Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10673 |
| ensemblid | ENSG00000102524.12 |
| hgncid | 11929 |
| symbol | TNFSF13B |
| name | TNF superfamily member 13b |
| refseq_nuc | NM_006573.5 |
| refseq_prot | NP_006564.1 |
| ensembl_nuc | ENST00000375887.9 |
| ensembl_prot | ENSP00000365048.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 108269718 |
| end | 108308478 |
| strand | + |
| ver | v1.2 |
| region | chr13:108269718-108308478 |
| region5000 | chr13:108264718-108313478 |
| regionname0 | TNFSF13B_chr13_108269718_108308478 |
| regionname5000 | TNFSF13B_chr13_108264718_108313478 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 285 | 383 | 90 | 77 | 160 | 18 | 36 | 118 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | MDDST others(280): Show |
chr13 | 108264718 | 108313478 |
| a0002 | 0/0 | 285 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | MDDST others(280): Show |
chr13 | 108264718 | 108313478 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 855 | 380 | 87 | 77 | 160 | 18 | 36 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | ATGGA others(850): Show |
chr13 | 108264718 | 108313478 | ||
| a0001c0002 | 0/0 | 855 | 3 | 3 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | ATGGA others(850): Show |
chr13 | 108264718 | 108313478 | ||
| a0002c0003 | 0/0 | 855 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | ATGGA others(850): Show |
chr13 | 108264718 | 108313478 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2572 | 54 | 26 | 16 | 2 | 4 | 6 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2567): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0002 | 1/1 | 2576 | 46 | 9 | 9 | 12 | 6 | 8 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2571): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0003 | 0/0 | 2563 | 45 | 0 | 6 | 35 | 1 | 3 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2558): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0004 | 0/0 | 2573 | 44 | 0 | 1 | 41 | 0 | 2 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2568): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0005 | 0/0 | 2574 | 38 | 1 | 10 | 24 | 2 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2569): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0006 | 0/0 | 2571 | 37 | 27 | 8 | 1 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2566): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0007 | 0/0 | 2573 | 29 | 2 | 5 | 21 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2568): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0008 | 0/0 | 2577 | 22 | 2 | 5 | 7 | 1 | 7 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2572): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0009 | 0/0 | 2575 | 11 | 2 | 2 | 7 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2570): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0010 | 0/0 | 2575 | 7 | 0 | 2 | 2 | 1 | 2 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2570): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0011 | 0/0 | 2575 | 6 | 0 | 5 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2570): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0012 | 0/0 | 2573 | 5 | 3 | 1 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2568): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0013 | 0/0 | 2565 | 5 | 5 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2560): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0014 | 0/0 | 2572 | 4 | 0 | 0 | 3 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2567): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0015 | 0/0 | 2574 | 3 | 1 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2569): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0016 | 0/0 | 2574 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2569): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0017 | 0/0 | 2576 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2571): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0018 | 0/0 | 2576 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2571): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0019 | 0/0 | 2571 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2566): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0020 | 0/0 | 2567 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2562): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0022 | 0/0 | 2577 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2572): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0023 | 0/0 | 2576 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2571): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0024 | 0/0 | 2576 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2571): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0025 | 0/0 | 2574 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2569): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0026 | 0/0 | 2574 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2569): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0027 | 0/0 | 2574 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2569): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0028 | 0/0 | 2574 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2569): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0029 | 0/0 | 2574 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2569): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0030 | 0/0 | 2573 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2568): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0031 | 0/0 | 2572 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2567): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0032 | 0/0 | 2572 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2567): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0033 | 0/0 | 2571 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2566): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0034 | 0/0 | 2564 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2559): Show |
chr13 | 108264718 | 108313478 |
| a0001c0001t0035 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2568): Show |
chr13 | 108264718 | 108313478 |
| a0001c0002t0002 | 0/0 | 2576 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2571): Show |
chr13 | 108264718 | 108313478 |
| a0001c0002t0021 | 0/0 | 2569 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2564): Show |
chr13 | 108264718 | 108313478 |
| a0002c0003t0002 | 0/0 | 2576 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | AGGGG others(2571): Show |
chr13 | 108264718 | 108313478 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0301 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0005g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0006g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0007g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0008g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0009g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0010g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0010g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0010g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0010g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0011g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0011g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0011g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0011g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0012g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0012g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0013g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0013g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0014g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0014g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0014g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0014g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0015g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0015g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0015g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0016g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0016g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0017g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0017g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0018g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0018g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0019g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0019g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0020g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0020g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0022g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0023g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0024g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0025g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0026g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0027g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0028g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0029g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0030g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0031g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0032g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0033g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0034g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0001t0035g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0002t0021g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0001c0002t0021g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| a0002c0003t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0033 | g0158 | EUR | GBR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0274 | EUR | GBR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0182 | EUR | GBR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0067 | EUR | GBR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0316 | EUR | FIN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0233 | EUR | FIN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0206 | EUR | FIN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | FIN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0334 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00597 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0079 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0308 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0231 | EAS | CHS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00639 | hp1 | a0001 | c0001 | t0017 | g0313 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00738 | hp1 | a0001 | c0001 | t0008 | g0127 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0330 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01069 | hp1 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0331 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0021 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01071 | hp1 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0021 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0293 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0087 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0197 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0329 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01168 | hp1 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01168 | hp2 | a0001 | c0001 | t0009 | g0311 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01169 | hp1 | a0001 | c0001 | t0018 | g0312 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01175 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01192 | hp1 | a0001 | c0001 | t0029 | g0289 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0184 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0273 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0300 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0317 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01256 | hp2 | a0001 | c0001 | t0026 | g0022 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01257 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01258 | hp1 | a0001 | c0001 | t0011 | g0022 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01261 | hp2 | a0001 | c0001 | t0032 | g0290 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0328 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0047 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0342 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0119 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0196 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0065 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01934 | hp1 | a0002 | c0003 | t0002 | g0082 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0060 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0276 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01952 | hp1 | a0001 | c0001 | t0012 | g0314 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0222 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0058 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0318 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0348 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01981 | hp2 | a0001 | c0001 | t0017 | g0016 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01993 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02004 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02015 | hp2 | a0001 | c0001 | t0025 | g0051 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02027 | hp1 | a0001 | c0001 | t0010 | g0268 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02055 | hp2 | a0001 | c0001 | t0016 | g0188 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0140 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0350 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0241 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0128 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0141 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0215 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0072 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02155 | hp1 | a0001 | c0001 | t0015 | g0229 | EAS | CDX | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | CDX | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0254 | EAS | CDX | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | CDX | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02258 | hp1 | a0001 | c0001 | t0012 | g0101 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0338 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PEL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0077 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | KHV | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0070 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02647 | hp1 | a0001 | c0001 | t0028 | g0123 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02647 | hp2 | a0001 | c0001 | t0008 | g0191 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02698 | hp2 | a0001 | c0001 | t0034 | g0236 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02717 | hp1 | a0001 | c0002 | t0021 | g0323 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0201 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0166 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0186 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02970 | hp1 | a0001 | c0001 | t0013 | g0136 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02970 | hp2 | a0001 | c0001 | t0020 | g0155 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0240 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0277 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0183 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03195 | hp1 | a0001 | c0002 | t0021 | g0230 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03195 | hp2 | a0001 | c0001 | t0031 | g0223 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03225 | hp1 | a0001 | c0001 | t0015 | g0309 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03225 | hp2 | a0001 | c0001 | t0019 | g0121 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03239 | hp1 | a0001 | c0001 | t0027 | g0019 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0279 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03486 | hp1 | a0001 | c0001 | t0013 | g0171 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0103 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0165 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0135 | AFR | ESN | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0194 | AFR | GWD | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0023 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0108 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0345 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0120 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03704 | hp1 | a0001 | c0001 | t0014 | g0042 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03704 | hp2 | a0001 | c0001 | t0008 | g0049 | SAS | PJL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03831 | hp1 | a0001 | c0001 | t0023 | g0109 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0291 