Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 399939 |
| ensemblid | ENSG00000223417.9 |
| hgncid | 43973 |
| symbol | TRIM49D1 |
| name | tripartite motif containing 49D1 |
| refseq_nuc | NM_001384911.1 |
| refseq_prot | NP_001371840.1 |
| ensembl_nuc | ENST00000420869.3 |
| ensembl_prot | ENSP00000474678.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 89911409 |
| end | 89922245 |
| strand | - |
| ver | v1.2 |
| region | chr11:89911409-89922245 |
| region5000 | chr11:89906409-89927245 |
| regionname0 | TRIM49D1_chr11_89911409_89922245 |
| regionname5000 | TRIM49D1_chr11_89906409_89927245 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 452 | 112 | 24 | 25 | 49 | 4 | 10 | 31 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| a0002 | 1/1 | 452 | 71 | 20 | 17 | 20 | 2 | 10 | 13 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| a0003 | 0/0 | 452 | 11 | 0 | 0 | 11 | 0 | 0 | 8 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| a0004 | 0/0 | 452 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| a0005 | 0/0 | 452 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| a0006 | 0/0 | 452 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| a0007 | 0/0 | 452 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| a0008 | 0/0 | 452 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| a0009 | 0/0 | 452 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| a0010 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | MNSGI others(447): Show |
chr11 | 89906409 | 89927245 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1356 | 92 | 23 | 17 | 40 | 2 | 10 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0001c0003 | 0/0 | 1356 | 20 | 1 | 8 | 9 | 2 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0002c0002 | 1/1 | 1356 | 70 | 19 | 17 | 20 | 2 | 10 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0002c0012 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0003c0004 | 0/0 | 1356 | 11 | 0 | 0 | 11 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0004c0005 | 0/0 | 1356 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0005c0006 | 0/0 | 1356 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0006c0007 | 0/0 | 1356 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0007c0008 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0007c0010 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0008c0009 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0009c0011 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 | ||
| a0010c0013 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | ATGAA others(1351): Show |
chr11 | 89906409 | 89927245 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2146 | 45 | 18 | 6 | 16 | 1 | 4 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0001c0001t0002 | 0/0 | 2146 | 45 | 5 | 10 | 24 | 1 | 5 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0001c0001t0008 | 0/0 | 2146 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0001c0001t0009 | 0/0 | 2146 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0001c0003t0001 | 0/0 | 2146 | 20 | 1 | 8 | 9 | 2 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0002c0002t0001 | 1/1 | 2146 | 56 | 15 | 15 | 17 | 1 | 6 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0002c0002t0003 | 0/0 | 2146 | 6 | 0 | 2 | 0 | 1 | 3 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0002c0002t0005 | 0/0 | 2146 | 4 | 2 | 0 | 1 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0002c0002t0006 | 0/0 | 2146 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0002c0002t0007 | 0/0 | 2146 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0002c0002t0010 | 0/0 | 2146 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0002c0012t0001 | 0/0 | 2146 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0003c0004t0001 | 0/0 | 2146 | 11 | 0 | 0 | 11 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0004c0005t0004 | 0/0 | 2146 | 5 | 5 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0005c0006t0006 | 0/0 | 2146 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0006c0007t0001 | 0/0 | 2146 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0007c0008t0002 | 0/0 | 2146 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0007c0010t0002 | 0/0 | 2146 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0008c0009t0001 | 0/0 | 2146 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0009c0011t0001 | 0/0 | 2146 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| a0010c0013t0001 | 0/0 | 2146 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | AGGCT others(2141): Show |
chr11 | 89906409 | 89927245 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 8 | 1 | 4 | 2 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0007 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0001 | 0/0 | 24 | 3 | 4 | 15 | 1 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0008 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0001t0009g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0004 | 0/0 | 6 | 0 | 3 | 2 | 1 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0002 | 0/0 | 9 | 0 | 2 | 5 | 0 | 2 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0003g0005 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0005g0012 