Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57093 |
| ensemblid | ENSG00000168930.13 |
| hgncid | 13431 |
| symbol | TRIM49 |
| name | tripartite motif containing 49 |
| refseq_nuc | NM_020358.2 |
| refseq_prot | NP_065091.1 |
| ensembl_nuc | ENST00000329758.5 |
| ensembl_prot | ENSP00000327604.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 89797655 |
| end | 89808575 |
| strand | - |
| ver | v1.2 |
| region | chr11:89797655-89808575 |
| region5000 | chr11:89792655-89813575 |
| regionname0 | TRIM49_chr11_89797655_89808575 |
| regionname5000 | TRIM49_chr11_89792655_89813575 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 452 | 69 | 7 | 16 | 28 | 5 | 12 | 22 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0002 | 0/0 | 452 | 69 | 2 | 16 | 37 | 6 | 8 | 25 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0003 | 0/0 | 452 | 49 | 16 | 9 | 18 | 1 | 5 | 12 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0004 | 0/0 | 452 | 33 | 1 | 4 | 25 | 0 | 3 | 24 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0005 | 0/0 | 452 | 11 | 0 | 0 | 7 | 0 | 4 | 7 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0006 | 0/0 | 452 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0007 | 0/0 | 452 | 4 | 0 | 0 | 0 | 2 | 2 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0008 | 0/0 | 452 | 3 | 1 | 0 | 1 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0009 | 0/0 | 452 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0010 | 0/0 | 452 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0011 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0012 | 0/0 | 452 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0013 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| a0014 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | MNSGI others(447): Show |
chr11 | 89792655 | 89813575 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 1356 | 65 | 6 | 14 | 27 | 5 | 12 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0001c0007 | 0/0 | 1356 | 4 | 1 | 2 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0002c0001 | 0/0 | 1356 | 69 | 2 | 16 | 37 | 6 | 8 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0003c0003 | 0/0 | 1356 | 45 | 12 | 9 | 18 | 1 | 5 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0003c0009 | 0/0 | 1356 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0003c0018 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0004c0004 | 0/0 | 1356 | 33 | 1 | 4 | 25 | 0 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0005c0005 | 0/0 | 1356 | 11 | 0 | 0 | 7 | 0 | 4 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0006c0008 | 0/0 | 1356 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0006c0013 | 0/0 | 1356 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0006c0014 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0007c0006 | 0/0 | 1356 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0008c0012 | 0/0 | 1356 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0008c0017 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0009c0011 | 0/0 | 1356 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0010c0010 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0011c0020 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0012c0015 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0013c0019 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 | ||
| a0014c0016 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | ATGAA others(1351): Show |
chr11 | 89792655 | 89813575 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 1/0 | 2163 | 63 | 5 | 14 | 26 | 5 | 12 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0001c0002t0004 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0001c0002t0013 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0001c0007t0004 | 0/0 | 2163 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0001c0007t0009 | 0/0 | 2163 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0002c0001t0001 | 0/0 | 2163 | 68 | 2 | 16 | 37 | 6 | 7 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0002c0001t0009 | 0/0 | 2163 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0003c0003t0002 | 0/0 | 2163 | 13 | 8 | 1 | 1 | 0 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0003c0003t0003 | 0/0 | 2163 | 22 | 0 | 7 | 13 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0003c0003t0005 | 0/0 | 2163 | 6 | 4 | 1 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0003c0003t0006 | 0/0 | 2164 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2159): Show |
chr11 | 89792655 | 89813575 |
| a0003c0009t0002 | 0/0 | 2163 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0003c0018t0002 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0004c0004t0002 | 0/0 | 2163 | 32 | 1 | 4 | 24 | 0 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0004c0004t0012 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0005c0005t0004 | 0/0 | 2163 | 11 | 0 | 0 | 7 | 0 | 4 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0006c0008t0004 | 0/0 | 2163 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0006c0013t0010 | 0/0 | 2163 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0006c0014t0011 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0007c0006t0007 | 0/0 | 2163 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0008c0012t0008 | 0/0 | 2163 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0008c0017t0008 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0009c0011t0001 | 0/0 | 2163 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0010c0010t0006 | 0/0 | 2164 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2159): Show |
chr11 | 89792655 | 89813575 |
| a0011c0020t0002 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0012c0015t0004 | 0/0 | 2163 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0013c0019t0001 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| a0014c0016t0002 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | CTAAT others(2158): Show |
chr11 | 89792655 | 89813575 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0002 | 1/0 | 22 | 1 | 7 | 7 | 3 | 3 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0004 | 0/0 | 8 | 1 | 0 | 2 | 1 | 4 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0008 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0002t0013g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0007t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0007t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0007t0009g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0001c0007t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0001 | 0/0 | 36 | 1 | 9 | 18 | 4 | 4 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0002c0001t0009g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0002g0009 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0006 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0006g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0003t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0009t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0009t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0009t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0003c0018t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0003 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0004c0004t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0005c0005t0004g0007 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0005c0005t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0005c0005t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0005c0005t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0005c0005t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0005c0005t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0006c0008t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0006c0008t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0006c0008t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0006c0008t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0006c0013t0010g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0006c0014t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0007c0006t0007g0011 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0008c0012t0008g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0008c0017t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0009c0011t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0010c0010t0006g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0011c0020t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0012c0015t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0013c0019t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| a0014c0016t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0013 | EUR | GBR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0008 | EUR | GBR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00280 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | FIN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00408 | hp2 | a0003 | c0003 | t0006 | g0071 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00609 | hp1 | a0003 | c0003 | t0003 | g0025 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00621 | hp1 | a0003 | c0003 | t0003 | g0063 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0090 