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03927 | hp1 | a0001 | c0001 | t0030 | g0179 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03942 | hp1 | a0001 | c0001 | t0008 | g0280 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0198 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG04115 | hp2 | a0001 | c0001 | t0010 | g0046 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0244 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG04184 | hp2 | a0001 | c0001 | t0012 | g0224 | SAS | BEB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG04204 | hp2 | a0001 | c0001 | t0010 | g0069 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | STU | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | CHB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | CHB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | CHB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0227 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18939 | hp1 | a0001 | c0001 | t0022 | g0105 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0083 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18942 | hp1 | a0001 | c0001 | t0014 | g0137 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18944 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18951 | hp1 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18953 | hp1 | a0001 | c0001 | t0007 | g0255 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18954 | hp1 | a0001 | c0001 | t0007 | g0269 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0344 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0354 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18962 | hp1 | a0001 | c0001 | t0014 | g0097 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0271 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0355 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18964 | hp1 | a0001 | c0001 | t0009 | g0220 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18964 | hp2 | a0001 | c0001 | t0035 | g0305 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18965 | hp1 | a0001 | c0001 | t0008 | g0270 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18974 | hp2 | a0001 | c0001 | t0009 | g0325 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18977 | hp1 | a0001 | c0001 | t0009 | g0242 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18979 | hp2 | a0001 | c0001 | t0008 | g0347 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18980 | hp2 | a0001 | c0001 | t0010 | g0232 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18984 | hp2 | a0001 | c0001 | t0009 | g0257 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18989 | hp2 | a0001 | c0001 | t0007 | g0213 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0258 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18993 | hp2 | a0001 | c0001 | t0007 | g0284 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18997 | hp1 | a0001 | c0001 | t0008 | g0174 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18997 | hp2 | a0001 | c0001 | t0009 | g0177 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0346 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19004 | hp1 | a0001 | c0001 | t0014 | g0351 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19004 | hp2 | a0001 | c0001 | t0007 | g0248 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19005 | hp1 | a0001 | c0001 | t0008 | g0092 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0349 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | LWK | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19043 | hp2 | a0001 | c0001 | t0019 | g0200 | AFR | LWK | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0251 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19059 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0209 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19068 | hp1 | a0001 | c0001 | t0008 | g0089 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19070 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0084 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19079 | hp2 | a0001 | c0001 | t0008 | g0337 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19080 | hp2 | a0001 | c0001 | t0015 | g0050 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19084 | hp2 | a0001 | c0001 | t0009 | g0146 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19087 | hp1 | a0001 | c0001 | t0007 | g0247 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19088 | hp1 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0056 | AFR | YRI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ASW | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ASW | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0125 | EUR | TSI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20752 | hp2 | a0001 | c0001 | t0011 | g0019 | EUR | TSI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0302 | EUR | TSI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0031 | EUR | TSI | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | GIH | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0252 | SAS | GIH | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01123 | hp1 | a0001 | c0001 | t0010 | g0059 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0195 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0216 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0272 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0091 | AFR | ACB | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03471 | hp1 | a0001 | c0001 | t0024 | g0285 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0099 | AFR | MSL | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG06807 | hp1 | a0001 | c0001 | t0013 | g0090 | AFR | USA | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0306 | AFR | USA | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA20300 | hp2 | a0001 | c0001 | t0020 | g0286 | AFR | USA | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | LWK | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0301 | REF | REF | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0071 | REF | REF | TNFSF13B_chr13_108264718_108313478 | TNFSF13B | chr13 | 108264718 | 108313478 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:108270208 | G | A | 1 | a0002 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.313G>A | p.Ala105Thr | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 1/6 | 491/2576 | 313/858 | 105/285 | chr13 | 108270208 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:108303585 | T | C | 1 | a0001c0002 | 3 | HG02280.hp1 HG02717.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.726T>C | p.Asn242Asn | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/6 | 904/2576 | 726/858 | 242/285 | chr13 | 108303585 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:108269850 | G | T | 1 | a0001c0001t0035 | 1 | NA18964.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 1/6 | chr13 | 108269850 | |||||||
| chr13:108307016 | C | CA | 2 | a0001c0001t0008 a0001c0001t0022 |
23 | HG00280.hp2 HG00738.hp1 HG01070.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*109dupA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 110 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | |||||
| chr13:108307016 | CA | C | 3 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0011 |
24 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*109delA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 109 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | |||||
| chr13:108307016 | CAA | C | 6 | a0001c0001t0005 a0001c0001t0025 a0001c0001t0026 others(3): Show |
43 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*108_*109delAA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 108 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | |||||
| chr13:108307016 | CAAA | C | 5 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0015 others(2): Show |
54 | HG00423.hp2 HG00544.hp2 HG01255.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*107_*109delAAA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 107 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | |||||
| chr13:108307016 | CAAAA | C | 5 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0014 others(2): Show |
89 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*106_*109delAAAA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 106 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | |||||
| chr13:108307016 | CAAAAA | C | 3 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0033 |
40 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*105_*109delAAAAA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 105 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | |||||
| chr13:108307016 | CAAAAAAA | C | 3 | a0001c0001t0013 a0001c0001t0020 a0001c0002t0021 |
9 | HG02717.hp1 HG02970.hp1 HG02970.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*103_*109delAAAAAA others(1): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 103 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | |||||
| chr13:108307016 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0034 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98_*109delAAAAAAA others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 98 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | |||||
| chr13:108307016 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003 | 45 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*97_*109delAAAAAAA others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 97 | INFO_REALIGN_3_PRIME | chr13 | 108307016 | |||||
| chr13:108307102 | C | T | 1 | a0001c0001t0029 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*164C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 164 | chr13 | 108307102 | ||||||
| chr13:108307259 | C | A | 1 | a0001c0001t0025 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 321 | chr13 | 108307259 | ||||||
| chr13:108307523 | C | T | 1 | a0001c0001t0019 | 2 | HG03225.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*585C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 585 | chr13 | 108307523 | ||||||
| chr13:108307597 | A | AT | 2 | a0001c0001t0007 a0001c0001t0015 |
32 | HG00408.hp1 HG00597.hp1 HG01496.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*666dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 667 | INFO_REALIGN_3_PRIME | chr13 | 108307597 | |||||
| chr13:108307609 | GGA | G | 3 | a0001c0001t0013 a0001c0001t0016 a0001c0001t0020 |
9 | HG01884.hp1 HG02055.hp2 HG02970.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*680_*681delGA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 680 | INFO_REALIGN_3_PRIME | chr13 | 108307609 | |||||
| chr13:108307641 | C | T | 1 | a0001c0001t0030 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 703 | chr13 | 108307641 | ||||||
| chr13:108307709 | G | A | 3 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0026 |
9 | HG00639.hp1 HG00741.hp2 HG01069.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*771G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 771 | chr13 | 108307709 | ||||||
| chr13:108307840 | T | A | 14 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0010 others(11): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*902T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 902 | chr13 | 108307840 | ||||||
| chr13:108308037 | T | A | 1 | a0001c0001t0027 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1099T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1099 | chr13 | 108308037 | ||||||
| chr13:108308067 | C | T | 1 | a0001c0001t0018 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1129C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1129 | chr13 | 108308067 | ||||||
| chr13:108308102 | GTT | G | 1 | a0001c0001t0013 | 5 | HG02970.hp1 HG03041.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1166_*1167delTT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1166 | INFO_REALIGN_3_PRIME | chr13 | 108308102 | |||||
| chr13:108308379 | G | A | 2 | a0001c0001t0024 a0001c0001t0031 |
2 | HG03195.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1441G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1441 | chr13 | 108308379 | ||||||
| chr13:108308401 | G | A | 1 | a0001c0001t0019 | 2 | HG03225.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1463G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1463 | chr13 | 108308401 | ||||||
| chr13:108308473 | C | T | 2 | a0001c0001t0032 a0001c0001t0033 |
2 | HG00099.hp1 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1535C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 6/6 | 1535 | chr13 | 108308473 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:108270295 | C | G | 37 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0001g0339 others(34): Show |
39 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.340-45C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 1/5 | chr13 | 108270295 | |||||||
| chr13:108270749 | A | G | 13 | a0001c0001t0001g0320 a0001c0001t0002g0315 a0001c0001t0002g0319 others(10): Show |
14 | HG00280.hp1 HG00639.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.424+325A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108270749 | |||||||
| chr13:108270893 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+469A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108270893 | |||||||
| chr13:108270931 | T | C | 1 | a0001c0001t0007g0023 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.424+507T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108270931 | |||||||
| chr13:108270950 | T | TAC | 19 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0320 others(16): Show |
22 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+545_424+546dup others(2): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | ||||||
| chr13:108270950 | T | TACACACA others(1): Show |
29 | a0001c0001t0001g0339 a0001c0001t0002g0333 a0001c0001t0002g0340 others(26): Show |
31 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.424+539_424+546dup others(8): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | ||||||
| chr13:108270950 | T | TACACACA others(3): Show |
3 | a0001c0001t0004g0326 a0001c0001t0004g0327 a0001c0001t0009g0325 |
3 | NA18974.hp2 NA18993.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.424+537_424+546dup others(10): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | ||||||
| chr13:108270950 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+535_424+546dup others(12): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | ||||||
| chr13:108270950 | T | TACACACA others(7): Show |
2 | a0001c0001t0002g0322 a0001c0002t0021g0323 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.424+533_424+546dup others(14): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | ||||||
| chr13:108270950 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0321 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.424+531_424+546dup others(16): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108270950 | ||||||
| chr13:108271101 | G | T | 2 | a0001c0001t0001g0320 a0001c0001t0002g0319 |
2 | HG01167.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.424+677G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271101 | |||||||
| chr13:108271379 | A | G | 1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+955A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271379 | |||||||
| chr13:108271429 | C | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0027 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.424+1005C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271429 | |||||||
| chr13:108271444 | T | TCA | 20 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0027 others(17): Show |
21 | HG00423.hp1 HG01496.hp1 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+1064_424+1065d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | T | TCACA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0002g0029 others(7): Show |
10 | HG00642.hp2 HG00741.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+1062_424+1065d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | TCA | T | 52 | a0001c0001t0001g0114 a0001c0001t0001g0124 a0001c0001t0001g0154 others(49): Show |
55 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.424+1064_424+1065d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | TCACA | T | 67 | a0001c0001t0001g0162 a0001c0001t0001g0167 a0001c0001t0001g0170 others(64): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.424+1062_424+1065d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | TCACACA | T | 96 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0025 others(93): Show |
104 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.424+1060_424+1065d others(8): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | TCACACAC others(1): Show |
T | 46 | a0001c0001t0001g0020 a0001c0001t0001g0294 a0001c0001t0001g0295 others(43): Show |
52 | HG00408.hp2 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.424+1058_424+1065d others(10): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | TCACACAC others(3): Show |
T | 5 | a0001c0001t0001g0303 a0001c0001t0002g0302 a0001c0001t0002g0304 others(2): Show |
