Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51463 |
|---|---|
| ensemblid | ENSG00000188092.15 |
| hgncid | 13840 |
| symbol | GPR89B |
| name | G protein-coupled receptor 89B |
| refseq_nuc | NM_016334.5 |
| refseq_prot | NP_057418.1 |
| ensembl_nuc | ENST00000314163.12 |
| ensembl_prot | ENSP00000358233.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 147928420 |
| end | 147993592 |
| strand | + |
| ver | v1.2 |
| region | chr1:147928420-147993592 |
| region5000 | chr1:147923420-147998592 |
| regionname0 | GPR89B_chr1_147928420_147993592 |
| regionname5000 | GPR89B_chr1_147923420_147998592 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 455 | 268 | 68 | 48 | 113 | 10 | 27 | 83 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0002 | 0/0 | 455 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0003 | 0/0 | 127 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0004 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0005 | 0/0 | 455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1368 | 217 | 54 | 43 | 90 | 9 | 19 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| c0002 | 0/0 | 1368 | 29 | 6 | 2 | 12 | 1 | 8 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| c0003 | 0/0 | 1368 | 21 | 7 | 3 | 11 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| c0004 | 0/0 | 1368 | 3 | 3 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| c0005 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| c0006 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| c0007 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| c0008 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 793 | 240 | 55 | 43 | 102 | 10 | 28 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| t0002 | 0/0 | 793 | 14 | 3 | 0 | 11 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| t0003 | 0/0 | 793 | 10 | 7 | 3 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| t0004 | 0/0 | 794 | 6 | 5 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| t0005 | 0/0 | 793 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| t0006 | 0/0 | 793 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| t0007 | 0/0 | 793 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| t0008 | 0/0 | 793 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1368 | 217 | 54 | 43 | 90 | 9 | 19 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0002 | 0/0 | 1368 | 29 | 6 | 2 | 12 | 1 | 8 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0003 | 0/0 | 1368 | 21 | 7 | 3 | 11 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0006 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0002c0004 | 0/0 | 1368 | 3 | 3 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0003c0008 | 0/0 | 1368 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0004c0007 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0005c0005 | 0/0 | 1368 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2160 | 208 | 48 | 41 | 89 | 9 | 19 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0001t0004 | 0/0 | 2161 | 6 | 5 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0001t0005 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0001t0006 | 0/0 | 2160 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0001t0008 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0002t0001 | 0/0 | 2160 | 29 | 6 | 2 | 12 | 1 | 8 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0003t0002 | 0/0 | 2160 | 11 | 0 | 0 | 11 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0003t0003 | 0/0 | 2160 | 10 | 7 | 3 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0001c0006t0007 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0002c0004t0002 | 0/0 | 2160 | 3 | 3 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0003c0008t0001 | 0/0 | 2160 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0004c0007t0001 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| a0005c0005t0001 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | copy fasta | chr1 | 147923420 | 147998592 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0008g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0006t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0002c0004t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0002c0004t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0002c0004t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0003c0008t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0004c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0005c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0068 | EUR | GBR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00423 | hp2 | a0001 | c0003 | t0002 | g0231 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0225 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0232 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0220 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0238 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0237 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0155 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0236 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0224 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02055 | hp1 | a0001 | c0006 | t0007 | g0256 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02055 | hp2 | a0001 | c0003 | t0003 | g0240 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0244 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0241 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0239 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02735 | hp2 | a0003 | c0008 | t0001 | g0089 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0243 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02886 | hp2 | a0002 | c0004 | t0002 | g0234 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0091 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03453 | hp2 | a0001 | c0003 | t0003 | g0242 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03486 | hp1 | a0002 | c0004 | t0002 | g0228 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0086 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0189 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0230 | EAS | CHB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18906 | hp1 | a0002 | c0004 | t0002 | g0227 | AFR | YRI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18944 | hp1 | a0001 | c0003 | t0002 | g0229 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18974 | hp1 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18974 | hp2 | a0004 | c0007 | t0001 | g0092 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0222 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18986 | hp1 | a0001 | c0003 | t0002 | g0221 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19006 | hp1 | a0001 | c0003 | t0002 | g0223 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19007 | hp1 | a0001 | c0003 | t0002 | g0233 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0215 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0235 | AFR | ASW | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | GIH | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | GIH | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02109 | hp2 | a0005 | c0005 | t0001 | g0115 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | USA | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0136 | REF | REF | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0079 | REF | REF | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147944065
|
G | T | 1 | a0003 | 1 | HG02735.hp2 | stop_gained | HIGH | c.382G>T | p.Gly128* | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/14 | 499/2160 | 382/1368 | 128/455 | chr1 | 147944065 | ||
| chr1:147954366
|
T | C | 1 | a0005 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.581T>C | p.Leu194Pro | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/14 | 698/2160 | 581/1368 | 194/455 | chr1 | 147954366 | ||
| chr1:147966594
|
G | A | 1 | a0002 | 3 | HG02886.hp2 HG03486.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.658G>A | p.Val220Met | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/14 | 775/2160 | 658/1368 | 220/455 | chr1 | 147966594 | ||
| chr1:147969869
|
G | T | 1 | a0004 | 1 | NA18974.hp2 | missense_variant&splice_region_variant | MODERATE | c.819G>T | p.Glu273Asp | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/14 | 936/2160 | 819/1368 | 273/455 | chr1 | 147969869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147943471
|
T | C | 2 | a0001c0003a0002c0004 | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
synonymous_variant | LOW | c.240T>C | p.Cys80Cys | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/14 | 357/2160 | 240/1368 | 80/455 | chr1 | 147943471 | ||
| chr1:147954337
|
G | A | 2 | a0001c0003a0002c0004 | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
synonymous_variant | LOW | c.552G>A | p.Thr184Thr | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/14 | 669/2160 | 552/1368 | 184/455 | chr1 | 147954337 | ||
| chr1:147988461
|
C | T | 2 | a0001c0003a0002c0004 | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
synonymous_variant | LOW | c.1035C>T | p.Phe345Phe | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/14 | 1152/2160 | 1035/1368 | 345/455 | chr1 | 147988461 | ||
| chr1:147992555
|
A | G | 3 | a0001c0002a0004c0007a0005c0005 | 31 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
synonymous_variant | LOW | c.1149A>G | p.Leu383Leu | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 13/14 | 1266/2160 | 1149/1368 | 383/455 | chr1 | 147992555 | ||
| chr1:147992848
|
C | T | 1 | a0001c0006 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1299C>T | p.Ser433Ser | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 1416/2160 | 1299/1368 | 433/455 | chr1 | 147992848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147928427
|
C | G | 1 | a0001c0001t0008 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/14 | 110 | chr1 | 147928427 | |||||
| chr1:147992979
|
G | GA | 1 | a0001c0001t0004 | 6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*67dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 68 | INFO_REALIGN_3_PRIME | chr1 | 147992979 | ||||
| chr1:147993201
|
G | T | 1 | a0001c0006t0007 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*284G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 284 | chr1 | 147993201 | |||||
| chr1:147993259
|
G | A | 1 | a0001c0001t0005 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*342G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 342 | chr1 | 147993259 | |||||
| chr1:147993414
|
C | T | 3 | a0001c0003t0002a0001c0003t0003a0002c0004t0002 | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*497C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 497 | chr1 | 147993414 | |||||
| chr1:147993478
|
C | T | 3 | a0001c0001t0006a0001c0003t0002a0002c0004t0002 | 15 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*561C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 561 | chr1 | 147993478 | |||||
| chr1:147993532
|
T | G | 3 | a0001c0003t0002a0001c0003t0003a0002c0004t0002 | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*615T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 615 | chr1 | 147993532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147928621
|
C | T | 11 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(8): Show | 11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+43C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928621 | ||||||
| chr1:147928646
|
C | G | 3 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG01109.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.42+68C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928646 | ||||||
| chr1:147928667
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.42+89G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928667 | ||||||
| chr1:147928671
|
C | G | 1 | a0001c0002t0001g0006 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.42+93C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928671 | ||||||
| chr1:147928711
|
A | C | 43 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(40): Show | 43 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.42+133A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928711 | ||||||
| chr1:147928833
|
G | T | 10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+255G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928833 | ||||||
| chr1:147928941
|
C | T | 9 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0266others(6): Show | 9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.42+363C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928941 | ||||||
| chr1:147928960
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+382G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928960 | ||||||
| chr1:147928974
|
G | T | 1 | a0001c0002t0001g0220 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.42+396G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928974 | ||||||
| chr1:147929088
|
A | G | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | HG00140.hp1 HG00673.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+510A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929088 | ||||||
| chr1:147929157
|
C | T | 1 | a0001c0001t0008g0215 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.42+579C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929157 | ||||||
| chr1:147929356
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.42+778C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929356 | ||||||
| chr1:147929420
|
C | G | 1 | a0001c0002t0001g0213 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.42+842C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929420 | ||||||
| chr1:147929790
|
G | GT | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 129 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.42+1217dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147929790 | |||||
| chr1:147929820
|
C | G | 1 | a0001c0001t0008g0215 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.42+1242C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929820 | ||||||
| chr1:147929838
|
T | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1260T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929838 | ||||||
| chr1:147929853
|
G | T | 10 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(7): Show | 10 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+1275G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929853 | ||||||
| chr1:147929934
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.42+1356C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929934 | ||||||
| chr1:147930107
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0129others(5): Show | 8 | HG01175.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.42+1529A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930107 | ||||||
| chr1:147930192
|
A | T | 1 | a0001c0002t0001g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.42+1614A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930192 | ||||||
| chr1:147930287
|
T | C | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+1709T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930287 | ||||||
| chr1:147930421
|
T | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1843T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930421 | ||||||
| chr1:147930724
|
T | TGCCTTTT others(15): Show |
4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2146_42+2147ins others(22): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930724 | ||||||
| chr1:147930996
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.42+2418A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930996 | ||||||
| chr1:147931044
|
T | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(36): Show | 39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.42+2466T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931044 | ||||||
| chr1:147931063
|
C | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.42+2485C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931063 | ||||||
| chr1:147931234
|
GC | G | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2657delC | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931234 | ||||||
| chr1:147931324
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+2746A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931324 | ||||||
| chr1:147931341
|
A | G | 15 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(12): Show | 15 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.42+2763A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931341 | ||||||
| chr1:147931413
|
A | G | 1 | a0001c0001t0004g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.42+2835A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931413 | ||||||
| chr1:147931440
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.42+2862G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931440 | ||||||
| chr1:147931585
|
CT | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+3019delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147931585 | |||||
| chr1:147931623
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.42+3045G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931623 | ||||||
| chr1:147931692
|
G | A | 10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+3114G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931692 | ||||||
| chr1:147931846
|
C | A | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+3268C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931846 | ||||||
| chr1:147931876
|
G | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+3298G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931876 | ||||||
| chr1:147931893
|
G | A | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.42+3315G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931893 | ||||||
| chr1:147932078
|
A | AT | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+3511dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147932078 | |||||
| chr1:147932215
|
C | T | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+3637C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932215 | ||||||
| chr1:147932216
|
G | A | 17 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(14): Show | 17 | HG00408.hp1 HG00609.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.42+3638G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932216 | ||||||
| chr1:147932281
|
T | G | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.42+3703T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932281 | ||||||
| chr1:147932337
|
G | A | 1 | a0001c0002t0001g0024 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.42+3759G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932337 | ||||||
| chr1:147932355
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+3777G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932355 | ||||||
| chr1:147932553
|
C | G | 1 | a0002c0004t0002g0234 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.42+3975C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932553 | ||||||
| chr1:147932592
|
T | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42+4014T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932592 | ||||||
| chr1:147932612
|
G | A | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-4015G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932612 | ||||||
| chr1:147932739
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.43-3888G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932739 | ||||||
| chr1:147932847
|
G | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-3780G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932847 | ||||||
| chr1:147932882
|
T | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG01175.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.43-3745T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932882 | ||||||
| chr1:147933160
|
G | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 183 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.43-3467G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933160 | ||||||
| chr1:147933242
|
T | C | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-3385T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933242 | ||||||
| chr1:147933250
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-3377C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933250 | ||||||
| chr1:147933435
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.43-3192G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933435 | ||||||
