Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4982 |
| ensemblid | ENSG00000164761.9 |
| hgncid | 11909 |
| symbol | TNFRSF11B |
| name | TNF receptor superfamily member 11b |
| refseq_nuc | NM_002546.4 |
| refseq_prot | NP_002537.3 |
| ensembl_nuc | ENST00000297350.9 |
| ensembl_prot | ENSP00000297350.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 118923557 |
| end | 118951885 |
| strand | - |
| ver | v1.2 |
| region | chr8:118923557-118951885 |
| region5000 | chr8:118918557-118956885 |
| regionname0 | TNFRSF11B_chr8_118923557_118951885 |
| regionname5000 | TNFRSF11B_chr8_118918557_118956885 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 401 | 320 | 89 | 31 | 170 | 4 | 26 | 129 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | MNKLL others(396): Show |
chr8 | 118918557 | 118956885 |
| a0002 | 1/1 | 401 | 107 | 5 | 31 | 44 | 4 | 21 | 39 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | MNNLL others(396): Show |
chr8 | 118918557 | 118956885 |
| a0003 | 0/0 | 401 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | MNKLL others(396): Show |
chr8 | 118918557 | 118956885 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1203 | 270 | 43 | 27 | 170 | 4 | 26 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 | ||
| a0001c0003 | 0/0 | 1203 | 34 | 33 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 | ||
| a0001c0005 | 0/0 | 1203 | 10 | 9 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 | ||
| a0001c0006 | 0/0 | 1203 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 | ||
| a0001c0007 | 0/0 | 1203 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 | ||
| a0001c0009 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 | ||
| a0001c0010 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 | ||
| a0002c0002 | 1/1 | 1203 | 92 | 1 | 26 | 44 | 3 | 16 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 | ||
| a0002c0004 | 0/0 | 1203 | 15 | 4 | 5 | 0 | 1 | 5 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 | ||
| a0003c0008 | 0/0 | 1203 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | ATGAA others(1198): Show |
chr8 | 118918557 | 118956885 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2087 | 263 | 39 | 27 | 167 | 4 | 26 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0001t0005 | 0/0 | 2088 | 4 | 3 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2083): Show |
chr8 | 118918557 | 118956885 |
| a0001c0001t0006 | 0/0 | 2087 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0001t0007 | 0/0 | 2087 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0003t0002 | 0/0 | 2087 | 13 | 12 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0003t0003 | 0/0 | 2087 | 12 | 12 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0003t0004 | 0/0 | 2088 | 8 | 8 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2083): Show |
chr8 | 118918557 | 118956885 |
| a0001c0003t0008 | 0/0 | 2088 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2083): Show |
chr8 | 118918557 | 118956885 |
| a0001c0005t0001 | 0/0 | 2087 | 9 | 8 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0005t0010 | 0/0 | 2087 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0006t0001 | 0/0 | 2087 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0007t0002 | 0/0 | 2087 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0009t0009 | 0/0 | 2087 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0001c0010t0001 | 0/0 | 2087 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0002c0002t0001 | 1/1 | 2087 | 90 | 1 | 25 | 43 | 3 | 16 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0002c0002t0005 | 0/0 | 2088 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2083): Show |
chr8 | 118918557 | 118956885 |
| a0002c0002t0011 | 0/0 | 2087 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0002c0004t0001 | 0/0 | 2087 | 15 | 4 | 5 | 0 | 1 | 5 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| a0003c0008t0001 | 0/0 | 2087 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | GGAGA others(2082): Show |
chr8 | 118918557 | 118956885 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 27 | 0 | 1 | 22 | 0 | 4 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0003 | 0/0 | 23 | 0 | 5 | 18 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0004 | 0/0 | 19 | 0 | 0 | 12 | 1 | 6 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0006 | 0/0 | 10 | 1 | 1 | 7 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0011 | 0/0 | 7 | 1 | 1 | 3 | 0 | 2 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0012 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0013 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0054 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0006g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0002g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0002g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0003g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0004g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0003t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0005t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0005t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0005t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0005t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0006t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0007t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0007t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0009t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0001c0010t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0001 | 0/0 | 40 | 1 | 10 | 21 | 0 | 8 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0009 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0014 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0002t0011g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0002c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| a0003c0008t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0001 | g0028 | EUR | GBR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0070 | EUR | FIN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0107 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00642 | hp1 | a0002 | c0004 | t0001 | g0057 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01167 | hp1 | a0001 | c0006 | t0001 | g0037 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01168 | hp2 | a0002 | c0004 | t0001 | g0058 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01169 | hp1 | a0001 | c0006 | t0001 | g0037 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01169 | hp2 | a0002 | c0004 | t0001 | g0055 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0059 | AMR | PUR | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01257 | hp2 | a0002 | c0004 | t0001 | g0028 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01261 | hp2 | a0001 | c0005 | t0001 | g0021 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0063 | EUR | IBS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0014 | EUR | IBS | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0108 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0035 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01981 | hp2 | a0002 | c0002 | t0011 | g0085 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02055 | hp1 | a0001 | c0003 | t0008 | g0125 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02145 | hp2 | a0001 | c0003 | t0003 | g0041 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CDX | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02258 | hp1 | a0002 | c0004 | t0001 | g0027 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02258 | hp2 | a0001 | c0003 | t0004 | g0022 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0142 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0104 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0114 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02622 | hp2 | a0002 | c0004 | t0001 | g0029 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02683 | hp1 | a0002 | c0004 | t0001 | g0056 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0075 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0076 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02717 | hp2 | a0001 | c0010 | t0001 | g0169 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0148 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0110 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02896 | hp1 | a0001 | c0003 | t0004 | g0045 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02897 | hp1 | a0001 | c0003 | t0004 | g0045 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02897 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02922 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02965 | hp1 | a0001 | c0003 | t0004 | g0040 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02976 | hp1 | a0001 | c0003 | t0003 | g0145 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0016 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0016 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03130 | hp1 | a0001 | c0003 | t0002 | g0015 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03139 | hp1 | a0001 | c0007 | t0002 | g0186 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03139 | hp2 | a0001 | c0003 | t0004 | g0022 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03195 | hp1 | a0002 | c0004 | t0001 | g0060 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0099 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03209 | hp2 | a0001 | c0009 | t0009 | g0197 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0113 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03490 | hp1 | a0002 | c0004 | t0001 | g0026 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03492 | hp2 | a0002 | c0004 | t0001 | g0026 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | GWD | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0025 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03654 | hp1 | a0003 | c0008 | t0001 | g0156 