5 | HG01261.hp1 HG02148.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+1056_424+1065d others(12): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | TCACACAC others(5): Show |
T | 2 | a0001c0001t0004g0355 a0001c0001t0006g0306 |
2 | NA18963.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.424+1054_424+1065d others(14): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | TCACACAC others(7): Show |
T | 4 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0322 others(1): Show |
4 | HG02717.hp1 HG03139.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+1052_424+1065d others(16): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | TCACACAC others(9): Show |
T | 2 | a0001c0001t0005g0307 a0001c0001t0005g0308 |
2 | HG00621.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.424+1050_424+1065d others(18): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271444 | TCACACAC others(13): Show |
T | 1 | a0001c0001t0015g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.424+1046_424+1065d others(22): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108271444 | ||||||
| chr13:108271480 | A | T | 1 | a0001c0001t0001g0020 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.424+1056A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271480 | |||||||
| chr13:108271512 | A | G | 1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+1088A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271512 | |||||||
| chr13:108271570 | A | G | 37 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0001g0339 others(34): Show |
39 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.424+1146A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271570 | |||||||
| chr13:108271586 | G | A | 1 | a0001c0001t0004g0225 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.424+1162G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271586 | |||||||
| chr13:108271610 | A | G | 3 | a0001c0001t0004g0110 a0001c0001t0007g0161 a0001c0001t0012g0224 |
3 | HG04184.hp2 NA18747.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.424+1186A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271610 | |||||||
| chr13:108271692 | G | A | 36 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0001g0339 others(33): Show |
38 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.424+1268G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271692 | |||||||
| chr13:108271737 | C | T | 3 | a0001c0001t0005g0108 a0001c0001t0023g0109 a0001c0001t0031g0223 |
3 | HG03195.hp2 HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.424+1313C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271737 | |||||||
| chr13:108271931 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.424+1507T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108271931 | |||||||
| chr13:108272006 | T | C | 3 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0163 |
3 | NA18998.hp1 NA19059.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.424+1582T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272006 | |||||||
| chr13:108272233 | C | T | 1 | a0001c0001t0004g0287 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.424+1809C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272233 | |||||||
| chr13:108272404 | T | C | 3 | a0001c0001t0003g0112 a0001c0001t0004g0111 a0001c0001t0005g0113 |
3 | NA18948.hp1 NA19081.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.424+1980T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272404 | |||||||
| chr13:108272566 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.424+2142T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272566 | |||||||
| chr13:108272812 | C | G | 1 | a0001c0001t0020g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.424+2388C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108272812 | |||||||
| chr13:108272859 | TA | T | 5 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0322 others(2): Show |
5 | HG02717.hp1 HG03139.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2444delA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108272859 | ||||||
| chr13:108273215 | T | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0167 a0001c0001t0002g0164 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+2791T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273215 | |||||||
| chr13:108273485 | G | GAAATGGA others(40): Show |
1 | a0001c0001t0009g0325 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.424+3064_424+3110d others(49): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108273485 | ||||||
| chr13:108273486 | A | G | 1 | a0001c0002t0021g0323 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424+3062A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273486 | |||||||
| chr13:108273549 | T | C | 1 | a0001c0001t0006g0168 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.424+3125T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273549 | |||||||
| chr13:108273755 | C | A | 1 | a0001c0001t0003g0169 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.424+3331C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273755 | |||||||
| chr13:108273932 | C | T | 1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+3508C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108273932 | |||||||
| chr13:108274047 | A | T | 211 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0057 others(208): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.424+3623A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274047 | |||||||
| chr13:108274122 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.424+3698G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274122 | |||||||
| chr13:108274139 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0013g0056 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.424+3715G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274139 | |||||||
| chr13:108274267 | G | C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0167 a0001c0001t0002g0164 others(5): Show |
8 | HG01884.hp2 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+3843G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274267 | |||||||
| chr13:108274278 | TATACATA others(6): Show |
T | 2 | a0001c0001t0007g0012 a0001c0001t0015g0229 |
3 | HG00597.hp1 HG02155.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.424+3876_424+3888d others(15): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108274278 | ||||||
| chr13:108274283 | A | T | 1 | a0001c0001t0002g0160 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+3859A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274283 | |||||||
| chr13:108274290 | C | CAATACAT others(22): Show |
5 | a0001c0001t0002g0119 a0001c0001t0002g0122 a0001c0001t0002g0126 others(2): Show |
5 | HG00639.hp2 HG01081.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+3878_424+3879i others(31): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108274290 | ||||||
| chr13:108274366 | AAT | A | 225 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0025 others(222): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.424+3956_424+3957d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108274366 | ||||||
| chr13:108274366 | AATAT | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0167 a0001c0001t0001g0321 others(10): Show |
13 | HG01884.hp2 HG01891.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+3954_424+3957d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108274366 | ||||||
| chr13:108274549 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+4125G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274549 | |||||||
| chr13:108274641 | T | C | 32 | a0001c0001t0001g0339 a0001c0001t0002g0333 a0001c0001t0002g0340 others(29): Show |
34 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+4217T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274641 | |||||||
| chr13:108274731 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.424+4307C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108274731 | |||||||
| chr13:108275155 | G | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0320 others(17): Show |
23 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.424+4731G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275155 | |||||||
| chr13:108275361 | C | G | 1 | a0001c0001t0002g0160 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+4937C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275361 | |||||||
| chr13:108275366 | A | C | 1 | a0001c0001t0002g0160 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+4942A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275366 | |||||||
| chr13:108275401 | T | C | 4 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0322 others(1): Show |
4 | HG02717.hp1 HG03139.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4977T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275401 | |||||||
| chr13:108275404 | T | A | 1 | a0001c0001t0002g0160 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+4980T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275404 | |||||||
| chr13:108275457 | C | A | 1 | a0001c0001t0004g0044 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.424+5033C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275457 | |||||||
| chr13:108275507 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.424+5083T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275507 | |||||||
| chr13:108275518 | A | C | 1 | a0001c0001t0002g0160 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424+5094A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275518 | |||||||
| chr13:108275550 | A | C | 1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+5126A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275550 | |||||||
| chr13:108275580 | G | A | 1 | a0001c0001t0013g0056 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.424+5156G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275580 | |||||||
| chr13:108275836 | G | A | 1 | a0001c0001t0005g0231 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.424+5412G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275836 | |||||||
| chr13:108275897 | AT | A | 3 | a0001c0001t0002g0160 a0001c0001t0009g0325 a0001c0001t0010g0232 |
3 | NA18974.hp2 NA18980.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.424+5479delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108275897 | ||||||
| chr13:108275947 | T | C | 1 | a0001c0001t0007g0128 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.424+5523T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275947 | |||||||
| chr13:108275967 | A | G | 1 | a0001c0001t0008g0222 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.424+5543A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275967 | |||||||
| chr13:108275992 | G | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0167 a0001c0001t0001g0228 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+5568G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108275992 | |||||||
| chr13:108276145 | G | A | 1 | a0001c0001t0013g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.424+5721G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276145 | |||||||
| chr13:108276155 | C | T | 1 | a0001c0001t0035g0305 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.424+5731C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276155 | |||||||
| chr13:108276388 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.424+5964A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276388 | |||||||
| chr13:108276420 | T | A | 1 | a0001c0001t0003g0169 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.424+5996T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276420 | |||||||
| chr13:108276502 | G | C | 87 | a0001c0001t0001g0162 a0001c0001t0001g0175 a0001c0001t0001g0176 others(84): Show |
96 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.424+6078G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276502 | |||||||
| chr13:108276531 | G | A | 1 | a0001c0001t0008g0233 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.424+6107G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276531 | |||||||
| chr13:108276590 | C | CA | 23 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0180 others(20): Show |
27 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.424+6173dupA | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108276590 | ||||||
| chr13:108276691 | T | A | 1 | a0001c0001t0004g0332 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.424+6267T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276691 | |||||||
| chr13:108276718 | C | G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0180 others(21): Show |
28 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.424+6294C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108276718 | |||||||
| chr13:108276766 | A | AT | 13 | a0001c0001t0001g0011 a0001c0001t0001g0167 a0001c0001t0001g0228 others(10): Show |
13 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+6350dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108276766 | ||||||
| chr13:108277069 | TACAGAGA others(5): Show |
T | 1 | a0001c0001t0010g0069 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.424+6650_424+6661d others(14): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108277069 | ||||||
| chr13:108277207 | G | C | 1 | a0001c0001t0015g0229 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.424+6783G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108277207 | |||||||
| chr13:108277315 | C | T | 243 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(240): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.424+6891C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108277315 | |||||||
| chr13:108277926 | A | G | 1 | a0001c0001t0030g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.424+7502A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108277926 | |||||||
| chr13:108278540 | T | G | 4 | a0001c0001t0001g0180 a0001c0001t0006g0070 a0001c0001t0006g0306 others(1): Show |
4 | HG02258.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+8116T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278540 | |||||||
| chr13:108278572 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0002g0159 a0001c0001t0033g0158 |
3 | HG00099.hp1 HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.424+8148C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278572 | |||||||
| chr13:108278578 | C | CTCCTCCT others(270): Show |
1 | a0001c0001t0003g0169 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(279): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(445): Show |
1 | a0001c0001t0003g0038 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(454): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(779): Show |
1 | a0001c0001t0007g0209 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(788): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(781): Show |
1 | a0001c0001t0006g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(790): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(694): Show |
1 | a0001c0001t0003g0037 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(703): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(627): Show |
1 | a0001c0001t0005g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(636): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(614): Show |
1 | a0001c0001t0003g0172 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(611): Show |
2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(669): Show |
1 | a0001c0001t0009g0293 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(678): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(270): Show |
1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(279): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(626): Show |
1 | a0001c0001t0024g0285 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(445): Show |
1 | a0001c0001t0003g0039 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(454): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(591): Show |
1 | a0001c0001t0003g0234 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(600): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(690): Show |
1 | a0001c0001t0007g0047 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(699): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(646): Show |
3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0002g0029 |
3 | HG00642.hp2 HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(655): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(631): Show |
2 | a0001c0001t0001g0057 a0001c0001t0013g0056 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(640): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(613): Show |
2 | a0001c0001t0006g0276 a0001c0001t0006g0277 |
2 | HG01943.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(622): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(634): Show |
2 | a0001c0001t0002g0235 a0001c0001t0034g0236 |
2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(643): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(657): Show |
2 | a0001c0001t0001g0294 a0001c0001t0002g0237 |
2 | HG01993.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(666): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(777): Show |
