Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8600 |
| ensemblid | ENSG00000120659.16 |
| hgncid | 11926 |
| symbol | TNFSF11 |
| name | TNF superfamily member 11 |
| refseq_nuc | NM_003701.4 |
| refseq_prot | NP_003692.1 |
| ensembl_nuc | ENST00000398795.7 |
| ensembl_prot | ENSP00000381775.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 42574152 |
| end | 42608013 |
| strand | + |
| ver | v1.2 |
| region | chr13:42574152-42608013 |
| region5000 | chr13:42569152-42613013 |
| regionname0 | TNFSF11_chr13_42574152_42608013 |
| regionname5000 | TNFSF11_chr13_42569152_42613013 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 317 | 406 | 84 | 73 | 204 | 11 | 32 | 162 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | MRRAS others(312): Show |
chr13 | 42569152 | 42613013 |
| a0002 | 0/0 | 317 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | MRRAS others(312): Show |
chr13 | 42569152 | 42613013 |
| a0003 | 0/0 | 317 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | MRRAS others(312): Show |
chr13 | 42569152 | 42613013 |
| a0004 | 0/0 | 317 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | MRRAS others(312): Show |
chr13 | 42569152 | 42613013 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 951 | 221 | 36 | 39 | 121 | 4 | 19 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 | ||
| a0001c0002 | 0/0 | 951 | 158 | 38 | 33 | 69 | 7 | 11 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 | ||
| a0001c0003 | 0/0 | 951 | 16 | 1 | 0 | 14 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 | ||
| a0001c0004 | 0/0 | 951 | 7 | 6 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 | ||
| a0001c0005 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 | ||
| a0001c0007 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 | ||
| a0001c0008 | 0/0 | 951 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 | ||
| a0002c0006 | 0/0 | 951 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 | ||
| a0003c0009 | 0/0 | 951 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 | ||
| a0004c0010 | 0/0 | 951 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | ATGCG others(946): Show |
chr13 | 42569152 | 42613013 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2201 | 210 | 30 | 37 | 119 | 4 | 19 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0001t0005 | 1/0 | 2201 | 4 | 3 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0001t0006 | 0/0 | 2201 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0001t0009 | 0/0 | 2201 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0001t0010 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0001t0012 | 0/0 | 2201 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0002t0001 | 0/0 | 2201 | 143 | 29 | 32 | 64 | 7 | 11 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0002t0003 | 0/0 | 2201 | 8 | 7 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0002t0004 | 0/0 | 2201 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0002t0006 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0002t0011 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0003t0002 | 0/0 | 2201 | 14 | 1 | 0 | 12 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0003t0007 | 0/0 | 2201 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0004t0001 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0004t0002 | 0/0 | 2201 | 5 | 4 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0005t0008 | 0/0 | 2201 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0007t0002 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0001c0008t0002 | 0/0 | 2201 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0002c0006t0001 | 0/0 | 2201 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0003c0009t0001 | 0/0 | 2201 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| a0004c0010t0001 | 0/0 | 2201 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | GCCCG others(2196): Show |
chr13 | 42569152 | 42613013 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 2 | 1 | 0 | 4 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0008 | 0/1 | 5 | 0 | 1 | 1 | 0 | 2 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0005g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0009g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0010g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0001t0012g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0003 | 0/0 | 7 | 0 | 2 | 4 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0002t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0007g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0003t0007g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0004t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0004t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0004t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0004t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0004t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0005t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0005t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0007t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0001c0008t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0002c0006t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0002c0006t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0003c0009t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| a0004c0010t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0123 | EUR | GBR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0119 | EUR | GBR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0118 | EUR | FIN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00280 | hp2 | a0003 | c0009 | t0001 | g0083 | EUR | FIN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00438 | hp2 | a0001 | c0002 | t0004 | g0007 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00621 | hp1 | a0001 | c0001 | t0010 | g0016 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00639 | hp1 | a0002 | c0006 | t0001 | g0300 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0293 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0044 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01071 | hp2 | a0001 | c0001 | t0009 | g0044 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0296 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01256 | hp1 | a0001 | c0008 | t0002 | g0278 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0209 | AMR | CLM | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0099 | EUR | IBS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0060 | EUR | IBS | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01884 | hp2 | a0001 | c0002 | t0011 | g0215 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02055 | hp1 | a0001 | c0004 | t0002 | g0250 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02129 | hp1 | a0001 | c0002 | t0004 | g0013 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0064 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | CDX | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0203 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02572 | hp1 | a0001 | c0004 | t0002 | g0022 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0206 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0219 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0102 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02717 | hp1 | a0001 | c0007 | t0002 | g0273 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0207 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0205 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0175 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02895 | hp2 | a0001 | c0004 | t0002 | g0251 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0217 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02922 | hp1 | a0001 | c0005 | t0008 | g0298 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02922 | hp2 | a0004 | c0010 | t0001 | g0056 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0212 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0208 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0210 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03453 | hp1 | a0001 | c0004 | t0002 | g0252 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0213 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03540 | hp2 | a0001 | c0005 | t0008 | g0299 | AFR | GWD | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0290 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | BEB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0277 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | BEB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG04199 | hp1 | a0001 | c0004 | t0002 | g0078 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0138 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18939 | hp1 | a0001 | c0003 | t0002 | g0291 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18944 | hp1 | a0001 | c0003 | t0002 | g0289 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18962 | hp1 | a0001 | c0003 | t0002 | g0282 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18964 | hp2 | a0001 | c0001 | t0012 | g0263 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18965 | hp1 | a0001 | c0003 | t0007 | g0287 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18979 | hp1 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18980 | hp1 | a0001 | c0003 | t0002 | g0284 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18981 | hp1 | a0001 | c0003 | t0002 | g0283 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18985 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18995 | hp1 | a0001 | c0003 | t0002 | g0280 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0211 | AFR | LWK | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | LWK | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19064 | hp1 | a0001 | c0003 | t0007 | g0286 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19066 | hp1 | a0001 | c0003 | t0002 | g0288 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19075 | hp2 | a0001 | c0003 | t0002 | g0279 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19080 | hp2 | a0001 | c0003 | t0002 | g0281 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0292 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19085 | hp2 | a0001 | c0003 | t0002 | g0285 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0152 | AFR | YRI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0022 | AFR | ASW | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ASW | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | TSI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0098 | EUR | TSI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | GIH | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | MSL | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0022 | AFR | USA | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | USA | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20300 | hp1 | a0002 | c0006 | t0001 | g0253 | AFR | USA | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | USA | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | LWK | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0008 | REF | REF | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0065 | REF | REF | TNFSF11_chr13_42569152_42613013 | TNFSF11 | chr13 | 42569152 | 42613013 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42574410 | C | G | 1 | a0002 | 2 | HG00639.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.107C>G | p.Pro36Arg | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 259/2201 | 107/954 | 36/317 | chr13 | 42574410 | |||
| chr13:42581145 | C | T | 1 | a0004 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.239C>T | p.Ser80Leu | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/5 | 391/2201 | 239/954 | 80/317 | chr13 | 42581145 | |||
| chr13:42600784 | C | G | 1 | a0003 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.420C>G | p.Ile140Met | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 3/5 | 572/2201 | 420/954 | 140/317 | chr13 | 42600784 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42574348 | G | A | 1 | a0001c0007 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.45G>A | p.Ser15Ser | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 197/2201 | 45/954 | 15/317 | chr13 | 42574348 | |||