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03669 | hp1 | a0002 | c0004 | t0001 | g0029 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0071 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03710 | hp2 | a0002 | c0004 | t0001 | g0061 | SAS | PJL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0088 | SAS | BEB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0021 | AFR | YRI | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18522 | hp2 | a0001 | c0005 | t0010 | g0105 | AFR | YRI | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19001 | hp2 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19076 | hp1 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19082 | hp2 | a0002 | c0002 | t0005 | g0091 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0017 | AFR | YRI | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA20129 | hp1 | a0001 | c0005 | t0001 | g0035 | AFR | ASW | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0041 | AFR | ASW | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | GIH | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0040 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0025 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02559 | hp1 | a0001 | c0003 | t0003 | g0112 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0021 | AFR | ACB | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0025 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0147 | AFR | MSL | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG06807 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | USA | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | USA | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | USA | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | USA | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0027 | AFR | LWK | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| NA21309 | hp2 | a0001 | c0007 | t0002 | g0185 | AFR | LWK | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0065 | REF | REF | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0081 | REF | REF | TNFRSF11B_chr8_118918557_118956885 | TNFRSF11B | chr8 | 118918557 | 118956885 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:118924739 | C | T | 1 | a0003 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.841G>A | p.Val281Met | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 905/2087 | 841/1206 | 281/401 | chr8 | 118924739 | |||
| chr8:118951813 | G | C | 2 | a0001 a0003 |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
missense_variant | MODERATE | c.9C>G | p.Asn3Lys | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/5 | 73/2087 | 9/1206 | 3/401 | chr8 | 118951813 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:118924430 | A | G | 2 | a0001c0003 a0001c0007 |
36 | HG00639.hp1 HG02055.hp1 HG02109.hp1 others(33): Show |
synonymous_variant | LOW | c.1150T>C | p.Leu384Leu | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 1214/2087 | 1150/1206 | 384/401 | chr8 | 118924430 | |||
| chr8:118926543 | T | C | 2 | a0001c0006 a0002c0004 |
17 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(14): Show |
synonymous_variant | LOW | c.768A>G | p.Leu256Leu | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/5 | 832/2087 | 768/1206 | 256/401 | chr8 | 118926543 | |||
| chr8:118926597 | C | T | 1 | a0001c0005 | 10 | HG01261.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
synonymous_variant | LOW | c.714G>A | p.Glu238Glu | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/5 | 778/2087 | 714/1206 | 238/401 | chr8 | 118926597 | |||
| chr8:118928772 | G | A | 2 | a0001c0007 a0001c0009 |
3 | HG03139.hp1 HG03209.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.558C>T | p.Ser186Ser | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/5 | 622/2087 | 558/1206 | 186/401 | chr8 | 118928772 | |||
| chr8:118933145 | G | A | 1 | a0001c0010 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.186C>T | p.Cys62Cys | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/5 | 250/2087 | 186/1206 | 62/401 | chr8 | 118933145 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:118923668 | A | G | 1 | a0002c0002t0011 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*706T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 706 | chr8 | 118923668 | ||||||
| chr8:118923686 | A | G | 1 | a0001c0001t0006 | 2 | NA18952.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*688T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 688 | chr8 | 118923686 | ||||||
| chr8:118923754 | A | G | 1 | a0001c0005t0010 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*620T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 620 | chr8 | 118923754 | ||||||
| chr8:118923791 | A | T | 2 | a0001c0003t0002 a0001c0007t0002 |
15 | HG00639.hp1 HG02280.hp2 HG02486.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*583T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 583 | chr8 | 118923791 | ||||||
| chr8:118924002 | G | T | 1 | a0001c0009t0009 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 372 | chr8 | 118924002 | ||||||
| chr8:118924007 | C | T | 5 | a0001c0003t0002 a0001c0003t0003 a0001c0003t0004 others(2): Show |
36 | HG00639.hp1 HG02055.hp1 HG02109.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*367G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 367 | chr8 | 118924007 | ||||||
| chr8:118924055 | G | C | 1 | a0001c0003t0008 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*319C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 319 | chr8 | 118924055 | ||||||
| chr8:118924091 | G | GT | 4 | a0001c0001t0005 a0001c0003t0004 a0001c0003t0008 others(1): Show |
14 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*282dupA | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 282 | chr8 | 118924091 | ||||||
| chr8:118924352 | A | G | 1 | a0001c0001t0007 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 5/5 | 22 | chr8 | 118924352 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:118924811 | C | A | 1 | a0001c0001t0001g0052 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.818-49G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118924811 | |||||||
| chr8:118924890 | T | G | 1 | a0001c0001t0001g0195 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.818-128A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118924890 | |||||||
| chr8:118925042 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0098 others(4): Show |
9 | HG00099.hp2 HG00741.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.818-280T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925042 | |||||||
| chr8:118925086 | T | C | 1 | a0001c0003t0004g0040 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.818-324A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925086 | |||||||
| chr8:118925175 | C | T | 11 | a0001c0006t0001g0037 a0002c0004t0001g0026 a0002c0004t0001g0027 others(8): Show |
16 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.818-413G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925175 | |||||||
| chr8:118925200 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0140 |
3 | HG00544.hp2 HG02056.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.818-438T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925200 | |||||||
| chr8:118925201 | T | C | 1 | a0002c0002t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.818-439A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925201 | |||||||
| chr8:118925209 | G | C | 2 | a0001c0007t0002g0185 a0001c0007t0002g0186 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.818-447C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925209 | |||||||
| chr8:118925370 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.818-608A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925370 | |||||||
| chr8:118925390 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.818-628C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925390 | |||||||
| chr8:118925424 | T | A | 11 | a0001c0006t0001g0037 a0002c0004t0001g0026 a0002c0004t0001g0027 others(8): Show |
16 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.818-662A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925424 | |||||||
| chr8:118925458 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.818-696C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925458 | |||||||
| chr8:118925458 | G | GA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
10 | HG01167.hp2 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.818-697_818-696ins others(1): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925458 | |||||||
| chr8:118925502 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0032 others(27): Show |
62 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.818-740G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925502 | |||||||
| chr8:118925601 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.818-839A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925601 | |||||||
| chr8:118925812 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.817+682C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118925812 | |||||||
| chr8:118926308 | A | G | 13 | a0001c0003t0002g0015 a0001c0003t0002g0017 a0001c0003t0002g0025 others(10): Show |
27 | HG00639.hp1 HG02145.hp2 HG02280.hp2 others(24): Show |
intron_variant | MODIFIER | c.817+186T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118926308 | |||||||
| chr8:118926314 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.817+180A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118926314 | |||||||
| chr8:118926396 | G | A | 2 | a0002c0004t0001g0055 a0002c0004t0001g0058 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.817+98C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118926396 | |||||||
| chr8:118926486 | T | G | 12 | a0001c0006t0001g0037 a0002c0004t0001g0026 a0002c0004t0001g0027 others(9): Show |
17 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(14): Show |
