Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 729384 |
| ensemblid | ENSG00000233802.8 |
| hgncid | 37217 |
| symbol | TRIM49D2 |
| name | tripartite motif containing 49D2 |
| refseq_nuc | NM_001105522.1 |
| refseq_prot | NP_001098992.1 |
| ensembl_nuc | ENST00000623787.3 |
| ensembl_prot | ENSP00000485097.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 89924064 |
| end | 89933063 |
| strand | + |
| ver | v1.2 |
| region | chr11:89924064-89933063 |
| region5000 | chr11:89919064-89938063 |
| regionname0 | TRIM49D2_chr11_89924064_89933063 |
| regionname5000 | TRIM49D2_chr11_89919064_89938063 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 452 | 145 | 22 | 32 | 71 | 5 | 15 | 52 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0002 | 0/0 | 452 | 88 | 33 | 15 | 28 | 5 | 7 | 21 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0003 | 0/0 | 452 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0004 | 0/0 | 452 | 6 | 0 | 0 | 5 | 0 | 1 | 2 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0005 | 0/0 | 452 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0006 | 0/0 | 452 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0007 | 0/0 | 452 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0008 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0009 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0010 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| a0011 | 0/0 | 12 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MPKDN others(7): Show |
chr11 | 89919064 | 89938063 |
| a0012 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | MNSGI others(447): Show |
chr11 | 89919064 | 89938063 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1356 | 119 | 22 | 22 | 57 | 3 | 15 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0001c0003 | 0/0 | 1356 | 24 | 0 | 10 | 12 | 2 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0001c0011 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0001c0015 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0002c0002 | 0/0 | 1356 | 86 | 31 | 15 | 28 | 5 | 7 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0002c0006 | 0/0 | 1356 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0003c0004 | 0/0 | 1356 | 7 | 6 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0004c0005 | 0/0 | 1356 | 6 | 0 | 0 | 5 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0005c0007 | 0/0 | 1356 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0006c0009 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0006c0010 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0007c0012 | 0/0 | 1356 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0008c0013 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0009c0016 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0010c0017 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0011c0008 | 0/0 | 1356 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ACGAA others(1351): Show |
chr11 | 89919064 | 89938063 | ||
| a0012c0014 | 0/0 | 1356 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | ATGAA others(1351): Show |
chr11 | 89919064 | 89938063 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1651 | 119 | 22 | 22 | 57 | 3 | 15 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0001c0003t0001 | 0/0 | 1651 | 24 | 0 | 10 | 12 | 2 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0001c0011t0001 | 0/0 | 1651 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0001c0015t0001 | 0/0 | 1651 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0002c0002t0001 | 0/0 | 1651 | 83 | 28 | 15 | 28 | 5 | 7 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0002c0002t0003 | 0/0 | 1651 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0002c0002t0004 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0002c0006t0001 | 0/0 | 1651 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0003c0004t0002 | 0/0 | 1651 | 7 | 6 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0004c0005t0001 | 0/0 | 1651 | 6 | 0 | 0 | 5 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0005c0007t0001 | 0/0 | 1651 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0006c0009t0001 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0006c0010t0001 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0007c0012t0001 | 0/0 | 1651 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0008c0013t0001 | 0/0 | 1651 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0009c0016t0001 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0010c0017t0001 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0011c0008t0003 | 0/0 | 1651 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| a0012c0014t0001 | 0/0 | 1651 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | GGTGA others(1646): Show |
chr11 | 89919064 | 89938063 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 37 | 5 | 12 | 18 | 1 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0003 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0005 | 0/0 | 8 | 1 | 0 | 2 | 1 | 4 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0007 | 0/0 | 7 | 1 | 3 | 2 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0014 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0024 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0003t0001g0004 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0003t0001g0006 | 0/0 | 7 | 0 | 3 | 3 | 1 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0003t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0003t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0011t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0001c0015t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0002 | 0/0 | 15 | 0 | 4 | 7 | 2 | 2 