1 | a0001c0001t0004g0075 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(786): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(777): Show |
1 | a0001c0001t0004g0048 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(786): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(776): Show |
30 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0002g0210 others(27): Show |
31 | HG00423.hp2 HG00597.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(785): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(614): Show |
1 | a0001c0001t0008g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(591): Show |
1 | a0001c0001t0008g0021 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(600): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(630): Show |
1 | a0001c0001t0004g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(639): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(611): Show |
135 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0061 others(132): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(631): Show |
1 | a0001c0001t0004g0173 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(640): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(686): Show |
1 | a0001c0001t0025g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(695): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(708): Show |
1 | a0001c0001t0002g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(717): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(669): Show |
17 | a0001c0001t0001g0034 a0001c0001t0001g0055 a0001c0001t0001g0102 others(14): Show |
17 | HG01192.hp2 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(678): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(689): Show |
27 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0002g0031 others(24): Show |
30 | HG00408.hp1 HG00621.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(698): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(724): Show |
1 | a0001c0001t0007g0035 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(733): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(885): Show |
1 | a0001c0001t0005g0036 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(894): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(648): Show |
2 | a0001c0001t0001g0180 a0001c0001t0031g0223 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(657): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(626): Show |
1 | a0001c0001t0002g0282 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(635): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(684): Show |
4 | a0001c0001t0001g0218 a0001c0001t0001g0310 a0001c0001t0006g0217 others(1): Show |
4 | HG03130.hp1 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(693): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(663): Show |
1 | a0001c0001t0001g0228 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(672): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(611): Show |
1 | a0001c0001t0013g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(619): Show |
1 | a0001c0001t0014g0137 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(628): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(614): Show |
2 | a0001c0001t0003g0010 a0001c0001t0008g0222 |
3 | HG01361.hp2 HG01928.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(634): Show |
23 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0138 others(20): Show |
24 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(643): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(615): Show |
1 | a0001c0001t0005g0328 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(624): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(611): Show |
1 | a0001c0001t0002g0178 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(720): Show |
2 | a0001c0001t0002g0343 a0001c0001t0003g0342 |
2 | HG01496.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(729): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(638): Show |
1 | a0001c0001t0004g0225 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(647): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(614): Show |
19 | a0001c0001t0001g0157 a0001c0001t0002g0159 a0001c0001t0002g0353 others(16): Show |
21 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(634): Show |
4 | a0001c0001t0003g0292 a0001c0001t0004g0327 a0001c0001t0005g0344 others(1): Show |
4 | NA18957.hp2 NA18965.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(643): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(613): Show |
1 | a0001c0001t0009g0325 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(622): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(611): Show |
1 | a0001c0001t0001g0006 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(609): Show |
1 | a0001c0001t0007g0271 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(618): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(610): Show |
1 | a0001c0001t0006g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(619): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(689): Show |
1 | a0001c0001t0007g0284 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(698): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(611): Show |
1 | a0001c0001t0008g0272 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(614): Show |
7 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0002g0187 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(630): Show |
2 | a0001c0001t0006g0197 a0001c0001t0008g0198 |
2 | HG01099.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.424+8165_424+8166i others(639): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(611): Show |
14 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0002g0126 others(11): Show |
14 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(684): Show |
1 | a0001c0001t0006g0221 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(693): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(633): Show |
1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(642): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(631): Show |
1 | a0001c0001t0005g0274 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(640): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(799): Show |
1 | a0001c0001t0001g0154 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(808): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(772): Show |
1 | a0001c0001t0022g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(781): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(630): Show |
1 | a0001c0001t0006g0306 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(639): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(645): Show |
7 | a0001c0001t0001g0011 a0001c0001t0002g0164 a0001c0001t0006g0011 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(654): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(662): Show |
1 | a0001c0001t0001g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(671): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(608): Show |
1 | a0001c0001t0001g0207 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(617): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(611): Show |
1 | a0001c0001t0006g0208 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278578 | C | CTCCTCCT others(611): Show |
1 | a0001c0001t0020g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.424+8165_424+8166i others(620): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278578 | ||||||
| chr13:108278580 | C | CCTCCTCC others(614): Show |
1 | a0001c0001t0006g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278580 | ||||||
| chr13:108278587 | C | CTCTTCCT others(614): Show |
5 | a0001c0001t0001g0193 a0001c0001t0009g0194 a0001c0001t0009g0195 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8165_424+8166i others(623): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278587 | ||||||
| chr13:108278588 | T | TCTTCCTC others(612): Show |
1 | a0001c0001t0001g0124 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.424+8165_424+8166i others(621): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278588 | ||||||
| chr13:108278590 | C | T | 1 | a0001c0001t0006g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.424+8166C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278590 | |||||||
| chr13:108278623 | C | T | 4 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0043 others(1): Show |
4 | HG00423.hp1 NA18998.hp1 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-8180C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278623 | |||||||
| chr13:108278632 | T | C | 2 | a0001c0001t0001g0356 a0001c0001t0003g0169 |
2 | HG02630.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.425-8171T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278632 | |||||||
| chr13:108278646 | A | C | 1 | a0001c0001t0006g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-8157A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278646 | |||||||
| chr13:108278646 | A | G | 2 | a0001c0001t0001g0356 a0001c0001t0003g0169 |
2 | HG02630.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.425-8157A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278646 | |||||||
| chr13:108278655 | T | C | 1 | a0001c0001t0006g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-8148T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278655 | |||||||
| chr13:108278658 | C | CCTCCTCC others(1): Show |
13 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0193 others(10): Show |
13 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-8128_425-8121d others(10): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278658 | ||||||
| chr13:108278658 | C | CCTCCTCC others(383): Show |
1 | a0001c0001t0003g0169 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.425-8136_425-8135i others(392): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278658 | ||||||
| chr13:108278666 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.425-8137T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278666 | |||||||
| chr13:108278666 | T | TCCCCTCC others(200): Show |
1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-8136_425-8135i others(209): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278666 | ||||||
| chr13:108278683 | T | C | 1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-8120T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278683 | |||||||
| chr13:108278696 | T | C | 1 | a0001c0001t0007g0271 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.425-8107T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278696 | |||||||
| chr13:108278719 | T | C | 1 | a0001c0001t0022g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.425-8084T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278719 | |||||||
| chr13:108278720 | C | T | 1 | a0001c0001t0022g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.425-8083C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278720 | |||||||
| chr13:108278726 | C | CCCCTTCT others(129): Show |
1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-8076_425-8075i others(138): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108278726 | ||||||
| chr13:108278728 | T | C | 1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-8075T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278728 | |||||||
| chr13:108278885 | T | G | 1 | a0001c0001t0003g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.425-7918T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278885 | |||||||
| chr13:108278896 | G | A | 3 | a0001c0001t0002g0138 a0001c0001t0003g0139 a0001c0001t0005g0140 |
3 | HG00609.hp1 HG02056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.425-7907G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108278896 | |||||||
| chr13:108279026 | T | G | 1 | a0001c0001t0003g0129 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.425-7777T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279026 | |||||||
| chr13:108279068 | A | ATTTGTT | 28 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0138 others(25): Show |
30 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-7735_425-7734i others(8): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279068 | |||||||
| chr13:108279069 | C | A | 28 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0138 others(25): Show |
30 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-7734C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279069 | |||||||
| chr13:108279069 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-7734C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279069 | |||||||
| chr13:108279070 | C | G | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-7733C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279070 | |||||||
| chr13:108279070 | C | T | 28 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0138 others(25): Show |
30 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-7733C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279070 | |||||||
| chr13:108279071 | C | G | 28 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0138 others(25): Show |
30 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-7732C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279071 | |||||||
| chr13:108279071 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-7732C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279071 | |||||||
| chr13:108279072 | C | T | 29 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0138 others(26): Show |
31 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.425-7731C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279072 | |||||||
| chr13:108279074 | T | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0167 a0001c0001t0001g0218 others(14): Show |
17 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.425-7729T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279074 | |||||||
| chr13:108279199 | G | A | 1 | a0001c0001t0006g0276 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.425-7604G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279199 | |||||||
| chr13:108279210 | T | A | 2 | a0001c0001t0006g0276 a0001c0001t0006g0277 |
2 | HG01943.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.425-7593T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279210 | |||||||
| chr13:108279215 | C | G | 1 | a0001c0001t0001g0356 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425-7588C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279215 | |||||||
| chr13:108279224 | A | T | 1 | a0001c0001t0003g0094 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.425-7579A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279224 | |||||||
| chr13:108279255 | C | T | 1 | a0001c0001t0013g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.425-7548C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279255 | |||||||
| chr13:108279324 | G | A | 1 | a0001c0001t0010g0059 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.425-7479G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279324 | |||||||
| chr13:108279462 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-7341G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279462 | |||||||
| chr13:108279463 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-7340A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279463 | |||||||
| chr13:108279631 | T | A | 1 | a0001c0001t0006g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.425-7172T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279631 | |||||||
| chr13:108279769 | G | T | 12 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0002g0206 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-7034G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279769 | |||||||
| chr13:108279773 | C | G | 3 | a0001c0001t0001g0356 a0001c0001t0006g0276 a0001c0001t0006g0277 |
3 | HG01943.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.425-7030C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279773 | |||||||
| chr13:108279892 | T | A | 1 | a0001c0001t0003g0169 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.425-6911T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279892 | |||||||
| chr13:108279897 | T | G | 2 | a0001c0001t0006g0276 a0001c0001t0006g0277 |
2 | HG01943.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.425-6906T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279897 | |||||||
| chr13:108279961 | C | T | 1 | a0001c0001t0015g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425-6842C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108279961 | |||||||
| chr13:108280040 | A | G | 1 | a0001c0001t0013g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.425-6763A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280040 | |||||||
| chr13:108280063 | C | T | 2 | a0001c0001t0006g0166 a0001c0001t0012g0165 |
2 | HG02723.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.425-6740C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280063 | |||||||
| chr13:108280069 | C | CT | 100 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0054 others(97): Show |
105 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.425-6716dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280069 | ||||||
