| geneid | 9687 |
|---|---|
| ensemblid | ENSG00000196208.14 |
| hgncid | 24885 |
| symbol | GREB1 |
| name | growth regulating estrogen receptor binding 1 |
| refseq_nuc | NM_014668.4 |
| refseq_prot | NP_055483.2 |
| ensembl_nuc | ENST00000381486.7 |
| ensembl_prot | ENSP00000370896.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 11534045 |
| end | 11642788 |
| strand | + |
| ver | v1.2 |
| region | chr2:11534045-11642788 |
| region5000 | chr2:11529045-11647788 |
| regionname0 | GREB1_chr2_11534045_11642788 |
| regionname5000 | GREB1_chr2_11529045_11647788 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1949 | 53 | 1 | 11 | 34 | 0 | 7 | 24 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002 | 0/0 | 1949 | 41 | 14 | 2 | 21 | 0 | 4 | 17 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003 | 1/0 | 1949 | 31 | 4 | 9 | 14 | 2 | 1 | 13 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004 | 0/0 | 1949 | 31 | 1 | 8 | 15 | 2 | 5 | 11 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005 | 0/0 | 1949 | 29 | 5 | 5 | 14 | 4 | 1 | 10 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006 | 0/0 | 1949 | 16 | 4 | 1 | 9 | 0 | 2 | 9 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007 | 0/0 | 1949 | 12 | 9 | 0 | 3 | 0 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008 | 0/0 | 1949 | 12 | 8 | 2 | 0 | 1 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009 | 0/0 | 1949 | 9 | 6 | 0 | 1 | 0 | 2 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0010 | 0/0 | 1949 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0011 | 0/0 | 1949 | 5 | 3 | 1 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0012 | 0/0 | 1949 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0013 | 0/0 | 1949 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0014 | 0/0 | 1949 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0015 | 0/0 | 1949 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0016 | 0/0 | 1949 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0017 | 0/0 | 1949 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0018 | 0/0 | 1949 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0019 | 0/0 | 1949 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0020 | 0/0 | 1949 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0021 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0022 | 0/0 | 1949 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0023 | 0/0 | 1949 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0024 | 0/0 | 1949 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0025 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0026 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0027 | 0/0 | 1949 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0028 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0029 | 0/0 | 1949 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0030 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0031 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0032 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0033 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0034 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0035 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0036 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0037 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0038 | 0/0 | 1949 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0039 | 0/0 | 1949 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0040 | 0/0 | 1851 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0041 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0042 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0043 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0044 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0045 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0046 | 0/0 | 1949 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0047 | 0/0 | 1949 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0048 | 0/0 | 1949 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0049 | 0/0 | 1949 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0050 | 0/0 | 1949 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0051 | 0/0 | 1949 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0052 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0053 | 0/0 | 1949 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0054 | 0/1 | 1949 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0055 | 0/0 | 1949 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0056 | 0/0 | 1949 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 5850 | 48 | 1 | 10 | 32 | 0 | 5 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0002 | 0/0 | 5850 | 27 | 4 | 5 | 13 | 4 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0003 | 0/0 | 5850 | 23 | 0 | 7 | 13 | 2 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0004 | 0/0 | 5850 | 23 | 1 | 7 | 10 | 2 | 3 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0005 | 0/0 | 5850 | 17 | 0 | 0 | 14 | 0 | 3 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0006 | 0/0 | 5850 | 10 | 6 | 2 | 0 | 1 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0007 | 0/0 | 5850 | 6 | 4 | 0 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0008 | 0/0 | 5850 | 5 | 3 | 1 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0009 | 1/0 | 5850 | 5 | 4 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0010 | 0/0 | 5850 | 5 | 0 | 5 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0011 | 0/0 | 5850 | 5 | 0 | 2 | 2 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0012 | 0/0 | 5850 | 4 | 4 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0013 | 0/0 | 5850 | 4 | 0 | 0 | 2 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0014 | 0/0 | 5850 | 4 | 0 | 0 | 4 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0015 | 0/0 | 5850 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0016 | 0/0 | 5850 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0017 | 0/0 | 5850 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0018 | 0/0 | 5850 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0019 | 0/0 | 5850 | 3 | 1 | 0 | 0 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0020 | 0/0 | 5850 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0021 | 0/0 | 5850 | 3 | 2 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0022 | 0/0 | 5850 | 3 | 1 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0023 | 0/0 | 5850 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0024 | 0/0 | 5850 | 3 | 0 | 3 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0025 | 0/0 | 5850 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0026 | 0/0 | 5850 | 3 | 0 | 0 | 1 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0027 | 0/0 | 5850 | 3 | 0 | 0 | 2 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0028 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0029 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0030 | 0/0 | 5850 | 2 | 1 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0031 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0032 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0033 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0034 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0035 | 0/0 | 5850 | 2 | 1 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0036 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0037 | 0/0 | 5850 | 2 | 1 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0038 | 0/0 | 5850 | 2 | 0 | 2 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0039 | 0/0 | 5850 | 2 | 0 | 0 | 1 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0040 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0041 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0042 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0043 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0044 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0045 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0046 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0047 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0048 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0049 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0050 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0051 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0052 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0053 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0054 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0055 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0056 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0057 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0058 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0059 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0060 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0061 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0062 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0063 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0064 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0065 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0066 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0067 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0068 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0069 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0070 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0071 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0072 | 0/0 | 5819 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0073 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0074 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0075 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0076 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0077 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0078 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0079 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0080 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0081 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0082 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0083 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0084 | 0/1 | 5850 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0085 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0086 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0087 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0088 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0089 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0090 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0091 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0092 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0093 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0094 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0095 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0096 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0097 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| c0098 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2721 | 42 | 8 | 8 | 21 | 1 | 4 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0002 | 0/1 | 2721 | 42 | 0 | 16 | 17 | 0 | 8 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0003 | 0/0 | 2716 | 26 | 6 | 1 | 16 | 2 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0004 | 0/0 | 2716 | 17 | 2 | 3 | 9 | 0 | 3 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0005 | 0/0 | 2708 | 14 | 0 | 4 | 10 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0006 | 0/0 | 2726 | 12 | 0 | 3 | 7 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0007 | 0/0 | 2726 | 11 | 0 | 0 | 11 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0008 | 0/0 | 2706 | 10 | 1 | 3 | 5 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0009 | 0/0 | 2706 | 8 | 0 | 2 | 3 | 1 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0010 | 0/0 | 2710 | 7 | 1 | 3 | 0 | 2 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0011 | 0/0 | 2708 | 7 | 0 | 0 | 3 | 0 | 4 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0012 | 0/0 | 2716 | 6 | 5 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0013 | 0/0 | 2710 | 6 | 0 | 3 | 0 | 0 | 3 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0014 | 0/0 | 2707 | 5 | 4 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0015 | 0/0 | 2716 | 5 | 5 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0016 | 0/0 | 2706 | 5 | 1 | 0 | 3 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0017 | 0/0 | 2721 | 4 | 4 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0018 | 0/0 | 2706 | 4 | 0 | 2 | 0 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0019 | 0/0 | 2721 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0020 | 0/0 | 2716 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0021 | 0/0 | 2716 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0022 | 0/0 | 2711 | 3 | 2 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0023 | 0/0 | 2716 | 3 | 2 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0024 | 0/0 | 2721 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0025 | 0/0 | 2706 | 3 | 0 | 2 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0026 | 0/0 | 2708 | 2 | 0 | 0 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0027 | 0/0 | 2716 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0028 | 0/0 | 2721 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0029 | 1/0 | 2706 | 2 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0030 | 0/0 | 2708 | 2 | 0 | 0 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0031 | 0/0 | 2716 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0032 | 0/0 | 2731 | 2 | 0 | 0 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0033 | 0/0 | 2716 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0034 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0035 | 0/0 | 2716 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0036 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0037 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0038 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0039 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0040 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0041 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0042 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0043 | 0/0 | 2710 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0044 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0045 | 0/0 | 2710 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0046 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0047 | 0/0 | 2725 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0048 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0049 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0050 | 0/0 | 2710 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0051 | 0/0 | 2731 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0052 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0053 | 0/0 | 2722 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0054 | 0/0 | 2711 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0055 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0056 | 0/0 | 2706 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0057 | 0/0 | 2726 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0058 | 0/0 | 2710 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0059 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0060 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0061 | 0/0 | 2711 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0062 | 0/0 | 2720 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0063 | 0/0 | 2710 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0064 | 0/0 | 2726 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0065 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0066 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0067 | 0/0 | 2708 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0068 | 0/0 | 2706 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0069 | 0/0 | 2720 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0070 | 0/0 | 2716 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0071 | 0/0 | 2711 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0072 | 0/0 | 2708 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0073 | 0/0 | 2708 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| t0074 | 0/0 | 2706 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 5850 | 48 | 1 | 10 | 32 | 0 | 5 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0013 | 0/0 | 5850 | 4 | 0 | 0 | 2 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0089 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0005 | 0/0 | 5850 | 17 | 0 | 0 | 14 | 0 | 3 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0007 | 0/0 | 5850 | 6 | 4 | 0 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0011 | 0/0 | 5850 | 5 | 0 | 2 | 2 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0012 | 0/0 | 5850 | 4 | 4 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0020 | 0/0 | 5850 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0034 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0053 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0055 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0057 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0061 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0003 | 0/0 | 5850 | 23 | 0 | 7 | 13 | 2 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0009 | 1/0 | 5850 | 5 | 4 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0038 | 0/0 | 5850 | 2 | 0 | 2 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0076 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0004 | 0/0 | 5850 | 23 | 1 | 7 | 10 | 2 | 3 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0025 | 0/0 | 5850 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0026 | 0/0 | 5850 | 3 | 0 | 0 | 1 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0082 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0088 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002 | 0/0 | 5850 | 27 | 4 | 5 | 13 | 4 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0066 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0073 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0014 | 0/0 | 5850 | 4 | 0 | 0 | 4 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0027 | 0/0 | 5850 | 3 | 0 | 0 | 2 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0033 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0054 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0056 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0063 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0064 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0065 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0097 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0098 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0015 | 0/0 | 5850 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0016 | 0/0 | 5850 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0017 | 0/0 | 5850 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0043 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0044 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0058 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0006 | 0/0 | 5850 | 10 | 6 | 2 | 0 | 1 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0049 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0060 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0019 | 0/0 | 5850 | 3 | 1 | 0 | 0 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0028 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0029 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0030 | 0/0 | 5850 | 2 | 1 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0010c0031 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0010c0032 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0010c0035 | 0/0 | 5850 | 2 | 1 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0011c0008 | 0/0 | 5850 | 5 | 3 | 1 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0012c0010 | 0/0 | 5850 | 5 | 0 | 5 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0013c0018 | 0/0 | 5850 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0013c0052 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0014c0023 | 0/0 | 5850 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0015c0022 | 0/0 | 5850 | 3 | 1 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0016c0021 | 0/0 | 5850 | 3 | 2 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0017c0024 | 0/0 | 5850 | 3 | 0 | 3 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0018c0037 | 0/0 | 5850 | 2 | 1 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0019c0036 | 0/0 | 5850 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0020c0039 | 0/0 | 5850 | 2 | 0 | 0 | 1 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0021c0040 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0022c0059 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0023c0045 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0024c0094 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0025c0093 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0026c0092 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0027c0096 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0028c0062 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0029c0095 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0030c0051 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0031c0050 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0032c0048 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0033c0047 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0034c0046 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0035c0042 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0036c0041 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0037c0067 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0038c0071 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0039c0074 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0040c0072 | 0/0 | 5819 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0041c0075 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0042c0070 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0043c0069 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0044c0068 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0045c0090 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0046c0078 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0047c0077 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0048c0079 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0049c0081 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0050c0087 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0051c0086 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0052c0085 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0053c0083 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0054c0084 | 0/1 | 5850 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0055c0080 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0056c0091 | 0/0 | 5850 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8570 | 3 | 0 | 0 | 2 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0002 | 0/0 | 8570 | 19 | 0 | 6 | 11 | 0 | 2 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0004 | 0/0 | 8565 | 4 | 1 | 0 | 2 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0005 | 0/0 | 8557 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0006 | 0/0 | 8575 | 7 | 0 | 2 | 5 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0007 | 0/0 | 8575 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0011 | 0/0 | 8557 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0018 | 0/0 | 8555 | 2 | 0 | 2 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0030 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0032 | 0/0 | 8580 | 2 | 0 | 0 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0069 | 0/0 | 8569 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0072 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0001t0073 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0013t0002 | 0/0 | 8570 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0013t0006 | 0/0 | 8575 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0013t0011 | 0/0 | 8557 | 2 | 0 | 0 | 1 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0001c0089t0002 | 0/0 | 8570 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0005t0001 | 0/0 | 8570 | 7 | 0 | 0 | 6 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0005t0005 | 0/0 | 8557 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0005t0006 | 0/0 | 8575 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0005t0007 | 0/0 | 8575 | 4 | 0 | 0 | 4 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0005t0011 | 0/0 | 8557 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0005t0051 | 0/0 | 8580 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0007t0001 | 0/0 | 8570 | 2 | 1 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0007t0007 | 0/0 | 8575 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0007t0020 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0007t0037 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0007t0052 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0011t0001 | 0/0 | 8570 | 2 | 0 | 0 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0011t0002 | 0/0 | 8570 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0011t0005 | 0/0 | 8557 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0011t0009 | 0/0 | 8555 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0012t0023 | 0/0 | 8565 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0012t0024 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0012t0065 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0020t0026 | 0/0 | 8557 | 2 | 0 | 0 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0020t0067 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0034t0019 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0034t0031 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0053t0019 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0055t0044 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0057t0059 | 0/0 | 8555 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0002c0061t0062 | 0/0 | 8569 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0003t0001 | 0/0 | 8570 | 11 | 0 | 3 | 6 | 1 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0003t0002 | 0/0 | 8570 | 2 | 0 | 2 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0003t0005 | 0/0 | 8557 | 4 | 0 | 2 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0003t0006 | 0/0 | 8575 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0003t0007 | 0/0 | 8575 | 2 | 0 | 0 | 2 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0003t0022 | 0/0 | 8560 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0003t0030 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0003t0057 | 0/0 | 8575 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0009t0001 | 0/0 | 8570 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0009t0015 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0009t0021 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0009t0029 | 1/0 | 8555 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0038t0001 | 0/0 | 8570 | 2 | 0 | 2 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0003c0076t0007 | 0/0 | 8575 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0004t0002 | 0/0 | 8570 | 8 | 0 | 2 | 3 | 0 | 3 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0004t0004 | 0/0 | 8565 | 8 | 1 | 3 | 4 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0004t0008 | 0/0 | 8555 | 4 | 0 | 1 | 2 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0004t0011 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0004t0013 | 0/0 | 8559 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0004t0025 | 0/0 | 8555 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0025t0008 | 0/0 | 8555 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0026t0004 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0026t0013 | 0/0 | 8559 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0026t0016 | 0/0 | 8555 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0082t0002 | 0/0 | 8570 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0004c0088t0025 | 0/0 | 8555 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0001 | 0/0 | 8570 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0003 | 0/0 | 8565 | 12 | 1 | 0 | 10 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0009 | 0/0 | 8555 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0010 | 0/0 | 8559 | 5 | 1 | 2 | 0 | 2 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0013 | 0/0 | 8559 | 2 | 0 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0016 | 0/0 | 8555 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0048 | 0/0 | 8564 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0050 | 0/0 | 8559 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0055 | 0/0 | 8555 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0056 | 0/0 | 8555 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0002t0071 | 0/0 | 8560 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0066t0022 | 0/0 | 8560 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0005c0073t0016 | 0/0 | 8555 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0014t0003 | 0/0 | 8565 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0014t0005 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0027t0003 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0027t0004 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0027t0009 | 0/0 | 8555 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0033t0003 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0033t0034 | 0/0 | 8560 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0054t0043 | 0/0 | 8559 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0056t0070 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0063t0063 | 0/0 | 8559 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0064t0012 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0065t0033 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0097t0016 | 0/0 | 8555 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0006c0098t0068 | 0/0 | 8555 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0015t0021 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0015t0027 | 0/0 | 8565 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0016t0001 | 0/0 | 8570 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0016t0015 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0017t0001 | 0/0 | 8570 | 3 | 0 | 0 | 3 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0043t0035 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0044t0039 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0007c0058t0024 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0006t0005 | 0/0 | 8557 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0006t0009 | 0/0 | 8555 | 2 | 0 | 0 | 0 | 1 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0006t0012 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0006t0015 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0006t0017 | 0/0 | 8570 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0006t0019 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0006t0024 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0006t0054 | 0/0 | 8560 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0049t0015 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0008c0060t0061 | 0/0 | 8560 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0019t0012 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0019t0066 | 0/0 | 8555 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0019t0074 | 0/0 | 8555 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0028t0003 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0028t0020 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0029t0020 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0029t0041 | 0/0 | 8555 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0030t0003 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0009c0030t0016 | 0/0 | 8555 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0010c0031t0038 | 0/0 | 8560 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0010c0031t0046 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0010c0032t0028 | 0/0 | 8570 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0010c0035t0060 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0010c0035t0064 | 0/0 | 8575 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0011c0008t0003 | 0/0 | 8565 | 2 | 0 | 1 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0011c0008t0012 | 0/0 | 8565 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0011c0008t0045 | 0/0 | 8559 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0012c0010t0002 | 0/0 | 8570 | 4 | 0 | 4 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0012c0010t0006 | 0/0 | 8575 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0013c0018t0003 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0013c0018t0022 | 0/0 | 8560 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0013c0018t0047 | 0/0 | 8574 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0013c0052t0049 | 0/0 | 8564 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0014c0023t0014 | 0/0 | 8556 | 3 | 3 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0015c0022t0001 | 0/0 | 8570 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0015c0022t0010 | 0/0 | 8559 | 2 | 0 | 1 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0016c0021t0001 | 0/0 | 8570 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0016c0021t0017 | 0/0 | 8570 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0017c0024t0008 | 0/0 | 8555 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0017c0024t0013 | 0/0 | 8559 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0017c0024t0025 | 0/0 | 8555 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0018c0037t0003 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0018c0037t0053 | 0/0 | 8571 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0019c0036t0001 | 0/0 | 8570 | 2 | 2 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0020c0039t0004 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0020c0039t0009 | 0/0 | 8555 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0021c0040t0036 | 0/0 | 8555 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0022c0059t0023 | 0/0 | 8565 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0023c0045t0001 | 0/0 | 8570 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0024c0094t0001 | 0/0 | 8570 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0025c0093t0002 | 0/0 | 8570 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0026c0092t0018 | 0/0 | 8555 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0027c0096t0005 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0028c0062t0040 | 0/0 | 8560 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0029c0095t0003 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0030c0051t0042 | 0/0 | 8555 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0031c0050t0006 | 0/0 | 8575 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0032c0048t0014 | 0/0 | 8556 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0033c0047t0031 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0034c0046t0012 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0035c0042t0029 | 0/0 | 8555 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0036c0041t0003 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0037c0067t0021 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0038c0071t0009 | 0/0 | 8555 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0039c0074t0014 | 0/0 | 8556 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0040c0072t0058 | 0/0 | 8528 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0041c0075t0001 | 0/0 | 8570 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0042c0070t0015 | 0/0 | 8565 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0043c0069t0003 | 0/0 | 8565 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0044c0068t0009 | 0/0 | 8555 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0045c0090t0013 | 0/0 | 8559 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0046c0078t0011 | 0/0 | 8557 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0047c0077t0002 | 0/0 | 8570 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0048c0079t0004 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0049c0081t0002 | 0/0 | 8570 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0050c0087t0004 | 0/0 | 8565 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0051c0086t0008 | 0/0 | 8555 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0052c0085t0011 | 0/0 | 8557 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0053c0083t0008 | 0/0 | 8555 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0054c0084t0002 | 0/1 | 8570 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0055c0080t0018 | 0/0 | 8555 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| a0056c0091t0002 | 0/0 | 8570 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | copy fasta | chr2 | 11529045 | 11647788 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0011g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0018g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0018g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0030g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0032g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0032g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0069g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0072g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0001t0073g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0013t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0013t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0013t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0013t0011g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0001c0089t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0006g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0011g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0005t0051g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0007t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0007t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0007t0020g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0007t0037g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0007t0052g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0011t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0011t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0011t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0011t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0011t0009g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0012t0023g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0012t0023g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0012t0024g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0012t0065g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0020t0026g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0020t0026g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0020t0067g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0034t0019g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0034t0031g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0053t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0055t0044g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0057t0059g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0002c0061t0062g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0022g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0030g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0003t0057g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0009t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0009t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0009t0015g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0009t0021g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0009t0029g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0038t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0038t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0003c0076t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0008g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0008g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0011g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0013g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0004t0025g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0025t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0025t0008g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0025t0008g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0026t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0026t0013g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0026t0016g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0082t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0004c0088t0025g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0009g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0010g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0010g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0010g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0010g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0013g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0013g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0016g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0048g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0050g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0055g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0056g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0002t0071g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0066t0022g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0005c0073t0016g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0014t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0014t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0014t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0014t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0027t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0027t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0027t0009g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0033t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0033t0034g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0054t0043g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0056t0070g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0063t0063g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0064t0012g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0065t0033g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0097t0016g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0006c0098t0068g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0015t0021g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0015t0027g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0015t0027g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0016t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0016t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0016t0015g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0017t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0017t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0017t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0043t0035g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0044t0039g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0007c0058t0024g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0009g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0009g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0012g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0015g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0017g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0017g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0019g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0024g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0006t0054g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0049t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0008c0060t0061g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0009c0019t0012g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0009c0019t0066g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0009c0019t0074g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0009c0028t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0009c0028t0020g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0009c0029t0020g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0009c0029t0041g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0009c0030t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0009c0030t0016g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0010c0031t0038g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0010c0031t0046g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0010c0032t0028g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0010c0032t0028g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0010c0035t0060g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0010c0035t0064g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0011c0008t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0011c0008t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0011c0008t0012g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0011c0008t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0011c0008t0045g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0012c0010t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0012c0010t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0012c0010t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0012c0010t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0012c0010t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0013c0018t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0013c0018t0022g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0013c0018t0047g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0013c0052t0049g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0014c0023t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0014c0023t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0014c0023t0014g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0015c0022t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0015c0022t0010g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0015c0022t0010g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0016c0021t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0016c0021t0017g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0016c0021t0017g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0017c0024t0008g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0017c0024t0013g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0017c0024t0025g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0018c0037t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0018c0037t0053g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0019c0036t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0019c0036t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0020c0039t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0020c0039t0009g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0021c0040t0036g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0022c0059t0023g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0023c0045t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0024c0094t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0025c0093t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0026c0092t0018g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0027c0096t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0028c0062t0040g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0029c0095t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0030c0051t0042g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0031c0050t0006g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0032c0048t0014g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0033c0047t0031g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0034c0046t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0035c0042t0029g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0036c0041t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0037c0067t0021g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0038c0071t0009g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0039c0074t0014g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0040c0072t0058g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0041c0075t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0042c0070t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0043c0069t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0044c0068t0009g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0045c0090t0013g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0046c0078t0011g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0047c0077t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0048c0079t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0049c0081t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0050c0087t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0051c0086t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0052c0085t0011g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0053c0083t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0054c0084t0002g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0055c0080t0018g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| a0056c0091t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0005 | c0002 | t0010 | g0119 | EUR | GBR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00099 | hp2 | a0005 | c0002 | t0071 | g0185 | EUR | GBR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00140 | hp1 | a0008 | c0006 | t0009 | g0264 | EUR | GBR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00140 | hp2 | a0004 | c0004 | t0008 | g0246 | EUR | GBR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00408 | hp1 | a0004 | c0004 | t0004 | g0197 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00408 | hp2 | a0004 | c0004 | t0002 | g0196 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00423 | hp2 | a0009 | c0030 | t0003 | g0169 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00558 | hp1 | a0003 | c0003 | t0005 | g0158 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00558 | hp2 | a0005 | c0002 | t0003 | g0114 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00621 | hp1 | a0007 | c0017 | t0001 | g0170 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00621 | hp2 | a0002 | c0005 | t0001 | g0057 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00639 | hp1 | a0010 | c0035 | t0064 | g0128 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00639 | hp2 | a0016 | c0021 | t0001 | g0137 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00673 | hp1 | a0004 | c0025 | t0008 | g0277 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00673 | hp2 | a0002 | c0020 | t0067 | g0171 | EAS | CHS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00733 | hp1 | a0024 | c0094 | t0001 | g0048 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00733 | hp2 | a0005 | c0002 | t0010 | g0124 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00735 | hp1 | a0053 | c0083 | t0008 | g0256 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00735 | hp2 | a0012 | c0010 | t0002 | g0184 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00741 | hp1 | a0011 | c0008 | t0003 | g0297 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG00741 | hp2 | a0001 | c0001 | t0018 | g0235 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01070 | hp1 | a0003 | c0038 | t0001 | g0083 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01070 | hp2 | a0039 | c0074 | t0014 | g0301 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01071 | hp1 | a0005 | c0002 | t0010 | g0123 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01071 | hp2 | a0003 | c0038 | t0001 | g0088 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01074 | hp1 | a0003 | c0003 | t0002 | g0225 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01081 | hp1 | a0001 | c0089 | t0002 | g0189 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01081 | hp2 | a0005 | c0002 | t0013 | g0188 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01099 | hp1 | a0017 | c0024 | t0025 | g0233 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01099 | hp2 | a0001 | c0001 | t0018 | g0258 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01106 | hp1 | a0012 | c0010 | t0006 | g0227 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01106 | hp2 | a0012 | c0010 | t0002 | g0224 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01109 | hp1 | a0006 | c0054 | t0043 | g0002 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01109 | hp2 | a0008 | c0006 | t0054 | g0018 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0257 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0148 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01168 | hp2 | a0004 | c0004 | t0004 | g0239 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01169 | hp1 | a0004 | c0004 | t0004 | g0242 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01175 | hp1 | a0040 | c0072 | t0058 | g0111 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01175 | hp2 | a0022 | c0059 | t0023 | g0110 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01192 | hp1 | a0038 | c0071 | t0009 | g0122 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01192 | hp2 | a0008 | c0006 | t0005 | g0121 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01243 | hp1 | a0004 | c0004 | t0002 | g0202 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01243 | hp2 | a0004 | c0004 | t0002 | g0295 | AMR | PUR | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01256 | hp1 | a0056 | c0091 | t0002 | g0209 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0147 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01257 | hp1 | a0015 | c0022 | t0010 | g0140 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01257 | hp2 | a0004 | c0004 | t0004 | g0244 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01261 | hp1 | a0018 | c0037 | t0053 | g0067 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01261 | hp2 | a0004 | c0004 | t0008 | g0173 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01361 | hp1 | a0002 | c0011 | t0009 | g0043 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01361 | hp2 | a0017 | c0024 | t0008 | g0234 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01433 | hp1 | a0004 | c0088 | t0025 | g0223 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01433 | hp2 | a0017 | c0024 | t0013 | g0228 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01496 | hp1 | a0003 | c0003 | t0005 | g0270 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01496 | hp2 | a0005 | c0002 | t0050 | g0084 | AMR | CLM | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01516 | hp1 | a0003 | c0003 | t0022 | g0120 | EUR | IBS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01516 | hp2 | a0004 | c0004 | t0025 | g0248 | EUR | IBS | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01884 | hp1 | a0010 | c0031 | t0046 | g0096 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01884 | hp2 | a0009 | c0030 | t0016 | g0077 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01981 | hp1 | a0004 | c0004 | t0013 | g0296 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01993 | hp1 | a0003 | c0003 | t0001 | g0141 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02004 | hp1 | a0012 | c0010 | t0002 | g0190 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02004 | hp2 | a0002 | c0011 | t0005 | g0135 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02040 | hp1 | a0002 | c0007 | t0007 | g0150 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02040 | hp2 | a0001 | c0013 | t0006 | g0181 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02056 | hp1 | a0002 | c0005 | t0007 | g0049 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0217 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02071 | hp1 | a0005 | c0002 | t0003 | g0117 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02080 | hp1 | a0005 | c0002 | t0056 | g0129 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0037 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02083 | hp1 | a0004 | c0004 | t0008 | g0273 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0138 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02135 | hp1 | a0001 | c0001 | t0072 | g0254 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02135 | hp2 | a0005 | c0002 | t0003 | g0152 | EAS | KHV | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02145 | hp1 | a0002 | c0034 | t0019 | g0026 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02145 | hp2 | a0013 | c0018 | t0003 | g0019 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02148 | hp1 | a0012 | c0010 | t0002 | g0226 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02148 | hp2 | a0003 | c0003 | t0005 | g0130 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02258 | hp1 | a0005 | c0066 | t0022 | g0072 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02258 | hp2 | a0005 | c0002 | t0048 | g0269 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02273 | hp2 | a0005 | c0002 | t0001 | g0142 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02280 | hp1 | a0002 | c0007 | t0052 | g0075 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02280 | hp2 | a0005 | c0002 | t0010 | g0101 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0294 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0212 | AMR | PEL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02451 | hp1 | a0010 | c0035 | t0060 | g0126 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02451 | hp2 | a0010 | c0031 | t0038 | g0029 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02572 | hp1 | a0006 | c0033 | t0003 | g0266 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02572 | hp2 | a0037 | c0067 | t0021 | g0070 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02602 | hp1 | a0004 | c0004 | t0002 | g0237 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02602 | hp2 | a0001 | c0013 | t0002 | g0194 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02615 | hp1 | a0009 | c0028 | t0003 | g0260 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02615 | hp2 | a0006 | c0064 | t0012 | g0078 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02622 | hp1 | a0007 | c0016 | t0001 | g0013 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02622 | hp2 | a0008 | c0049 | t0015 | g0006 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02630 | hp1 | a0007 | c0043 | t0035 | g0095 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02630 | hp2 | a0013 | c0052 | t0049 | g0261 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02647 | hp1 | a0008 | c0006 | t0017 | g0259 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02647 | hp2 | a0008 | c0006 | t0015 | g0005 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02698 | hp1 | a0005 | c0002 | t0013 | g0187 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02723 | hp1 | a0008 | c0006 | t0012 | g0112 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02723 | hp2 | a0008 | c0006 | t0019 | g0076 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02735 | hp1 | a0002 | c0011 | t0002 | g0275 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02735 | hp2 | a0015 | c0022 | t0010 | g0132 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02738 | hp1 | a0055 | c0080 | t0018 | g0236 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02738 | hp2 | a0008 | c0006 | t0009 | g0265 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02809 | hp1 | a0002 | c0007 | t0001 | g0104 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02809 | hp2 | a0021 | c0040 | t0036 | g0089 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02818 | hp1 | a0002 | c0012 | t0065 | g0103 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02818 | hp2 | a0009 | c0028 | t0020 | g0304 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02895 | hp1 | a0002 | c0012 | t0024 | g0127 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02895 | hp2 | a0010 | c0032 | t0028 | g0007 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02896 | hp1 | a0011 | c0008 | t0012 | g0094 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02896 | hp2 | a0003 | c0009 | t0015 | g0105 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02897 | hp1 | a0011 | c0008 | t0012 | g0093 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02897 | hp2 | a0010 | c0032 | t0028 | g0009 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02922 | hp1 | a0030 | c0051 | t0042 | g0306 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02922 | hp2 | a0014 | c0023 | t0014 | g0073 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02965 | hp1 | a0019 | c0036 | t0001 | g0300 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02965 | hp2 | a0007 | c0044 | t0039 | g0011 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02976 | hp1 | a0003 | c0009 | t0001 | g0144 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02976 | hp2 | a0008 | c0006 | t0024 | g0143 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03017 | hp1 | a0009 | c0019 | t0012 | g0161 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03017 | hp2 | a0052 | c0085 | t0011 | g0280 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03041 | hp1 | a0033 | c0047 | t0031 | g0107 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03041 | hp2 | a0002 | c0007 | t0037 | g0023 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03098 | hp1 | a0034 | c0046 | t0012 | g0097 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03098 | hp2 | a0007 | c0015 | t0027 | g0024 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03130 | hp1 | a0009 | c0029 | t0020 | g0016 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03130 | hp2 | a0006 | c0033 | t0034 | g0302 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03139 | hp1 | a0003 | c0009 | t0001 | g0109 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03139 | hp2 | a0005 | c0002 | t0055 | g0014 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03195 | hp1 | a0019 | c0036 | t0001 | g0299 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03195 | hp2 | a0036 | c0041 | t0003 | g0091 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03209 | hp1 | a0006 | c0063 | t0063 | g0106 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03209 | hp2 | a0013 | c0018 | t0022 | g0030 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03239 | hp1 | a0004 | c0026 | t0013 | g0204 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03239 | hp2 | a0044 | c0068 | t0009 | g0080 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03453 | hp1 | a0007 | c0058 | t0024 | g0125 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03453 | hp2 | a0032 | c0048 | t0014 | g0008 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03486 | hp1 | a0028 | c0062 | t0040 | g0025 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03486 | hp2 | a0002 | c0055 | t0044 | g0003 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03516 | hp1 | a0002 | c0007 | t0020 | g0307 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03516 | hp2 | a0014 | c0023 | t0014 | g0071 | AFR | ESN | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03540 | hp1 | a0007 | c0016 | t0015 | g0017 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03540 | hp2 | a0002 | c0034 | t0031 | g0263 | AFR | GWD | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03579 | hp1 | a0003 | c0009 | t0021 | g0308 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03579 | hp2 | a0042 | c0070 | t0015 | g0010 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03654 | hp1 | a0001 | c0001 | t0011 | g0205 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03654 | hp2 | a0031 | c0050 | t0006 | g0238 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03669 | hp1 | a0045 | c0090 | t0013 | g0243 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03669 | hp2 | a0025 | c0093 | t0002 | g0178 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03710 | hp1 | a0001 | c0013 | t0011 | g0218 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03710 | hp2 | a0006 | c0098 | t0068 | g0052 | SAS | PJL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03831 | hp1 | a0041 | c0075 | t0001 | g0153 | SAS | BEB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03831 | hp2 | a0009 | c0019 | t0074 | g0284 | SAS | BEB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03927 | hp1 | a0020 | c0039 | t0004 | g0283 | SAS | BEB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03927 | hp2 | a0026 | c0092 | t0018 | g0249 | SAS | BEB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0267 | SAS | STU | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0186 | SAS | STU | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04184 | hp1 | a0043 | c0069 | t0003 | g0154 | SAS | BEB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04199 | hp1 | a0002 | c0005 | t0011 | g0250 | SAS | STU | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04199 | hp2 | a0002 | c0005 | t0001 | g0034 | SAS | STU | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04204 | hp1 | a0006 | c0027 | t0004 | g0177 | SAS | STU | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04204 | hp2 | a0004 | c0026 | t0016 | g0041 | SAS | STU | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | STU | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG04228 | hp2 | a0004 | c0004 | t0002 | g0281 | SAS | STU | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18522 | hp1 | a0009 | c0019 | t0066 | g0108 | AFR | YRI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18522 | hp2 | a0007 | c0015 | t0027 | g0004 | AFR | YRI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18612 | hp1 | a0001 | c0001 | t0007 | g0062 | EAS | CHB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18612 | hp2 | a0050 | c0087 | t0004 | g0172 | EAS | CHB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18906 | hp1 | a0018 | c0037 | t0003 | g0298 | AFR | YRI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18906 | hp2 | a0002 | c0061 | t0062 | g0134 | AFR | YRI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18939 | hp1 | a0049 | c0081 | t0002 | g0199 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0278 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18940 | hp1 | a0005 | c0002 | t0009 | g0079 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18940 | hp2 | a0002 | c0005 | t0005 | g0063 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18941 | hp1 | a0005 | c0002 | t0003 | g0098 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18941 | hp2 | a0004 | c0004 | t0008 | g0292 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18942 | hp1 | a0047 | c0077 | t0002 | g0174 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18942 | hp2 | a0005 | c0073 | t0016 | g0162 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18945 | hp1 | a0004 | c0025 | t0008 | g0279 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18945 | hp2 | a0002 | c0005 | t0001 | g0035 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18950 | hp1 | a0005 | c0002 | t0003 | g0151 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18950 | hp2 | a0002 | c0005 | t0001 | g0036 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18952 | hp1 | a0004 | c0004 | t0002 | g0215 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0145 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18953 | hp1 | a0002 | c0020 | t0026 | g0219 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18953 | hp2 | a0001 | c0001 | t0069 | g0288 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18956 | hp1 | a0001 | c0001 | t0032 | g0251 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18956 | hp2 | a0006 | c0014 | t0003 | g0060 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18959 | hp1 | a0003 | c0003 | t0057 | g0059 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18959 | hp2 | a0004 | c0004 | t0002 | g0183 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18960 | hp1 | a0003 | c0003 | t0001 | g0115 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18961 | hp1 | a0001 | c0001 | t0032 | g0201 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18961 | hp2 | a0003 | c0003 | t0030 | g0056 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18962 | hp2 | a0002 | c0020 | t0026 | g0221 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18966 | hp1 | a0005 | c0002 | t0003 | g0001 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18966 | hp2 | a0002 | c0005 | t0001 | g0066 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18970 | hp1 | a0001 | c0001 | t0030 | g0087 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0214 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18973 | hp2 | a0003 | c0003 | t0006 | g0191 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18975 | hp1 | a0005 | c0002 | t0003 | g0116 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18977 | hp1 | a0006 | c0014 | t0003 | g0054 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18979 | hp1 | a0002 | c0005 | t0005 | g0046 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18979 | hp2 | a0006 | c0056 | t0070 | g0179 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18981 | hp1 | a0001 | c0001 | t0073 | g0253 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18981 | hp2 | a0002 | c0005 | t0001 | g0033 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18982 | hp2 | a0006 | c0027 | t0003 | g0272 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18984 | hp1 | a0004 | c0004 | t0004 | g0195 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18984 | hp2 | a0002 | c0005 | t0005 | g0065 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18986 | hp1 | a0005 | c0002 | t0003 | g0156 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18987 | hp1 | a0006 | c0027 | t0009 | g0053 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18988 | hp1 | a0004 | c0025 | t0008 | g0285 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18988 | hp2 | a0002 | c0011 | t0001 | g0271 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18989 | hp2 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18995 | hp1 | a0004 | c0026 | t0004 | g0290 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0255 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA18998 | hp2 | a0029 | c0095 | t0003 | g0038 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19000 | hp1 | a0002 | c0007 | t0001 | g0262 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19000 | hp2 | a0046 | c0078 | t0011 | g0176 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19002 | hp2 | a0003 | c0003 | t0005 | g0113 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19003 | hp1 | a0003 | c0076 | t0007 | g0102 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19003 | hp2 | a0005 | c0002 | t0016 | g0164 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19004 | hp1 | a0007 | c0017 | t0001 | g0167 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19004 | hp2 | a0005 | c0002 | t0003 | g0118 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19010 | hp1 | a0002 | c0005 | t0007 | g0061 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19010 | hp2 | a0003 | c0003 | t0007 | g0163 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19011 | hp1 | a0005 | c0002 | t0003 | g0082 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19011 | hp2 | a0002 | c0011 | t0001 | g0040 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19012 | hp1 | a0001 | c0013 | t0011 | g0200 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19012 | hp2 | a0003 | c0003 | t0007 | g0159 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19030 | hp1 | a0014 | c0023 | t0014 | g0068 | AFR | LWK | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19030 | hp2 | a0007 | c0015 | t0021 | g0069 | AFR | LWK | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19043 | hp1 | a0011 | c0008 | t0045 | g0022 | AFR | LWK | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19043 | hp2 | a0002 | c0053 | t0019 | g0090 | AFR | LWK | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19056 | hp1 | a0007 | c0017 | t0001 | g0157 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19056 | hp2 | a0027 | c0096 | t0005 | g0074 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19057 | hp1 | a0023 | c0045 | t0001 | g0165 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19057 | hp2 | a0004 | c0082 | t0002 | g0216 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19060 | hp1 | a0004 | c0004 | t0004 | g0289 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19063 | hp1 | a0020 | c0039 | t0009 | g0050 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19063 | hp2 | a0006 | c0014 | t0003 | g0051 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19065 | hp1 | a0006 | c0014 | t0005 | g0039 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0136 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19067 | hp1 | a0002 | c0005 | t0007 | g0064 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19070 | hp1 | a0002 | c0005 | t0001 | g0045 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19070 | hp2 | a0006 | c0065 | t0033 | g0220 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19085 | hp1 | a0048 | c0079 | t0004 | g0213 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19086 | hp1 | a0006 | c0097 | t0016 | g0058 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19088 | hp1 | a0004 | c0004 | t0011 | g0211 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19088 | hp2 | a0002 | c0005 | t0051 | g0055 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19091 | hp1 | a0004 | c0004 | t0004 | g0198 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19091 | hp2 | a0002 | c0005 | t0007 | g0031 | EAS | JPT | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19240 | hp1 | a0008 | c0006 | t0017 | g0015 | AFR | YRI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA19240 | hp2 | a0035 | c0042 | t0029 | g0020 | AFR | YRI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20129 | hp1 | a0002 | c0012 | t0023 | g0085 | AFR | ASW | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20129 | hp2 | a0005 | c0002 | t0003 | g0133 | AFR | ASW | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20752 | hp1 | a0005 | c0002 | t0003 | g0139 | EUR | TSI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0268 | EUR | TSI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20805 | hp1 | a0005 | c0002 | t0010 | g0100 | EUR | TSI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20805 | hp2 | a0011 | c0008 | t0003 | g0027 | EUR | TSI | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20905 | hp1 | a0002 | c0005 | t0006 | g0293 | SAS | GIH | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20905 | hp2 | a0004 | c0004 | t0002 | g0230 | SAS | GIH | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02486 | hp1 | a0002 | c0057 | t0059 | g0021 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02486 | hp2 | a0009 | c0029 | t0041 | g0028 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02559 | hp1 | a0008 | c0060 | t0061 | g0305 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG02559 | hp2 | a0002 | c0012 | t0023 | g0086 | AFR | ACB | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03471 | hp1 | a0007 | c0016 | t0001 | g0012 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG03471 | hp2 | a0016 | c0021 | t0017 | g0092 | AFR | MSL | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG06807 | hp1 | a0015 | c0022 | t0001 | g0081 | AFR | USA | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| HG06807 | hp2 | a0013 | c0018 | t0047 | g0303 | AFR | USA | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | USA | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA20300 | hp2 | a0016 | c0021 | t0017 | g0099 | AFR | USA | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA21309 | hp1 | a0004 | c0004 | t0004 | g0240 | AFR | LWK | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| NA21309 | hp2 | a0051 | c0086 | t0008 | g0245 | AFR | LWK | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| homoSapiens_chm13v2 | hp1 | a0054 | c0084 | t0002 | g0208 | REF | REF | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| homoSapiens_grch38 | hp1 | a0003 | c0009 | t0029 | g0149 | REF | REF | GREB1_chr2_11529045_11647788 | GREB1 | chr2 | 11529045 | 11647788 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:11562500
|
G | C | 1 | a0021 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.195G>C | p.Glu65Asp | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/33 | 566/8555 | 195/5850 | 65/1949 | chr2 | 11562500 | ||
| chr2:11562535
|
A | C | 17 | a0001a0004a0012others(14): Show | 106 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
missense_variant | MODERATE | c.230A>C | p.Asn77Thr | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/33 | 601/8555 | 230/5850 | 77/1949 | chr2 | 11562535 | ||
| chr2:11566546
|
C | T | 1 | a0056 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.344C>T | p.Ala115Val | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/33 | 715/8555 | 344/5850 | 115/1949 | chr2 | 11566546 | ||
| chr2:11566567
|
T | C | 25 | a0002a0006a0007others(22): Show | 123 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(120): Show |
missense_variant | MODERATE | c.365T>C | p.Val122Ala | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/33 | 736/8555 | 365/5850 | 122/1949 | chr2 | 11566567 | ||
| chr2:11566585
|
C | T | 1 | a0045 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.383C>T | p.Pro128Leu | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/33 | 754/8555 | 383/5850 | 128/1949 | chr2 | 11566585 | ||
| chr2:11578373
|
C | A | 1 | a0036 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.714C>A | p.Phe238Leu | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/33 | 1085/8555 | 714/5850 | 238/1949 | chr2 | 11578373 | ||
| chr2:11580760
|
G | A | 2 | a0019a0035 | 3 | HG02965.hp1 HG03195.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.829G>A | p.Gly277Ser | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/33 | 1200/8555 | 829/5850 | 277/1949 | chr2 | 11580760 | ||
| chr2:11585782
|
G | A | 11 | a0007a0009a0018others(8): Show | 32 | HG00423.hp2 HG00621.hp1 HG01175.hp2 others(29): Show |
missense_variant | MODERATE | c.1036G>A | p.Val346Met | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/33 | 1407/8555 | 1036/5850 | 346/1949 | chr2 | 11585782 | ||
| chr2:11585821
|
T | C | 13 | a0008a0011a0015others(10): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
missense_variant | MODERATE | c.1075T>C | p.Phe359Leu | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/33 | 1446/8555 | 1075/5850 | 359/1949 | chr2 | 11585821 | ||
| chr2:11592826
|
T | C | 1 | a0049 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.1396T>C | p.Ser466Pro | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/33 | 1767/8555 | 1396/5850 | 466/1949 | chr2 | 11592826 | ||
| chr2:11596179
|
G | A | 27 | a0007a0008a0009others(24): Show | 77 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(74): Show |
missense_variant | MODERATE | c.1894G>A | p.Ala632Thr | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/33 | 2265/8555 | 1894/5850 | 632/1949 | chr2 | 11596179 | ||
| chr2:11600835
|
C | T | 1 | a0012 | 5 | HG00735.hp2 HG01106.hp1 HG01106.hp2 others(2): Show |
missense_variant | MODERATE | c.2369C>T | p.Pro790Leu | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/33 | 2740/8555 | 2369/5850 | 790/1949 | chr2 | 11600835 | ||
| chr2:11610939
|
G | A | 2 | a0046a0047 | 2 | NA18942.hp1 NA19000.hp2 |
missense_variant | MODERATE | c.2918G>A | p.Arg973Gln | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/33 | 3289/8555 | 2918/5850 | 973/1949 | chr2 | 11610939 | ||
| chr2:11616660
|
A | G | 1 | a0050 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.3352A>G | p.Lys1118Glu | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/33 | 3723/8555 | 3352/5850 | 1118/1949 | chr2 | 11616660 | ||
| chr2:11618303
|
G | A | 2 | a0024a0038 | 2 | HG00733.hp1 HG01192.hp1 |
missense_variant | MODERATE | c.3428G>A | p.Gly1143Asp | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 3799/8555 | 3428/5850 | 1143/1949 | chr2 | 11618303 | ||
| chr2:11618305
|
G | A | 4 | a0016a0033a0034others(1): Show | 6 | HG00639.hp2 HG03041.hp1 HG03098.hp1 others(3): Show |
missense_variant | MODERATE | c.3430G>A | p.Glu1144Lys | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 3801/8555 | 3430/5850 | 1144/1949 | chr2 | 11618305 | ||
| chr2:11618333
|
C | T | 1 | a0039 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.3458C>T | p.Pro1153Leu | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 3829/8555 | 3458/5850 | 1153/1949 | chr2 | 11618333 | ||
| chr2:11618365
|
C | T | 5 | a0014a0022a0030others(2): Show | 7 | HG01070.hp2 HG01175.hp2 HG02922.hp1 others(4): Show |
missense_variant | MODERATE | c.3490C>T | p.Arg1164Cys | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 3861/8555 | 3490/5850 | 1164/1949 | chr2 | 11618365 | ||
| chr2:11618386
|
A | G | 1 | a0052 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.3511A>G | p.Arg1171Gly | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 3882/8555 | 3511/5850 | 1171/1949 | chr2 | 11618386 | ||
| chr2:11618390
|
C | G | 2 | a0041a0054 | 2 | HG03831.hp1 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.3515C>G | p.Ala1172Gly | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 3886/8555 | 3515/5850 | 1172/1949 | chr2 | 11618390 | ||
| chr2:11618410
|
C | A | 1 | a0053 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.3535C>A | p.Pro1179Thr | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 3906/8555 | 3535/5850 | 1179/1949 | chr2 | 11618410 | ||
| chr2:11618552
|
C | T | 1 | a0025 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3677C>T | p.Ser1226Leu | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 4048/8555 | 3677/5850 | 1226/1949 | chr2 | 11618552 | ||
| chr2:11618605
|
G | A | 1 | a0029 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.3730G>A | p.Ala1244Thr | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 4101/8555 | 3730/5850 | 1244/1949 | chr2 | 11618605 | ||
| chr2:11627097
|
G | A | 1 | a0026 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.4442G>A | p.Arg1481His | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/33 | 4813/8555 | 4442/5850 | 1481/1949 | chr2 | 11627097 | ||
| chr2:11632014
|
G | A | 1 | a0027 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.4717G>A | p.Val1573Met | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/33 | 5088/8555 | 4717/5850 | 1573/1949 | chr2 | 11632014 | ||
| chr2:11633029
|
G | A | 1 | a0028 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.4957G>A | p.Val1653Met | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/33 | 5328/8555 | 4957/5850 | 1653/1949 | chr2 | 11633029 | ||
| chr2:11634198
|
G | A | 26 | a0004a0005a0006others(23): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(118): Show |
missense_variant | MODERATE | c.5059G>A | p.Asp1687Asn | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/33 | 5430/8555 | 5059/5850 | 1687/1949 | chr2 | 11634198 | ||
| chr2:11634250
|
G | A | 1 | a0037 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.5111G>A | p.Arg1704Gln | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/33 | 5482/8555 | 5111/5850 | 1704/1949 | chr2 | 11634250 | ||
| chr2:11634265
|
A | G | 3 | a0014a0032a0039 | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
missense_variant | MODERATE | c.5126A>G | p.Gln1709Arg | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/33 | 5497/8555 | 5126/5850 | 1709/1949 | chr2 | 11634265 | ||
| chr2:11638660
|
TTCTTTTT others(34): Show |
T | 1 | a0040 | 1 | HG01175.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.5548-10_5578delTCT others(38): Show |
p.Ile1850fs | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/33 | 5548/5850 | 1850/1949 | chr2 | 11638660 | |||
| chr2:11640319
|
C | A | 1 | a0040 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.5715C>A | p.Asp1905Glu | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 6086/8555 | 5715/5850 | 1905/1949 | chr2 | 11640319 | ||
| chr2:11640438
|
C | T | 1 | a0023 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.5834C>T | p.Thr1945Met | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 6205/8555 | 5834/5850 | 1945/1949 | chr2 | 11640438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:11556680
|
C | T | 11 | a0002c0005a0002c0011a0006c0014others(8): Show | 36 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(33): Show |
synonymous_variant | LOW | c.66C>T | p.Ile22Ile | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/33 | 437/8555 | 66/5850 | 22/1949 | chr2 | 11556680 | ||
| chr2:11566604
|
C | T | 13 | a0002c0012a0002c0020a0002c0057others(10): Show | 21 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(18): Show |
synonymous_variant | LOW | c.402C>T | p.Cys134Cys | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/33 | 773/8555 | 402/5850 | 134/1949 | chr2 | 11566604 | ||
| chr2:11580774
|
G | A | 2 | a0002c0057a0005c0066 | 2 | HG02258.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.843G>A | p.Pro281Pro | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/33 | 1214/8555 | 843/5850 | 281/1949 | chr2 | 11580774 | ||
| chr2:11593008
|
C | G | 16 | a0001c0013a0002c0005a0002c0020others(13): Show | 43 | HG00621.hp2 HG00673.hp2 HG00733.hp1 others(40): Show |
synonymous_variant | LOW | c.1578C>G | p.Ala526Ala | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/33 | 1949/8555 | 1578/5850 | 526/1949 | chr2 | 11593008 | ||
| chr2:11597965
|
T | C | 79 | a0001c0001a0001c0013a0001c0089others(76): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
synonymous_variant | LOW | c.2139T>C | p.His713His | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 14/33 | 2510/8555 | 2139/5850 | 713/1949 | chr2 | 11597965 | ||
| chr2:11598825
|
C | T | 3 | a0001c0089a0003c0038a0004c0088 | 4 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(1): Show |
synonymous_variant | LOW | c.2298C>T | p.Val766Val | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/33 | 2669/8555 | 2298/5850 | 766/1949 | chr2 | 11598825 | ||
| chr2:11610706
|
C | T | 2 | a0001c0089a0041c0075 | 2 | HG01081.hp1 HG03831.hp1 |
synonymous_variant | LOW | c.2685C>T | p.Ser895Ser | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/33 | 3056/8555 | 2685/5850 | 895/1949 | chr2 | 11610706 | ||
| chr2:11610793
|
G | A | 1 | a0013c0052 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.2772G>A | p.Thr924Thr | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/33 | 3143/8555 | 2772/5850 | 924/1949 | chr2 | 11610793 | ||
| chr2:11610853
|
C | T | 3 | a0002c0055a0006c0054a0006c0064 | 3 | HG01109.hp1 HG02615.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.2832C>T | p.Cys944Cys | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/33 | 3203/8555 | 2832/5850 | 944/1949 | chr2 | 11610853 | ||
| chr2:11610892
|
G | A | 1 | a0004c0082 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.2871G>A | p.Ser957Ser | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/33 | 3242/8555 | 2871/5850 | 957/1949 | chr2 | 11610892 | ||
| chr2:11612509
|
T | C | 91 | a0001c0001a0001c0013a0001c0089others(88): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
synonymous_variant | LOW | c.3021T>C | p.Ile1007Ile | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/33 | 3392/8555 | 3021/5850 | 1007/1949 | chr2 | 11612509 | ||
| chr2:11615190
|
C | T | 9 | a0002c0012a0002c0034a0005c0066others(6): Show | 17 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(14): Show |
synonymous_variant | LOW | c.3222C>T | p.Asn1074Asn | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/33 | 3593/8555 | 3222/5850 | 1074/1949 | chr2 | 11615190 | ||
| chr2:11618475
|
C | T | 1 | a0006c0098 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.3600C>T | p.Pro1200Pro | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 3971/8555 | 3600/5850 | 1200/1949 | chr2 | 11618475 | ||
| chr2:11618577
|
G | A | 3 | a0002c0053a0002c0061a0006c0064 | 3 | HG02615.hp2 NA18906.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.3702G>A | p.Ala1234Ala | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 4073/8555 | 3702/5850 | 1234/1949 | chr2 | 11618577 | ||
| chr2:11618763
|
C | T | 1 | a0052c0085 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.3888C>T | p.Arg1296Arg | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/33 | 4259/8555 | 3888/5850 | 1296/1949 | chr2 | 11618763 | ||
| chr2:11633016
|
C | T | 1 | a0037c0067 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.4944C>T | p.Cys1648Cys | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/33 | 5315/8555 | 4944/5850 | 1648/1949 | chr2 | 11633016 | ||
| chr2:11634257
|
C | T | 3 | a0004c0025a0005c0073a0006c0097 | 5 | HG00673.hp1 NA18942.hp2 NA18945.hp1 others(2): Show |
synonymous_variant | LOW | c.5118C>T | p.Ser1706Ser | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/33 | 5489/8555 | 5118/5850 | 1706/1949 | chr2 | 11634257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:11534155
|
G | A | 2 | a0002c0020t0026a0006c0065t0033 | 3 | NA18953.hp1 NA18962.hp2 NA19070.hp2 |
5_prime_UTR_variant | MODIFIER | c.-261G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/33 | 22460 | chr2 | 11534155 | |||||
| chr2:11534169
|
A | C | 57 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(54): Show | 112 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(109): Show |
5_prime_UTR_variant | MODIFIER | c.-247A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/33 | 22446 | chr2 | 11534169 | |||||
| chr2:11534226
|
A | G | 1 | a0006c0098t0068 | 1 | HG03710.hp2 | 5_prime_UTR_variant | MODIFIER | c.-190A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/33 | 22389 | chr2 | 11534226 | |||||
| chr2:11556499
|
G | A | 5 | a0002c0007t0037a0006c0033t0034a0007c0015t0027others(2): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-116G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/33 | 116 | chr2 | 11556499 | |||||
| chr2:11556511
|
G | A | 11 | a0002c0007t0020a0002c0034t0019a0002c0053t0019others(8): Show | 11 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-104G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/33 | 104 | chr2 | 11556511 | |||||
| chr2:11556548
|
C | T | 24 | a0002c0012t0023a0002c0012t0024a0002c0012t0065others(21): Show | 27 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-67C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/33 | 67 | chr2 | 11556548 | |||||
| chr2:11556610
|
T | G | 2 | a0002c0055t0044a0006c0054t0043 | 2 | HG01109.hp1 HG03486.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-5T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/33 | chr2 | 11556610 | ||||||
| chr2:11640468
|
G | T | 1 | a0040c0072t0058 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*14G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 14 | chr2 | 11640468 | |||||
| chr2:11640550
|
G | A | 3 | a0014c0023t0014a0032c0048t0014a0039c0074t0014 | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*96G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 96 | chr2 | 11640550 | |||||
| chr2:11640609
|
C | T | 1 | a0003c0003t0057 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*155C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 155 | chr2 | 11640609 | |||||
| chr2:11640637
|
G | A | 1 | a0006c0033t0034 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 183 | chr2 | 11640637 | |||||
| chr2:11640749
|
T | C | 2 | a0002c0057t0059a0011c0008t0045 | 2 | HG02486.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*295T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 295 | chr2 | 11640749 | |||||
| chr2:11640865
|
T | C | 2 | a0010c0031t0046a0010c0035t0060 | 2 | HG01884.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*411T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 411 | chr2 | 11640865 | |||||
| chr2:11640949
|
T | C | 2 | a0002c0057t0059a0011c0008t0045 | 2 | HG02486.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*495T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 495 | chr2 | 11640949 | |||||
| chr2:11640969
|
A | G | 6 | a0002c0007t0037a0002c0012t0024a0007c0058t0024others(3): Show | 8 | HG02647.hp1 HG02895.hp1 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*515A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 515 | chr2 | 11640969 | |||||
| chr2:11641134
|
G | A | 2 | a0008c0060t0061a0010c0031t0038 | 2 | HG02451.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*680G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 680 | chr2 | 11641134 | |||||
| chr2:11641135
|