splice_region_variant&intron_variant | LOW | c.817+8A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 4/4 | chr8 | 118926486 | |||||||
| chr8:118926835 | C | T | 5 | a0001c0003t0004g0022 a0001c0003t0004g0040 a0001c0003t0004g0045 others(2): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.593-117G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118926835 | |||||||
| chr8:118926918 | T | G | 1 | a0002c0002t0001g0083 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.593-200A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118926918 | |||||||
| chr8:118927026 | C | T | 38 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(35): Show |
68 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.593-308G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927026 | |||||||
| chr8:118927223 | C | T | 20 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(17): Show |
32 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.593-505G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927223 | |||||||
| chr8:118927240 | A | C | 8 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
15 | HG01167.hp2 HG01884.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.593-522T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927240 | |||||||
| chr8:118927261 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.593-543T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927261 | |||||||
| chr8:118927265 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.593-547C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927265 | |||||||
| chr8:118927514 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.593-796A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927514 | |||||||
| chr8:118927551 | A | AT | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(105): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.593-834dupA | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927551 | |||||||
| chr8:118927551 | A | ATT | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0024 others(34): Show |
76 | HG00408.hp1 HG00642.hp1 HG01099.hp2 others(73): Show |
intron_variant | MODIFIER | c.593-835_593-834dup others(2): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927551 | |||||||
| chr8:118927551 | A | ATTT | 16 | a0001c0001t0001g0012 a0001c0001t0001g0176 a0001c0001t0001g0177 others(13): Show |
26 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.593-836_593-834dup others(3): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927551 | |||||||
| chr8:118927620 | A | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.593-902T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927620 | |||||||
| chr8:118927701 | C | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(21): Show |
52 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.593-983G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927701 | |||||||
| chr8:118927811 | T | C | 12 | a0001c0006t0001g0037 a0002c0004t0001g0026 a0002c0004t0001g0027 others(9): Show |
17 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.592+927A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118927811 | |||||||
| chr8:118928012 | A | ATG | 31 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0053 others(28): Show |
65 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.592+724_592+725dup others(2): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928012 | |||||||
| chr8:118928012 | A | ATGTG | 16 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0024 others(13): Show |
32 | HG00597.hp2 HG01099.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.592+722_592+725dup others(4): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928012 | |||||||
| chr8:118928012 | A | ATGTGTG | 8 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0160 others(5): Show |
17 | HG02132.hp2 HG03225.hp1 NA18949.hp2 others(14): Show |
intron_variant | MODIFIER | c.592+720_592+725dup others(6): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928012 | |||||||
| chr8:118928012 | A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0146 a0001c0001t0001g0166 a0001c0001t0006g0048 |
4 | HG01071.hp2 NA18952.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+718_592+725dup others(8): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928012 | |||||||
| chr8:118928012 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0165 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.592+716_592+725dup others(10): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928012 | |||||||
| chr8:118928012 | ATG | A | 18 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0133 others(15): Show |
24 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.592+724_592+725del others(2): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928012 | |||||||
| chr8:118928127 | G | A | 2 | a0002c0002t0001g0075 a0002c0002t0001g0088 |
2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.592+611C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928127 | |||||||
| chr8:118928178 | T | C | 38 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(35): Show |
68 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.592+560A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928178 | |||||||
| chr8:118928262 | T | TCTGCCTA | 10 | a0002c0004t0001g0026 a0002c0004t0001g0028 a0002c0004t0001g0029 others(7): Show |
13 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+469_592+475dup others(7): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928262 | |||||||
| chr8:118928404 | A | G | 1 | a0001c0005t0001g0035 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.592+334T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928404 | |||||||
| chr8:118928419 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.592+319C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928419 | |||||||
| chr8:118928681 | CAG | C | 38 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(35): Show |
68 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.592+55_592+56delCT | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 3/4 | chr8 | 118928681 | |||||||
| chr8:118928934 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(372): Show |
splice_region_variant&intron_variant | LOW | c.401-5T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118928934 | |||||||
| chr8:118929038 | A | G | 47 | a0001c0001t0001g0046 a0001c0001t0001g0129 a0001c0001t0001g0138 others(44): Show |
106 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.401-109T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118929038 | |||||||
| chr8:118929068 | T | G | 1 | a0001c0001t0007g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.401-139A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118929068 | |||||||
| chr8:118929125 | C | T | 18 | a0001c0003t0002g0015 a0001c0003t0002g0017 a0001c0003t0002g0025 others(15): Show |
36 | HG00639.hp1 HG02055.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.401-196G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118929125 | |||||||
| chr8:118929231 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.401-302C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118929231 | |||||||
| chr8:118929541 | C | T | 7 | a0001c0005t0001g0021 a0001c0005t0001g0035 a0001c0005t0001g0099 others(4): Show |
10 | HG01261.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.401-612G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118929541 | |||||||
| chr8:118929591 | A | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0032 others(27): Show |
62 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.401-662T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118929591 | |||||||
| chr8:118930177 | G | A | 1 | a0002c0002t0001g0077 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.401-1248C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930177 | |||||||
| chr8:118930268 | A | G | 1 | a0002c0004t0001g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.401-1339T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930268 | |||||||
| chr8:118930374 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.401-1445G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930374 | |||||||
| chr8:118930404 | T | G | 47 | a0001c0001t0001g0046 a0001c0001t0001g0129 a0001c0001t0001g0138 others(44): Show |
106 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.401-1475A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930404 | |||||||
| chr8:118930406 | G | A | 12 | a0001c0006t0001g0037 a0002c0004t0001g0026 a0002c0004t0001g0027 others(9): Show |
17 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.401-1477C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930406 | |||||||
| chr8:118930433 | C | T | 1 | a0001c0001t0007g0110 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.401-1504G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930433 | |||||||
| chr8:118930497 | C | T | 18 | a0001c0003t0002g0015 a0001c0003t0002g0017 a0001c0003t0002g0025 others(15): Show |
36 | HG00639.hp1 HG02055.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.401-1568G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930497 | |||||||
| chr8:118930548 | G | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(36): Show |
90 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.401-1619C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930548 | |||||||
| chr8:118930591 | T | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.401-1662A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930591 | |||||||
| chr8:118930707 | G | A | 2 | a0002c0002t0001g0019 a0002c0002t0005g0091 |
4 | NA18954.hp1 NA18969.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-1778C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930707 | |||||||
| chr8:118930758 | TCTC | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
15 | HG01167.hp2 HG01884.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.401-1832_401-1830d others(5): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930758 | |||||||