| chr1:147933617
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43-3010A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933617 | ||||||
| chr1:147933845
|
C | T | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.43-2782C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933845 | ||||||
| chr1:147933981
|
A | G | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-2646A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933981 | ||||||
| chr1:147933998
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43-2629A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933998 | ||||||
| chr1:147934210
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.43-2417T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934210 | ||||||
| chr1:147934378
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.43-2249C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934378 | ||||||
| chr1:147934382
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.43-2245G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934382 | ||||||
| chr1:147934449
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18952.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.43-2178C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934449 | ||||||
| chr1:147934470
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-2157C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934470 | ||||||
| chr1:147934526
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.43-2101C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934526 | ||||||
| chr1:147934566
|
A | C | 1 | a0001c0001t0001g0211 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.43-2061A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934566 | ||||||
| chr1:147934700
|
T | C | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.43-1927T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934700 | ||||||
| chr1:147934747
|
ATTATG | A | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-1875_43-1871del others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147934747 | |||||
| chr1:147934953
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.43-1674G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934953 | ||||||
| chr1:147935180
|
G | A | 6 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-1447G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935180 | ||||||
| chr1:147935238
|
C | T | 1 | a0001c0001t0004g0262 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.43-1389C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935238 | ||||||
| chr1:147935297
|
G | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-1330G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935297 | ||||||
| chr1:147935516
|
G | A | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-1111G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935516 | ||||||
| chr1:147935595
|
T | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-1032T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935595 | ||||||
| chr1:147935814
|
A | C | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.43-813A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935814 | ||||||
| chr1:147935901
|
A | G | 2 | a0001c0001t0001g0218a0001c0002t0001g0121 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.43-726A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935901 | ||||||
| chr1:147936178
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.43-449A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147936178 | ||||||
| chr1:147936200
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-427C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147936200 | ||||||
| chr1:147936264
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01169.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.43-363G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147936264 | ||||||
| chr1:147936313
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-314C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147936313 | ||||||
| chr1:147936560
|
AAG | A | 4 | a0001c0003t0002g0230a0001c0003t0002g0231a0001c0003t0002g0232others(1): Show | 4 | HG00423.hp2 HG00621.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-64_43-63delAG | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147936560 | |||||
| chr1:147936945
|
A | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+259A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147936945 | ||||||
| chr1:147937028
|
CTTATA | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+348_102+352del others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 147937028 | |||||
| chr1:147937163
|
A | G | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0266 | 3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.102+477A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937163 | ||||||
| chr1:147937196
|
A | G | 19 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(16): Show | 19 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.102+510A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937196 | ||||||
| chr1:147937223
|
C | T | 1 | a0001c0003t0002g0229 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.102+537C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937223 | ||||||
| chr1:147937239
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0266 | 3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.102+553C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937239 | ||||||
| chr1:147937278
|
T | C | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.102+592T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937278 | ||||||
| chr1:147937557
|
G | A | 23 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+871G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937557 | ||||||
| chr1:147937689
|
T | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+1003T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937689 | ||||||
| chr1:147937720
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.103-994C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937720 | ||||||
| chr1:147937820
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.103-894G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937820 | ||||||
| chr1:147937872
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.103-842C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937872 | ||||||
| chr1:147938061
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.103-653T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938061 | ||||||
| chr1:147938090
|
G | T | 1 | a0001c0001t0001g0120 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-624G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938090 | ||||||
| chr1:147938403
|
G | A | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.103-311G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938403 | ||||||
| chr1:147938430
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.103-284A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938430 | ||||||
| chr1:147938518
|
A | G | 11 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(8): Show | 11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-196A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938518 | ||||||
| chr1:147938548
|
A | G | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.103-166A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938548 | ||||||
| chr1:147938636
|
C | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.103-78C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938636 | ||||||
| chr1:147938900
|
GA | G | 13 | a0001c0001t0001g0022a0001c0001t0001g0082a0001c0001t0001g0248others(10): Show | 13 | HG02055.hp2 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.206+96delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 147938900 | |||||
| chr1:147938900
|
GAA | G | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.206+95_206+96delAA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 147938900 | |||||
| chr1:147938912
|
A | C | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206+95A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147938912 | ||||||
| chr1:147939058
|
A | G | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+241A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939058 | ||||||
| chr1:147939133
|
G | T | 1 | a0001c0001t0004g0261 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.206+316G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939133 | ||||||
| chr1:147939429
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.206+612C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939429 | ||||||
| chr1:147939494
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.206+677C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939494 | ||||||
| chr1:147939638
|
G | A | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG03688.hp2 HG03710.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.206+821G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939638 | ||||||
| chr1:147939852
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.206+1035C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939852 | ||||||
| chr1:147939871
|
A | C | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.206+1054A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939871 | ||||||
| chr1:147939872
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0080 | 2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.206+1055C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939872 | ||||||
| chr1:147939943
|
G | A | 26 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0003t0002g0221others(23): Show | 26 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.206+1126G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939943 | ||||||
| chr1:147940130
|
G | A | 5 | a0001c0001t0001g0023a0001c0003t0003g0235a0001c0003t0003g0236others(2): Show | 5 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.206+1313G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940130 | ||||||
| chr1:147940132
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | NA19063.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.206+1315G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940132 | ||||||
| chr1:147940200
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.206+1383A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940200 | ||||||
| chr1:147940214
|
T | C | 2 | a0001c0003t0003g0235a0001c0003t0003g0236 | 2 | HG01934.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.206+1397T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940214 | ||||||
| chr1:147940230
|
C | T | 1 | a0001c0003t0002g0233 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.206+1413C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940230 | ||||||
| chr1:147940264
|
A | G | 7 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(4): Show | 7 | HG01934.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.206+1447A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940264 | ||||||
| chr1:147940298
|
G | A | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.206+1481G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940298 | ||||||
| chr1:147940320
|
C | G | 5 | a0001c0002t0001g0006a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 6 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.206+1503C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940320 | ||||||
| chr1:147940328
|
A | G | 4 | a0001c0003t0003g0240a0001c0003t0003g0241a0001c0003t0003g0242others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.206+1511A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940328 | ||||||
| chr1:147940353
|
A | G | 1 | a0001c0002t0001g0006 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.206+1536A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940353 | ||||||
| chr1:147940357
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0266 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.206+1540T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940357 | ||||||
| chr1:147940359
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0266 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.206+1542T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940359 | ||||||
| chr1:147940565
|
T | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.206+1748T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940565 | ||||||
| chr1:147940588
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.206+1771T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940588 | ||||||
| chr1:147940658
|
C | A | 1 | a0001c0003t0003g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.206+1841C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940658 | ||||||
| chr1:147940663
|
G | A | 1 | a0001c0003t0003g0235 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.206+1846G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940663 | ||||||
| chr1:147940664
|
C | A | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.206+1847C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940664 | ||||||
| chr1:147940880
|
T | C | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.206+2063T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940880 | ||||||
| chr1:147940901
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.206+2084C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940901 | ||||||
| chr1:147941099
|
G | A | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.206+2282G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147941099 | ||||||
| chr1:147941354
|
A | G | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0266 | 3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.207-2084A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147941354 | ||||||
| chr1:147941430
|
C | CA | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.207-2004dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 147941430 | |||||
| chr1:147941879
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.207-1559T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147941879 | ||||||
| chr1:147942110
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.207-1328C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147942110 | ||||||
| chr1:147942293
|
C | CA | 23 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.207-1135dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 147942293 | |||||
| chr1:147942780
|
CAG | C | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.207-657_207-656del others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147942780 | ||||||
| chr1:147943028
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG00438.hp1 NA18947.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.207-410A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147943028 | ||||||
| chr1:147943149
|
A | G | 1 | a0001c0003t0002g0232 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.207-289A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147943149 | ||||||
| chr1:147943281
|
C | T | 4 | a0001c0003t0003g0240a0001c0003t0003g0241a0001c0003t0003g0242others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.207-157C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147943281 | ||||||
| chr1:147943571
|
G | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.313+27G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943571 | ||||||
| chr1:147943644
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.313+100T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943644 | ||||||
| chr1:147943786
|
A | G | 8 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.314-211A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943786 | ||||||
| chr1:147943836
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.314-161C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943836 | ||||||
| chr1:147943959
|
A | G | 6 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-38A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943959 | ||||||
| chr1:147944137
|
A | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG00408.hp2 NA18957.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+39A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944137 | ||||||
| chr1:147944361
|
A | G | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.415+263A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944361 | ||||||
| chr1:147944502
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0074a0001c0001t0001g0075others(2): Show | 6 | HG01256.hp1 HG01346.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+404A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944502 | ||||||
| chr1:147944545
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.415+447A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944545 | ||||||
| chr1:147944714
|
C | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415+616C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944714 | ||||||
| chr1:147944715
|
AG | A | 4 | a0001c0003t0003g0240a0001c0003t0003g0241a0001c0003t0003g0242others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+618delG | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944715 | ||||||
| chr1:147944798
|
TGAATCTA others(15): Show |
T | 12 | a0001c0001t0001g0156a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00673.hp1 HG02080.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+725_415+746del others(22): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147944798 | |||||
| chr1:147944813
|
A | T | 1 | a0001c0001t0001g0200 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.415+715A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944813 | ||||||
| chr1:147944872
|
T | G | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+774T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944872 | ||||||
| chr1:147944973
|
A | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+875A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944973 | ||||||
| chr1:147944991
|
C | G | 4 | a0001c0003t0002g0230a0001c0003t0002g0231a0001c0003t0002g0232others(1): Show | 4 | HG00423.hp2 HG00621.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+893C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944991 | ||||||
| chr1:147945031
|
CT | C | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG03688.hp2 HG03710.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+936delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147945031 | |||||
| chr1:147945067
|
A | G | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+969A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945067 | ||||||
| chr1:147945251
|
T | C | 1 | a0003c0008t0001g0089 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.415+1153T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945251 | ||||||
| chr1:147945701
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+1603C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945701 | ||||||
| chr1:147945724
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.415+1626T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945724 | ||||||
| chr1:147945844
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+1746C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945844 | ||||||
| chr1:147945887
|
G | T | 5 | a0001c0001t0001g0218a0001c0002t0001g0006a0001c0002t0001g0116others(2): Show | 6 | HG00140.hp1 HG00741.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+1789G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945887 | ||||||
| chr1:147945927
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.415+1829C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945927 | ||||||
| chr1:147946183
|
A | G | 4 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+2085A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946183 | ||||||
| chr1:147946273
|
G | C | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415+2175G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946273 | ||||||
| chr1:147946279
|
T | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG01255.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.415+2181T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946279 | ||||||
| chr1:147946564
|
T | C | 29 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(26): Show | 29 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.415+2466T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946564 | ||||||
| chr1:147946964
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+2866C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946964 | ||||||
| chr1:147947135
|