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00735 | hp1 | a0002 | c0001 | t0001 | g0013 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0078 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01081 | hp2 | a0006 | c0008 | t0004 | g0111 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01099 | hp2 | a0003 | c0003 | t0002 | g0035 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0091 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0052 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01192 | hp1 | a0002 | c0001 | t0001 | g0079 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01192 | hp2 | a0003 | c0003 | t0005 | g0039 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01243 | hp2 | a0001 | c0007 | t0009 | g0105 | AMR | PUR | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01257 | hp2 | a0003 | c0003 | t0003 | g0056 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01261 | hp1 | a0001 | c0007 | t0004 | g0116 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01261 | hp2 | a0002 | c0001 | t0001 | g0092 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01361 | hp2 | a0004 | c0004 | t0002 | g0024 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01496 | hp1 | a0003 | c0003 | t0003 | g0006 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01496 | hp2 | a0004 | c0004 | t0002 | g0024 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0013 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01515 | hp2 | a0002 | c0001 | t0001 | g0001 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01516 | hp2 | a0007 | c0006 | t0007 | g0011 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01517 | hp1 | a0007 | c0006 | t0007 | g0011 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | IBS | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01884 | hp1 | a0003 | c0003 | t0002 | g0054 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01891 | hp2 | a0003 | c0003 | t0002 | g0036 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01975 | hp1 | a0003 | c0003 | t0003 | g0017 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01975 | hp2 | a0003 | c0003 | t0003 | g0065 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01981 | hp2 | a0004 | c0004 | t0002 | g0015 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01993 | hp1 | a0003 | c0003 | t0003 | g0072 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01993 | hp2 | a0003 | c0003 | t0003 | g0017 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02004 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02004 | hp2 | a0004 | c0004 | t0002 | g0051 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02015 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02040 | hp1 | a0003 | c0003 | t0003 | g0064 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02056 | hp2 | a0003 | c0003 | t0003 | g0070 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0098 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0086 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0083 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02129 | hp1 | a0002 | c0001 | t0001 | g0102 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02129 | hp2 | a0008 | c0012 | t0008 | g0019 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02132 | hp2 | a0004 | c0004 | t0002 | g0046 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02135 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02293 | hp1 | a0003 | c0003 | t0003 | g0067 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PEL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02602 | hp2 | a0005 | c0005 | t0004 | g0119 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02683 | hp2 | a0005 | c0005 | t0004 | g0114 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02738 | hp2 | a0009 | c0011 | t0001 | g0029 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02809 | hp1 | a0001 | c0007 | t0004 | g0110 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02809 | hp2 | a0003 | c0009 | t0002 | g0076 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02886 | hp1 | a0003 | c0009 | t0002 | g0075 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02886 | hp2 | a0003 | c0003 | t0002 | g0010 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02895 | hp1 | a0003 | c0003 | t0002 | g0009 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02895 | hp2 | a0006 | c0008 | t0004 | g0109 | AFR | GWD | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0112 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02922 | hp2 | a0006 | c0013 | t0010 | g0031 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02965 | hp1 | a0006 | c0008 | t0004 | g0107 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02965 | hp2 | a0003 | c0003 | t0002 | g0010 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03017 | hp1 | a0005 | c0005 | t0004 | g0007 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0027 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03130 | hp1 | a0006 | c0014 | t0011 | g0042 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03130 | hp2 | a0011 | c0020 | t0002 | g0057 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03195 | hp1 | a0003 | c0018 | t0002 | g0043 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03195 | hp2 | a0003 | c0003 | t0005 | g0020 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03225 | hp1 | a0003 | c0003 | t0002 | g0032 | AFR | MSL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | MSL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03516 | hp1 | a0003 | c0003 | t0002 | g0010 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03516 | hp2 | a0006 | c0008 | t0004 | g0108 | AFR | ESN | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0013 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03654 | hp2 | a0009 | c0011 | t0001 | g0029 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0095 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03669 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0096 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03688 | hp2 | a0008 | c0012 | t0008 | g0019 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03704 | hp1 | a0007 | c0006 | t0007 | g0011 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03710 | hp2 | a0003 | c0003 | t0002 | g0009 | SAS | PJL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03831 | hp1 | a0005 | c0005 | t0004 | g0115 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03927 | hp2 | a0004 | c0004 | t0002 | g0015 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03942 | hp2 | a0003 | c0003 | t0002 | g0009 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG04115 | hp1 | a0012 | c0015 | t0004 | g0120 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG04115 | hp2 | a0003 | c0003 | t0003 | g0068 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG04184 | hp1 | a0003 | c0003 | t0003 | g0006 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG04184 | hp2 | a0004 | c0004 | t0002 | g0003 | SAS | BEB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG04199 | hp2 | a0002 | c0001 | t0009 | g0113 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0097 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG04228 | hp2 | a0003 | c0003 | t0002 | g0037 | SAS | STU | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | CHB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18939 | hp2 | a0004 | c0004 | t0002 | g0022 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18949 | hp2 | a0004 | c0004 | t0012 | g0047 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18950 | hp1 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18950 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18953 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18953 | hp2 | a0004 | c0004 | t0002 | g0016 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18954 | hp1 | a0013 | c0019 | t0001 | g0104 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18959 | hp2 | a0003 | c0003 | t0006 | g0021 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18960 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18960 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18961 | hp1 | a0010 | c0010 | t0006 | g0026 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18964 | hp1 | a0004 | c0004 | t0002 | g0049 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18964 | hp2 | a0004 | c0004 | t0002 | g0044 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0085 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18965 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18966 | hp1 | a0003 | c0003 | t0006 | g0021 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18968 | hp1 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18973 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18977 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18977 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18978 | hp2 | a0004 | c0004 | t0002 | g0016 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18981 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18981 | hp2 | a0014 | c0016 | t0002 | g0045 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18982 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18992 | hp1 | a0005 | c0005 | t0004 | g0117 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18992 | hp2 | a0004 | c0004 | t0002 | g0015 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18993 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18994 | hp1 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18994 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18998 | hp2 | a0003 | c0003 | t0006 | g0073 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18999 | hp1 | a0003 | c0003 | t0003 | g0025 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19001 | hp1 | a0005 | c0005 | t0004 | g0118 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19004 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19004 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19005 | hp1 | a0003 | c0003 | t0003 | g0066 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19005 | hp2 | a0001 | c0002 | t0013 | g0074 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19007 | hp1 | a0010 | c0010 | t0006 | g0026 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19007 | hp2 | a0004 | c0004 | t0002 | g0012 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19009 | hp2 | a0001 | c0007 | t0009 | g0106 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19011 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | LWK | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19030 | hp2 | a0004 | c0004 | t0002 | g0048 | AFR | LWK | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19057 | hp1 | a0002 | c0001 | t0001 | g0089 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19057 | hp2 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19063 | hp1 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19065 | hp1 | a0002 | c0001 | t0001 | g0088 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19065 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19070 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19074 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19074 | hp2 | a0004 | c0004 | t0002 | g0016 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19076 | hp1 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19077 | hp1 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19077 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19079 | hp2 | a0003 | c0003 | t0003 | g0017 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19084 | hp1 | a0003 | c0003 | t0003 | g0006 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19087 | hp1 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19087 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19088 | hp2 | a0004 | c0004 | t0002 | g0003 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19091 | hp1 | a0005 | c0005 | t0004 | g0007 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA19091 | hp2 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ASW | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ASW | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0001 | EUR | TSI | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20805 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | TSI | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20805 | hp2 | a0003 | c0003 | t0005 | g0040 | EUR | TSI | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20905 | hp1 | a0004 | c0004 | t0002 | g0050 | SAS | GIH | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20905 | hp2 | a0007 | c0006 | t0007 | g0011 | SAS | GIH | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG01123 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | CLM | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02486 | hp1 | a0003 | c0003 | t0005 | g0041 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02486 | hp2 | a0003 | c0009 | t0002 | g0077 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0027 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG02559 | hp2 | a0003 | c0003 | t0005 | g0038 | AFR | ACB | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03471 | hp1 | a0008 | c0017 | t0008 | g0034 | AFR | MSL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| HG03471 | hp2 | a0003 | c0003 | t0005 | g0020 | AFR | MSL | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18955 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA18955 | hp2 | a0004 | c0004 | t0002 | g0022 | EAS | JPT | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20300 | hp1 | a0006 | c0013 | t0010 | g0031 | AFR | USA | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| NA20300 | hp2 | a0003 | c0003 | t0002 | g0010 | AFR | USA | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0002 | REF | REF | TRIM49_chr11_89792655_89813575 | TRIM49 | chr11 | 89792655 | 89813575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89798152 | A | T | 1 | a0012 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1337T>A | p.Ile446Asn | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1666/2163 | 1337/1359 | 446/452 | chr11 | 89798152 | |||
| chr11:89798308 | G | T | 2 | a0004 a0014 |
34 | HG01361.hp2 HG01496.hp2 HG01981.hp2 others(31): Show |
missense_variant | MODERATE | c.1181C>A | p.Thr394Asn | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1510/2163 | 1181/1359 | 394/452 | chr11 | 89798308 | |||
| chr11:89798342 | C | T | 6 | a0003 a0004 a0006 others(3): Show |
93 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
missense_variant | MODERATE | c.1147G>A | p.Val383Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1476/2163 | 1147/1359 | 383/452 | chr11 | 89798342 | |||
| chr11:89798365 | G | T | 6 | a0003 a0004 a0006 others(3): Show |
93 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
missense_variant | MODERATE | c.1124C>A | p.Ala375Glu | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1453/2163 | 1124/1359 | 375/452 | chr11 | 89798365 | |||
| chr11:89798372 | C | T | 3 | a0002 a0009 a0013 |
72 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(69): Show |
missense_variant | MODERATE | c.1117G>A | p.Gly373Arg | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1446/2163 | 1117/1359 | 373/452 | chr11 | 89798372 | |||
| chr11:89798596 | T | C | 7 | a0003 a0004 a0006 others(4): Show |
96 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(93): Show |
missense_variant | MODERATE | c.893A>G | p.Asn298Ser | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1222/2163 | 893/1359 | 298/452 | chr11 | 89798596 | |||
| chr11:89798612 | G | C | 5 | a0003 a0004 a0010 others(2): Show |
86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
missense_variant | MODERATE | c.877C>G | p.His293Asp | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1206/2163 | 877/1359 | 293/452 | chr11 | 89798612 | |||
| chr11:89801771 | C | T | 1 | a0009 | 2 | HG02738.hp2 HG03654.hp2 |
missense_variant | MODERATE | c.669G>A | p.Met223Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/8 | 998/2163 | 669/1359 | 223/452 | chr11 | 89801771 | |||
| chr11:89803741 | T | C | 1 | a0013 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.464A>G | p.His155Arg | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/8 | 793/2163 | 464/1359 | 155/452 | chr11 | 89803741 | |||
| chr11:89803762 | C | A | 2 | a0005 a0012 |
12 | HG02602.hp2 HG02683.hp2 HG03017.hp1 others(9): Show |
missense_variant | MODERATE | c.443G>T | p.Trp148Leu | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/8 | 772/2163 | 443/1359 | 148/452 | chr11 | 89803762 | |||
| chr11:89804151 | C | G | 1 | a0010 | 2 | NA18961.hp1 NA19007.hp1 |
missense_variant | MODERATE | c.319G>C | p.Asp107His | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 648/2163 | 319/1359 | 107/452 | chr11 | 89804151 | |||
| chr11:89804164 | T | C | 1 | a0011 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.306A>G | p.Ile102Met | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 635/2163 | 306/1359 | 102/452 | chr11 | 89804164 | |||
| chr11:89804231 | A | G | 1 | a0014 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.239T>C | p.Val80Ala | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 568/2163 | 239/1359 | 80/452 | chr11 | 89804231 | |||
| chr11:89804285 | A | C | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.185T>G | p.Ile62Arg | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 514/2163 | 185/1359 | 62/452 | chr11 | 89804285 | |||
| chr11:89804291 | T | C | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.179A>G | p.Glu60Gly | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 508/2163 | 179/1359 | 60/452 | chr11 | 89804291 | |||
| chr11:89804292 | C | A | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
stop_gained | HIGH | c.178G>T | p.Glu60* | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 507/2163 | 178/1359 | 60/452 | chr11 | 89804292 | |||
| chr11:89804298 | A | T | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.172T>A | p.Ser58Thr | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 501/2163 | 172/1359 | 58/452 | chr11 | 89804298 | |||
| chr11:89804303 | G | A | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.167C>T | p.Thr56Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 496/2163 | 167/1359 | 56/452 | chr11 | 89804303 | |||
| chr11:89804312 | G | A | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.158C>T | p.Ser53Phe | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 487/2163 | 158/1359 | 53/452 | chr11 | 89804312 | |||