| chr8:118930917 | A | C | 1 | a0001c0007t0002g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.401-1988T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118930917 | |||||||
| chr8:118931099 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.400+1832G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118931099 | |||||||
| chr8:118931263 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(372): Show |
intron_variant | MODIFIER | c.400+1668A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118931263 | |||||||
| chr8:118931264 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0174 others(4): Show |
13 | HG01167.hp2 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.400+1667C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118931264 | |||||||
| chr8:118931361 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.400+1570A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118931361 | |||||||
| chr8:118931486 | A | G | 1 | a0002c0002t0001g0073 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.400+1445T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118931486 | |||||||
| chr8:118931632 | T | G | 12 | a0001c0006t0001g0037 a0002c0004t0001g0026 a0002c0004t0001g0027 others(9): Show |
17 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.400+1299A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118931632 | |||||||
| chr8:118931675 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0098 others(4): Show |
9 | HG00099.hp2 HG00741.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.400+1256T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118931675 | |||||||
| chr8:118931891 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.400+1040C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118931891 | |||||||
| chr8:118932051 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.400+880T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932051 | |||||||
| chr8:118932172 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.400+759T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932172 | |||||||
| chr8:118932212 | C | T | 18 | a0001c0003t0002g0015 a0001c0003t0002g0017 a0001c0003t0002g0025 others(15): Show |
36 | HG00639.hp1 HG02055.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.400+719G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932212 | |||||||
| chr8:118932555 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.400+376T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932555 | |||||||
| chr8:118932634 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.400+297G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932634 | |||||||
| chr8:118932640 | T | G | 1 | a0001c0003t0003g0041 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.400+291A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932640 | |||||||
| chr8:118932661 | T | TA | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.400+269dupT | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932661 | |||||||
| chr8:118932661 | TA | T | 19 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(16): Show |
30 | HG00099.hp1 HG00642.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.400+269delT | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932661 | |||||||
| chr8:118932728 | A | C | 1 | a0002c0002t0001g0018 | 3 | NA18974.hp1 NA19001.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.400+203T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932728 | |||||||
| chr8:118932764 | A | G | 12 | a0001c0006t0001g0037 a0002c0004t0001g0026 a0002c0004t0001g0027 others(9): Show |
17 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.400+167T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932764 | |||||||
| chr8:118932865 | C | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0193 |
3 | HG02074.hp2 HG02165.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.400+66G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932865 | |||||||
| chr8:118932927 | G | A | 12 | a0001c0006t0001g0037 a0002c0004t0001g0026 a0002c0004t0001g0027 others(9): Show |
17 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(14): Show |
splice_region_variant&intron_variant | LOW | c.400+4C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 2/4 | chr8 | 118932927 | |||||||
| chr8:118933307 | G | A | 13 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
24 | HG00639.hp1 HG01167.hp2 HG01884.hp1 others(21): Show |
splice_region_variant&intron_variant | LOW | c.31-7C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933307 | |||||||
| chr8:118933491 | G | A | 13 | a0001c0001t0001g0012 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
20 | HG01167.hp2 HG01884.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-191C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933491 | |||||||
| chr8:118933566 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.31-266T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933566 | |||||||
| chr8:118933694 | A | T | 2 | a0002c0002t0001g0089 a0002c0002t0001g0090 |
2 | HG00423.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.31-394T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933694 | |||||||
| chr8:118933740 | G | A | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(20): Show |
48 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.31-440C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933740 | |||||||
| chr8:118933770 | TTTAAAAC others(1): Show |
T | 12 | a0001c0006t0001g0037 a0002c0004t0001g0026 a0002c0004t0001g0027 others(9): Show |
17 | HG00099.hp1 HG00642.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-478_31-471delTG others(6): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933770 | |||||||
| chr8:118933795 | C | T | 1 | a0002c0002t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.31-495G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933795 | |||||||
| chr8:118933796 | G | A | 11 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0003t0003g0041 others(8): Show |
21 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-496C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933796 | |||||||
| chr8:118933902 | T | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(149): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.31-602A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933902 | |||||||
| chr8:118933933 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-633A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933933 | |||||||
| chr8:118933985 | C | T | 1 | a0002c0002t0001g0070 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.31-685G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118933985 | |||||||
| chr8:118934150 | T | G | 4 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0007t0002g0185 others(1): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-850A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934150 | |||||||
| chr8:118934321 | G | A | 1 | a0001c0006t0001g0037 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.31-1021C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934321 | |||||||
| chr8:118934371 | A | T | 5 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0003t0003g0041 others(2): Show |
11 | HG02145.hp2 HG02486.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-1071T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934371 | |||||||
| chr8:118934417 | C | A | 46 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0003t0003g0041 others(43): Show |
111 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.31-1117G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934417 | |||||||
| chr8:118934422 | C | T | 1 | a0001c0003t0003g0041 | 2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.31-1122G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934422 | |||||||
| chr8:118934568 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(89): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.31-1268C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934568 | |||||||
| chr8:118934719 | C | A | 6 | a0001c0003t0004g0022 a0001c0003t0004g0040 a0001c0003t0004g0045 others(3): Show |
10 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-1419G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934719 | |||||||
| chr8:118934854 | C | T | 4 | a0002c0004t0001g0028 a0002c0004t0001g0055 a0002c0004t0001g0057 others(1): Show |
5 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-1554G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934854 | |||||||
| chr8:118934963 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.31-1663C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934963 | |||||||
| chr8:118934972 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.31-1672C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118934972 | |||||||
| chr8:118935029 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.31-1729C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935029 | |||||||
| chr8:118935177 | G | A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(25): Show |
54 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.31-1877C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935177 | |||||||
| chr8:118935191 | T | A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0032 others(26): Show |
60 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.31-1891A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935191 | |||||||
| chr8:118935328 | C | A | 1 | a0002c0004t0001g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.31-2028G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935328 | |||||||
| chr8:118935337 | C | T | 1 | a0001c0003t0002g0025 | 3 | HG02486.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.31-2037G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935337 | |||||||
| chr8:118935344 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.31-2044A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935344 | |||||||
| chr8:118935412 | A | G | 35 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0014 others(32): Show |