G | A | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415+3037G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947135 | ||||||
| chr1:147947333
|
C | CA | 21 | a0001c0001t0001g0190a0001c0001t0001g0248a0001c0001t0001g0249others(18): Show | 21 | HG00738.hp1 HG02055.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.415+3252dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147947333 | |||||
| chr1:147947333
|
C | CAAA | 11 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(8): Show | 11 | HG00423.hp2 HG00597.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.415+3250_415+3252d others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147947333 | |||||
| chr1:147947352
|
A | G | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+3254A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947352 | ||||||
| chr1:147947359
|
C | G | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.415+3261C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947359 | ||||||
| chr1:147947389
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.415+3291C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947389 | ||||||
| chr1:147947410
|
T | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+3312T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947410 | ||||||
| chr1:147947523
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.415+3425C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947523 | ||||||
| chr1:147947649
|
T | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+3551T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947649 | ||||||
| chr1:147947748
|
A | G | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+3650A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947748 | ||||||
| chr1:147947997
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0080 | 2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.415+3899C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947997 | ||||||
| chr1:147948038
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.415+3940T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948038 | ||||||
| chr1:147948154
|
G | A | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+4056G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948154 | ||||||
| chr1:147948756
|
AT | A | 55 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0023others(52): Show | 56 | HG00323.hp2 HG00597.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.416-4567delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147948756 | |||||
| chr1:147948756
|
ATT | A | 20 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(17): Show | 20 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.416-4568_416-4567d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147948756 | |||||
| chr1:147948756
|
ATTT | A | 11 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(8): Show | 11 | HG00738.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-4569_416-4567d others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147948756 | |||||
| chr1:147948783
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.416-4562G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948783 | ||||||
| chr1:147948849
|
G | T | 10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-4496G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948849 | ||||||
| chr1:147948905
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.416-4440C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948905 | ||||||
| chr1:147949005
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0072others(1): Show | 4 | NA18939.hp2 NA18955.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-4340A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949005 | ||||||
| chr1:147949036
|
G | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(1): Show | 4 | HG02083.hp1 NA18952.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-4309G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949036 | ||||||
| chr1:147949047
|
G | A | 28 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(25): Show | 28 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.416-4298G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949047 | ||||||
| chr1:147949109
|
G | C | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.416-4236G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949109 | ||||||
| chr1:147949112
|
G | T | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-4233G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949112 | ||||||
| chr1:147949123
|
A | C | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.416-4222A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949123 | ||||||
| chr1:147949290
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-4055A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949290 | ||||||
| chr1:147949297
|
TGGCTGGG others(116): Show |
T | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-4041_416-3919d others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949297 | |||||
| chr1:147949332
|
G | A | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-4013G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949332 | ||||||
| chr1:147949335
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.416-4010G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949335 | ||||||
| chr1:147949348
|
T | C | 39 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(36): Show | 39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.416-3997T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949348 | ||||||
| chr1:147949363
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3982A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949363 | ||||||
| chr1:147949367
|
C | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3978C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949367 | ||||||
| chr1:147949371
|
T | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3974T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949371 | ||||||
| chr1:147949379
|
T | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3966T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949379 | ||||||
| chr1:147949384
|
G | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3961G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949384 | ||||||
| chr1:147949385
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3960G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949385 | ||||||
| chr1:147949393
|
AC | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3945delC | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949393 | |||||
| chr1:147949412
|
G | A | 10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-3933G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949412 | ||||||
| chr1:147949426
|
G | A | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3919G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949426 | ||||||
| chr1:147949428
|
C | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3917C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949428 | ||||||
| chr1:147949432
|
T | C | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3913T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949432 | ||||||
| chr1:147949447
|
C | CCCACCTC others(412): Show |
1 | a0001c0003t0003g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.416-3897_416-3896i others(421): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | |||||
| chr1:147949447
|
C | CCCACCTC others(413): Show |
1 | a0001c0003t0003g0238 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.416-3897_416-3896i others(422): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | |||||
| chr1:147949447
|
C | CCCACCTC others(111): Show |
20 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(17): Show | 20 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.416-3897_416-3896i others(120): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | |||||
| chr1:147949447
|
C | CCCACCTC others(412): Show |
2 | a0001c0003t0003g0235a0001c0003t0003g0236 | 2 | HG01934.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.416-3897_416-3896i others(421): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | |||||
| chr1:147949447
|
C | CCCACCTC others(111): Show |
232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.416-3897_416-3896i others(120): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | |||||
| chr1:147949447
|
C | CCCACCTC others(112): Show |
1 | a0001c0001t0001g0009 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.416-3897_416-3896i others(121): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | |||||
| chr1:147949447
|
C | CCCACCTC others(110): Show |
2 | a0001c0001t0001g0002a0001c0001t0001g0019 | 3 | HG03491.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.416-3897_416-3896i others(119): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | |||||
| chr1:147949464
|
C | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3881C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949464 | ||||||
| chr1:147949472
|
C | T | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3873C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949472 | ||||||
| chr1:147949485
|
C | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3860C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949485 | ||||||
| chr1:147949497
|
C | A | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3848C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949497 | ||||||
| chr1:147949534
|
C | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3811C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949534 | ||||||
| chr1:147949550
|
C | T | 4 | a0001c0003t0003g0240a0001c0003t0003g0241a0001c0003t0003g0242others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-3795C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949550 | ||||||
| chr1:147949551
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.416-3794G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949551 | ||||||
| chr1:147949552
|
G | A | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3793G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949552 | ||||||
| chr1:147949554
|
G | A | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3791G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949554 | ||||||
| chr1:147949555
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3790C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949555 | ||||||
| chr1:147949568
|
G | A | 2 | a0001c0003t0003g0239a0001c0006t0007g0256 | 2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.416-3777G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949568 | ||||||
| chr1:147949568
|
G | C | 5 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3777G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949568 | ||||||
| chr1:147949569
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3776G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949569 | ||||||
| chr1:147949577
|
ACCCCCCC others(345): Show |
A | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-3761_416-3410d others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949577 | |||||
| chr1:147949589
|
C | CCCTCCCG others(71): Show |
1 | a0001c0001t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3751_416-3750i others(80): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949589 | |||||
| chr1:147949594
|
CAGGACCG others(91): Show |
C | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3750_416-3653d others(100): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949594 | ||||||
| chr1:147949595
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3750A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949595 | ||||||
| chr1:147949595
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3750A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949595 | ||||||
| chr1:147949600
|
C | G | 40 | a0001c0001t0001g0071a0001c0001t0001g0248a0001c0001t0001g0249others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.416-3745C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949600 | ||||||
| chr1:147949605
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3740A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949605 | ||||||
| chr1:147949610
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3735A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949610 | ||||||
| chr1:147949611
|
C | T | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-3734C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949611 | ||||||
| chr1:147949612
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3733G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949612 | ||||||
| chr1:147949616
|
C | T | 1 | a0001c0002t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.416-3729C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949616 | ||||||
| chr1:147949694
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3651G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949694 | ||||||
| chr1:147949707
|
G | T | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3638G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949707 | ||||||
| chr1:147949722
|
A | C | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3623A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949722 | ||||||
| chr1:147949744
|
A | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3601A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949744 | ||||||
| chr1:147949771
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0266 | 3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.416-3574C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949771 | ||||||
| chr1:147949776
|
A | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3569A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949776 | ||||||
| chr1:147949778
|
A | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3567A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949778 | ||||||
| chr1:147949787
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3558C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949787 | ||||||
| chr1:147949792
|
A | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3553A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949792 | ||||||
| chr1:147949808
|
G | C | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.416-3537G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949808 | ||||||
| chr1:147949813
|
CCCTCCCG others(71): Show |
C | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3516_416-3439d others(80): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949813 | |||||
| chr1:147949829
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3516A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949829 | ||||||
| chr1:147949836
|
C | T | 2 | a0001c0001t0001g0205a0001c0001t0001g0206 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.416-3509C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949836 | ||||||
| chr1:147949837
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.416-3508G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949837 | ||||||
| chr1:147949884
|
G | A | 5 | a0001c0001t0001g0044a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 5 | HG03688.hp2 HG03710.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3461G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949884 | ||||||
| chr1:147949906
|
C | CGGCTGGC others(42): Show |
10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-3393_416-3392i others(51): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949906 | |||||
| chr1:147949906
|
C | T | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3439C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949906 | ||||||
| chr1:147949919
|
G | GGGGGGCT others(42): Show |
4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG02965.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-3393_416-3392i others(51): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949919 | |||||
| chr1:147949919
|
G | GGGGGGCT others(43): Show |
1 | a0001c0001t0001g0251 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.416-3410_416-3409i others(52): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949919 | |||||
| chr1:147949929
|
CCCCCCCA others(140): Show |
C | 1 | a0001c0001t0001g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.416-3392_416-3246d others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949929 | |||||
| chr1:147949946
|
C | CGGACGGG others(42): Show |
1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-3393_416-3392i others(51): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949946 | |||||
| chr1:147949953
|
T | G | 27 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(24): Show | 27 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.416-3392T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949953 | ||||||
| chr1:147949955
|
C | T | 23 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.416-3390C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949955 | ||||||
| chr1:147949967
|
T | C | 23 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.416-3378T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949967 | ||||||
| chr1:147949969
|
T | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3376T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949969 | ||||||
| chr1:147949980
|
CCCCCACC others(42): Show |
C | 1 | a0001c0002t0001g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.416-3331_416-3283d others(51): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949980 | |||||
| chr1:147949996
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.416-3349G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949996 | ||||||
| chr1:147950002
|
G | T | 18 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(15): Show | 18 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.416-3343G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950002 | ||||||
| chr1:147950004
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-3341C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950004 | ||||||
| chr1:147950016
|
C | T | 23 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.416-3329C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950016 | ||||||
| chr1:147950029
|
T | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3316T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950029 | ||||||
| chr1:147950054
|
G | A | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3291G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950054 | ||||||
| chr1:147950063
|
T | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3282T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950063 | ||||||
| chr1:147950076
|
T | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3269T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950076 | ||||||
| chr1:147950082
|
C | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.416-3263C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950082 | ||||||
| chr1:147950113
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3232C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950113 | ||||||
| chr1:147950115
|
G | C | 1 | a0001c0001t0005g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.416-3230G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950115 | ||||||
| chr1:147950126
|
C | G | 1 | a0005c0005t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.416-3219C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950126 | ||||||
| chr1:147950190
|
A | G | 3 | a0001c0003t0002g0231a0001c0003t0002g0232a0001c0003t0002g0233 | 3 | HG00423.hp2 HG00621.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.416-3155A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950190 | ||||||
| chr1:147950194
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.416-3151G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950194 | ||||||
| chr1:147950196
|
A | G | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-3149A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950196 | ||||||
| chr1:147950293
|
A | ACGGGGCG others(1): Show |
14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3045_416-3038d others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147950293 | |||||
| chr1:147950294
|
C | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-3051C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950294 | ||||||
| chr1:147950311
|
G | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3034G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950311 | ||||||
| chr1:147950338
|