| chr13:42574429 | T | C | 6 | a0001c0002 a0001c0003 a0001c0007 others(3): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
synonymous_variant | LOW | c.126T>C | p.Pro42Pro | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 278/2201 | 126/954 | 42/317 | chr13 | 42574429 | |||
| chr13:42574450 | C | T | 1 | a0001c0005 | 2 | HG02922.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.147C>T | p.Phe49Phe | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 299/2201 | 147/954 | 49/317 | chr13 | 42574450 | |||
| chr13:42581230 | T | C | 1 | a0001c0008 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.324T>C | p.Asp108Asp | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/5 | 476/2201 | 324/954 | 108/317 | chr13 | 42581230 | |||
| chr13:42600760 | A | G | 1 | a0004c0010 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.396A>G | p.Gln132Gln | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 3/5 | 548/2201 | 396/954 | 132/317 | chr13 | 42600760 | |||
| chr13:42606888 | T | C | 4 | a0001c0003 a0001c0004 a0001c0007 others(1): Show |
25 | HG00673.hp1 HG01256.hp1 HG02055.hp1 others(22): Show |
synonymous_variant | LOW | c.924T>C | p.Phe308Phe | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 1076/2201 | 924/954 | 308/317 | chr13 | 42606888 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42574163 | C | T | 1 | a0001c0002t0004 | 5 | HG00438.hp2 HG02129.hp1 NA18971.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-141C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | chr13 | 42574163 | |||||||
| chr13:42574177 | C | G | 20 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(17): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
5_prime_UTR_variant | MODIFIER | c.-127C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 127 | chr13 | 42574177 | ||||||
| chr13:42574300 | C | T | 1 | a0001c0001t0012 | 1 | NA18964.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/5 | 4 | chr13 | 42574300 | ||||||
| chr13:42606966 | T | C | 1 | a0001c0002t0003 | 8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*48T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 48 | chr13 | 42606966 | ||||||
| chr13:42606992 | A | G | 1 | a0001c0002t0011 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 74 | chr13 | 42606992 | ||||||
| chr13:42607074 | C | T | 1 | a0001c0001t0009 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*156C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 156 | chr13 | 42607074 | ||||||
| chr13:42607077 | G | A | 1 | a0001c0003t0007 | 2 | NA18965.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*159G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 159 | chr13 | 42607077 | ||||||
| chr13:42607182 | G | T | 19 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(16): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 264 | chr13 | 42607182 | ||||||
| chr13:42607301 | C | T | 5 | a0001c0003t0002 a0001c0003t0007 a0001c0004t0002 others(2): Show |
23 | HG00673.hp1 HG01256.hp1 HG02055.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*383C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 383 | chr13 | 42607301 | ||||||
| chr13:42607458 | A | G | 1 | a0001c0001t0010 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*540A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 540 | chr13 | 42607458 | ||||||
| chr13:42607622 | G | A | 1 | a0001c0005t0008 | 2 | HG02922.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*704G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 704 | chr13 | 42607622 | ||||||
| chr13:42607660 | G | A | 2 | a0001c0001t0006 a0001c0002t0006 |
4 | HG02622.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*742G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 742 | chr13 | 42607660 | ||||||
| chr13:42607866 | G | T | 4 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0004 others(1): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*948G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 948 | chr13 | 42607866 | ||||||
| chr13:42607917 | T | C | 1 | a0001c0002t0001 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 5/5 | 999 | chr13 | 42607917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:42574538 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.219+16C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574538 | |||||||
| chr13:42574596 | T | A | 9 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(6): Show |
9 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+74T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574596 | |||||||
| chr13:42574708 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.219+186G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574708 | |||||||
| chr13:42574757 | G | A | 2 | a0001c0002t0001g0058 a0001c0002t0001g0059 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.219+235G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574757 | |||||||
| chr13:42574926 | G | A | 9 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(6): Show |
9 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+404G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42574926 | |||||||
| chr13:42575100 | C | T | 1 | a0002c0006t0001g0300 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.219+578C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575100 | |||||||
| chr13:42575661 | A | T | 2 | a0001c0005t0008g0298 a0001c0005t0008g0299 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.219+1139A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575661 | |||||||
| chr13:42575753 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.219+1231A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575753 | |||||||
| chr13:42575822 | A | T | 2 | a0001c0002t0001g0295 a0001c0002t0001g0296 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.219+1300A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575822 | |||||||
| chr13:42575881 | A | G | 1 | a0001c0002t0001g0294 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219+1359A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575881 | |||||||
| chr13:42575974 | C | G | 16 | a0001c0003t0002g0279 a0001c0003t0002g0280 a0001c0003t0002g0281 others(13): Show |
16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.219+1452C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42575974 | |||||||
| chr13:42576033 | A | G | 1 | a0001c0002t0001g0277 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.219+1511A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576033 | |||||||
| chr13:42576149 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.219+1627A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576149 | |||||||
| chr13:42576225 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219+1703G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576225 | |||||||
| chr13:42576264 | G | A | 2 | a0001c0002t0001g0060 a0001c0002t0001g0061 |
2 | HG01243.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.219+1742G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576264 | |||||||
| chr13:42576360 | C | T | 1 | a0001c0002t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.219+1838C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576360 | |||||||
| chr13:42576499 | A | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(298): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.219+1977A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576499 | |||||||
| chr13:42576552 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+2030C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576552 | |||||||
| chr13:42576866 | T | C | 1 | a0001c0008t0002g0278 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.219+2344T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576866 | |||||||
| chr13:42576939 | C | T | 1 | a0001c0007t0002g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.219+2417C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576939 | |||||||
| chr13:42576962 | A | G | 1 | a0001c0002t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.219+2440A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42576962 | |||||||
| chr13:42577050 | T | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(19): Show |
34 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.219+2528T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577050 | |||||||
| chr13:42577061 | T | C | 1 | a0001c0003t0002g0279 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.219+2539T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577061 | |||||||
| chr13:42577364 | G | A | 96 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(93): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.219+2842G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577364 | |||||||
| chr13:42577424 | C | T | 1 | a0001c0007t0002g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.219+2902C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577424 | |||||||
| chr13:42577500 | GA | G | 10 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(7): Show |
10 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+2986delA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42577500 | ||||||
| chr13:42577693 | G | A | 2 | a0001c0005t0008g0298 a0001c0005t0008g0299 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.219+3171G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577693 | |||||||
| chr13:42577864 | C | T | 1 | a0004c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.220-3262C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577864 | |||||||
| chr13:42577968 | G | C | 2 | a0001c0003t0002g0279 a0001c0003t0002g0280 |
2 | NA18995.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.220-3158G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42577968 | |||||||
| chr13:42578043 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220-3083A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578043 | |||||||
| chr13:42578196 | G | T | 1 | a0001c0002t0001g0150 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.220-2930G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578196 | |||||||
| chr13:42578433 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.220-2693T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578433 | |||||||
| chr13:42578514 | C | T | 16 | a0001c0003t0002g0279 a0001c0003t0002g0280 a0001c0003t0002g0281 others(13): Show |
16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.220-2612C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578514 | |||||||
| chr13:42578585 | A | C | 1 | a0001c0001t0012g0263 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.220-2541A>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578585 | |||||||
| chr13:42578627 | C | T | 96 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(93): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.220-2499C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578627 | |||||||
| chr13:42578751 | G | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.220-2375G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42578751 | |||||||
| chr13:42579006 | T | C | 1 | a0001c0002t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220-2120T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579006 | |||||||
| chr13:42579022 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.220-2104A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579022 | |||||||
| chr13:42579119 | G | A | 1 | a0001c0002t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220-2007G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579119 | |||||||
| chr13:42579415 | C | CA | 170 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(167): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.220-1695dupA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579415 | ||||||
| chr13:42579415 | CA | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0256 others(10): Show |
