | T | 2 | a0001c0001t0007 a0002c0003t0007 |
8 | HG02074.hp1 NA18949.hp2 NA18967.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1638G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1638 | chr9 | 114902293 | ||||||
| chr9:114902336 | T | G | 1 | a0001c0002t0019 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1595A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1595 | chr9 | 114902336 | ||||||
| chr9:114902377 | T | A | 1 | a0001c0002t0011 | 4 | HG00733.hp1 HG02004.hp2 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1554A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1554 | chr9 | 114902377 | ||||||
| chr9:114902461 | A | G | 1 | a0001c0001t0024 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1470T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1470 | chr9 | 114902461 | ||||||
| chr9:114902470 | G | A | 1 | a0001c0001t0005 | 12 | HG01496.hp1 HG01884.hp1 HG02572.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1461C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1461 | chr9 | 114902470 | ||||||
| chr9:114902613 | C | G | 1 | a0001c0001t0023 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1318G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1318 | chr9 | 114902613 | ||||||
| chr9:114902654 | T | A | 1 | a0001c0001t0030 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1277A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1277 | chr9 | 114902654 | ||||||
| chr9:114902907 | A | G | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(17): Show |
230 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*1024T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1024 | chr9 | 114902907 | ||||||
| chr9:114902913 | C | T | 3 | a0001c0001t0007 a0001c0001t0009 a0002c0003t0007 |
13 | HG02074.hp1 HG02074.hp2 NA18949.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1018G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 1018 | chr9 | 114902913 | ||||||
| chr9:114903050 | G | T | 1 | a0001c0001t0026 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*881C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 881 | chr9 | 114903050 | ||||||
| chr9:114903077 | C | T | 1 | a0001c0001t0009 | 5 | HG02074.hp2 NA18950.hp2 NA19000.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*854G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 854 | chr9 | 114903077 | ||||||
| chr9:114903081 | C | A | 1 | a0001c0001t0032 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 850 | chr9 | 114903081 | ||||||
| chr9:114903099 | A | G | 19 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(16): Show |
229 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*832T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 832 | chr9 | 114903099 | ||||||
| chr9:114903155 | A | G | 26 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(23): Show |
247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*776T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 776 | chr9 | 114903155 | ||||||
| chr9:114903290 | C | G | 11 | a0001c0001t0018 a0001c0002t0002 a0001c0002t0008 others(8): Show |
125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*641G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 641 | chr9 | 114903290 | ||||||
| chr9:114903320 | G | A | 1 | a0001c0001t0031 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*611C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 611 | chr9 | 114903320 | ||||||
| chr9:114903423 | GGA | G | 3 | a0001c0002t0008 a0001c0002t0011 a0001c0002t0012 |
11 | HG00733.hp1 HG01358.hp2 HG01515.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*506_*507delTC | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 506 | chr9 | 114903423 | ||||||
| chr9:114903427 | G | C | 3 | a0001c0002t0008 a0001c0002t0011 a0001c0002t0012 |
11 | HG00733.hp1 HG01358.hp2 HG01515.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*504C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 504 | chr9 | 114903427 | ||||||
| chr9:114903429 | T | C | 3 | a0001c0002t0008 a0001c0002t0011 a0001c0002t0012 |
11 | HG00733.hp1 HG01358.hp2 HG01515.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*502A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 502 | chr9 | 114903429 | ||||||
| chr9:114903454 | G | A | 1 | a0001c0002t0020 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*477C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 477 | chr9 | 114903454 | ||||||
| chr9:114903472 | T | C | 11 | a0001c0001t0018 a0001c0002t0002 a0001c0002t0008 others(8): Show |
125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*459A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 459 | chr9 | 114903472 | ||||||
| chr9:114903568 | C | T | 1 | a0001c0001t0021 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 363 | chr9 | 114903568 | ||||||
| chr9:114903586 | G | A | 11 | a0001c0001t0018 a0001c0002t0002 a0001c0002t0008 others(8): Show |
125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*345C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 345 | chr9 | 114903586 | ||||||
| chr9:114903605 | G | A | 4 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0032 others(1): Show |
41 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*326C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 326 | chr9 | 114903605 | ||||||
| chr9:114903651 | A | T | 11 | a0001c0001t0018 a0001c0002t0002 a0001c0002t0008 others(8): Show |
125 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*280T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 280 | chr9 | 114903651 | ||||||
| chr9:114903917 | C | T | 1 | a0001c0001t0015 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 4/4 | 14 | chr9 | 114903917 | ||||||
| chr9:114930390 | C | T | 1 | a0001c0002t0014 | 1 | HG01167.hp1 | 5_prime_UTR_variant | MODIFIER | c.-87G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/4 | 87 | chr9 | 114930390 | ||||||
| chr9:114930508 | T | G | 3 | a0001c0001t0007 a0001c0002t0010 a0002c0003t0007 |
13 | HG02074.hp1 NA18949.hp2 NA18957.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-205A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/4 | 205 | chr9 | 114930508 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:114904342 | A | G | 1 | a0001c0002t0002g0204 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.311-17T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904342 | |||||||
| chr9:114904375 | G | A | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.311-50C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904375 | |||||||
| chr9:114904398 | G | A | 135 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(132): Show |
243 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.311-73C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904398 | |||||||
| chr9:114904496 | G | A | 71 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(68): Show |
124 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.311-171C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904496 | |||||||
| chr9:114904644 | A | T | 138 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(135): Show |
246 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.311-319T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904644 | |||||||
| chr9:114904746 | T | C | 1 | a0001c0001t0001g0031 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.311-421A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904746 | |||||||
| chr9:114904849 | C | G | 1 | a0001c0001t0027g0068 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.311-524G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904849 | |||||||
| chr9:114904881 | A | G | 71 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(68): Show |
124 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.311-556T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904881 | |||||||
| chr9:114904962 | C | T | 71 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(68): Show |
124 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.311-637G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114904962 | |||||||
| chr9:114905163 | T | C | 66 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(63): Show |
121 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(118): Show |
intron_variant | MODIFIER | c.310+665A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905163 | |||||||
| chr9:114905169 | C | T | 2 | a0001c0002t0011g0024 a0001c0002t0011g0185 |
4 | HG00733.hp1 HG02004.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.310+659G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905169 | |||||||
| chr9:114905172 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.310+656C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905172 | |||||||
| chr9:114905183 | A | C | 15 | a0001c0001t0004g0001 a0001c0001t0004g0052 a0001c0001t0004g0053 others(12): Show |
36 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.310+645T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905183 | |||||||
| chr9:114905491 | T | C | 139 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(136): Show |
247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.310+337A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905491 | |||||||
| chr9:114905569 | G | A | 1 | a0001c0001t0021g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.310+259C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905569 | |||||||
| chr9:114905608 | G | T | 9 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0130 others(6): Show |
13 | HG00738.hp1 HG01070.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.310+220C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905608 | |||||||
| chr9:114905657 | G | A | 1 | a0001c0002t0002g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.310+171C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905657 | |||||||
| chr9:114905657 | G | T | 16 | a0001c0001t0004g0001 a0001c0001t0004g0052 a0001c0001t0004g0053 others(13): Show |
41 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.310+171C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905657 | |||||||
| chr9:114905713 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0150 |
2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.310+115T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905713 | |||||||
| chr9:114905774 | A | G | 1 | a0001c0001t0015g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.310+54T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 3/3 | chr9 | 114905774 | |||||||
| chr9:114905939 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.239-40C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114905939 | |||||||