| chr11:89804321 | A | G | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.149T>C | p.Val50Ala | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 478/2163 | 149/1359 | 50/452 | chr11 | 89804321 | |||
| chr11:89804322 | C | T | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.148G>A | p.Val50Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 477/2163 | 148/1359 | 50/452 | chr11 | 89804322 | |||
| chr11:89804328 | A | T | 1 | a0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
missense_variant | MODERATE | c.142T>A | p.Phe48Ile | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 471/2163 | 142/1359 | 48/452 | chr11 | 89804328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89798400 | T | C | 2 | a0006c0008 a0006c0013 |
6 | HG01081.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.1089A>G | p.Lys363Lys | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1418/2163 | 1089/1359 | 363/452 | chr11 | 89798400 | |||
| chr11:89798451 | A | G | 6 | a0003c0003 a0003c0009 a0004c0004 others(3): Show |
86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
synonymous_variant | LOW | c.1038T>C | p.His346His | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 1367/2163 | 1038/1359 | 346/452 | chr11 | 89798451 | |||
| chr11:89804167 | C | T | 1 | a0003c0009 | 3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.303G>A | p.Lys101Lys | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 632/2163 | 303/1359 | 101/452 | chr11 | 89804167 | |||
| chr11:89804272 | G | A | 1 | a0007c0006 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
synonymous_variant | LOW | c.198C>T | p.Thr66Thr | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 527/2163 | 198/1359 | 66/452 | chr11 | 89804272 | |||
| chr11:89804293 | G | T | 6 | a0001c0007 a0005c0005 a0006c0008 others(3): Show |
25 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(22): Show |
synonymous_variant | LOW | c.177C>A | p.Thr59Thr | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 506/2163 | 177/1359 | 59/452 | chr11 | 89804293 | |||
| chr11:89804302 | T | C | 1 | a0007c0006 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
synonymous_variant | LOW | c.168A>G | p.Thr56Thr | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 497/2163 | 168/1359 | 56/452 | chr11 | 89804302 | |||
| chr11:89804320 | G | A | 1 | a0007c0006 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
synonymous_variant | LOW | c.150C>T | p.Val50Val | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/8 | 479/2163 | 150/1359 | 50/452 | chr11 | 89804320 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89797665 | A | C | 11 | a0003c0003t0002 a0003c0003t0003 a0003c0003t0005 others(8): Show |
86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*465T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 465 | chr11 | 89797665 | ||||||
| chr11:89797673 | A | T | 1 | a0003c0003t0003 | 22 | HG00609.hp1 HG00621.hp1 HG01257.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*457T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 457 | chr11 | 89797673 | ||||||
| chr11:89797748 | T | C | 11 | a0003c0003t0002 a0003c0003t0003 a0003c0003t0005 others(8): Show |
86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*382A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 382 | chr11 | 89797748 | ||||||
| chr11:89797791 | G | A | 1 | a0006c0013t0010 | 2 | HG02922.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*339C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 339 | chr11 | 89797791 | ||||||
| chr11:89797795 | G | C | 11 | a0003c0003t0002 a0003c0003t0003 a0003c0003t0005 others(8): Show |
87 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*335C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 335 | chr11 | 89797795 | ||||||
| chr11:89797795 | G | T | 1 | a0004c0004t0012 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 335 | chr11 | 89797795 | ||||||
| chr11:89797830 | T | A | 11 | a0003c0003t0002 a0003c0003t0003 a0003c0003t0005 others(8): Show |
86 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*300A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 300 | chr11 | 89797830 | ||||||
| chr11:89797869 | G | GA | 2 | a0003c0003t0006 a0010c0010t0006 |
6 | HG00408.hp2 NA18959.hp2 NA18961.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*260dupT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 260 | chr11 | 89797869 | ||||||
| chr11:89798047 | T | C | 2 | a0008c0012t0008 a0008c0017t0008 |
3 | HG02129.hp2 HG03471.hp1 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*83A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 8/8 | 83 | chr11 | 89798047 | ||||||
| chr11:89807166 | A | G | 5 | a0001c0007t0009 a0002c0001t0009 a0003c0003t0005 others(2): Show |
12 | HG01192.hp2 HG01243.hp2 HG02486.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-72T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/8 | 2697 | chr11 | 89807166 | ||||||
| chr11:89807169 | A | G | 1 | a0007c0006t0007 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-75T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/8 | 2700 | chr11 | 89807169 | ||||||
| chr11:89807206 | G | A | 1 | a0001c0002t0013 | 1 | NA19005.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/8 | 2737 | chr11 | 89807206 | ||||||
| chr11:89808448 | A | G | 8 | a0001c0002t0004 a0001c0007t0004 a0001c0007t0009 others(5): Show |
24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-202T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/8 | 3979 | chr11 | 89808448 | ||||||
| chr11:89808450 | C | A | 1 | a0006c0013t0010 | 2 | HG02922.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-204G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/8 | 3981 | chr11 | 89808450 | ||||||
| chr11:89808486 | T | C | 8 | a0001c0002t0004 a0001c0007t0004 a0001c0007t0009 others(5): Show |
24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-240A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/8 | 4017 | chr11 | 89808486 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89798633 | C | CA | 38 | a0001c0002t0001g0093 a0001c0007t0009g0105 a0001c0007t0009g0106 others(35): Show |
62 | HG01081.hp2 HG01099.hp2 HG01192.hp2 others(59): Show |
splice_region_variant&intron_variant | LOW | c.860-5dupT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798633 | |||||||
| chr11:89798633 | C | CAA | 14 | a0001c0002t0001g0023 a0001c0007t0004g0110 a0001c0007t0004g0116 others(11): Show |
26 | HG00408.hp2 HG01261.hp1 HG02293.hp2 others(23): Show |
splice_region_variant&intron_variant | LOW | c.860-6_860-5dupTT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798633 | |||||||
| chr11:89798633 | C | CAAA | 7 | a0001c0002t0001g0005 a0001c0002t0001g0055 a0001c0002t0001g0058 others(4): Show |
13 | HG00544.hp2 HG01257.hp1 HG02132.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.860-7_860-5dupTTT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798633 | |||||||
| chr11:89798673 | A | G | 1 | a0011c0020t0002g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.860-44T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798673 | |||||||
| chr11:89798735 | T | A | 68 | a0001c0007t0004g0116 a0001c0007t0009g0105 a0001c0007t0009g0106 others(65): Show |
115 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.860-106A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798735 | |||||||
| chr11:89798813 | A | G | 1 | a0003c0018t0002g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.860-184T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798813 | |||||||
| chr11:89798818 | G | GT | 5 | a0003c0009t0002g0075 a0003c0009t0002g0076 a0003c0009t0002g0077 others(2): Show |
5 | HG02132.hp2 HG02486.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-190dupA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798818 | |||||||
| chr11:89798818 | G | GTT | 45 | a0003c0003t0002g0009 a0003c0003t0002g0010 a0003c0003t0002g0032 others(42): Show |
82 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.860-191_860-190dup others(2): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798818 | |||||||
| chr11:89798818 | GT | G | 7 | a0001c0002t0001g0005 a0001c0002t0001g0023 a0001c0002t0001g0055 others(4): Show |
14 | HG00544.hp2 HG01257.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.860-190delA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89798818 | |||||||
| chr11:89799039 | A | G | 31 | a0003c0003t0002g0009 a0003c0003t0002g0010 a0003c0003t0002g0035 others(28): Show |
61 | HG00408.hp2 HG01099.hp2 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.860-410T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799039 | |||||||
| chr11:89799050 | T | C | 3 | a0003c0009t0002g0075 a0003c0009t0002g0076 a0003c0009t0002g0077 |
3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.860-421A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799050 | |||||||
| chr11:89799133 | G | T | 1 | a0010c0010t0006g0026 | 2 | NA18961.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.860-504C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799133 | |||||||
| chr11:89799234 | T | C | 26 | a0003c0003t0002g0009 a0003c0003t0002g0010 a0003c0003t0002g0035 others(23): Show |