15 | HG01361.hp2 HG02451.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.220-1695delA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579415 | ||||||
| chr13:42579704 | C | CTTTTT | 8 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0265 others(5): Show |
8 | HG00099.hp1 HG01884.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-1402_220-1398d others(7): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579704 | C | CTTTTTT | 39 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0035 others(36): Show |
52 | HG00642.hp1 HG01192.hp1 HG01433.hp2 others(49): Show |
intron_variant | MODIFIER | c.220-1403_220-1398d others(8): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579704 | C | CTTTTTTT | 22 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0015 others(19): Show |
41 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.220-1404_220-1398d others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579704 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0040 a0001c0001t0001g0188 a0001c0001t0001g0189 others(3): Show |
7 | HG00408.hp1 HG00423.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-1405_220-1398d others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579704 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0193 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.220-1408_220-1398d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579704 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220-1411_220-1398d others(16): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579704 | CT | C | 35 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0045 others(32): Show |
43 | HG00597.hp1 HG00673.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.220-1398delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579704 | CTT | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.220-1399_220-1398d others(4): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579704 | CTTT | C | 11 | a0001c0001t0001g0046 a0001c0001t0001g0256 a0001c0001t0001g0257 others(8): Show |
12 | HG01361.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.220-1400_220-1398d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579704 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.220-1408_220-1398d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr13 | 42579704 | ||||||
| chr13:42579733 | A | T | 2 | a0002c0006t0001g0253 a0002c0006t0001g0300 |
2 | HG00639.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.220-1393A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579733 | |||||||
| chr13:42579824 | A | G | 1 | a0001c0002t0001g0132 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.220-1302A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579824 | |||||||
| chr13:42579975 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.220-1151C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42579975 | |||||||
| chr13:42580224 | C | T | 4 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0004t0002g0251 others(1): Show |
5 | HG02572.hp1 HG02895.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-902C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580224 | |||||||
| chr13:42580349 | G | A | 14 | a0001c0003t0002g0279 a0001c0003t0002g0280 a0001c0003t0002g0281 others(11): Show |
14 | HG01256.hp1 HG03654.hp1 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-777G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580349 | |||||||
| chr13:42580368 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220-758A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580368 | |||||||
| chr13:42580409 | G | A | 1 | a0001c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220-717G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580409 | |||||||
| chr13:42580460 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.220-666A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580460 | |||||||
| chr13:42580670 | G | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
108 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.220-456G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580670 | |||||||
| chr13:42580823 | T | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0133 |
2 | NA18980.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.220-303T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580823 | |||||||
| chr13:42580823 | T | G | 94 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(91): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.220-303T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42580823 | |||||||
| chr13:42581032 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.220-94G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42581032 | |||||||
| chr13:42581051 | T | G | 3 | a0001c0002t0001g0084 a0001c0002t0001g0134 a0003c0009t0001g0083 |
3 | HG00280.hp2 HG02602.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.220-75T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42581051 | |||||||
| chr13:42581101 | C | T | 1 | a0001c0002t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220-25C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 1/4 | chr13 | 42581101 | |||||||
| chr13:42581307 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+14G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581307 | |||||||
| chr13:42581395 | T | G | 1 | a0001c0002t0006g0219 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.387+102T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581395 | |||||||
| chr13:42581585 | G | A | 1 | a0001c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+292G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581585 | |||||||
| chr13:42581695 | C | T | 1 | a0001c0002t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.387+402C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581695 | |||||||
| chr13:42581696 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+403A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42581696 | |||||||
| chr13:42582016 | G | A | 302 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(299): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.387+723G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582016 | |||||||
| chr13:42582140 | G | C | 2 | a0001c0005t0008g0298 a0001c0005t0008g0299 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.387+847G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582140 | |||||||
| chr13:42582164 | C | T | 2 | a0001c0002t0001g0214 a0001c0002t0011g0215 |
2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.387+871C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582164 | |||||||
| chr13:42582222 | A | G | 1 | a0001c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+929A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582222 | |||||||
| chr13:42582289 | A | T | 1 | a0001c0002t0001g0131 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.387+996A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582289 | |||||||
| chr13:42582377 | G | A | 2 | a0001c0002t0001g0085 a0001c0002t0001g0086 |
2 | NA18987.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.387+1084G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582377 | |||||||
| chr13:42582422 | C | CGA | 3 | a0001c0001t0001g0035 a0001c0001t0001g0155 a0001c0001t0001g0177 |
4 | NA18944.hp2 NA18953.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+1129_387+1130i others(4): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582422 | |||||||
| chr13:42582458 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG03490.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.387+1165T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582458 | |||||||
| chr13:42582560 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+1267G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582560 | |||||||
| chr13:42582602 | G | A | 6 | a0001c0002t0001g0017 a0001c0002t0001g0026 a0001c0002t0001g0087 others(3): Show |
9 | NA18948.hp1 NA18990.hp2 NA19005.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+1309G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582602 | |||||||
| chr13:42582629 | T | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA18969.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.387+1336T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582629 | |||||||
| chr13:42582698 | A | G | 1 | a0001c0007t0002g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.387+1405A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582698 | |||||||
| chr13:42582961 | A | C | 1 | a0001c0002t0001g0130 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.387+1668A>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42582961 | |||||||
| chr13:42583008 | G | A | 1 | a0001c0002t0001g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.387+1715G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583008 | |||||||
| chr13:42583067 | T | A | 5 | a0001c0002t0001g0203 a0001c0002t0001g0204 a0001c0002t0001g0216 others(2): Show |
5 | HG02451.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+1774T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583067 | |||||||
| chr13:42583122 | C | T | 1 | a0001c0002t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.387+1829C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583122 | |||||||
| chr13:42583131 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+1838G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583131 | |||||||
| chr13:42583176 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+1883C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583176 | |||||||
| chr13:42583304 | C | G | 1 | a0001c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+2011C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583304 | |||||||
| chr13:42583358 | G | A | 5 | a0001c0002t0001g0203 a0001c0002t0001g0204 a0001c0002t0001g0216 others(2): Show |
5 | HG02451.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2065G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583358 | |||||||
| chr13:42583359 | C | T | 5 | a0001c0002t0001g0203 a0001c0002t0001g0204 a0001c0002t0001g0216 others(2): Show |
5 | HG02451.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+2066C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583359 | |||||||
| chr13:42583417 | T | TA | 58 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
90 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.387+2145dupA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA | 7 | a0001c0002t0001g0086 a0001c0002t0001g0127 a0001c0002t0001g0128 others(4): Show |
7 | HG00733.hp2 HG01168.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.387+2139_387+2145d others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(1): Show |
57 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(54): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.387+2138_387+2145d others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(2): Show |
33 | a0001c0002t0001g0012 a0001c0002t0001g0013 a0001c0002t0001g0028 others(30): Show |
41 | HG00597.hp1 HG00738.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.387+2137_387+2145d others(11): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(3): Show |
10 | a0001c0002t0001g0087 a0001c0002t0001g0093 a0001c0002t0001g0094 others(7): Show |
10 | HG01106.hp1 HG01109.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.387+2136_387+2145d others(12): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(4): Show |
9 | a0001c0002t0001g0027 a0001c0002t0001g0048 a0001c0002t0001g0053 others(6): Show |
10 | HG01169.hp2 HG02622.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.387+2135_387+2145d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(5): Show |
8 | a0001c0002t0001g0052 a0001c0002t0001g0091 a0001c0002t0001g0217 others(5): Show |
8 | HG00673.hp1 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.387+2134_387+2145d others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(6): Show |
4 | a0001c0002t0003g0208 a0001c0002t0003g0209 a0001c0002t0003g0210 others(1): Show |
4 | HG01496.hp2 HG03041.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+2133_387+2145d others(15): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(7): Show |