| chr9:114906081 | A | T | 69 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(66): Show |
125 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(122): Show |
intron_variant | MODIFIER | c.239-182T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906081 | |||||||
| chr9:114906239 | GAGGGGTA others(28): Show |
G | 1 | a0001c0002t0002g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.239-375_239-341del others(35): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906239 | |||||||
| chr9:114906273 | A | G | 1 | a0001c0001t0003g0014 | 4 | HG01243.hp2 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-374T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906273 | |||||||
| chr9:114906827 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0244 |
3 | NA18971.hp1 NA18972.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.239-928T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906827 | |||||||
| chr9:114906990 | C | T | 25 | a0001c0001t0004g0001 a0001c0001t0004g0052 a0001c0001t0004g0053 others(22): Show |
52 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.239-1091G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114906990 | |||||||
| chr9:114907019 | A | G | 138 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(135): Show |
246 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.239-1120T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907019 | |||||||
| chr9:114907035 | G | A | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.239-1136C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907035 | |||||||
| chr9:114907037 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239-1138G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907037 | |||||||
| chr9:114907129 | G | A | 1 | a0001c0002t0002g0208 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.239-1230C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907129 | |||||||
| chr9:114907305 | C | T | 229 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0017 others(226): Show |
363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.239-1406G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907305 | |||||||
| chr9:114907352 | G | A | 1 | a0001c0001t0004g0249 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.239-1453C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907352 | |||||||
| chr9:114907419 | A | T | 69 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(66): Show |
125 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(122): Show |
intron_variant | MODIFIER | c.239-1520T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907419 | |||||||
| chr9:114907462 | C | T | 1 | a0001c0001t0015g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.239-1563G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907462 | |||||||
| chr9:114907534 | C | G | 68 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(65): Show |
119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.239-1635G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907534 | |||||||
| chr9:114907585 | C | T | 2 | a0001c0001t0013g0231 a0001c0001t0013g0253 |
2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.239-1686G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907585 | |||||||
| chr9:114907660 | C | T | 1 | a0001c0001t0003g0219 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239-1761G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907660 | |||||||
| chr9:114907673 | T | C | 1 | a0001c0001t0003g0236 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.239-1774A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907673 | |||||||
| chr9:114907685 | C | T | 1 | a0001c0001t0004g0055 | 2 | NA18953.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.239-1786G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907685 | |||||||
| chr9:114907978 | G | C | 1 | a0001c0002t0002g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.239-2079C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907978 | |||||||
| chr9:114907994 | C | T | 5 | a0001c0001t0007g0058 a0001c0001t0007g0257 a0001c0001t0007g0259 others(2): Show |
6 | NA18949.hp2 NA18967.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-2095G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114907994 | |||||||
| chr9:114908107 | C | T | 2 | a0001c0001t0013g0231 a0001c0001t0013g0253 |
2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.239-2208G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908107 | |||||||
| chr9:114908384 | A | T | 138 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(135): Show |
246 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.239-2485T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908384 | |||||||
| chr9:114908469 | T | A | 1 | a0001c0002t0002g0204 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.239-2570A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908469 | |||||||
| chr9:114908645 | G | GA | 71 | a0001c0001t0001g0137 a0001c0001t0003g0008 a0001c0001t0003g0013 others(68): Show |
127 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(124): Show |
intron_variant | MODIFIER | c.239-2747dupT | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908645 | |||||||
| chr9:114908964 | A | C | 1 | a0001c0001t0025g0134 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.239-3065T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114908964 | |||||||
| chr9:114909156 | C | T | 1 | a0001c0002t0002g0198 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.239-3257G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909156 | |||||||
| chr9:114909245 | G | T | 259 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(256): Show |
401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.239-3346C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909245 | |||||||
| chr9:114909335 | G | A | 1 | a0001c0002t0002g0190 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.239-3436C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909335 | |||||||
| chr9:114909413 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.239-3514T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909413 | |||||||
| chr9:114909419 | G | A | 12 | a0001c0001t0003g0048 a0001c0001t0003g0228 a0001c0001t0003g0236 others(9): Show |
20 | HG01496.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.239-3520C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909419 | |||||||
| chr9:114909515 | G | A | 2 | a0001c0001t0013g0231 a0001c0001t0013g0253 |
2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.239-3616C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909515 | |||||||
| chr9:114909697 | C | T | 1 | a0001c0002t0002g0205 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.239-3798G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909697 | |||||||
| chr9:114909964 | T | C | 43 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(40): Show |
72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.239-4065A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909964 | |||||||
| chr9:114909973 | C | G | 2 | a0001c0002t0002g0166 a0001c0002t0002g0180 |
2 | HG01943.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.239-4074G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909973 | |||||||
| chr9:114909992 | A | C | 1 | a0001c0001t0003g0049 | 2 | HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.239-4093T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114909992 | |||||||
| chr9:114910033 | A | G | 1 | a0001c0001t0004g0246 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.239-4134T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910033 | |||||||
| chr9:114910386 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.239-4487C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910386 | |||||||
| chr9:114910452 | C | G | 1 | a0001c0001t0003g0215 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239-4553G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910452 | |||||||
| chr9:114910480 | T | C | 139 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(136): Show |
247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.239-4581A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910480 | |||||||
| chr9:114910651 | A | T | 1 | a0001c0001t0003g0228 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-4752T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910651 | |||||||
| chr9:114910854 | C | T | 1 | a0001c0001t0015g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.239-4955G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910854 | |||||||
| chr9:114910866 | A | C | 70 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(67): Show |
127 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(124): Show |
intron_variant | MODIFIER | c.239-4967T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114910866 | |||||||
| chr9:114911189 | C | T | 1 | a0001c0001t0003g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-5290G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911189 | |||||||
| chr9:114911190 | G | A | 1 | a0001c0002t0002g0195 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-5291C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911190 | |||||||
| chr9:114911293 | C | T | 1 | a0001c0002t0002g0132 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.239-5394G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911293 | |||||||
| chr9:114911307 | A | G | 2 | a0001c0001t0003g0048 a0001c0001t0003g0228 |
3 | HG02109.hp1 HG02486.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.239-5408T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911307 | |||||||
| chr9:114911330 | G | A | 2 | a0001c0002t0002g0194 a0001c0002t0002g0195 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.239-5431C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911330 | |||||||
| chr9:114911692 | G | A | 1 | a0001c0002t0017g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.239-5793C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911692 | |||||||
| chr9:114911731 | C | T | 1 | a0001c0001t0007g0261 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.239-5832G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911731 | |||||||
| chr9:114911873 | T | C | 2 | a0001c0001t0003g0216 a0001c0001t0003g0221 |
2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.239-5974A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911873 | |||||||
| chr9:114911895 | A | G | 1 | a0001c0002t0002g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.239-5996T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911895 | |||||||