54 | HG01099.hp2 HG01192.hp2 HG01361.hp2 others(51): Show |
intron_variant | MODIFIER | c.859+482A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799234 | |||||||
| chr11:89799290 | A | G | 13 | a0003c0003t0003g0006 a0003c0003t0003g0017 a0003c0003t0003g0025 others(10): Show |
21 | HG00609.hp1 HG01257.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.859+426T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799290 | |||||||
| chr11:89799375 | C | A | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+341G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799375 | |||||||
| chr11:89799637 | A | T | 1 | a0003c0018t0002g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.859+79T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799637 | |||||||
| chr11:89799675 | T | A | 2 | a0003c0003t0003g0025 a0003c0003t0003g0063 |
3 | HG00609.hp1 HG00621.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.859+41A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799675 | |||||||
| chr11:89799691 | G | A | 1 | a0001c0007t0009g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.859+25C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 7/7 | chr11 | 89799691 | |||||||
| chr11:89799826 | A | G | 1 | a0002c0001t0001g0089 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.762-13T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89799826 | |||||||
| chr11:89799895 | A | T | 21 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(18): Show |
31 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.762-82T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89799895 | |||||||
| chr11:89799937 | A | T | 10 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0005c0005t0004g0007 others(7): Show |
15 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.762-124T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89799937 | |||||||
| chr11:89799991 | G | A | 2 | a0002c0001t0001g0013 a0002c0001t0001g0052 |
5 | HG00099.hp1 HG00735.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.762-178C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89799991 | |||||||
| chr11:89800024 | C | CT | 20 | a0001c0002t0001g0033 a0001c0002t0001g0053 a0003c0003t0003g0056 others(17): Show |
40 | HG01243.hp1 HG01257.hp2 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.762-212dupA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800024 | |||||||
| chr11:89800024 | CTTT | C | 13 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(10): Show |
21 | HG01243.hp2 HG01261.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.762-214_762-212del others(3): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800024 | |||||||
| chr11:89800024 | CTTTT | C | 7 | a0001c0007t0009g0106 a0002c0001t0009g0113 a0006c0008t0004g0107 others(4): Show |
8 | HG01081.hp2 HG02895.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.762-215_762-212del others(4): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800024 | |||||||
| chr11:89800076 | G | A | 1 | a0003c0003t0003g0070 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.762-263C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800076 | |||||||
| chr11:89800154 | C | T | 17 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(14): Show |
23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.762-341G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800154 | |||||||
| chr11:89800156 | G | T | 1 | a0005c0005t0004g0117 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.762-343C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800156 | |||||||
| chr11:89800248 | C | T | 10 | a0001c0007t0009g0105 a0001c0007t0009g0106 a0002c0001t0009g0113 others(7): Show |
14 | HG01081.hp2 HG01243.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.762-435G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800248 | |||||||
| chr11:89800302 | G | A | 1 | a0002c0001t0001g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.762-489C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800302 | |||||||
| chr11:89800345 | A | G | 18 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(15): Show |
24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.762-532T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800345 | |||||||
| chr11:89800397 | A | T | 2 | a0006c0014t0011g0042 a0007c0006t0007g0011 |
5 | HG01516.hp2 HG01517.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.761+569T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800397 | |||||||
| chr11:89800407 | A | C | 8 | a0001c0007t0004g0116 a0005c0005t0004g0007 a0005c0005t0004g0114 others(5): Show |
13 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.761+559T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800407 | |||||||
| chr11:89800410 | A | C | 10 | a0001c0007t0009g0105 a0001c0007t0009g0106 a0002c0001t0009g0113 others(7): Show |
14 | HG01081.hp2 HG01243.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.761+556T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800410 | |||||||
| chr11:89800414 | A | ACT | 10 | a0001c0007t0009g0105 a0001c0007t0009g0106 a0002c0001t0009g0113 others(7): Show |
14 | HG01081.hp2 HG01243.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.761+550_761+551dup others(2): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800414 | |||||||
| chr11:89800414 | A | C | 1 | a0002c0001t0001g0083 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.761+552T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800414 | |||||||
| chr11:89800430 | T | G | 2 | a0006c0014t0011g0042 a0007c0006t0007g0011 |
5 | HG01516.hp2 HG01517.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.761+536A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800430 | |||||||
| chr11:89800446 | A | G | 1 | a0006c0014t0011g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.761+520T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800446 | |||||||
| chr11:89800470 | G | A | 19 | a0001c0002t0001g0081 a0001c0007t0004g0110 a0001c0007t0004g0116 others(16): Show |
25 | HG00741.hp1 HG01081.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.761+496C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800470 | |||||||
| chr11:89800545 | C | G | 1 | a0003c0003t0003g0069 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.761+421G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800545 | |||||||
| chr11:89800612 | G | A | 2 | a0006c0014t0011g0042 a0007c0006t0007g0011 |
5 | HG01516.hp2 HG01517.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.761+354C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800612 | |||||||
| chr11:89800636 | G | A | 1 | a0006c0014t0011g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.761+330C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800636 | |||||||
| chr11:89800682 | T | G | 49 | a0001c0002t0001g0101 a0001c0007t0004g0116 a0001c0007t0009g0105 others(46): Show |
106 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.761+284A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800682 | |||||||
| chr11:89800736 | C | G | 1 | a0002c0001t0009g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.761+230G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800736 | |||||||
| chr11:89800742 | CA | C | 20 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(17): Show |
29 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.761+223delT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800742 | |||||||
| chr11:89800758 | G | C | 14 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0002c0001t0009g0113 others(11): Show |
19 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.761+208C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800758 | |||||||
| chr11:89800842 | G | C | 1 | a0001c0007t0009g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.761+124C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800842 | |||||||
| chr11:89800871 | A | G | 1 | a0005c0005t0004g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.761+95T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800871 | |||||||
| chr11:89800921 | G | A | 1 | a0002c0001t0001g0085 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.761+45C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 6/7 | chr11 | 89800921 | |||||||
| chr11:89800991 | G | GA | 3 | a0001c0007t0009g0105 a0002c0001t0001g0014 a0003c0003t0005g0020 |
7 | HG01243.hp2 HG03195.hp2 HG03471.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.739-4dupT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89800991 | |||||||
| chr11:89800991 | GA | G | 9 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0003c0003t0002g0035 others(6): Show |
16 | HG01099.hp2 HG01261.hp1 HG02602.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.739-4delT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89800991 | |||||||
| chr11:89800991 | GAA | G | 3 | a0005c0005t0004g0117 a0005c0005t0004g0118 a0007c0006t0007g0011 |
6 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.739-5_739-4delTT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89800991 | |||||||
| chr11:89801023 | T | G | 11 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0005c0005t0004g0007 others(8): Show |
19 | HG01261.hp1 HG01516.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.739-35A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801023 | |||||||