3 | a0001c0002t0001g0216 a0001c0002t0003g0206 a0001c0002t0003g0207 |
3 | HG02572.hp2 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.387+2132_387+2145d others(16): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(8): Show |
1 | a0001c0002t0001g0055 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.387+2131_387+2145d others(17): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(9): Show |
6 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+2130_387+2145d others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(10): Show |
1 | a0001c0002t0003g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.387+2129_387+2145d others(19): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583417 | T | TAAAAAAA others(11): Show |
1 | a0001c0002t0001g0203 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.387+2128_387+2145d others(20): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583417 | ||||||
| chr13:42583433 | A | AAAAAAAA others(1): Show |
5 | a0001c0001t0001g0046 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
6 | HG02647.hp1 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+2145_387+2146i others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583433 | ||||||
| chr13:42583433 | A | AAAAAAAG | 36 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(33): Show |
49 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.387+2145_387+2146i others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583433 | ||||||
| chr13:42583434 | A | AAAAAAG | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(32): Show |
56 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.387+2145_387+2146i others(8): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42583434 | ||||||
| chr13:42583439 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.387+2146G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583439 | |||||||
| chr13:42583443 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
162 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.387+2150G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583443 | |||||||
| chr13:42583444 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.387+2151G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583444 | |||||||
| chr13:42583447 | G | A | 1 | a0001c0001t0001g0047 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.387+2154G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583447 | |||||||
| chr13:42583448 | A | G | 96 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(93): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.387+2155A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583448 | |||||||
| chr13:42583763 | G | A | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.387+2470G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583763 | |||||||
| chr13:42583779 | G | A | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.387+2486G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583779 | |||||||
| chr13:42583797 | G | A | 1 | a0001c0002t0006g0219 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.387+2504G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583797 | |||||||
| chr13:42583903 | G | T | 1 | a0001c0007t0002g0273 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.387+2610G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583903 | |||||||
| chr13:42583966 | A | G | 1 | a0001c0002t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.387+2673A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583966 | |||||||
| chr13:42583996 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.387+2703C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42583996 | |||||||
| chr13:42584083 | A | G | 1 | a0001c0002t0001g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.387+2790A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584083 | |||||||
| chr13:42584252 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.387+2959G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584252 | |||||||
| chr13:42584365 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+3072T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584365 | |||||||
| chr13:42584451 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.387+3158A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584451 | |||||||
| chr13:42584460 | C | A | 1 | a0001c0002t0001g0087 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.387+3167C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584460 | |||||||
| chr13:42584491 | C | G | 3 | a0001c0001t0001g0154 a0001c0001t0001g0184 a0001c0001t0001g0187 |
3 | NA18987.hp2 NA18997.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.387+3198C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584491 | |||||||
| chr13:42584598 | C | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.387+3305C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584598 | |||||||
| chr13:42584599 | T | A | 1 | a0001c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+3306T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584599 | |||||||
| chr13:42584617 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.387+3324G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584617 | |||||||
| chr13:42584660 | C | T | 1 | a0001c0002t0001g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.387+3367C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584660 | |||||||
| chr13:42584736 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.387+3443C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584736 | |||||||
| chr13:42584955 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+3662G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584955 | |||||||
| chr13:42584999 | G | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.387+3706G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42584999 | |||||||
| chr13:42585031 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.387+3738G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585031 | |||||||
| chr13:42585041 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG00642.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.387+3748C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585041 | |||||||
| chr13:42585111 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.387+3818A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585111 | |||||||
| chr13:42585138 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.387+3845G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585138 | |||||||
| chr13:42585215 | G | A | 2 | a0001c0002t0001g0048 a0001c0002t0001g0053 |
2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.387+3922G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585215 | |||||||
| chr13:42585225 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.387+3932G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585225 | |||||||
| chr13:42585265 | G | A | 96 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(93): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.387+3972G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585265 | |||||||
| chr13:42585380 | T | C | 97 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(94): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.387+4087T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585380 | |||||||
| chr13:42585413 | T | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0262 |
2 | HG03139.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.387+4120T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585413 | |||||||
| chr13:42585525 | C | G | 1 | a0001c0002t0001g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.387+4232C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585525 | |||||||
| chr13:42585668 | G | A | 129 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(126): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.387+4375G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585668 | |||||||
| chr13:42585789 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.387+4496G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42585789 | |||||||
| chr13:42586247 | G | A | 4 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0004t0002g0251 others(1): Show |
5 | HG02572.hp1 HG02895.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+4954G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586247 | |||||||
| chr13:42586441 | A | T | 1 | a0004c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387+5148A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586441 | |||||||
| chr13:42586544 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.387+5251A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586544 | |||||||
| chr13:42586583 | G | A | 4 | a0001c0002t0001g0030 a0001c0002t0001g0095 a0001c0002t0001g0107 others(1): Show |
5 | HG02647.hp2 HG02976.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+5290G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586583 | |||||||
| chr13:42586584 | A | T | 9 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(6): Show |
9 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.387+5291A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586584 | |||||||
| chr13:42586794 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.387+5501A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586794 | |||||||
| chr13:42586828 | T | G | 1 | a0001c0002t0001g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.387+5535T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586828 | |||||||
| chr13:42586993 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.387+5700T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42586993 | |||||||
| chr13:42587082 | G | A | 1 | a0004c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387+5789G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587082 | |||||||
| chr13:42587230 | T | C | 5 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0004t0002g0251 others(2): Show |
6 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+5937T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587230 | |||||||
| chr13:42587245 | T | G | 1 | a0001c0001t0005g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.387+5952T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587245 | |||||||
| chr13:42587455 | A | G | 1 | a0001c0002t0001g0275 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.387+6162A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587455 | |||||||
| chr13:42587543 | T | C | 1 | a0001c0008t0002g0278 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.387+6250T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587543 | |||||||
| chr13:42587597 | G | C | 1 | a0001c0002t0001g0089 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.387+6304G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587597 | |||||||
| chr13:42587603 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.387+6310A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587603 | |||||||
| chr13:42587767 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.387+6474A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587767 | |||||||
| chr13:42587894 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.387+6601A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587894 | |||||||
| chr13:42587927 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(77): Show |
115 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.387+6634G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42587927 | |||||||
| chr13:42588058 | T | C | 1 | a0001c0001t0005g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.387+6765T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42588058 | |||||||
| chr13:42588062 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.387+6769C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42588062 | |||||||
| chr13:42588549 | G | A | 5 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0004t0002g0251 others(2): Show |
6 | HG02572.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+7256G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42588549 | |||||||