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0008 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0019 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0002c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0003c0004t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0003c0004t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0003c0004t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0003c0004t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0003c0004t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0003c0004t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0004c0005t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0004c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0004c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0005c0007t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0005c0007t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0006c0009t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0006c0010t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0007c0012t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0008c0013t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0009c0016t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0010c0017t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0011c0008t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| a0012c0014t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0006 | EUR | GBR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0083 | EUR | FIN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0040 | EUR | FIN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00438 | hp1 | a0004 | c0005 | t0001 | g0017 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01109 | hp2 | a0007 | c0012 | t0001 | g0004 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01243 | hp1 | a0003 | c0004 | t0002 | g0065 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0033 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01261 | hp2 | a0005 | c0007 | t0001 | g0028 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0032 | EUR | IBS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0008 | EUR | IBS | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0071 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0033 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02071 | hp2 | a0008 | c0013 | t0001 | g0106 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02074 | hp2 | a0004 | c0005 | t0001 | g0017 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02083 | hp1 | a0004 | c0005 | t0001 | g0017 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | CDX | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02280 | hp1 | a0002 | c0002 | t0003 | g0038 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02280 | hp2 | a0009 | c0016 | t0001 | g0061 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PEL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | KHV | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02647 | hp1 | a0002 | c0002 | t0004 | g0057 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02698 | hp2 | a0004 | c0005 | t0001 | g0105 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02723 | hp1 | a0002 | c0006 | t0001 | g0062 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02886 | hp1 | a0003 | c0004 | t0002 | g0066 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0038 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02897 | hp2 | a0003 | c0004 | t0002 | g0067 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02965 | hp2 | a0003 | c0004 | t0002 | g0068 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03139 | hp2 | a0002 | c0006 | t0001 | g0063 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03195 | hp1 | a0006 | c0009 | t0001 | g0082 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | ESN | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03209 | hp2 | a0006 | c0010 | t0001 | g0023 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03453 | hp1 | a0003 | c0004 | t0002 | g0031 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03540 | hp2 | a0003 | c0004 | t0002 | g0031 | AFR | GWD | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0027 | SAS | STU | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03834 | hp2 | a0011 | c0008 | t0003 | g0108 | SAS | BEB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | STU | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | YRI | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | YRI | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | CHB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | YRI | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18947 | hp1 | a0004 | c0005 | t0001 | g0017 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18947 | hp2 | a0004 | c0005 | t0001 | g0037 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18970 | hp1 | a0001 | c0015 | t0001 | g0003 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18971 | hp2 | a0001 | c0011 | t0001 | g0087 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | LWK | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19043 | hp2 | a0005 | c0007 | t0001 | g0056 | AFR | LWK | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19067 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19085 | hp2 | a0012 | c0014 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19089 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02109 | hp2 | a0003 | c0004 | t0002 | g0064 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03471 | hp1 | a0010 | c0017 | t0001 | g0092 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | MSL | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TRIM49D2_chr11_89919064_89938063 | TRIM49D2 | chr11 | 89919064 | 89938063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89924172 | C | A | 1 | a0002 | 1 | HG02647.hp1 | splice_region_variant | LOW | c.-6C>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/7 | chr11 | 89924172 | |||||||