GT | G | 16 | a0002c0061t0062a0004c0004t0013a0004c0026t0013others(13): Show | 22 | HG00099.hp1 HG00733.hp2 HG01071.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*687delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 687 | INFO_REALIGN_3_PRIME | chr2 | 11641135 | ||||
| chr2:11641142
|
G | T | 20 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(17): Show | 29 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*688G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 688 | chr2 | 11641142 | |||||
| chr2:11641143
|
G | A | 1 | a0002c0057t0059 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*689G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 689 | chr2 | 11641143 | |||||
| chr2:11641153
|
T | TGG | 19 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(16): Show | 28 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*700_*701dupGG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 702 | INFO_REALIGN_3_PRIME | chr2 | 11641153 | ||||
| chr2:11641156
|
C | G | 19 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(16): Show | 28 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*702C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 702 | chr2 | 11641156 | |||||
| chr2:11641198
|
C | G | 1 | a0001c0001t0073 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*744C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 744 | chr2 | 11641198 | |||||
| chr2:11641324
|
G | C | 19 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(16): Show | 28 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*870G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 870 | chr2 | 11641324 | |||||
| chr2:11641467
|
G | GGTTTT | 21 | a0003c0003t0022a0004c0004t0013a0004c0026t0013others(18): Show | 27 | HG00099.hp1 HG00099.hp2 HG00733.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1044_*1048dupGTTT others(1): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1049 | INFO_REALIGN_3_PRIME | chr2 | 11641467 | ||||
| chr2:11641467
|
G | GGTTTTGT others(3): Show |
45 | a0001c0001t0004a0002c0007t0020a0002c0012t0023others(42): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1039_*1048dupGTTT others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1049 | INFO_REALIGN_3_PRIME | chr2 | 11641467 | ||||
| chr2:11641467
|
G | GGTTTTGT others(8): Show |
48 | a0001c0001t0001a0001c0001t0002a0001c0001t0069others(45): Show | 106 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*1034_*1048dupGTTT others(11): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1049 | INFO_REALIGN_3_PRIME | chr2 | 11641467 | ||||
| chr2:11641467
|
G | GGTTTTGT others(13): Show |
14 | a0001c0001t0006a0001c0001t0007a0001c0013t0006others(11): Show | 26 | HG00639.hp1 HG01106.hp1 HG02040.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1029_*1048dupGTTT others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1049 | INFO_REALIGN_3_PRIME | chr2 | 11641467 | ||||
| chr2:11641467
|
G | GGTTTTGT others(18): Show |
2 | a0001c0001t0032a0002c0005t0051 | 3 | NA18956.hp1 NA18961.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1024_*1048dupGTTT others(21): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1049 | INFO_REALIGN_3_PRIME | chr2 | 11641467 | ||||
| chr2:11641468
|
G | T | 19 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(16): Show | 28 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1014G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1014 | chr2 | 11641468 | |||||
| chr2:11641492
|
T | C | 3 | a0014c0023t0014a0032c0048t0014a0039c0074t0014 | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1038T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1038 | chr2 | 11641492 | |||||
| chr2:11641517
|
G | T | 35 | a0002c0012t0023a0002c0012t0065a0002c0034t0031others(32): Show | 43 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1063G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1063 | chr2 | 11641517 | |||||
| chr2:11641525
|
A | G | 1 | a0005c0002t0050 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1071 | chr2 | 11641525 | |||||
| chr2:11641544
|
G | A | 19 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(16): Show | 28 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1090G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1090 | chr2 | 11641544 | |||||
| chr2:11641635
|
A | G | 3 | a0001c0001t0030a0001c0001t0072a0003c0003t0030 | 3 | HG02135.hp1 NA18961.hp2 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1181A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1181 | chr2 | 11641635 | |||||
| chr2:11641640
|
C | T | 3 | a0001c0001t0030a0001c0001t0072a0003c0003t0030 | 3 | HG02135.hp1 NA18961.hp2 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1186C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1186 | chr2 | 11641640 | |||||
| chr2:11641679
|
G | A | 3 | a0005c0002t0055a0006c0033t0034a0021c0040t0036 | 3 | HG02809.hp2 HG03130.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1225G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1225 | chr2 | 11641679 | |||||
| chr2:11641737
|
C | T | 2 | a0002c0061t0062a0013c0018t0047 | 2 | HG06807.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1283C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1283 | chr2 | 11641737 | |||||
| chr2:11641833
|
G | A | 1 | a0013c0018t0047 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1379G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1379 | chr2 | 11641833 | |||||
| chr2:11642065
|
C | A | 20 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(17): Show | 29 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1611C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1611 | chr2 | 11642065 | |||||
| chr2:11642120
|
C | CT | 20 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(17): Show | 29 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1676dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1677 | INFO_REALIGN_3_PRIME | chr2 | 11642120 | ||||
| chr2:11642132
|
G | T | 20 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(17): Show | 29 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1678G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1678 | chr2 | 11642132 | |||||
| chr2:11642184
|
C | T | 176 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(173): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*1730C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1730 | chr2 | 11642184 | |||||
| chr2:11642188
|
G | A | 20 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(17): Show | 29 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1734G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1734 | chr2 | 11642188 | |||||
| chr2:11642263
|
C | T | 20 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(17): Show | 29 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1809C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1809 | chr2 | 11642263 | |||||
| chr2:11642264
|
G | A | 2 | a0006c0056t0070a0006c0065t0033 | 2 | NA18979.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1810G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1810 | chr2 | 11642264 | |||||
| chr2:11642293
|
A | AT | 4 | a0014c0023t0014a0018c0037t0053a0032c0048t0014others(1): Show | 6 | HG01070.hp2 HG01261.hp1 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1851dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1852 | INFO_REALIGN_3_PRIME | chr2 | 11642293 | ||||
| chr2:11642293
|
AT | A | 21 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(18): Show | 30 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1851delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 1851 | INFO_REALIGN_3_PRIME | chr2 | 11642293 | ||||
| chr2:11642659
|
A | G | 20 | a0001c0001t0005a0001c0001t0011a0001c0001t0030others(17): Show | 29 | HG00558.hp1 HG00673.hp2 HG01109.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2205A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 2205 | chr2 | 11642659 | |||||
| chr2:11642681
|
C | G | 9 | a0002c0007t0052a0002c0012t0023a0002c0012t0065others(6): Show | 11 | HG01175.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2227C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 2227 | chr2 | 11642681 | |||||
| chr2:11642723
|
G | A | 1 | a0040c0072t0058 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 33/33 | 2269 | chr2 | 11642723 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:11534295
|
T | C | 1 | a0005c0002t0003g0001 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-162+41T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534295 | ||||||
| chr2:11534533
|
T | C | 25 | a0002c0007t0037g0023a0002c0034t0019g0026a0002c0055t0044g0003others(22): Show | 25 | HG01109.hp1 HG01109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.-162+279T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534533 | ||||||
| chr2:11534536
|
G | A | 4 | a0009c0029t0041g0028a0010c0031t0038g0029a0011c0008t0003g0027others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+282G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534536 | ||||||
| chr2:11534571
|
C | G | 32 | a0002c0007t0020g0307a0002c0007t0037g0023a0002c0034t0019g0026others(29): Show | 32 | HG01109.hp1 HG01109.hp2 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.-162+317C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534571 | ||||||
| chr2:11534580
|
T | C | 36 | a0002c0007t0020g0307a0002c0007t0037g0023a0002c0034t0019g0026others(33): Show | 36 | HG01109.hp1 HG01109.hp2 HG02145.hp1 others(33): Show |
intron_variant | MODIFIER | c.-162+326T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534580 | ||||||
| chr2:11534665
|
G | T | 1 | a0039c0074t0014g0301 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-162+411G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534665 | ||||||
| chr2:11534689
|
C | G | 4 | a0009c0029t0041g0028a0010c0031t0038g0029a0011c0008t0003g0027others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+435C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534689 | ||||||
| chr2:11534707
|
A | G | 3 | a0018c0037t0003g0298a0019c0036t0001g0299a0019c0036t0001g0300 | 3 | HG02965.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-162+453A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534707 | ||||||
| chr2:11534776
|
C | T | 1 | a0011c0008t0003g0297 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-162+522C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534776 | ||||||
| chr2:11534875
|
G | C | 1 | a0002c0005t0007g0031 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-162+621G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534875 | ||||||
| chr2:11534999
|
C | T | 3 | a0001c0001t0006g0294a0004c0004t0002g0295a0004c0004t0013g0296 | 3 | HG01243.hp2 HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-162+745C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11534999 | ||||||
| chr2:11535020
|
G | C | 48 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(45): Show | 48 | HG00621.hp2 HG00733.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.-162+766G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535020 | ||||||
| chr2:11535117
|
G | GGAGCTAC others(8): Show |
1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-162+875_-162+876i others(17): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11535117 | |||||
| chr2:11535131
|
T | C | 7 | a0002c0007t0020g0307a0003c0009t0021g0308a0006c0033t0034g0302others(4): Show | 7 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-162+877T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535131 | ||||||
| chr2:11535153
|
A | T | 21 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0282others(18): Show | 21 | HG00423.hp1 HG00673.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.-162+899A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535153 | ||||||
| chr2:11535346
|
C | T | 97 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0005g0047others(94): Show | 97 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.-162+1092C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535346 | ||||||
| chr2:11535384
|
CTTAT | C | 96 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0005g0047others(93): Show | 96 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.-162+1153_-162+115 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11535384 | |||||
| chr2:11535463
|
A | G | 97 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0005g0047others(94): Show | 97 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.-162+1209A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535463 | ||||||
| chr2:11535537
|
T | TTTCCTC | 210 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(207): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-162+1284_-162+128 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11535537 | |||||
| chr2:11535617
|
G | A | 3 | a0002c0055t0044g0003a0006c0054t0043g0002a0007c0015t0027g0004 | 3 | HG01109.hp1 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+1363G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535617 | ||||||
| chr2:11535669
|
G | A | 1 | a0050c0087t0004g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-162+1415G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535669 | ||||||
| chr2:11535780
|
A | G | 3 | a0002c0055t0044g0003a0006c0054t0043g0002a0007c0015t0027g0004 | 3 | HG01109.hp1 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+1526A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535780 | ||||||
| chr2:11535786
|
A | G | 6 | a0002c0034t0019g0026a0009c0029t0041g0028a0010c0031t0038g0029others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+1532A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535786 | ||||||
| chr2:11535913
|
C | T | 2 | a0002c0007t0037g0023a0007c0015t0027g0024 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-162+1659C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535913 | ||||||
| chr2:11535939
|
A | G | 95 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(92): Show | 95 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.-162+1685A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11535939 | ||||||
| chr2:11536028
|
G | T | 5 | a0002c0007t0020g0307a0003c0009t0021g0308a0008c0060t0061g0305others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+1774G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536028 | ||||||
| chr2:11536088
|
C | A | 1 | a0004c0004t0008g0173 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-162+1834C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536088 | ||||||
| chr2:11536180
|
A | G | 3 | a0002c0011t0001g0271a0003c0003t0005g0270a0006c0027t0003g0272 | 3 | HG01496.hp1 NA18982.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-162+1926A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536180 | ||||||
| chr2:11536185
|
T | A | 95 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(92): Show | 95 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.-162+1931T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536185 | ||||||
| chr2:11536237
|
T | A | 5 | a0008c0006t0015g0005a0008c0049t0015g0006a0010c0032t0028g0007others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+1983T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536237 | ||||||
| chr2:11536341
|
G | A | 3 | a0002c0055t0044g0003a0006c0054t0043g0002a0007c0015t0027g0004 | 3 | HG01109.hp1 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+2087G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536341 | ||||||
| chr2:11536388
|
T | A | 2 | a0002c0007t0037g0023a0007c0015t0027g0024 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-162+2134T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536388 | ||||||
| chr2:11536790
|
AG | A | 95 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(92): Show | 95 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.-162+2537delG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536790 | ||||||
| chr2:11536862
|
G | A | 1 | a0008c0006t0019g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-162+2608G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536862 | ||||||
| chr2:11536932
|
T | TCTTTCA | 95 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(92): Show | 95 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.-162+2681_-162+268 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11536932 | |||||
| chr2:11536969
|
T | C | 1 | a0011c0008t0003g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-162+2715T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536969 | ||||||
| chr2:11536970
|
A | C | 1 | a0027c0096t0005g0074 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-162+2716A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11536970 | ||||||
| chr2:11537002
|
G | A | 5 | a0008c0006t0015g0005a0008c0049t0015g0006a0010c0032t0028g0007others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+2748G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11537002 | ||||||
| chr2:11537323
|
A | G | 95 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(92): Show | 95 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.-162+3069A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11537323 | ||||||
| chr2:11537356
|
T | C | 6 | a0002c0034t0019g0026a0009c0029t0041g0028a0010c0031t0038g0029others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+3102T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11537356 | ||||||
| chr2:11537363
|
T | G | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-162+3109T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11537363 | ||||||
| chr2:11537514
|
C | G | 1 | a0002c0005t0006g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-162+3260C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11537514 | ||||||
| chr2:11537668
|
ATATTT | A | 15 | a0002c0055t0044g0003a0002c0057t0059g0021a0005c0002t0055g0014others(12): Show | 15 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-162+3418_-162+342 others(9): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11537668 | |||||
| chr2:11537690
|
C | G | 2 | a0002c0007t0037g0023a0007c0015t0027g0024 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-162+3436C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11537690 | ||||||
| chr2:11537714
|
T | C | 1 | a0009c0030t0016g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-162+3460T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11537714 | ||||||
| chr2:11537728
|
A | G | 95 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(92): Show | 95 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.-162+3474A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11537728 | ||||||
| chr2:11537771
|
A | G | 6 | a0001c0001t0002g0287a0001c0001t0004g0291a0001c0001t0069g0288others(3): Show | 6 | NA18941.hp2 NA18953.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+3517A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11537771 | ||||||
| chr2:11538163
|
T | C | 3 | a0001c0001t0004g0175a0046c0078t0011g0176a0047c0077t0002g0174 | 3 | NA18942.hp1 NA19000.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-162+3909T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538163 | ||||||
| chr2:11538180
|
G | A | 1 | a0006c0064t0012g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-162+3926G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538180 | ||||||
| chr2:11538247
|
C | T | 17 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0020t0067g0171others(14): Show | 17 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.-162+3993C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538247 | ||||||
| chr2:11538371
|
C | CT | 125 | a0001c0001t0002g0032a0001c0001t0002g0182a0001c0001t0002g0192others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-162+4124dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538371 | |||||
| chr2:11538609
|
G | GTTTC | 5 | a0002c0007t0007g0150a0005c0002t0003g0151a0005c0002t0003g0152others(2): Show | 5 | HG01884.hp2 HG02040.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+4432_-162+443 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
G | GTTTCTTT others(1): Show |
4 | a0001c0001t0005g0168a0002c0020t0067g0171a0007c0017t0001g0170others(1): Show | 4 | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+4428_-162+443 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTC | G | 26 | a0001c0001t0005g0131a0001c0001t0007g0138a0002c0011t0005g0135others(23): Show | 26 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.-162+4432_-162+443 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTCTTT others(1): Show |
G | 39 | a0002c0007t0001g0104a0002c0012t0065g0103a0003c0003t0001g0115others(36): Show | 39 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.-162+4428_-162+443 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTCTTT others(5): Show |
G | 20 | a0002c0053t0019g0090a0003c0038t0001g0088a0005c0002t0003g0098others(17): Show | 20 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-162+4424_-162+443 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTCTTT others(9): Show |
G | 9 | a0001c0001t0030g0087a0002c0012t0023g0085a0002c0012t0023g0086others(6): Show | 9 | HG01070.hp1 HG01261.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.-162+4420_-162+443 others(20): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTCTTT others(11): Show |
G | 1 | a0005c0002t0009g0079 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-162+4357_-162+437 others(22): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTCTTT others(13): Show |
G | 3 | a0005c0002t0003g0082a0015c0022t0001g0081a0044c0068t0009g0080 | 3 | HG03239.hp2 HG06807.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-162+4416_-162+443 others(24): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTCTTT others(25): Show |
G | 1 | a0011c0008t0045g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-162+4404_-162+443 others(36): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTCTTT others(41): Show |
G | 3 | a0002c0007t0037g0023a0007c0015t0027g0004a0007c0015t0027g0024 | 3 | HG03041.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+4388_-162+443 others(52): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTCTTT others(45): Show |
G | 162 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.-162+4384_-162+443 others(56): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538609
|
GTTTCTTT others(49): Show |
G | 16 | a0002c0007t0001g0262a0002c0034t0019g0026a0002c0034t0031g0263others(13): Show | 16 | HG00140.hp1 HG01109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-162+4380_-162+443 others(60): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538609 | |||||
| chr2:11538672
|
TCTTTCTT others(17): Show |
T | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-162+4420_-162+444 others(28): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538672 | |||||
| chr2:11538674
|
TTTCTTTC others(9): Show |
T | 1 | a0007c0016t0015g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-162+4424_-162+443 others(20): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538674 | |||||
| chr2:11538678
|
TTTCTTTC others(5): Show |
T | 2 | a0008c0006t0054g0018a0013c0018t0003g0019 | 2 | HG01109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-162+4428_-162+443 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538678 | |||||
| chr2:11538686
|
T | C | 24 | a0002c0007t0001g0262a0002c0007t0020g0307a0002c0007t0037g0023others(21): Show | 24 | HG00140.hp1 HG02258.hp2 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.-162+4432T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538686 | ||||||
| chr2:11538689
|
C | CTTTCTTT others(7): Show |
1 | a0043c0069t0003g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-162+4435_-162+443 others(18): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538689 | ||||||
| chr2:11538696
|
C | T | 156 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-162+4442C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538696 | ||||||
| chr2:11538700
|
C | T | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-162+4446C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538700 | ||||||
| chr2:11538743
|
CCTTCTTT others(54): Show |
C | 5 | a0002c0007t0020g0307a0003c0009t0021g0308a0008c0060t0061g0305others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+4494_-162+455 others(65): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538743 | |||||
| chr2:11538747
|
C | T | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-162+4493C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538747 | ||||||
| chr2:11538748
|
T | C | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-162+4494T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538748 | ||||||
| chr2:11538748
|
T | TTTCCTTC others(5): Show |
14 | a0002c0055t0044g0003a0005c0066t0022g0072a0006c0054t0043g0002others(11): Show | 14 | HG01070.hp2 HG01109.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.-162+4505_-162+451 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538748 | |||||
| chr2:11538754
|
TCCTTTCT others(34): Show |
T | 1 | a0006c0033t0034g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-162+4505_-162+454 others(45): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538754 | |||||
| chr2:11538755
|
CCTTTCTT others(42): Show |
C | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-162+4505_-162+455 others(53): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538755 | |||||
| chr2:11538759
|
T | C | 6 | a0005c0002t0055g0014a0007c0016t0001g0012a0007c0016t0001g0013others(3): Show | 6 | HG02622.hp1 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+4505T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538759 | ||||||
| chr2:11538759
|
TCTTCCTT others(1): Show |
T | 9 | a0002c0007t0001g0262a0002c0034t0031g0263a0003c0003t0001g0267others(6): Show | 9 | HG00140.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+4515_-162+452 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538759 | |||||
| chr2:11538763
|
CCTTCCTT others(34): Show |
C | 150 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-162+4523_-162+456 others(45): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538763 | |||||
| chr2:11538767
|
CCTTCCTT others(16): Show |
C | 6 | a0005c0002t0055g0014a0007c0016t0001g0012a0007c0016t0001g0013others(3): Show | 6 | HG02622.hp1 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+4515_-162+453 others(27): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538767 | |||||
| chr2:11538769
|
T | C | 12 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0015g0005others(9): Show | 12 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-162+4515T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538769 | ||||||
| chr2:11538771
|
C | T | 12 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0015g0005others(9): Show | 12 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-162+4517C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538771 | ||||||
| chr2:11538775
|
CCCGT | C | 12 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0015g0005others(9): Show | 12 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-162+4523_-162+452 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538775 | |||||
| chr2:11538776
|
CCGTCTTC others(6): Show |
C | 3 | a0001c0001t0006g0294a0004c0004t0002g0295a0004c0004t0013g0296 | 3 | HG01243.hp2 HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-162+4523_-162+453 others(17): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538776 | ||||||
| chr2:11538778
|
G | T | 9 | a0002c0007t0001g0262a0002c0034t0031g0263a0003c0003t0001g0267others(6): Show | 9 | HG00140.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+4524G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538778 | ||||||
| chr2:11538779
|
TCTTCCTT others(18): Show |
T | 3 | a0002c0007t0037g0023a0007c0015t0027g0004a0007c0015t0027g0024 | 3 | HG03041.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+4540_-162+456 others(29): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538779 | |||||
| chr2:11538788
|
C | T | 9 | a0002c0007t0001g0262a0002c0034t0031g0263a0003c0003t0001g0267others(6): Show | 9 | HG00140.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+4534C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538788 | ||||||
| chr2:11538793
|
T | C | 15 | a0001c0001t0006g0294a0002c0057t0059g0021a0004c0004t0002g0295others(12): Show | 15 | HG01109.hp2 HG01243.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.-162+4539T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538793 | ||||||
| chr2:11538794
|
TC | T | 21 | a0002c0007t0001g0262a0002c0034t0031g0263a0002c0057t0059g0021others(18): Show | 21 | HG00140.hp1 HG01109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-162+4543delC | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538794 | |||||
| chr2:11538794
|
TCC | T | 6 | a0005c0002t0055g0014a0007c0016t0001g0012a0007c0016t0001g0013others(3): Show | 6 | HG02622.hp1 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+4542_-162+454 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538794 | |||||
| chr2:11538796
|
C | CCTT | 19 | a0002c0034t0019g0026a0002c0055t0044g0003a0005c0066t0022g0072others(16): Show | 19 | HG01070.hp2 HG01109.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.-162+4546_-162+454 others(7): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538796 | |||||
| chr2:11538796
|
C | T | 12 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0015g0005others(9): Show | 12 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-162+4542C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538796 | ||||||
| chr2:11538798
|
T | G | 1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-162+4544T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538798 | ||||||
| chr2:11538800
|
CTTTA | C | 3 | a0001c0001t0006g0294a0004c0004t0002g0295a0004c0004t0013g0296 | 3 | HG01243.hp2 HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-162+4547_-162+455 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538800 | ||||||
| chr2:11538807
|
T | C | 3 | a0001c0001t0006g0294a0004c0004t0002g0295a0004c0004t0013g0296 | 3 | HG01243.hp2 HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-162+4553T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538807 | ||||||
| chr2:11538811
|
T | C | 3 | a0001c0001t0006g0294a0004c0004t0002g0295a0004c0004t0013g0296 | 3 | HG01243.hp2 HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-162+4557T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538811 | ||||||
| chr2:11538815
|
T | C | 3 | a0001c0001t0006g0294a0004c0004t0002g0295a0004c0004t0013g0296 | 3 | HG01243.hp2 HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-162+4561T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538815 | ||||||
| chr2:11538817
|
C | A | 3 | a0001c0001t0006g0294a0004c0004t0002g0295a0004c0004t0013g0296 | 3 | HG01243.hp2 HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-162+4563C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538817 | ||||||
| chr2:11538885
|
C | A | 1 | a0007c0016t0001g0013 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-162+4631C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538885 | ||||||
| chr2:11538887
|
C | CTT | 6 | a0002c0007t0020g0307a0003c0009t0021g0308a0006c0033t0034g0302others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+4634_-162+463 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538887 | |||||
| chr2:11538893
|
C | T | 6 | a0002c0007t0020g0307a0003c0009t0021g0308a0006c0033t0034g0302others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+4639C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538893 | ||||||
| chr2:11538894
|
T | C | 6 | a0002c0007t0020g0307a0003c0009t0021g0308a0006c0033t0034g0302others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+4640T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538894 | ||||||
| chr2:11538895
|
T | C | 6 | a0002c0007t0020g0307a0003c0009t0021g0308a0006c0033t0034g0302others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-162+4641T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538895 | ||||||
| chr2:11538895
|
T | TTTCC | 193 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(190): Show | 193 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-162+4654_-162+465 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538895 | |||||
| chr2:11538910
|
C | CCTTCCCC others(17): Show |
1 | a0004c0004t0008g0273 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-162+4657_-162+465 others(28): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538910 | |||||
| chr2:11538910
|
C | CCTTCCCC others(37): Show |
1 | a0001c0001t0006g0180 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-162+4657_-162+465 others(48): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538910 | |||||
| chr2:11538910
|
CCCCCTCC others(13): Show |
C | 1 | a0002c0020t0067g0171 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-162+4689_-162+470 others(24): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538910 | |||||
| chr2:11538927
|
G | C | 306 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.-162+4673G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538927 | ||||||
| chr2:11538934
|
C | CTCCCCTC others(8): Show |
10 | a0003c0003t0001g0141a0003c0003t0001g0148a0003c0003t0022g0120others(7): Show | 10 | HG00099.hp1 HG00733.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-162+4692_-162+469 others(19): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538934 | |||||
| chr2:11538934
|
CTCCCCTC others(8): Show |
C | 3 | a0018c0037t0003g0298a0019c0036t0001g0299a0019c0036t0001g0300 | 3 | HG02965.hp1 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-162+4693_-162+470 others(19): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538934 | |||||
| chr2:11538947
|
G | C | 304 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-162+4693G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538947 | ||||||
| chr2:11538949
|
G | GTCCCC | 31 | a0001c0001t0006g0180a0002c0007t0052g0075a0002c0055t0044g0003others(28): Show | 31 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-162+4704_-162+470 others(9): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538949 | |||||
| chr2:11538949
|
G | GTCCCCTC others(18): Show |
21 | a0001c0001t0002g0182a0001c0001t0002g0274a0001c0001t0002g0287others(18): Show | 21 | HG00423.hp1 HG01243.hp2 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.-162+4708_-162+470 others(29): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538949 | |||||
| chr2:11538949
|
G | GTCCCCTC others(39): Show |
1 | a0002c0005t0001g0033 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-162+4708_-162+470 others(50): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538949 | |||||
| chr2:11538949
|
G | GTCCCCTC others(38): Show |
1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-162+4708_-162+470 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538949 | |||||
| chr2:11538949
|
G | GTCCCCTC others(38): Show |
141 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.-162+4708_-162+470 others(49): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538949 | |||||
| chr2:11538949
|
G | GTCCCCTC others(58): Show |
1 | a0002c0005t0001g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-162+4708_-162+470 others(69): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538949 | |||||
| chr2:11538949
|
G | GTCCCCTC others(78): Show |
1 | a0006c0033t0034g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-162+4708_-162+470 others(89): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538949 | |||||
| chr2:11538957
|
C | CCCTCT | 9 | a0002c0007t0001g0262a0002c0034t0031g0263a0003c0003t0001g0267others(6): Show | 9 | HG00140.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+4707_-162+470 others(9): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538957 | |||||
| chr2:11538958
|
C | CCTCCCCT others(63): Show |
1 | a0004c0004t0002g0183 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-162+4708_-162+470 others(74): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538958 | |||||
| chr2:11538964
|
C | G | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4710C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538964 | ||||||
| chr2:11538972
|
C | T | 1 | a0007c0015t0021g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-162+4718C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538972 | ||||||
| chr2:11538974
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4720T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538974 | ||||||
| chr2:11538985
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4731T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538985 | ||||||
| chr2:11538987
|
C | CTCTCTTC others(40): Show |
8 | a0005c0002t0055g0014a0007c0016t0001g0012a0007c0016t0001g0013others(5): Show | 8 | HG01070.hp2 HG02622.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-162+4743_-162+478 others(51): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538987 | |||||
| chr2:11538990
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4736T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538990 | ||||||
| chr2:11538990
|
T | TCTTCTCC others(3): Show |
9 | a0002c0007t0001g0262a0002c0034t0031g0263a0003c0003t0001g0267others(6): Show | 9 | HG00140.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+4737_-162+474 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11538990 | |||||
| chr2:11538992
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4738T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538992 | ||||||
| chr2:11538995
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4741T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11538995 | ||||||
| chr2:11539002
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4748T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539002 | ||||||
| chr2:11539007
|
CCTTCTCC others(6): Show |
C | 1 | a0012c0010t0002g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-162+4756_-162+476 others(17): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539007 | |||||
| chr2:11539012
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4758T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539012 | ||||||
| chr2:11539013
|
CCTCCCTT others(5): Show |
C | 1 | a0053c0083t0008g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-162+4763_-162+477 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539013 | |||||
| chr2:11539017
|
C | CCTTCT | 28 | a0001c0001t0007g0138a0001c0001t0030g0087a0002c0011t0005g0135others(25): Show | 28 | HG00558.hp2 HG00639.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-162+4812_-162+481 others(9): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
C | CCTTCTCT others(3): Show |
8 | a0003c0003t0001g0141a0005c0002t0003g0116a0005c0002t0003g0117others(5): Show | 8 | HG00733.hp2 HG01993.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-162+4807_-162+481 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
C | CCTTCTCT others(8): Show |
2 | a0005c0002t0003g0118a0009c0030t0016g0077 | 2 | HG01884.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-162+4802_-162+481 others(19): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
C | CCTTCTCT others(18): Show |
2 | a0002c0055t0044g0003a0009c0028t0020g0304 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-162+4792_-162+481 others(29): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
C | CCTTCTCT others(45): Show |
1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-162+4789_-162+479 others(56): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
C | CCTTCTCT others(23): Show |
4 | a0002c0007t0020g0307a0006c0033t0034g0302a0008c0060t0061g0305others(1): Show | 4 | HG02559.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+4787_-162+481 others(34): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
C | CCTTCTCT others(50): Show |
1 | a0011c0008t0045g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-162+4794_-162+479 others(61): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
C | CCTTCTCT others(33): Show |
2 | a0002c0007t0052g0075a0003c0009t0021g0308 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-162+4777_-162+481 others(44): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
CCTTCT | C | 32 | a0001c0001t0002g0252a0001c0001t0005g0168a0001c0001t0006g0180others(29): Show | 32 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-162+4812_-162+481 others(9): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
CCTTCTCT others(3): Show |
C | 34 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0005g0047others(31): Show | 34 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.-162+4807_-162+481 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
CCTTCTCT others(8): Show |
C | 15 | a0001c0001t0002g0032a0001c0001t0002g0241a0001c0001t0002g0247others(12): Show | 15 | HG00140.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-162+4802_-162+481 others(19): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539017
|
CCTTCTCT others(13): Show |
C | 85 | a0001c0001t0002g0182a0001c0001t0002g0192a0001c0001t0002g0193others(82): Show | 85 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-162+4797_-162+481 others(24): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539017 | |||||
| chr2:11539022
|
T | TCTTCTCT others(35): Show |
1 | a0019c0036t0001g0299 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-162+4789_-162+479 others(46): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539022 | |||||
| chr2:11539024
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4770T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539024 | ||||||
| chr2:11539025
|
T | C | 1 | a0012c0010t0002g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-162+4771T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539025 | ||||||
| chr2:11539027
|
T | TCTTCTCT others(25): Show |
2 | a0018c0037t0053g0067a0037c0067t0021g0070 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-162+4784_-162+478 others(36): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539027 | |||||
| chr2:11539027
|
T | TCTTCTCT others(30): Show |
2 | a0008c0006t0015g0005a0008c0049t0015g0006 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-162+4789_-162+479 others(41): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539027 | |||||
| chr2:11539032
|
T | TCTTCTCT others(25): Show |
7 | a0005c0066t0022g0072a0007c0015t0021g0069a0010c0032t0028g0007others(4): Show | 7 | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-162+4789_-162+479 others(36): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539032 | |||||
| chr2:11539032
|
T | TCTTCTCT others(40): Show |
2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-162+4789_-162+479 others(51): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539032 | |||||
| chr2:11539034
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4780T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539034 | ||||||
| chr2:11539037
|
T | C | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4783T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539037 | ||||||
| chr2:11539037
|
T | TCTTCTCC others(20): Show |
5 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0054g0018others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+4789_-162+479 others(31): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539037 | |||||
| chr2:11539038
|
C | T | 2 | a0001c0001t0018g0258a0003c0003t0002g0257 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-162+4784C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539038 | ||||||
| chr2:11539062
|
T | TCTTCC | 5 | a0002c0007t0001g0262a0002c0034t0031g0263a0006c0056t0070g0179others(2): Show | 5 | HG00140.hp1 HG02738.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+4812_-162+481 others(9): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539062 | |||||
| chr2:11539062
|
T | TCTTCTCT others(3): Show |
4 | a0003c0003t0001g0267a0003c0003t0001g0268a0005c0002t0048g0269others(1): Show | 4 | HG02258.hp2 HG02572.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-162+4816_-162+481 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539062 | |||||
| chr2:11539062
|
T | TCTTCTCT others(8): Show |
3 | a0002c0034t0019g0026a0009c0029t0041g0028a0028c0062t0040g0025 | 3 | HG02145.hp1 HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-162+4816_-162+481 others(19): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539062 | |||||
| chr2:11539062
|
T | TCTTCTCT others(13): Show |
1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162+4816_-162+481 others(24): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539062 | |||||
| chr2:11539062
|
T | TCTTCTCT others(23): Show |
3 | a0002c0007t0037g0023a0007c0015t0027g0004a0013c0018t0022g0030 | 3 | HG03041.hp2 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+4816_-162+481 others(34): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539062 | |||||
| chr2:11539062
|
T | TCTTCTCT others(28): Show |
1 | a0007c0015t0027g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-162+4816_-162+481 others(39): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539062 | |||||
| chr2:11539300
|
C | T | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-162+5046C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539300 | ||||||
| chr2:11539314
|
GTGC | G | 9 | a0001c0001t0002g0229a0001c0001t0002g0231a0001c0001t0002g0232others(6): Show | 9 | HG00741.hp2 HG01074.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+5063_-162+506 others(7): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539314 | |||||
| chr2:11539427
|
C | T | 7 | a0002c0007t0020g0307a0003c0009t0021g0308a0006c0033t0034g0302others(4): Show | 7 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-162+5173C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539427 | ||||||
| chr2:11539480
|
G | T | 3 | a0002c0007t0037g0023a0007c0015t0027g0004a0007c0015t0027g0024 | 3 | HG03041.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+5226G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539480 | ||||||
| chr2:11539795
|
A | AT | 150 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-162+5563dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539795 | |||||
| chr2:11539795
|
A | ATT | 19 | a0001c0001t0006g0255a0001c0001t0007g0037a0002c0005t0001g0057others(16): Show | 19 | HG00621.hp2 HG01106.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.-162+5562_-162+556 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539795 | |||||
| chr2:11539795
|
AT | A | 15 | a0002c0007t0001g0104a0002c0057t0059g0021a0003c0003t0001g0148others(12): Show | 15 | HG00741.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-162+5563delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539795 | |||||
| chr2:11539795
|
ATT | A | 10 | a0002c0007t0037g0023a0007c0015t0021g0069a0007c0015t0027g0004others(7): Show | 10 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-162+5562_-162+556 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539795 | |||||