| chr13:42588998 | C | T | 1 | a0001c0002t0001g0203 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.387+7705C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42588998 | |||||||
| chr13:42589145 | G | A | 1 | a0001c0003t0002g0281 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.387+7852G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589145 | |||||||
| chr13:42589159 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.387+7866C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589159 | |||||||
| chr13:42589234 | G | T | 9 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(6): Show |
9 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.387+7941G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589234 | |||||||
| chr13:42589390 | C | A | 8 | a0001c0002t0003g0205 a0001c0002t0003g0206 a0001c0002t0003g0207 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.387+8097C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589390 | |||||||
| chr13:42589401 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(296): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.387+8108C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589401 | |||||||
| chr13:42589443 | C | A | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+8150C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589443 | |||||||
| chr13:42589461 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.387+8168C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589461 | |||||||
| chr13:42589466 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.387+8173C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589466 | |||||||
| chr13:42589501 | T | C | 1 | a0001c0002t0001g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.387+8208T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589501 | |||||||
| chr13:42589505 | T | G | 15 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(12): Show |
15 | HG01496.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.387+8212T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589505 | |||||||
| chr13:42589645 | C | T | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.387+8352C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589645 | |||||||
| chr13:42589663 | G | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(215): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.387+8370G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589663 | |||||||
| chr13:42589720 | A | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(296): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.387+8427A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589720 | |||||||
| chr13:42589743 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.387+8450G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589743 | |||||||
| chr13:42589814 | G | A | 303 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(300): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.387+8521G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42589814 | |||||||
| chr13:42590011 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+8718C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590011 | |||||||
| chr13:42590035 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+8742T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590035 | |||||||
| chr13:42590405 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.387+9112G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590405 | |||||||
| chr13:42590450 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.387+9157T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590450 | |||||||
| chr13:42590488 | C | T | 16 | a0001c0003t0002g0279 a0001c0003t0002g0280 a0001c0003t0002g0281 others(13): Show |
16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.387+9195C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590488 | |||||||
| chr13:42590559 | A | G | 16 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(13): Show |
16 | HG01496.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.387+9266A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590559 | |||||||
| chr13:42590574 | C | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.387+9281C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590574 | |||||||
| chr13:42590592 | A | G | 1 | a0004c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387+9299A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590592 | |||||||
| chr13:42590730 | G | A | 1 | a0004c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.387+9437G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590730 | |||||||
| chr13:42590816 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.387+9523T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590816 | |||||||
| chr13:42590914 | A | G | 1 | a0001c0003t0002g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.387+9621A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42590914 | |||||||
| chr13:42591006 | T | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0077 |
2 | HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.387+9713T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591006 | |||||||
| chr13:42591022 | G | T | 3 | a0001c0002t0001g0216 a0001c0002t0001g0217 a0001c0002t0001g0218 |
3 | HG02818.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.387+9729G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591022 | |||||||
| chr13:42591246 | G | T | 96 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0007 others(93): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.388-9506G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591246 | |||||||
| chr13:42591332 | A | G | 66 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
99 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.388-9420A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591332 | |||||||
| chr13:42591369 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.388-9383C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591369 | |||||||
| chr13:42591372 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0066 others(1): Show |
12 | NA18939.hp2 NA18941.hp1 NA18955.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-9380C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591372 | |||||||
| chr13:42591399 | T | A | 1 | a0004c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.388-9353T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591399 | |||||||
| chr13:42591567 | C | T | 16 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(13): Show |
16 | HG01496.hp2 HG02280.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.388-9185C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591567 | |||||||
| chr13:42591602 | A | G | 1 | a0001c0003t0002g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.388-9150A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591602 | |||||||
| chr13:42591824 | G | C | 3 | a0001c0002t0001g0216 a0001c0002t0001g0217 a0001c0002t0001g0218 |
3 | HG02818.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.388-8928G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42591824 | |||||||
| chr13:42592027 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.388-8725G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592027 | |||||||
| chr13:42592110 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.388-8642C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592110 | |||||||
| chr13:42592148 | G | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.388-8604G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592148 | |||||||
| chr13:42592159 | A | G | 76 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.388-8593A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592159 | |||||||
| chr13:42592222 | G | C | 2 | a0001c0002t0001g0097 a0001c0002t0001g0109 |
2 | HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.388-8530G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592222 | |||||||
| chr13:42592233 | C | G | 16 | a0001c0003t0002g0279 a0001c0003t0002g0280 a0001c0003t0002g0281 others(13): Show |
16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.388-8519C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592233 | |||||||
| chr13:42592488 | C | G | 1 | a0001c0003t0002g0213 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.388-8264C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592488 | |||||||
| chr13:42592645 | G | A | 16 | a0001c0003t0002g0279 a0001c0003t0002g0280 a0001c0003t0002g0281 others(13): Show |
16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.388-8107G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592645 | |||||||
| chr13:42592797 | C | T | 4 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-7955C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592797 | |||||||
| chr13:42592810 | A | G | 76 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.388-7942A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42592810 | |||||||
| chr13:42593078 | G | A | 2 | a0001c0005t0008g0298 a0001c0005t0008g0299 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.388-7674G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593078 | |||||||
| chr13:42593078 | G | C | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-7674G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593078 | |||||||
| chr13:42593197 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(214): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.388-7555T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593197 | |||||||
| chr13:42593262 | T | C | 8 | a0001c0002t0003g0205 a0001c0002t0003g0206 a0001c0002t0003g0207 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.388-7490T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593262 | |||||||
| chr13:42593338 | A | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
109 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.388-7414A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593338 | |||||||
| chr13:42593377 | A | G | 66 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
99 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.388-7375A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593377 | |||||||
| chr13:42593925 | T | A | 3 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 |
3 | HG02630.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.388-6827T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593925 | |||||||
| chr13:42593937 | C | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0269 |
2 | HG02896.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.388-6815C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593937 | |||||||
| chr13:42593938 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG00735.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.388-6814A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42593938 | |||||||
| chr13:42594172 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.388-6580C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594172 | |||||||
| chr13:42594365 | G | C | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.388-6387G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594365 | |||||||
| chr13:42594402 | G | A | 129 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(126): Show |
164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.388-6350G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594402 | |||||||
| chr13:42594524 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
124 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.388-6228G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594524 | |||||||
| chr13:42594723 | G | C | 1 | a0001c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.388-6029G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594723 | |||||||
| chr13:42594752 | C | T | 1 | a0001c0002t0003g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.388-6000C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594752 | |||||||
| chr13:42594892 | C | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(296): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.388-5860C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594892 | |||||||