| chr9:114911912 | C | T | 1 | a0001c0001t0003g0214 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-6013G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911912 | |||||||
| chr9:114911930 | G | T | 1 | a0001c0001t0003g0054 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.239-6031C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911930 | |||||||
| chr9:114911970 | A | G | 43 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(40): Show |
72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.239-6071T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114911970 | |||||||
| chr9:114912040 | C | T | 39 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0025 others(36): Show |
66 | HG00558.hp1 HG00597.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.238+6056G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912040 | |||||||
| chr9:114912096 | G | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0036 a0001c0001t0001g0109 others(1): Show |
7 | HG02698.hp2 HG03017.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+6000C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912096 | |||||||
| chr9:114912253 | A | C | 1 | a0001c0002t0002g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+5843T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912253 | |||||||
| chr9:114912333 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.238+5763T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912333 | |||||||
| chr9:114912452 | C | T | 1 | a0001c0001t0004g0052 | 2 | NA18956.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.238+5644G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912452 | |||||||
| chr9:114912493 | G | T | 5 | a0001c0001t0001g0123 a0001c0001t0001g0150 a0001c0001t0001g0172 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+5603C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912493 | |||||||
| chr9:114912499 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.238+5597G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912499 | |||||||
| chr9:114912503 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.238+5593G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912503 | |||||||
| chr9:114912522 | T | G | 1 | a0001c0001t0015g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.238+5574A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912522 | |||||||
| chr9:114912534 | C | T | 68 | a0001c0001t0018g0199 a0001c0002t0002g0002 a0001c0002t0002g0003 others(65): Show |
118 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.238+5562G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912534 | |||||||
| chr9:114912546 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG02015.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.238+5550A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912546 | |||||||
| chr9:114912556 | A | C | 1 | a0001c0001t0003g0214 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.238+5540T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912556 | |||||||
| chr9:114912564 | A | AT | 30 | a0001c0001t0003g0214 a0001c0001t0004g0001 a0001c0001t0004g0052 others(27): Show |
58 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.238+5531dupA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912564 | |||||||
| chr9:114912568 | T | C | 1 | a0001c0002t0002g0207 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.238+5528A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912568 | |||||||
| chr9:114912673 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.238+5423G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912673 | |||||||
| chr9:114912691 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0172 |
3 | HG03516.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.238+5405C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912691 | |||||||
| chr9:114912698 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.238+5398G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912698 | |||||||
| chr9:114912721 | T | A | 1 | a0001c0002t0002g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+5375A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114912721 | |||||||
| chr9:114913160 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.238+4936G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913160 | |||||||
| chr9:114913165 | A | G | 8 | a0001c0001t0003g0013 a0001c0001t0003g0015 a0001c0001t0003g0051 others(5): Show |
15 | HG01109.hp2 HG02055.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.238+4931T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913165 | |||||||
| chr9:114913170 | G | A | 1 | a0001c0001t0004g0249 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.238+4926C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913170 | |||||||
| chr9:114913174 | A | G | 69 | a0001c0001t0018g0199 a0001c0002t0002g0002 a0001c0002t0002g0003 others(66): Show |
120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.238+4922T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913174 | |||||||
| chr9:114913190 | C | T | 1 | a0001c0001t0015g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.238+4906G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913190 | |||||||
| chr9:114913221 | T | G | 1 | a0001c0002t0002g0181 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.238+4875A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913221 | |||||||
| chr9:114913533 | G | A | 68 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(65): Show |
119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.238+4563C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913533 | |||||||
| chr9:114913622 | T | A | 1 | a0001c0002t0002g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+4474A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913622 | |||||||
| chr9:114913727 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.238+4369C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913727 | |||||||
| chr9:114913869 | A | G | 1 | a0001c0001t0023g0213 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.238+4227T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913869 | |||||||
| chr9:114913870 | C | T | 1 | a0001c0001t0007g0255 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.238+4226G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913870 | |||||||
| chr9:114913999 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.238+4097C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114913999 | |||||||
| chr9:114914006 | G | T | 1 | a0001c0002t0002g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+4090C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914006 | |||||||
| chr9:114914034 | T | C | 137 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(134): Show |
245 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.238+4062A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914034 | |||||||
| chr9:114914238 | T | C | 137 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(134): Show |
245 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.238+3858A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914238 | |||||||
| chr9:114914247 | A | G | 1 | a0001c0001t0003g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.238+3849T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914247 | |||||||
| chr9:114914261 | A | G | 67 | a0001c0001t0018g0199 a0001c0002t0002g0002 a0001c0002t0002g0003 others(64): Show |
118 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.238+3835T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914261 | |||||||
| chr9:114914495 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0154 |
3 | NA18945.hp1 NA19000.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.238+3601C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914495 | |||||||
| chr9:114914550 | G | A | 136 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(133): Show |
244 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.238+3546C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914550 | |||||||
| chr9:114914553 | A | C | 137 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(134): Show |
245 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.238+3543T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914553 | |||||||
| chr9:114914651 | G | C | 69 | a0001c0001t0018g0199 a0001c0002t0002g0002 a0001c0002t0002g0003 others(66): Show |
120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.238+3445C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914651 | |||||||
| chr9:114914937 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.238+3159G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914937 | |||||||
| chr9:114914983 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.238+3113G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114914983 | |||||||
| chr9:114915025 | A | C | 136 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(133): Show |
244 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.238+3071T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915025 | |||||||
| chr9:114915036 | C | T | 1 | a0001c0002t0002g0165 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.238+3060G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915036 | |||||||
| chr9:114915078 | A | G | 2 | a0001c0002t0002g0045 a0001c0002t0002g0204 |
3 | NA18939.hp1 NA18984.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.238+3018T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915078 | |||||||
| chr9:114915080 | C | T | 1 | a0001c0001t0015g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.238+3016G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915080 | |||||||
| chr9:114915126 | G | A | 27 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(24): Show |
55 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.238+2970C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915126 | |||||||
| chr9:114915149 | T | A | 1 | a0001c0001t0028g0113 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+2947A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915149 | |||||||
| chr9:114915286 | A | G | 27 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0034 others(24): Show |
36 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.238+2810T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915286 | |||||||
| chr9:114915337 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.238+2759C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915337 | |||||||
| chr9:114915339 | C | T | 1 | a0001c0002t0002g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.238+2757G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915339 | |||||||