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0002t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0002c0012t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0003c0004t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0003c0004t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0003c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0003c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0003c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0003c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0004c0005t0004g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0004c0005t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0004c0005t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0005c0006t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0005c0006t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0006c0007t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0006c0007t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0007c0008t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0007c0010t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0008c0009t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0009c0011t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| a0010c0013t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0004 | EUR | GBR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0044 | EUR | GBR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00323 | hp1 | a0002 | c0002 | t0003 | g0005 | EUR | FIN | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0092 | EUR | FIN | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00438 | hp1 | a0003 | c0004 | t0001 | g0014 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | CHS | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01109 | hp1 | a0008 | c0009 | t0001 | g0089 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01243 | hp1 | a0009 | c0011 | t0001 | g0095 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0035 | AMR | PUR | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0040 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0086 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01884 | hp1 | a0005 | c0006 | t0006 | g0031 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0070 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0013 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0087 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02083 | hp1 | a0003 | c0004 | t0001 | g0014 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02132 | hp2 | a0003 | c0004 | t0001 | g0113 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02155 | hp2 | a0002 | c0002 | t0007 | g0033 | EAS | CDX | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0088 | EAS | CDX | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0091 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02280 | hp1 | a0002 | c0002 | t0005 | g0079 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02280 | hp2 | a0006 | c0007 | t0001 | g0077 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | PEL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | KHV | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02647 | hp1 | a0002 | c0002 | t0010 | g0065 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02717 | hp1 | a0005 | c0006 | t0006 | g0029 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0034 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02886 | hp2 | a0004 | c0005 | t0004 | g0009 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02895 | hp1 | a0004 | c0005 | t0004 | g0009 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02897 | hp1 | a0004 | c0005 | t0004 | g0009 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02897 | hp2 | a0002 | c0002 | t0005 | g0012 | AFR | GWD | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | ESN | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03139 | hp1 | a0002 | c0012 | t0001 | g0038 | AFR | ESN | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0076 | AFR | ESN | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0064 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03453 | hp1 | a0004 | c0005 | t0004 | g0037 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0071 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0061 | SAS | STU | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0005 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03834 | hp1 | a0002 | c0002 | t0003 | g0005 | SAS | BEB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03834 | hp2 | a0002 | c0002 | t0005 | g0012 | SAS | BEB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | STU | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | YRI | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18522 | hp2 | a0002 | c0002 | t0006 | g0030 | AFR | YRI | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | CHB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | YRI | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0093 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18947 | hp1 | a0003 | c0004 | t0001 | g0014 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18947 | hp2 | a0003 | c0004 | t0001 | g0114 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18979 | hp1 | a0003 | c0004 | t0001 | g0015 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18980 | hp1 | a0003 | c0004 | t0001 | g0015 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18990 | hp1 | a0003 | c0004 | t0001 | g0111 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18995 | hp2 | a0003 | c0004 | t0001 | g0110 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18998 | hp1 | a0002 | c0002 | t0005 | g0012 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19009 | hp1 | a0002 | c0002 | t0007 | g0032 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19009 | hp2 | a0003 | c0004 | t0001 | g0015 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | LWK | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19043 | hp2 | a0010 | c0013 | t0001 | g0058 | AFR | LWK | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19085 | hp1 | a0007 | c0008 | t0002 | g0115 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19085 | hp2 | a0007 | c0010 | t0002 | g0121 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19090 | hp1 | a0003 | c0004 | t0001 | g0112 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19240 | hp1 | a0006 | c0007 | t0001 | g0078 | AFR | YRI | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02109 | hp2 | a0004 | c0005 | t0004 | g0036 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | MSL | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | LWK | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0097 | AFR | LWK | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0059 | REF | REF | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0045 | REF | REF | TRIM49D1_chr11_89906409_89927245 | TRIM49D1 | chr11 | 89906409 | 89927245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89911723 | T | A | 1 | a0007 | 2 | NA19085.hp1 NA19085.hp2 |
missense_variant | MODERATE | c.1223A>T | p.His408Leu | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 8/8 | 1832/2146 | 1223/1359 | 408/452 | chr11 | 89911723 | |||
| chr11:89911942 | G | A | 1 | a0008 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1004C>T | p.Thr335Ile | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 8/8 | 1613/2146 | 1004/1359 | 335/452 | chr11 | 89911942 | |||
| chr11:89911993 | G | A | 1 | a0005 | 2 | HG01884.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.953C>T | p.Ala318Val | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 8/8 | 1562/2146 | 953/1359 | 318/452 | chr11 | 89911993 | |||
| chr11:89912039 | G | A | 1 | a0009 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.907C>T | p.Arg303Cys | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 8/8 | 1516/2146 | 907/1359 | 303/452 | chr11 | 89912039 | |||
| chr11:89913279 | T | C | 1 | a0010 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.784A>G | p.Met262Val | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/8 | 1393/2146 | 784/1359 | 262/452 | chr11 | 89913279 | |||
| chr11:89915018 | C | T | 1 | a0004 | 5 | HG02109.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.632G>A | p.Arg211Gln | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 5/8 | 1241/2146 | 632/1359 | 211/452 | chr11 | 89915018 | |||
| chr11:89915029 | A | T | 5 | a0001 a0003 a0007 others(2): Show |
127 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
missense_variant | MODERATE | c.621T>A | p.Asp207Glu | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 5/8 | 1230/2146 | 621/1359 | 207/452 | chr11 | 89915029 | |||
| chr11:89917405 | T | C | 1 | a0006 | 2 | HG02280.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.306A>G | p.Ile102Met | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 3/8 | 915/2146 | 306/1359 | 102/452 | chr11 | 89917405 | |||
| chr11:89917580 | T | C | 1 | a0003 | 11 | HG00438.hp1 HG02083.hp1 HG02132.hp2 others(8): Show |
missense_variant | MODERATE | c.131A>G | p.Gln44Arg | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 3/8 | 740/2146 | 131/1359 | 44/452 | chr11 | 89917580 | |||
| chr11:89920300 | G | T | 1 | a0002 | 1 | HG02647.hp1 | splice_region_variant | LOW | c.-6C>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/8 | chr11 | 89920300 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89911932 | A | G | 2 | a0002c0012 a0004c0005 |
6 | HG02109.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
synonymous_variant | LOW | c.1014T>C | p.Ser338Ser | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 8/8 | 1623/2146 | 1014/1359 | 338/452 | chr11 | 89911932 | |||
| chr11:89912085 | C | T | 2 | a0001c0003 a0008c0009 |
21 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(18): Show |
splice_region_variant&synonymous_variant | LOW | c.861G>A | p.Val287Val | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 8/8 | 1470/2146 | 861/1359 | 287/452 | chr11 | 89912085 | |||
| chr11:89917513 | A | G | 1 | a0007c0008 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.198T>C | p.Thr66Thr | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 3/8 | 807/2146 | 198/1359 | 66/452 | chr11 | 89917513 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89911494 | G | C | 1 | a0004c0005t0004 | 5 | HG02109.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*93C>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 8/8 | 93 | chr11 | 89911494 | ||||||
| chr11:89920327 | T | C | 1 | a0002c0002t0005 | 4 | HG02280.hp1 HG02897.hp2 HG03834.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-33A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/8 | 2617 | chr11 | 89920327 | ||||||
| chr11:89920332 | C | T | 1 | a0002c0002t0003 | 6 | HG00323.hp1 HG01106.hp1 HG01255.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-38G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/8 | 2622 | chr11 | 89920332 | ||||||
| chr11:89920423 | T | C | 4 | a0001c0001t0002 a0001c0001t0008 a0007c0008t0002 others(1): Show |
48 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-129A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/8 | 2713 | chr11 | 89920423 | ||||||