C | T | 1 | a0001c0003t0002g0230 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.416-3007C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950338 | ||||||
| chr1:147950352
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.416-2993C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950352 | ||||||
| chr1:147950421
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.416-2924C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950421 | ||||||
| chr1:147950526
|
C | CG | 4 | a0001c0001t0001g0156a0001c0001t0001g0200a0001c0001t0001g0219others(1): Show | 4 | HG00673.hp1 HG01109.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-2815dupG | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147950526 | |||||
| chr1:147950572
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-2773C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950572 | ||||||
| chr1:147950581
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(73): Show | 81 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.416-2764C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950581 | ||||||
| chr1:147950621
|
G | A | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.416-2724G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950621 | ||||||
| chr1:147950688
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-2657C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950688 | ||||||
| chr1:147950714
|
C | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-2631C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950714 | ||||||
| chr1:147950724
|
AGCTGGAG others(5): Show |
A | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-2620_416-2609d others(14): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950724 | ||||||
| chr1:147950751
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 122 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.416-2594T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950751 | ||||||
| chr1:147950760
|
G | C | 1 | a0001c0002t0001g0006 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.416-2585G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950760 | ||||||
| chr1:147950768
|
CA | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-2570delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147950768 | |||||
| chr1:147950801
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-2544C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950801 | ||||||
| chr1:147950825
|
C | T | 6 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-2520C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950825 | ||||||
| chr1:147950861
|
G | T | 2 | a0001c0003t0003g0235a0001c0003t0003g0236 | 2 | HG01934.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.416-2484G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950861 | ||||||
| chr1:147950926
|
A | AGAGAGG | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-2408_416-2403d others(8): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147950926 | |||||
| chr1:147951283
|
T | C | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-2062T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951283 | ||||||
| chr1:147951381
|
A | G | 3 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG01109.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.416-1964A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951381 | ||||||
| chr1:147951436
|
G | C | 1 | a0001c0002t0001g0006 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.416-1909G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951436 | ||||||
| chr1:147951446
|
A | G | 25 | a0001c0001t0001g0263a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.416-1899A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951446 | ||||||
| chr1:147951482
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1863T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951482 | ||||||
| chr1:147951496
|
A | C | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1849A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951496 | ||||||
| chr1:147951554
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.416-1791G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951554 | ||||||
| chr1:147951628
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1717A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951628 | ||||||
| chr1:147951690
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1655T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951690 | ||||||
| chr1:147951710
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.416-1635G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951710 | ||||||
| chr1:147951778
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.416-1567C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951778 | ||||||
| chr1:147951859
|
T | C | 25 | a0001c0001t0001g0263a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.416-1486T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951859 | ||||||
| chr1:147951977
|
C | A | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-1368C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951977 | ||||||
| chr1:147952000
|
TGTAGAGT others(14): Show |
T | 3 | a0001c0001t0001g0170a0001c0001t0001g0263a0001c0001t0004g0258 | 3 | HG02809.hp1 HG02896.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.416-1326_416-1306d others(23): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147952000 | |||||
| chr1:147952112
|
G | A | 1 | a0004c0007t0001g0092 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.416-1233G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952112 | ||||||
| chr1:147952121
|
A | G | 25 | a0001c0001t0001g0263a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.416-1224A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952121 | ||||||
| chr1:147952125
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1220G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952125 | ||||||
| chr1:147952193
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1152T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952193 | ||||||
| chr1:147952232
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1113T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952232 | ||||||
| chr1:147952244
|
A | G | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-1101A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952244 | ||||||
| chr1:147952283
|
G | T | 1 | a0001c0002t0001g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.416-1062G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952283 | ||||||
| chr1:147952455
|
G | C | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-890G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952455 | ||||||
| chr1:147952619
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-726A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952619 | ||||||
| chr1:147952668
|
A | G | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-677A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952668 | ||||||
| chr1:147952928
|
A | G | 1 | a0001c0002t0001g0101 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.416-417A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952928 | ||||||
| chr1:147952997
|
G | GT | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0112others(6): Show | 9 | HG01175.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-333dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147952997 | |||||
| chr1:147953029
|
A | G | 9 | a0001c0001t0001g0257a0001c0001t0001g0264a0001c0001t0001g0266others(6): Show | 9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-316A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147953029 | ||||||
| chr1:147953078
|
A | G | 1 | a0001c0002t0001g0111 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.416-267A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147953078 | ||||||
| chr1:147953200
|
A | C | 1 | a0001c0002t0001g0006 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.416-145A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147953200 | ||||||
| chr1:147953207
|
A | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-138A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147953207 | ||||||
| chr1:147953672
|
A | G | 1 | a0001c0002t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.536+207A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147953672 | ||||||
| chr1:147953749
|
C | T | 23 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.536+284C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147953749 | ||||||
| chr1:147953909
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.537-413C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147953909 | ||||||
| chr1:147954080
|
T | C | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.537-242T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147954080 | ||||||
| chr1:147954229
|
A | G | 11 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(8): Show | 11 | HG00438.hp1 HG00735.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.537-93A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147954229 | ||||||
| chr1:147954513
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.617+111G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954513 | ||||||
| chr1:147954589
|
G | A | 1 | a0001c0001t0004g0261 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.617+187G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954589 | ||||||
| chr1:147954686
|
T | A | 1 | a0001c0001t0001g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.617+284T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954686 | ||||||
| chr1:147954825
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+423A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954825 | ||||||
| chr1:147954873
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+471G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954873 | ||||||
| chr1:147954877
|
G | A | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.617+475G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954877 | ||||||
| chr1:147954966
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+564C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954966 | ||||||
| chr1:147955013
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.617+611C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955013 | ||||||
| chr1:147955209
|
T | C | 25 | a0001c0001t0001g0263a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+807T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955209 | ||||||
| chr1:147955267
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+865G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955267 | ||||||
| chr1:147955284
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+882T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955284 | ||||||
| chr1:147955287
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+885C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955287 | ||||||
| chr1:147955339
|
G | A | 25 | a0001c0001t0001g0263a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+937G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955339 | ||||||
| chr1:147955471
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+1069G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955471 | ||||||
| chr1:147955497
|
G | A | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.617+1095G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955497 | ||||||
| chr1:147955521
|
A | C | 17 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(14): Show | 17 | HG00741.hp2 HG01099.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.617+1119A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955521 | ||||||
| chr1:147955568
|
T | C | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.617+1166T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955568 | ||||||
| chr1:147955636
|
T | C | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(1): Show | 4 | NA18957.hp2 NA18963.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+1234T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955636 | ||||||
| chr1:147955700
|
C | G | 4 | a0001c0003t0003g0240a0001c0003t0003g0241a0001c0003t0003g0242others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+1298C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955700 | ||||||
| chr1:147955822
|
T | C | 2 | a0001c0002t0001g0024a0001c0002t0001g0162 | 2 | NA18942.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.617+1420T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955822 | ||||||
| chr1:147955975
|
T | C | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+1573T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955975 | ||||||
| chr1:147956207
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+1805A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956207 | ||||||
| chr1:147956226
|
G | T | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.617+1824G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956226 | ||||||
| chr1:147956435
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.617+2033G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956435 | ||||||
| chr1:147956452
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+2050G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956452 | ||||||
| chr1:147956467
|
A | C | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+2065A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956467 | ||||||
| chr1:147956581
|
G | C | 1 | a0001c0001t0001g0040 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.617+2179G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956581 | ||||||
| chr1:147956655
|
A | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.617+2253A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956655 | ||||||
| chr1:147956657
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+2255G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956657 | ||||||
| chr1:147956686
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+2284T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956686 | ||||||
| chr1:147956741
|
A | AT | 11 | a0001c0001t0001g0018a0001c0001t0001g0257a0001c0001t0001g0264others(8): Show | 11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+2353dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147956741 | |||||
| chr1:147956741
|
AT | A | 24 | a0001c0001t0001g0146a0001c0003t0002g0221a0001c0003t0002g0222others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.617+2353delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147956741 | |||||
| chr1:147956770
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.617+2368C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956770 | ||||||
| chr1:147956833
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.617+2431A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956833 | ||||||
| chr1:147956836
|
C | A | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.617+2434C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956836 | ||||||
| chr1:147956836
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.617+2434C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956836 | ||||||
| chr1:147956953
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.617+2551G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956953 | ||||||
| chr1:147956965
|
T | C | 11 | a0001c0001t0001g0263a0001c0001t0004g0258a0001c0001t0004g0259others(8): Show | 11 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.617+2563T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956965 | ||||||
| chr1:147956981
|
T | C | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.617+2579T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956981 | ||||||
| chr1:147956986
|
A | C | 9 | a0001c0001t0001g0257a0001c0001t0001g0264a0001c0001t0001g0266others(6): Show | 9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+2584A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956986 | ||||||
| chr1:147957004
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.617+2602G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957004 | ||||||
| chr1:147957085
|
A | C | 1 | a0002c0004t0002g0234 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.617+2683A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957085 | ||||||
| chr1:147957160
|
T | A | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+2758T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957160 | ||||||
| chr1:147957162
|
T | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+2760T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957162 | ||||||
| chr1:147957192
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.617+2790G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957192 | ||||||
| chr1:147957238
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.617+2836A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957238 | ||||||
| chr1:147957259
|
G | T | 1 | a0001c0003t0003g0243 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.617+2857G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957259 | ||||||
| chr1:147957285
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.617+2883T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957285 | ||||||
| chr1:147957309
|
G | A | 9 | a0001c0001t0001g0257a0001c0001t0001g0264a0001c0001t0001g0266others(6): Show | 9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+2907G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957309 | ||||||
| chr1:147957331
|
G | C | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.617+2929G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957331 | ||||||
| chr1:147957392
|
G | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0166others(2): Show | 6 | HG01891.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.617+2990G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957392 | ||||||
| chr1:147957540
|
C | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+3138C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957540 | ||||||
| chr1:147957546
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3144A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957546 | ||||||
| chr1:147957559
|
T | C | 4 | a0001c0003t0003g0240a0001c0003t0003g0241a0001c0003t0003g0242others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+3157T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957559 | ||||||
| chr1:147957706
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.617+3304T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957706 | ||||||
| chr1:147957715
|
C | G | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.617+3313C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957715 | ||||||
| chr1:147957722
|
A | G | 2 | a0001c0001t0001g0263a0001c0003t0003g0244 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.617+3320A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957722 | ||||||
| chr1:147957755
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.617+3353T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957755 | ||||||
| chr1:147957790
|
C | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3388C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957790 | ||||||
| chr1:147957798
|
C | G | 1 | a0001c0001t0001g0119 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.617+3396C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957798 | ||||||
| chr1:147957835
|
C | T | 12 | a0001c0001t0001g0156a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00673.hp1 HG02080.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+3433C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957835 | ||||||
| chr1:147957880
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 7 | HG00323.hp2 HG01243.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+3478C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957880 | ||||||
| chr1:147957962
|
A | G | 25 | a0001c0001t0001g0263a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+3560A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957962 | ||||||
| chr1:147957969
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.617+3567C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957969 | ||||||
| chr1:147957977
|
C | T | 25 | a0001c0001t0001g0263a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+3575C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957977 | ||||||
| chr1:147958015
|
C | G | 25 | a0001c0001t0001g0263a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+3613C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958015 | ||||||
| chr1:147958021
|