| chr2:11539795
|
ATTTTTT | A | 9 | a0005c0066t0022g0072a0014c0023t0014g0068a0014c0023t0014g0071others(6): Show | 9 | HG01070.hp2 HG01261.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-162+5558_-162+556 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11539795 | |||||
| chr2:11539931
|
C | T | 5 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0054g0018others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+5677C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11539931 | ||||||
| chr2:11540026
|
C | A | 5 | a0002c0055t0044g0003a0005c0002t0055g0014a0006c0054t0043g0002others(2): Show | 5 | HG01109.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-162+5772C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540026 | ||||||
| chr2:11540129
|
C | A | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-162+5875C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540129 | ||||||
| chr2:11540139
|
C | T | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-162+5885C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540139 | ||||||
| chr2:11540145
|
T | C | 3 | a0008c0006t0017g0259a0009c0028t0003g0260a0013c0052t0049g0261 | 3 | HG02615.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-162+5891T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540145 | ||||||
| chr2:11540256
|
G | A | 1 | a0004c0004t0004g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-162+6002G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540256 | ||||||
| chr2:11540277
|
C | T | 175 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-162+6023C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540277 | ||||||
| chr2:11540314
|
A | G | 8 | a0002c0007t0037g0023a0002c0057t0059g0021a0007c0015t0027g0004others(5): Show | 8 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-162+6060A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540314 | ||||||
| chr2:11540408
|
A | C | 2 | a0018c0037t0053g0067a0037c0067t0021g0070 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-162+6154A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540408 | ||||||
| chr2:11540421
|
G | A | 6 | a0007c0016t0001g0012a0007c0016t0001g0013a0008c0006t0017g0015others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-162+6167G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540421 | ||||||
| chr2:11540463
|
A | G | 1 | a0002c0011t0001g0040 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-162+6209A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540463 | ||||||
| chr2:11540586
|
C | T | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-162+6332C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540586 | ||||||
| chr2:11540770
|
CAA | C | 177 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(174): Show | 177 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-162+6518_-162+651 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11540770 | |||||
| chr2:11540817
|
C | T | 2 | a0004c0004t0002g0237a0055c0080t0018g0236 | 2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-162+6563C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540817 | ||||||
| chr2:11540836
|
T | C | 10 | a0002c0034t0019g0026a0002c0055t0044g0003a0005c0002t0055g0014others(7): Show | 10 | HG01109.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-162+6582T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540836 | ||||||
| chr2:11540877
|
C | G | 10 | a0002c0034t0019g0026a0002c0055t0044g0003a0005c0002t0055g0014others(7): Show | 10 | HG01109.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-162+6623C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540877 | ||||||
| chr2:11540892
|
G | A | 10 | a0002c0034t0019g0026a0002c0055t0044g0003a0005c0002t0055g0014others(7): Show | 10 | HG01109.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-162+6638G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540892 | ||||||
| chr2:11540917
|
G | T | 187 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(184): Show | 187 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.-162+6663G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540917 | ||||||
| chr2:11540936
|
A | C | 3 | a0005c0002t0055g0014a0007c0044t0039g0011a0009c0029t0020g0016 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-162+6682A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540936 | ||||||
| chr2:11540974
|
A | G | 1 | a0006c0033t0034g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-162+6720A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11540974 | ||||||
| chr2:11541139
|
G | A | 1 | a0006c0033t0034g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-162+6885G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541139 | ||||||
| chr2:11541165
|
G | C | 10 | a0002c0034t0019g0026a0002c0055t0044g0003a0005c0002t0055g0014others(7): Show | 10 | HG01109.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-162+6911G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541165 | ||||||
| chr2:11541170
|
AG | A | 3 | a0002c0007t0037g0023a0007c0015t0027g0004a0007c0015t0027g0024 | 3 | HG03041.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+6918delG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11541170 | |||||
| chr2:11541312
|
A | G | 207 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(204): Show | 207 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.-162+7058A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541312 | ||||||
| chr2:11541404
|
C | T | 7 | a0002c0007t0020g0307a0003c0009t0021g0308a0006c0033t0034g0302others(4): Show | 7 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-162+7150C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541404 | ||||||
| chr2:11541423
|
C | T | 2 | a0011c0008t0012g0093a0011c0008t0012g0094 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-162+7169C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541423 | ||||||
| chr2:11541442
|
T | C | 208 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.-162+7188T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541442 | ||||||
| chr2:11541444
|
A | AG | 12 | a0001c0001t0004g0186a0001c0001t0018g0258a0001c0001t0072g0254others(9): Show | 12 | HG01074.hp1 HG01099.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-162+7191dupG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11541444 | |||||
| chr2:11541445
|
GA | G | 42 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0005g0047others(39): Show | 42 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(39): Show |
intron_variant | MODIFIER | c.-162+7192delA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541445 | ||||||
| chr2:11541446
|
A | G | 163 | a0001c0001t0002g0032a0001c0001t0002g0182a0001c0001t0002g0192others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-162+7192A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541446 | ||||||
| chr2:11541453
|
C | G | 205 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-162+7199C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541453 | ||||||
| chr2:11541460
|
G | C | 3 | a0002c0007t0001g0262a0002c0034t0031g0263a0006c0056t0070g0179 | 3 | HG03540.hp2 NA18979.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-162+7206G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541460 | ||||||
| chr2:11541606
|
A | G | 1 | a0011c0008t0003g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-162+7352A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541606 | ||||||
| chr2:11541671
|
G | A | 1 | a0011c0008t0012g0093 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-162+7417G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541671 | ||||||
| chr2:11541833
|
G | A | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-162+7579G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541833 | ||||||
| chr2:11541892
|
G | A | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.-162+7638G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541892 | ||||||
| chr2:11541968
|
C | T | 1 | a0011c0008t0003g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-162+7714C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11541968 | ||||||
| chr2:11542245
|
C | T | 3 | a0002c0007t0037g0023a0007c0015t0027g0004a0007c0015t0027g0024 | 3 | HG03041.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+7991C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542245 | ||||||
| chr2:11542330
|
A | C | 5 | a0002c0034t0019g0026a0009c0029t0041g0028a0010c0031t0038g0029others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+8076A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542330 | ||||||
| chr2:11542338
|
C | T | 1 | a0038c0071t0009g0122 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-162+8084C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542338 | ||||||
| chr2:11542425
|
A | G | 1 | a0005c0002t0055g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-162+8171A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542425 | ||||||
| chr2:11542628
|
C | CG | 192 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-162+8380dupG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11542628 | |||||
| chr2:11542628
|
C | G | 1 | a0001c0001t0002g0222 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-162+8374C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542628 | ||||||
| chr2:11542666
|
T | G | 5 | a0008c0006t0015g0005a0008c0049t0015g0006a0010c0032t0028g0007others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+8412T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542666 | ||||||
| chr2:11542670
|
A | T | 205 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-162+8416A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542670 | ||||||
| chr2:11542712
|
G | A | 7 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(4): Show | 7 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-162+8458G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542712 | ||||||
| chr2:11542722
|
G | A | 1 | a0012c0010t0002g0224 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-162+8468G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542722 | ||||||
| chr2:11542809
|
A | G | 10 | a0005c0066t0022g0072a0014c0023t0014g0068a0014c0023t0014g0071others(7): Show | 10 | HG01070.hp2 HG01261.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-162+8555A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542809 | ||||||
| chr2:11542911
|
C | T | 3 | a0002c0020t0026g0219a0002c0020t0026g0221a0006c0065t0033g0220 | 3 | NA18953.hp1 NA18962.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-162+8657C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542911 | ||||||
| chr2:11542948
|
T | G | 204 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.-162+8694T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11542948 | ||||||
| chr2:11543036
|
G | A | 22 | a0002c0007t0001g0262a0002c0007t0037g0023a0002c0034t0019g0026others(19): Show | 22 | HG00140.hp1 HG01109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.-162+8782G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543036 | ||||||
| chr2:11543167
|
G | T | 5 | a0002c0034t0019g0026a0009c0029t0041g0028a0010c0031t0038g0029others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+8913G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543167 | ||||||
| chr2:11543198
|
G | A | 210 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(207): Show | 210 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-162+8944G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543198 | ||||||
| chr2:11543278
|
G | T | 5 | a0002c0034t0019g0026a0009c0029t0041g0028a0010c0031t0038g0029others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-162+9024G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543278 | ||||||
| chr2:11543297
|
G | T | 205 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-162+9043G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543297 | ||||||
| chr2:11543324
|
T | C | 205 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-162+9070T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543324 | ||||||
| chr2:11543505
|
A | G | 205 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-162+9251A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543505 | ||||||
| chr2:11543772
|
C | A | 211 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(208): Show | 211 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-162+9518C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543772 | ||||||
| chr2:11543819
|
G | A | 7 | a0007c0015t0021g0069a0008c0006t0015g0005a0008c0049t0015g0006others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-162+9565G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543819 | ||||||
| chr2:11543839
|
C | T | 190 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(187): Show | 190 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.-162+9585C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543839 | ||||||
| chr2:11543862
|
G | A | 1 | a0021c0040t0036g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-162+9608G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543862 | ||||||
| chr2:11543881
|
C | G | 163 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(160): Show | 163 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.-162+9627C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543881 | ||||||
| chr2:11543882
|
G | C | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-162+9628G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11543882 | ||||||
| chr2:11544040
|
A | G | 1 | a0011c0008t0003g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-162+9786A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544040 | ||||||
| chr2:11544187
|
C | G | 4 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0034t0031g0263others(1): Show | 4 | HG02809.hp1 HG03540.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+9933C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544187 | ||||||
| chr2:11544189
|
C | T | 201 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-162+9935C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544189 | ||||||
| chr2:11544279
|
T | C | 202 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-162+10025T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544279 | ||||||
| chr2:11544358
|
A | G | 106 | a0001c0001t0002g0032a0001c0001t0002g0182a0001c0001t0002g0192others(103): Show | 106 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-162+10104A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544358 | ||||||
| chr2:11544421
|
C | T | 3 | a0002c0007t0037g0023a0007c0015t0027g0004a0007c0015t0027g0024 | 3 | HG03041.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+10167C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544421 | ||||||
| chr2:11544512
|
G | C | 1 | a0001c0001t0002g0222 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-162+10258G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544512 | ||||||
| chr2:11544565
|
G | C | 1 | a0002c0007t0001g0262 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-162+10311G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544565 | ||||||
| chr2:11544565
|
G | T | 1 | a0001c0001t0002g0222 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-162+10311G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544565 | ||||||
| chr2:11544600
|
C | T | 10 | a0005c0066t0022g0072a0014c0023t0014g0068a0014c0023t0014g0071others(7): Show | 10 | HG01070.hp2 HG01261.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-162+10346C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544600 | ||||||
| chr2:11544726
|
C | T | 184 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(181): Show | 184 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.-162+10472C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544726 | ||||||
| chr2:11544745
|
CCT | C | 11 | a0002c0007t0052g0075a0005c0066t0022g0072a0014c0023t0014g0068others(8): Show | 11 | HG01070.hp2 HG01261.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-162+10492_-162+10 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544745 | ||||||
| chr2:11544767
|
C | G | 2 | a0006c0027t0004g0177a0025c0093t0002g0178 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-162+10513C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544767 | ||||||
| chr2:11544789
|
C | G | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-162+10535C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544789 | ||||||
| chr2:11544907
|
C | T | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-162+10653C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11544907 | ||||||
| chr2:11545120
|
C | T | 4 | a0002c0034t0019g0026a0009c0029t0041g0028a0010c0031t0038g0029others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162+10866C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545120 | ||||||
| chr2:11545205
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-162+10951G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545205 | ||||||
| chr2:11545212
|
G | A | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-162+10958G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545212 | ||||||
| chr2:11545259
|
G | A | 3 | a0003c0038t0001g0083a0003c0038t0001g0088a0044c0068t0009g0080 | 3 | HG01070.hp1 HG01071.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-162+11005G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545259 | ||||||
| chr2:11545322
|
G | A | 7 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(4): Show | 7 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-162+11068G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545322 | ||||||
| chr2:11545325
|
T | A | 1 | a0043c0069t0003g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-162+11071T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545325 | ||||||
| chr2:11545351
|
C | T | 3 | a0002c0007t0037g0023a0007c0015t0027g0004a0007c0015t0027g0024 | 3 | HG03041.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-162+11097C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545351 | ||||||
| chr2:11545401
|
G | A | 1 | a0011c0008t0003g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-161-11053G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545401 | ||||||
| chr2:11545432
|
A | G | 199 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.-161-11022A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545432 | ||||||
| chr2:11545496
|
A | T | 1 | a0001c0001t0002g0222 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-161-10958A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545496 | ||||||
| chr2:11545527
|
G | A | 2 | a0001c0001t0002g0241a0001c0001t0002g0252 | 2 | NA18975.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-161-10927G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545527 | ||||||
| chr2:11545568
|
A | C | 169 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(166): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-161-10886A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545568 | ||||||
| chr2:11545595
|
G | A | 1 | a0012c0010t0002g0224 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-161-10859G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545595 | ||||||
| chr2:11545605
|
T | C | 169 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(166): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-161-10849T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545605 | ||||||
| chr2:11545899
|
C | T | 6 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0054g0018others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-10555C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545899 | ||||||
| chr2:11545915
|
C | T | 1 | a0015c0022t0001g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-161-10539C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545915 | ||||||
| chr2:11545920
|
G | A | 5 | a0002c0034t0019g0026a0009c0029t0041g0028a0010c0031t0038g0029others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-10534G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11545920 | ||||||
| chr2:11546066
|
A | C | 169 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(166): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-161-10388A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546066 | ||||||
| chr2:11546117
|
C | T | 10 | a0005c0066t0022g0072a0014c0023t0014g0068a0014c0023t0014g0071others(7): Show | 10 | HG01070.hp2 HG01261.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-161-10337C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546117 | ||||||
| chr2:11546126
|
G | C | 6 | a0003c0003t0001g0267a0003c0003t0001g0268a0005c0002t0048g0269others(3): Show | 6 | HG00140.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-10328G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546126 | ||||||
| chr2:11546172
|
G | A | 154 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(151): Show | 154 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.-161-10282G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546172 | ||||||
| chr2:11546189
|
T | TA | 197 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-161-10256dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11546189 | |||||
| chr2:11546195
|
A | C | 1 | a0003c0003t0001g0115 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-161-10259A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546195 | ||||||
| chr2:11546316
|
T | C | 1 | a0031c0050t0006g0238 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-161-10138T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546316 | ||||||
| chr2:11546641
|
G | GGTTCTGG others(23): Show |
1 | a0001c0001t0002g0222 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-161-9811_-161-978 others(34): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11546641 | |||||
| chr2:11546696
|
C | T | 7 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(4): Show | 7 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-161-9758C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546696 | ||||||
| chr2:11546746
|
T | C | 186 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(183): Show | 186 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-161-9708T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546746 | ||||||
| chr2:11546750
|
T | G | 10 | a0005c0066t0022g0072a0014c0023t0014g0068a0014c0023t0014g0071others(7): Show | 10 | HG01070.hp2 HG01261.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-161-9704T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546750 | ||||||
| chr2:11546863
|
G | A | 1 | a0003c0003t0002g0257 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-161-9591G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11546863 | ||||||
| chr2:11546943
|
C | CT | 8 | a0002c0007t0037g0023a0002c0012t0065g0103a0007c0015t0027g0004others(5): Show | 8 | HG01175.hp1 HG01175.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-9491dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11546943 | |||||
| chr2:11546943
|
CT | C | 29 | a0001c0001t0004g0186a0001c0001t0006g0180a0001c0013t0011g0218others(26): Show | 29 | HG00673.hp2 HG00741.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.-161-9491delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11546943 | |||||
| chr2:11546943
|
CTT | C | 153 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(150): Show | 153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.-161-9492_-161-949 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11546943 | |||||
| chr2:11547007
|
G | A | 1 | a0002c0053t0019g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-161-9447G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11547007 | ||||||
| chr2:11547061
|
C | T | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-161-9393C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11547061 | ||||||
| chr2:11547150
|
C | T | 7 | a0007c0015t0021g0069a0008c0006t0015g0005a0008c0049t0015g0006others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-161-9304C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11547150 | ||||||
| chr2:11547380
|
A | G | 186 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(183): Show | 186 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-161-9074A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11547380 | ||||||
| chr2:11547601
|
A | G | 1 | a0001c0001t0002g0282 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-161-8853A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11547601 | ||||||
| chr2:11547713
|
G | A | 1 | a0004c0004t0002g0295 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-161-8741G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11547713 | ||||||
| chr2:11547727
|
T | C | 6 | a0003c0003t0001g0267a0003c0003t0001g0268a0005c0002t0048g0269others(3): Show | 6 | HG00140.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-8727T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11547727 | ||||||
| chr2:11547970
|
C | T | 1 | a0002c0005t0001g0057 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-161-8484C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11547970 | ||||||
| chr2:11547994
|
C | T | 1 | a0005c0002t0010g0123 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-161-8460C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11547994 | ||||||
| chr2:11548168
|
C | A | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-161-8286C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11548168 | ||||||
| chr2:11548176
|
C | CA | 13 | a0001c0001t0001g0042a0002c0007t0020g0307a0003c0003t0001g0141others(10): Show | 13 | HG00735.hp2 HG01993.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.-161-8265dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11548176 | |||||
| chr2:11548176
|
CA | C | 6 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0054g0018others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-8265delA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11548176 | |||||
| chr2:11548258
|
GCA | G | 6 | a0002c0007t0020g0307a0003c0009t0021g0308a0008c0060t0061g0305others(3): Show | 6 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-8189_-161-818 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11548258 | |||||
| chr2:11548291
|
C | CAT | 256 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(253): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.-161-8163_-161-816 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11548291 | ||||||
| chr2:11548320
|
GCACACAC others(49): Show |
G | 10 | a0002c0034t0019g0026a0005c0002t0055g0014a0007c0044t0039g0011others(7): Show | 10 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-161-8123_-161-806 others(60): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11548320 | |||||
| chr2:11548469
|
C | T | 5 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0054t0043g0002others(2): Show | 5 | HG01109.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-7985C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11548469 | ||||||
| chr2:11548635
|
G | A | 10 | a0002c0034t0019g0026a0005c0002t0055g0014a0007c0044t0039g0011others(7): Show | 10 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-161-7819G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11548635 | ||||||
| chr2:11548816
|
T | C | 1 | a0001c0089t0002g0189 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-161-7638T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11548816 | ||||||
| chr2:11548922
|
T | G | 60 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0007t0001g0104others(57): Show | 60 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-161-7532T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11548922 | ||||||
| chr2:11548956
|
C | G | 60 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0007t0001g0104others(57): Show | 60 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-161-7498C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11548956 | ||||||
| chr2:11548965
|
T | A | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.-161-7489T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11548965 | ||||||
| chr2:11549246
|
T | C | 1 | a0009c0030t0016g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-161-7208T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11549246 | ||||||
| chr2:11549356
|
C | T | 8 | a0002c0034t0019g0026a0007c0044t0039g0011a0008c0006t0019g0076others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-7098C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11549356 | ||||||
| chr2:11549537
|
T | G | 52 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0007t0001g0104others(49): Show | 52 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-161-6917T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11549537 | ||||||
| chr2:11549698
|
C | T | 5 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0054t0043g0002others(2): Show | 5 | HG01109.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-6756C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11549698 | ||||||
| chr2:11549709
|
T | C | 3 | a0007c0044t0039g0011a0008c0006t0019g0076a0009c0029t0020g0016 | 3 | HG02723.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-161-6745T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11549709 | ||||||
| chr2:11549892
|
T | C | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-161-6562T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11549892 | ||||||
| chr2:11550074
|
C | G | 4 | a0002c0007t0020g0307a0008c0060t0061g0305a0009c0028t0020g0304others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-161-6380C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550074 | ||||||
| chr2:11550204
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-161-6250C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550204 | ||||||
| chr2:11550228
|
A | G | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.-161-6226A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550228 | ||||||
| chr2:11550266
|
G | A | 14 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0037g0023others(11): Show | 14 | HG00140.hp1 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-161-6188G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550266 | ||||||
| chr2:11550537
|
G | T | 1 | a0003c0009t0015g0105 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-161-5917G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550537 | ||||||
| chr2:11550564
|
C | T | 5 | a0002c0034t0019g0026a0009c0029t0041g0028a0010c0031t0038g0029others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-5890C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550564 | ||||||
| chr2:11550717
|
G | A | 8 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0032g0251others(5): Show | 8 | HG00735.hp2 HG01106.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-5737G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550717 | ||||||
| chr2:11550748
|
A | C | 1 | a0001c0001t0073g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-161-5706A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550748 | ||||||
| chr2:11550864
|
C | T | 14 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0037g0023others(11): Show | 14 | HG00140.hp1 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-161-5590C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550864 | ||||||
| chr2:11550980
|
A | C | 5 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0054g0018others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-5474A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11550980 | ||||||
| chr2:11551007
|
T | A | 6 | a0005c0066t0022g0072a0018c0037t0003g0298a0018c0037t0053g0067others(3): Show | 6 | HG01261.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-5447T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551007 | ||||||
| chr2:11551089
|
C | A | 46 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0012t0023g0085others(43): Show | 46 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-161-5365C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551089 | ||||||
| chr2:11551098
|
T | C | 233 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(230): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.-161-5356T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551098 | ||||||
| chr2:11551124
|
C | G | 46 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0012t0023g0085others(43): Show | 46 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-161-5330C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551124 | ||||||
| chr2:11551376
|
G | T | 2 | a0008c0006t0012g0112a0034c0046t0012g0097 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-161-5078G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551376 | ||||||
| chr2:11551640
|
C | A | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-161-4814C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551640 | ||||||
| chr2:11551688
|
T | C | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-161-4766T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551688 | ||||||
| chr2:11551691
|
A | G | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-161-4763A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551691 | ||||||
| chr2:11551740
|
G | A | 2 | a0011c0008t0003g0027a0011c0008t0003g0297 | 2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-161-4714G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551740 | ||||||
| chr2:11551762
|
C | T | 1 | a0004c0004t0002g0281 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-161-4692C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551762 | ||||||
| chr2:11551763
|
G | T | 14 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0037g0023others(11): Show | 14 | HG00140.hp1 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-161-4691G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551763 | ||||||
| chr2:11551796
|
C | T | 1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-161-4658C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551796 | ||||||
| chr2:11551960
|
A | G | 1 | a0003c0003t0002g0257 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-161-4494A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551960 | ||||||
| chr2:11551980
|
A | C | 40 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0012t0023g0085others(37): Show | 40 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-161-4474A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551980 | ||||||
| chr2:11551993
|
G | C | 14 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0037g0023others(11): Show | 14 | HG00140.hp1 HG01109.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-161-4461G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11551993 | ||||||
| chr2:11552002
|
A | G | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-161-4452A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552002 | ||||||
| chr2:11552009
|
G | A | 5 | a0002c0057t0059g0021a0007c0016t0015g0017a0008c0006t0054g0018others(2): Show | 5 | HG01109.hp2 HG02145.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-161-4445G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552009 | ||||||
| chr2:11552110
|
C | T | 157 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(154): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.-161-4344C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552110 | ||||||
| chr2:11552171
|
C | T | 1 | a0002c0005t0007g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-161-4283C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552171 | ||||||
| chr2:11552251
|
G | A | 1 | a0035c0042t0029g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-161-4203G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552251 | ||||||
| chr2:11552346
|
A | G | 198 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(195): Show | 198 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.-161-4108A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552346 | ||||||
| chr2:11552374
|
C | T | 1 | a0005c0002t0016g0164 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-161-4080C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552374 | ||||||
| chr2:11552480
|
G | T | 44 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0020g0307others(41): Show | 44 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.-161-3974G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552480 | ||||||
| chr2:11552538
|
C | A | 229 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(226): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.-161-3916C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552538 | ||||||
| chr2:11552608
|
A | G | 1 | a0005c0002t0048g0269 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-161-3846A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552608 | ||||||
| chr2:11552609
|
C | G | 4 | a0002c0007t0037g0023a0006c0033t0034g0302a0007c0015t0027g0004others(1): Show | 4 | HG03041.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161-3845C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552609 | ||||||
| chr2:11552665
|
G | C | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.-161-3789G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552665 | ||||||
| chr2:11552733
|
C | T | 3 | a0001c0001t0002g0193a0001c0001t0006g0217a0001c0001t0006g0255 | 3 | HG02056.hp2 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-161-3721C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552733 | ||||||
| chr2:11552737
|
C | A | 5 | a0002c0007t0037g0023a0007c0015t0027g0004a0007c0015t0027g0024others(2): Show | 5 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-3717C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552737 | ||||||
| chr2:11552737
|
C | T | 30 | a0001c0001t0001g0166a0001c0001t0005g0047a0001c0001t0006g0214others(27): Show | 30 | HG00639.hp1 HG01070.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-161-3717C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552737 | ||||||
| chr2:11552738
|
G | A | 2 | a0001c0001t0006g0217a0001c0001t0006g0255 | 2 | HG02056.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-161-3716G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552738 | ||||||
| chr2:11552739
|
C | T | 28 | a0001c0001t0002g0193a0001c0001t0006g0212a0001c0001t0007g0037others(25): Show | 28 | HG00621.hp2 HG02056.hp1 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.-161-3715C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552739 | ||||||
| chr2:11552752
|
C | T | 1 | a0006c0033t0034g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-161-3702C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552752 | ||||||
| chr2:11552757
|
A | G | 2 | a0002c0055t0044g0003a0006c0054t0043g0002 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-161-3697A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552757 | ||||||
| chr2:11552781
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-161-3673G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552781 | ||||||
| chr2:11552782
|
C | T | 7 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(4): Show | 7 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-161-3672C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552782 | ||||||
| chr2:11552786
|
C | T | 6 | a0002c0034t0019g0026a0002c0053t0019g0090a0005c0002t0003g0133others(3): Show | 6 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-3668C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552786 | ||||||
| chr2:11552799
|
C | T | 5 | a0002c0034t0019g0026a0002c0053t0019g0090a0009c0029t0041g0028others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-161-3655C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552799 | ||||||
| chr2:11552871
|
A | G | 11 | a0002c0007t0037g0023a0002c0034t0019g0026a0002c0053t0019g0090others(8): Show | 11 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-161-3583A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552871 | ||||||
| chr2:11552872
|
T | C | 6 | a0002c0007t0037g0023a0006c0033t0034g0302a0007c0015t0027g0004others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-3582T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552872 | ||||||
| chr2:11552880
|
C | G | 1 | a0001c0089t0002g0189 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-161-3574C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552880 | ||||||
| chr2:11552881
|
A | G | 1 | a0001c0089t0002g0189 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-161-3573A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552881 | ||||||
| chr2:11552882
|
C | T | 6 | a0001c0089t0002g0189a0002c0034t0019g0026a0002c0053t0019g0090others(3): Show | 6 | HG01081.hp1 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-3572C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552882 | ||||||
| chr2:11552903
|
G | T | 3 | a0001c0001t0006g0278a0004c0025t0008g0279a0004c0025t0008g0285 | 3 | NA18939.hp2 NA18945.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-161-3551G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552903 | ||||||
| chr2:11552957
|
T | C | 1 | a0009c0030t0016g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-161-3497T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552957 | ||||||
| chr2:11552958
|
C | A | 16 | a0002c0007t0001g0104a0002c0007t0001g0262a0003c0003t0001g0267others(13): Show | 16 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.-161-3496C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552958 | ||||||
| chr2:11552965
|
G | C | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161-3489G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552965 | ||||||
| chr2:11552969
|
C | T | 3 | a0001c0001t0004g0175a0046c0078t0011g0176a0047c0077t0002g0174 | 3 | NA18942.hp1 NA19000.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-161-3485C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552969 | ||||||
| chr2:11552976
|
C | G | 1 | a0001c0001t0030g0087 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-161-3478C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552976 | ||||||
| chr2:11552988
|
C | T | 1 | a0013c0018t0022g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-161-3466C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552988 | ||||||
| chr2:11552999
|
A | G | 32 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0005t0005g0063others(29): Show | 32 | HG00099.hp1 HG00639.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.-161-3455A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11552999 | ||||||
| chr2:11553005
|
G | A | 22 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0012t0023g0085others(19): Show | 22 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-161-3449G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553005 | ||||||
| chr2:11553009
|
C | CA | 8 | a0001c0001t0002g0222a0001c0001t0002g0286a0001c0001t0002g0287others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-3428dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11553009 | |||||
| chr2:11553009
|
C | CAA | 8 | a0002c0005t0005g0046a0002c0011t0002g0275a0002c0034t0019g0026others(5): Show | 8 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-161-3429_-161-342 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11553009 | |||||
| chr2:11553009
|
C | CAAA | 66 | a0001c0001t0006g0212a0001c0001t0007g0037a0001c0001t0007g0062others(63): Show | 66 | HG00140.hp1 HG00621.hp2 HG01070.hp2 others(63): Show |
intron_variant | MODIFIER | c.-161-3430_-161-342 others(7): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11553009 | |||||
| chr2:11553009
|
C | CAAAA | 45 | a0001c0001t0001g0166a0001c0001t0005g0168a0002c0007t0001g0104others(42): Show | 45 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-161-3431_-161-342 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11553009 | |||||
| chr2:11553009
|
C | CAAAAA | 6 | a0006c0056t0070g0179a0008c0006t0024g0143a0010c0035t0060g0126others(3): Show | 6 | HG02451.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-161-3432_-161-342 others(9): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11553009 | |||||
| chr2:11553032
|
G | A | 1 | a0004c0004t0004g0195 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-161-3422G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553032 | ||||||
| chr2:11553187
|
G | A | 1 | a0004c0004t0002g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-161-3267G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553187 | ||||||
| chr2:11553371
|
T | C | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.-161-3083T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553371 | ||||||
| chr2:11553487
|
AAAAC | A | 39 | a0002c0007t0020g0307a0002c0012t0023g0085a0002c0012t0023g0086others(36): Show | 39 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.-161-2955_-161-295 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11553487 | |||||
| chr2:11553522
|
T | C | 105 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(102): Show | 105 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.-161-2932T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553522 | ||||||
| chr2:11553600
|
C | A | 2 | a0002c0055t0044g0003a0006c0054t0043g0002 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-161-2854C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553600 | ||||||
| chr2:11553691
|
T | C | 106 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(103): Show | 106 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.-161-2763T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553691 | ||||||
| chr2:11553710
|
G | A | 21 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(18): Show | 21 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-161-2744G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553710 | ||||||
| chr2:11553762
|
T | C | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.-161-2692T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553762 | ||||||
| chr2:11553778
|
A | G | 1 | a0005c0002t0001g0142 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-161-2676A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553778 | ||||||
| chr2:11553880
|
T | C | 105 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(102): Show | 105 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.-161-2574T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553880 | ||||||
| chr2:11553892
|
T | C | 105 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(102): Show | 105 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.-161-2562T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553892 | ||||||
| chr2:11553911
|
T | C | 61 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(58): Show | 61 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-161-2543T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11553911 | ||||||
| chr2:11553930
|
AAAGCTTC others(14): Show |