| chr9:114915450 | G | T | 1 | a0001c0002t0010g0056 | 2 | NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.238+2646C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915450 | |||||||
| chr9:114915545 | G | A | 41 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(38): Show |
70 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.238+2551C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915545 | |||||||
| chr9:114915773 | A | AG | 139 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(136): Show |
247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.238+2322_238+2323i others(3): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915773 | |||||||
| chr9:114915847 | T | C | 1 | a0001c0002t0002g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.238+2249A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915847 | |||||||
| chr9:114915859 | C | T | 1 | a0001c0002t0002g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.238+2237G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915859 | |||||||
| chr9:114915860 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+2236C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915860 | |||||||
| chr9:114915924 | T | A | 1 | a0001c0002t0002g0192 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.238+2172A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915924 | |||||||
| chr9:114915956 | T | C | 139 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(136): Show |
247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.238+2140A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114915956 | |||||||
| chr9:114916025 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.238+2071G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916025 | |||||||
| chr9:114916073 | G | T | 1 | a0001c0001t0003g0233 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.238+2023C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916073 | |||||||
| chr9:114916527 | C | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1569G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916527 | |||||||
| chr9:114916529 | G | C | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1567C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916529 | |||||||
| chr9:114916530 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1566C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916530 | |||||||
| chr9:114916531 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1565C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916531 | |||||||
| chr9:114916532 | T | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1564A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916532 | |||||||
| chr9:114916533 | G | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1563C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916533 | |||||||
| chr9:114916551 | G | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1545C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916551 | |||||||
| chr9:114916552 | T | A | 2 | a0001c0002t0002g0187 a0001c0002t0002g0193 |
2 | NA18975.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.238+1544A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916552 | |||||||
| chr9:114916553 | G | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1543C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916553 | |||||||
| chr9:114916556 | A | C | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1540T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916556 | |||||||
| chr9:114916557 | G | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1539C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916557 | |||||||
| chr9:114916559 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1537C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916559 | |||||||
| chr9:114916560 | G | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1536C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916560 | |||||||
| chr9:114916562 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1534C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916562 | |||||||
| chr9:114916564 | G | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1532C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916564 | |||||||
| chr9:114916565 | G | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1531C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916565 | |||||||
| chr9:114916568 | C | A | 1 | a0001c0001t0004g0242 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.238+1528G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916568 | |||||||
| chr9:114916575 | T | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1521A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916575 | |||||||
| chr9:114916577 | T | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1519A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916577 | |||||||
| chr9:114916589 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.238+1507G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916589 | |||||||
| chr9:114916598 | T | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1498A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916598 | |||||||
| chr9:114916599 | T | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1497A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916599 | |||||||
| chr9:114916600 | T | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1496A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916600 | |||||||
| chr9:114916602 | C | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1494G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916602 | |||||||
| chr9:114916603 | A | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1493T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916603 | |||||||
| chr9:114916605 | A | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1491T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916605 | |||||||
| chr9:114916607 | C | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1489G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916607 | |||||||
| chr9:114916609 | C | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1487G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916609 | |||||||
| chr9:114916611 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1485C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916611 | |||||||
| chr9:114916612 | T | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1484A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916612 | |||||||
| chr9:114916613 | G | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1483C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916613 | |||||||
| chr9:114916615 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1481C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916615 | |||||||
| chr9:114916619 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1477C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916619 | |||||||
| chr9:114916622 | C | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1474G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916622 | |||||||
| chr9:114916624 | T | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1472A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916624 | |||||||
| chr9:114916626 | A | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1470T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916626 | |||||||
| chr9:114916629 | T | C | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1467A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916629 | |||||||
| chr9:114916633 | T | C | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1463A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916633 | |||||||
| chr9:114916639 | A | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1457T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916639 | |||||||
| chr9:114916642 | C | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1454G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916642 | |||||||
| chr9:114916644 | T | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1452A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916644 | |||||||
| chr9:114916652 | C | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1444G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916652 | |||||||
| chr9:114916657 | C | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1439G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916657 | |||||||
| chr9:114916660 | G | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1436C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916660 | |||||||
| chr9:114916661 | C | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1435G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916661 | |||||||
| chr9:114916666 | A | AATATAAC others(3): Show |
1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1429_238+1430i others(12): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916666 | |||||||
| chr9:114916668 | T | C | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1428A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916668 | |||||||
| chr9:114916674 | A | C | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1422T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916674 | |||||||
| chr9:114916676 | T | C | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1420A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916676 | |||||||
| chr9:114916679 | A | C | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1417T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916679 | |||||||
| chr9:114916680 | T | C | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1416A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916680 | |||||||
| chr9:114916686 | A | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1410T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916686 | |||||||
| chr9:114916687 | A | G | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1409T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916687 | |||||||
| chr9:114916688 | A | T | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1408T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916688 | |||||||
| chr9:114916726 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.238+1370C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916726 | |||||||
| chr9:114916998 | G | A | 1 | a0001c0002t0002g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.238+1098C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114916998 | |||||||