| chr11:89920495 | A | G | 2 | a0001c0001t0009 a0004c0005t0004 |
6 | HG01243.hp2 HG02109.hp2 HG02886.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-201T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/8 | 2785 | chr11 | 89920495 | ||||||
| chr11:89921907 | C | T | 1 | a0001c0001t0008 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-271G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/8 | 4197 | chr11 | 89921907 | ||||||
| chr11:89921945 | C | G | 1 | a0002c0002t0007 | 2 | HG02155.hp2 NA19009.hp1 |
5_prime_UTR_variant | MODIFIER | c.-309G>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/8 | 4235 | chr11 | 89921945 | ||||||
| chr11:89921966 | C | T | 2 | a0002c0002t0006 a0005c0006t0006 |
3 | HG01884.hp1 HG02717.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-330G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/8 | 4256 | chr11 | 89921966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89912091 | A | AAAAT | 13 | a0001c0001t0001g0021 a0001c0001t0001g0096 a0001c0001t0001g0107 others(10): Show |
15 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.860-9_860-6dupATTT | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912091 | |||||||
| chr11:89912091 | AAAAT | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0104 a0001c0001t0002g0016 others(9): Show |
18 | HG00323.hp1 HG00423.hp1 HG01106.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.860-9_860-6delATTT | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912091 | |||||||
| chr11:89912091 | AAAATAAA others(1): Show |
A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0099 a0001c0001t0001g0105 others(3): Show |
7 | HG01891.hp2 HG02155.hp2 HG02895.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.860-13_860-6delATT others(5): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912091 | |||||||
| chr11:89912091 | AAAATAAA others(5): Show |
A | 1 | a0006c0007t0001g0078 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.860-17_860-6delATT others(9): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912091 | |||||||
| chr11:89912131 | T | A | 16 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0011 others(13): Show |
30 | HG00140.hp2 HG00408.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.860-45A>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912131 | |||||||
| chr11:89912131 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.860-45A>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912131 | |||||||
| chr11:89912131 | T | TAAAA | 3 | a0002c0002t0001g0046 a0002c0002t0001g0050 a0002c0012t0001g0038 |
3 | HG00741.hp2 HG03139.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.860-46_860-45insTT others(2): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912131 | |||||||
| chr11:89912131 | TAGAA | T | 2 | a0001c0001t0001g0106 a0002c0002t0001g0066 |
2 | HG03098.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.860-49_860-46delTT others(2): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912131 | |||||||
| chr11:89912133 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.860-47C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912133 | |||||||
| chr11:89912135 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.860-49T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912135 | |||||||
| chr11:89912137 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.860-51C>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912137 | |||||||
| chr11:89912144 | A | C | 1 | a0003c0004t0001g0112 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.860-58T>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912144 | |||||||
| chr11:89912309 | A | G | 1 | a0002c0012t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.860-223T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912309 | |||||||
| chr11:89912327 | A | G | 2 | a0004c0005t0004g0009 a0004c0005t0004g0037 |
4 | HG02886.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-241T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912327 | |||||||
| chr11:89912389 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.860-303T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912389 | |||||||
| chr11:89912392 | T | A | 18 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0011 others(15): Show |
32 | HG00140.hp2 HG00408.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.860-306A>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89912392 | |||||||
| chr11:89913071 | G | C | 1 | a0001c0003t0001g0094 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.859+133C>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89913071 | |||||||
| chr11:89913163 | A | T | 8 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0066 others(5): Show |
12 | HG00323.hp1 HG01106.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.859+41T>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 7/7 | chr11 | 89913163 | |||||||
| chr11:89913344 | A | G | 1 | a0003c0004t0001g0112 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.762-43T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 6/7 | chr11 | 89913344 | |||||||
| chr11:89913456 | C | T | 1 | a0002c0002t0007g0032 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.762-155G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 6/7 | chr11 | 89913456 | |||||||
| chr11:89913463 | C | T | 1 | a0001c0003t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.762-162G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 6/7 | chr11 | 89913463 | |||||||