90 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.31-2112T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935412 | |||||||
| chr8:118935437 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.31-2137C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935437 | |||||||
| chr8:118935499 | A | G | 2 | a0001c0003t0003g0016 a0001c0003t0003g0142 |
6 | HG02451.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-2199T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935499 | |||||||
| chr8:118935534 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.31-2234A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935534 | |||||||
| chr8:118935561 | ACTTTC | A | 46 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0003t0003g0041 others(43): Show |
111 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.31-2266_31-2262del others(5): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935561 | |||||||
| chr8:118935571 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(89): Show |
192 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.31-2271G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935571 | |||||||
| chr8:118935576 | ATAAT | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0179 |
3 | HG02257.hp2 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.31-2280_31-2277del others(4): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935576 | |||||||
| chr8:118935589 | C | T | 45 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0003t0003g0041 others(42): Show |
110 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.31-2289G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935589 | |||||||
| chr8:118935594 | A | T | 1 | a0002c0002t0001g0069 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.31-2294T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935594 | |||||||
| chr8:118935682 | T | G | 1 | a0002c0002t0001g0078 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.31-2382A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935682 | |||||||
| chr8:118935807 | AGAGG | A | 35 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0014 others(32): Show |
90 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.31-2511_31-2508del others(4): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935807 | |||||||
| chr8:118935834 | C | T | 1 | a0001c0005t0001g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.31-2534G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935834 | |||||||
| chr8:118935871 | G | C | 1 | a0002c0002t0001g0079 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.31-2571C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118935871 | |||||||
| chr8:118936023 | T | G | 1 | a0002c0002t0001g0079 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.31-2723A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936023 | |||||||
| chr8:118936164 | G | A | 11 | a0002c0004t0001g0026 a0002c0004t0001g0027 a0002c0004t0001g0028 others(8): Show |
15 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-2864C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936164 | |||||||
| chr8:118936212 | C | G | 2 | a0001c0003t0003g0016 a0001c0003t0003g0142 |
6 | HG02451.hp1 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-2912G>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936212 | |||||||
| chr8:118936301 | T | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0032 others(44): Show |
88 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.31-3001A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936301 | |||||||
| chr8:118936520 | C | T | 1 | a0002c0002t0001g0083 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.31-3220G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936520 | |||||||
| chr8:118936521 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.31-3221C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936521 | |||||||
| chr8:118936561 | T | A | 1 | a0002c0002t0001g0080 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.31-3261A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936561 | |||||||
| chr8:118936618 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0171 |
3 | NA18953.hp2 NA18998.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.31-3318A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936618 | |||||||
| chr8:118936667 | C | CCTT | 4 | a0001c0003t0003g0112 a0001c0003t0003g0113 a0001c0003t0003g0114 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3370_31-3368dup others(3): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936667 | |||||||
| chr8:118936759 | G | A | 6 | a0001c0003t0004g0022 a0001c0003t0004g0040 a0001c0003t0004g0045 others(3): Show |
10 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-3459C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936759 | |||||||
| chr8:118936781 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.31-3481G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936781 | |||||||
| chr8:118936838 | C | T | 1 | a0002c0002t0001g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.31-3538G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936838 | |||||||
| chr8:118936872 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(92): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.31-3572T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936872 | |||||||
| chr8:118936926 | T | C | 57 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0003t0003g0041 others(54): Show |
126 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.31-3626A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118936926 | |||||||
| chr8:118937086 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-3786G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118937086 | |||||||
| chr8:118937207 | G | C | 11 | a0002c0004t0001g0026 a0002c0004t0001g0027 a0002c0004t0001g0028 others(8): Show |
15 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-3907C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118937207 | |||||||
| chr8:118937269 | T | A | 1 | a0002c0002t0001g0080 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.31-3969A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118937269 | |||||||
| chr8:118937513 | C | T | 1 | a0002c0002t0001g0067 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.31-4213G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118937513 | |||||||
| chr8:118937517 | A | C | 57 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0003t0003g0041 others(54): Show |
126 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.31-4217T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118937517 | |||||||
| chr8:118937529 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0033 others(21): Show |
54 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.31-4229T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118937529 | |||||||
| chr8:118937873 | A | C | 1 | a0001c0003t0004g0040 | 2 | HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.31-4573T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118937873 | |||||||
| chr8:118937955 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.31-4655T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118937955 | |||||||
| chr8:118937968 | TATA | T | 7 | a0001c0001t0001g0106 a0001c0005t0001g0021 a0001c0005t0001g0035 others(4): Show |
11 | HG01167.hp1 HG01169.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-4671_31-4669del others(3): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118937968 | |||||||
| chr8:118938429 | C | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0032 others(101): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.31-5129G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938429 | |||||||
| chr8:118938458 | C | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0032 others(44): Show |
88 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.31-5158G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938458 | |||||||
| chr8:118938542 | C | T | 57 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0003t0003g0041 others(54): Show |
126 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.31-5242G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938542 | |||||||
| chr8:118938543 | A | C | 11 | a0002c0004t0001g0026 a0002c0004t0001g0027 a0002c0004t0001g0028 others(8): Show |
15 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-5243T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938543 | |||||||
| chr8:118938543 | A | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(138): Show |
308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.31-5243T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938543 | |||||||
| chr8:118938549 | T | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0032 others(44): Show |
88 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.31-5249A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938549 | |||||||
| chr8:118938634 | T | G | 3 | a0001c0005t0001g0021 a0001c0005t0001g0035 a0001c0005t0001g0099 |
6 | HG01261.hp2 HG01891.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-5334A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938634 | |||||||
| chr8:118938766 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(178): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(375): Show |
intron_variant | MODIFIER | c.31-5466T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938766 | |||||||
| chr8:118938825 | T | G | 11 | a0002c0004t0001g0026 a0002c0004t0001g0027 a0002c0004t0001g0028 others(8): Show |
15 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-5525A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938825 | |||||||
| chr8:118938832 | G | A | 2 | a0002c0002t0001g0082 a0002c0002t0001g0083 |
2 | NA18982.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.31-5532C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938832 | |||||||
| chr8:118938902 | C | T | 1 | a0001c0003t0003g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.31-5602G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938902 | |||||||