A | 61 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(58): Show | 61 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-161-2518_-161-249 others(25): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr2 | 11553930 | |||||
| chr2:11554005
|
G | A | 1 | a0004c0004t0004g0197 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-161-2449G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554005 | ||||||
| chr2:11554075
|
C | A | 4 | a0008c0006t0017g0259a0009c0028t0003g0260a0010c0031t0046g0096others(1): Show | 4 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-161-2379C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554075 | ||||||
| chr2:11554125
|
A | G | 107 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-161-2329A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554125 | ||||||
| chr2:11554156
|
G | T | 1 | a0004c0004t0011g0211 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-161-2298G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554156 | ||||||
| chr2:11554244
|
A | G | 18 | a0002c0007t0001g0104a0002c0007t0001g0262a0003c0003t0001g0267others(15): Show | 18 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-2210A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554244 | ||||||
| chr2:11554280
|
C | T | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.-161-2174C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554280 | ||||||
| chr2:11554441
|
A | G | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-161-2013A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554441 | ||||||
| chr2:11554550
|
C | T | 104 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.-161-1904C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554550 | ||||||
| chr2:11554624
|
A | G | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.-161-1830A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554624 | ||||||
| chr2:11554656
|
T | C | 122 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-161-1798T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554656 | ||||||
| chr2:11554763
|
C | T | 1 | a0005c0002t0003g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-161-1691C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554763 | ||||||
| chr2:11554913
|
C | G | 32 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(29): Show | 32 | HG00639.hp1 HG00673.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.-161-1541C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554913 | ||||||
| chr2:11554976
|
G | A | 27 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(24): Show | 27 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.-161-1478G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554976 | ||||||
| chr2:11554983
|
T | C | 6 | a0007c0015t0021g0069a0008c0006t0015g0005a0008c0049t0015g0006others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-1471T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11554983 | ||||||
| chr2:11555034
|
A | G | 41 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(38): Show | 41 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.-161-1420A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555034 | ||||||
| chr2:11555180
|
G | A | 18 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(15): Show | 18 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-1274G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555180 | ||||||
| chr2:11555309
|
G | A | 1 | a0015c0022t0010g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-161-1145G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555309 | ||||||
| chr2:11555313
|
G | A | 18 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(15): Show | 18 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-1141G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555313 | ||||||
| chr2:11555448
|
G | A | 3 | a0002c0007t0020g0307a0009c0028t0020g0304a0030c0051t0042g0306 | 3 | HG02818.hp2 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-161-1006G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555448 | ||||||
| chr2:11555501
|
T | C | 18 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(15): Show | 18 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-953T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555501 | ||||||
| chr2:11555609
|
G | A | 1 | a0035c0042t0029g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-161-845G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555609 | ||||||
| chr2:11555809
|
A | G | 18 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(15): Show | 18 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-645A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555809 | ||||||
| chr2:11555866
|
A | T | 6 | a0002c0007t0037g0023a0006c0033t0034g0302a0007c0015t0027g0004others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-161-588A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555866 | ||||||
| chr2:11555889
|
T | C | 18 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(15): Show | 18 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-565T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555889 | ||||||
| chr2:11555930
|
G | C | 40 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(37): Show | 40 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.-161-524G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11555930 | ||||||
| chr2:11556205
|
C | T | 18 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(15): Show | 18 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-161-249C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11556205 | ||||||
| chr2:11556217
|
G | A | 1 | a0012c0010t0002g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-161-237G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 1/32 | chr2 | 11556217 | ||||||
| chr2:11556868
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.157+97C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11556868 | ||||||
| chr2:11557080
|
G | A | 122 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.157+309G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557080 | ||||||
| chr2:11557157
|
G | A | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+386G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557157 | ||||||
| chr2:11557170
|
T | C | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+399T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557170 | ||||||
| chr2:11557197
|
CA | C | 11 | a0002c0007t0020g0307a0002c0034t0019g0026a0002c0053t0019g0090others(8): Show | 11 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.157+430delA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr2 | 11557197 | |||||
| chr2:11557245
|
A | G | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+474A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557245 | ||||||
| chr2:11557401
|
T | C | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.157+630T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557401 | ||||||
| chr2:11557489
|
A | G | 2 | a0002c0007t0052g0075a0013c0018t0022g0030 | 2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.157+718A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557489 | ||||||
| chr2:11557497
|
C | A | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+726C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557497 | ||||||
| chr2:11557497
|
C | T | 1 | a0001c0001t0018g0258 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.157+726C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557497 | ||||||
| chr2:11557676
|
T | G | 1 | a0004c0004t0002g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.157+905T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557676 | ||||||
| chr2:11557688
|
C | T | 1 | a0007c0015t0021g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.157+917C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557688 | ||||||
| chr2:11557717
|
T | C | 15 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(12): Show | 15 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.157+946T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557717 | ||||||
| chr2:11557818
|
C | T | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+1047C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557818 | ||||||
| chr2:11557819
|
A | G | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+1048A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557819 | ||||||
| chr2:11557864
|
A | G | 1 | a0017c0024t0013g0228 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.157+1093A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11557864 | ||||||
| chr2:11558007
|
G | A | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+1236G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558007 | ||||||
| chr2:11558183
|
T | C | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+1412T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558183 | ||||||
| chr2:11558208
|
G | A | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+1437G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558208 | ||||||
| chr2:11558249
|
C | G | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.157+1478C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558249 | ||||||
| chr2:11558408
|
G | A | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+1637G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558408 | ||||||
| chr2:11558447
|
G | A | 6 | a0002c0007t0037g0023a0006c0033t0034g0302a0007c0015t0027g0004others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+1676G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558447 | ||||||
| chr2:11558531
|
A | G | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.157+1760A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558531 | ||||||
| chr2:11558552
|
A | G | 3 | a0007c0016t0001g0012a0007c0016t0001g0013a0008c0006t0017g0015 | 3 | HG02622.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.157+1781A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558552 | ||||||
| chr2:11558728
|
C | T | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.157+1957C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558728 | ||||||
| chr2:11558743
|
A | T | 123 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.157+1972A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558743 | ||||||
| chr2:11558842
|
C | T | 1 | a0016c0021t0017g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.157+2071C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11558842 | ||||||
| chr2:11559000
|
G | T | 1 | a0006c0014t0003g0051 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.157+2229G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559000 | ||||||
| chr2:11559027
|
A | G | 7 | a0007c0015t0021g0069a0008c0006t0015g0005a0008c0049t0015g0006others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.157+2256A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559027 | ||||||
| chr2:11559444
|
T | A | 41 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(38): Show | 41 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.157+2673T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559444 | ||||||
| chr2:11559551
|
G | A | 2 | a0002c0055t0044g0003a0006c0054t0043g0002 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.157+2780G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559551 | ||||||
| chr2:11559621
|
G | A | 18 | a0002c0007t0001g0104a0002c0007t0001g0262a0003c0003t0001g0267others(15): Show | 18 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.158-2842G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559621 | ||||||
| chr2:11559721
|
C | T | 1 | a0001c0001t0006g0217 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.158-2742C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559721 | ||||||
| chr2:11559767
|
G | A | 10 | a0005c0066t0022g0072a0014c0023t0014g0068a0014c0023t0014g0071others(7): Show | 10 | HG01070.hp2 HG01261.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-2696G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559767 | ||||||
| chr2:11559804
|
G | A | 1 | a0005c0002t0003g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.158-2659G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559804 | ||||||
| chr2:11559820
|
G | A | 15 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(12): Show | 15 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.158-2643G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559820 | ||||||
| chr2:11559838
|
C | A | 2 | a0002c0055t0044g0003a0006c0054t0043g0002 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.158-2625C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559838 | ||||||
| chr2:11559895
|
A | G | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.158-2568A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559895 | ||||||
| chr2:11559908
|
G | A | 2 | a0005c0002t0010g0101a0005c0002t0050g0084 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.158-2555G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559908 | ||||||
| chr2:11559944
|
A | G | 15 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(12): Show | 15 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.158-2519A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559944 | ||||||
| chr2:11559952
|
C | G | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.158-2511C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559952 | ||||||
| chr2:11559971
|
G | A | 4 | a0001c0001t0006g0214a0004c0004t0002g0215a0004c0082t0002g0216others(1): Show | 4 | NA18952.hp1 NA18970.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-2492G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11559971 | ||||||
| chr2:11560436
|
C | T | 1 | a0001c0013t0002g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.158-2027C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11560436 | ||||||
| chr2:11560461
|
G | A | 1 | a0001c0001t0069g0288 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.158-2002G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11560461 | ||||||
| chr2:11560462
|
A | G | 1 | a0001c0001t0069g0288 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.158-2001A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11560462 | ||||||
| chr2:11560490
|
C | G | 1 | a0006c0064t0012g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.158-1973C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11560490 | ||||||
| chr2:11560649
|
T | C | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.158-1814T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11560649 | ||||||
| chr2:11560701
|
C | CA | 71 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(68): Show | 71 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.158-1751dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr2 | 11560701 | |||||
| chr2:11560701
|
C | CAA | 6 | a0007c0016t0015g0017a0008c0006t0054g0018a0013c0018t0003g0019others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-1752_158-1751d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr2 | 11560701 | |||||
| chr2:11560864
|
C | T | 15 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(12): Show | 15 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.158-1599C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11560864 | ||||||
| chr2:11560958
|
A | G | 28 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(25): Show | 28 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.158-1505A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11560958 | ||||||
| chr2:11561045
|
C | T | 1 | a0008c0006t0054g0018 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.158-1418C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561045 | ||||||
| chr2:11561083
|
T | C | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.158-1380T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561083 | ||||||
| chr2:11561166
|
A | G | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.158-1297A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561166 | ||||||
| chr2:11561193
|
C | T | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.158-1270C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561193 | ||||||
| chr2:11561196
|
T | C | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.158-1267T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561196 | ||||||
| chr2:11561302
|
T | A | 1 | a0001c0001t0006g0212 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.158-1161T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561302 | ||||||
| chr2:11561319
|
T | TGTGTGTC others(5): Show |
1 | a0001c0001t0069g0288 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.158-1139_158-1128d others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr2 | 11561319 | |||||
| chr2:11561360
|
T | TA | 60 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(57): Show | 60 | HG00099.hp1 HG00621.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.158-1102dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr2 | 11561360 | |||||
| chr2:11561361
|
A | AAT | 48 | a0002c0005t0001g0036a0002c0005t0007g0031a0002c0007t0001g0104others(45): Show | 48 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.158-1102_158-1101i others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561361 | ||||||
| chr2:11561361
|
ATTT | A | 10 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(7): Show | 10 | HG01109.hp1 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-1085_158-1083d others(5): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr2 | 11561361 | |||||
| chr2:11561362
|
T | A | 113 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(110): Show | 113 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.158-1101T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561362 | ||||||
| chr2:11561363
|
T | A | 1 | a0001c0089t0002g0189 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.158-1100T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561363 | ||||||
| chr2:11561365
|
T | A | 10 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(7): Show | 10 | HG01109.hp1 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-1098T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561365 | ||||||
| chr2:11561366
|
T | A | 5 | a0008c0006t0015g0005a0008c0049t0015g0006a0010c0032t0028g0007others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-1097T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561366 | ||||||
| chr2:11561394
|
T | TA | 15 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(12): Show | 15 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.158-1069_158-1068i others(3): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561394 | ||||||
| chr2:11561467
|
A | G | 17 | a0002c0007t0037g0023a0002c0055t0044g0003a0005c0002t0010g0119others(14): Show | 17 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.158-996A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561467 | ||||||
| chr2:11561607
|
C | T | 28 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(25): Show | 28 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.158-856C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561607 | ||||||
| chr2:11561683
|
C | T | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.158-780C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561683 | ||||||
| chr2:11561716
|
C | T | 11 | a0002c0007t0020g0307a0002c0034t0019g0026a0002c0053t0019g0090others(8): Show | 11 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.158-747C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561716 | ||||||
| chr2:11561717
|
G | A | 13 | a0003c0003t0001g0141a0003c0003t0001g0148a0003c0003t0002g0225others(10): Show | 13 | HG00099.hp2 HG01071.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-746G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561717 | ||||||
| chr2:11561877
|
A | G | 1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.158-586A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561877 | ||||||
| chr2:11561976
|
A | G | 1 | a0001c0001t0073g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.158-487A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11561976 | ||||||
| chr2:11562113
|
C | T | 15 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(12): Show | 15 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.158-350C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11562113 | ||||||
| chr2:11562358
|
C | T | 9 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(6): Show | 9 | HG00639.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-105C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11562358 | ||||||
| chr2:11562455
|
G | C | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
splice_region_variant&intron_variant | LOW | c.158-8G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 2/32 | chr2 | 11562455 | ||||||
| chr2:11562736
|
C | T | 8 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(5): Show | 8 | HG01109.hp1 HG02630.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+154C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11562736 | ||||||
| chr2:11562834
|
T | C | 122 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.277+252T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11562834 | ||||||
| chr2:11562966
|
A | ATCTTTCT others(1): Show |
56 | a0002c0007t0020g0307a0002c0012t0023g0085a0002c0012t0023g0086others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.277+394_277+401dup others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr2 | 11562966 | |||||
| chr2:11562980
|
C | CTTTCTTT others(2): Show |
6 | a0002c0007t0037g0023a0006c0033t0034g0302a0007c0015t0027g0004others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+401_277+402ins others(9): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr2 | 11562980 | |||||
| chr2:11562984
|
T | C | 1 | a0005c0002t0003g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.277+402T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11562984 | ||||||
| chr2:11563209
|
G | C | 1 | a0003c0003t0005g0270 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.277+627G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563209 | ||||||
| chr2:11563362
|
G | A | 1 | a0002c0005t0001g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.277+780G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563362 | ||||||
| chr2:11563443
|
T | C | 2 | a0005c0002t0013g0187a0005c0002t0013g0188 | 2 | HG01081.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.277+861T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563443 | ||||||
| chr2:11563461
|
C | G | 1 | a0008c0060t0061g0305 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.277+879C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563461 | ||||||
| chr2:11563502
|
T | G | 1 | a0001c0001t0005g0168 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.277+920T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563502 | ||||||
| chr2:11563643
|
C | T | 1 | a0011c0008t0003g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.277+1061C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563643 | ||||||
| chr2:11563710
|
A | G | 3 | a0007c0016t0001g0012a0007c0016t0001g0013a0008c0006t0017g0015 | 3 | HG02622.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.277+1128A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563710 | ||||||
| chr2:11563812
|
A | G | 6 | a0002c0007t0037g0023a0006c0033t0034g0302a0007c0015t0027g0004others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+1230A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563812 | ||||||
| chr2:11563862
|
T | G | 3 | a0003c0038t0001g0083a0003c0038t0001g0088a0044c0068t0009g0080 | 3 | HG01070.hp1 HG01071.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.277+1280T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563862 | ||||||
| chr2:11563930
|
A | G | 1 | a0009c0030t0016g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.277+1348A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11563930 | ||||||
| chr2:11564085
|
T | C | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.277+1503T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564085 | ||||||
| chr2:11564117
|
C | T | 24 | a0002c0007t0020g0307a0002c0007t0037g0023a0002c0055t0044g0003others(21): Show | 24 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.277+1535C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564117 | ||||||
| chr2:11564158
|
G | A | 36 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(33): Show | 36 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.277+1576G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564158 | ||||||
| chr2:11564300
|
C | G | 18 | a0002c0007t0001g0104a0002c0007t0001g0262a0003c0003t0001g0267others(15): Show | 18 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.277+1718C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564300 | ||||||
| chr2:11564321
|
G | A | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.277+1739G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564321 | ||||||
| chr2:11564330
|
G | GAGGT | 24 | a0002c0007t0020g0307a0002c0007t0037g0023a0002c0055t0044g0003others(21): Show | 24 | HG00099.hp1 HG00733.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.277+1752_277+1755d others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr2 | 11564330 | |||||
| chr2:11564620
|
C | T | 31 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(28): Show | 31 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.278-1860C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564620 | ||||||
| chr2:11564660
|
G | T | 3 | a0007c0016t0015g0017a0013c0018t0003g0019a0035c0042t0029g0020 | 3 | HG02145.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.278-1820G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564660 | ||||||
| chr2:11564710
|
G | T | 103 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(100): Show | 103 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.278-1770G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564710 | ||||||
| chr2:11564843
|
C | T | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.278-1637C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564843 | ||||||
| chr2:11564844
|
G | A | 2 | a0007c0043t0035g0095a0021c0040t0036g0089 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.278-1636G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564844 | ||||||
| chr2:11564846
|
G | A | 1 | a0002c0007t0001g0262 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.278-1634G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564846 | ||||||
| chr2:11564954
|
T | C | 18 | a0002c0034t0031g0263a0007c0015t0021g0069a0007c0044t0039g0011others(15): Show | 18 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.278-1526T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564954 | ||||||
| chr2:11564988
|
G | A | 2 | a0005c0002t0010g0119a0005c0002t0010g0124 | 2 | HG00099.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.278-1492G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11564988 | ||||||
| chr2:11565143
|
T | C | 1 | a0012c0010t0002g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.278-1337T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11565143 | ||||||
| chr2:11565598
|
A | G | 76 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(73): Show | 76 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.278-882A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11565598 | ||||||
| chr2:11565613
|
T | C | 106 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(103): Show | 106 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.278-867T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11565613 | ||||||
| chr2:11565670
|
A | G | 3 | a0007c0044t0039g0011a0008c0006t0019g0076a0009c0029t0020g0016 | 3 | HG02723.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.278-810A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11565670 | ||||||
| chr2:11565721
|
C | T | 2 | a0007c0058t0024g0125a0022c0059t0023g0110 | 2 | HG01175.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.278-759C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11565721 | ||||||
| chr2:11565770
|
C | A | 18 | a0002c0007t0001g0104a0002c0007t0001g0262a0003c0003t0002g0257others(15): Show | 18 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.278-710C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11565770 | ||||||
| chr2:11565770
|
C | T | 1 | a0009c0028t0003g0260 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.278-710C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11565770 | ||||||
| chr2:11565887
|
CTTGT | C | 3 | a0003c0003t0001g0148a0005c0002t0010g0123a0015c0022t0010g0140 | 3 | HG01071.hp1 HG01168.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.278-590_278-587del others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr2 | 11565887 | |||||
| chr2:11565925
|
T | G | 1 | a0009c0019t0012g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.278-555T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11565925 | ||||||
| chr2:11566005
|
G | A | 12 | a0002c0055t0044g0003a0006c0054t0043g0002a0008c0006t0012g0112others(9): Show | 12 | HG01109.hp1 HG01884.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.278-475G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11566005 | ||||||
| chr2:11566019
|
T | TTATATA | 58 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(55): Show | 58 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.278-449_278-444dup others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr2 | 11566019 | |||||
| chr2:11566019
|
T | TTATATAT others(1): Show |
27 | a0002c0005t0001g0066a0002c0005t0005g0046a0002c0007t0001g0104others(24): Show | 27 | HG00639.hp1 HG00733.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.278-451_278-444dup others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr2 | 11566019 | |||||
| chr2:11566019
|
T | TTATATAT others(3): Show |
6 | a0002c0012t0024g0127a0002c0012t0065g0103a0002c0020t0067g0171others(3): Show | 6 | HG00673.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-453_278-444dup others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr2 | 11566019 | |||||
| chr2:11566019
|
T | TTATATAT others(5): Show |
2 | a0002c0007t0020g0307a0002c0007t0052g0075 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.278-455_278-444dup others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | INFO_REALIGN_3_PRIME | chr2 | 11566019 | |||||
| chr2:11566200
|
G | A | 7 | a0001c0001t0002g0247a0004c0004t0004g0239a0004c0004t0004g0242others(4): Show | 7 | HG00735.hp1 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-280G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11566200 | ||||||
| chr2:11566209
|
G | A | 8 | a0002c0055t0044g0003a0006c0054t0043g0002a0008c0006t0012g0112others(5): Show | 8 | HG01109.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.278-271G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11566209 | ||||||
| chr2:11566213
|
C | T | 1 | a0004c0025t0008g0277 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.278-267C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11566213 | ||||||
| chr2:11566276
|
C | T | 1 | a0003c0076t0007g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.278-204C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11566276 | ||||||
| chr2:11566352
|
T | C | 45 | a0002c0007t0020g0307a0002c0007t0037g0023a0002c0012t0023g0085others(42): Show | 45 | HG00639.hp1 HG00673.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.278-128T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11566352 | ||||||
| chr2:11566367
|
C | T | 1 | a0017c0024t0013g0228 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.278-113C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11566367 | ||||||
| chr2:11566451
|
A | C | 1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.278-29A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 3/32 | chr2 | 11566451 | ||||||
| chr2:11566766
|
C | G | 77 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(74): Show | 77 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.454+110C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11566766 | ||||||
| chr2:11566818
|
G | A | 1 | a0002c0005t0051g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.454+162G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11566818 | ||||||
| chr2:11566954
|
C | T | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.454+298C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11566954 | ||||||
| chr2:11566965
|
C | T | 2 | a0008c0006t0005g0121a0031c0050t0006g0238 | 2 | HG01192.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.454+309C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11566965 | ||||||
| chr2:11566996
|
A | G | 5 | a0008c0006t0015g0005a0008c0049t0015g0006a0010c0032t0028g0007others(2): Show | 5 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+340A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11566996 | ||||||
| chr2:11567013
|
GTTGCTGC others(1): Show |
G | 20 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0052g0075others(17): Show | 20 | HG00423.hp2 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.454+359_454+366del others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr2 | 11567013 | |||||
| chr2:11567283
|
T | C | 99 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(96): Show | 99 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.454+627T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11567283 | ||||||
| chr2:11567345
|
G | A | 39 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(36): Show | 39 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.454+689G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11567345 | ||||||
| chr2:11567530
|
T | G | 20 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0052g0075others(17): Show | 20 | HG00423.hp2 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.454+874T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11567530 | ||||||
| chr2:11567759
|
C | T | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.454+1103C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11567759 | ||||||
| chr2:11567760
|
G | A | 3 | a0002c0007t0037g0023a0007c0015t0027g0004a0007c0015t0027g0024 | 3 | HG03041.hp2 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.454+1104G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11567760 | ||||||
| chr2:11567889
|
T | C | 1 | a0005c0002t0003g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.454+1233T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11567889 | ||||||
| chr2:11567935
|
C | T | 2 | a0001c0001t0002g0210a0001c0001t0002g0222 | 2 | NA18977.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.454+1279C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11567935 | ||||||
| chr2:11567964
|
C | T | 1 | a0044c0068t0009g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.454+1308C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11567964 | ||||||
| chr2:11568070
|
C | T | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.454+1414C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11568070 | ||||||
| chr2:11568183
|
A | G | 1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.454+1527A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11568183 | ||||||
| chr2:11568279
|
A | T | 1 | a0003c0003t0001g0147 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.454+1623A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11568279 | ||||||
| chr2:11568379
|
C | T | 1 | a0012c0010t0006g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.454+1723C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11568379 | ||||||
| chr2:11568442
|
T | G | 4 | a0007c0016t0015g0017a0008c0006t0054g0018a0013c0018t0003g0019others(1): Show | 4 | HG01109.hp2 HG02145.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+1786T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11568442 | ||||||
| chr2:11568625
|
G | A | 26 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0037g0023others(23): Show | 26 | HG00423.hp2 HG00621.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.454+1969G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11568625 | ||||||
| chr2:11568707
|
G | C | 239 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(236): Show | 239 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.454+2051G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11568707 | ||||||
| chr2:11568979
|
G | A | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.454+2323G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11568979 | ||||||
| chr2:11569021
|
G | A | 14 | a0002c0007t0037g0023a0002c0055t0044g0003a0006c0033t0034g0302others(11): Show | 14 | HG01109.hp1 HG02630.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.454+2365G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569021 | ||||||
| chr2:11569028
|
A | G | 8 | a0002c0055t0044g0003a0006c0054t0043g0002a0008c0006t0012g0112others(5): Show | 8 | HG01109.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.454+2372A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569028 | ||||||
| chr2:11569066
|
G | A | 1 | a0006c0014t0003g0051 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.454+2410G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569066 | ||||||
| chr2:11569071
|
T | C | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.454+2415T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569071 | ||||||
| chr2:11569096
|
T | C | 1 | a0013c0018t0022g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.454+2440T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569096 | ||||||
| chr2:11569169
|
C | T | 2 | a0015c0022t0010g0132a0041c0075t0001g0153 | 2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.454+2513C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569169 | ||||||
| chr2:11569197
|
T | C | 1 | a0015c0022t0010g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.454+2541T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569197 | ||||||
| chr2:11569278
|
C | T | 19 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0052g0075others(16): Show | 19 | HG00423.hp2 HG00621.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.454+2622C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569278 | ||||||
| chr2:11569324
|
A | G | 6 | a0002c0007t0037g0023a0006c0033t0034g0302a0007c0015t0027g0004others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+2668A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569324 | ||||||
| chr2:11569333
|
G | T | 21 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(18): Show | 21 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.454+2677G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569333 | ||||||
| chr2:11569460
|
A | C | 21 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(18): Show | 21 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.454+2804A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569460 | ||||||
| chr2:11569558
|
A | G | 17 | a0002c0007t0001g0104a0002c0007t0001g0262a0006c0056t0070g0179others(14): Show | 17 | HG00423.hp2 HG00621.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.454+2902A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569558 | ||||||
| chr2:11569769
|
C | T | 1 | a0001c0001t0006g0212 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.454+3113C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569769 | ||||||
| chr2:11569840
|
G | A | 7 | a0007c0015t0021g0069a0008c0006t0015g0005a0008c0049t0015g0006others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.454+3184G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569840 | ||||||
| chr2:11569843
|
A | G | 2 | a0005c0002t0010g0101a0005c0002t0050g0084 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.454+3187A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569843 | ||||||
| chr2:11569862
|
G | A | 8 | a0002c0055t0044g0003a0006c0054t0043g0002a0008c0006t0012g0112others(5): Show | 8 | HG01109.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.454+3206G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11569862 | ||||||
| chr2:11570097
|
C | T | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.454+3441C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11570097 | ||||||
| chr2:11570177
|
G | A | 7 | a0001c0001t0002g0210a0001c0001t0002g0222a0001c0001t0006g0217others(4): Show | 7 | HG00408.hp1 HG02056.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.454+3521G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11570177 | ||||||
| chr2:11570228
|
G | A | 1 | a0001c0001t0069g0288 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.454+3572G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11570228 | ||||||
| chr2:11570360
|
G | A | 1 | a0004c0004t0008g0273 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.454+3704G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11570360 | ||||||
| chr2:11570401
|
T | TA | 36 | a0002c0005t0001g0066a0002c0007t0020g0307a0002c0007t0052g0075others(33): Show | 36 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.454+3761dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr2 | 11570401 | |||||
| chr2:11570401
|
T | TAA | 18 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(15): Show | 18 | HG00639.hp1 HG00673.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.454+3760_454+3761d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr2 | 11570401 | |||||
| chr2:11570401
|
TAAA | T | 11 | a0002c0007t0001g0104a0002c0007t0001g0262a0006c0056t0070g0179others(8): Show | 11 | HG00423.hp2 HG00621.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.454+3759_454+3761d others(5): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr2 | 11570401 | |||||
| chr2:11570401
|
TAAAA | T | 6 | a0007c0015t0021g0069a0008c0006t0015g0005a0008c0049t0015g0006others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.454+3758_454+3761d others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr2 | 11570401 | |||||
| chr2:11570523
|
CT | C | 6 | a0002c0020t0026g0219a0003c0076t0007g0102a0004c0004t0004g0289others(3): Show | 6 | HG02922.hp2 NA18953.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.454+3879delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr2 | 11570523 | |||||
| chr2:11570575
|
A | G | 40 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(37): Show | 40 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.454+3919A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11570575 | ||||||
| chr2:11570590
|
A | G | 243 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(240): Show | 243 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.454+3934A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11570590 | ||||||
| chr2:11571014
|
C | G | 1 | a0013c0018t0022g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.454+4358C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571014 | ||||||
| chr2:11571034
|
T | C | 1 | a0001c0001t0032g0251 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.454+4378T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571034 | ||||||
| chr2:11571038
|
G | GAT | 21 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(18): Show | 21 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.454+4396_454+4397d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr2 | 11571038 | |||||
| chr2:11571041
|
A | G | 5 | a0001c0001t0002g0192a0012c0010t0002g0184a0012c0010t0002g0190others(2): Show | 5 | HG00735.hp2 HG01106.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.454+4385A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571041 | ||||||
| chr2:11571096
|
A | C | 84 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(81): Show | 84 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.454+4440A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571096 | ||||||
| chr2:11571126
|
G | A | 21 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(18): Show | 21 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.454+4470G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571126 | ||||||
| chr2:11571207
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.454+4551T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571207 | ||||||
| chr2:11571373
|
A | G | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.454+4717A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571373 | ||||||
| chr2:11571430
|
A | G | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.454+4774A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571430 | ||||||
| chr2:11571488
|
A | G | 3 | a0002c0007t0020g0307a0009c0028t0020g0304a0030c0051t0042g0306 | 3 | HG02818.hp2 HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.454+4832A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571488 | ||||||
| chr2:11571532
|
C | T | 1 | a0005c0002t0048g0269 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.455-4821C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571532 | ||||||
| chr2:11571586
|
A | C | 1 | a0001c0089t0002g0189 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.455-4767A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571586 | ||||||
| chr2:11571603
|
C | T | 15 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0037g0023others(12): Show | 15 | HG00423.hp2 HG00621.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.455-4750C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571603 | ||||||
| chr2:11571657
|
A | G | 8 | a0002c0055t0044g0003a0006c0054t0043g0002a0008c0006t0012g0112others(5): Show | 8 | HG01109.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-4696A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571657 | ||||||
| chr2:11571733
|
C | T | 1 | a0039c0074t0014g0301 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.455-4620C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571733 | ||||||
| chr2:11571737
|
G | A | 39 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(36): Show | 39 | HG00621.hp2 HG00733.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.455-4616G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571737 | ||||||
| chr2:11571742
|
G | A | 1 | a0005c0002t0003g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.455-4611G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571742 | ||||||
| chr2:11571772
|
G | A | 1 | a0008c0060t0061g0305 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.455-4581G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571772 | ||||||
| chr2:11571811
|
C | T | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-4542C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571811 | ||||||
| chr2:11571860
|
A | G | 21 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(18): Show | 21 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.455-4493A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571860 | ||||||
| chr2:11571900
|
A | G | 21 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(18): Show | 21 | HG00639.hp1 HG00673.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.455-4453A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571900 | ||||||