| chr13:108280069 | C | CTT | 23 | a0001c0001t0002g0160 a0001c0001t0002g0353 a0001c0001t0003g0292 others(20): Show |
25 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.425-6717_425-6716d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280069 | ||||||
| chr13:108280072 | T | C | 1 | a0001c0001t0022g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.425-6731T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280072 | |||||||
| chr13:108280236 | G | A | 1 | a0001c0001t0010g0125 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425-6567G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280236 | |||||||
| chr13:108280245 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-6558A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280245 | |||||||
| chr13:108280513 | T | C | 1 | a0001c0001t0002g0333 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.425-6290T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280513 | |||||||
| chr13:108280561 | G | A | 1 | a0001c0001t0004g0052 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.425-6242G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280561 | |||||||
| chr13:108280716 | C | CT | 34 | a0001c0001t0002g0353 a0001c0001t0003g0037 a0001c0001t0003g0068 others(31): Show |
36 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.425-6074dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280716 | ||||||
| chr13:108280716 | CT | C | 26 | a0001c0001t0001g0321 a0001c0001t0001g0324 a0001c0001t0002g0045 others(23): Show |
28 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.425-6074delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280716 | ||||||
| chr13:108280725 | T | G | 20 | a0001c0001t0002g0138 a0001c0001t0002g0143 a0001c0001t0002g0153 others(17): Show |
22 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.425-6078T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280725 | |||||||
| chr13:108280820 | G | C | 2 | a0001c0001t0001g0124 a0001c0001t0006g0199 |
2 | HG02559.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.425-5983G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280820 | |||||||
| chr13:108280829 | C | T | 1 | a0001c0001t0013g0171 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.425-5974C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280829 | |||||||
| chr13:108280866 | A | G | 1 | a0001c0001t0015g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425-5937A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280866 | |||||||
| chr13:108280891 | A | G | 1 | a0001c0001t0008g0222 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.425-5912A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108280891 | |||||||
| chr13:108280958 | T | TATTAGAG others(3): Show |
2 | a0001c0001t0002g0007 a0001c0001t0002g0027 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.425-5834_425-5825d others(12): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108280958 | ||||||
| chr13:108281007 | G | A | 12 | a0001c0001t0001g0011 a0001c0001t0001g0167 a0001c0001t0001g0218 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-5796G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281007 | |||||||
| chr13:108281115 | A | G | 1 | a0001c0001t0002g0267 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.425-5688A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281115 | |||||||
| chr13:108281129 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.425-5674C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281129 | |||||||
| chr13:108281153 | A | C | 1 | a0001c0001t0001g0303 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.425-5650A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281153 | |||||||
| chr13:108281315 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-5488T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281315 | |||||||
| chr13:108281601 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0002g0206 |
2 | HG00323.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.425-5202A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281601 | |||||||
| chr13:108281663 | A | G | 26 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0102 others(23): Show |
27 | HG00642.hp2 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.425-5140A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281663 | |||||||
| chr13:108281697 | G | A | 236 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0025 others(233): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.425-5106G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281697 | |||||||
| chr13:108281867 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-4936T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281867 | |||||||
| chr13:108281948 | C | T | 9 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0003g0266 others(6): Show |
9 | HG02109.hp1 HG02258.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-4855C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108281948 | |||||||
| chr13:108282055 | G | A | 6 | a0001c0001t0001g0228 a0001c0001t0006g0024 a0001c0001t0006g0106 others(3): Show |
6 | HG01243.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-4748G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282055 | |||||||
| chr13:108282260 | ATG | A | 7 | a0001c0001t0001g0073 a0001c0001t0002g0288 a0001c0001t0006g0276 others(4): Show |
7 | HG01943.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-4541_425-4540d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108282260 | ||||||
| chr13:108282266 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-4537T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282266 | |||||||
| chr13:108282272 | G | A | 98 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(95): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.425-4531G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282272 | |||||||
| chr13:108282276 | A | G | 7 | a0001c0001t0009g0195 a0001c0001t0015g0309 a0001c0001t0016g0188 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.425-4527A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282276 | |||||||
| chr13:108282346 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-4457A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282346 | |||||||
| chr13:108282550 | G | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0256 a0001c0001t0001g0275 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-4253G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282550 | |||||||
| chr13:108282735 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.425-4068T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282735 | |||||||
| chr13:108282803 | G | A | 7 | a0001c0001t0001g0228 a0001c0001t0006g0024 a0001c0001t0006g0106 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-4000G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282803 | |||||||
| chr13:108282886 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-3917T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282886 | |||||||
| chr13:108282960 | A | C | 9 | a0001c0001t0001g0249 a0001c0001t0001g0296 a0001c0001t0001g0303 others(6): Show |
10 | HG00741.hp2 HG01123.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.425-3843A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108282960 | |||||||
| chr13:108283099 | C | T | 100 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(97): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.425-3704C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283099 | |||||||
| chr13:108283147 | G | C | 1 | a0001c0001t0005g0262 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.425-3656G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283147 | |||||||
| chr13:108283209 | G | A | 99 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(96): Show |
105 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.425-3594G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283209 | |||||||
| chr13:108283221 | C | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0162 |
2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.425-3582C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283221 | |||||||
| chr13:108283341 | A | G | 104 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(101): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-3462A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283341 | |||||||
| chr13:108283375 | T | G | 34 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(31): Show |
34 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.425-3428T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283375 | |||||||
| chr13:108283443 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0256 a0001c0001t0001g0275 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-3360A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283443 | |||||||
| chr13:108283554 | A | T | 101 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(98): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-3249A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283554 | |||||||
| chr13:108283573 | T | A | 1 | a0001c0001t0012g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.425-3230T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283573 | |||||||
| chr13:108283580 | A | G | 1 | a0001c0001t0014g0097 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.425-3223A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283580 | |||||||
| chr13:108283588 | T | C | 1 | a0001c0001t0004g0132 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.425-3215T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283588 | |||||||
| chr13:108283688 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-3115A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283688 | |||||||
| chr13:108283733 | C | T | 8 | a0001c0001t0001g0157 a0001c0001t0001g0295 a0001c0001t0002g0002 others(5): Show |
9 | HG00140.hp1 HG01074.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-3070C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283733 | |||||||
| chr13:108283813 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2990T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283813 | |||||||
| chr13:108283822 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2981T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283822 | |||||||
| chr13:108283823 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2980A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283823 | |||||||
| chr13:108283824 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2979G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283824 | |||||||
| chr13:108283839 | T | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0228 a0001c0001t0001g0256 others(48): Show |
54 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.425-2964T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283839 | |||||||
| chr13:108283914 | T | C | 101 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(98): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-2889T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283914 | |||||||
| chr13:108283987 | T | A | 1 | a0001c0001t0007g0284 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.425-2816T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108283987 | |||||||
| chr13:108284025 | G | C | 2 | a0001c0001t0005g0080 a0001c0001t0009g0257 |
2 | NA18983.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.425-2778G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284025 | |||||||
| chr13:108284091 | G | C | 1 | a0001c0001t0012g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.425-2712G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284091 | |||||||
| chr13:108284094 | G | C | 1 | a0001c0001t0001g0299 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.425-2709G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284094 | |||||||
| chr13:108284100 | T | C | 101 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(98): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-2703T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284100 | |||||||
| chr13:108284201 | C | G | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2602C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284201 | |||||||
| chr13:108284202 | A | C | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2601A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284202 | |||||||
| chr13:108284203 | C | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2600C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284203 | |||||||
| chr13:108284277 | T | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0324 a0001c0001t0006g0091 others(1): Show |
4 | HG02559.hp2 HG02615.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2526T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284277 | |||||||
| chr13:108284303 | T | C | 1 | a0001c0001t0005g0354 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.425-2500T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284303 | |||||||
| chr13:108284307 | C | A | 1 | a0001c0001t0005g0081 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.425-2496C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284307 | |||||||
| chr13:108284351 | TAAATGAA others(17): Show |
T | 101 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(98): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-2448_425-2425d others(26): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108284351 | ||||||
| chr13:108284352 | A | G | 4 | a0001c0001t0006g0189 a0001c0001t0009g0194 a0001c0001t0028g0123 others(1): Show |
4 | HG00099.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-2451A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284352 | |||||||
| chr13:108284355 | TGAATAAA others(5): Show |
T | 1 | a0001c0001t0033g0158 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.425-2447_425-2436d others(14): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284355 | |||||||
| chr13:108284356 | G | A | 3 | a0001c0001t0006g0189 a0001c0001t0009g0194 a0001c0001t0028g0123 |
3 | HG02622.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.425-2447G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284356 | |||||||
| chr13:108284356 | GAATA | G | 36 | a0001c0001t0001g0339 a0001c0001t0003g0010 a0001c0001t0003g0037 others(33): Show |
37 | HG01069.hp2 HG01257.hp2 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.425-2440_425-2437d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108284356 | ||||||
| chr13:108284359 | T | C | 3 | a0001c0001t0006g0189 a0001c0001t0009g0194 a0001c0001t0028g0123 |
3 | HG02622.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.425-2444T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284359 | |||||||
| chr13:108284363 | T | C | 9 | a0001c0001t0001g0228 a0001c0001t0004g0173 a0001c0001t0004g0336 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-2440T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284363 | |||||||
| chr13:108284363 | T | TAAAC | 5 | a0001c0001t0001g0006 a0001c0001t0001g0256 a0001c0001t0001g0275 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-2417_425-2414d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108284363 | ||||||
| chr13:108284363 | TAAAC | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0085 a0001c0001t0001g0086 others(8): Show |
12 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-2417_425-2414d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108284363 | ||||||
| chr13:108284367 | C | T | 84 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0055 others(81): Show |
87 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.425-2436C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284367 | |||||||
| chr13:108284371 | C | T | 8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0185 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-2432C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284371 | |||||||
| chr13:108284383 | C | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2420C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284383 | |||||||
| chr13:108284384 | A | C | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2419A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284384 | |||||||
| chr13:108284387 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2416C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284387 | |||||||
| chr13:108284496 | T | C | 1 | a0001c0001t0003g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.425-2307T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284496 | |||||||
| chr13:108284623 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-2180T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284623 | |||||||
| chr13:108284690 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.425-2113C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284690 | |||||||
| chr13:108284820 | G | T | 41 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0190 others(38): Show |
44 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.425-1983G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284820 | |||||||
| chr13:108284965 | T | C | 6 | a0001c0001t0001g0025 a0001c0001t0002g0156 a0001c0001t0002g0164 others(3): Show |