| chr11:89913617 | C | T | 2 | a0002c0002t0005g0012 a0002c0002t0005g0079 |
4 | HG02280.hp1 HG02897.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.762-316G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 6/7 | chr11 | 89913617 | |||||||
| chr11:89913624 | C | T | 1 | a0002c0012t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.762-323G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 6/7 | chr11 | 89913624 | |||||||
| chr11:89913965 | A | AT | 12 | a0001c0001t0002g0118 a0001c0003t0001g0013 a0001c0003t0001g0022 others(9): Show |
19 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.761+209dupA | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 6/7 | chr11 | 89913965 | |||||||
| chr11:89913974 | T | TA | 1 | a0004c0005t0004g0009 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.761+200dupT | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 6/7 | chr11 | 89913974 | |||||||
| chr11:89913974 | T | TG | 88 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(85): Show |
150 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.761+200_761+201ins others(1): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 6/7 | chr11 | 89913974 | |||||||
| chr11:89914056 | C | T | 1 | a0002c0002t0001g0041 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.761+119G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 6/7 | chr11 | 89914056 | |||||||
| chr11:89914201 | T | TA | 8 | a0001c0001t0001g0084 a0001c0001t0002g0122 a0002c0002t0001g0020 others(5): Show |
9 | HG01243.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.739-5dupT | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 5/7 | chr11 | 89914201 | |||||||
| chr11:89914201 | TA | T | 6 | a0001c0001t0001g0096 a0002c0002t0001g0044 a0004c0005t0004g0009 others(3): Show |
8 | HG00140.hp2 HG01884.hp1 HG02109.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.739-5delT | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 5/7 | chr11 | 89914201 | |||||||
| chr11:89914559 | G | T | 3 | a0004c0005t0004g0009 a0004c0005t0004g0036 a0004c0005t0004g0037 |
5 | HG02109.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.738+353C>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 5/7 | chr11 | 89914559 | |||||||
| chr11:89914618 | T | C | 1 | a0002c0002t0001g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.738+294A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 5/7 | chr11 | 89914618 | |||||||
| chr11:89914790 | G | A | 3 | a0004c0005t0004g0009 a0004c0005t0004g0036 a0004c0005t0004g0037 |
5 | HG02109.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.738+122C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 5/7 | chr11 | 89914790 | |||||||
| chr11:89914828 | G | A | 8 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0066 others(5): Show |
12 | HG00323.hp1 HG01106.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.738+84C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 5/7 | chr11 | 89914828 | |||||||
| chr11:89915223 | G | A | 1 | a0001c0003t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.508-81C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915223 | |||||||
| chr11:89915329 | T | C | 4 | a0002c0002t0003g0005 a0002c0002t0003g0064 a0002c0002t0007g0032 others(1): Show |
8 | HG00323.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.508-187A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915329 | |||||||
| chr11:89915370 | T | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0025 others(12): Show |
31 | HG00438.hp1 HG01123.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.508-228A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915370 | |||||||
| chr11:89915377 | T | TA | 7 | a0001c0001t0001g0027 a0001c0001t0001g0080 a0002c0002t0001g0055 others(4): Show |
11 | HG00323.hp1 HG01106.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.508-236dupT | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915377 | |||||||
| chr11:89915377 | TA | T | 23 | a0001c0003t0001g0004 a0001c0003t0001g0091 a0002c0002t0001g0019 others(20): Show |
28 | HG01256.hp2 HG01261.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.508-236delT | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915377 | |||||||
| chr11:89915383 | A | C | 2 | a0002c0002t0007g0032 a0002c0002t0007g0033 |
2 | HG02155.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.508-241T>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915383 | |||||||
| chr11:89915388 | A | C | 1 | a0002c0002t0001g0076 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.508-246T>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915388 | |||||||
| chr11:89915479 | C | T | 1 | a0002c0002t0001g0039 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.508-337G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915479 | |||||||
| chr11:89915515 | G | A | 15 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0057 others(12): Show |
17 | HG01261.hp1 HG01261.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-373C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915515 | |||||||
| chr11:89915520 | A | G | 1 | a0002c0002t0001g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.508-378T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915520 | |||||||
| chr11:89915570 | G | A | 3 | a0002c0002t0001g0076 a0006c0007t0001g0077 a0006c0007t0001g0078 |
3 | HG02280.hp2 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.508-428C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915570 | |||||||