| chr11:89801123 | G | A | 19 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(16): Show |
28 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.739-135C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801123 | |||||||
| chr11:89801136 | A | T | 19 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(16): Show |
28 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.739-148T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801136 | |||||||
| chr11:89801204 | T | C | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-216A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801204 | |||||||
| chr11:89801285 | T | G | 1 | a0001c0007t0009g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.739-297A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801285 | |||||||
| chr11:89801391 | A | C | 1 | a0003c0009t0002g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.738+311T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801391 | |||||||
| chr11:89801459 | T | C | 30 | a0001c0002t0001g0095 a0001c0007t0004g0110 a0001c0007t0009g0105 others(27): Show |
58 | HG01099.hp2 HG01192.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.738+243A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801459 | |||||||
| chr11:89801526 | G | C | 10 | a0001c0007t0009g0106 a0002c0001t0001g0086 a0002c0001t0009g0113 others(7): Show |
14 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.738+176C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801526 | |||||||
| chr11:89801614 | T | G | 4 | a0003c0009t0002g0075 a0003c0009t0002g0076 a0003c0009t0002g0077 others(1): Show |
4 | HG02486.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.738+88A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 5/7 | chr11 | 89801614 | |||||||
| chr11:89802122 | G | A | 9 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0005c0005t0004g0007 others(6): Show |
14 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.508-190C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802122 | |||||||
| chr11:89802166 | C | T | 10 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0005c0005t0004g0007 others(7): Show |
16 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.508-234G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802166 | |||||||
| chr11:89802301 | C | A | 18 | a0001c0002t0001g0094 a0001c0007t0004g0110 a0001c0007t0004g0116 others(15): Show |
24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.508-369G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802301 | |||||||
| chr11:89802405 | T | G | 12 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(9): Show |
18 | HG01243.hp2 HG01261.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.508-473A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802405 | |||||||
| chr11:89802491 | T | C | 17 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(14): Show |
23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.508-559A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802491 | |||||||
| chr11:89802536 | G | A | 18 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(15): Show |
27 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.508-604C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802536 | |||||||
| chr11:89802541 | C | G | 1 | a0001c0002t0001g0100 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.508-609G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802541 | |||||||
| chr11:89802568 | T | A | 1 | a0012c0015t0004g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.508-636A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802568 | |||||||
| chr11:89802570 | C | T | 1 | a0004c0004t0002g0046 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.508-638G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802570 | |||||||
| chr11:89802580 | CACAT | C | 34 | a0001c0002t0001g0005 a0001c0002t0001g0023 a0001c0002t0001g0055 others(31): Show |
53 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-652_508-649del others(4): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802580 | |||||||
| chr11:89802580 | CACATACA others(1): Show |
C | 17 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(14): Show |
25 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.508-656_508-649del others(8): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802580 | |||||||
| chr11:89802588 | T | C | 1 | a0006c0013t0010g0031 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.508-656A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802588 | |||||||
| chr11:89802671 | C | T | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-739G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802671 | |||||||
| chr11:89802699 | C | G | 14 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(11): Show |
19 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.508-767G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802699 | |||||||
| chr11:89802750 | C | T | 2 | a0006c0008t0004g0107 a0006c0008t0004g0109 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.508-818G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802750 | |||||||
| chr11:89802829 | C | G | 2 | a0003c0009t0002g0075 a0003c0009t0002g0077 |
2 | HG02486.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.507+869G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802829 | |||||||
| chr11:89802883 | A | C | 20 | a0001c0002t0001g0008 a0001c0002t0001g0081 a0001c0007t0004g0110 others(17): Show |
33 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.507+815T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802883 | |||||||
| chr11:89802906 | G | A | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+792C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802906 | |||||||
| chr11:89802999 | T | G | 1 | a0006c0014t0011g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.507+699A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89802999 | |||||||
| chr11:89803019 | G | A | 3 | a0003c0009t0002g0075 a0003c0009t0002g0076 a0003c0009t0002g0077 |
3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.507+679C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803019 | |||||||
| chr11:89803048 | G | A | 18 | a0001c0002t0001g0030 a0001c0007t0004g0110 a0001c0007t0004g0116 others(15): Show |
28 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.507+650C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803048 | |||||||
| chr11:89803090 | T | G | 1 | a0002c0001t0001g0091 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.507+608A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803090 | |||||||
| chr11:89803110 | A | C | 3 | a0003c0003t0006g0021 a0003c0003t0006g0073 a0003c0018t0002g0043 |
4 | HG03195.hp1 NA18959.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.507+588T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803110 | |||||||
| chr11:89803160 | G | A | 1 | a0002c0001t0001g0087 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.507+538C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803160 | |||||||
| chr11:89803171 | C | T | 1 | a0002c0001t0001g0103 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.507+527G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803171 | |||||||
| chr11:89803184 | G | A | 26 | a0001c0002t0001g0061 a0002c0001t0001g0001 a0002c0001t0001g0013 others(23): Show |
72 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.507+514C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803184 | |||||||
| chr11:89803237 | T | C | 1 | a0006c0013t0010g0031 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.507+461A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803237 | |||||||
| chr11:89803374 | C | G | 1 | a0003c0009t0002g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.507+324G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803374 | |||||||
| chr11:89803385 | G | A | 3 | a0003c0009t0002g0075 a0003c0009t0002g0076 a0003c0009t0002g0077 |
3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.507+313C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803385 | |||||||
| chr11:89803398 | C | T | 1 | a0003c0009t0002g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.507+300G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803398 | |||||||
| chr11:89803540 | A | G | 6 | a0001c0002t0001g0059 a0002c0001t0009g0113 a0006c0008t0004g0107 others(3): Show |
6 | HG01081.hp2 HG02132.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+158T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803540 | |||||||
| chr11:89803563 | C | T | 3 | a0001c0007t0009g0105 a0001c0007t0009g0106 a0006c0013t0010g0031 |
4 | HG01243.hp2 HG02922.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.507+135G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803563 | |||||||
| chr11:89803567 | G | A | 6 | a0002c0001t0009g0113 a0006c0008t0004g0107 a0006c0008t0004g0108 others(3): Show |
9 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+131C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803567 | |||||||
| chr11:89803578 | C | T | 2 | a0006c0008t0004g0107 a0006c0008t0004g0109 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.507+120G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 4/7 | chr11 | 89803578 | |||||||