| chr9:114917067 | G | T | 1 | a0001c0002t0002g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238+1029C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917067 | |||||||
| chr9:114917090 | G | C | 139 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(136): Show |
247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.238+1006C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917090 | |||||||
| chr9:114917194 | C | T | 24 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0007 others(21): Show |
48 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.238+902G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917194 | |||||||
| chr9:114917205 | C | T | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.238+891G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917205 | |||||||
| chr9:114917450 | G | C | 17 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(14): Show |
42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.238+646C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917450 | |||||||
| chr9:114917491 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0003g0237 a0001c0001t0003g0252 others(1): Show |
4 | HG01891.hp2 HG02132.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+605C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917491 | |||||||
| chr9:114917522 | G | A | 68 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(65): Show |
125 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(122): Show |
intron_variant | MODIFIER | c.238+574C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917522 | |||||||
| chr9:114917870 | T | A | 1 | a0001c0001t0003g0014 | 4 | HG01243.hp2 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+226A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917870 | |||||||
| chr9:114917956 | A | G | 1 | a0001c0002t0002g0203 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.238+140T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114917956 | |||||||
| chr9:114918067 | C | T | 1 | a0001c0002t0002g0128 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.238+29G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 2/3 | chr9 | 114918067 | |||||||
| chr9:114918452 | A | G | 38 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(35): Show |
67 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.196-314T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918452 | |||||||
| chr9:114918453 | CT | C | 67 | a0001c0001t0001g0147 a0001c0001t0004g0250 a0001c0002t0002g0002 others(64): Show |
117 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.196-316delA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918453 | |||||||
| chr9:114918471 | A | G | 1 | a0001c0001t0004g0245 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.196-333T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918471 | |||||||
| chr9:114918552 | C | T | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-414G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918552 | |||||||
| chr9:114918688 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.196-550C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918688 | |||||||
| chr9:114918791 | G | A | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-653C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918791 | |||||||
| chr9:114918848 | C | T | 1 | a0001c0001t0023g0213 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196-710G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918848 | |||||||
| chr9:114918969 | T | C | 1 | a0001c0002t0002g0182 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.196-831A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918969 | |||||||
| chr9:114918976 | C | A | 1 | a0001c0002t0002g0045 | 2 | NA18939.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.196-838G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114918976 | |||||||
| chr9:114919020 | G | GT | 57 | a0001c0001t0001g0028 a0001c0001t0001g0063 a0001c0001t0001g0066 others(54): Show |
89 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.196-883dupA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919020 | |||||||
| chr9:114919072 | C | T | 71 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(68): Show |
128 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(125): Show |
intron_variant | MODIFIER | c.196-934G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919072 | |||||||
| chr9:114919097 | C | T | 27 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(24): Show |
55 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.196-959G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919097 | |||||||
| chr9:114919243 | C | T | 71 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(68): Show |
128 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(125): Show |
intron_variant | MODIFIER | c.196-1105G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919243 | |||||||
| chr9:114919282 | A | G | 27 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(24): Show |
55 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.196-1144T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919282 | |||||||
| chr9:114919299 | A | G | 2 | a0001c0001t0006g0076 a0001c0001t0006g0077 |
2 | NA18982.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.196-1161T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919299 | |||||||
| chr9:114919590 | G | T | 67 | a0001c0001t0018g0199 a0001c0002t0002g0002 a0001c0002t0002g0003 others(64): Show |
117 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.196-1452C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919590 | |||||||
| chr9:114919652 | T | C | 1 | a0001c0001t0003g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.196-1514A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919652 | |||||||
| chr9:114919757 | C | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0137 |
2 | HG00597.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.196-1619G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919757 | |||||||
| chr9:114919797 | G | C | 112 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(109): Show |
192 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.196-1659C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114919797 | |||||||
| chr9:114920212 | C | T | 68 | a0001c0001t0018g0199 a0001c0002t0002g0002 a0001c0002t0002g0003 others(65): Show |
119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.196-2074G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920212 | |||||||
| chr9:114920228 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.196-2090T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920228 | |||||||
| chr9:114920265 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.196-2127T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920265 | |||||||
| chr9:114920768 | G | T | 1 | a0001c0001t0007g0259 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.196-2630C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920768 | |||||||
| chr9:114920934 | G | T | 1 | a0001c0001t0003g0218 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.196-2796C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114920934 | |||||||
| chr9:114921186 | AC | A | 10 | a0001c0001t0007g0058 a0001c0001t0007g0255 a0001c0001t0007g0257 others(7): Show |
13 | HG02074.hp1 NA18949.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-3049delG | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921186 | |||||||
| chr9:114921259 | C | G | 1 | a0001c0001t0023g0213 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196-3121G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921259 | |||||||
| chr9:114921355 | A | C | 1 | a0001c0001t0025g0134 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.196-3217T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921355 | |||||||
| chr9:114921484 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.196-3346T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921484 | |||||||
| chr9:114921675 | G | T | 2 | a0001c0001t0004g0243 a0001c0001t0004g0254 |
2 | HG00609.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.196-3537C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921675 | |||||||
| chr9:114921722 | A | C | 1 | a0001c0002t0016g0164 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.196-3584T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921722 | |||||||
| chr9:114921808 | C | T | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-3670G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921808 | |||||||
| chr9:114921934 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0122 |
3 | HG00280.hp1 HG00642.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.196-3796T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114921934 | |||||||
| chr9:114922072 | CT | C | 25 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0007 others(22): Show |
49 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.196-3935delA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922072 | |||||||
| chr9:114922267 | C | T | 68 | a0001c0001t0024g0212 a0001c0002t0002g0002 a0001c0002t0002g0003 others(65): Show |
119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.196-4129G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922267 | |||||||
| chr9:114922430 | G | A | 2 | a0001c0001t0003g0237 a0001c0001t0021g0238 |
2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.196-4292C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922430 | |||||||
| chr9:114922651 | G | C | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-4513C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922651 | |||||||
| chr9:114922669 | C | T | 2 | a0001c0002t0010g0056 a0001c0002t0010g0256 |
3 | NA18969.hp1 NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.196-4531G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922669 | |||||||
| chr9:114922675 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.196-4537T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922675 | |||||||
| chr9:114922796 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.196-4658C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114922796 | |||||||
| chr9:114923006 | G | C | 1 | a0001c0002t0002g0208 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-4868C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923006 | |||||||
| chr9:114923069 | A | G | 1 | a0001c0002t0002g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.196-4931T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923069 | |||||||
| chr9:114923118 | A | G | 138 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(135): Show |