| chr2:11571949
|
G | T | 102 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(99): Show | 102 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.455-4404G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571949 | ||||||
| chr2:11571962
|
G | C | 84 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(81): Show | 84 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.455-4391G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11571962 | ||||||
| chr2:11572031
|
A | G | 1 | a0015c0022t0001g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.455-4322A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11572031 | ||||||
| chr2:11572292
|
G | C | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-4061G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11572292 | ||||||
| chr2:11572489
|
A | G | 8 | a0007c0015t0021g0069a0008c0006t0015g0005a0008c0049t0015g0006others(5): Show | 8 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.455-3864A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11572489 | ||||||
| chr2:11572764
|
C | T | 1 | a0005c0002t0003g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.455-3589C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11572764 | ||||||
| chr2:11573078
|
GCCTCACA others(3): Show |
G | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-3271_455-3262d others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | INFO_REALIGN_3_PRIME | chr2 | 11573078 | |||||
| chr2:11573139
|
T | C | 1 | a0006c0033t0003g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.455-3214T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573139 | ||||||
| chr2:11573146
|
T | C | 1 | a0006c0014t0003g0060 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.455-3207T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573146 | ||||||
| chr2:11573238
|
C | T | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-3115C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573238 | ||||||
| chr2:11573371
|
T | C | 8 | a0002c0055t0044g0003a0006c0054t0043g0002a0008c0006t0012g0112others(5): Show | 8 | HG01109.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-2982T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573371 | ||||||
| chr2:11573784
|
G | A | 8 | a0002c0055t0044g0003a0006c0054t0043g0002a0008c0006t0012g0112others(5): Show | 8 | HG01109.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-2569G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573784 | ||||||
| chr2:11573811
|
G | A | 6 | a0008c0006t0012g0112a0008c0006t0024g0143a0011c0008t0012g0093others(3): Show | 6 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-2542G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573811 | ||||||
| chr2:11573823
|
G | A | 1 | a0009c0019t0074g0284 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.455-2530G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573823 | ||||||
| chr2:11573864
|
A | C | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-2489A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573864 | ||||||
| chr2:11573961
|
G | C | 8 | a0002c0055t0044g0003a0006c0054t0043g0002a0008c0006t0012g0112others(5): Show | 8 | HG01109.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.455-2392G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573961 | ||||||
| chr2:11573986
|
C | T | 1 | a0052c0085t0011g0280 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.455-2367C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11573986 | ||||||
| chr2:11574022
|
C | T | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-2331C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11574022 | ||||||
| chr2:11574135
|
C | T | 1 | a0001c0001t0018g0235 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.455-2218C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11574135 | ||||||
| chr2:11574238
|
C | T | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-2115C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11574238 | ||||||
| chr2:11574245
|
A | G | 1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.455-2108A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11574245 | ||||||
| chr2:11574300
|
A | G | 13 | a0002c0007t0020g0307a0002c0034t0019g0026a0002c0053t0019g0090others(10): Show | 13 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.455-2053A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11574300 | ||||||
| chr2:11574431
|
G | A | 9 | a0002c0007t0001g0104a0002c0007t0001g0262a0006c0056t0070g0179others(6): Show | 9 | HG00423.hp2 HG00621.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.455-1922G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11574431 | ||||||
| chr2:11574694
|
C | G | 1 | a0006c0033t0003g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.455-1659C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11574694 | ||||||
| chr2:11575052
|
A | C | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455-1301A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11575052 | ||||||
| chr2:11575416
|
A | G | 42 | a0002c0005t0001g0033a0002c0005t0001g0034a0002c0005t0001g0035others(39): Show | 42 | HG00621.hp2 HG00733.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.455-937A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11575416 | ||||||
| chr2:11575473
|
G | A | 1 | a0003c0003t0001g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.455-880G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11575473 | ||||||
| chr2:11575551
|
G | A | 7 | a0007c0015t0021g0069a0008c0006t0015g0005a0008c0049t0015g0006others(4): Show | 7 | HG02622.hp2 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.455-802G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11575551 | ||||||
| chr2:11575650
|
G | A | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-703G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11575650 | ||||||
| chr2:11575933
|
C | T | 14 | a0002c0007t0020g0307a0002c0034t0019g0026a0002c0053t0019g0090others(11): Show | 14 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.455-420C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11575933 | ||||||
| chr2:11575934
|
A | G | 24 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0007t0020g0307others(21): Show | 24 | HG00423.hp2 HG00621.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.455-419A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11575934 | ||||||
| chr2:11576113
|
G | A | 3 | a0007c0016t0015g0017a0013c0018t0003g0019a0035c0042t0029g0020 | 3 | HG02145.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.455-240G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11576113 | ||||||
| chr2:11576235
|
A | G | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.455-118A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11576235 | ||||||
| chr2:11576235
|
A | T | 1 | a0003c0003t0007g0159 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.455-118A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11576235 | ||||||
| chr2:11576250
|
C | T | 1 | a0006c0033t0003g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.455-103C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11576250 | ||||||
| chr2:11576303
|
A | G | 3 | a0008c0006t0017g0259a0009c0028t0003g0260a0013c0052t0049g0261 | 3 | HG02615.hp1 HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.455-50A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 4/32 | chr2 | 11576303 | ||||||
| chr2:11576652
|
A | G | 3 | a0007c0016t0015g0017a0013c0018t0003g0019a0035c0042t0029g0020 | 3 | HG02145.hp2 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.637+117A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11576652 | ||||||
| chr2:11576793
|
A | T | 235 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(232): Show | 235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.637+258A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11576793 | ||||||
| chr2:11576892
|
G | A | 1 | a0002c0061t0062g0134 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637+357G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11576892 | ||||||
| chr2:11576928
|
G | A | 1 | a0002c0005t0051g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.637+393G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11576928 | ||||||
| chr2:11576965
|
G | A | 4 | a0002c0005t0001g0045a0002c0005t0005g0046a0002c0005t0005g0063others(1): Show | 4 | NA18940.hp2 NA18979.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+430G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11576965 | ||||||
| chr2:11577055
|
C | T | 1 | a0005c0002t0003g0152 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.637+520C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577055 | ||||||
| chr2:11577071
|
G | A | 3 | a0002c0034t0019g0026a0002c0053t0019g0090a0010c0031t0038g0029 | 3 | HG02145.hp1 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.637+536G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577071 | ||||||
| chr2:11577099
|
C | T | 1 | a0007c0015t0021g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.637+564C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577099 | ||||||
| chr2:11577104
|
A | G | 5 | a0002c0007t0020g0307a0002c0034t0019g0026a0002c0053t0019g0090others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+569A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577104 | ||||||
| chr2:11577169
|
A | G | 2 | a0010c0031t0046g0096a0015c0022t0001g0081 | 2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.637+634A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577169 | ||||||
| chr2:11577213
|
TCAAGA | T | 4 | a0005c0002t0050g0084a0007c0016t0015g0017a0013c0018t0003g0019others(1): Show | 4 | HG01496.hp2 HG02145.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+683_637+687del others(5): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr2 | 11577213 | |||||
| chr2:11577303
|
A | G | 241 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(238): Show | 241 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.637+768A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577303 | ||||||
| chr2:11577485
|
T | C | 4 | a0005c0066t0022g0072a0006c0033t0034g0302a0018c0037t0053g0067others(1): Show | 4 | HG01261.hp1 HG02258.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-812T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577485 | ||||||
| chr2:11577630
|
C | T | 2 | a0008c0060t0061g0305a0021c0040t0036g0089 | 2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.638-667C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577630 | ||||||
| chr2:11577849
|
G | A | 1 | a0005c0002t0056g0129 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.638-448G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577849 | ||||||
| chr2:11577933
|
C | T | 2 | a0011c0008t0003g0027a0011c0008t0003g0297 | 2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.638-364C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11577933 | ||||||
| chr2:11578010
|
C | T | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.638-287C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11578010 | ||||||
| chr2:11578242
|
C | T | 1 | a0015c0022t0001g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.638-55C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11578242 | ||||||
| chr2:11578275
|
C | T | 5 | a0008c0006t0054g0018a0010c0035t0060g0126a0010c0035t0064g0128others(2): Show | 5 | HG00639.hp1 HG01109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-22C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11578275 | ||||||
| chr2:11578289
|
C | A | 6 | a0002c0007t0037g0023a0006c0033t0034g0302a0009c0029t0041g0028others(3): Show | 6 | HG02451.hp2 HG02486.hp2 HG02895.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.638-8C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 5/32 | chr2 | 11578289 | ||||||
| chr2:11578465
|
C | T | 147 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(144): Show | 147 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.772+34C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11578465 | ||||||
| chr2:11578473
|
G | A | 1 | a0043c0069t0003g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.772+42G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11578473 | ||||||
| chr2:11578648
|
A | C | 1 | a0002c0005t0051g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.772+217A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11578648 | ||||||
| chr2:11578680
|
A | G | 3 | a0002c0055t0044g0003a0011c0008t0045g0022a0013c0018t0022g0030 | 3 | HG03209.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.772+249A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11578680 | ||||||
| chr2:11578712
|
G | A | 1 | a0003c0003t0001g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.772+281G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11578712 | ||||||
| chr2:11578732
|
T | C | 136 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(133): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.772+301T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11578732 | ||||||
| chr2:11579072
|
C | T | 6 | a0010c0035t0060g0126a0010c0035t0064g0128a0011c0008t0045g0022others(3): Show | 6 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.772+641C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579072 | ||||||
| chr2:11579095
|
T | G | 1 | a0004c0004t0008g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.772+664T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579095 | ||||||
| chr2:11579167
|
T | C | 1 | a0004c0088t0025g0223 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.772+736T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579167 | ||||||
| chr2:11579170
|
C | A | 1 | a0006c0063t0063g0106 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.772+739C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579170 | ||||||
| chr2:11579284
|
C | T | 1 | a0001c0001t0002g0287 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.772+853C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579284 | ||||||
| chr2:11579439
|
GAATT | G | 15 | a0003c0038t0001g0083a0003c0038t0001g0088a0008c0006t0005g0121others(12): Show | 15 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.772+1011_772+1014d others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr2 | 11579439 | |||||
| chr2:11579453
|
G | A | 1 | a0009c0029t0020g0016 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.772+1022G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579453 | ||||||
| chr2:11579718
|
GAC | G | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.773-985_773-984del others(2): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579718 | ||||||
| chr2:11579723
|
G | A | 21 | a0002c0012t0065g0103a0007c0016t0001g0012a0007c0016t0001g0013others(18): Show | 21 | HG01070.hp2 HG01175.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.773-981G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579723 | ||||||
| chr2:11579750
|
C | T | 1 | a0033c0047t0031g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.773-954C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579750 | ||||||
| chr2:11579771
|
C | T | 1 | a0005c0002t0055g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.773-933C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579771 | ||||||
| chr2:11579832
|
T | C | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.773-872T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579832 | ||||||
| chr2:11579875
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.773-829C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579875 | ||||||
| chr2:11579990
|
G | T | 2 | a0006c0056t0070g0179a0006c0065t0033g0220 | 2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.773-714G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11579990 | ||||||
| chr2:11580084
|
C | A | 1 | a0002c0011t0009g0043 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.773-620C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11580084 | ||||||
| chr2:11580156
|
A | G | 29 | a0003c0038t0001g0083a0003c0038t0001g0088a0008c0006t0005g0121others(26): Show | 29 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.773-548A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11580156 | ||||||
| chr2:11580173
|
C | T | 34 | a0003c0038t0001g0083a0003c0038t0001g0088a0007c0044t0039g0011others(31): Show | 34 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.773-531C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11580173 | ||||||
| chr2:11580235
|
C | T | 1 | a0005c0002t0010g0101 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.773-469C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11580235 | ||||||
| chr2:11580516
|
G | A | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.773-188G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11580516 | ||||||
| chr2:11580543
|
C | T | 1 | a0013c0052t0049g0261 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.773-161C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11580543 | ||||||
| chr2:11580596
|
G | C | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.773-108G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 6/32 | chr2 | 11580596 | ||||||
| chr2:11580860
|
G | A | 13 | a0003c0038t0001g0083a0003c0038t0001g0088a0008c0006t0005g0121others(10): Show | 13 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.901+28G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11580860 | ||||||
| chr2:11581130
|
G | A | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.901+298G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581130 | ||||||
| chr2:11581203
|
A | G | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.901+371A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581203 | ||||||
| chr2:11581409
|
T | G | 120 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.901+577T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581409 | ||||||
| chr2:11581503
|
G | C | 1 | a0007c0015t0027g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.901+671G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581503 | ||||||
| chr2:11581642
|
T | G | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.901+810T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581642 | ||||||
| chr2:11581651
|
G | A | 1 | a0001c0001t0002g0241 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.901+819G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581651 | ||||||
| chr2:11581675
|
G | A | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.901+843G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581675 | ||||||
| chr2:11581690
|
A | G | 37 | a0002c0012t0065g0103a0007c0015t0021g0069a0007c0015t0027g0004others(34): Show | 37 | HG00423.hp2 HG00621.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.901+858A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581690 | ||||||
| chr2:11581821
|
G | T | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.901+989G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581821 | ||||||
| chr2:11581877
|
C | T | 3 | a0001c0001t0006g0278a0004c0025t0008g0279a0004c0025t0008g0285 | 3 | NA18939.hp2 NA18945.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.901+1045C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581877 | ||||||
| chr2:11581886
|
C | G | 170 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.901+1054C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581886 | ||||||
| chr2:11581956
|
C | T | 199 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.901+1124C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581956 | ||||||
| chr2:11581976
|
A | T | 206 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.901+1144A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11581976 | ||||||
| chr2:11582062
|
C | CA | 63 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(60): Show | 63 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.901+1230_901+1231i others(3): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582062 | ||||||
| chr2:11582062
|
C | CG | 143 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.901+1232dupG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr2 | 11582062 | |||||
| chr2:11582063
|
G | C | 63 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(60): Show | 63 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.901+1231G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582063 | ||||||
| chr2:11582082
|
AC | A | 19 | a0003c0038t0001g0083a0003c0038t0001g0088a0008c0006t0005g0121others(16): Show | 19 | HG00140.hp1 HG00741.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.901+1253delC | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr2 | 11582082 | |||||
| chr2:11582327
|
A | G | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.901+1495A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582327 | ||||||
| chr2:11582336
|
C | T | 24 | a0002c0012t0065g0103a0007c0015t0021g0069a0007c0015t0027g0004others(21): Show | 24 | HG01070.hp2 HG01175.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.901+1504C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582336 | ||||||
| chr2:11582342
|
G | A | 61 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(58): Show | 61 | HG00099.hp2 HG00558.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.901+1510G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582342 | ||||||
| chr2:11582449
|
A | G | 205 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.901+1617A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582449 | ||||||
| chr2:11582464
|
G | A | 11 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(8): Show | 11 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.901+1632G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582464 | ||||||
| chr2:11582493
|
G | A | 76 | a0002c0012t0065g0103a0003c0038t0001g0083a0003c0038t0001g0088others(73): Show | 76 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.901+1661G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582493 | ||||||
| chr2:11582702
|
G | A | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.901+1870G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582702 | ||||||
| chr2:11582735
|
C | T | 2 | a0007c0016t0015g0017a0009c0029t0041g0028 | 2 | HG02486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.901+1903C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582735 | ||||||
| chr2:11582821
|
G | A | 4 | a0002c0034t0031g0263a0010c0031t0038g0029a0010c0032t0028g0007others(1): Show | 4 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+1989G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582821 | ||||||
| chr2:11582833
|
A | G | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.901+2001A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582833 | ||||||
| chr2:11582895
|
C | T | 207 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.901+2063C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582895 | ||||||
| chr2:11582965
|
CA | C | 6 | a0005c0002t0055g0014a0010c0031t0046g0096a0013c0018t0022g0030others(3): Show | 6 | HG01884.hp1 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.901+2134delA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582965 | ||||||
| chr2:11582984
|
G | A | 112 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.901+2152G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582984 | ||||||
| chr2:11582998
|
C | G | 90 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.902-2163C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11582998 | ||||||
| chr2:11583020
|
T | TA | 6 | a0005c0002t0055g0014a0010c0031t0046g0096a0013c0018t0022g0030others(3): Show | 6 | HG01884.hp1 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.902-2140dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr2 | 11583020 | |||||
| chr2:11583073
|
T | G | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.902-2088T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583073 | ||||||
| chr2:11583147
|
C | T | 1 | a0038c0071t0009g0122 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.902-2014C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583147 | ||||||
| chr2:11583185
|
C | T | 90 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.902-1976C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583185 | ||||||
| chr2:11583204
|
G | A | 26 | a0002c0012t0065g0103a0007c0015t0021g0069a0007c0015t0027g0004others(23): Show | 26 | HG01070.hp2 HG01175.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.902-1957G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583204 | ||||||
| chr2:11583256
|
C | A | 1 | a0003c0009t0021g0308 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.902-1905C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583256 | ||||||
| chr2:11583381
|
A | C | 6 | a0005c0002t0055g0014a0010c0031t0046g0096a0013c0018t0022g0030others(3): Show | 6 | HG01884.hp1 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.902-1780A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583381 | ||||||
| chr2:11583406
|
G | A | 1 | a0001c0001t0032g0251 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.902-1755G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583406 | ||||||
| chr2:11583501
|
AT | A | 26 | a0002c0012t0065g0103a0007c0015t0021g0069a0007c0015t0027g0004others(23): Show | 26 | HG01070.hp2 HG01175.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.902-1650delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr2 | 11583501 | |||||
| chr2:11583501
|
ATT | A | 64 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(61): Show | 64 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.902-1651_902-1650d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr2 | 11583501 | |||||
| chr2:11583544
|
C | G | 3 | a0005c0002t0055g0014a0013c0018t0047g0303a0036c0041t0003g0091 | 3 | HG03139.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.902-1617C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583544 | ||||||
| chr2:11583557
|
G | A | 1 | a0044c0068t0009g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.902-1604G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583557 | ||||||
| chr2:11583610
|
G | A | 90 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.902-1551G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583610 | ||||||
| chr2:11583716
|
G | A | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.902-1445G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583716 | ||||||
| chr2:11583732
|
G | A | 118 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.902-1429G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583732 | ||||||
| chr2:11583850
|
ACT | A | 57 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(54): Show | 57 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.902-1308_902-1307d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr2 | 11583850 | |||||
| chr2:11583912
|
G | A | 1 | a0005c0002t0013g0187 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.902-1249G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583912 | ||||||
| chr2:11583999
|
G | A | 1 | a0003c0003t0001g0141 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.902-1162G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11583999 | ||||||
| chr2:11584018
|
G | A | 4 | a0007c0015t0021g0069a0007c0015t0027g0004a0007c0015t0027g0024others(1): Show | 4 | HG02630.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.902-1143G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584018 | ||||||
| chr2:11584033
|
A | G | 57 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(54): Show | 57 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.902-1128A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584033 | ||||||
| chr2:11584073
|
G | A | 1 | a0005c0073t0016g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.902-1088G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584073 | ||||||
| chr2:11584192
|
G | C | 1 | a0020c0039t0009g0050 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.902-969G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584192 | ||||||
| chr2:11584289
|
A | G | 2 | a0004c0004t0004g0239a0004c0004t0004g0242 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.902-872A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584289 | ||||||
| chr2:11584303
|
G | A | 1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.902-858G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584303 | ||||||
| chr2:11584303
|
G | C | 2 | a0010c0031t0046g0096a0013c0018t0022g0030 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.902-858G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584303 | ||||||
| chr2:11584349
|
A | G | 207 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.902-812A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584349 | ||||||
| chr2:11584369
|
T | G | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.902-792T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584369 | ||||||
| chr2:11584371
|
T | A | 1 | a0001c0001t0007g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.902-790T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584371 | ||||||
| chr2:11584418
|
A | G | 1 | a0007c0015t0021g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.902-743A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584418 | ||||||
| chr2:11584454
|
G | T | 107 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.902-707G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584454 | ||||||
| chr2:11584558
|
A | G | 207 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.902-603A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584558 | ||||||
| chr2:11584734
|
G | C | 1 | a0009c0028t0003g0260 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.902-427G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584734 | ||||||
| chr2:11584813
|
G | GGAGGCT | 25 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.902-340_902-335dup others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr2 | 11584813 | |||||
| chr2:11584923
|
T | C | 214 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.902-238T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584923 | ||||||
| chr2:11584968
|
C | T | 32 | a0007c0015t0021g0069a0007c0015t0027g0004a0007c0015t0027g0024others(29): Show | 32 | HG00423.hp2 HG00621.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.902-193C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584968 | ||||||
| chr2:11584998
|
T | G | 1 | a0041c0075t0001g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.902-163T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11584998 | ||||||
| chr2:11585053
|
G | GA | 119 | a0001c0001t0001g0166a0001c0001t0002g0032a0001c0001t0002g0192others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.902-97dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr2 | 11585053 | |||||
| chr2:11585060
|
A | AC | 3 | a0002c0007t0001g0104a0002c0061t0062g0134a0013c0052t0049g0261 | 3 | HG02630.hp2 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.902-101_902-100ins others(1): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11585060 | ||||||
| chr2:11585060
|
A | C | 8 | a0007c0017t0001g0157a0007c0017t0001g0167a0007c0017t0001g0170others(5): Show | 8 | HG00423.hp2 HG00621.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.902-101A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11585060 | ||||||
| chr2:11585065
|
C | A | 3 | a0010c0031t0046g0096a0013c0018t0022g0030a0030c0051t0042g0306 | 3 | HG01884.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.902-96C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11585065 | ||||||
| chr2:11585100
|
G | A | 13 | a0005c0002t0055g0014a0010c0031t0038g0029a0010c0031t0046g0096others(10): Show | 13 | HG01070.hp2 HG01884.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.902-61G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11585100 | ||||||
| chr2:11585115
|
G | A | 118 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.902-46G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11585115 | ||||||
| chr2:11585132
|
G | A | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.902-29G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 7/32 | chr2 | 11585132 | ||||||
| chr2:11585361
|
C | T | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015+87C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 8/32 | chr2 | 11585361 | ||||||
| chr2:11585369
|
C | T | 25 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1015+95C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 8/32 | chr2 | 11585369 | ||||||
| chr2:11585384
|
G | A | 25 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1015+110G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 8/32 | chr2 | 11585384 | ||||||
| chr2:11585605
|
C | T | 25 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1016-157C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 8/32 | chr2 | 11585605 | ||||||
| chr2:11585737
|
C | T | 25 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1016-25C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 8/32 | chr2 | 11585737 | ||||||
| chr2:11585925
|
G | A | 1 | a0001c0001t0002g0287 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1159+20G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11585925 | ||||||
| chr2:11585935
|
G | GA | 59 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(56): Show | 59 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1159+31dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11585935 | |||||
| chr2:11585951
|
G | A | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1159+46G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11585951 | ||||||
| chr2:11586229
|
G | T | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1159+324G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586229 | ||||||
| chr2:11586247
|
G | A | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+342G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586247 | ||||||
| chr2:11586288
|
T | C | 59 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(56): Show | 59 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.1159+383T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586288 | ||||||
| chr2:11586438
|
C | T | 2 | a0013c0018t0047g0303a0036c0041t0003g0091 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1159+533C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586438 | ||||||
| chr2:11586450
|
G | A | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1159+545G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586450 | ||||||
| chr2:11586764
|
C | A | 25 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1159+859C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586764 | ||||||
| chr2:11586764
|
C | T | 33 | a0008c0006t0005g0121a0008c0006t0009g0264a0008c0006t0009g0265others(30): Show | 33 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1159+859C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586764 | ||||||
| chr2:11586765
|
A | C | 25 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1159+860A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586765 | ||||||
| chr2:11586778
|
G | A | 46 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(43): Show | 46 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1159+873G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586778 | ||||||
| chr2:11586858
|
G | A | 2 | a0013c0018t0047g0303a0036c0041t0003g0091 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1159+953G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586858 | ||||||
| chr2:11586932
|
G | T | 1 | a0008c0006t0024g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1159+1027G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586932 | ||||||
| chr2:11586961
|
G | T | 62 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(59): Show | 62 | HG00099.hp2 HG00558.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1159+1056G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11586961 | ||||||
| chr2:11587008
|
G | A | 1 | a0003c0009t0021g0308 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1159+1103G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587008 | ||||||
| chr2:11587067
|
G | A | 2 | a0001c0001t0002g0241a0003c0003t0007g0159 | 2 | NA18986.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1159+1162G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587067 | ||||||
| chr2:11587112
|
G | A | 1 | a0004c0004t0013g0296 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1159+1207G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587112 | ||||||
| chr2:11587123
|
G | A | 1 | a0005c0002t0050g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1159+1218G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587123 | ||||||
| chr2:11587138
|
C | T | 4 | a0007c0015t0021g0069a0007c0015t0027g0004a0007c0015t0027g0024others(1): Show | 4 | HG02630.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+1233C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587138 | ||||||
| chr2:11587150
|
G | A | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1159+1245G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587150 | ||||||
| chr2:11587167
|
C | T | 3 | a0001c0013t0011g0218a0004c0026t0016g0041a0009c0019t0012g0161 | 3 | HG03017.hp1 HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1159+1262C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587167 | ||||||
| chr2:11587267
|
TG | T | 33 | a0008c0006t0005g0121a0008c0006t0009g0264a0008c0006t0009g0265others(30): Show | 33 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1159+1363delG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587267 | ||||||
| chr2:11587373
|
C | A | 2 | a0007c0016t0015g0017a0009c0029t0041g0028 | 2 | HG02486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1160-1373C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587373 | ||||||
| chr2:11587381
|
G | A | 216 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1160-1365G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587381 | ||||||
| chr2:11587496
|
C | A | 1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1160-1250C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587496 | ||||||
| chr2:11587572
|
G | A | 2 | a0013c0018t0047g0303a0036c0041t0003g0091 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1160-1174G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587572 | ||||||
| chr2:11587693
|
TAA | T | 6 | a0007c0016t0001g0012a0007c0016t0001g0013a0007c0058t0024g0125others(3): Show | 6 | HG01175.hp2 HG02622.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160-1052_1160-105 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587693 | ||||||
| chr2:11587693
|
TAACA | T | 8 | a0002c0007t0001g0262a0003c0003t0001g0136a0007c0017t0001g0157others(5): Show | 8 | HG01884.hp2 HG02559.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160-1052_1160-104 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587693 | ||||||
| chr2:11587693
|
TAACACA | T | 11 | a0007c0016t0015g0017a0007c0017t0001g0167a0007c0017t0001g0170others(8): Show | 11 | HG00423.hp2 HG00621.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1160-1052_1160-104 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587693 | ||||||
| chr2:11587693
|
TAACACAC others(3): Show |
T | 13 | a0008c0006t0005g0121a0008c0006t0009g0264a0008c0006t0009g0265others(10): Show | 13 | HG00140.hp1 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1160-1052_1160-104 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587693 | ||||||
| chr2:11587693
|
TAACACAC others(5): Show |
T | 5 | a0008c0006t0015g0005a0008c0049t0015g0006a0011c0008t0003g0027others(2): Show | 5 | HG00741.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-1052_1160-104 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587693 | ||||||
| chr2:11587693
|
TAACACAC others(7): Show |
T | 12 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(9): Show | 12 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1160-1052_1160-103 others(18): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587693 | ||||||
| chr2:11587693
|
TAACACAC others(17): Show |
T | 5 | a0018c0037t0053g0067a0019c0036t0001g0299a0019c0036t0001g0300others(2): Show | 5 | HG01261.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-1052_1160-102 others(28): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587693 | ||||||
| chr2:11587694
|
A | AAC | 16 | a0001c0001t0002g0032a0001c0001t0002g0247a0001c0001t0006g0180others(13): Show | 16 | HG00408.hp1 HG00408.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1160-1005_1160-100 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587694 | |||||
| chr2:11587694
|
A | C | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1160-1052A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587694 | ||||||
| chr2:11587694
|
AAC | A | 10 | a0002c0011t0002g0275a0002c0053t0019g0090a0003c0009t0015g0105others(7): Show | 10 | HG01243.hp1 HG02630.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-1005_1160-100 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587694 | |||||
| chr2:11587694
|
AACAC | A | 44 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0207others(41): Show | 44 | HG00423.hp1 HG00639.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.1160-1007_1160-100 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587694 | |||||
| chr2:11587694
|
AACACAC | A | 5 | a0007c0043t0035g0095a0014c0023t0014g0068a0014c0023t0014g0071others(2): Show | 5 | HG01070.hp2 HG02630.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-1009_1160-100 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587694 | |||||
| chr2:11587694
|
AACACACA others(1): Show |
A | 3 | a0001c0001t0032g0251a0004c0025t0008g0277a0054c0084t0002g0208 | 3 | HG00673.hp1 NA18956.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1160-1011_1160-100 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587694 | |||||
| chr2:11587694
|
AACACACA others(3): Show |
A | 2 | a0013c0018t0047g0303a0036c0041t0003g0091 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1160-1013_1160-100 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587694 | |||||
| chr2:11587732
|
C | T | 1 | a0056c0091t0002g0209 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1160-1014C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587732 | ||||||
| chr2:11587735
|
A | G | 3 | a0002c0007t0001g0104a0002c0061t0062g0134a0013c0052t0049g0261 | 3 | HG02630.hp2 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1160-1011A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587735 | ||||||
| chr2:11587737
|
A | G | 9 | a0001c0001t0002g0203a0002c0007t0001g0104a0002c0057t0059g0021others(6): Show | 9 | HG02486.hp1 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-1009A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587737 | ||||||
| chr2:11587739
|
A | ACGCG | 3 | a0001c0013t0011g0200a0002c0020t0026g0219a0002c0020t0026g0221 | 3 | NA18953.hp1 NA18962.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1160-1006_1160-100 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587739 | |||||
| chr2:11587739
|
A | G | 11 | a0001c0001t0002g0203a0002c0007t0001g0104a0002c0057t0059g0021others(8): Show | 11 | HG02080.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1160-1007A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587739 | ||||||
| chr2:11587740
|
C | T | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1006C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587740 | ||||||
| chr2:11587741
|
A | ACACACAC others(29): Show |
1 | a0004c0004t0002g0295 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(40): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(31): Show |
1 | a0001c0001t0030g0087 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(42): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(27): Show |
2 | a0005c0002t0009g0079a0020c0039t0004g0283 | 2 | HG03927.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(38): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(23): Show |
1 | a0002c0011t0005g0135 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(34): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(25): Show |
3 | a0001c0001t0002g0192a0003c0003t0001g0155a0003c0003t0005g0113 | 3 | HG01993.hp2 NA18989.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(36): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(21): Show |
2 | a0002c0011t0001g0271a0005c0002t0003g0152 | 2 | HG02135.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(32): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(23): Show |
1 | a0005c0002t0001g0142 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(34): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(25): Show |
1 | a0005c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(36): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(21): Show |
4 | a0003c0003t0001g0147a0005c0002t0010g0119a0005c0073t0016g0162others(1): Show | 4 | HG00099.hp1 HG01256.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(32): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(23): Show |
1 | a0050c0087t0004g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(34): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(25): Show |
1 | a0025c0093t0002g0178 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(36): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(19): Show |
14 | a0001c0001t0002g0229a0002c0005t0001g0057a0003c0003t0001g0115others(11): Show | 14 | HG00621.hp2 HG01168.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(30): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(21): Show |
1 | a0005c0002t0003g0082 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(32): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(25): Show |
1 | a0002c0007t0020g0307 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(36): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(15): Show |
4 | a0005c0002t0003g0114a0005c0002t0071g0185a0006c0027t0003g0272others(1): Show | 4 | HG00099.hp2 HG00558.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(26): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(17): Show |
10 | a0001c0001t0002g0232a0002c0034t0031g0263a0003c0003t0005g0130others(7): Show | 10 | HG01074.hp2 HG01175.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(28): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(19): Show |
1 | a0001c0001t0073g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(30): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(21): Show |
2 | a0006c0027t0004g0177a0051c0086t0008g0245 | 2 | HG04204.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(32): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(13): Show |
1 | a0002c0007t0007g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(24): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(15): Show |