| chr11:89926763 | T | C | 1 | a0011 | 1 | HG03834.hp2 | start_lost | HIGH | c.2T>C | p.Met1? | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 2/7 | 116/1651 | 2/1359 | 1/452 | chr11 | 89926763 | |||
| chr11:89926892 | A | G | 1 | a0004 | 6 | HG00438.hp1 HG02074.hp2 HG02083.hp1 others(3): Show |
missense_variant | MODERATE | c.131A>G | p.Gln44Arg | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 2/7 | 245/1651 | 131/1359 | 44/452 | chr11 | 89926892 | |||
| chr11:89926903 | A | T | 1 | a0010 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.142A>T | p.Ile48Phe | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 2/7 | 256/1651 | 142/1359 | 48/452 | chr11 | 89926903 | |||
| chr11:89927067 | A | G | 1 | a0009 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.306A>G | p.Ile102Met | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 2/7 | 420/1651 | 306/1359 | 102/452 | chr11 | 89927067 | |||
| chr11:89927117 | T | A | 1 | a0006 | 2 | HG03195.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.356T>A | p.Leu119Gln | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 2/7 | 470/1651 | 356/1359 | 119/452 | chr11 | 89927117 | |||
| chr11:89929443 | T | A | 7 | a0001 a0004 a0006 others(4): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(154): Show |
missense_variant | MODERATE | c.621T>A | p.Asp207Glu | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/7 | 735/1651 | 621/1359 | 207/452 | chr11 | 89929443 | |||
| chr11:89929454 | G | A | 1 | a0003 | 7 | HG01243.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
missense_variant | MODERATE | c.632G>A | p.Arg211Gln | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/7 | 746/1651 | 632/1359 | 211/452 | chr11 | 89929454 | |||
| chr11:89931193 | A | G | 1 | a0005 | 2 | HG01261.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.784A>G | p.Met262Val | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/7 | 898/1651 | 784/1359 | 262/452 | chr11 | 89931193 | |||
| chr11:89932482 | C | A | 1 | a0008 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.956C>A | p.Pro319His | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 7/7 | 1070/1651 | 956/1359 | 319/452 | chr11 | 89932482 | |||
| chr11:89932530 | C | T | 1 | a0007 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1004C>T | p.Thr335Ile | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 7/7 | 1118/1651 | 1004/1359 | 335/452 | chr11 | 89932530 | |||
| chr11:89932749 | A | T | 1 | a0012 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1223A>T | p.His408Leu | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 7/7 | 1337/1651 | 1223/1359 | 408/452 | chr11 | 89932749 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89927133 | C | T | 1 | a0001c0015 | 1 | NA18970.hp1 | synonymous_variant | LOW | c.372C>T | p.His124His | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 2/7 | 486/1651 | 372/1359 | 124/452 | chr11 | 89927133 | |||
| chr11:89931171 | G | A | 1 | a0001c0011 | 1 | NA18971.hp2 | splice_region_variant&synonymous_variant | LOW | c.762G>A | p.Arg254Arg | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/7 | 876/1651 | 762/1359 | 254/452 | chr11 | 89931171 | |||
| chr11:89932387 | G | A | 3 | a0001c0003 a0006c0009 a0007c0012 |
26 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(23): Show |
splice_region_variant&synonymous_variant | LOW | c.861G>A | p.Val287Val | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 7/7 | 975/1651 | 861/1359 | 287/452 | chr11 | 89932387 | |||
| chr11:89932540 | T | C | 2 | a0002c0006 a0003c0004 |
9 | HG01243.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
synonymous_variant | LOW | c.1014T>C | p.Ser338Ser | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 7/7 | 1128/1651 | 1014/1359 | 338/452 | chr11 | 89932540 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89924145 | A | G | 2 | a0002c0002t0003 a0011c0008t0003 |
3 | HG02280.hp1 HG02897.hp1 HG03834.hp2 |
5_prime_UTR_variant | MODIFIER | c.-33A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/7 | 2617 | chr11 | 89924145 | ||||||
| chr11:89932978 | C | G | 1 | a0003c0004t0002 | 7 | HG01243.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*93C>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 7/7 | 93 | chr11 | 89932978 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:89924205 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-5+32C>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89924205 | |||||||
| chr11:89924558 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(59): Show |
160 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-5+385C>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89924558 | |||||||
| chr11:89924574 | T | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(56): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.-5+401T>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89924574 | |||||||
| chr11:89924641 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-5+468A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89924641 | |||||||
| chr11:89924669 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-5+496G>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89924669 | |||||||
| chr11:89924724 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-5+551T>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89924724 | |||||||