6 | HG00099.hp1 HG00735.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-1838T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108284965 | |||||||
| chr13:108285033 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-1770C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285033 | |||||||
| chr13:108285104 | T | A | 103 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(100): Show |
109 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.425-1699T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285104 | |||||||
| chr13:108285143 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0356 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.425-1660G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285143 | |||||||
| chr13:108285160 | T | C | 1 | a0001c0001t0012g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.425-1643T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285160 | |||||||
| chr13:108285212 | A | AAGG | 352 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(349): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.425-1589_425-1588i others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108285212 | ||||||
| chr13:108285380 | A | T | 1 | a0001c0001t0030g0179 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.425-1423A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285380 | |||||||
| chr13:108285396 | A | C | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-1407A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285396 | |||||||
| chr13:108285485 | A | G | 104 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(101): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-1318A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285485 | |||||||
| chr13:108285492 | A | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0175 a0001c0001t0001g0249 others(38): Show |
44 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.425-1311A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285492 | |||||||
| chr13:108285524 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.425-1279A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285524 | |||||||
| chr13:108285589 | G | A | 1 | a0001c0001t0012g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.425-1214G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285589 | |||||||
| chr13:108285687 | A | G | 1 | a0001c0001t0004g0281 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.425-1116A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285687 | |||||||
| chr13:108285751 | T | C | 1 | a0001c0001t0006g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.425-1052T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285751 | |||||||
| chr13:108285821 | A | G | 1 | a0001c0001t0002g0302 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.425-982A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285821 | |||||||
| chr13:108285905 | T | C | 33 | a0001c0001t0002g0143 a0001c0001t0002g0160 a0001c0001t0002g0340 others(30): Show |
36 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.425-898T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108285905 | |||||||
| chr13:108286003 | A | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0163 |
5 | NA18971.hp1 NA18983.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-800A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286003 | |||||||
| chr13:108286070 | G | T | 4 | a0001c0001t0009g0195 a0001c0001t0015g0309 a0001c0001t0019g0121 others(1): Show |
4 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-733G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286070 | |||||||
| chr13:108286228 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0162 |
2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.425-575C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286228 | |||||||
| chr13:108286321 | G | A | 1 | a0001c0001t0004g0332 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.425-482G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286321 | |||||||
| chr13:108286346 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0013g0171 a0001c0001t0031g0223 |
3 | HG02055.hp1 HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.425-457G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286346 | |||||||
| chr13:108286349 | T | C | 104 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(101): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-454T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286349 | |||||||
| chr13:108286354 | AT | A | 12 | a0001c0001t0001g0073 a0001c0001t0001g0256 a0001c0001t0002g0288 others(9): Show |
12 | HG01074.hp2 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-438delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108286354 | ||||||
| chr13:108286373 | T | G | 104 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(101): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-430T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286373 | |||||||
| chr13:108286379 | T | A | 104 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(101): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.425-424T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286379 | |||||||
| chr13:108286386 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-417T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286386 | |||||||
| chr13:108286600 | A | G | 4 | a0001c0001t0002g0237 a0001c0001t0008g0233 a0001c0001t0008g0252 others(1): Show |
4 | HG00280.hp2 HG02486.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-203A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286600 | |||||||
| chr13:108286628 | CAT | C | 102 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(99): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.425-167_425-166del others(2): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108286628 | ||||||
| chr13:108286636 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.425-167T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286636 | |||||||
| chr13:108286700 | AATTG | A | 4 | a0001c0001t0009g0195 a0001c0001t0015g0309 a0001c0001t0019g0121 others(1): Show |
4 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-99_425-96delGA others(2): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 108286700 | ||||||
| chr13:108286735 | G | A | 1 | a0001c0001t0005g0334 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.425-68G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286735 | |||||||
| chr13:108286750 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0012g0103 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.425-53T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 2/5 | chr13 | 108286750 | |||||||
| chr13:108286986 | C | G | 3 | a0001c0001t0006g0024 a0001c0001t0006g0070 a0001c0001t0006g0186 |
3 | HG02630.hp1 HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.481+127C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108286986 | |||||||
| chr13:108287051 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+192A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287051 | |||||||
| chr13:108287108 | C | T | 2 | a0001c0001t0005g0349 a0001c0001t0009g0325 |
2 | NA18974.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.481+249C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287108 | |||||||
| chr13:108287121 | G | A | 1 | a0001c0001t0004g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.481+262G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287121 | |||||||
| chr13:108287132 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0030g0179 |
2 | HG02055.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.481+273A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287132 | |||||||
| chr13:108287133 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.481+274G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287133 | |||||||
| chr13:108287139 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+280A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287139 | |||||||
| chr13:108287253 | T | G | 1 | a0001c0001t0002g0267 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.481+394T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287253 | |||||||
| chr13:108287306 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+447T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287306 | |||||||
| chr13:108287327 | A | G | 4 | a0001c0001t0003g0172 a0001c0001t0004g0052 a0001c0001t0005g0098 others(1): Show |
4 | HG00544.hp1 HG02015.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+468A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287327 | |||||||
| chr13:108287357 | A | C | 102 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(99): Show |
108 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.481+498A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287357 | |||||||
| chr13:108287415 | A | T | 1 | a0001c0001t0002g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481+556A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287415 | |||||||
| chr13:108287508 | C | T | 1 | a0001c0001t0012g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.481+649C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287508 | |||||||
| chr13:108287574 | A | G | 21 | a0001c0001t0001g0006 a0001c0001t0001g0228 a0001c0001t0001g0256 others(18): Show |
22 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.481+715A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108287574 | |||||||
| chr13:108288060 | G | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0063 others(119): Show |
128 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.481+1201G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288060 | |||||||
| chr13:108288101 | G | A | 7 | a0001c0001t0003g0037 a0001c0001t0004g0032 a0001c0001t0004g0332 others(4): Show |
7 | HG02071.hp1 NA18962.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+1242G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288101 | |||||||
| chr13:108288210 | A | G | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.481+1351A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288210 | |||||||
| chr13:108288400 | C | A | 342 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(339): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.481+1541C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288400 | |||||||
| chr13:108288571 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.481+1712A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288571 | |||||||
| chr13:108288596 | T | C | 1 | a0001c0001t0004g0273 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.481+1737T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288596 | |||||||
| chr13:108288633 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.481+1774A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288633 | |||||||
| chr13:108288822 | C | T | 1 | a0001c0001t0007g0248 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.481+1963C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288822 | |||||||
| chr13:108288823 | G | A | 8 | a0001c0001t0001g0228 a0001c0001t0006g0106 a0001c0001t0006g0189 others(5): Show |
8 | HG01243.hp2 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.481+1964G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288823 | |||||||
| chr13:108288852 | G | A | 1 | a0001c0001t0004g0291 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.481+1993G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288852 | |||||||
| chr13:108288955 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0027 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.481+2096G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288955 | |||||||
| chr13:108288966 | T | A | 3 | a0001c0001t0016g0188 a0001c0001t0016g0196 a0001c0001t0020g0155 |
3 | HG01884.hp1 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.481+2107T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108288966 | |||||||
| chr13:108289067 | G | C | 4 | a0001c0001t0009g0195 a0001c0001t0015g0309 a0001c0001t0019g0121 others(1): Show |
4 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+2208G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289067 | |||||||
| chr13:108289091 | C | CAGA | 104 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(101): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.481+2236_481+2238d others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108289091 | ||||||
| chr13:108289249 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.481+2390C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289249 | |||||||
| chr13:108289347 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0256 a0001c0001t0001g0275 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+2488C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289347 | |||||||
| chr13:108289431 | A | G | 1 | a0001c0001t0008g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.481+2572A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289431 | |||||||
| chr13:108289458 | A | G | 1 | a0001c0001t0008g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.481+2599A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289458 | |||||||
| chr13:108289599 | TATA | T | 14 | a0001c0001t0001g0228 a0001c0001t0006g0087 a0001c0001t0006g0106 others(11): Show |
14 | HG01081.hp1 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.481+2747_481+2749d others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108289599 | ||||||
| chr13:108289634 | T | A | 104 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(101): Show |
110 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.481+2775T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289634 | |||||||
| chr13:108289675 | T | G | 1 | a0001c0001t0003g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.481+2816T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289675 | |||||||
| chr13:108289684 | A | G | 2 | a0001c0001t0013g0090 a0001c0001t0013g0240 |
2 | HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.481+2825A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289684 | |||||||
| chr13:108289801 | T | C | 1 | a0001c0001t0003g0234 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.481+2942T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108289801 | |||||||
| chr13:108290248 | A | G | 102 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(99): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.481+3389A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290248 | |||||||
| chr13:108290440 | G | C | 67 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0054 others(64): Show |
73 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.481+3581G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290440 | |||||||
| chr13:108290528 | T | G | 1 | a0001c0001t0006g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.481+3669T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290528 | |||||||
| chr13:108290631 | G | A | 1 | a0001c0001t0006g0276 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.481+3772G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290631 | |||||||
| chr13:108290681 | A | C | 3 | a0001c0001t0006g0189 a0001c0001t0009g0194 a0001c0001t0028g0123 |
3 | HG02622.hp2 HG02647.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.481+3822A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290681 | |||||||
| chr13:108290686 | A | G | 102 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(99): Show |
107 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.481+3827A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290686 | |||||||
| chr13:108290720 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0228 a0001c0001t0001g0256 others(18): Show |
22 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.481+3861C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290720 | |||||||
| chr13:108290869 | C | A | 101 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(98): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.481+4010C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290869 | |||||||
| chr13:108290967 | G | A | 2 | a0001c0001t0002g0304 a0001c0001t0008g0198 |
2 | HG01261.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.481+4108G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290967 | |||||||
| chr13:108290990 | C | T | 2 | a0001c0001t0003g0134 a0001c0001t0007g0133 |
2 | NA19057.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.481+4131C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108290990 | |||||||
| chr13:108291267 | A | T | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.481+4408A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291267 | |||||||
| chr13:108291327 | C | G | 1 | a0001c0001t0006g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.481+4468C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291327 | |||||||
| chr13:108291382 | T | G | 360 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(357): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.481+4523T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291382 | |||||||
| chr13:108291395 | T | C | 2 | a0001c0001t0006g0087 a0001c0001t0006g0277 |
2 | HG01081.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.481+4536T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291395 | |||||||