10 | a0001c0001t0002g0241a0001c0001t0072g0254a0002c0005t0006g0293others(7): Show | 10 | HG01074.hp1 HG01081.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(26): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(17): Show |
1 | a0002c0005t0001g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(28): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(11): Show |
1 | a0005c0002t0003g0139 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(22): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(13): Show |
5 | a0002c0005t0001g0036a0004c0026t0013g0204a0005c0002t0003g0118others(2): Show | 5 | HG01192.hp1 HG03239.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(24): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(15): Show |
1 | a0006c0098t0068g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(26): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(17): Show |
1 | a0005c0002t0003g0151 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(28): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(11): Show |
10 | a0001c0001t0002g0231a0001c0001t0006g0294a0001c0013t0006g0181others(7): Show | 10 | HG00733.hp1 HG01071.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(22): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(13): Show |
2 | a0004c0026t0016g0041a0005c0002t0010g0124 | 2 | HG00733.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(24): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(9): Show |
8 | a0001c0001t0006g0212a0002c0005t0001g0035a0002c0005t0007g0031others(5): Show | 8 | HG02258.hp2 HG02300.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(20): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(11): Show |
3 | a0002c0005t0001g0034a0003c0003t0057g0059a0021c0040t0036g0089 | 3 | HG02809.hp2 HG04199.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(22): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(3): Show |
1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(5): Show |
1 | a0006c0054t0043g0002 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(7): Show |
2 | a0001c0013t0011g0218a0006c0097t0016g0058 | 2 | HG03710.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(18): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(9): Show |
3 | a0002c0005t0005g0065a0003c0003t0007g0159a0003c0003t0022g0120 | 3 | HG01516.hp1 NA18984.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(20): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(3): Show |
1 | a0002c0055t0044g0003 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(5): Show |
4 | a0002c0005t0001g0033a0002c0005t0051g0055a0003c0003t0001g0146others(1): Show | 4 | NA18961.hp2 NA18981.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACAC others(7): Show |
2 | a0004c0026t0004g0290a0005c0002t0010g0101 | 2 | HG02280.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(18): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACGC others(3): Show |
2 | a0002c0005t0007g0064a0002c0020t0067g0171 | 2 | HG00673.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1160-1004_1160-100 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACACGC others(5): Show |
1 | a0005c0002t0050g0084 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACACGCGC others(5): Show |
1 | a0002c0005t0011g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1160-1004_1160-100 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACGCGCG | 4 | a0002c0005t0001g0045a0002c0005t0005g0046a0002c0007t0052g0075others(1): Show | 4 | HG02280.hp1 NA18939.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160-1002_1160-100 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | ACGCGCGC others(3): Show |
1 | a0001c0013t0002g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1160-1002_1160-100 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11587741 | |||||
| chr2:11587741
|
A | G | 18 | a0001c0001t0002g0203a0001c0013t0011g0200a0002c0007t0001g0104others(15): Show | 18 | HG01070.hp2 HG02080.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1160-1005A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587741 | ||||||
| chr2:11587862
|
G | C | 217 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1160-884G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587862 | ||||||
| chr2:11587938
|
C | A | 13 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(10): Show | 13 | HG00639.hp2 HG01109.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1160-808C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587938 | ||||||
| chr2:11587954
|
G | A | 110 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1160-792G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587954 | ||||||
| chr2:11587963
|
C | T | 132 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1160-783C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11587963 | ||||||
| chr2:11588078
|
T | C | 32 | a0008c0006t0005g0121a0008c0006t0009g0264a0008c0006t0009g0265others(29): Show | 32 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1160-668T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588078 | ||||||
| chr2:11588085
|
G | A | 2 | a0005c0002t0013g0187a0005c0002t0013g0188 | 2 | HG01081.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1160-661G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588085 | ||||||
| chr2:11588099
|
C | T | 1 | a0007c0017t0001g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1160-647C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588099 | ||||||
| chr2:11588134
|
T | G | 3 | a0001c0001t0073g0253a0005c0002t0003g0082a0005c0002t0003g0098 | 3 | NA18941.hp1 NA18981.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1160-612T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588134 | ||||||
| chr2:11588227
|
C | CA | 8 | a0003c0003t0001g0145a0003c0003t0001g0146a0005c0002t0003g0117others(5): Show | 8 | HG01884.hp1 HG02071.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.1160-506dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | INFO_REALIGN_3_PRIME | chr2 | 11588227 | |||||
| chr2:11588255
|
T | C | 159 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1160-491T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588255 | ||||||
| chr2:11588262
|
T | C | 120 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1160-484T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588262 | ||||||
| chr2:11588398
|
C | T | 1 | a0009c0029t0020g0016 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1160-348C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588398 | ||||||
| chr2:11588521
|
A | G | 2 | a0001c0001t0002g0207a0001c0001t0005g0047 | 2 | NA18962.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1160-225A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588521 | ||||||
| chr2:11588669
|
C | T | 4 | a0007c0015t0021g0069a0007c0015t0027g0004a0007c0015t0027g0024others(1): Show | 4 | HG02630.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-77C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588669 | ||||||
| chr2:11588728
|
G | A | 6 | a0001c0001t0002g0247a0004c0004t0004g0239a0004c0004t0004g0242others(3): Show | 6 | HG00735.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1160-18G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 9/32 | chr2 | 11588728 | ||||||
| chr2:11588970
|
G | A | 54 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(51): Show | 54 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1345+39G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11588970 | ||||||
| chr2:11589006
|
G | A | 3 | a0002c0007t0001g0104a0002c0061t0062g0134a0013c0052t0049g0261 | 3 | HG02630.hp2 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1345+75G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589006 | ||||||
| chr2:11589263
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0007g0138 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1345+332G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589263 | ||||||
| chr2:11589480
|
A | G | 67 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1345+549A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589480 | ||||||
| chr2:11589597
|
A | G | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1345+666A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589597 | ||||||
| chr2:11589670
|
C | T | 2 | a0018c0037t0053g0067a0037c0067t0021g0070 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1345+739C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589670 | ||||||
| chr2:11589673
|
A | G | 2 | a0008c0060t0061g0305a0011c0008t0045g0022 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1345+742A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589673 | ||||||
| chr2:11589686
|
GAGAA | G | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1345+759_1345+762d others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr2 | 11589686 | |||||
| chr2:11589803
|
G | A | 1 | a0002c0007t0001g0262 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1345+872G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589803 | ||||||
| chr2:11589832
|
A | G | 1 | a0003c0003t0001g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1345+901A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589832 | ||||||
| chr2:11589857
|
G | A | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1345+926G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589857 | ||||||
| chr2:11589906
|
G | A | 9 | a0001c0013t0006g0181a0002c0005t0001g0066a0002c0005t0007g0031others(6): Show | 9 | HG02040.hp2 HG02056.hp1 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.1345+975G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589906 | ||||||
| chr2:11589969
|
G | A | 3 | a0010c0031t0046g0096a0013c0018t0022g0030a0030c0051t0042g0306 | 3 | HG01884.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1345+1038G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589969 | ||||||
| chr2:11589973
|
T | C | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345+1042T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11589973 | ||||||
| chr2:11590035
|
G | T | 1 | a0008c0060t0061g0305 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1345+1104G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590035 | ||||||
| chr2:11590104
|
A | G | 1 | a0004c0026t0013g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1345+1173A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590104 | ||||||
| chr2:11590178
|
C | G | 1 | a0001c0013t0011g0218 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1345+1247C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590178 | ||||||
| chr2:11590204
|
A | G | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345+1273A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590204 | ||||||
| chr2:11590215
|
C | T | 1 | a0005c0002t0016g0164 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1345+1284C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590215 | ||||||
| chr2:11590216
|
G | A | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345+1285G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590216 | ||||||
| chr2:11590268
|
C | T | 32 | a0007c0016t0001g0012a0007c0016t0001g0013a0007c0016t0015g0017others(29): Show | 32 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1345+1337C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590268 | ||||||
| chr2:11590351
|
C | T | 2 | a0006c0027t0004g0177a0025c0093t0002g0178 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1345+1420C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590351 | ||||||
| chr2:11590367
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1345+1436G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590367 | ||||||
| chr2:11590612
|
A | G | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345+1681A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590612 | ||||||
| chr2:11590754
|
T | C | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345+1823T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11590754 | ||||||
| chr2:11591145
|
C | T | 13 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(10): Show | 13 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1346-1631C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11591145 | ||||||
| chr2:11591381
|
C | T | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1346-1395C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11591381 | ||||||
| chr2:11591565
|
G | A | 1 | a0007c0015t0021g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1346-1211G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11591565 | ||||||
| chr2:11591590
|
G | A | 1 | a0005c0002t0055g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1346-1186G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11591590 | ||||||
| chr2:11591648
|
T | G | 214 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1346-1128T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11591648 | ||||||
| chr2:11591658
|
T | C | 3 | a0010c0031t0046g0096a0013c0018t0022g0030a0030c0051t0042g0306 | 3 | HG01884.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1346-1118T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11591658 | ||||||
| chr2:11591720
|
T | C | 214 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1346-1056T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11591720 | ||||||
| chr2:11592114
|
C | T | 1 | a0011c0008t0045g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1346-662C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592114 | ||||||
| chr2:11592187
|
C | CT | 10 | a0005c0002t0003g0152a0007c0017t0001g0157a0007c0017t0001g0167others(7): Show | 10 | HG00423.hp2 HG01884.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1346-573dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr2 | 11592187 | |||||
| chr2:11592187
|
CT | C | 9 | a0001c0001t0002g0282a0002c0005t0001g0033a0002c0007t0037g0023others(6): Show | 9 | HG01167.hp2 HG01256.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1346-573delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr2 | 11592187 | |||||
| chr2:11592201
|
TTTAAC | T | 30 | a0008c0006t0005g0121a0008c0006t0009g0264a0008c0006t0009g0265others(27): Show | 30 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1346-574_1346-570d others(7): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592201 | ||||||
| chr2:11592202
|
TTAAC | T | 19 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(16): Show | 19 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1346-573_1346-570d others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592202 | ||||||
| chr2:11592329
|
AT | A | 55 | a0001c0001t0002g0193a0001c0001t0002g0203a0001c0001t0002g0276others(52): Show | 55 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1346-430delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr2 | 11592329 | |||||
| chr2:11592329
|
ATT | A | 25 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(22): Show | 25 | HG00639.hp1 HG01175.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1346-431_1346-430d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr2 | 11592329 | |||||
| chr2:11592346
|
T | A | 7 | a0001c0013t0011g0200a0002c0020t0026g0219a0002c0020t0026g0221others(4): Show | 7 | HG00673.hp2 NA18939.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1346-430T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592346 | ||||||
| chr2:11592346
|
TA | T | 6 | a0002c0057t0059g0021a0005c0002t0003g0098a0005c0002t0003g0133others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1346-425delA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr2 | 11592346 | |||||
| chr2:11592347
|
A | T | 1 | a0002c0005t0005g0046 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1346-429A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592347 | ||||||
| chr2:11592348
|
A | T | 2 | a0002c0057t0059g0021a0005c0066t0022g0072 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1346-428A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592348 | ||||||
| chr2:11592405
|
G | A | 12 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(9): Show | 12 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1346-371G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592405 | ||||||
| chr2:11592421
|
G | GAATCAC | 119 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.1346-354_1346-349d others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr2 | 11592421 | |||||
| chr2:11592557
|
C | A | 1 | a0008c0060t0061g0305 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1346-219C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592557 | ||||||
| chr2:11592563
|
G | GA | 23 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(20): Show | 23 | HG00639.hp1 HG01070.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1346-206dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | INFO_REALIGN_3_PRIME | chr2 | 11592563 | |||||
| chr2:11592641
|
T | C | 2 | a0006c0056t0070g0179a0006c0065t0033g0220 | 2 | NA18979.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1346-135T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592641 | ||||||
| chr2:11592705
|
A | T | 8 | a0008c0006t0012g0112a0008c0006t0024g0143a0011c0008t0012g0093others(5): Show | 8 | HG00639.hp2 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1346-71A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592705 | ||||||
| chr2:11592713
|
A | G | 25 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(22): Show | 25 | HG00639.hp1 HG01070.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1346-63A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592713 | ||||||
| chr2:11592714
|
C | T | 5 | a0011c0008t0045g0022a0014c0023t0014g0068a0014c0023t0014g0071others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346-62C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592714 | ||||||
| chr2:11592757
|
C | T | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1346-19C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 10/32 | chr2 | 11592757 | ||||||
| chr2:11593134
|
C | G | 1 | a0001c0001t0073g0253 | 1 | NA18981.hp1 | splice_region_variant&intron_variant | LOW | c.1696+8C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593134 | ||||||
| chr2:11593150
|
C | A | 29 | a0007c0016t0001g0012a0007c0016t0001g0013a0007c0016t0015g0017others(26): Show | 29 | HG00423.hp2 HG00621.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.1696+24C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593150 | ||||||
| chr2:11593362
|
G | T | 133 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.1696+236G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593362 | ||||||
| chr2:11593419
|
A | AACTC | 147 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.1696+293_1696+294i others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593419 | ||||||
| chr2:11593419
|
A | C | 1 | a0005c0002t0003g0152 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1696+293A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593419 | ||||||
| chr2:11593478
|
C | G | 1 | a0002c0007t0020g0307 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1696+352C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593478 | ||||||
| chr2:11593751
|
G | A | 4 | a0007c0015t0021g0069a0007c0015t0027g0004a0007c0015t0027g0024others(1): Show | 4 | HG02630.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696+625G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593751 | ||||||
| chr2:11593759
|
G | A | 1 | a0041c0075t0001g0153 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1696+633G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593759 | ||||||
| chr2:11593776
|
T | C | 8 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(5): Show | 8 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1696+650T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593776 | ||||||
| chr2:11593876
|
T | C | 1 | a0001c0001t0007g0138 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1696+750T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593876 | ||||||
| chr2:11593890
|
G | T | 1 | a0006c0033t0003g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1696+764G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593890 | ||||||
| chr2:11593908
|
G | T | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1696+782G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593908 | ||||||
| chr2:11593999
|
A | G | 8 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(5): Show | 8 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1696+873A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11593999 | ||||||
| chr2:11594132
|
G | A | 37 | a0008c0006t0005g0121a0008c0006t0009g0264a0008c0006t0009g0265others(34): Show | 37 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1696+1006G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594132 | ||||||
| chr2:11594175
|
T | C | 1 | a0013c0052t0049g0261 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1696+1049T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594175 | ||||||
| chr2:11594189
|
T | C | 185 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1697-1062T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594189 | ||||||
| chr2:11594209
|
A | C | 214 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1697-1042A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594209 | ||||||
| chr2:11594331
|
A | G | 7 | a0001c0001t0002g0192a0001c0001t0002g0231a0003c0003t0001g0147others(4): Show | 7 | HG01256.hp2 HG01496.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1697-920A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594331 | ||||||
| chr2:11594362
|
C | CT | 174 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1697-879dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr2 | 11594362 | |||||
| chr2:11594596
|
C | G | 1 | a0001c0001t0018g0258 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1697-655C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594596 | ||||||
| chr2:11594688
|
T | TTTG | 214 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1697-554_1697-552d others(5): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr2 | 11594688 | |||||
| chr2:11594754
|
A | G | 180 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1697-497A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594754 | ||||||
| chr2:11594779
|
G | A | 170 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1697-472G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594779 | ||||||
| chr2:11594783
|
C | G | 170 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1697-468C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594783 | ||||||
| chr2:11594843
|
G | A | 1 | a0004c0004t0002g0281 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1697-408G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594843 | ||||||
| chr2:11594935
|
C | A | 132 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1697-316C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594935 | ||||||
| chr2:11594989
|
T | C | 208 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1697-262T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11594989 | ||||||
| chr2:11594993
|
C | CT | 172 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1697-243dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | INFO_REALIGN_3_PRIME | chr2 | 11594993 | |||||
| chr2:11595009
|
A | T | 170 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1697-242A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11595009 | ||||||
| chr2:11595125
|
A | G | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1697-126A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11595125 | ||||||
| chr2:11595202
|
G | A | 1 | a0002c0011t0005g0135 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1697-49G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 11/32 | chr2 | 11595202 | ||||||
| chr2:11595417
|
A | G | 1 | a0001c0001t0073g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1825+38A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 12/32 | chr2 | 11595417 | ||||||
| chr2:11595701
|
C | T | 1 | a0005c0002t0010g0123 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1825+322C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 12/32 | chr2 | 11595701 | ||||||
| chr2:11595739
|
C | T | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1825+360C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 12/32 | chr2 | 11595739 | ||||||
| chr2:11595911
|
A | G | 210 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1826-200A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 12/32 | chr2 | 11595911 | ||||||
| chr2:11596022
|
C | T | 3 | a0009c0028t0003g0260a0009c0028t0020g0304a0011c0008t0045g0022 | 3 | HG02615.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1826-89C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 12/32 | chr2 | 11596022 | ||||||
| chr2:11596340
|
C | T | 2 | a0003c0003t0007g0159a0043c0069t0003g0154 | 2 | HG04184.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1954+101C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596340 | ||||||
| chr2:11596447
|
A | AG | 28 | a0006c0097t0016g0058a0007c0016t0001g0012a0007c0016t0001g0013others(25): Show | 28 | HG00423.hp2 HG00621.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1954+214dupG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr2 | 11596447 | |||||
| chr2:11596467
|
ATGCACAG others(21): Show |
A | 2 | a0002c0005t0001g0045a0003c0003t0007g0163 | 2 | NA19010.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1954+249_1954+276d others(30): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr2 | 11596467 | |||||
| chr2:11596467
|
ATGCACAG others(50): Show |
A | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1954+249_1954+305d others(59): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr2 | 11596467 | |||||
| chr2:11596483
|
T | G | 2 | a0003c0003t0001g0155a0006c0097t0016g0058 | 2 | NA18989.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1954+244T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596483 | ||||||
| chr2:11596483
|
T | TG | 273 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1954+248dupG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr2 | 11596483 | |||||
| chr2:11596506
|
GGGGGTGG others(21): Show |
G | 1 | a0022c0059t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1954+272_1954+299d others(30): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr2 | 11596506 | |||||
| chr2:11596535
|
GGGGGTGG others(24): Show |
G | 26 | a0007c0016t0001g0012a0007c0016t0001g0013a0007c0016t0015g0017others(23): Show | 26 | HG00423.hp2 HG00621.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.1954+310_1954+340d others(33): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr2 | 11596535 | |||||
| chr2:11596564
|
GAA | G | 3 | a0007c0044t0039g0011a0009c0029t0020g0016a0022c0059t0023g0110 | 3 | HG01175.hp2 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1954+326_1954+327d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596564 | ||||||
| chr2:11596595
|
C | T | 2 | a0001c0001t0001g0166a0008c0060t0061g0305 | 2 | HG02129.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1954+356C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596595 | ||||||
| chr2:11596744
|
GA | G | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1954+506delA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596744 | ||||||
| chr2:11596769
|
CAGTG | C | 13 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(10): Show | 13 | HG00639.hp2 HG01109.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1954+533_1954+536d others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | INFO_REALIGN_3_PRIME | chr2 | 11596769 | |||||
| chr2:11596785
|
G | A | 13 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(10): Show | 13 | HG00639.hp2 HG01109.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1954+546G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596785 | ||||||
| chr2:11596853
|
G | A | 2 | a0010c0031t0046g0096a0013c0018t0022g0030 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1954+614G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596853 | ||||||
| chr2:11596934
|
G | A | 3 | a0008c0006t0017g0015a0008c0006t0017g0259a0008c0006t0019g0076 | 3 | HG02647.hp1 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1954+695G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596934 | ||||||
| chr2:11596968
|
G | A | 2 | a0001c0001t0002g0210a0001c0001t0002g0222 | 2 | NA18977.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1954+729G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596968 | ||||||
| chr2:11596990
|
T | C | 6 | a0010c0035t0060g0126a0010c0035t0064g0128a0013c0018t0003g0019others(3): Show | 6 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1954+751T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11596990 | ||||||
| chr2:11597029
|
A | G | 1 | a0005c0002t0055g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1955-752A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597029 | ||||||
| chr2:11597103
|
C | T | 37 | a0001c0001t0002g0192a0001c0001t0002g0231a0001c0001t0002g0232others(34): Show | 37 | HG00099.hp2 HG00558.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1955-678C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597103 | ||||||
| chr2:11597116
|
G | C | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1955-665G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597116 | ||||||
| chr2:11597148
|
C | T | 2 | a0011c0008t0045g0022a0015c0022t0001g0081 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1955-633C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597148 | ||||||
| chr2:11597196
|
A | T | 6 | a0002c0034t0031g0263a0005c0066t0022g0072a0007c0015t0021g0069others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1955-585A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597196 | ||||||
| chr2:11597243
|
A | G | 15 | a0002c0007t0037g0023a0006c0033t0034g0302a0008c0006t0012g0112others(12): Show | 15 | HG00639.hp2 HG01109.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1955-538A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597243 | ||||||
| chr2:11597328
|
G | A | 11 | a0007c0016t0001g0012a0007c0016t0001g0013a0007c0016t0015g0017others(8): Show | 11 | HG01175.hp2 HG02486.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1955-453G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597328 | ||||||
| chr2:11597349
|
A | G | 3 | a0010c0031t0038g0029a0010c0032t0028g0007a0010c0032t0028g0009 | 3 | HG02451.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1955-432A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597349 | ||||||
| chr2:11597427
|
T | C | 1 | a0009c0029t0020g0016 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1955-354T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597427 | ||||||
| chr2:11597737
|
G | T | 1 | a0003c0003t0005g0130 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1955-44G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 13/32 | chr2 | 11597737 | ||||||
| chr2:11598041
|
TGGGTGTT others(28): Show |
T | 12 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(9): Show | 12 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2152+67_2152+101de others(36): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 14/32 | INFO_REALIGN_3_PRIME | chr2 | 11598041 | |||||
| chr2:11598234
|
C | T | 6 | a0010c0035t0060g0126a0010c0035t0064g0128a0013c0018t0003g0019others(3): Show | 6 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2152+256C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 14/32 | chr2 | 11598234 | ||||||
| chr2:11598250
|
G | T | 1 | a0028c0062t0040g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2152+272G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 14/32 | chr2 | 11598250 | ||||||
| chr2:11598252
|
A | G | 274 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2152+274A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 14/32 | chr2 | 11598252 | ||||||
| chr2:11598639
|
C | T | 274 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2153-41C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 14/32 | chr2 | 11598639 | ||||||
| chr2:11599062
|
T | A | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2333+202T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599062 | ||||||
| chr2:11599242
|
G | T | 108 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(105): Show | 108 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.2333+382G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599242 | ||||||
| chr2:11599289
|
G | A | 9 | a0001c0001t0002g0247a0004c0004t0004g0239a0004c0004t0004g0242others(6): Show | 9 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.2333+429G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599289 | ||||||
| chr2:11599315
|
C | T | 1 | a0004c0026t0004g0290 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2333+455C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599315 | ||||||
| chr2:11599332
|
C | CT | 14 | a0001c0001t0002g0182a0001c0001t0007g0138a0002c0034t0031g0263others(11): Show | 14 | HG01109.hp2 HG01243.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2333+488dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr2 | 11599332 | |||||
| chr2:11599332
|
CT | C | 8 | a0003c0003t0001g0115a0007c0044t0039g0011a0009c0029t0020g0016others(5): Show | 8 | HG00639.hp1 HG02145.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2333+488delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr2 | 11599332 | |||||
| chr2:11599362
|
C | T | 1 | a0003c0003t0002g0225 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2333+502C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599362 | ||||||
| chr2:11599379
|
G | A | 1 | a0006c0056t0070g0179 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2333+519G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599379 | ||||||
| chr2:11599442
|
C | A | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2333+582C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599442 | ||||||
| chr2:11599450
|
C | T | 6 | a0002c0034t0031g0263a0005c0066t0022g0072a0007c0015t0021g0069others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2333+590C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599450 | ||||||
| chr2:11599493
|
C | T | 1 | a0005c0002t0048g0269 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2333+633C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599493 | ||||||
| chr2:11599519
|
A | AT | 44 | a0001c0001t0002g0210a0001c0001t0002g0232a0001c0001t0002g0247others(41): Show | 44 | HG00099.hp1 HG00741.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.2333+677dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr2 | 11599519 | |||||
| chr2:11599519
|
A | ATTTTTT | 6 | a0010c0035t0060g0126a0010c0035t0064g0128a0013c0018t0003g0019others(3): Show | 6 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2333+672_2333+677d others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr2 | 11599519 | |||||
| chr2:11599519
|
AT | A | 93 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2333+677delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr2 | 11599519 | |||||
| chr2:11599550
|
C | T | 1 | a0004c0004t0008g0173 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2333+690C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599550 | ||||||
| chr2:11599559
|
G | A | 1 | a0008c0006t0015g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2333+699G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599559 | ||||||
| chr2:11599590
|
C | G | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2333+730C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599590 | ||||||
| chr2:11599666
|
G | A | 195 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(192): Show | 195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.2333+806G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599666 | ||||||
| chr2:11599680
|
C | G | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2333+820C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599680 | ||||||
| chr2:11599766
|
C | T | 8 | a0007c0044t0039g0011a0009c0029t0020g0016a0010c0035t0060g0126others(5): Show | 8 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2333+906C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599766 | ||||||
| chr2:11599779
|
C | G | 7 | a0001c0001t0002g0192a0001c0001t0002g0231a0001c0001t0072g0254others(4): Show | 7 | HG01256.hp2 HG01496.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.2333+919C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599779 | ||||||
| chr2:11599842
|
T | C | 8 | a0007c0044t0039g0011a0009c0029t0020g0016a0010c0035t0060g0126others(5): Show | 8 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2334-958T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599842 | ||||||
| chr2:11599906
|
C | T | 1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2334-894C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11599906 | ||||||
| chr2:11600051
|
G | A | 43 | a0001c0001t0002g0232a0001c0001t0002g0247a0002c0007t0020g0307others(40): Show | 43 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.2334-749G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11600051 | ||||||
| chr2:11600145
|
C | T | 8 | a0007c0044t0039g0011a0009c0029t0020g0016a0010c0035t0060g0126others(5): Show | 8 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2334-655C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11600145 | ||||||
| chr2:11600398
|
C | G | 1 | a0005c0073t0016g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2334-402C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11600398 | ||||||
| chr2:11600450
|
T | G | 1 | a0002c0007t0052g0075 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2334-350T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11600450 | ||||||
| chr2:11600511
|
A | G | 1 | a0003c0003t0001g0267 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2334-289A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11600511 | ||||||
| chr2:11600643
|
G | A | 1 | a0001c0001t0006g0278 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2334-157G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 15/32 | chr2 | 11600643 | ||||||
| chr2:11601031
|
A | G | 32 | a0001c0001t0002g0232a0001c0001t0002g0247a0002c0007t0020g0307others(29): Show | 32 | HG00099.hp1 HG00741.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.2529+36A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601031 | ||||||
| chr2:11601067
|
C | A | 274 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2529+72C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601067 | ||||||
| chr2:11601157
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2529+162T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601157 | ||||||
| chr2:11601215
|
C | T | 1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2529+220C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601215 | ||||||
| chr2:11601264
|
T | C | 276 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.2529+269T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601264 | ||||||
| chr2:11601319
|
G | A | 1 | a0006c0098t0068g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2529+324G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601319 | ||||||
| chr2:11601580
|
A | G | 10 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2529+585A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601580 | ||||||
| chr2:11601603
|
C | T | 19 | a0002c0057t0059g0021a0005c0002t0003g0133a0005c0002t0010g0101others(16): Show | 19 | HG00639.hp1 HG01070.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.2529+608C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601603 | ||||||
| chr2:11601606
|
C | T | 1 | a0004c0004t0002g0202 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2529+611C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601606 | ||||||
| chr2:11601681
|
T | C | 4 | a0002c0057t0059g0021a0005c0002t0003g0133a0008c0049t0015g0006others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2529+686T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601681 | ||||||
| chr2:11601733
|
G | A | 11 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(8): Show | 11 | HG02145.hp1 HG02559.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.2530-673G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601733 | ||||||
| chr2:11601915
|
A | G | 4 | a0012c0010t0002g0184a0012c0010t0002g0190a0012c0010t0002g0226others(1): Show | 4 | HG00735.hp2 HG01106.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2530-491A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11601915 | ||||||
| chr2:11602003
|
G | A | 8 | a0007c0044t0039g0011a0009c0029t0020g0016a0010c0035t0060g0126others(5): Show | 8 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2530-403G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11602003 | ||||||
| chr2:11602145
|
T | G | 1 | a0003c0076t0007g0102 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2530-261T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11602145 | ||||||
| chr2:11602249
|
G | T | 1 | a0020c0039t0004g0283 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2530-157G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11602249 | ||||||
| chr2:11602332
|
A | G | 108 | a0001c0001t0002g0192a0001c0001t0002g0210a0001c0001t0002g0222others(105): Show | 108 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.2530-74A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11602332 | ||||||
| chr2:11602356
|
C | T | 6 | a0010c0035t0060g0126a0010c0035t0064g0128a0013c0018t0003g0019others(3): Show | 6 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2530-50C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11602356 | ||||||
| chr2:11602360
|
C | T | 4 | a0002c0057t0059g0021a0005c0002t0003g0133a0008c0049t0015g0006others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2530-46C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11602360 | ||||||
| chr2:11602370
|
C | T | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2530-36C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11602370 | ||||||
| chr2:11602371
|
A | G | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2530-35A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 16/32 | chr2 | 11602371 | ||||||
| chr2:11602582
|
G | A | 4 | a0002c0057t0059g0021a0005c0002t0003g0133a0008c0049t0015g0006others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2666+40G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11602582 | ||||||
| chr2:11602728
|
C | A | 60 | a0001c0001t0002g0192a0001c0001t0002g0210a0001c0001t0002g0222others(57): Show | 60 | HG00099.hp2 HG00733.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.2666+186C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11602728 | ||||||
| chr2:11602768
|
A | G | 3 | a0005c0002t0010g0101a0005c0002t0050g0084a0021c0040t0036g0089 | 3 | HG01496.hp2 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2666+226A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11602768 | ||||||
| chr2:11602882
|
TTTG | T | 5 | a0002c0034t0031g0263a0005c0066t0022g0072a0007c0015t0021g0069others(2): Show | 5 | HG02258.hp1 HG03098.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2666+343_2666+345d others(5): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11602882 | |||||
| chr2:11602906
|
C | G | 1 | a0002c0034t0031g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2666+364C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11602906 | ||||||
| chr2:11602966
|
G | T | 3 | a0010c0035t0060g0126a0010c0035t0064g0128a0013c0018t0003g0019 | 3 | HG00639.hp1 HG02145.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2666+424G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11602966 | ||||||
| chr2:11603024
|
G | A | 1 | a0003c0003t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2666+482G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603024 | ||||||
| chr2:11603170
|
A | G | 1 | a0026c0092t0018g0249 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2666+628A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603170 | ||||||
| chr2:11603191
|
G | A | 1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2666+649G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603191 | ||||||
| chr2:11603393
|
T | G | 3 | a0005c0002t0010g0101a0005c0002t0050g0084a0021c0040t0036g0089 | 3 | HG01496.hp2 HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2666+851T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603393 | ||||||
| chr2:11603627
|
T | C | 2 | a0008c0006t0015g0005a0032c0048t0014g0008 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2666+1085T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603627 | ||||||
| chr2:11603631
|
C | G | 1 | a0002c0012t0024g0127 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2666+1089C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603631 | ||||||
| chr2:11603678
|
A | G | 1 | a0001c0001t0002g0282 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2666+1136A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603678 | ||||||
| chr2:11603754
|
C | T | 2 | a0005c0002t0010g0101a0005c0002t0050g0084 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2666+1212C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603754 | ||||||
| chr2:11603940
|
G | A | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2666+1398G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603940 | ||||||
| chr2:11603966
|
G | T | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2666+1424G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603966 | ||||||
| chr2:11603968
|
T | A | 1 | a0002c0007t0037g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2666+1426T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11603968 | ||||||
| chr2:11604015
|
C | T | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2666+1473C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11604015 | ||||||
| chr2:11604106
|
C | T | 234 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(231): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.2666+1564C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11604106 | ||||||
| chr2:11604171
|
C | T | 1 | a0005c0002t0055g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2666+1629C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11604171 | ||||||
| chr2:11604350
|
C | G | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2666+1808C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11604350 | ||||||
| chr2:11604447
|
G | A | 89 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(86): Show | 89 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.2666+1905G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11604447 | ||||||
| chr2:11604568
|
C | T | 67 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(64): Show | 67 | HG00099.hp2 HG00733.hp2 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.2666+2026C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11604568 | ||||||