| chr13:42594905 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.388-5847G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42594905 | |||||||
| chr13:42594945 | AT | A | 75 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
108 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.388-5804delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42594945 | ||||||
| chr13:42594948 | T | TA | 8 | a0001c0002t0001g0084 a0001c0002t0001g0099 a0001c0002t0001g0110 others(5): Show |
8 | HG00280.hp2 HG01099.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-5793dupA | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42594948 | ||||||
| chr13:42595059 | A | T | 1 | a0001c0001t0001g0183 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.388-5693A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595059 | |||||||
| chr13:42595255 | T | A | 1 | a0001c0002t0001g0057 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.388-5497T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595255 | |||||||
| chr13:42595305 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.388-5447T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595305 | |||||||
| chr13:42595435 | A | T | 1 | a0001c0002t0001g0105 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.388-5317A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595435 | |||||||
| chr13:42595611 | T | G | 10 | a0001c0001t0001g0301 a0001c0002t0001g0048 a0001c0002t0001g0049 others(7): Show |
10 | HG01109.hp2 HG01192.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-5141T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595611 | |||||||
| chr13:42595956 | C | G | 2 | a0001c0002t0001g0111 a0001c0002t0001g0150 |
2 | HG01099.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.388-4796C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42595956 | |||||||
| chr13:42596079 | G | A | 1 | a0001c0002t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.388-4673G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596079 | |||||||
| chr13:42596081 | G | A | 6 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0004t0002g0250 others(3): Show |
7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-4671G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596081 | |||||||
| chr13:42596303 | C | T | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-4449C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596303 | |||||||
| chr13:42596443 | T | C | 1 | a0001c0002t0001g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.388-4309T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596443 | |||||||
| chr13:42596637 | C | G | 1 | a0001c0001t0009g0044 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.388-4115C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596637 | |||||||
| chr13:42596720 | G | A | 8 | a0001c0002t0001g0084 a0001c0002t0001g0099 a0001c0002t0001g0110 others(5): Show |
8 | HG00280.hp2 HG01099.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-4032G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596720 | |||||||
| chr13:42596751 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.388-4001G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596751 | |||||||
| chr13:42596942 | T | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.388-3810T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596942 | |||||||
| chr13:42596962 | G | A | 8 | a0001c0002t0003g0205 a0001c0002t0003g0206 a0001c0002t0003g0207 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.388-3790G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42596962 | |||||||
| chr13:42597050 | G | A | 6 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0004t0002g0250 others(3): Show |
7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.388-3702G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597050 | |||||||
| chr13:42597175 | T | TACATGTC | 273 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(270): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.388-3577_388-3576i others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597175 | |||||||
| chr13:42597246 | C | A | 20 | a0001c0001t0001g0041 a0001c0001t0001g0172 a0001c0001t0001g0195 others(17): Show |
21 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.388-3506C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597246 | |||||||
| chr13:42597311 | A | G | 1 | a0001c0002t0004g0032 | 2 | NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.388-3441A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597311 | |||||||
| chr13:42597340 | C | CT | 39 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0156 others(36): Show |
41 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.388-3391dupT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597340 | ||||||
| chr13:42597340 | C | CTT | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.388-3392_388-3391d others(4): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597340 | ||||||
| chr13:42597340 | C | CTTT | 21 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0159 others(18): Show |
23 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.388-3393_388-3391d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597340 | ||||||
| chr13:42597340 | CTTTTTTT others(3): Show |
C | 20 | a0001c0001t0001g0041 a0001c0001t0001g0172 a0001c0001t0001g0195 others(17): Show |
21 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.388-3400_388-3391d others(12): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597340 | ||||||
| chr13:42597432 | G | A | 16 | a0001c0003t0002g0279 a0001c0003t0002g0280 a0001c0003t0002g0281 others(13): Show |
16 | HG00673.hp1 HG01256.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.388-3320G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597432 | |||||||
| chr13:42597514 | TC | T | 4 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-3235delC | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42597514 | ||||||
| chr13:42597530 | C | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
87 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.388-3222C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597530 | |||||||
| chr13:42597801 | G | A | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.388-2951G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597801 | |||||||
| chr13:42597823 | G | A | 9 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(6): Show |
9 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.388-2929G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597823 | |||||||
| chr13:42597855 | C | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.388-2897C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597855 | |||||||
| chr13:42597873 | G | A | 1 | a0001c0002t0001g0116 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.388-2879G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597873 | |||||||
| chr13:42597949 | A | T | 8 | a0001c0002t0003g0205 a0001c0002t0003g0206 a0001c0002t0003g0207 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.388-2803A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42597949 | |||||||
| chr13:42598006 | T | G | 1 | a0001c0003t0002g0282 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.388-2746T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598006 | |||||||
| chr13:42598421 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(296): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.388-2331T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598421 | |||||||
| chr13:42598476 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0230 a0001c0001t0001g0234 others(1): Show |
4 | NA18947.hp2 NA18951.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-2276G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598476 | |||||||
| chr13:42598659 | A | T | 1 | a0001c0008t0002g0278 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.388-2093A>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598659 | |||||||
| chr13:42598741 | G | A | 9 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(6): Show |
9 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.388-2011G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598741 | |||||||
| chr13:42598742 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.388-2010C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598742 | |||||||
| chr13:42598921 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.388-1831G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42598921 | |||||||
| chr13:42599062 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
226 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.388-1690T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599062 | |||||||
| chr13:42599077 | G | C | 1 | a0004c0010t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.388-1675G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599077 | |||||||
| chr13:42599174 | A | G | 1 | a0001c0002t0001g0052 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.388-1578A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599174 | |||||||
| chr13:42599303 | CTCTA | C | 4 | a0001c0001t0005g0063 a0001c0001t0005g0064 a0001c0001t0006g0174 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1406_388-1403d others(6): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599303 | ||||||
| chr13:42599321 | C | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0254 a0001c0001t0001g0255 |
5 | NA18953.hp1 NA18960.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.388-1431C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599321 | |||||||
| chr13:42599329 | CTATCTAT others(2): Show |
C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0232 |
3 | HG01070.hp2 HG01071.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.388-1422_388-1414d others(11): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599329 | |||||||
| chr13:42599330 | T | TATCTATC others(4): Show |
1 | a0001c0002t0001g0129 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.388-1421_388-1411d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599330 | ||||||
| chr13:42599330 | T | TATCTATC others(8): Show |
1 | a0001c0005t0008g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.388-1421_388-1407d others(17): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599330 | ||||||
| chr13:42599333 | CT | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | NA18947.hp2 NA18951.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.388-1418delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599333 | |||||||
| chr13:42599333 | CTATCT | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0297 |
3 | HG00423.hp2 HG02132.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.388-1418_388-1414d others(7): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599333 | |||||||
| chr13:42599334 | T | TATCTATC others(4): Show |
5 | a0001c0001t0001g0159 a0001c0001t0001g0183 a0001c0002t0001g0051 others(2): Show |
5 | HG03041.hp2 HG03540.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-1417_388-1407d others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599334 | ||||||
| chr13:42599337 | CT | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0080 others(3): Show |
6 | HG02004.hp1 HG02165.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.388-1414delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599337 | |||||||
| chr13:42599338 | T | TATC | 26 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0024 others(23): Show |
31 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.388-1413_388-1411d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599338 | ||||||
| chr13:42599338 | T | TATCATCT others(31): Show |
1 | a0001c0001t0001g0248 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.388-1411_388-1410i others(40): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599338 | ||||||
| chr13:42599338 | T | TATCTATC | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(21): Show |
31 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.388-1413_388-1407d others(9): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599338 | ||||||