| chr13:108291441 | A | G | 33 | a0001c0001t0001g0339 a0001c0001t0003g0010 a0001c0001t0003g0037 others(30): Show |
35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.481+4582A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291441 | |||||||
| chr13:108291842 | T | C | 1 | a0001c0001t0005g0344 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.481+4983T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291842 | |||||||
| chr13:108291922 | C | T | 1 | a0001c0001t0006g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.481+5063C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291922 | |||||||
| chr13:108291927 | A | G | 7 | a0001c0001t0002g0007 a0001c0001t0002g0027 a0001c0001t0002g0119 others(4): Show |
8 | HG01099.hp1 HG01169.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.481+5068A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291927 | |||||||
| chr13:108291955 | C | T | 1 | a0001c0001t0008g0021 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.481+5096C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108291955 | |||||||
| chr13:108292059 | ACT | A | 101 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(98): Show |
106 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.481+5207_481+5208d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108292059 | ||||||
| chr13:108292108 | A | G | 41 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0190 others(38): Show |
44 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.481+5249A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292108 | |||||||
| chr13:108292171 | T | C | 33 | a0001c0001t0001g0339 a0001c0001t0003g0010 a0001c0001t0003g0037 others(30): Show |
35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.481+5312T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292171 | |||||||
| chr13:108292423 | A | G | 1 | a0001c0001t0002g0030 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.481+5564A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292423 | |||||||
| chr13:108292693 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.481+5834T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292693 | |||||||
| chr13:108292795 | A | G | 1 | a0001c0001t0020g0286 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.481+5936A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108292795 | |||||||
| chr13:108293265 | T | C | 1 | a0001c0001t0002g0160 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.481+6406T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293265 | |||||||
| chr13:108293287 | C | T | 1 | a0001c0001t0006g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.481+6428C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293287 | |||||||
| chr13:108293437 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.481+6578G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293437 | |||||||
| chr13:108293592 | A | C | 2 | a0001c0001t0006g0141 a0001c0001t0006g0182 |
2 | HG00140.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.481+6733A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293592 | |||||||
| chr13:108293654 | T | C | 3 | a0001c0001t0006g0070 a0001c0001t0006g0186 a0001c0001t0009g0293 |
3 | HG01074.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.481+6795T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293654 | |||||||
| chr13:108293783 | G | A | 5 | a0001c0001t0001g0073 a0001c0001t0013g0090 a0001c0001t0013g0171 others(2): Show |
5 | HG02055.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.481+6924G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293783 | |||||||
| chr13:108293894 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0256 a0001c0001t0001g0275 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.481+7035T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293894 | |||||||
| chr13:108293951 | C | T | 1 | a0001c0001t0008g0021 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.481+7092C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108293951 | |||||||
| chr13:108294183 | A | AT | 108 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0102 others(105): Show |
114 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.481+7338dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294183 | ||||||
| chr13:108294183 | A | ATT | 7 | a0001c0001t0001g0011 a0001c0001t0006g0011 a0001c0001t0006g0226 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+7337_481+7338d others(4): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294183 | ||||||
| chr13:108294183 | AT | A | 42 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0190 others(39): Show |
45 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.481+7338delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294183 | ||||||
| chr13:108294242 | T | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0228 a0001c0001t0001g0256 others(19): Show |
23 | HG01081.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.481+7383T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294242 | |||||||
| chr13:108294324 | C | T | 4 | a0001c0001t0009g0195 a0001c0001t0015g0309 a0001c0001t0019g0121 others(1): Show |
4 | HG02109.hp2 HG03225.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+7465C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294324 | |||||||
| chr13:108294380 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.481+7521A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294380 | |||||||
| chr13:108294381 | T | C | 1 | a0001c0001t0005g0262 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.481+7522T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294381 | |||||||
| chr13:108294427 | GC | G | 33 | a0001c0001t0001g0339 a0001c0001t0003g0010 a0001c0001t0003g0037 others(30): Show |
35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.481+7570delC | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294427 | ||||||
| chr13:108294524 | C | T | 1 | a0001c0001t0013g0136 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.481+7665C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294524 | |||||||
| chr13:108294550 | A | AT | 7 | a0001c0001t0003g0112 a0001c0001t0006g0040 a0001c0001t0006g0041 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+7701dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294550 | ||||||
| chr13:108294550 | AT | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0256 a0001c0001t0001g0275 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.481+7701delT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294550 | ||||||
| chr13:108294671 | G | A | 3 | a0001c0001t0006g0070 a0001c0001t0006g0186 a0001c0001t0009g0293 |
3 | HG01074.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.481+7812G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294671 | |||||||
| chr13:108294672 | T | C | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7813T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294672 | |||||||
| chr13:108294677 | T | G | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7818T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294677 | |||||||
| chr13:108294678 | T | TTCAC | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7820_481+7821i others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108294678 | ||||||
| chr13:108294683 | G | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7824G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294683 | |||||||
| chr13:108294684 | G | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7825G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294684 | |||||||
| chr13:108294685 | T | A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7826T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294685 | |||||||
| chr13:108294687 | T | TA | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7828_481+7829i others(3): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294687 | |||||||
| chr13:108294688 | C | A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7829C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294688 | |||||||
| chr13:108294692 | G | T | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7833G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294692 | |||||||
| chr13:108294697 | GCAT | G | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7839_481+7841d others(5): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294697 | |||||||
| chr13:108294702 | GATATCAG others(4751): Show |
G | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.481+7844_482-3793d others(2): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294702 | |||||||
| chr13:108294862 | T | C | 1 | a0001c0001t0007g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.481+8003T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294862 | |||||||
| chr13:108294864 | G | T | 1 | a0001c0001t0007g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.481+8005G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108294864 | |||||||
| chr13:108295282 | C | T | 1 | a0001c0001t0007g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.482-7971C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295282 | |||||||
| chr13:108295283 | T | C | 1 | a0001c0001t0007g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.482-7970T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295283 | |||||||
| chr13:108295393 | A | G | 223 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0054 others(220): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.482-7860A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295393 | |||||||
| chr13:108295480 | C | T | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-7773C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295480 | |||||||
| chr13:108295492 | T | C | 1 | a0001c0001t0007g0255 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.482-7761T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295492 | |||||||
| chr13:108295782 | T | C | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-7471T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295782 | |||||||
| chr13:108295843 | T | G | 3 | a0001c0001t0016g0188 a0001c0001t0016g0196 a0001c0001t0020g0155 |
3 | HG01884.hp1 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.482-7410T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295843 | |||||||
| chr13:108295968 | G | T | 2 | a0001c0001t0005g0058 a0001c0001t0005g0338 |
2 | HG01978.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.482-7285G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108295968 | |||||||
| chr13:108296247 | A | G | 1 | a0001c0001t0004g0281 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.482-7006A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296247 | |||||||
| chr13:108296259 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.482-6994A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296259 | |||||||
| chr13:108296305 | G | A | 33 | a0001c0001t0001g0339 a0001c0001t0003g0010 a0001c0001t0003g0037 others(30): Show |
35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.482-6948G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296305 | |||||||
| chr13:108296544 | C | T | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-6709C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296544 | |||||||
| chr13:108296635 | A | C | 1 | a0001c0001t0015g0309 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.482-6618A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296635 | |||||||
| chr13:108296722 | T | C | 1 | a0001c0001t0012g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.482-6531T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296722 | |||||||
| chr13:108296891 | A | G | 8 | a0001c0001t0001g0073 a0001c0001t0001g0321 a0001c0001t0002g0288 others(5): Show |
8 | HG01943.hp1 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-6362A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108296891 | |||||||
| chr13:108297003 | C | T | 3 | a0001c0001t0006g0070 a0001c0001t0006g0186 a0001c0001t0009g0293 |
3 | HG01074.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.482-6250C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297003 | |||||||
| chr13:108297060 | T | C | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-6193T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297060 | |||||||
| chr13:108297099 | T | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0154 a0001c0001t0001g0256 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-6154T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297099 | |||||||
| chr13:108297102 | A | G | 1 | a0001c0001t0011g0019 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.482-6151A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297102 | |||||||
| chr13:108297375 | C | T | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-5878C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297375 | |||||||
| chr13:108297519 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.482-5734C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297519 | |||||||
| chr13:108297616 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0356 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.482-5637T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297616 | |||||||
| chr13:108297638 | T | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0154 a0001c0001t0001g0256 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-5615T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297638 | |||||||
| chr13:108297658 | T | A | 2 | a0001c0001t0006g0087 a0001c0001t0006g0277 |
2 | HG01081.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.482-5595T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297658 | |||||||
| chr13:108297735 | G | A | 6 | a0001c0001t0001g0055 a0001c0001t0001g0074 a0001c0001t0001g0190 others(3): Show |
6 | HG02622.hp1 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-5518G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297735 | |||||||
| chr13:108297736 | G | A | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.482-5517G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297736 | |||||||
| chr13:108297796 | A | C | 1 | a0001c0001t0006g0182 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.482-5457A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108297796 | |||||||
| chr13:108298013 | A | G | 1 | a0001c0001t0012g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.482-5240A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298013 | |||||||
| chr13:108298021 | G | A | 331 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0033 others(328): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.482-5232G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298021 | |||||||
| chr13:108298102 | G | A | 1 | a0001c0001t0025g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.482-5151G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298102 | |||||||
| chr13:108298179 | G | A | 30 | a0001c0001t0002g0143 a0001c0001t0002g0160 a0001c0001t0003g0076 others(27): Show |
33 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.482-5074G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298179 | |||||||
| chr13:108298199 | T | G | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-5054T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298199 | |||||||
| chr13:108298270 | G | T | 105 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0057 others(102): Show |
114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.482-4983G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298270 | |||||||
| chr13:108298489 | A | G | 1 | a0001c0001t0008g0092 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.482-4764A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298489 | |||||||
| chr13:108298704 | C | T | 1 | a0001c0001t0012g0165 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.482-4549C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298704 | |||||||
| chr13:108298729 | C | A | 7 | a0001c0001t0001g0339 a0001c0001t0003g0010 a0001c0001t0003g0088 others(4): Show |
8 | HG01069.hp2 HG01257.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-4524C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298729 | |||||||
| chr13:108298828 | C | T | 32 | a0001c0001t0001g0339 a0001c0001t0003g0010 a0001c0001t0003g0037 others(29): Show |
33 | HG01069.hp2 HG01257.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.482-4425C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298828 | |||||||
| chr13:108298863 | C | T | 1 | a0001c0001t0007g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.482-4390C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298863 | |||||||
| chr13:108298879 | G | A | 4 | a0001c0001t0006g0106 a0001c0002t0002g0026 a0001c0002t0021g0230 others(1): Show |
4 | HG02280.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-4374G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298879 | |||||||
| chr13:108298949 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0356 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.482-4304G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108298949 | |||||||
| chr13:108298968 | A | AAAAC | 3 | a0001c0001t0007g0008 a0001c0001t0007g0047 a0001c0001t0007g0065 |