| chr8:118938980 | T | C | 2 | a0001c0003t0002g0017 a0001c0003t0002g0025 |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-5680A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118938980 | |||||||
| chr8:118939096 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.31-5796C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939096 | |||||||
| chr8:118939096 | G | C | 1 | a0001c0001t0001g0008 | 8 | NA18945.hp1 NA18960.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-5796C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939096 | |||||||
| chr8:118939280 | C | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0032 others(41): Show |
84 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.31-5980G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939280 | |||||||
| chr8:118939417 | G | A | 1 | a0001c0001t0001g0008 | 8 | NA18945.hp1 NA18960.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-6117C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939417 | |||||||
| chr8:118939453 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.31-6153A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939453 | |||||||
| chr8:118939534 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(94): Show |
213 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.31-6234C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939534 | |||||||
| chr8:118939543 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.31-6243C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939543 | |||||||
| chr8:118939606 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0109 a0001c0001t0001g0111 others(1): Show |
5 | HG00639.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-6306C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939606 | |||||||
| chr8:118939661 | A | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
228 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.31-6361T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939661 | |||||||
| chr8:118939684 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.31-6384C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939684 | |||||||
| chr8:118939780 | G | A | 1 | a0001c0009t0009g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.31-6480C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939780 | |||||||
| chr8:118939887 | T | A | 11 | a0002c0004t0001g0026 a0002c0004t0001g0027 a0002c0004t0001g0028 others(8): Show |
15 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-6587A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939887 | |||||||
| chr8:118939973 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(92): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.31-6673T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118939973 | |||||||
| chr8:118940018 | A | T | 1 | a0001c0005t0001g0104 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.31-6718T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940018 | |||||||
| chr8:118940186 | G | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(38): Show |
93 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.31-6886C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940186 | |||||||
| chr8:118940264 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.31-6964C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940264 | |||||||
| chr8:118940266 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.31-6966C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940266 | |||||||
| chr8:118940438 | T | C | 4 | a0001c0003t0003g0112 a0001c0003t0003g0113 a0001c0003t0003g0114 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-7138A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940438 | |||||||
| chr8:118940511 | A | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.31-7211T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940511 | |||||||
| chr8:118940526 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.31-7226G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940526 | |||||||
| chr8:118940581 | A | G | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(25): Show |
54 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.31-7281T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940581 | |||||||
| chr8:118940792 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.31-7492C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940792 | |||||||
| chr8:118940919 | A | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(18): Show |
44 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.31-7619T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118940919 | |||||||
| chr8:118941040 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.31-7740A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941040 | |||||||
| chr8:118941129 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.31-7829C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941129 | |||||||
| chr8:118941229 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(88): Show |
191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.31-7929T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941229 | |||||||
| chr8:118941326 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-8026C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941326 | |||||||
| chr8:118941411 | T | C | 6 | a0001c0003t0004g0022 a0001c0003t0004g0040 a0001c0003t0004g0045 others(3): Show |
10 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-8111A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941411 | |||||||
| chr8:118941504 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0128 others(3): Show |
15 | HG02040.hp1 HG02523.hp1 NA18940.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-8204T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941504 | |||||||
| chr8:118941687 | CAATT | C | 6 | a0001c0003t0004g0022 a0001c0003t0004g0040 a0001c0003t0004g0045 others(3): Show |
10 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-8391_31-8388del others(4): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941687 | |||||||
| chr8:118941726 | A | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0178 others(1): Show |
6 | HG02257.hp2 HG02622.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-8426T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941726 | |||||||
| chr8:118941727 | C | A | 1 | a0002c0002t0001g0083 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.31-8427G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941727 | |||||||
| chr8:118941740 | CAAG | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(23): Show |
52 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.31-8443_31-8441del others(3): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941740 | |||||||
| chr8:118941807 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.31-8507A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941807 | |||||||
| chr8:118941869 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
263 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.31-8569C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118941869 | |||||||
| chr8:118942040 | G | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.31-8740C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942040 | |||||||
| chr8:118942238 | GCC | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.31-8940_31-8939del others(2): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942238 | |||||||
| chr8:118942245 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.31-8945G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942245 | |||||||
| chr8:118942444 | T | C | 3 | a0001c0003t0004g0045 a0001c0003t0004g0148 a0001c0005t0001g0147 |
4 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-9144A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942444 | |||||||
| chr8:118942603 | T | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.30+9189A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942603 | |||||||
| chr8:118942711 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0134 |
4 | HG00438.hp2 NA18972.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9081C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942711 | |||||||
| chr8:118942756 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(18): Show |
44 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.30+9036G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942756 | |||||||
| chr8:118942789 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.30+9003C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942789 | |||||||
| chr8:118942828 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.30+8964C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942828 | |||||||
| chr8:118942841 | A | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02165.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.30+8951T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942841 | |||||||
| chr8:118942872 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.30+8920C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942872 | |||||||
| chr8:118942900 | T | C | 1 | a0001c0006t0001g0037 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.30+8892A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942900 | |||||||
| chr8:118942938 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+8854A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942938 | |||||||
| chr8:118942940 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+8852A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942940 | |||||||
| chr8:118942941 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+8851A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942941 | |||||||
| chr8:118942950 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.30+8842G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942950 | |||||||
| chr8:118942985 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.30+8807G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118942985 | |||||||