G | A | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+3619G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958021 | ||||||
| chr1:147958070
|
G | GA | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.617+3679dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958070 | |||||
| chr1:147958140
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3738A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958140 | ||||||
| chr1:147958141
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3739G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958141 | ||||||
| chr1:147958142
|
TAAAGACA others(10): Show |
T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3742_617+3758d others(19): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958142 | |||||
| chr1:147958253
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3851A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958253 | ||||||
| chr1:147958271
|
A | G | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+3869A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958271 | ||||||
| chr1:147958287
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3885A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958287 | ||||||
| chr1:147958385
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.617+3983G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958385 | ||||||
| chr1:147958410
|
G | A | 12 | a0001c0001t0001g0156a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00673.hp1 HG02080.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+4008G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958410 | ||||||
| chr1:147958529
|
CT | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 239 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.617+4130delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958529 | |||||
| chr1:147958604
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+4202C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958604 | ||||||
| chr1:147958638
|
C | CA | 6 | a0001c0001t0001g0219a0001c0001t0001g0248a0001c0001t0001g0249others(3): Show | 6 | HG00673.hp1 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+4250dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958638 | |||||
| chr1:147958638
|
CA | C | 25 | a0001c0001t0001g0263a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+4250delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958638 | |||||
| chr1:147958660
|
C | T | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+4258C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958660 | ||||||
| chr1:147958668
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4266A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958668 | ||||||
| chr1:147958736
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4334G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958736 | ||||||
| chr1:147958745
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.617+4343A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958745 | ||||||
| chr1:147958782
|
A | G | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.617+4380A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958782 | ||||||
| chr1:147958834
|
C | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.617+4432C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958834 | ||||||
| chr1:147958853
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4451G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958853 | ||||||
| chr1:147958855
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0263 | 2 | HG01099.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.617+4453A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958855 | ||||||
| chr1:147958863
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4461A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958863 | ||||||
| chr1:147958867
|
CCA | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+4468_617+4469d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958867 | |||||
| chr1:147958923
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.617+4521A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958923 | ||||||
| chr1:147958974
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4572A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958974 | ||||||
| chr1:147959016
|
A | AT | 23 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.617+4622dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147959016 | |||||
| chr1:147959207
|
T | A | 1 | a0001c0001t0001g0193 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.617+4805T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959207 | ||||||
| chr1:147959222
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4820G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959222 | ||||||
| chr1:147959283
|
A | G | 3 | a0002c0004t0002g0227a0002c0004t0002g0228a0002c0004t0002g0234 | 3 | HG02886.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.617+4881A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959283 | ||||||
| chr1:147959292
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.617+4890G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959292 | ||||||
| chr1:147959325
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4923C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959325 | ||||||
| chr1:147959418
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5016A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959418 | ||||||
| chr1:147959548
|
A | C | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5146A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959548 | ||||||
| chr1:147959553
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5151C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959553 | ||||||
| chr1:147959563
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0008g0215 | 2 | NA19058.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.617+5161A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959563 | ||||||
| chr1:147959656
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5254G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959656 | ||||||
| chr1:147959739
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5337T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959739 | ||||||
| chr1:147959752
|
G | T | 1 | a0002c0004t0002g0228 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.617+5350G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959752 | ||||||
| chr1:147959762
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5360A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959762 | ||||||
| chr1:147959871
|
G | T | 1 | a0001c0001t0001g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.617+5469G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959871 | ||||||
| chr1:147959874
|
T | G | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.617+5472T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959874 | ||||||
| chr1:147959961
|
A | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+5559A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959961 | ||||||
| chr1:147960046
|
G | A | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+5644G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960046 | ||||||
| chr1:147960179
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5777G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960179 | ||||||
| chr1:147960189
|
T | A | 1 | a0001c0003t0002g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.617+5787T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960189 | ||||||
| chr1:147960280
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5878C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960280 | ||||||
| chr1:147960497
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.618-6057G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960497 | ||||||
| chr1:147960618
|
C | T | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618-5936C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960618 | ||||||
| chr1:147960882
|
T | G | 1 | a0001c0003t0003g0240 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.618-5672T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960882 | ||||||
| chr1:147960993
|
C | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-5561C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960993 | ||||||
| chr1:147961042
|
G | A | 7 | a0001c0002t0001g0093a0001c0002t0001g0094a0001c0002t0001g0101others(4): Show | 7 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-5512G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961042 | ||||||
| chr1:147961161
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.618-5393A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961161 | ||||||
| chr1:147961258
|
A | G | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.618-5296A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961258 | ||||||
| chr1:147961275
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.618-5279A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961275 | ||||||
| chr1:147961537
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0266 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.618-5017T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961537 | ||||||
| chr1:147961622
|
C | A | 7 | a0001c0001t0001g0159a0001c0001t0004g0258a0001c0001t0004g0259others(4): Show | 7 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-4932C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961622 | ||||||
| chr1:147961646
|
T | C | 5 | a0001c0001t0001g0103a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.618-4908T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961646 | ||||||
| chr1:147961657
|
T | A | 1 | a0001c0002t0001g0118 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.618-4897T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961657 | ||||||
| chr1:147961775
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-4779G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961775 | ||||||
| chr1:147961917
|
A | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.618-4637A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961917 | ||||||
| chr1:147962081
|
T | A | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-4473T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962081 | ||||||
| chr1:147962178
|
C | G | 1 | a0001c0002t0001g0068 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.618-4376C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962178 | ||||||
| chr1:147962313
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.618-4241A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962313 | ||||||
| chr1:147962421
|
CT | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-4132delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962421 | ||||||
| chr1:147962423
|
C | CA | 18 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(15): Show | 21 | HG00735.hp1 HG01243.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.618-4115dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147962423 | |||||
| chr1:147962423
|
CA | C | 27 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(24): Show | 27 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.618-4115delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147962423 | |||||
| chr1:147962424
|
A | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-4130A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962424 | ||||||
| chr1:147962553
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-4001C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962553 | ||||||
| chr1:147962567
|
A | C | 1 | a0001c0003t0002g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.618-3987A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962567 | ||||||
| chr1:147962595
|
C | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.618-3959C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962595 | ||||||
| chr1:147962668
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.618-3886G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962668 | ||||||
| chr1:147962743
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-3811A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962743 | ||||||
| chr1:147962755
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.618-3799C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962755 | ||||||
| chr1:147962792
|
G | A | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-3762G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962792 | ||||||
| chr1:147962820
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-3734C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962820 | ||||||
| chr1:147962890
|
C | T | 1 | a0001c0002t0001g0116 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.618-3664C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962890 | ||||||
| chr1:147962891
|
G | A | 4 | a0001c0003t0003g0240a0001c0003t0003g0241a0001c0003t0003g0242others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-3663G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962891 | ||||||
| chr1:147962896
|
A | G | 1 | a0001c0002t0001g0133 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618-3658A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962896 | ||||||
| chr1:147962900
|
A | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.618-3654A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962900 | ||||||
| chr1:147962941
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0166others(2): Show | 6 | HG01891.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.618-3613A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962941 | ||||||
| chr1:147962953
|
GA | G | 31 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(28): Show | 31 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.618-3589delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147962953 | |||||
| chr1:147963174
|
A | G | 11 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(8): Show | 11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-3380A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963174 | ||||||
| chr1:147963205
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255 | 3 | HG01109.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.618-3349G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963205 | ||||||
| chr1:147963256
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.618-3298A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963256 | ||||||
| chr1:147963359
|
G | A | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-3195G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963359 | ||||||
| chr1:147963375
|
TA | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 137 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.618-3161delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147963375 | |||||
| chr1:147963375
|
TAA | T | 10 | a0001c0001t0001g0252a0001c0003t0003g0235a0001c0003t0003g0236others(7): Show | 10 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.618-3162_618-3161d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147963375 | |||||
| chr1:147963377
|
A | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.618-3177A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963377 | ||||||
| chr1:147963548
|
T | C | 1 | a0001c0002t0001g0189 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.618-3006T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963548 | ||||||
| chr1:147963575
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.618-2979T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963575 | ||||||
| chr1:147963587
|
A | G | 1 | a0005c0005t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.618-2967A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963587 | ||||||
| chr1:147963880
|
A | C | 1 | a0001c0001t0001g0201 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.618-2674A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963880 | ||||||
| chr1:147963943
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.618-2611G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963943 | ||||||
| chr1:147964025
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.618-2529A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964025 | ||||||
| chr1:147964032
|
G | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.618-2522G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964032 | ||||||
| chr1:147964194
|
T | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-2360T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964194 | ||||||
| chr1:147964215
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0209 | 2 | NA18986.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.618-2339T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964215 | ||||||
| chr1:147964323
|
T | C | 3 | a0001c0002t0001g0117a0001c0002t0001g0118a0005c0005t0001g0115 | 3 | HG02109.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.618-2231T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964323 | ||||||
| chr1:147964364
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-2190C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964364 | ||||||
| chr1:147964437
|
T | C | 4 | a0001c0001t0001g0157a0001c0001t0001g0173a0001c0001t0001g0210others(1): Show | 4 | NA18944.hp2 NA18952.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-2117T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964437 | ||||||
| chr1:147964580
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.618-1974A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964580 | ||||||
| chr1:147965032
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-1522A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965032 | ||||||
| chr1:147965307
|
C | G | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.618-1247C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965307 | ||||||
| chr1:147965506
|
A | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-1048A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965506 | ||||||
| chr1:147965787
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-767G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965787 | ||||||
| chr1:147965792
|
A | G | 39 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(36): Show | 39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.618-762A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965792 | ||||||
| chr1:147966037
|
G | C | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-517G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966037 | ||||||
| chr1:147966055
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.618-499C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966055 | ||||||
| chr1:147966207
|
A | AG | 7 | a0001c0001t0001g0058a0001c0001t0001g0148a0001c0001t0001g0149others(4): Show | 7 | HG00408.hp1 HG00609.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-346dupG | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147966207 | |||||
| chr1:147966237
|
A | G | 16 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0003t0002g0221others(13): Show | 16 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.618-317A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966237 | ||||||
| chr1:147966312
|
TAGC | T | 19 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(16): Show | 19 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.618-239_618-237del others(3): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147966312 | |||||
| chr1:147966440
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.618-114C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966440 | ||||||
| chr1:147966521
|
C | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0072others(1): Show | 4 | NA18939.hp2 NA18955.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-33C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966521 | ||||||
| chr1:147966689
|
C | A | 1 | a0001c0001t0001g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.727+26C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147966689 | ||||||
| chr1:147967001
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.727+338A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967001 | ||||||
| chr1:147967069
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(3): Show | 7 | HG00323.hp2 HG01243.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.727+406T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967069 | ||||||
| chr1:147967173
|
T | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.727+510T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967173 | ||||||
| chr1:147967465
|