246 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.196-4980T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923118 | |||||||
| chr9:114923137 | T | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0150 |
2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.196-4999A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923137 | |||||||
| chr9:114923223 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.196-5085G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923223 | |||||||
| chr9:114923268 | G | A | 1 | a0001c0001t0015g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.196-5130C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923268 | |||||||
| chr9:114923397 | A | C | 1 | a0001c0001t0003g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.196-5259T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923397 | |||||||
| chr9:114923472 | C | T | 1 | a0001c0002t0002g0184 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.196-5334G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923472 | |||||||
| chr9:114923473 | T | C | 1 | a0001c0002t0002g0184 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.196-5335A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923473 | |||||||
| chr9:114923478 | T | TTCTTTCT others(3): Show |
1 | a0001c0001t0001g0144 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.196-5341_196-5340i others(12): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | T | TTCTTTTT others(5): Show |
1 | a0001c0001t0001g0105 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.196-5341_196-5340i others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | T | TTTTC | 17 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0001g0063 others(14): Show |
19 | HG00597.hp2 HG00609.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-5344_196-5341d others(6): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | T | TTTTCTTT others(1): Show |
22 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0020 others(19): Show |
33 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.196-5348_196-5341d others(10): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | T | TTTTCTTT others(5): Show |
14 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0032 others(11): Show |
20 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.196-5352_196-5341d others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | T | TTTTCTTT others(9): Show |
12 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0092 others(9): Show |
12 | HG00423.hp2 HG01069.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-5356_196-5341d others(18): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | T | TTTTCTTT others(13): Show |
4 | a0001c0001t0001g0071 a0001c0001t0001g0095 a0001c0001t0001g0143 others(1): Show |
4 | HG00438.hp1 HG02615.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-5360_196-5341d others(22): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | TTTTC | T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0110 a0001c0001t0001g0111 others(7): Show |
11 | HG01261.hp2 HG01891.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-5344_196-5341d others(6): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | TTTTCTTT others(1): Show |
T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0028 others(7): Show |
17 | HG00558.hp2 HG02015.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.196-5348_196-5341d others(10): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | TTTTCTTT others(5): Show |
T | 1 | a0001c0001t0001g0149 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.196-5352_196-5341d others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923478 | TTTTCTTT others(9): Show |
T | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196-5356_196-5341d others(18): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923478 | |||||||
| chr9:114923507 | TTTCTTTC others(8): Show |
T | 8 | a0001c0001t0007g0255 a0001c0001t0007g0257 a0001c0001t0007g0258 others(5): Show |
10 | HG02074.hp1 NA18949.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-5384_196-5370d others(17): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923507 | |||||||
| chr9:114923508 | TTCTTTCT others(3): Show |
T | 1 | a0001c0002t0002g0184 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.196-5380_196-5371d others(12): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923508 | |||||||
| chr9:114923508 | TTCTTTCT others(7): Show |
T | 15 | a0001c0002t0002g0002 a0001c0002t0002g0025 a0001c0002t0002g0026 others(12): Show |
26 | HG00558.hp1 HG00597.hp1 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-5384_196-5371d others(16): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923508 | |||||||
| chr9:114923509 | TCTTTCTT others(6): Show |
T | 1 | a0001c0002t0002g0002 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.196-5384_196-5372d others(15): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923509 | |||||||
| chr9:114923511 | TTTCTTTC others(4): Show |
T | 5 | a0001c0001t0003g0232 a0001c0001t0007g0058 a0001c0001t0007g0259 others(2): Show |
6 | HG01192.hp1 HG02074.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-5384_196-5374d others(13): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923511 | |||||||
| chr9:114923514 | CTTTCTTT others(5): Show |
C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0125 |
2 | HG02056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.196-5388_196-5377d others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923514 | |||||||
| chr9:114923515 | TTTCTTTC | T | 11 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(8): Show |
26 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-5384_196-5378d others(9): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923515 | |||||||
| chr9:114923519 | TTTC | T | 12 | a0001c0001t0001g0115 a0001c0001t0003g0013 a0001c0001t0003g0015 others(9): Show |
19 | HG01496.hp1 HG02280.hp1 HG02965.hp2 others(16): Show |
intron_variant | MODIFIER | c.196-5384_196-5382d others(5): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923519 | |||||||
| chr9:114923520 | TTC | T | 7 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0202 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-5384_196-5383d others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923520 | |||||||
| chr9:114923522 | C | CT | 9 | a0001c0001t0003g0013 a0001c0001t0003g0015 a0001c0001t0003g0048 others(6): Show |
10 | HG01109.hp1 HG01109.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-5385dupA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTT | 7 | a0001c0002t0002g0004 a0001c0002t0002g0177 a0001c0002t0002g0198 others(4): Show |
10 | HG01175.hp2 HG01255.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-5386_196-5385d others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCT | 11 | a0001c0001t0001g0116 a0001c0001t0003g0015 a0001c0001t0003g0046 others(8): Show |
13 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(7): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTT | 14 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0006 others(11): Show |
19 | HG01255.hp2 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(8): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT | 8 | a0001c0002t0002g0003 a0001c0002t0002g0006 a0001c0002t0002g0007 others(5): Show |
8 | HG01433.hp2 HG01516.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(9): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(2): Show |
17 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(14): Show |
21 | HG00733.hp2 HG01891.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(11): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(3): Show |
10 | a0001c0002t0002g0003 a0001c0002t0002g0006 a0001c0002t0002g0007 others(7): Show |
14 | HG00642.hp2 HG00733.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(12): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(4): Show |
5 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0022 others(2): Show |
5 | HG00323.hp1 HG02451.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(13): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(6): Show |
14 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0001t0003g0008 others(11): Show |
17 | HG01069.hp2 HG01071.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(15): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(7): Show |
8 | a0001c0001t0003g0008 a0001c0002t0002g0003 a0001c0002t0002g0004 others(5): Show |
11 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(16): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(8): Show |
1 | a0001c0002t0002g0197 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.196-5385_196-5384i others(17): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(10): Show |
5 | a0001c0001t0003g0014 a0001c0001t0003g0049 a0001c0001t0003g0050 others(2): Show |
5 | HG01243.hp2 HG02257.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(19): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(11): Show |
5 | a0001c0002t0002g0007 a0001c0002t0002g0132 a0001c0002t0002g0161 others(2): Show |
5 | HG00099.hp1 HG01070.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-5385_196-5384i others(20): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(12): Show |
2 | a0001c0002t0002g0004 a0001c0002t0002g0160 |
2 | HG02886.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.196-5385_196-5384i others(21): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(15): Show |
1 | a0001c0002t0002g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.196-5385_196-5384i others(24): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923522 | C | CTTTCTTT others(5): Show |
1 | a0001c0002t0002g0004 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.196-5385_196-5384i others(14): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923522 | |||||||
| chr9:114923523 | T | TTTCTTTC others(4): Show |
1 | a0001c0001t0005g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-5386_196-5385i others(13): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923523 | |||||||
| chr9:114923523 | T | TTTCTTTC others(8): Show |
1 | a0001c0002t0002g0175 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196-5386_196-5385i others(17): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923523 | |||||||
| chr9:114923523 | T | TTTCTTTC others(12): Show |
1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.196-5386_196-5385i others(21): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923523 | |||||||
| chr9:114923524 | T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196-5387_196-5386i others(16): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923524 | |||||||