| chr11:89803847 | G | C | 1 | a0002c0001t0001g0088 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.412-54C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89803847 | |||||||
| chr11:89803871 | C | A | 2 | a0004c0004t0002g0003 a0004c0004t0002g0044 |
2 | NA18950.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.412-78G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89803871 | |||||||
| chr11:89803982 | T | C | 1 | a0002c0001t0009g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.411+77A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89803982 | |||||||
| chr11:89803984 | C | T | 6 | a0002c0001t0009g0113 a0006c0008t0004g0107 a0006c0008t0004g0108 others(3): Show |
9 | HG01081.hp2 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.411+75G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89803984 | |||||||
| chr11:89804021 | T | C | 12 | a0001c0002t0001g0005 a0001c0002t0001g0023 a0001c0002t0001g0055 others(9): Show |
21 | HG00544.hp2 HG00621.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.411+38A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89804021 | |||||||
| chr11:89804036 | C | A | 1 | a0002c0001t0001g0089 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.411+23G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 3/7 | chr11 | 89804036 | |||||||
| chr11:89804489 | A | C | 12 | a0001c0002t0001g0080 a0001c0007t0004g0110 a0001c0007t0004g0116 others(9): Show |
17 | HG01261.hp1 HG01884.hp2 HG02293.hp1 others(14): Show |
intron_variant | MODIFIER | c.-4-16T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804489 | |||||||
| chr11:89804523 | C | G | 69 | a0001c0002t0001g0033 a0001c0002t0001g0053 a0001c0002t0001g0055 others(66): Show |
112 | HG00408.hp2 HG00609.hp1 HG01081.hp2 others(109): Show |
intron_variant | MODIFIER | c.-4-50G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804523 | |||||||
| chr11:89804538 | G | C | 11 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(8): Show |
16 | HG01243.hp2 HG01261.hp1 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4-65C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804538 | |||||||
| chr11:89804617 | A | G | 1 | a0011c0020t0002g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-4-144T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804617 | |||||||
| chr11:89804651 | C | A | 16 | a0001c0007t0009g0105 a0002c0001t0009g0113 a0003c0003t0003g0006 others(13): Show |
22 | HG00609.hp1 HG01081.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.-4-178G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804651 | |||||||
| chr11:89804669 | C | T | 10 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0106 others(7): Show |
15 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.-4-196G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804669 | |||||||
| chr11:89804695 | C | T | 1 | a0005c0005t0004g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4-222G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804695 | |||||||
| chr11:89804713 | A | G | 2 | a0006c0008t0004g0107 a0006c0008t0004g0109 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-4-240T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804713 | |||||||
| chr11:89804718 | A | G | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-245T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804718 | |||||||
| chr11:89804746 | A | G | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-273T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804746 | |||||||
| chr11:89804829 | A | G | 1 | a0005c0005t0004g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-4-356T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804829 | |||||||
| chr11:89804862 | C | T | 14 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0002c0001t0009g0113 others(11): Show |
19 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.-4-389G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804862 | |||||||
| chr11:89804865 | G | A | 14 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0002c0001t0009g0113 others(11): Show |
19 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.-4-392C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804865 | |||||||
| chr11:89804865 | GGGCCAAA others(15): Show |
G | 1 | a0003c0003t0005g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-4-414_-4-393delAT others(20): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804865 | |||||||
| chr11:89804935 | A | G | 44 | a0001c0002t0001g0095 a0001c0007t0004g0110 a0001c0007t0004g0116 others(41): Show |
76 | HG01081.hp2 HG01099.hp2 HG01192.hp2 others(73): Show |
intron_variant | MODIFIER | c.-4-462T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804935 | |||||||
| chr11:89804950 | G | A | 1 | a0001c0007t0009g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-4-477C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804950 | |||||||
| chr11:89804967 | C | T | 1 | a0001c0007t0009g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-4-494G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804967 | |||||||
| chr11:89804977 | C | T | 16 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(13): Show |
21 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.-4-504G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89804977 | |||||||
| chr11:89805066 | T | A | 48 | a0001c0002t0001g0033 a0001c0002t0001g0053 a0001c0002t0001g0055 others(45): Show |
84 | HG00609.hp1 HG01099.hp2 HG01192.hp2 others(81): Show |
intron_variant | MODIFIER | c.-4-593A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805066 | |||||||
| chr11:89805117 | T | C | 17 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(14): Show |
25 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.-4-644A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805117 | |||||||
| chr11:89805182 | C | T | 1 | a0001c0007t0009g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-4-709G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805182 | |||||||
| chr11:89805273 | C | A | 1 | a0011c0020t0002g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-4-800G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805273 | |||||||
| chr11:89805289 | A | G | 10 | a0001c0002t0001g0055 a0003c0003t0003g0006 a0003c0003t0003g0025 others(7): Show |
16 | HG00609.hp1 HG01257.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-4-816T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805289 | |||||||
| chr11:89805395 | C | T | 13 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0005c0005t0004g0007 others(10): Show |
18 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4-922G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805395 | |||||||
| chr11:89805458 | C | T | 1 | a0002c0001t0001g0079 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-4-985G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805458 | |||||||
| chr11:89805477 | G | T | 1 | a0001c0002t0001g0058 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-4-1004C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805477 | |||||||
| chr11:89805517 | T | A | 1 | a0003c0003t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-1044A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805517 | |||||||
| chr11:89805517 | T | C | 13 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0005c0005t0004g0007 others(10): Show |
18 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.-4-1044A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805517 | |||||||
| chr11:89805526 | C | G | 11 | a0001c0007t0009g0105 a0001c0007t0009g0106 a0002c0001t0001g0078 others(8): Show |
16 | HG00639.hp1 HG00741.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.-4-1053G>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805526 | |||||||
| chr11:89805556 | G | A | 2 | a0004c0004t0002g0050 a0004c0004t0002g0051 |
2 | HG02004.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-4-1083C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805556 | |||||||
| chr11:89805613 | A | C | 1 | a0003c0003t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-4-1140T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805613 | |||||||
| chr11:89805639 | A | G | 2 | a0001c0002t0001g0033 a0001c0002t0001g0053 |
2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-4-1166T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805639 | |||||||
| chr11:89805697 | G | A | 17 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(14): Show |
23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-1224C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805697 | |||||||
| chr11:89805723 | G | T | 20 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(17): Show |
27 | HG00639.hp1 HG01081.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-4-1250C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805723 | |||||||
| chr11:89805723 | GT | G | 50 | a0001c0002t0001g0033 a0001c0002t0001g0053 a0001c0002t0001g0055 others(47): Show |
86 | HG00408.hp2 HG00609.hp1 HG01099.hp2 others(83): Show |
intron_variant | MODIFIER | c.-4-1251delA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805723 | |||||||
| chr11:89805724 | T | G | 15 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(12): Show |
21 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.-4-1251A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805724 | |||||||