| chr13:42599338 | T | TATCTATC others(4): Show |
2 | a0001c0003t0002g0279 a0001c0003t0002g0280 |
2 | NA18995.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.388-1407_388-1406i others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599338 | ||||||
| chr13:42599341 | CT | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0045 others(54): Show |
84 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.388-1410delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599341 | |||||||
| chr13:42599342 | T | TATC | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(35): Show |
48 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.388-1409_388-1407d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599342 | ||||||
| chr13:42599345 | CT | C | 12 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0244 others(9): Show |
13 | HG01081.hp2 HG02622.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.388-1406delT | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599345 | |||||||
| chr13:42599346 | TATC | T | 24 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0067 others(21): Show |
27 | HG00423.hp2 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.388-1402_388-1400d others(5): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599346 | ||||||
| chr13:42599349 | C | CATCCATC others(5): Show |
3 | a0001c0003t0002g0281 a0001c0003t0002g0283 a0001c0003t0002g0285 |
3 | NA18981.hp1 NA19080.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.388-1400_388-1399i others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | ||||||
| chr13:42599349 | C | CATCCATC others(9): Show |
2 | a0001c0003t0002g0284 a0001c0003t0002g0291 |
2 | NA18939.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.388-1400_388-1399i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | ||||||
| chr13:42599349 | C | CATCCATC others(17): Show |
1 | a0001c0004t0002g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.388-1400_388-1399i others(26): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | ||||||
| chr13:42599349 | C | CATCT | 10 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0182 others(7): Show |
12 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.388-1370_388-1367d others(6): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | ||||||
| chr13:42599349 | C | CATCTATC others(1): Show |
33 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0015 others(30): Show |
50 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.388-1374_388-1367d others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | ||||||
| chr13:42599349 | C | CATCTATC others(5): Show |
21 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0036 others(18): Show |
27 | HG00140.hp2 HG00408.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.388-1378_388-1367d others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | ||||||
| chr13:42599349 | C | CATCTATC others(9): Show |
1 | a0001c0001t0001g0187 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.388-1382_388-1367d others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | ||||||
| chr13:42599349 | C | CATCTATC others(13): Show |
1 | a0001c0001t0001g0188 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.388-1386_388-1367d others(22): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599349 | ||||||
| chr13:42599349 | C | CT | 146 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(3): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCATC others(12): Show |
1 | a0001c0003t0002g0213 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.388-1403_388-1402i others(21): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCATC others(9): Show |
2 | a0001c0003t0002g0292 a0001c0008t0002g0278 |
2 | HG01256.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.388-1403_388-1402i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCATC others(13): Show |
2 | a0001c0003t0002g0282 a0001c0003t0002g0289 |
2 | NA18944.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.388-1403_388-1402i others(22): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCATC others(17): Show |
1 | a0001c0003t0007g0286 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.388-1403_388-1402i others(26): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCATC others(21): Show |
1 | a0001c0003t0002g0288 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.388-1403_388-1402i others(30): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCATC others(1): Show |
4 | a0001c0001t0001g0071 a0001c0002t0001g0048 a0001c0002t0001g0050 others(1): Show |
4 | HG00140.hp1 HG02129.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(10): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCATC others(5): Show |
17 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0068 others(14): Show |
20 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCATC others(9): Show |
7 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0161 others(4): Show |
10 | HG00597.hp2 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCATC others(13): Show |
3 | a0001c0001t0001g0198 a0001c0001t0001g0229 a0001c0002t0001g0055 |
3 | HG01975.hp1 HG02257.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.388-1403_388-1402i others(22): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCTAT others(21): Show |
1 | a0001c0003t0007g0287 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.388-1403_388-1402i others(30): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCTAT others(9): Show |
2 | a0001c0001t0001g0246 a0001c0002t0003g0209 |
2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.388-1403_388-1402i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCTAT others(9): Show |
1 | a0001c0001t0001g0254 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.388-1403_388-1402i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599349 | C | CTATCTAT others(13): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0255 |
4 | NA18953.hp1 NA18960.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1403_388-1402i others(22): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599349 | |||||||
| chr13:42599372 | C | CTATCTAT others(9): Show |
4 | a0001c0001t0001g0041 a0001c0001t0001g0196 a0001c0001t0001g0247 others(1): Show |
5 | HG00735.hp1 HG00741.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-1367_388-1366i others(18): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599372 | ||||||
| chr13:42599372 | C | CTATCTAT others(5): Show |
4 | a0001c0001t0001g0172 a0001c0001t0001g0197 a0001c0001t0001g0199 others(1): Show |
4 | HG01361.hp1 HG04204.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1369_388-1368i others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599372 | ||||||
| chr13:42599372 | C | T | 2 | a0001c0001t0001g0195 a0001c0005t0008g0299 |
2 | HG03540.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.388-1380C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599372 | |||||||
| chr13:42599380 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.388-1372C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599380 | |||||||
| chr13:42599382 | A | ATCTATCT others(5): Show |
3 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0007t0002g0273 |
4 | HG02572.hp1 HG02717.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1367_388-1366i others(14): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr13 | 42599382 | ||||||
| chr13:42599382 | A | G | 4 | a0001c0003t0002g0213 a0001c0004t0002g0250 a0001c0004t0002g0251 others(1): Show |
4 | HG02055.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1370A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599382 | |||||||
| chr13:42599454 | C | T | 4 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.388-1298C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599454 | |||||||
| chr13:42599505 | G | C | 4 | a0001c0002t0003g0205 a0001c0002t0003g0206 a0001c0002t0003g0207 others(1): Show |
4 | HG02572.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-1247G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599505 | |||||||
| chr13:42599519 | G | A | 11 | a0001c0001t0001g0301 a0001c0002t0001g0048 a0001c0002t0001g0049 others(8): Show |
11 | HG01109.hp2 HG01192.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.388-1233G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599519 | |||||||
| chr13:42599521 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.388-1231G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599521 | |||||||
| chr13:42599677 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.388-1075C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599677 | |||||||
| chr13:42599678 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0198 |
2 | NA18981.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.388-1074G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599678 | |||||||
| chr13:42599754 | G | A | 14 | a0001c0003t0002g0279 a0001c0003t0002g0280 a0001c0003t0002g0281 others(11): Show |
14 | HG01256.hp1 HG03654.hp1 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.388-998G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599754 | |||||||
| chr13:42599842 | T | C | 2 | a0001c0002t0001g0295 a0001c0002t0001g0296 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.388-910T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599842 | |||||||
| chr13:42599880 | T | A | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.388-872T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599880 | |||||||
| chr13:42599901 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.388-851T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599901 | |||||||
| chr13:42599964 | A | G | 135 | a0001c0001t0001g0041 a0001c0001t0001g0172 a0001c0001t0001g0195 others(132): Show |
171 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.388-788A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42599964 | |||||||
| chr13:42600353 | C | A | 10 | a0001c0001t0001g0041 a0001c0001t0001g0172 a0001c0001t0001g0195 others(7): Show |
11 | HG00735.hp1 HG00741.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.388-399C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600353 | |||||||
| chr13:42600361 | G | A | 23 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(20): Show |
24 | HG01496.hp2 HG02055.hp1 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.388-391G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600361 | |||||||
| chr13:42600473 | G | C | 1 | a0001c0002t0001g0120 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.388-279G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600473 | |||||||
| chr13:42600544 | T | C | 1 | a0001c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.388-208T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600544 | |||||||
| chr13:42600719 | T | C | 1 | a0001c0002t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.388-33T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 2/4 | chr13 | 42600719 | |||||||
| chr13:42601085 | C | T | 18 | a0001c0003t0002g0213 a0001c0003t0002g0279 a0001c0003t0002g0280 others(15): Show |
18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.532+104C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601085 | |||||||
| chr13:42601208 | A | G | 3 | a0001c0003t0002g0292 a0001c0003t0002g0293 a0001c0004t0002g0078 |
3 | HG00673.hp1 HG04199.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.532+227A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601208 | |||||||
| chr13:42601326 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(299): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.532+345A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601326 | |||||||
| chr13:42601464 | G | C | 1 | a0001c0002t0001g0102 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.532+483G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601464 | |||||||
| chr13:42601591 | C | A | 1 | a0001c0002t0001g0120 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.532+610C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601591 | |||||||