4 | HG01496.hp1 HG01928.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-4265_482-4262d others(6): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108298968 | ||||||
| chr13:108298972 | CAAACAAA others(12): Show |
C | 33 | a0001c0001t0001g0339 a0001c0001t0003g0010 a0001c0001t0003g0037 others(30): Show |
35 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.482-4260_482-4242d others(21): Show |
TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108298972 | ||||||
| chr13:108299158 | G | A | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-4095G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299158 | |||||||
| chr13:108299163 | A | C | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-4090A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299163 | |||||||
| chr13:108299251 | G | A | 2 | a0001c0001t0006g0040 a0001c0001t0006g0041 |
2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482-4002G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299251 | |||||||
| chr13:108299297 | G | A | 1 | a0001c0001t0002g0138 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.482-3956G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299297 | |||||||
| chr13:108299462 | G | C | 29 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0034 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-3791G>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299462 | |||||||
| chr13:108299495 | G | A | 1 | a0001c0001t0010g0069 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.482-3758G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299495 | |||||||
| chr13:108299537 | T | C | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.482-3716T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299537 | |||||||
| chr13:108299651 | T | C | 24 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0085 others(21): Show |
24 | HG00099.hp1 HG00735.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.482-3602T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299651 | |||||||
| chr13:108299962 | G | A | 1 | a0001c0001t0006g0276 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.482-3291G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299962 | |||||||
| chr13:108299994 | T | C | 2 | a0001c0001t0004g0096 a0001c0001t0004g0327 |
2 | NA18957.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.482-3259T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108299994 | |||||||
| chr13:108300010 | G | A | 4 | a0001c0001t0006g0024 a0001c0001t0006g0070 a0001c0001t0006g0186 others(1): Show |
4 | HG01074.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-3243G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300010 | |||||||
| chr13:108300159 | C | G | 52 | a0001c0001t0001g0054 a0001c0001t0001g0261 a0001c0001t0002g0181 others(49): Show |
55 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.482-3094C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300159 | |||||||
| chr13:108300204 | A | G | 1 | a0001c0001t0004g0246 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.482-3049A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300204 | |||||||
| chr13:108300205 | T | C | 2 | a0001c0001t0001g0207 a0001c0001t0006g0208 |
2 | HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.482-3048T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300205 | |||||||
| chr13:108300343 | C | T | 1 | a0001c0001t0006g0106 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.482-2910C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300343 | |||||||
| chr13:108300354 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.482-2899A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300354 | |||||||
| chr13:108300420 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0256 a0001c0001t0001g0275 others(3): Show |
7 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.482-2833C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300420 | |||||||
| chr13:108300430 | A | G | 1 | a0001c0001t0005g0113 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.482-2823A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300430 | |||||||
| chr13:108300665 | T | C | 1 | a0001c0001t0003g0348 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.482-2588T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300665 | |||||||
| chr13:108300949 | A | G | 2 | a0001c0001t0004g0110 a0001c0001t0004g0132 |
2 | HG02040.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.482-2304A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300949 | |||||||
| chr13:108300968 | G | A | 1 | a0001c0001t0005g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.482-2285G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108300968 | |||||||
| chr13:108301127 | A | G | 1 | a0001c0001t0006g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.482-2126A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301127 | |||||||
| chr13:108301481 | C | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0275 a0001c0001t0001g0303 |
4 | HG01167.hp2 HG01169.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.482-1772C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301481 | |||||||
| chr13:108301503 | A | G | 3 | a0001c0001t0016g0188 a0001c0001t0016g0196 a0001c0001t0020g0155 |
3 | HG01884.hp1 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.482-1750A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301503 | |||||||
| chr13:108301601 | A | G | 1 | a0001c0001t0011g0018 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.482-1652A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301601 | |||||||
| chr13:108301611 | A | G | 1 | a0001c0001t0006g0135 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.482-1642A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301611 | |||||||
| chr13:108301643 | C | T | 89 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0261 others(86): Show |
92 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.482-1610C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301643 | |||||||
| chr13:108301714 | A | G | 1 | a0001c0001t0003g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.482-1539A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301714 | |||||||
| chr13:108301878 | A | G | 5 | a0001c0001t0006g0024 a0001c0001t0006g0070 a0001c0001t0006g0091 others(2): Show |
5 | HG02559.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.482-1375A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301878 | |||||||
| chr13:108301904 | T | G | 1 | a0001c0001t0024g0285 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.482-1349T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301904 | |||||||
| chr13:108301943 | G | A | 8 | a0001c0001t0001g0114 a0001c0001t0001g0162 a0001c0001t0001g0167 others(5): Show |
8 | HG01192.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.482-1310G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301943 | |||||||
| chr13:108301956 | A | C | 83 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0176 others(80): Show |
87 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.482-1297A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108301956 | |||||||
| chr13:108302085 | C | T | 2 | a0001c0001t0006g0166 a0001c0001t0006g0221 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.482-1168C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302085 | |||||||
| chr13:108302232 | A | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0185 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1021A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302232 | |||||||
| chr13:108302387 | A | C | 1 | a0001c0001t0031g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.482-866A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302387 | |||||||
| chr13:108302396 | C | T | 2 | a0001c0001t0004g0111 a0001c0001t0004g0281 |
2 | NA18948.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.482-857C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302396 | |||||||
| chr13:108302537 | TC | T | 266 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(263): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.482-710delC | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 108302537 | ||||||
| chr13:108302552 | A | G | 1 | a0001c0001t0024g0285 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.482-701A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302552 | |||||||
| chr13:108302674 | C | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0319 |
2 | HG02300.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.482-579C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302674 | |||||||
| chr13:108302728 | G | A | 1 | a0001c0001t0005g0067 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.482-525G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302728 | |||||||
| chr13:108302771 | C | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0054 others(17): Show |
21 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.482-482C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108302771 | |||||||
| chr13:108303054 | A | C | 1 | a0001c0001t0006g0087 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.482-199A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108303054 | |||||||
| chr13:108303116 | C | G | 278 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(275): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.482-137C>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108303116 | |||||||
| chr13:108303181 | C | A | 1 | a0001c0001t0002g0181 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.482-72C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108303181 | |||||||
| chr13:108303227 | C | T | 8 | a0001c0001t0013g0056 a0001c0001t0013g0090 a0001c0001t0013g0136 others(5): Show |
8 | HG01884.hp1 HG02055.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.482-26C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 3/5 | chr13 | 108303227 | |||||||
| chr13:108303801 | T | A | 2 | a0001c0001t0012g0101 a0001c0001t0012g0165 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.745+197T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303801 | |||||||
| chr13:108303814 | A | G | 1 | a0001c0001t0005g0204 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.745+210A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303814 | |||||||
| chr13:108303815 | T | C | 1 | a0001c0001t0013g0136 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.745+211T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303815 | |||||||
| chr13:108303821 | T | A | 280 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(277): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.745+217T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303821 | |||||||
| chr13:108303958 | T | C | 1 | a0001c0001t0035g0305 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.745+354T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303958 | |||||||
| chr13:108303969 | G | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0025 others(36): Show |
41 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.745+365G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108303969 | |||||||
| chr13:108304140 | G | T | 5 | a0001c0001t0001g0102 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01081.hp1 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.745+536G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304140 | |||||||
| chr13:108304191 | C | A | 1 | a0001c0001t0031g0223 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.745+587C>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304191 | |||||||
| chr13:108304284 | A | C | 2 | a0001c0001t0001g0124 a0001c0001t0031g0223 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.745+680A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304284 | |||||||
| chr13:108304325 | A | G | 1 | a0001c0001t0012g0224 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.745+721A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304325 | |||||||
| chr13:108304410 | C | T | 281 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(278): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.745+806C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304410 | |||||||
| chr13:108304446 | A | G | 277 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(274): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.745+842A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304446 | |||||||
| chr13:108304478 | G | T | 276 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.745+874G>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304478 | |||||||
| chr13:108304489 | G | A | 2 | a0001c0001t0019g0121 a0001c0001t0019g0200 |
2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.745+885G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304489 | |||||||
| chr13:108304552 | A | C | 1 | a0001c0001t0001g0025 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.745+948A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304552 | |||||||
| chr13:108304642 | C | T | 276 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(273): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.745+1038C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304642 | |||||||
| chr13:108304715 | A | G | 100 | a0001c0001t0004g0009 a0001c0001t0004g0013 a0001c0001t0004g0015 others(97): Show |
106 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.745+1111A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108304715 | |||||||
| chr13:108305015 | G | A | 2 | a0001c0001t0006g0166 a0001c0001t0006g0221 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.745+1411G>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305015 | |||||||
| chr13:108305250 | A | G | 1 | a0001c0001t0009g0220 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.746-1576A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305250 | |||||||
| chr13:108305287 | A | G | 5 | a0001c0001t0003g0116 a0001c0001t0003g0129 a0001c0001t0003g0169 others(2): Show |
5 | HG02080.hp2 NA18946.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-1539A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305287 | |||||||
| chr13:108305361 | T | C | 1 | a0001c0001t0008g0174 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.746-1465T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305361 | |||||||
| chr13:108305594 | T | A | 277 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(274): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.746-1232T>A | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305594 | |||||||
| chr13:108305644 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.746-1182A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305644 | |||||||
| chr13:108305728 | A | G | 2 | a0001c0001t0005g0274 a0001c0001t0005g0328 |
2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.746-1098A>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108305728 | |||||||
| chr13:108306017 | C | T | 28 | a0001c0001t0007g0003 a0001c0001t0007g0008 a0001c0001t0007g0012 others(25): Show |
32 | HG00408.hp1 HG00597.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.746-809C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306017 | |||||||
| chr13:108306020 | C | T | 1 | a0001c0001t0004g0332 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.746-806C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306020 | |||||||
| chr13:108306560 | T | C | 2 | a0001c0001t0004g0078 a0001c0001t0035g0305 |
2 | NA18612.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.746-266T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306560 | |||||||
| chr13:108306654 | A | T | 28 | a0001c0001t0007g0003 a0001c0001t0007g0008 a0001c0001t0007g0012 others(25): Show |
32 | HG00408.hp1 HG00597.hp1 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.746-172A>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306654 | |||||||
| chr13:108306732 | A | AT | 258 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(255): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.746-84dupT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr13 | 108306732 | ||||||
| chr13:108306732 | A | ATT | 20 | a0001c0001t0004g0048 a0001c0001t0004g0075 a0001c0001t0004g0077 others(17): Show |
20 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.746-85_746-84dupTT | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr13 | 108306732 | ||||||
| chr13:108306737 | T | G | 1 | a0001c0001t0016g0188 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.746-89T>G | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306737 | |||||||
| chr13:108306759 | T | C | 1 | a0001c0001t0004g0355 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.746-67T>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306759 | |||||||
| chr13:108306765 | A | C | 2 | a0001c0001t0005g0274 a0001c0001t0005g0328 |
2 | HG00099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.746-61A>C | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306765 | |||||||
| chr13:108306804 | C | T | 1 | a0001c0001t0008g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.746-22C>T | TNFSF13B | ENSG00000102524.12 | transcript | ENST00000375887.9 | protein_coding | 5/5 | chr13 | 108306804 |