| chr8:118943101 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.30+8691C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118943101 | |||||||
| chr8:118943111 | A | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+8681T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118943111 | |||||||
| chr8:118943336 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.30+8456A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118943336 | |||||||
| chr8:118943551 | G | T | 4 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0007t0002g0185 others(1): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+8241C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118943551 | |||||||
| chr8:118943613 | T | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+8179A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118943613 | |||||||
| chr8:118943657 | G | A | 1 | a0001c0001t0001g0050 | 2 | NA19003.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.30+8135C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118943657 | |||||||
| chr8:118943703 | T | C | 1 | a0002c0002t0001g0084 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.30+8089A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118943703 | |||||||
| chr8:118943710 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0187 others(6): Show |
32 | HG01069.hp1 HG01109.hp1 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.30+8082G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118943710 | |||||||
| chr8:118943804 | A | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+7988T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118943804 | |||||||
| chr8:118944015 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.30+7777C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944015 | |||||||
| chr8:118944020 | TGAA | T | 4 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0007t0002g0185 others(1): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+7769_30+7771del others(3): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944020 | |||||||
| chr8:118944039 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.30+7753C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944039 | |||||||
| chr8:118944066 | T | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0047 others(14): Show |
45 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.30+7726A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944066 | |||||||
| chr8:118944080 | T | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+7712A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944080 | |||||||
| chr8:118944139 | G | T | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(23): Show |
52 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.30+7653C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944139 | |||||||
| chr8:118944266 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(17): Show |
49 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.30+7526C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944266 | |||||||
| chr8:118944287 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.30+7505T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944287 | |||||||
| chr8:118944311 | T | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
10 | HG01167.hp2 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+7481A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944311 | |||||||
| chr8:118944367 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.30+7425G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944367 | |||||||
| chr8:118944467 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+7325C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944467 | |||||||
| chr8:118944538 | A | G | 11 | a0002c0004t0001g0026 a0002c0004t0001g0027 a0002c0004t0001g0028 others(8): Show |
15 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+7254T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944538 | |||||||
| chr8:118944666 | G | A | 10 | a0002c0004t0001g0026 a0002c0004t0001g0028 a0002c0004t0001g0029 others(7): Show |
13 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+7126C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944666 | |||||||
| chr8:118944694 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0133 |
3 | HG00408.hp2 HG00621.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.30+7098G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944694 | |||||||
| chr8:118944773 | C | T | 1 | a0002c0004t0001g0026 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.30+7019G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944773 | |||||||
| chr8:118944774 | G | A | 3 | a0002c0002t0001g0009 a0002c0002t0001g0086 a0002c0002t0011g0085 |
9 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+7018C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944774 | |||||||
| chr8:118944822 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.30+6970T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944822 | |||||||
| chr8:118944847 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.30+6945T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944847 | |||||||
| chr8:118944934 | G | A | 1 | a0001c0007t0002g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.30+6858C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118944934 | |||||||
| chr8:118945209 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+6583G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945209 | |||||||
| chr8:118945276 | T | TTG | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0098 others(3): Show |
8 | HG00099.hp2 HG00741.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+6514_30+6515dup others(2): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945276 | |||||||
| chr8:118945276 | T | TTGTGTG | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
255 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.30+6510_30+6515dup others(6): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945276 | |||||||
| chr8:118945280 | G | GT | 4 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0007t0002g0185 others(1): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+6511dupA | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945280 | |||||||
| chr8:118945281 | T | TC | 20 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(17): Show |
49 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.30+6510_30+6511ins others(1): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945281 | |||||||
| chr8:118945382 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.30+6410T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945382 | |||||||
| chr8:118945386 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.30+6406T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945386 | |||||||
| chr8:118945400 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0096 others(9): Show |
37 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.30+6392A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945400 | |||||||
| chr8:118945476 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.30+6316T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945476 | |||||||
| chr8:118945903 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.30+5889C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118945903 | |||||||
| chr8:118946180 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.30+5612A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118946180 | |||||||
| chr8:118946316 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.30+5476G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118946316 | |||||||
| chr8:118946360 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA18966.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.30+5432G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118946360 | |||||||
| chr8:118946468 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.30+5324G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118946468 | |||||||
| chr8:118946518 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.30+5274A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118946518 | |||||||
| chr8:118946684 | G | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.30+5108C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118946684 | |||||||
| chr8:118946686 | C | T | 1 | a0002c0004t0001g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.30+5106G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118946686 | |||||||
| chr8:118946837 | G | T | 1 | a0002c0002t0001g0089 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.30+4955C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118946837 | |||||||
| chr8:118947039 | A | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(17): Show |
49 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.30+4753T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947039 | |||||||
| chr8:118947150 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+4642C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947150 | |||||||
| chr8:118947189 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.30+4603T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947189 | |||||||
| chr8:118947212 | CTGGCAGT others(38): Show |
C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.30+4535_30+4579del others(45): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947212 | |||||||
| chr8:118947244 | A | G | 4 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0007t0002g0185 others(1): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+4548T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947244 | |||||||
| chr8:118947355 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0122 a0001c0001t0001g0126 others(1): Show |
10 | HG00544.hp1 HG02080.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+4437T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947355 | |||||||
| chr8:118947377 | A | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0178 others(1): Show |