| chr13:42601782 | A | G | 4 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.532+801A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601782 | |||||||
| chr13:42601934 | A | G | 1 | a0001c0002t0001g0124 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.532+953A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601934 | |||||||
| chr13:42601975 | C | T | 57 | a0001c0001t0001g0227 a0001c0002t0001g0007 a0001c0002t0001g0012 others(54): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.532+994C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42601975 | |||||||
| chr13:42602016 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.532+1035A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602016 | |||||||
| chr13:42602308 | C | G | 1 | a0001c0002t0001g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.532+1327C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602308 | |||||||
| chr13:42602328 | T | G | 8 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(5): Show |
8 | HG01975.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.532+1347T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602328 | |||||||
| chr13:42602337 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.532+1356T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602337 | |||||||
| chr13:42602462 | G | A | 18 | a0001c0003t0002g0213 a0001c0003t0002g0279 a0001c0003t0002g0280 others(15): Show |
18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.532+1481G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602462 | |||||||
| chr13:42602466 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.532+1485C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602466 | |||||||
| chr13:42602579 | A | G | 25 | a0001c0001t0001g0041 a0001c0001t0001g0195 a0001c0001t0001g0196 others(22): Show |
26 | HG00673.hp1 HG00735.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.532+1598A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602579 | |||||||
| chr13:42602683 | T | C | 1 | a0001c0002t0001g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.532+1702T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602683 | |||||||
| chr13:42602691 | G | A | 1 | a0001c0002t0001g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.532+1710G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602691 | |||||||
| chr13:42602794 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.532+1813C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602794 | |||||||
| chr13:42602977 | G | A | 2 | a0001c0005t0008g0298 a0001c0005t0008g0299 |
2 | HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.532+1996G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42602977 | |||||||
| chr13:42603027 | T | C | 19 | a0001c0001t0001g0041 a0001c0001t0001g0195 a0001c0001t0001g0196 others(16): Show |
20 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.532+2046T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603027 | |||||||
| chr13:42603033 | T | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(42): Show |
66 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.532+2052T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603033 | |||||||
| chr13:42603116 | C | T | 15 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(12): Show |
15 | HG01496.hp2 HG02572.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.532+2135C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603116 | |||||||
| chr13:42603128 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.532+2147A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603128 | |||||||
| chr13:42603487 | G | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
5 | HG01361.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.532+2506G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603487 | |||||||
| chr13:42603852 | A | C | 1 | a0001c0001t0001g0046 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.533-2645A>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603852 | |||||||
| chr13:42603853 | G | C | 6 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0004t0002g0250 others(3): Show |
7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.533-2644G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603853 | |||||||
| chr13:42603858 | C | A | 18 | a0001c0003t0002g0213 a0001c0003t0002g0279 a0001c0003t0002g0280 others(15): Show |
18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-2639C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42603858 | |||||||
| chr13:42604002 | G | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0225 |
2 | HG00140.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.533-2495G>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604002 | |||||||
| chr13:42604324 | G | A | 18 | a0001c0003t0002g0213 a0001c0003t0002g0279 a0001c0003t0002g0280 others(15): Show |
18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-2173G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604324 | |||||||
| chr13:42604447 | C | T | 59 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
92 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.533-2050C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604447 | |||||||
| chr13:42604469 | T | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0179 |
2 | HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.533-2028T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604469 | |||||||
| chr13:42604503 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.533-1994G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604503 | |||||||
| chr13:42604516 | C | A | 1 | a0001c0002t0001g0123 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.533-1981C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604516 | |||||||
| chr13:42604535 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
216 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.533-1962G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604535 | |||||||
| chr13:42604546 | G | A | 3 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 |
3 | HG02630.hp2 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.533-1951G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604546 | |||||||
| chr13:42604605 | T | G | 5 | a0001c0001t0001g0039 a0001c0001t0001g0160 a0001c0001t0001g0166 others(2): Show |
6 | NA18943.hp1 NA18992.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-1892T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604605 | |||||||
| chr13:42604728 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.533-1769C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604728 | |||||||
| chr13:42604832 | G | A | 96 | a0001c0001t0001g0227 a0001c0002t0001g0002 a0001c0002t0001g0003 others(93): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.533-1665G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604832 | |||||||
| chr13:42604865 | C | A | 4 | a0001c0001t0006g0174 a0001c0001t0006g0175 a0001c0001t0006g0185 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-1632C>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604865 | |||||||
| chr13:42604925 | G | A | 9 | a0001c0001t0001g0041 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
10 | HG00735.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.533-1572G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604925 | |||||||
| chr13:42604939 | G | A | 18 | a0001c0003t0002g0213 a0001c0003t0002g0279 a0001c0003t0002g0280 others(15): Show |
18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-1558G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42604939 | |||||||
| chr13:42605005 | G | A | 8 | a0001c0002t0003g0205 a0001c0002t0003g0206 a0001c0002t0003g0207 others(5): Show |
8 | HG01496.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.533-1492G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605005 | |||||||
| chr13:42605019 | A | G | 6 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0004t0002g0250 others(3): Show |
7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.533-1478A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605019 | |||||||
| chr13:42605127 | T | C | 18 | a0001c0003t0002g0213 a0001c0003t0002g0279 a0001c0003t0002g0280 others(15): Show |
18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-1370T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605127 | |||||||
| chr13:42605149 | G | A | 7 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(4): Show |
7 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.533-1348G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605149 | |||||||
| chr13:42605250 | A | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.533-1247A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605250 | |||||||
| chr13:42605303 | C | G | 6 | a0001c0004t0001g0022 a0001c0004t0002g0022 a0001c0004t0002g0250 others(3): Show |
7 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.533-1194C>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605303 | |||||||
| chr13:42605499 | G | C | 3 | a0001c0002t0001g0216 a0001c0002t0001g0217 a0001c0002t0001g0218 |
3 | HG02818.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.533-998G>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605499 | |||||||
| chr13:42605579 | GAAGGTTC others(6): Show |
G | 7 | a0001c0001t0001g0041 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
8 | HG00735.hp1 HG00741.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.533-915_533-903del others(13): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr13 | 42605579 | ||||||
| chr13:42605945 | T | G | 1 | a0001c0001t0001g0047 | 2 | NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.533-552T>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605945 | |||||||
| chr13:42605948 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.533-549A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605948 | |||||||
| chr13:42605958 | CAT | C | 18 | a0001c0003t0002g0213 a0001c0003t0002g0279 a0001c0003t0002g0280 others(15): Show |
18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-538_533-537del others(2): Show |
TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42605958 | |||||||
| chr13:42606081 | C | T | 24 | a0001c0003t0002g0213 a0001c0003t0002g0279 a0001c0003t0002g0280 others(21): Show |
25 | HG00673.hp1 HG01256.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.533-416C>T | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606081 | |||||||
| chr13:42606174 | A | G | 3 | a0001c0002t0001g0152 a0001c0002t0001g0202 a0001c0002t0001g0214 |
3 | HG02280.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.533-323A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606174 | |||||||
| chr13:42606185 | T | C | 1 | a0001c0002t0003g0205 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.533-312T>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606185 | |||||||
| chr13:42606203 | A | G | 1 | a0001c0002t0001g0142 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.533-294A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606203 | |||||||
| chr13:42606296 | G | A | 2 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.533-201G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606296 | |||||||
| chr13:42606367 | G | A | 9 | a0001c0001t0001g0041 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
10 | HG00735.hp1 HG00741.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.533-130G>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606367 | |||||||
| chr13:42606404 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.533-93A>G | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606404 | |||||||
| chr13:42606440 | A | C | 18 | a0001c0003t0002g0213 a0001c0003t0002g0279 a0001c0003t0002g0280 others(15): Show |
18 | HG00673.hp1 HG01256.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.533-57A>C | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606440 | |||||||
| chr13:42606463 | T | A | 10 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0001g0050 others(7): Show |
10 | HG01109.hp2 HG01975.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.533-34T>A | TNFSF11 | ENSG00000120659.16 | transcript | ENST00000398795.7 | protein_coding | 4/4 | chr13 | 42606463 |