A | G | 10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.727+802A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967465 | ||||||
| chr1:147967478
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.727+815T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967478 | ||||||
| chr1:147967743
|
G | A | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0266 | 3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.727+1080G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967743 | ||||||
| chr1:147967797
|
T | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.728-1078T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967797 | ||||||
| chr1:147967849
|
A | G | 4 | a0001c0003t0003g0240a0001c0003t0003g0241a0001c0003t0003g0242others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-1026A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967849 | ||||||
| chr1:147967921
|
G | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-954G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967921 | ||||||
| chr1:147968040
|
G | A | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.728-835G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968040 | ||||||
| chr1:147968240
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0134 | 2 | HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.728-635G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968240 | ||||||
| chr1:147968539
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.728-336A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968539 | ||||||
| chr1:147968707
|
A | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0204 | 2 | HG00408.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.728-168A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968707 | ||||||
| chr1:147968744
|
A | G | 1 | a0001c0001t0001g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.728-131A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968744 | ||||||
| chr1:147969015
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.816+52G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969015 | ||||||
| chr1:147969024
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.816+61T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969024 | ||||||
| chr1:147969151
|
T | G | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.816+188T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969151 | ||||||
| chr1:147969354
|
A | G | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+391A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969354 | ||||||
| chr1:147969413
|
A | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.816+450A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969413 | ||||||
| chr1:147969462
|
T | G | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-405T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969462 | ||||||
| chr1:147969751
|
G | A | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.817-116G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969751 | ||||||
| chr1:147970003
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+44C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970003 | ||||||
| chr1:147970026
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.909+67A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970026 | ||||||
| chr1:147970115
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.909+156A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970115 | ||||||
| chr1:147970162
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.909+203C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970162 | ||||||
| chr1:147970271
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.909+312A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970271 | ||||||
| chr1:147970453
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.909+494C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970453 | ||||||
| chr1:147970482
|
T | C | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.909+523T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970482 | ||||||
| chr1:147970491
|
A | ATC | 52 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0015others(49): Show | 53 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.909+574_909+575dup others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
A | ATCTC | 16 | a0001c0001t0001g0010a0001c0001t0001g0045a0001c0001t0001g0046others(13): Show | 16 | HG00323.hp1 HG00438.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.909+572_909+575dup others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
A | ATCTCTC | 29 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0025others(26): Show | 33 | HG00323.hp2 HG00408.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.909+570_909+575dup others(6): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
A | ATCTCTCT others(1): Show |
11 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0141others(8): Show | 11 | HG00140.hp1 HG01928.hp2 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+568_909+575dup others(8): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
A | ATCTCTCT others(3): Show |
12 | a0001c0001t0001g0028a0001c0001t0001g0058a0001c0001t0001g0100others(9): Show | 12 | HG00408.hp1 HG00438.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+566_909+575dup others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
A | ATCTCTCT others(5): Show |
4 | a0001c0001t0001g0039a0001c0001t0001g0137a0001c0001t0001g0180others(1): Show | 4 | HG01243.hp2 HG02027.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+564_909+575dup others(12): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
A | ATCTCTCT others(7): Show |
1 | a0001c0001t0001g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.909+562_909+575dup others(14): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
A | ATCTCTCT others(11): Show |
1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.909+558_909+575dup others(18): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
A | ATCTCTCT others(13): Show |
1 | a0001c0001t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.909+556_909+575dup others(20): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
ATC | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 6 | HG00741.hp2 HG02083.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+574_909+575del others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
ATCTC | A | 14 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0078others(11): Show | 14 | HG01074.hp2 HG02015.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.909+572_909+575del others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
ATCTCTCT others(3): Show |
A | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+566_909+575del others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970491
|
ATCTCTCT others(7): Show |
A | 10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.909+562_909+575del others(14): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | |||||
| chr1:147970521
|
C | A | 1 | a0001c0001t0004g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.909+562C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970521 | ||||||
| chr1:147970525
|
CTCTCTCT others(3): Show |
C | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+572_909+581del others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970525 | |||||
| chr1:147970527
|
C | A | 1 | a0001c0001t0004g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.909+568C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970527 | ||||||
| chr1:147970535
|
A | C | 20 | a0001c0001t0001g0182a0001c0001t0004g0260a0001c0003t0002g0221others(17): Show | 20 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.909+576A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970535 | ||||||
| chr1:147970541
|
A | C | 15 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(12): Show | 15 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.909+582A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970541 | ||||||
| chr1:147970543
|
CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0004g0260 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.909+596_909+607del others(12): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970543 | |||||
| chr1:147970545
|
C | A | 8 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(5): Show | 8 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+586C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970545 | ||||||
| chr1:147970547
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.909+588C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970547 | ||||||
| chr1:147970549
|
C | A | 14 | a0001c0003t0002g0221a0001c0003t0002g0224a0001c0003t0003g0235others(11): Show | 14 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.909+590C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970549 | ||||||
| chr1:147970549
|
C | CTA | 3 | a0001c0003t0002g0222a0001c0003t0002g0223a0002c0004t0002g0227 | 3 | NA18906.hp1 NA18982.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.909+591_909+592ins others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970549 | |||||
| chr1:147970549
|
C | CTCTCTCT others(3): Show |
1 | a0001c0003t0002g0231 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.909+595_909+596ins others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970549 | |||||
| chr1:147970549
|
C | CTCTCTCT others(9): Show |
1 | a0001c0003t0002g0225 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.909+595_909+596ins others(16): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970549 | |||||
| chr1:147970549
|
C | CTCTCTCT others(11): Show |
1 | a0001c0003t0002g0229 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.909+595_909+596ins others(18): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970549 | |||||
| chr1:147970549
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0065 | 2 | HG02155.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.909+590C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970549 | ||||||
| chr1:147970555
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.909+596A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970555 | ||||||
| chr1:147970567
|
C | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0263a0001c0001t0001g0264others(4): Show | 8 | HG01099.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+608C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970567 | ||||||
| chr1:147970569
|
C | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0048others(53): Show | 57 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.909+610C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970569 | ||||||
| chr1:147970571
|
A | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0156others(14): Show | 17 | HG00673.hp1 HG00673.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.909+612A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970571 | ||||||
| chr1:147970584
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.909+625A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970584 | ||||||
| chr1:147970599
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | HG02083.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.909+640A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970599 | ||||||
| chr1:147970617
|
T | C | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+658T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970617 | ||||||
| chr1:147970706
|
C | G | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.909+747C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970706 | ||||||
| chr1:147970841
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.909+882T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970841 | ||||||
| chr1:147970931
|
C | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+972C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970931 | ||||||
| chr1:147971141
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.909+1182G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971141 | ||||||
| chr1:147971157
|
C | CTT | 38 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(35): Show | 38 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.909+1208_909+1209d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971157 | |||||
| chr1:147971182
|
C | T | 1 | a0001c0003t0002g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.909+1223C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971182 | ||||||
| chr1:147971230
|
A | C | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+1271A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971230 | ||||||
| chr1:147971230
|
A | G | 1 | a0001c0002t0001g0116 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.909+1271A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971230 | ||||||
| chr1:147971256
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.909+1297T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971256 | ||||||
| chr1:147971300
|
C | A | 1 | a0001c0001t0001g0123 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.909+1341C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971300 | ||||||
| chr1:147971302
|
G | A | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.909+1343G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971302 | ||||||
| chr1:147971314
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.909+1355T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971314 | ||||||
| chr1:147971464
|
C | CT | 40 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0026others(37): Show | 40 | HG00323.hp1 HG00673.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.909+1530dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971464 | |||||
| chr1:147971464
|
C | CTTT | 9 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0224others(6): Show | 9 | HG02040.hp1 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.909+1528_909+1530d others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971464 | |||||
| chr1:147971464
|
C | CTTTT | 8 | a0001c0003t0002g0223a0001c0003t0002g0231a0001c0003t0002g0232others(5): Show | 8 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1527_909+1530d others(6): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971464 | |||||
| chr1:147971464
|
C | CTTTTT | 11 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(8): Show | 11 | HG00597.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.909+1526_909+1530d others(7): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971464 | |||||
| chr1:147971562
|
C | T | 1 | a0001c0003t0002g0230 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.909+1603C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971562 | ||||||
| chr1:147971678
|
C | T | 23 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.909+1719C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971678 | ||||||
| chr1:147971766
|
C | T | 3 | a0001c0002t0001g0093a0001c0002t0001g0094a0001c0002t0001g0101 | 3 | NA18965.hp2 NA18971.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.909+1807C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971766 | ||||||
| chr1:147972079
|
A | G | 23 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(20): Show | 23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.909+2120A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972079 | ||||||
| chr1:147972176
|
G | T | 11 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(8): Show | 11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+2217G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972176 | ||||||
| chr1:147972302
|
T | G | 18 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(15): Show | 18 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.909+2343T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972302 | ||||||
| chr1:147972371
|
A | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0132a0001c0003t0003g0244 | 3 | HG01175.hp1 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.909+2412A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972371 | ||||||
| chr1:147972375
|
A | G | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+2416A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972375 | ||||||
| chr1:147972437
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.909+2478C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972437 | ||||||
| chr1:147972528
|
G | A | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.909+2569G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972528 | ||||||
| chr1:147972665
|
A | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0026others(5): Show | 8 | HG01175.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+2706A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972665 | ||||||
| chr1:147972739
|
G | T | 6 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(3): Show | 6 | HG00735.hp2 HG01074.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+2780G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972739 | ||||||
| chr1:147972748
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+2789G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972748 | ||||||
| chr1:147972790
|
A | AT | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.909+2834dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147972790 | |||||
| chr1:147972804
|
C | T | 4 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0085others(1): Show | 4 | HG03688.hp2 HG03710.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+2845C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972804 | ||||||
| chr1:147972887
|
A | G | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+2928A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972887 | ||||||
| chr1:147973129
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.909+3170A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147973129 | ||||||
| chr1:147973538
|
G | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0174a0001c0001t0001g0178others(3): Show | 6 | HG00438.hp2 HG02027.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+3579G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147973538 | ||||||
| chr1:147973766
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.909+3807G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147973766 | ||||||
| chr1:147973781
|
T | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+3822T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147973781 | ||||||
| chr1:147974149
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.909+4190C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974149 | ||||||
| chr1:147974305
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.909+4346A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974305 | ||||||
| chr1:147974654
|
A | G | 1 | a0001c0003t0002g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.909+4695A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974654 | ||||||
| chr1:147974713
|
A | G | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.909+4754A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974713 | ||||||
| chr1:147974737
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.909+4778C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974737 | ||||||
| chr1:147974943
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+4984C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974943 | ||||||
| chr1:147975102
|
T | A | 1 | a0001c0001t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.909+5143T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147975102 | ||||||
| chr1:147975186
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.909+5227A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147975186 | ||||||
| chr1:147975844
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.909+5885C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147975844 | ||||||
| chr1:147976064
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.909+6105A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976064 | ||||||
| chr1:147976104
|
G | A | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+6145G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976104 | ||||||
| chr1:147976155
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0209 | 2 | NA18986.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.909+6196A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976155 | ||||||
| chr1:147976238
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.909+6279C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976238 | ||||||
| chr1:147976268