| chr11:89924881 | G | T | 1 | a0002c0002t0001g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-5+708G>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89924881 | |||||||
| chr11:89924908 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
213 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-5+735T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89924908 | |||||||
| chr11:89924983 | T | C | 1 | a0002c0002t0001g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-5+810T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89924983 | |||||||
| chr11:89925029 | A | G | 1 | a0009c0016t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-5+856A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925029 | |||||||
| chr11:89925133 | T | C | 2 | a0002c0002t0001g0020 a0002c0002t0001g0069 |
4 | HG00408.hp1 HG02080.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+960T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925133 | |||||||
| chr11:89925171 | T | A | 1 | a0003c0004t0002g0031 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-5+998T>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925171 | |||||||
| chr11:89925201 | G | GTATAT | 2 | a0002c0002t0001g0008 a0002c0002t0001g0040 |
6 | HG00323.hp2 HG00642.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.-5+1030_-5+1034dup others(5): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr11 | 89925201 | ||||||
| chr11:89925284 | G | A | 3 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0041 |
5 | HG01074.hp2 HG02055.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5+1111G>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925284 | |||||||
| chr11:89925288 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-5+1115T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925288 | |||||||
| chr11:89925357 | G | GA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(91): Show |
211 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.-5+1195dupA | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr11 | 89925357 | ||||||
| chr11:89925410 | T | C | 1 | a0002c0002t0001g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-5+1237T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925410 | |||||||
| chr11:89925477 | G | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.-4-1281G>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925477 | |||||||
| chr11:89925504 | T | C | 1 | a0002c0002t0001g0044 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-4-1254T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925504 | |||||||
| chr11:89925545 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-4-1213C>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925545 | |||||||
| chr11:89925735 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
213 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-4-1023T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925735 | |||||||
| chr11:89925770 | T | C | 5 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0041 others(2): Show |
7 | HG01074.hp2 HG02055.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-4-988T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89925770 | |||||||
| chr11:89926134 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0075 a0001c0001t0001g0077 others(1): Show |
7 | HG00423.hp2 HG00544.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4-624T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89926134 | |||||||
| chr11:89926200 | G | T | 1 | a0002c0002t0001g0060 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-4-558G>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89926200 | |||||||
| chr11:89926249 | T | TGTGCAGG others(37): Show |
1 | a0001c0001t0001g0079 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-4-505_-4-462dupCA others(42): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr11 | 89926249 | ||||||
| chr11:89926317 | G | GTCTC | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
213 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.-4-438_-4-435dupTC others(2): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr11 | 89926317 | ||||||
| chr11:89926375 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.-4-383G>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89926375 | |||||||
| chr11:89926464 | A | G | 4 | a0001c0001t0001g0037 a0004c0005t0001g0017 a0004c0005t0001g0037 others(1): Show |
7 | HG00438.hp1 HG02074.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4-294A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89926464 | |||||||
| chr11:89926661 | T | G | 1 | a0002c0002t0001g0040 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-4-97T>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89926661 | |||||||
| chr11:89926669 | A | C | 4 | a0003c0004t0002g0031 a0003c0004t0002g0066 a0003c0004t0002g0067 others(1): Show |
5 | HG02886.hp1 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4-89A>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 1/6 | chr11 | 89926669 | |||||||
| chr11:89927183 | C | T | 6 | a0003c0004t0002g0031 a0003c0004t0002g0064 a0003c0004t0002g0065 others(3): Show |
7 | HG01243.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.411+11C>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 2/6 | chr11 | 89927183 | |||||||
| chr11:89927266 | T | C | 1 | a0002c0002t0001g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.411+94T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 2/6 | chr11 | 89927266 | |||||||
| chr11:89927655 | C | CA | 8 | a0001c0003t0001g0022 a0001c0003t0001g0083 a0002c0002t0001g0011 others(5): Show |
16 | HG00323.hp1 HG01884.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.507+122dupA | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89927655 | ||||||