| chr11:89915748 | T | C | 1 | a0002c0002t0007g0033 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.508-606A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915748 | |||||||
| chr11:89915774 | T | TAC | 2 | a0002c0002t0001g0047 a0002c0002t0001g0072 |
2 | HG03492.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.508-634_508-633dup others(2): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915774 | |||||||
| chr11:89915774 | T | TACAC | 2 | a0002c0002t0001g0051 a0002c0002t0001g0067 |
2 | HG02027.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.508-636_508-633dup others(4): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915774 | |||||||
| chr11:89915774 | TAC | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0084 a0001c0001t0001g0105 others(11): Show |
29 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.508-634_508-633del others(2): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915774 | |||||||
| chr11:89915774 | TACAC | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0023 others(26): Show |
64 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.508-636_508-633del others(4): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915774 | |||||||
| chr11:89915774 | TACACAC | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0027 others(26): Show |
42 | HG00438.hp1 HG00741.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.508-638_508-633del others(6): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915774 | |||||||
| chr11:89915774 | TACACACA others(1): Show |
T | 20 | a0001c0001t0001g0100 a0001c0001t0002g0028 a0001c0003t0001g0004 others(17): Show |
33 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.508-640_508-633del others(8): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915774 | |||||||
| chr11:89915774 | TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0106 others(6): Show |
12 | HG01884.hp1 HG01891.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.508-642_508-633del others(10): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915774 | |||||||
| chr11:89915774 | TACACACA others(11): Show |
T | 4 | a0002c0002t0005g0012 a0002c0002t0005g0079 a0006c0007t0001g0077 others(1): Show |
6 | HG02280.hp1 HG02280.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.508-650_508-633del others(18): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915774 | |||||||
| chr11:89915774 | TACACACA others(15): Show |
T | 1 | a0002c0002t0001g0076 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.508-654_508-633del others(22): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915774 | |||||||
| chr11:89915808 | CACACACA others(3): Show |
C | 2 | a0001c0003t0001g0097 a0002c0002t0001g0041 |
2 | NA18998.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.508-676_508-667del others(10): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915808 | |||||||
| chr11:89915817 | A | ACAC | 2 | a0002c0002t0001g0066 a0002c0002t0001g0069 |
2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.508-676_508-675ins others(3): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915817 | |||||||
| chr11:89915939 | A | G | 11 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0066 others(8): Show |
17 | HG00323.hp1 HG01106.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.508-797T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915939 | |||||||
| chr11:89915941 | CT | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(94): Show |
168 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.508-800delA | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89915941 | |||||||
| chr11:89916011 | T | A | 1 | a0004c0005t0004g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.508-869A>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916011 | |||||||
| chr11:89916069 | A | G | 1 | a0002c0002t0001g0020 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.507+850T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916069 | |||||||
| chr11:89916092 | C | T | 1 | a0001c0003t0001g0088 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.507+827G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916092 | |||||||
| chr11:89916218 | A | G | 1 | a0001c0001t0001g0025 | 2 | NA19011.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.507+701T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916218 | |||||||
| chr11:89916269 | A | T | 3 | a0004c0005t0004g0009 a0004c0005t0004g0036 a0004c0005t0004g0037 |
5 | HG02109.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+650T>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916269 | |||||||
| chr11:89916569 | T | C | 4 | a0002c0002t0001g0020 a0002c0002t0006g0030 a0005c0006t0006g0029 others(1): Show |
5 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+350A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916569 | |||||||
| chr11:89916762 | G | T | 1 | a0001c0001t0002g0116 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.507+157C>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916762 | |||||||
| chr11:89916781 | G | GTTTTC | 29 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
67 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.507+133_507+137dup others(5): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916781 | |||||||
| chr11:89916796 | C | CT | 13 | a0001c0003t0001g0092 a0001c0003t0001g0093 a0001c0003t0001g0094 others(10): Show |