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0164a0001c0001t0001g0166others(2): Show | 6 | HG01891.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+6309T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976268 | ||||||
| chr1:147976660
|
G | T | 1 | a0001c0002t0001g0189 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.909+6701G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976660 | ||||||
| chr1:147976922
|
T | G | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.909+6963T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976922 | ||||||
| chr1:147976927
|
G | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+6968G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976927 | ||||||
| chr1:147977111
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+7152A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977111 | ||||||
| chr1:147977166
|
G | A | 11 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(8): Show | 11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+7207G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977166 | ||||||
| chr1:147977192
|
C | A | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+7233C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977192 | ||||||
| chr1:147977233
|
C | CA | 17 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0069others(14): Show | 17 | HG01109.hp2 HG01175.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.909+7303dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147977233 | |||||
| chr1:147977233
|
CA | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 171 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.909+7303delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147977233 | |||||
| chr1:147977233
|
CAA | C | 7 | a0001c0001t0001g0032a0001c0001t0001g0169a0001c0001t0001g0176others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+7302_909+7303d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147977233 | |||||
| chr1:147977252
|
A | C | 1 | a0001c0001t0001g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.909+7293A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977252 | ||||||
| chr1:147977253
|
A | C | 1 | a0001c0001t0001g0060 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.909+7294A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977253 | ||||||
| chr1:147977262
|
A | C | 2 | a0001c0001t0004g0262a0001c0003t0003g0244 | 2 | HG00738.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.909+7303A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977262 | ||||||
| chr1:147977448
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | NA18939.hp1 NA18962.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.909+7489G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977448 | ||||||
| chr1:147977523
|
G | A | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+7564G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977523 | ||||||
| chr1:147977563
|
C | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.909+7604C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977563 | ||||||
| chr1:147977589
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0021 | 2 | NA20805.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.909+7630C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977589 | ||||||
| chr1:147977596
|
G | A | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.909+7637G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977596 | ||||||
| chr1:147977631
|
G | A | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+7672G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977631 | ||||||
| chr1:147977672
|
T | C | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.909+7713T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977672 | ||||||
| chr1:147977744
|
A | G | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.909+7785A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977744 | ||||||
| chr1:147977747
|
T | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0026others(5): Show | 8 | HG01175.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+7788T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977747 | ||||||
| chr1:147978135
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-8064C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978135 | ||||||
| chr1:147978146
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.910-8053G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978146 | ||||||
| chr1:147978437
|
T | TGGG | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-7761_910-7759d others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147978437 | |||||
| chr1:147978513
|
T | G | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-7686T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978513 | ||||||
| chr1:147978568
|
C | A | 1 | a0001c0001t0001g0158 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.910-7631C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978568 | ||||||
| chr1:147978628
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0161a0001c0001t0001g0168others(6): Show | 12 | HG00738.hp2 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-7571G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978628 | ||||||
| chr1:147978631
|
C | T | 2 | a0002c0004t0002g0227a0002c0004t0002g0234 | 2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.910-7568C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978631 | ||||||
| chr1:147978858
|
T | TTTGCCTC | 6 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-7341_910-7340i others(9): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978858 | ||||||
| chr1:147978859
|
G | C | 6 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-7340G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978859 | ||||||
| chr1:147978860
|
A | C | 6 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-7339A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978860 | ||||||
| chr1:147978860
|
A | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-7339A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978860 | ||||||
| chr1:147978861
|
T | G | 6 | a0001c0001t0004g0258a0001c0001t0004g0259a0001c0001t0004g0260others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-7338T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978861 | ||||||
| chr1:147978869
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-7330A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978869 | ||||||
| chr1:147978886
|
G | A | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.910-7313G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978886 | ||||||
| chr1:147979171
|
T | G | 1 | a0001c0003t0003g0242 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.910-7028T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979171 | ||||||
| chr1:147979307
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.910-6892C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979307 | ||||||
| chr1:147979310
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.910-6889C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979310 | ||||||
| chr1:147979407
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(72): Show | 80 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.910-6792C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979407 | ||||||
| chr1:147979458
|
T | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-6741T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979458 | ||||||
| chr1:147979459
|
T | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0212 | 2 | HG00738.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.910-6740T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979459 | ||||||
| chr1:147979677
|
T | C | 41 | a0001c0001t0001g0195a0001c0001t0001g0248a0001c0001t0001g0249others(38): Show | 41 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.910-6522T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979677 | ||||||
| chr1:147979699
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.910-6500A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979699 | ||||||
| chr1:147979788
|
C | T | 6 | a0001c0001t0001g0167a0001c0001t0001g0190a0001c0002t0001g0083others(3): Show | 6 | HG02129.hp1 HG02280.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-6411C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979788 | ||||||
| chr1:147979827
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.910-6372A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979827 | ||||||
| chr1:147979843
|
C | G | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-6356C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979843 | ||||||
| chr1:147979886
|
C | T | 3 | a0001c0001t0001g0053a0001c0002t0001g0090a0001c0006t0007g0256 | 3 | HG02015.hp1 HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.910-6313C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979886 | ||||||
| chr1:147979906
|
T | C | 18 | a0001c0001t0001g0103a0001c0001t0001g0248a0001c0001t0001g0249others(15): Show | 18 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.910-6293T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979906 | ||||||
| chr1:147980007
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.910-6192G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980007 | ||||||
| chr1:147980043
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0005g0091 | 2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.910-6156G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980043 | ||||||
| chr1:147980085
|
C | CA | 22 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.910-6100dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980085 | |||||
| chr1:147980151
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0043a0001c0001t0001g0150 | 3 | NA18943.hp1 NA18975.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.910-6048G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980151 | ||||||
| chr1:147980274
|
C | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.910-5925C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980274 | ||||||
| chr1:147980302
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.910-5897A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980302 | ||||||
| chr1:147980358
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.910-5841T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980358 | ||||||
| chr1:147980462
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0204 | 2 | HG00408.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.910-5737A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980462 | ||||||
| chr1:147980515
|
C | A | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-5684C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980515 | ||||||
| chr1:147980633
|
A | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0183 | 3 | HG00438.hp2 HG02040.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.910-5566A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980633 | ||||||
| chr1:147980768
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0135 | 2 | HG02602.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.910-5431G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980768 | ||||||
| chr1:147980776
|
G | A | 4 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(1): Show | 4 | NA18974.hp1 NA18982.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-5423G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980776 | ||||||
| chr1:147980788
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0001g0087a0001c0001t0001g0105 | 3 | HG02809.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.910-5411C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980788 | ||||||
| chr1:147980818
|
C | CA | 95 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 101 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.910-5353dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980818 | |||||
| chr1:147980818
|
C | CAA | 17 | a0001c0001t0001g0039a0001c0001t0001g0139a0001c0001t0001g0141others(14): Show | 17 | HG00323.hp2 HG01169.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.910-5354_910-5353d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980818 | |||||
| chr1:147980818
|
CAA | C | 13 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(10): Show | 13 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.910-5354_910-5353d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980818 | |||||
| chr1:147980818
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0003t0003g0240a0001c0003t0003g0241a0001c0003t0003g0243 | 3 | HG02055.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.910-5363_910-5353d others(13): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980818 | |||||
| chr1:147981023
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.910-5176A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981023 | ||||||
| chr1:147981028
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.910-5171G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981028 | ||||||
| chr1:147981037
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.910-5162G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981037 | ||||||
| chr1:147981078
|
A | G | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-5121A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981078 | ||||||
| chr1:147981295
|
C | T | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG01891.hp1 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.910-4904C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981295 | ||||||
| chr1:147981318
|
G | GAC | 8 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(5): Show | 8 | HG02258.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-4871_910-4870d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | |||||
| chr1:147981318
|
G | GACACACA others(3): Show |
3 | a0001c0003t0003g0240a0001c0003t0003g0242a0001c0003t0003g0243 | 3 | HG02055.hp2 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.910-4879_910-4870d others(12): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | |||||
| chr1:147981318
|
G | GACACACA others(5): Show |
2 | a0001c0003t0003g0239a0001c0003t0003g0241 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.910-4870_910-4869i others(14): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | |||||
| chr1:147981318
|
G | GACACACA others(7): Show |
1 | a0001c0003t0002g0222 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.910-4870_910-4869i others(16): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | |||||
| chr1:147981318
|
G | GACACACA others(9): Show |
4 | a0001c0003t0003g0235a0001c0003t0003g0237a0001c0003t0003g0238others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-4870_910-4869i others(18): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | |||||
| chr1:147981318
|
G | GACACACA others(11): Show |
10 | a0001c0003t0002g0221a0001c0003t0002g0223a0001c0003t0002g0224others(7): Show | 10 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.910-4870_910-4869i others(20): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | |||||
| chr1:147981318
|
G | GACACACA others(13): Show |
3 | a0002c0004t0002g0227a0002c0004t0002g0228a0002c0004t0002g0234 | 3 | HG02886.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.910-4870_910-4869i others(22): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | |||||
| chr1:147981330
|
T | C | 41 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(38): Show | 41 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.910-4869T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981330 | ||||||
| chr1:147981349
|
A | ACACACAC others(10): Show |
1 | a0001c0003t0003g0236 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.910-4850_910-4849i others(19): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981349 | ||||||
| chr1:147981453
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.910-4746G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981453 | ||||||
| chr1:147981469
|
A | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-4730A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981469 | ||||||
| chr1:147981500
|
A | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0099 | 2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.910-4699A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981500 | ||||||
| chr1:147981611
|
T | G | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-4588T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981611 | ||||||
| chr1:147981631
|
T | C | 3 | a0001c0003t0002g0224a0001c0003t0002g0225a0001c0003t0002g0229 | 3 | HG00597.hp1 HG02040.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.910-4568T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981631 | ||||||
| chr1:147981731
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.910-4468C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981731 | ||||||
| chr1:147981827
|
A | G | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-4372A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981827 | ||||||
| chr1:147982090
|
C | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-4109C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982090 | ||||||
| chr1:147982099
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.910-4100G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982099 | ||||||
| chr1:147982145
|
C | T | 9 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0266others(6): Show | 9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.910-4054C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982145 | ||||||
| chr1:147982193
|
C | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-4006C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982193 | ||||||
| chr1:147982221
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-3978G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982221 | ||||||
| chr1:147982302
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0134 | 2 | HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.910-3897T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982302 | ||||||
| chr1:147982306
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.910-3893C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982306 | ||||||
| chr1:147982349
|
T | G | 11 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(8): Show | 11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-3850T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982349 | ||||||
| chr1:147982427
|
G | T | 1 | a0001c0001t0001g0100 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.910-3772G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982427 | ||||||
| chr1:147982437
|
C | T | 2 | a0001c0001t0005g0091a0001c0001t0008g0215 | 2 | HG03139.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.910-3762C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982437 | ||||||
| chr1:147982469
|
A | C | 1 | a0001c0002t0001g0094 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.910-3730A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982469 | ||||||
| chr1:147982861
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG02602.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.910-3338C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982861 | ||||||
| chr1:147982863
|
T | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.910-3336T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982863 | ||||||
| chr1:147982987
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-3212C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982987 | ||||||
| chr1:147982988
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.910-3211A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982988 | ||||||
| chr1:147983019
|
G | A | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-3180G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983019 | ||||||
| chr1:147983229
|
AACCTAGG others(4): Show |
A | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-2966_910-2956d others(13): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147983229 | |||||
| chr1:147983237
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.910-2962C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983237 | ||||||
| chr1:147983262
|
G | A | 1 | a0002c0004t0002g0228 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.910-2937G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983262 | ||||||
| chr1:147983336
|
T | G | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-2863T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983336 | ||||||
| chr1:147983434