| chr9:114923524 | T | TTCTTTCT others(11): Show |
2 | a0001c0001t0006g0098 a0001c0001t0021g0238 |
2 | NA18965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.196-5387_196-5386i others(20): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923524 | |||||||
| chr9:114923525 | T | TCTTTCTT others(14): Show |
1 | a0001c0001t0001g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.196-5388_196-5387i others(23): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923525 | |||||||
| chr9:114923526 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.196-5388A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923526 | |||||||
| chr9:114923528 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0159 |
2 | HG00438.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.196-5390A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923528 | |||||||
| chr9:114923532 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.196-5394A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923532 | |||||||
| chr9:114923931 | T | C | 1 | a0001c0002t0002g0209 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.196-5793A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114923931 | |||||||
| chr9:114924029 | G | C | 8 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0130 others(5): Show |
12 | HG00738.hp1 HG01070.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.196-5891C>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924029 | |||||||
| chr9:114924138 | C | T | 1 | a0001c0001t0004g0242 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.195+5971G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924138 | |||||||
| chr9:114924177 | A | G | 111 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(108): Show |
191 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.195+5932T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924177 | |||||||
| chr9:114924201 | G | T | 1 | a0001c0001t0013g0231 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.195+5908C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924201 | |||||||
| chr9:114924215 | T | G | 1 | a0001c0002t0002g0184 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.195+5894A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924215 | |||||||
| chr9:114924234 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.195+5875A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924234 | |||||||
| chr9:114924321 | T | C | 17 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(14): Show |
42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.195+5788A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924321 | |||||||
| chr9:114924425 | T | TATTGAAT others(20): Show |
1 | a0001c0001t0001g0066 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.195+5657_195+5683d others(29): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924425 | |||||||
| chr9:114924452 | A | T | 68 | a0001c0001t0024g0212 a0001c0002t0002g0002 a0001c0002t0002g0003 others(65): Show |
119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.195+5657T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924452 | |||||||
| chr9:114924567 | C | A | 67 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(64): Show |
118 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.195+5542G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924567 | |||||||
| chr9:114924578 | C | G | 17 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(14): Show |
42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.195+5531G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924578 | |||||||
| chr9:114924756 | C | A | 67 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0004 others(64): Show |
118 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.195+5353G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924756 | |||||||
| chr9:114924835 | A | C | 1 | a0001c0001t0001g0170 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.195+5274T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924835 | |||||||
| chr9:114924871 | G | T | 68 | a0001c0001t0024g0212 a0001c0002t0002g0002 a0001c0002t0002g0003 others(65): Show |
119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.195+5238C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114924871 | |||||||
| chr9:114925128 | C | G | 1 | a0001c0002t0002g0177 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.195+4981G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925128 | |||||||
| chr9:114925130 | G | A | 1 | a0001c0002t0002g0197 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.195+4979C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925130 | |||||||
| chr9:114925131 | G | T | 1 | a0001c0001t0003g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.195+4978C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925131 | |||||||
| chr9:114925717 | T | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG00323.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.195+4392A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925717 | |||||||
| chr9:114925838 | A | G | 1 | a0001c0001t0003g0046 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.195+4271T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925838 | |||||||
| chr9:114925982 | TAAGAG | T | 17 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(14): Show |
42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.195+4122_195+4126d others(7): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114925982 | |||||||
| chr9:114926299 | G | A | 1 | a0001c0001t0013g0231 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.195+3810C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926299 | |||||||
| chr9:114926658 | G | A | 2 | a0001c0001t0013g0231 a0001c0001t0013g0253 |
2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.195+3451C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926658 | |||||||
| chr9:114926719 | A | C | 1 | a0001c0001t0003g0216 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.195+3390T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926719 | |||||||
| chr9:114926845 | A | T | 1 | a0001c0002t0002g0186 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.195+3264T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926845 | |||||||
| chr9:114926904 | A | G | 68 | a0001c0001t0018g0199 a0001c0002t0002g0002 a0001c0002t0002g0003 others(65): Show |
119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.195+3205T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926904 | |||||||
| chr9:114926953 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.195+3156T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926953 | |||||||
| chr9:114926982 | A | AATATTTA others(22): Show |
3 | a0001c0001t0003g0214 a0001c0001t0003g0228 a0001c0001t0003g0232 |
3 | HG01192.hp1 HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.195+3098_195+3126d others(31): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926982 | |||||||
| chr9:114926982 | A | AATATTTA others(25): Show |
24 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0007 others(21): Show |
48 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.195+3095_195+3126d others(34): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926982 | |||||||
| chr9:114926982 | A | AATATTTA others(57): Show |
4 | a0001c0002t0002g0161 a0001c0002t0002g0163 a0001c0002t0002g0175 others(1): Show |
4 | HG01346.hp1 HG03579.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+3126_195+3127i others(66): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926982 | |||||||
| chr9:114926993 | T | TATAAAAT others(25): Show |
1 | a0001c0001t0001g0041 | 2 | HG00558.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.195+3084_195+3115d others(34): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926993 | |||||||
| chr9:114926993 | TATAAAAT others(25): Show |
T | 1 | a0001c0002t0002g0210 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.195+3084_195+3115d others(34): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114926993 | |||||||
| chr9:114927009 | TATA | T | 35 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(32): Show |
60 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.195+3097_195+3099d others(5): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927009 | |||||||
| chr9:114927009 | TATAATAT others(28): Show |
T | 6 | a0001c0001t0003g0046 a0001c0001t0003g0047 a0001c0001t0003g0050 others(3): Show |
10 | HG02257.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.195+3065_195+3099d others(37): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927009 | |||||||
| chr9:114927025 | C | T | 105 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(102): Show |
181 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.195+3084G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927025 | |||||||
| chr9:114927025 | CATAAAAT others(25): Show |
C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0107 a0001c0001t0001g0123 others(5): Show |
9 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+3052_195+3083d others(34): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927025 | |||||||
| chr9:114927092 | A | G | 1 | a0001c0001t0023g0213 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.195+3017T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927092 | |||||||
| chr9:114927211 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.195+2898A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927211 | |||||||
| chr9:114927268 | T | C | 43 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(40): Show |
72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.195+2841A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927268 | |||||||
| chr9:114927352 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.195+2757G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927352 | |||||||
| chr9:114927482 | T | G | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+2627A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927482 | |||||||
| chr9:114927512 | G | A | 1 | a0001c0002t0008g0200 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.195+2597C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927512 | |||||||
| chr9:114927558 | A | G | 43 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(40): Show |
72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.195+2551T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927558 | |||||||
| chr9:114927598 | C | G | 17 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(14): Show |