| chr11:89805724 | T | TG | 4 | a0002c0001t0001g0090 a0002c0001t0001g0091 a0002c0001t0009g0113 others(1): Show |
5 | HG00639.hp1 HG01168.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-1252_-4-1251ins others(1): Show |
TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805724 | |||||||
| chr11:89805909 | G | C | 1 | a0006c0013t0010g0031 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-5+1190C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805909 | |||||||
| chr11:89805947 | T | G | 16 | a0001c0002t0001g0055 a0003c0003t0003g0006 a0003c0003t0003g0025 others(13): Show |
24 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-5+1152A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805947 | |||||||
| chr11:89805994 | C | A | 17 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(14): Show |
23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+1105G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89805994 | |||||||
| chr11:89806020 | C | A | 19 | a0001c0002t0001g0096 a0001c0007t0004g0110 a0001c0007t0004g0116 others(16): Show |
25 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.-5+1079G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806020 | |||||||
| chr11:89806221 | A | G | 18 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(15): Show |
24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.-5+878T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806221 | |||||||
| chr11:89806261 | C | A | 17 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(14): Show |
23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+838G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806261 | |||||||
| chr11:89806268 | G | C | 1 | a0003c0003t0002g0036 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-5+831C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806268 | |||||||
| chr11:89806273 | T | C | 19 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(16): Show |
26 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.-5+826A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806273 | |||||||
| chr11:89806339 | T | C | 2 | a0003c0003t0006g0073 a0003c0018t0002g0043 |
2 | HG03195.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-5+760A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806339 | |||||||
| chr11:89806542 | C | T | 1 | a0003c0009t0002g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-5+557G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806542 | |||||||
| chr11:89806575 | T | A | 21 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(18): Show |
30 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.-5+524A>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806575 | |||||||
| chr11:89806629 | A | G | 3 | a0003c0003t0002g0032 a0003c0003t0006g0021 a0003c0018t0002g0043 |
4 | HG03195.hp1 HG03225.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+470T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806629 | |||||||
| chr11:89806637 | T | C | 7 | a0001c0002t0001g0004 a0001c0002t0001g0030 a0001c0002t0001g0093 others(4): Show |
15 | HG00280.hp2 HG00544.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.-5+462A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806637 | |||||||
| chr11:89806652 | A | G | 13 | a0004c0004t0002g0003 a0004c0004t0002g0012 a0004c0004t0002g0015 others(10): Show |
32 | HG01981.hp2 HG02004.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.-5+447T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806652 | |||||||
| chr11:89806656 | T | C | 1 | a0011c0020t0002g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-5+443A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806656 | |||||||
| chr11:89806735 | C | A | 1 | a0003c0003t0002g0037 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-5+364G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806735 | |||||||
| chr11:89806832 | A | G | 2 | a0003c0003t0006g0021 a0003c0018t0002g0043 |
3 | HG03195.hp1 NA18959.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-5+267T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806832 | |||||||
| chr11:89806887 | A | G | 1 | a0007c0006t0007g0011 | 4 | HG01516.hp2 HG01517.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+212T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806887 | |||||||
| chr11:89806896 | G | T | 1 | a0001c0007t0004g0110 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-5+203C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806896 | |||||||
| chr11:89806932 | C | A | 1 | a0006c0008t0004g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-5+167G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89806932 | |||||||
| chr11:89807016 | C | A | 38 | a0001c0002t0001g0005 a0001c0002t0001g0058 a0001c0002t0001g0059 others(35): Show |
59 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-5+83G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89807016 | |||||||
| chr11:89807057 | T | G | 1 | a0001c0007t0009g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-5+42A>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 2/7 | chr11 | 89807057 | |||||||
| chr11:89807359 | A | G | 7 | a0003c0003t0002g0009 a0003c0003t0002g0010 a0003c0003t0002g0035 others(4): Show |
14 | HG01099.hp2 HG01891.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-190-75T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807359 | |||||||
| chr11:89807430 | C | T | 1 | a0001c0002t0004g0112 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-190-146G>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807430 | |||||||
| chr11:89807443 | T | C | 16 | a0001c0002t0001g0033 a0001c0007t0004g0110 a0001c0007t0004g0116 others(13): Show |
21 | HG01081.hp2 HG01261.hp1 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.-190-159A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807443 | |||||||
| chr11:89807460 | G | C | 1 | a0001c0007t0009g0106 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-190-176C>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807460 | |||||||
| chr11:89807560 | A | T | 1 | a0002c0001t0001g0102 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-190-276T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807560 | |||||||
| chr11:89807663 | C | A | 17 | a0001c0007t0004g0110 a0001c0007t0004g0116 a0001c0007t0009g0105 others(14): Show |
23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-190-379G>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807663 | |||||||
| chr11:89807686 | A | T | 4 | a0006c0008t0004g0107 a0006c0008t0004g0108 a0006c0008t0004g0109 others(1): Show |
4 | HG01081.hp2 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-190-402T>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807686 | |||||||
| chr11:89807721 | A | C | 14 | a0001c0002t0001g0033 a0001c0007t0004g0110 a0001c0007t0004g0116 others(11): Show |
19 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(16): Show |
intron_variant | MODIFIER | c.-190-437T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807721 | |||||||
| chr11:89807758 | A | G | 17 | a0001c0002t0004g0112 a0001c0007t0004g0110 a0001c0007t0004g0116 others(14): Show |
23 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.-190-474T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807758 | |||||||
| chr11:89807940 | T | C | 3 | a0003c0009t0002g0075 a0003c0009t0002g0076 a0003c0009t0002g0077 |
3 | HG02486.hp2 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-191+497A>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89807940 | |||||||
| chr11:89808025 | G | T | 117 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(114): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-191+412C>A | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808025 | |||||||
| chr11:89808183 | G | A | 18 | a0001c0002t0004g0112 a0001c0007t0004g0110 a0001c0007t0004g0116 others(15): Show |
24 | HG01081.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.-191+254C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808183 | |||||||
| chr11:89808204 | A | G | 1 | a0003c0003t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-191+233T>C | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808204 | |||||||
| chr11:89808221 | TA | T | 65 | a0001c0002t0001g0005 a0001c0002t0001g0023 a0001c0002t0001g0033 others(62): Show |
113 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.-191+215delT | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808221 | |||||||
| chr11:89808332 | A | C | 1 | a0001c0007t0009g0105 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-191+105T>G | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808332 | |||||||
| chr11:89808397 | G | A | 4 | a0002c0001t0001g0018 a0002c0001t0001g0102 a0002c0001t0001g0103 others(1): Show |
6 | HG02129.hp1 NA18612.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.-191+40C>T | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808397 | |||||||
| chr11:89808427 | CTT | C | 8 | a0001c0007t0004g0116 a0005c0005t0004g0007 a0005c0005t0004g0114 others(5): Show |
13 | HG01261.hp1 HG02602.hp2 HG02683.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.-191+8_-191+9delAA | TRIM49 | ENSG00000168930.13 | transcript | ENST00000329758.5 | protein_coding | 1/7 | chr11 | 89808427 |