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-2765G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983434 | ||||||
| chr1:147983496
|
C | A | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-2703C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983496 | ||||||
| chr1:147983512
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.910-2687C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983512 | ||||||
| chr1:147983555
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0206 | 2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.910-2644C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983555 | ||||||
| chr1:147983695
|
G | A | 10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.910-2504G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983695 | ||||||
| chr1:147983763
|
G | T | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-2436G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983763 | ||||||
| chr1:147983799
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-2400C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983799 | ||||||
| chr1:147983811
|
G | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-2388G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983811 | ||||||
| chr1:147983855
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.910-2344T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983855 | ||||||
| chr1:147983882
|
G | A | 3 | a0001c0003t0002g0224a0001c0003t0002g0225a0001c0003t0002g0229 | 3 | HG00597.hp1 HG02040.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.910-2317G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983882 | ||||||
| chr1:147983955
|
C | A | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-2244C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983955 | ||||||
| chr1:147984071
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.910-2128G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984071 | ||||||
| chr1:147984107
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-2092C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984107 | ||||||
| chr1:147984176
|
G | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-2023G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984176 | ||||||
| chr1:147984178
|
G | T | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02559.hp2 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.910-2021G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984178 | ||||||
| chr1:147984237
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0080 | 2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.910-1962T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984237 | ||||||
| chr1:147984243
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.910-1956G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984243 | ||||||
| chr1:147984244
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.910-1955G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984244 | ||||||
| chr1:147984257
|
G | A | 13 | a0001c0001t0001g0039a0001c0001t0001g0114a0001c0001t0001g0158others(10): Show | 13 | HG00438.hp2 HG01978.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.910-1942G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984257 | ||||||
| chr1:147984262
|
T | G | 1 | a0001c0002t0001g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.910-1937T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984262 | ||||||
| chr1:147984301
|
C | A | 5 | a0001c0002t0001g0024a0001c0002t0001g0090a0001c0002t0001g0097others(2): Show | 5 | HG00673.hp2 HG02015.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-1898C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984301 | ||||||
| chr1:147984306
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.910-1893A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984306 | ||||||
| chr1:147984397
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.910-1802G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984397 | ||||||
| chr1:147984456
|
T | G | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.910-1743T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984456 | ||||||
| chr1:147984542
|
C | G | 1 | a0001c0001t0005g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.910-1657C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984542 | ||||||
| chr1:147984578
|
A | G | 1 | a0001c0001t0005g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.910-1621A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984578 | ||||||
| chr1:147984838
|
T | G | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.910-1361T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984838 | ||||||
| chr1:147984854
|
G | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-1345G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984854 | ||||||
| chr1:147984890
|
T | C | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-1309T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984890 | ||||||
| chr1:147985120
|
T | C | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-1079T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985120 | ||||||
| chr1:147985125
|
A | G | 3 | a0001c0003t0002g0231a0001c0003t0002g0232a0001c0003t0002g0233 | 3 | HG00423.hp2 HG00621.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.910-1074A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985125 | ||||||
| chr1:147985138
|
G | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-1061G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985138 | ||||||
| chr1:147985385
|
A | C | 2 | a0001c0001t0001g0179a0001c0001t0001g0183 | 2 | HG02040.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.910-814A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985385 | ||||||
| chr1:147985412
|
T | G | 1 | a0001c0001t0001g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.910-787T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985412 | ||||||
| chr1:147985475
|
G | C | 25 | a0001c0001t0001g0067a0001c0003t0002g0221a0001c0003t0002g0222others(22): Show | 25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.910-724G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985475 | ||||||
| chr1:147985581
|
G | C | 1 | a0003c0008t0001g0089 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.910-618G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985581 | ||||||
| chr1:147985595
|
A | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-604A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985595 | ||||||
| chr1:147985614
|
T | G | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-585T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985614 | ||||||
| chr1:147985636
|
G | GT | 22 | a0001c0001t0001g0257a0001c0001t0001g0264a0001c0001t0004g0258others(19): Show | 22 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.910-552dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147985636 | |||||
| chr1:147985783
|
G | A | 1 | a0001c0001t0005g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.910-416G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985783 | ||||||
| chr1:147985953
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.910-246C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985953 | ||||||
| chr1:147986034
|
C | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-165C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147986034 | ||||||
| chr1:147986185
|
C | T | 10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.910-14C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147986185 | ||||||
| chr1:147986545
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1005+251C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147986545 | ||||||
| chr1:147986826
|
A | T | 1 | a0001c0001t0001g0070 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1005+532A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147986826 | ||||||
| chr1:147986842
|
G | A | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1005+548G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147986842 | ||||||
| chr1:147986959
|
C | T | 1 | a0001c0002t0001g0220 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1005+665C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147986959 | ||||||
| chr1:147987018
|
G | T | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1005+724G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987018 | ||||||
| chr1:147987173
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0014 | 3 | HG00741.hp2 HG01243.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1005+879T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987173 | ||||||
| chr1:147987519
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1006-913T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987519 | ||||||
| chr1:147987711
|
G | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0080 | 2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1006-721G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987711 | ||||||
| chr1:147987743
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1006-689T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987743 | ||||||
| chr1:147987754
|
G | T | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1006-678G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987754 | ||||||
| chr1:147987809
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1006-623A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987809 | ||||||
| chr1:147987896
|
A | G | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1006-536A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987896 | ||||||
| chr1:147988042
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-390C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988042 | ||||||
| chr1:147988062
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006-370G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988062 | ||||||
| chr1:147988098
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006-334G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988098 | ||||||
| chr1:147988107
|
C | T | 5 | a0001c0003t0003g0239a0001c0003t0003g0240a0001c0003t0003g0241others(2): Show | 5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-325C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988107 | ||||||
| chr1:147988122
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | NA18957.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1006-310G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988122 | ||||||
| chr1:147988410
|
T | A | 1 | a0001c0003t0003g0239 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1006-22T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988410 | ||||||
| chr1:147988588
|
G | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+67G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147988588 | ||||||
| chr1:147988589
|
G | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+68G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147988589 | ||||||
| chr1:147988666
|
C | T | 1 | a0001c0003t0003g0244 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1095+145C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147988666 | ||||||
| chr1:147988861
|
C | CA | 37 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0123others(34): Show | 37 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1095+353dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 147988861 | |||||
| chr1:147988861
|
C | CAA | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+352_1095+353d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 147988861 | |||||
| chr1:147989127
|
G | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+606G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989127 | ||||||
| chr1:147989234
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+713A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989234 | ||||||
| chr1:147989251
|
A | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0204 | 2 | HG00408.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1095+730A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989251 | ||||||
| chr1:147989322
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1095+801C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989322 | ||||||
| chr1:147989427
|
C | CT | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0053others(3): Show | 6 | HG02258.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+921dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 147989427 | |||||
| chr1:147989427
|
CT | C | 26 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0201others(23): Show | 26 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1095+921delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 147989427 | |||||
| chr1:147989443
|
A | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0198 | 2 | HG02080.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1095+922A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989443 | ||||||
| chr1:147989686
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1095+1165G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989686 | ||||||
| chr1:147989754
|
C | A | 1 | a0001c0001t0001g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1095+1233C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989754 | ||||||
| chr1:147989845
|
G | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+1324G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989845 | ||||||
| chr1:147989963
|
C | G | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1095+1442C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989963 | ||||||
| chr1:147990004
|
T | G | 10 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0001g0264others(7): Show | 10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1095+1483T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990004 | ||||||
| chr1:147990033
|
C | T | 1 | a0001c0001t0005g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1095+1512C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990033 | ||||||
| chr1:147990044
|
C | G | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1095+1523C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990044 | ||||||
| chr1:147990064
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1095+1543G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990064 | ||||||
| chr1:147990099
|
A | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+1578A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990099 | ||||||
| chr1:147990168
|
T | A | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+1647T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990168 | ||||||
| chr1:147990177
|
C | G | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+1656C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990177 | ||||||
| chr1:147990333
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1095+1812A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990333 | ||||||
| chr1:147990362
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0132 | 2 | HG01175.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1095+1841A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990362 | ||||||
| chr1:147990403
|
G | A | 1 | a0005c0005t0001g0115 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1095+1882G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990403 | ||||||
| chr1:147990451
|
C | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0132 | 2 | HG01175.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1095+1930C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990451 | ||||||
| chr1:147990496
|
T | C | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1095+1975T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990496 | ||||||
| chr1:147990591
|
T | G | 1 | a0001c0001t0001g0257 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1096-1911T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990591 | ||||||
| chr1:147990736
|
T | C | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1096-1766T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990736 | ||||||
| chr1:147990806
|
G | A | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1096-1696G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990806 | ||||||
| chr1:147990880
|
C | T | 4 | a0001c0003t0003g0235a0001c0003t0003g0236a0001c0003t0003g0237others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-1622C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990880 | ||||||
| chr1:147990959
|
G | A | 1 | a0001c0006t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1096-1543G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990959 | ||||||
| chr1:147991024
|
T | C | 13 | a0001c0001t0001g0047a0001c0001t0001g0106a0001c0001t0001g0107others(10): Show | 13 | HG00438.hp1 HG00735.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1096-1478T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991024 | ||||||
| chr1:147991031
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1096-1471C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991031 | ||||||
| chr1:147991057
|
A | T | 1 | a0001c0001t0001g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1096-1445A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991057 | ||||||
| chr1:147991080
|
A | G | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1096-1422A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991080 | ||||||
| chr1:147991101
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1096-1401G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991101 | ||||||
| chr1:147991120
|
G | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1096-1382G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991120 | ||||||
| chr1:147991166
|
C | T | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1096-1336C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991166 | ||||||
| chr1:147991183
|
C | A | 12 | a0001c0001t0001g0156a0001c0001t0001g0190a0001c0001t0001g0191others(9): Show | 12 | HG00673.hp1 HG02080.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096-1319C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991183 | ||||||
| chr1:147991208
|
C | A | 40 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(37): Show | 40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1096-1294C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991208 | ||||||
| chr1:147991413
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1096-1089C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991413 | ||||||
| chr1:147991461
|
C | T | 14 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(11): Show | 14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1096-1041C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991461 | ||||||
| chr1:147991493
|
A | G | 13 | a0001c0001t0001g0048a0001c0001t0001g0087a0001c0001t0001g0100others(10): Show | 13 | HG00323.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1096-1009A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991493 | ||||||
| chr1:147991494
|
G | C | 13 | a0001c0001t0001g0048a0001c0001t0001g0087a0001c0001t0001g0100others(10): Show | 13 | HG00323.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1096-1008G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991494 | ||||||
| chr1:147991665
|
G | T | 1 | a0001c0001t0001g0119 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1096-837G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991665 | ||||||
| chr1:147991666
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1096-836A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991666 | ||||||
| chr1:147991751
|
A | T | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-751A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991751 | ||||||
| chr1:147991832
|
C | T | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0266 | 3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1096-670C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991832 | ||||||
| chr1:147991878
|
T | C | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-624T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991878 | ||||||
| chr1:147992390
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-112G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147992390 | ||||||
| chr1:147992467
|
G | C | 24 | a0001c0003t0002g0221a0001c0003t0002g0222a0001c0003t0002g0223others(21): Show | 24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1096-35G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147992467 | ||||||
| chr1:147992585
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1161+18C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 13/13 | chr1 | 147992585 |