42 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.195+2511G>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114927598 | |||||||
| chr9:114928027 | A | G | 5 | a0001c0002t0002g0023 a0001c0002t0002g0132 a0001c0002t0002g0161 others(2): Show |
7 | HG01070.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+2082T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928027 | |||||||
| chr9:114928043 | T | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0033 others(5): Show |
13 | HG00673.hp1 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+2066A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928043 | |||||||
| chr9:114928410 | G | T | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1699C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928410 | |||||||
| chr9:114928452 | A | C | 3 | a0001c0002t0002g0006 a0001c0002t0002g0160 a0001c0002t0002g0175 |
9 | HG02280.hp2 HG02451.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.195+1657T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928452 | |||||||
| chr9:114928478 | T | C | 139 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(136): Show |
247 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.195+1631A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928478 | |||||||
| chr9:114928573 | T | G | 2 | a0001c0002t0002g0023 a0001c0002t0002g0132 |
4 | HG01070.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.195+1536A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928573 | |||||||
| chr9:114928584 | C | T | 27 | a0001c0001t0001g0244 a0001c0001t0004g0001 a0001c0001t0004g0052 others(24): Show |
55 | HG00423.hp1 HG00609.hp2 HG01167.hp2 others(52): Show |
intron_variant | MODIFIER | c.195+1525G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928584 | |||||||
| chr9:114928921 | C | T | 69 | a0001c0001t0018g0199 a0001c0001t0024g0212 a0001c0002t0002g0002 others(66): Show |
120 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.195+1188G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928921 | |||||||
| chr9:114928937 | T | G | 1 | a0001c0002t0002g0211 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.195+1172A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928937 | |||||||
| chr9:114928939 | A | G | 1 | a0001c0001t0015g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.195+1170T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928939 | |||||||
| chr9:114928990 | A | G | 112 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(109): Show |
192 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.195+1119T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928990 | |||||||
| chr9:114928995 | G | T | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1114C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928995 | |||||||
| chr9:114928996 | A | T | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+1113T>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114928996 | |||||||
| chr9:114929033 | T | C | 68 | a0001c0001t0018g0199 a0001c0002t0002g0002 a0001c0002t0002g0003 others(65): Show |
119 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.195+1076A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929033 | |||||||
| chr9:114929084 | T | A | 70 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(67): Show |
127 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(124): Show |
intron_variant | MODIFIER | c.195+1025A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929084 | |||||||
| chr9:114929095 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.195+1014T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929095 | |||||||
| chr9:114929278 | C | T | 71 | a0001c0001t0001g0073 a0001c0001t0001g0244 a0001c0001t0003g0008 others(68): Show |
128 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(125): Show |
intron_variant | MODIFIER | c.195+831G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929278 | |||||||
| chr9:114929288 | G | A | 1 | a0001c0001t0005g0229 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.195+821C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929288 | |||||||
| chr9:114929357 | C | CT | 20 | a0001c0001t0001g0072 a0001c0001t0001g0108 a0001c0001t0003g0214 others(17): Show |
22 | HG01192.hp1 HG01928.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.195+751dupA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929357 | |||||||
| chr9:114929357 | CT | C | 7 | a0001c0001t0001g0106 a0001c0001t0001g0124 a0001c0001t0001g0125 others(4): Show |
7 | HG01070.hp2 HG02451.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+751delA | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929357 | |||||||
| chr9:114929378 | C | T | 43 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0014 others(40): Show |
72 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.195+731G>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929378 | |||||||
| chr9:114929396 | G | A | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+713C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929396 | |||||||
| chr9:114929544 | A | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0107 a0001c0001t0001g0149 |
4 | HG02056.hp1 HG02602.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+565T>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929544 | |||||||
| chr9:114929874 | CAT | C | 70 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0021 others(67): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.195+233_195+234del others(2): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929874 | |||||||
| chr9:114929874 | CATAT | C | 109 | a0001c0001t0001g0244 a0001c0001t0003g0013 a0001c0001t0003g0015 others(106): Show |
186 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(183): Show |
intron_variant | MODIFIER | c.195+231_195+234del others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929874 | |||||||
| chr9:114929875 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.195+234T>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929875 | |||||||
| chr9:114929892 | T | C | 2 | a0001c0002t0008g0200 a0001c0002t0012g0044 |
3 | NA18945.hp2 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.195+217A>G | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929892 | |||||||
| chr9:114929962 | G | GTA | 3 | a0001c0001t0001g0126 a0001c0001t0005g0230 a0001c0001t0007g0255 |
3 | HG02074.hp1 NA18522.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.195+145_195+146dup others(2): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929962 | |||||||
| chr9:114929962 | G | GTATA | 7 | a0001c0002t0002g0127 a0001c0002t0002g0128 a0001c0002t0002g0129 others(4): Show |
7 | HG00597.hp1 HG01070.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+143_195+146dup others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929962 | |||||||
| chr9:114929962 | GTA | G | 2 | a0001c0002t0010g0056 a0001c0002t0010g0256 |
3 | NA18969.hp1 NA18974.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.195+145_195+146del others(2): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929962 | |||||||
| chr9:114929967 | T | A | 1 | a0001c0001t0004g0251 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.195+142A>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929967 | |||||||
| chr9:114929971 | T | TAGAG | 14 | a0001c0002t0002g0003 a0001c0002t0002g0045 a0001c0002t0002g0201 others(11): Show |
24 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.195+137_195+138ins others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929971 | |||||||
| chr9:114929973 | T | G | 17 | a0001c0001t0003g0252 a0001c0001t0004g0254 a0001c0001t0013g0253 others(14): Show |
27 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.195+136A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929973 | |||||||
| chr9:114929973 | T | TAGAG | 5 | a0001c0001t0018g0199 a0001c0002t0002g0026 a0001c0002t0002g0196 others(2): Show |
7 | HG01257.hp1 HG02896.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+135_195+136ins others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929973 | |||||||
| chr9:114929975 | T | G | 44 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(41): Show |
80 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.195+134A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929975 | |||||||
| chr9:114929975 | T | TAGAG | 16 | a0001c0002t0002g0025 a0001c0002t0002g0043 a0001c0002t0002g0183 others(13): Show |
21 | HG00558.hp1 HG00733.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.195+133_195+134ins others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929975 | |||||||
| chr9:114929975 | T | TAGAGAG | 2 | a0001c0002t0008g0200 a0001c0002t0012g0044 |
3 | NA18945.hp2 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.195+133_195+134ins others(6): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929975 | |||||||
| chr9:114929977 | T | G | 110 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(107): Show |
167 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.195+132A>C | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929977 | |||||||
| chr9:114929977 | T | TAGAG | 11 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0006 others(8): Show |
35 | HG00099.hp1 HG00323.hp1 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.195+128_195+131dup others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929977 | |||||||
| chr9:114929977 | T | TATAG | 13 | a0001c0002t0002g0007 a0001c0002t0002g0022 a0001c0002t0002g0023 others(10): Show |
22 | HG00738.hp1 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.195+131_195+132ins others(4): Show |
TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929977 | |||||||
| chr9:114929979 | G | T | 26 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0060 others(23): Show |
33 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.195+130C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929979 | |||||||
| chr9:114929981 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG00741.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.195+128C>A | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114929981 | |||||||
| chr9:114930062 | C | A | 1 | a0001c0001t0024g0212 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.195+47G>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114930062 | |||||||
| chr9:114930064 | G | A | 70 | a0001c0001t0001g0244 a0001c0001t0003g0008 a0001c0001t0003g0013 others(67): Show |
127 | HG00423.hp1 HG00609.hp2 HG01069.hp2 others(124): Show |
intron_variant | MODIFIER | c.195+45C>T | TNFSF8 | ENSG00000106952.8 | transcript | ENST00000223795.3 | protein_coding | 1/3 | chr9 | 114930064 |