| chr11:89927655 | C | CAA | 22 | a0001c0003t0001g0004 a0001c0003t0001g0006 a0001c0003t0001g0033 others(19): Show |
39 | HG00140.hp2 HG00438.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.507+121_507+122dup others(2): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89927655 | ||||||
| chr11:89927655 | C | CAAA | 4 | a0001c0001t0001g0080 a0002c0002t0001g0008 a0002c0002t0001g0040 others(1): Show |
8 | HG00323.hp2 HG00642.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.507+120_507+122dup others(3): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89927655 | ||||||
| chr11:89927655 | CA | C | 8 | a0002c0002t0001g0059 a0002c0002t0001g0073 a0002c0002t0001g0074 others(5): Show |
8 | HG01175.hp1 HG01243.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.507+122delA | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89927655 | ||||||
| chr11:89927655 | CAAAAAAA others(3): Show |
C | 2 | a0002c0002t0001g0042 a0002c0002t0001g0043 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.507+113_507+122del others(10): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89927655 | ||||||
| chr11:89927671 | A | AAAAAG | 23 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(20): Show |
79 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.507+133_507+137dup others(5): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89927671 | ||||||
| chr11:89927671 | A | AAAAG | 19 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(16): Show |
44 | HG00438.hp1 HG01123.hp1 HG01256.hp1 others(41): Show |
intron_variant | MODIFIER | c.507+121_507+122ins others(4): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89927671 | ||||||
| chr11:89927715 | C | A | 1 | a0002c0002t0004g0057 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.507+162C>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89927715 | |||||||
| chr11:89927903 | A | G | 3 | a0002c0002t0001g0046 a0002c0002t0001g0054 a0002c0002t0001g0055 |
3 | HG01884.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.507+350A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89927903 | |||||||
| chr11:89928203 | T | A | 5 | a0003c0004t0002g0031 a0003c0004t0002g0064 a0003c0004t0002g0066 others(2): Show |
6 | HG02109.hp2 HG02886.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.507+650T>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928203 | |||||||
| chr11:89928254 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.507+701T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928254 | |||||||
| chr11:89928360 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.507+807T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928360 | |||||||
| chr11:89928440 | A | G | 1 | a0002c0002t0001g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.507+887A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928440 | |||||||
| chr11:89928461 | A | T | 3 | a0003c0004t0002g0031 a0003c0004t0002g0067 a0003c0004t0002g0068 |
4 | HG02897.hp2 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-869A>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928461 | |||||||
| chr11:89928523 | GA | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(92): Show |
209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.508-800delA | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928523 | ||||||
| chr11:89928533 | T | C | 14 | a0002c0002t0001g0008 a0002c0002t0001g0011 a0002c0002t0001g0025 others(11): Show |
24 | HG00323.hp2 HG00642.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.508-797T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928533 | |||||||
| chr11:89928534 | T | C | 3 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0060 |
3 | HG02630.hp1 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.508-796T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928534 | |||||||
| chr11:89928654 | T | TTG | 4 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0053 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-634_508-633dup others(2): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928654 | ||||||
| chr11:89928654 | TTG | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0103 others(9): Show |
33 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.508-634_508-633del others(2): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928654 | ||||||
| chr11:89928654 | TTGTG | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(19): Show |
72 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.508-636_508-633del others(4): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928654 | ||||||
| chr11:89928654 | TTGTGTG | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(21): Show |
51 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.508-638_508-633del others(6): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928654 | ||||||
| chr11:89928654 | TTGTGTGT others(1): Show |
T | 25 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0085 others(22): Show |
48 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.508-640_508-633del others(8): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928654 | ||||||
| chr11:89928654 | TTGTGTGT others(3): Show |
T | 6 | a0001c0001t0001g0015 a0002c0002t0001g0011 a0002c0002t0001g0045 others(3): Show |
12 | HG01109.hp1 HG01123.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.508-642_508-633del others(10): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928654 | ||||||
| chr11:89928654 | TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0001g0091 a0002c0002t0001g0047 |
2 | HG00423.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508-644_508-633del others(12): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928654 | ||||||
| chr11:89928654 | TTGTGTGT others(7): Show |