15 | HG00323.hp2 HG00597.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.507+122dupA | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916796 | |||||||
| chr11:89916796 | C | CTT | 17 | a0001c0001t0001g0080 a0001c0003t0001g0004 a0001c0003t0001g0013 others(14): Show |
27 | HG00140.hp1 HG00438.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.507+121_507+122dup others(2): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916796 | |||||||
| chr11:89916796 | C | CTTT | 5 | a0001c0003t0001g0086 a0001c0003t0001g0087 a0002c0002t0003g0005 others(2): Show |
9 | HG00323.hp1 HG01106.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.507+120_507+122dup others(3): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916796 | |||||||
| chr11:89916796 | C | CTTTTCT | 5 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0096 others(2): Show |
5 | HG01243.hp1 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+122_507+123ins others(6): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916796 | |||||||
| chr11:89916796 | CT | C | 6 | a0002c0002t0001g0010 a0002c0002t0001g0046 a0002c0002t0001g0047 others(3): Show |
8 | HG00735.hp1 HG00741.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.507+122delA | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916796 | |||||||
| chr11:89916796 | CTTTTTTT others(3): Show |
C | 2 | a0002c0002t0001g0055 a0002c0002t0001g0056 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.507+113_507+122del others(10): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916796 | |||||||
| chr11:89916797 | T | TTTTC | 17 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0025 others(14): Show |
32 | HG00438.hp1 HG01123.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.507+121_507+122ins others(4): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 4/7 | chr11 | 89916797 | |||||||
| chr11:89917077 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.412-63T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 3/7 | chr11 | 89917077 | |||||||
| chr11:89917206 | A | G | 1 | a0002c0002t0001g0068 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.411+94T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 3/7 | chr11 | 89917206 | |||||||
| chr11:89917289 | G | A | 3 | a0004c0005t0004g0009 a0004c0005t0004g0036 a0004c0005t0004g0037 |
5 | HG02109.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+11C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 3/7 | chr11 | 89917289 | |||||||
| chr11:89917803 | T | G | 1 | a0004c0005t0004g0037 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-4-89A>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89917803 | |||||||
| chr11:89918008 | T | C | 7 | a0003c0004t0001g0014 a0003c0004t0001g0015 a0003c0004t0001g0110 others(4): Show |
11 | HG00438.hp1 HG02083.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.-4-294A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918008 | |||||||
| chr11:89918096 | G | A | 1 | a0002c0002t0001g0048 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-4-382C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918096 | |||||||
| chr11:89918097 | C | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(87): Show |
155 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-4-383G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918097 | |||||||
| chr11:89918148 | T | TGAGA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(95): Show |
167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-4-438_-4-435dupTC others(2): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918148 | |||||||
| chr11:89918181 | T | C | 1 | a0003c0004t0001g0015 | 3 | NA18979.hp1 NA18980.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-4-467A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918181 | |||||||
| chr11:89918338 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
6 | HG00423.hp2 HG00544.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-624T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918338 | |||||||
| chr11:89918702 | A | G | 4 | a0002c0002t0001g0055 a0002c0002t0001g0056 a0002c0002t0001g0066 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-4-988T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918702 | |||||||
| chr11:89918737 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(95): Show |
167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-4-1023T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918737 | |||||||
| chr11:89918844 | C | T | 2 | a0002c0002t0001g0057 a0010c0013t0001g0058 |
2 | HG01261.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-4-1130G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918844 | |||||||
| chr11:89918995 | C | A | 90 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(87): Show |
155 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-4-1281G>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89918995 | |||||||
| chr11:89919103 | A | AT | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(95): Show |
167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-5+1195dupA | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919103 | |||||||
| chr11:89919184 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(101): Show |
175 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.-5+1115T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919184 | |||||||
| chr11:89919188 | C | T | 2 | a0002c0002t0001g0066 a0002c0002t0001g0067 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-5+1111G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919188 | |||||||