6 | HG02257.hp2 HG02622.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+4415T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947377 | |||||||
| chr8:118947384 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.30+4408A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947384 | |||||||
| chr8:118947418 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.30+4374G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947418 | |||||||
| chr8:118947574 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(26): Show |
56 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.30+4218G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947574 | |||||||
| chr8:118947671 | C | T | 3 | a0001c0003t0004g0022 a0001c0003t0004g0040 a0001c0003t0008g0125 |
6 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+4121G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947671 | |||||||
| chr8:118947680 | T | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+4112A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947680 | |||||||
| chr8:118947682 | T | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.30+4110A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947682 | |||||||
| chr8:118947686 | A | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.30+4106T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947686 | |||||||
| chr8:118947691 | A | C | 1 | a0002c0002t0001g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.30+4101T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947691 | |||||||
| chr8:118947717 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA19072.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.30+4075T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947717 | |||||||
| chr8:118947816 | T | G | 11 | a0002c0004t0001g0026 a0002c0004t0001g0027 a0002c0004t0001g0028 others(8): Show |
15 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+3976A>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118947816 | |||||||
| chr8:118948097 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.30+3695T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948097 | |||||||
| chr8:118948112 | A | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+3680T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948112 | |||||||
| chr8:118948181 | T | A | 1 | a0003c0008t0001g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.30+3611A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948181 | |||||||
| chr8:118948189 | C | T | 1 | a0001c0005t0001g0099 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.30+3603G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948189 | |||||||
| chr8:118948194 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.30+3598C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948194 | |||||||
| chr8:118948308 | A | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.30+3484T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948308 | |||||||
| chr8:118948422 | C | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.30+3370G>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948422 | |||||||
| chr8:118948480 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.30+3312C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948480 | |||||||
| chr8:118948607 | T | TAAG | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.30+3182_30+3184dup others(3): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948607 | |||||||
| chr8:118948739 | C | T | 1 | a0002c0004t0001g0055 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.30+3053G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948739 | |||||||
| chr8:118948759 | TAAAAC | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0098 |
3 | HG00099.hp2 HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.30+3028_30+3032del others(5): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948759 | |||||||
| chr8:118948792 | C | A | 1 | a0002c0002t0001g0086 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.30+3000G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948792 | |||||||
| chr8:118948792 | C | CA | 139 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.30+2999dupT | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948792 | |||||||
| chr8:118948826 | G | A | 1 | a0002c0002t0001g0087 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.30+2966C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948826 | |||||||
| chr8:118948838 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.30+2954T>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948838 | |||||||
| chr8:118948879 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0023 others(26): Show |
55 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.30+2913C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948879 | |||||||
| chr8:118948980 | A | C | 1 | a0001c0001t0001g0038 | 2 | HG03490.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.30+2812T>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118948980 | |||||||
| chr8:118949199 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+2593G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118949199 | |||||||
| chr8:118949283 | A | G | 1 | a0002c0002t0001g0063 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.30+2509T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118949283 | |||||||
| chr8:118949781 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.30+2011C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118949781 | |||||||
| chr8:118949881 | T | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+1911A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118949881 | |||||||
| chr8:118949927 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.30+1865C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118949927 | |||||||
| chr8:118950050 | C | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
6 | HG01891.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+1742G>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950050 | |||||||
| chr8:118950060 | G | C | 11 | a0002c0004t0001g0026 a0002c0004t0001g0027 a0002c0004t0001g0028 others(8): Show |
15 | HG00099.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+1732C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950060 | |||||||
| chr8:118950177 | ATGTT | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
10 | HG01167.hp2 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+1611_30+1614del others(4): Show |
TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950177 | |||||||
| chr8:118950247 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
263 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.30+1545G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950247 | |||||||
| chr8:118950333 | C | A | 4 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0007t0002g0185 others(1): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+1459G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950333 | |||||||
| chr8:118950353 | A | G | 1 | a0002c0002t0001g0062 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.30+1439T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950353 | |||||||
| chr8:118950420 | T | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+1372A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950420 | |||||||
| chr8:118950486 | G | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0178 others(1): Show |
6 | HG02257.hp2 HG02622.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+1306C>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950486 | |||||||
| chr8:118950703 | T | C | 1 | a0001c0001t0001g0024 | 3 | NA18972.hp1 NA19010.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.30+1089A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950703 | |||||||
| chr8:118950824 | C | A | 4 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0007t0002g0185 others(1): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+968G>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118950824 | |||||||
| chr8:118951028 | T | C | 1 | a0001c0001t0001g0052 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.30+764A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951028 | |||||||
| chr8:118951186 | T | A | 1 | a0001c0001t0001g0180 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.30+606A>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951186 | |||||||
| chr8:118951246 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.30+546C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951246 | |||||||
| chr8:118951308 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.30+484T>C | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951308 | |||||||
| chr8:118951405 | T | C | 1 | a0002c0002t0001g0088 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.30+387A>G | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951405 | |||||||
| chr8:118951520 | T | TTC | 5 | a0001c0001t0001g0184 a0002c0002t0001g0019 a0002c0002t0001g0089 others(2): Show |
7 | HG00423.hp2 HG00673.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+270_30+271dupGA | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951520 | |||||||
| chr8:118951520 | TTC | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.30+270_30+271delGA | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951520 | |||||||
| chr8:118951604 | G | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0032 others(38): Show |
80 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.30+188C>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951604 | |||||||
| chr8:118951700 | C | T | 4 | a0001c0003t0002g0017 a0001c0003t0002g0025 a0001c0007t0002g0185 others(1): Show |
9 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+92G>A | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951700 | |||||||
| chr8:118951777 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0053 others(21): Show |
58 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+15C>T | TNFRSF11B | ENSG00000164761.9 | transcript | ENST00000297350.9 | protein_coding | 1/4 | chr8 | 118951777 |