T | 1 | a0002c0002t0001g0072 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.508-646_508-633del others(14): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928654 | ||||||
| chr11:89928654 | TTGTGTGT others(11): Show |
T | 5 | a0002c0002t0001g0030 a0002c0002t0001g0059 a0002c0002t0003g0038 others(2): Show |
7 | HG02280.hp1 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-650_508-633del others(18): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89928654 | ||||||
| chr11:89928721 | T | C | 1 | a0006c0009t0001g0082 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.508-609T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928721 | |||||||
| chr11:89928724 | A | G | 1 | a0002c0002t0001g0011 | 4 | HG02155.hp1 NA18985.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-606A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928724 | |||||||
| chr11:89928902 | C | T | 3 | a0002c0002t0001g0030 a0002c0002t0001g0059 a0009c0016t0001g0061 |
4 | HG02280.hp2 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-428C>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928902 | |||||||
| chr11:89928952 | T | C | 1 | a0002c0002t0001g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.508-378T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928952 | |||||||
| chr11:89928957 | C | T | 16 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0027 others(13): Show |
21 | HG01261.hp1 HG01261.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.508-373C>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928957 | |||||||
| chr11:89928993 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.508-337G>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89928993 | |||||||
| chr11:89929081 | G | GT | 8 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0093 others(5): Show |
12 | HG00323.hp2 HG00642.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.508-236dupT | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89929081 | ||||||
| chr11:89929081 | GT | G | 25 | a0001c0001t0001g0077 a0001c0003t0001g0033 a0002c0002t0001g0018 others(22): Show |
32 | HG01243.hp1 HG01256.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.508-236delT | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr11 | 89929081 | ||||||
| chr11:89929084 | T | G | 2 | a0002c0002t0001g0030 a0002c0002t0001g0059 |
3 | HG02809.hp2 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.508-246T>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89929084 | |||||||
| chr11:89929089 | T | G | 1 | a0002c0002t0001g0011 | 4 | HG02155.hp1 NA18985.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-241T>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89929089 | |||||||
| chr11:89929102 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(16): Show |
39 | HG00438.hp1 HG01123.hp1 HG01256.hp1 others(36): Show |
intron_variant | MODIFIER | c.508-228A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89929102 | |||||||
| chr11:89929134 | T | C | 1 | a0002c0002t0001g0047 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.508-196T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89929134 | |||||||
| chr11:89929143 | A | G | 3 | a0002c0002t0001g0008 a0002c0002t0001g0011 a0002c0002t0001g0040 |
10 | HG00323.hp2 HG00642.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.508-187A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89929143 | |||||||
| chr11:89929197 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.508-133A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89929197 | |||||||
| chr11:89929230 | G | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0095 |
2 | HG02074.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.508-100G>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 3/6 | chr11 | 89929230 | |||||||
| chr11:89929644 | C | T | 8 | a0002c0002t0001g0008 a0002c0002t0001g0011 a0002c0002t0001g0025 others(5): Show |
17 | HG00323.hp2 HG00642.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.738+84C>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | chr11 | 89929644 | |||||||
| chr11:89929682 | C | T | 6 | a0003c0004t0002g0031 a0003c0004t0002g0064 a0003c0004t0002g0065 others(3): Show |
7 | HG01243.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+122C>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | chr11 | 89929682 | |||||||
| chr11:89929854 | A | G | 1 | a0002c0002t0001g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.738+294A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | chr11 | 89929854 | |||||||
| chr11:89929896 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG00408.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.738+336G>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | chr11 | 89929896 | |||||||
| chr11:89929913 | C | A | 6 | a0003c0004t0002g0031 a0003c0004t0002g0064 a0003c0004t0002g0065 others(3): Show |
7 | HG01243.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+353C>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | chr11 | 89929913 | |||||||
| chr11:89930003 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.739-272C>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | chr11 | 89930003 | |||||||
| chr11:89930022 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.739-253A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | chr11 | 89930022 | |||||||
| chr11:89930165 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.739-110T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | chr11 | 89930165 | |||||||
| chr11:89930256 | A | AT | 6 | a0002c0002t0001g0027 a0002c0002t0001g0042 a0002c0002t0001g0043 others(3): Show |
8 | HG02280.hp1 HG02897.hp1 HG02976.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.739-5dupT | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 89930256 | ||||||