| chr11:89919264 | G | GAATAT | 2 | a0002c0002t0003g0005 a0002c0002t0003g0064 |
6 | HG00323.hp1 HG01106.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+1030_-5+1034dup others(5): Show |
TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919264 | |||||||
| chr11:89919339 | A | G | 2 | a0002c0002t0001g0018 a0002c0002t0005g0079 |
3 | HG00408.hp2 HG02280.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-5+960T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919339 | |||||||
| chr11:89919443 | T | C | 2 | a0006c0007t0001g0077 a0006c0007t0001g0078 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-5+856A>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919443 | |||||||
| chr11:89919564 | A | G | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(95): Show |
167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-5+735T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919564 | |||||||
| chr11:89919803 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(100): Show |
174 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-5+496G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919803 | |||||||
| chr11:89919898 | A | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(61): Show |
125 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-5+401T>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919898 | |||||||
| chr11:89919914 | G | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(63): Show |
129 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-5+385C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919914 | |||||||
| chr11:89919951 | G | A | 1 | a0003c0004t0001g0114 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-5+348C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 2/7 | chr11 | 89919951 | |||||||
| chr11:89920633 | T | A | 4 | a0002c0002t0003g0005 a0002c0002t0003g0064 a0002c0002t0007g0032 others(1): Show |
8 | HG00323.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.-215-124A>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89920633 | |||||||
| chr11:89920655 | C | A | 5 | a0002c0002t0001g0011 a0002c0002t0001g0018 a0002c0002t0001g0049 others(2): Show |
8 | HG00408.hp2 HG01928.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.-215-146G>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89920655 | |||||||
| chr11:89920928 | G | T | 2 | a0001c0001t0009g0035 a0004c0005t0004g0036 |
2 | HG01243.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-215-419C>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89920928 | |||||||
| chr11:89920976 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(99): Show |
173 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.-215-467T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89920976 | |||||||
| chr11:89921018 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0081 |
3 | HG00544.hp2 HG02523.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-215-509G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921018 | |||||||
| chr11:89921078 | G | T | 4 | a0002c0002t0003g0005 a0002c0002t0003g0064 a0002c0002t0007g0032 others(1): Show |
8 | HG00323.hp1 HG01106.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.-215-569C>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921078 | |||||||
| chr11:89921090 | G | A | 2 | a0002c0002t0005g0012 a0002c0002t0005g0079 |
4 | HG02280.hp1 HG02897.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-215-581C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921090 | |||||||
| chr11:89921173 | C | A | 1 | a0002c0002t0001g0052 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-215-664G>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921173 | |||||||
| chr11:89921181 | A | C | 7 | a0002c0002t0001g0019 a0002c0002t0001g0057 a0002c0002t0001g0060 others(4): Show |
8 | HG01261.hp1 HG01261.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-216+671T>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921181 | |||||||
| chr11:89921276 | A | G | 2 | a0002c0002t0001g0055 a0002c0002t0001g0056 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-216+576T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921276 | |||||||
| chr11:89921341 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-216+511A>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921341 | |||||||
| chr11:89921368 | T | A | 64 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(61): Show |
125 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-216+484A>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921368 | |||||||
| chr11:89921413 | A | G | 4 | a0001c0001t0009g0035 a0004c0005t0004g0009 a0004c0005t0004g0036 others(1): Show |
6 | HG01243.hp2 HG02109.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-216+439T>C | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921413 | |||||||
| chr11:89921545 | A | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(95): Show |
167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-216+307T>G | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921545 | |||||||
| chr11:89921567 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-216+285G>A | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921567 | |||||||
| chr11:89921729 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(95): Show |
167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-216+123C>T | TRIM49D1 | ENSG00000223417.9 | transcript | ENST00000420869.3 | protein_coding | 1/7 | chr11 | 89921729 |