| chr11:89930256 | A | ATT | 3 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0041 |
5 | HG01074.hp2 HG02055.hp1 HG02717.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.739-6_739-5dupTT | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 89930256 | ||||||
| chr11:89930256 | AT | A | 9 | a0001c0003t0001g0081 a0002c0002t0001g0009 a0003c0004t0002g0031 others(6): Show |
14 | HG01243.hp1 HG01981.hp2 HG02083.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.739-5delT | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr11 | 89930256 | ||||||
| chr11:89930497 | T | TA | 10 | a0001c0003t0001g0004 a0001c0003t0001g0022 a0001c0003t0001g0034 others(7): Show |
23 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.761+209dupA | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 89930497 | ||||||
| chr11:89930497 | T | TAA | 6 | a0003c0004t0002g0031 a0003c0004t0002g0064 a0003c0004t0002g0065 others(3): Show |
7 | HG01243.hp1 HG02109.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.761+208_761+209dup others(2): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr11 | 89930497 | ||||||
| chr11:89930497 | T | TC | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(86): Show |
193 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.761+200_761+201ins others(1): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 5/6 | chr11 | 89930497 | |||||||
| chr11:89930671 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.761+374A>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 5/6 | chr11 | 89930671 | |||||||
| chr11:89930848 | G | A | 2 | a0002c0006t0001g0062 a0002c0006t0001g0063 |
2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.762-323G>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 5/6 | chr11 | 89930848 | |||||||
| chr11:89930855 | G | A | 2 | a0002c0002t0003g0038 a0011c0008t0003g0108 |
3 | HG02280.hp1 HG02897.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.762-316G>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 5/6 | chr11 | 89930855 | |||||||
| chr11:89931009 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.762-162G>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 5/6 | chr11 | 89931009 | |||||||
| chr11:89931309 | T | A | 8 | a0002c0002t0001g0008 a0002c0002t0001g0011 a0002c0002t0001g0025 others(5): Show |
17 | HG00323.hp2 HG00642.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.859+41T>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89931309 | |||||||
| chr11:89932080 | T | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.860-306T>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89932080 | |||||||
| chr11:89932083 | T | C | 1 | a0008c0013t0001g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.860-303T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89932083 | |||||||
| chr11:89932145 | T | C | 4 | a0003c0004t0002g0031 a0003c0004t0002g0066 a0003c0004t0002g0067 others(1): Show |
5 | HG02886.hp1 HG02897.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-241T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89932145 | |||||||
| chr11:89932163 | T | C | 2 | a0002c0006t0001g0062 a0002c0006t0001g0063 |
2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.860-223T>C | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89932163 | |||||||
| chr11:89932171 | T | G | 1 | a0003c0004t0002g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.860-215T>G | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89932171 | |||||||
| chr11:89932175 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.860-211G>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89932175 | |||||||
| chr11:89932335 | CTTTCTTT others(5): Show |
C | 1 | a0002c0002t0001g0025 | 2 | HG01074.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.860-49_860-38delTT others(10): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 89932335 | ||||||
| chr11:89932339 | C | CTATT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(8): Show |
14 | HG01123.hp1 HG01123.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.860-46_860-45insAT others(2): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 89932339 | ||||||
| chr11:89932339 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.860-47C>T | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89932339 | |||||||
| chr11:89932339 | CTTTT | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0023 others(5): Show |
9 | HG00140.hp2 HG01074.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.860-45_860-42delTT others(2): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 89932339 | ||||||
| chr11:89932339 | CTTTTTAT others(1): Show |
C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0002c0002t0001g0008 others(6): Show |
17 | HG00323.hp2 HG00642.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.860-45_860-38delTT others(6): Show |
TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 89932339 | ||||||
| chr11:89932341 | T | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
189 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.860-45T>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89932341 | |||||||
| chr11:89932341 | T | TTTTA | 6 | a0001c0003t0001g0004 a0002c0002t0001g0002 a0002c0002t0001g0059 others(3): Show |
7 | HG02080.hp2 HG02723.hp1 HG02738.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.860-9_860-6dupATTT | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr11 | 89932341 | ||||||
| chr11:89932342 | T | A | 1 | a0002c0002t0001g0026 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.860-44T>A | TRIM49D2 | ENSG00000233802.8 | transcript | ENST00000623787.3 | protein_coding | 6/6 | chr11 | 89932342 |