| chr2:11604621
|
C | A | 16 | a0007c0016t0001g0012a0007c0016t0001g0013a0009c0019t0012g0161others(13): Show | 16 | HG01175.hp2 HG01261.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.2666+2079C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11604621 | ||||||
| chr2:11604874
|
C | T | 3 | a0002c0007t0001g0104a0002c0053t0019g0090a0002c0061t0062g0134 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2666+2332C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11604874 | ||||||
| chr2:11604979
|
A | C | 5 | a0002c0057t0059g0021a0005c0002t0003g0133a0007c0016t0015g0017others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2666+2437A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11604979 | ||||||
| chr2:11605081
|
C | G | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2666+2539C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11605081 | ||||||
| chr2:11605090
|
A | G | 1 | a0003c0009t0001g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2666+2548A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11605090 | ||||||
| chr2:11605144
|
C | CT | 35 | a0001c0001t0001g0042a0001c0001t0002g0193a0001c0001t0002g0207others(32): Show | 35 | HG00621.hp1 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.2666+2634dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTT | 8 | a0002c0007t0001g0262a0004c0004t0004g0244a0011c0008t0003g0297others(5): Show | 8 | HG00735.hp1 HG00741.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2666+2633_2666+263 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTT | 7 | a0001c0001t0002g0032a0001c0001t0002g0241a0002c0007t0001g0104others(4): Show | 7 | HG02809.hp1 HG03139.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.2666+2632_2666+263 others(7): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTT | 12 | a0002c0005t0005g0046a0002c0053t0019g0090a0006c0014t0005g0039others(9): Show | 12 | HG02615.hp1 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2666+2631_2666+263 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTTT | 30 | a0001c0001t0002g0276a0001c0013t0006g0181a0001c0013t0011g0200others(27): Show | 30 | HG00673.hp2 HG00733.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.2666+2630_2666+263 others(9): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTTTT | 16 | a0001c0001t0002g0274a0001c0001t0002g0286a0001c0013t0002g0194others(13): Show | 16 | HG00423.hp1 HG00621.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.2666+2629_2666+263 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTTTTT others(1): Show |
30 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0229others(27): Show | 30 | HG00099.hp2 HG00733.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2666+2627_2666+263 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTTTTT others(2): Show |
15 | a0001c0001t0030g0087a0001c0001t0073g0253a0002c0007t0007g0150others(12): Show | 15 | HG01167.hp2 HG01175.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.2666+2626_2666+263 others(13): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0002g0210a0001c0001t0072g0254a0003c0003t0030g0056others(5): Show | 8 | HG02080.hp1 HG02135.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.2666+2625_2666+263 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTTTTT others(4): Show |
1 | a0005c0002t0010g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2666+2624_2666+263 others(15): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTTTTT others(5): Show |
3 | a0003c0003t0001g0155a0003c0003t0057g0059a0005c0073t0016g0162 | 3 | NA18942.hp2 NA18959.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2666+2623_2666+263 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0002g0222a0002c0011t0009g0043 | 2 | HG01361.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.2666+2622_2666+263 others(17): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
C | CTTTTTTT others(8): Show |
1 | a0004c0004t0004g0198 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2666+2620_2666+263 others(19): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
CT | C | 10 | a0001c0001t0002g0282a0001c0001t0006g0278a0002c0007t0037g0023others(7): Show | 10 | HG00140.hp1 HG01070.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.2666+2634delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
CTT | C | 8 | a0002c0011t0002g0275a0002c0057t0059g0021a0005c0002t0003g0133others(5): Show | 8 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2666+2633_2666+263 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
CTTT | C | 10 | a0007c0043t0035g0095a0008c0006t0012g0112a0008c0006t0017g0015others(7): Show | 10 | HG00639.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2666+2632_2666+263 others(7): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
CTTTT | C | 7 | a0001c0001t0002g0287a0006c0027t0009g0053a0007c0044t0039g0011others(4): Show | 7 | HG02896.hp1 HG02965.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2666+2631_2666+263 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
CTTTTTTT others(4): Show |
C | 9 | a0002c0011t0001g0271a0007c0058t0024g0125a0010c0035t0060g0126others(6): Show | 9 | HG00639.hp1 HG01106.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2666+2624_2666+263 others(15): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
CTTTTTTT others(5): Show |
C | 1 | a0003c0003t0001g0141 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2666+2623_2666+263 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
CTTTTTTT others(6): Show |
C | 18 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(15): Show | 18 | HG00140.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2666+2622_2666+263 others(17): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605144
|
CTTTTTTT others(7): Show |
C | 1 | a0010c0032t0028g0009 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2666+2621_2666+263 others(18): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11605144 | |||||
| chr2:11605303
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2666+2761G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11605303 | ||||||
| chr2:11605363
|
T | C | 1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2666+2821T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11605363 | ||||||
| chr2:11605415
|
G | A | 1 | a0001c0001t0002g0282 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2666+2873G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11605415 | ||||||
| chr2:11605427
|
C | T | 10 | a0007c0044t0039g0011a0007c0058t0024g0125a0009c0029t0020g0016others(7): Show | 10 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2666+2885C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11605427 | ||||||
| chr2:11605583
|
G | C | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2666+3041G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11605583 | ||||||
| chr2:11605874
|
T | G | 10 | a0007c0044t0039g0011a0007c0058t0024g0125a0009c0029t0020g0016others(7): Show | 10 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2666+3332T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11605874 | ||||||
| chr2:11605877
|
G | A | 84 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(81): Show | 84 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2666+3335G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11605877 | ||||||
| chr2:11606048
|
T | C | 1 | a0001c0001t0002g0203 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2666+3506T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606048 | ||||||
| chr2:11606051
|
C | T | 84 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(81): Show | 84 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2666+3509C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606051 | ||||||
| chr2:11606061
|
A | G | 1 | a0001c0001t0006g0278 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2666+3519A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606061 | ||||||
| chr2:11606321
|
C | T | 1 | a0012c0010t0002g0224 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2666+3779C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606321 | ||||||
| chr2:11606345
|
G | C | 6 | a0002c0057t0059g0021a0005c0002t0003g0133a0007c0016t0015g0017others(3): Show | 6 | HG01109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2666+3803G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606345 | ||||||
| chr2:11606350
|
G | A | 12 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(9): Show | 12 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2666+3808G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606350 | ||||||
| chr2:11606363
|
T | C | 1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2666+3821T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606363 | ||||||
| chr2:11606448
|
A | G | 56 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(53): Show | 56 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2666+3906A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606448 | ||||||
| chr2:11606547
|
T | C | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2666+4005T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606547 | ||||||
| chr2:11606758
|
C | CATT | 45 | a0002c0007t0001g0104a0002c0012t0023g0085a0002c0012t0023g0086others(42): Show | 45 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.2667-3890_2667-388 others(7): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11606758 | |||||
| chr2:11606758
|
C | CATTATT | 17 | a0001c0001t0002g0247a0002c0053t0019g0090a0002c0055t0044g0003others(14): Show | 17 | HG00639.hp1 HG01257.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.2667-3893_2667-388 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11606758 | |||||
| chr2:11606758
|
C | CATTATTA others(2): Show |
8 | a0005c0002t0010g0101a0005c0002t0010g0119a0005c0002t0050g0084others(5): Show | 8 | HG00099.hp1 HG00741.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.2667-3896_2667-388 others(13): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11606758 | |||||
| chr2:11606758
|
C | CATTATTA others(5): Show |
1 | a0001c0001t0002g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2667-3899_2667-388 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11606758 | |||||
| chr2:11606758
|
C | CATTATTA others(8): Show |
1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2667-3902_2667-388 others(19): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11606758 | |||||
| chr2:11606758
|
C | T | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2667-3930C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606758 | ||||||
| chr2:11606758
|
CATT | C | 26 | a0001c0001t0002g0203a0001c0001t0002g0241a0001c0001t0011g0205others(23): Show | 26 | HG01168.hp1 HG02280.hp1 HG02922.hp2 others(23): Show |
intron_variant | MODIFIER | c.2667-3890_2667-388 others(7): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11606758 | |||||
| chr2:11606758
|
CATTATT | C | 45 | a0001c0001t0002g0192a0001c0001t0002g0210a0001c0001t0002g0222others(42): Show | 45 | HG00099.hp2 HG00733.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.2667-3893_2667-388 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11606758 | |||||
| chr2:11606758
|
CATTATTA others(8): Show |
C | 136 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.2667-3902_2667-388 others(19): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11606758 | |||||
| chr2:11606758
|
CATTATTA others(11): Show |
C | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2667-3905_2667-388 others(22): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11606758 | |||||
| chr2:11606818
|
C | T | 10 | a0007c0044t0039g0011a0007c0058t0024g0125a0009c0029t0020g0016others(7): Show | 10 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2667-3870C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606818 | ||||||
| chr2:11606845
|
T | C | 161 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(158): Show | 161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.2667-3843T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606845 | ||||||
| chr2:11606871
|
C | T | 3 | a0002c0007t0001g0104a0002c0053t0019g0090a0002c0061t0062g0134 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2667-3817C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606871 | ||||||
| chr2:11606876
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2667-3812G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606876 | ||||||
| chr2:11606878
|
G | A | 56 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(53): Show | 56 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2667-3810G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606878 | ||||||
| chr2:11606937
|
C | T | 56 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(53): Show | 56 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2667-3751C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606937 | ||||||
| chr2:11606975
|
G | T | 26 | a0001c0001t0002g0232a0001c0001t0002g0247a0002c0007t0020g0307others(23): Show | 26 | HG00099.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2667-3713G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11606975 | ||||||
| chr2:11607105
|
A | G | 56 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(53): Show | 56 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2667-3583A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607105 | ||||||
| chr2:11607149
|
T | C | 1 | a0003c0003t0005g0158 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2667-3539T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607149 | ||||||
| chr2:11607353
|
A | G | 2 | a0009c0019t0012g0161a0009c0019t0074g0284 | 2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2667-3335A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607353 | ||||||
| chr2:11607424
|
ATGTATGT others(1): Show |
A | 4 | a0005c0066t0022g0072a0007c0015t0021g0069a0007c0015t0027g0004others(1): Show | 4 | HG02258.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.2667-3260_2667-325 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607424 | |||||
| chr2:11607428
|
A | ATG | 4 | a0009c0029t0041g0028a0019c0036t0001g0299a0019c0036t0001g0300others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2667-3228_2667-322 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607428 | |||||
| chr2:11607428
|
ATG | A | 68 | a0001c0001t0002g0192a0001c0001t0002g0210a0001c0001t0002g0222others(65): Show | 68 | HG00099.hp2 HG00733.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.2667-3228_2667-322 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607428 | |||||
| chr2:11607428
|
ATGTG | A | 6 | a0002c0007t0037g0023a0006c0027t0004g0177a0006c0033t0034g0302others(3): Show | 6 | HG03041.hp2 HG03130.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.2667-3230_2667-322 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607428 | |||||
| chr2:11607428
|
ATGTGTG | A | 13 | a0001c0013t0011g0200a0002c0007t0001g0104a0002c0053t0019g0090others(10): Show | 13 | HG01109.hp2 HG02486.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2667-3232_2667-322 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607428 | |||||
| chr2:11607428
|
ATGTGTGT others(1): Show |
A | 40 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(37): Show | 40 | HG00423.hp1 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.2667-3234_2667-322 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607428 | |||||
| chr2:11607430
|
G | GTA | 5 | a0007c0058t0024g0125a0010c0035t0060g0126a0013c0018t0003g0019others(2): Show | 5 | HG02145.hp2 HG02451.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2667-3257_2667-325 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607430 | |||||
| chr2:11607432
|
G | A | 1 | a0011c0008t0045g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2667-3256G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607432 | ||||||
| chr2:11607434
|
G | A | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2667-3254G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607434 | ||||||
| chr2:11607448
|
GTGTGTGT others(9): Show |
G | 5 | a0001c0001t0002g0232a0004c0004t0025g0248a0005c0002t0010g0119others(2): Show | 5 | HG00099.hp1 HG01074.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2667-3238_2667-322 others(20): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607448 | |||||
| chr2:11607450
|
GTGTGTGT others(5): Show |
G | 3 | a0001c0001t0001g0166a0001c0001t0004g0206a0006c0033t0003g0266 | 3 | HG02129.hp2 HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2667-3236_2667-322 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607450 | |||||
| chr2:11607452
|
GTGTGTGT others(3): Show |
G | 74 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(71): Show | 74 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.2667-3234_2667-322 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607452 | |||||
| chr2:11607454
|
GTGTGTGT others(1): Show |
G | 19 | a0001c0001t0004g0186a0001c0013t0011g0218a0002c0005t0001g0034others(16): Show | 19 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(16): Show |
intron_variant | MODIFIER | c.2667-3232_2667-322 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607454 | |||||
| chr2:11607454
|
GTGTGTGT others(3): Show |
G | 2 | a0004c0025t0008g0277a0052c0085t0011g0280 | 2 | HG00673.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2667-3232_2667-322 others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607454 | |||||
| chr2:11607458
|
GTGTATA | G | 5 | a0002c0055t0044g0003a0005c0002t0010g0101a0005c0002t0050g0084others(2): Show | 5 | HG01109.hp1 HG01496.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2667-3228_2667-322 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607458 | |||||
| chr2:11607460
|
G | A | 1 | a0003c0003t0005g0113 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2667-3228G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607460 | ||||||
| chr2:11607460
|
GTA | G | 12 | a0001c0001t0002g0247a0002c0007t0020g0307a0002c0012t0023g0085others(9): Show | 12 | HG00741.hp1 HG01071.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2667-3217_2667-321 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607460 | |||||
| chr2:11607460
|
GTATA | G | 3 | a0013c0018t0022g0030a0032c0048t0014g0008a0044c0068t0009g0080 | 3 | HG03209.hp2 HG03239.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2667-3219_2667-321 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607460 | |||||
| chr2:11607462
|
A | G | 26 | a0002c0007t0052g0075a0002c0012t0023g0086a0002c0012t0024g0127others(23): Show | 26 | HG00639.hp1 HG01257.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.2667-3226A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607462 | ||||||
| chr2:11607464
|
A | G | 13 | a0001c0001t0002g0247a0002c0007t0020g0307a0002c0007t0052g0075others(10): Show | 13 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.2667-3224A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607464 | ||||||
| chr2:11607466
|
A | G | 1 | a0021c0040t0036g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2667-3222A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607466 | ||||||
| chr2:11607471
|
T | C | 6 | a0001c0001t0002g0232a0004c0004t0025g0248a0005c0002t0010g0119others(3): Show | 6 | HG00099.hp1 HG01074.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2667-3217T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607471 | ||||||
| chr2:11607475
|
CACACATA others(31): Show |
C | 1 | a0011c0008t0045g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2667-3209_2667-317 others(42): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607475 | |||||
| chr2:11607477
|
CACATACA others(29): Show |
C | 8 | a0007c0058t0024g0125a0009c0029t0020g0016a0010c0035t0060g0126others(5): Show | 8 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2667-3158_2667-312 others(40): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607477 | |||||
| chr2:11607483
|
C | T | 1 | a0053c0083t0008g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2667-3205C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607483 | ||||||
| chr2:11607483
|
CAT | C | 5 | a0001c0001t0002g0203a0001c0001t0002g0229a0001c0001t0006g0294others(2): Show | 5 | HG01243.hp2 HG01981.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.2667-3197_2667-319 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607483 | |||||
| chr2:11607497
|
T | C | 2 | a0002c0005t0051g0055a0004c0088t0025g0223 | 2 | HG01433.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2667-3191T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607497 | ||||||
| chr2:11607508
|
A | G | 6 | a0001c0001t0006g0217a0001c0001t0032g0201a0012c0010t0002g0184others(3): Show | 6 | HG00735.hp2 HG01106.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.2667-3180A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607508 | ||||||
| chr2:11607519
|
CAT | C | 6 | a0002c0057t0059g0021a0005c0002t0003g0133a0007c0016t0015g0017others(3): Show | 6 | HG01109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2667-3161_2667-316 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607519 | |||||
| chr2:11607525
|
TATAC | T | 56 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(53): Show | 56 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2667-3161_2667-315 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607525 | |||||
| chr2:11607526
|
A | G | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2667-3162A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607526 | ||||||
| chr2:11607530
|
A | G | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2667-3158A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607530 | ||||||
| chr2:11607531
|
C | T | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2667-3157C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607531 | ||||||
| chr2:11607531
|
CAT | C | 103 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2667-3149_2667-314 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607531 | |||||
| chr2:11607533
|
T | C | 63 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(60): Show | 63 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.2667-3155T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607533 | ||||||
| chr2:11607539
|
T | C | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2667-3149T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607539 | ||||||
| chr2:11607539
|
T | G | 1 | a0001c0001t0073g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2667-3149T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607539 | ||||||
| chr2:11607542
|
A | G | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2667-3146A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607542 | ||||||
| chr2:11607543
|
T | C | 27 | a0001c0001t0002g0232a0001c0001t0002g0247a0002c0007t0020g0307others(24): Show | 27 | HG00099.hp1 HG00741.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.2667-3145T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607543 | ||||||
| chr2:11607555
|
CAT | C | 3 | a0002c0005t0006g0293a0006c0097t0016g0058a0042c0070t0015g0010 | 3 | HG03579.hp2 NA19086.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2667-3125_2667-312 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607555 | |||||
| chr2:11607557
|
T | C | 2 | a0007c0044t0039g0011a0010c0031t0046g0096 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2667-3131T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607557 | ||||||
| chr2:11607566
|
G | A | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2667-3122G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607566 | ||||||
| chr2:11607567
|
C | T | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2667-3121C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607567 | ||||||
| chr2:11607577
|
C | T | 2 | a0007c0044t0039g0011a0010c0031t0046g0096 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2667-3111C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607577 | ||||||
| chr2:11607578
|
A | T | 1 | a0001c0001t0073g0253 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2667-3110A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607578 | ||||||
| chr2:11607581
|
T | G | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2667-3107T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607581 | ||||||
| chr2:11607585
|
C | CAT | 79 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(76): Show | 79 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.2667-3097_2667-309 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607585 | |||||
| chr2:11607591
|
T | G | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2667-3097T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607591 | ||||||
| chr2:11607592
|
A | ACATATAT others(39): Show |
44 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(41): Show | 44 | HG00423.hp1 HG00621.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.2667-3080_2667-307 others(50): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607592 | |||||
| chr2:11607592
|
A | ATACATAT others(31): Show |
12 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(9): Show | 12 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2667-3096_2667-309 others(42): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607592 | ||||||
| chr2:11607593
|
C | T | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2667-3095C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607593 | ||||||
| chr2:11607595
|
T | C | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2667-3093T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607595 | ||||||
| chr2:11607595
|
T | TAGATAC | 71 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(68): Show | 71 | HG00099.hp2 HG00733.hp2 HG01071.hp1 others(68): Show |
intron_variant | MODIFIER | c.2667-3092_2667-309 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607595 | |||||
| chr2:11607595
|
T | TATAGATA others(1): Show |
11 | a0002c0007t0001g0104a0002c0053t0019g0090a0002c0061t0062g0134others(8): Show | 11 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2667-3090_2667-308 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607595 | |||||
| chr2:11607595
|
T | TATATATA others(9): Show |
26 | a0001c0001t0002g0232a0001c0001t0002g0247a0002c0007t0020g0307others(23): Show | 26 | HG00099.hp1 HG00741.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2667-3082_2667-308 others(20): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607595 | |||||
| chr2:11607595
|
T | TATATATA others(11): Show |
122 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2667-3080_2667-307 others(22): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607595 | |||||
| chr2:11607599
|
T | TATACATA others(39): Show |
6 | a0002c0057t0059g0021a0005c0002t0003g0133a0007c0016t0015g0017others(3): Show | 6 | HG01109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2667-3080_2667-307 others(50): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607599 | |||||
| chr2:11607601
|
T | C | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2667-3087T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607601 | ||||||
| chr2:11607610
|
A | G | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2667-3078A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607610 | ||||||
| chr2:11607613
|
C | T | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2667-3075C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607613 | ||||||
| chr2:11607625
|
T | C | 1 | a0007c0044t0039g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2667-3063T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607625 | ||||||
| chr2:11607625
|
T | TATATAC | 277 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.2667-3057_2667-305 others(10): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11607625 | |||||
| chr2:11607652
|
G | T | 279 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.2667-3036G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607652 | ||||||
| chr2:11607657
|
G | A | 1 | a0004c0026t0004g0290 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2667-3031G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607657 | ||||||
| chr2:11607757
|
T | C | 2 | a0007c0058t0024g0125a0013c0018t0003g0019 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2667-2931T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607757 | ||||||
| chr2:11607834
|
T | C | 160 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.2667-2854T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607834 | ||||||
| chr2:11607911
|
G | A | 104 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.2667-2777G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11607911 | ||||||
| chr2:11608027
|
C | T | 1 | a0004c0004t0008g0292 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2667-2661C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11608027 | ||||||
| chr2:11608280
|
T | C | 160 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.2667-2408T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11608280 | ||||||
| chr2:11608387
|
A | G | 10 | a0002c0034t0031g0263a0002c0057t0059g0021a0005c0002t0003g0133others(7): Show | 10 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2667-2301A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11608387 | ||||||
| chr2:11608440
|
G | A | 2 | a0002c0005t0001g0035a0002c0005t0001g0036 | 2 | NA18945.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.2667-2248G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11608440 | ||||||
| chr2:11608459
|
C | A | 70 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(67): Show | 70 | HG00099.hp2 HG00733.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.2667-2229C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11608459 | ||||||
| chr2:11608464
|
C | A | 2 | a0002c0005t0001g0035a0002c0005t0001g0036 | 2 | NA18945.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.2667-2224C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11608464 | ||||||
| chr2:11608623
|
G | A | 1 | a0002c0011t0001g0271 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2667-2065G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11608623 | ||||||
| chr2:11608690
|
G | C | 3 | a0001c0001t0002g0207a0001c0001t0004g0291a0002c0005t0001g0033 | 3 | NA18960.hp2 NA18981.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.2667-1998G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11608690 | ||||||
| chr2:11608915
|
C | T | 294 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.2667-1773C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11608915 | ||||||
| chr2:11609085
|
C | T | 1 | a0002c0005t0005g0046 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2667-1603C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609085 | ||||||
| chr2:11609125
|
G | A | 55 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(52): Show | 55 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2667-1563G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609125 | ||||||
| chr2:11609224
|
T | C | 3 | a0002c0007t0001g0104a0002c0053t0019g0090a0002c0061t0062g0134 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2667-1464T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609224 | ||||||
| chr2:11609242
|
T | TTATTTAT others(7): Show |
1 | a0004c0004t0004g0240 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2667-1445_2667-144 others(18): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
T | TTTTA | 52 | a0001c0001t0002g0192a0001c0001t0002g0229a0001c0001t0002g0231others(49): Show | 52 | HG00741.hp2 HG01099.hp1 HG01099.hp2 others(49): Show |
intron_variant | MODIFIER | c.2667-1409_2667-140 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
T | TTTTATTT others(1): Show |
159 | a0001c0001t0001g0042a0001c0001t0001g0166a0001c0001t0002g0032others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.2667-1413_2667-140 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
T | TTTTATTT others(5): Show |
29 | a0001c0001t0001g0044a0001c0001t0002g0182a0001c0001t0002g0193others(26): Show | 29 | HG00735.hp1 HG01167.hp2 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.2667-1417_2667-140 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
T | TTTTTTTT others(1): Show |
23 | a0001c0001t0002g0276a0001c0001t0002g0286a0001c0013t0011g0200others(20): Show | 23 | HG00673.hp2 HG00733.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.2667-1443_2667-144 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
T | TTTTTTTT others(5): Show |
5 | a0002c0005t0001g0057a0002c0020t0026g0219a0002c0020t0026g0221others(2): Show | 5 | HG00621.hp2 HG03239.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.2667-1443_2667-144 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
T | TTTTTTTT others(9): Show |
1 | a0005c0002t0055g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2667-1443_2667-144 others(20): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
T | TTTTTTTT others(9): Show |
1 | a0001c0001t0002g0274 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2667-1443_2667-144 others(20): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
TTTTA | T | 8 | a0002c0007t0001g0104a0002c0053t0019g0090a0002c0061t0062g0134others(5): Show | 8 | HG01070.hp2 HG02809.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2667-1409_2667-140 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
TTTTATTT others(1): Show |
T | 3 | a0005c0002t0050g0084a0008c0006t0009g0264a0008c0006t0009g0265 | 3 | HG00140.hp1 HG01496.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2667-1413_2667-140 others(12): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609242
|
TTTTATTT others(5): Show |
T | 1 | a0002c0007t0037g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2667-1417_2667-140 others(16): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr2 | 11609242 | |||||
| chr2:11609350
|
C | G | 2 | a0002c0007t0020g0307a0008c0006t0054g0018 | 2 | HG01109.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2667-1338C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609350 | ||||||
| chr2:11609356
|
T | C | 56 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(53): Show | 56 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2667-1332T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609356 | ||||||
| chr2:11609441
|
G | C | 1 | a0006c0014t0005g0039 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2667-1247G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609441 | ||||||
| chr2:11609500
|
C | T | 4 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(1): Show | 4 | HG01070.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2667-1188C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609500 | ||||||
| chr2:11609671
|
C | T | 9 | a0007c0044t0039g0011a0007c0058t0024g0125a0009c0029t0020g0016others(6): Show | 9 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2667-1017C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609671 | ||||||
| chr2:11609709
|
G | T | 1 | a0005c0002t0003g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2667-979G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609709 | ||||||
| chr2:11609784
|
G | A | 1 | a0001c0001t0004g0206 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2667-904G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609784 | ||||||
| chr2:11609805
|
C | T | 1 | a0009c0019t0066g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2667-883C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609805 | ||||||
| chr2:11609848
|
G | C | 1 | a0011c0008t0045g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2667-840G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609848 | ||||||
| chr2:11609975
|
A | G | 163 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(160): Show | 163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.2667-713A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11609975 | ||||||
| chr2:11610095
|
C | T | 1 | a0006c0033t0003g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2667-593C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11610095 | ||||||
| chr2:11610216
|
G | A | 18 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(15): Show | 18 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2667-472G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11610216 | ||||||
| chr2:11610248
|
G | A | 55 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(52): Show | 55 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2667-440G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11610248 | ||||||
| chr2:11610403
|
T | C | 1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2667-285T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11610403 | ||||||
| chr2:11610528
|
G | A | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2667-160G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 17/32 | chr2 | 11610528 | ||||||
| chr2:11611040
|
C | T | 18 | a0001c0001t0002g0232a0001c0001t0002g0247a0004c0004t0004g0239others(15): Show | 18 | HG00099.hp1 HG00741.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.3006+13C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611040 | ||||||
| chr2:11611135
|
G | T | 59 | a0001c0001t0002g0192a0001c0001t0002g0210a0001c0001t0002g0222others(56): Show | 59 | HG01071.hp1 HG01074.hp1 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.3006+108G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611135 | ||||||
| chr2:11611161
|
G | C | 4 | a0007c0017t0001g0157a0007c0017t0001g0167a0009c0030t0003g0169others(1): Show | 4 | HG00423.hp2 NA19004.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.3006+134G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611161 | ||||||
| chr2:11611327
|
C | G | 117 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.3006+300C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611327 | ||||||
| chr2:11611374
|
G | A | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3006+347G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611374 | ||||||
| chr2:11611506
|
A | G | 118 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.3006+479A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611506 | ||||||
| chr2:11611516
|
G | A | 2 | a0002c0055t0044g0003a0006c0054t0043g0002 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3006+489G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611516 | ||||||
| chr2:11611526
|
AAACTCCT others(10): Show |
A | 2 | a0003c0003t0002g0225a0003c0003t0022g0120 | 2 | HG01074.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3006+503_3006+519d others(19): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr2 | 11611526 | |||||
| chr2:11611586
|
T | C | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3006+559T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611586 | ||||||
| chr2:11611614
|
C | G | 1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3006+587C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611614 | ||||||
| chr2:11611673
|
C | T | 92 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.3006+646C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611673 | ||||||
| chr2:11611729
|
G | A | 2 | a0002c0007t0001g0104a0002c0061t0062g0134 | 2 | HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3006+702G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11611729 | ||||||
| chr2:11612018
|
AC | A | 3 | a0001c0001t0002g0207a0001c0001t0004g0291a0002c0005t0001g0033 | 3 | NA18960.hp2 NA18981.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.3007-474delC | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr2 | 11612018 | |||||
| chr2:11612057
|
G | A | 6 | a0007c0058t0024g0125a0010c0035t0060g0126a0010c0035t0064g0128others(3): Show | 6 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.3007-438G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11612057 | ||||||
| chr2:11612193
|
C | CA | 24 | a0002c0007t0052g0075a0002c0055t0044g0003a0005c0002t0010g0101others(21): Show | 24 | HG00639.hp1 HG01109.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.3007-286dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr2 | 11612193 | |||||
| chr2:11612193
|
C | CAA | 7 | a0002c0005t0007g0031a0002c0020t0026g0221a0003c0076t0007g0102others(4): Show | 7 | HG02647.hp1 HG02965.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.3007-287_3007-286d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr2 | 11612193 | |||||
| chr2:11612193
|
C | CAAA | 165 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.3007-288_3007-286d others(5): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr2 | 11612193 | |||||
| chr2:11612193
|
C | CAAAA | 9 | a0001c0001t0011g0205a0001c0001t0018g0235a0002c0005t0001g0036others(6): Show | 9 | HG00741.hp2 HG01981.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.3007-289_3007-286d others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr2 | 11612193 | |||||
| chr2:11612247
|
C | T | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3007-248C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11612247 | ||||||
| chr2:11612342
|
T | A | 1 | a0001c0001t0032g0201 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3007-153T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 18/32 | chr2 | 11612342 | ||||||
| chr2:11612793
|
G | A | 164 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.3122+183G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11612793 | ||||||
| chr2:11612821
|
C | T | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3122+211C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11612821 | ||||||
| chr2:11612928
|
G | A | 1 | a0044c0068t0009g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3122+318G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11612928 | ||||||
| chr2:11613067
|
A | G | 127 | a0001c0001t0002g0232a0001c0001t0002g0247a0001c0001t0002g0274others(124): Show | 127 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.3122+457A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613067 | ||||||
| chr2:11613119
|
G | C | 3 | a0007c0043t0035g0095a0007c0044t0039g0011a0009c0029t0020g0016 | 3 | HG02630.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3122+509G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613119 | ||||||
| chr2:11613131
|
G | A | 12 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(9): Show | 12 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.3122+521G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613131 | ||||||
| chr2:11613159
|
A | G | 2 | a0007c0044t0039g0011a0009c0029t0020g0016 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3122+549A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613159 | ||||||
| chr2:11613222
|
G | A | 1 | a0028c0062t0040g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3122+612G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613222 | ||||||
| chr2:11613225
|
A | G | 1 | a0001c0001t0002g0282 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3122+615A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613225 | ||||||
| chr2:11613229
|
G | A | 1 | a0002c0005t0006g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3122+619G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613229 | ||||||
| chr2:11613316
|
G | A | 2 | a0010c0031t0046g0096a0013c0018t0022g0030 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3122+706G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613316 | ||||||
| chr2:11613571
|
C | T | 123 | a0001c0001t0002g0232a0001c0001t0002g0247a0001c0001t0002g0274others(120): Show | 123 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.3122+961C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613571 | ||||||
| chr2:11613758
|
C | G | 6 | a0007c0058t0024g0125a0010c0035t0060g0126a0010c0035t0064g0128others(3): Show | 6 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.3122+1148C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613758 | ||||||
| chr2:11613769
|
G | C | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3122+1159G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613769 | ||||||
| chr2:11613829
|
T | C | 53 | a0002c0007t0052g0075a0002c0012t0023g0085a0002c0012t0023g0086others(50): Show | 53 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.3122+1219T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613829 | ||||||
| chr2:11613967
|
G | T | 2 | a0008c0006t0009g0264a0008c0006t0009g0265 | 2 | HG00140.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.3123-1124G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613967 | ||||||
| chr2:11613989
|
A | T | 3 | a0010c0031t0046g0096a0013c0018t0022g0030a0030c0051t0042g0306 | 3 | HG01884.hp1 HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3123-1102A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11613989 | ||||||
| chr2:11614014
|
C | T | 2 | a0006c0027t0004g0177a0025c0093t0002g0178 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3123-1077C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614014 | ||||||
| chr2:11614117
|
G | A | 5 | a0002c0057t0059g0021a0005c0002t0048g0269a0010c0031t0046g0096others(2): Show | 5 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3123-974G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614117 | ||||||
| chr2:11614124
|
GA | G | 58 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(55): Show | 58 | HG01071.hp1 HG01081.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.3123-966delA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614124 | ||||||
| chr2:11614125
|
A | AT | 54 | a0001c0001t0001g0042a0001c0001t0002g0274a0001c0001t0002g0276others(51): Show | 54 | HG00423.hp1 HG00621.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.3123-947dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr2 | 11614125 | |||||
| chr2:11614125
|
A | ATT | 7 | a0001c0013t0011g0200a0002c0005t0007g0031a0002c0007t0001g0104others(4): Show | 7 | HG02809.hp1 HG03927.hp1 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.3123-948_3123-947d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr2 | 11614125 | |||||
| chr2:11614125
|
A | T | 4 | a0001c0001t0002g0229a0004c0004t0002g0295a0005c0002t0003g0116others(1): Show | 4 | HG01243.hp2 HG01981.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.3123-966A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614125 | ||||||
| chr2:11614125
|
AT | A | 21 | a0001c0001t0002g0232a0001c0001t0002g0247a0002c0007t0020g0307others(18): Show | 21 | HG00099.hp1 HG00741.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.3123-947delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr2 | 11614125 | |||||
| chr2:11614125
|
ATTTT | A | 51 | a0002c0007t0052g0075a0002c0012t0023g0085a0002c0012t0023g0086others(48): Show | 51 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.3123-950_3123-947d others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr2 | 11614125 | |||||
| chr2:11614181
|
C | T | 1 | a0006c0033t0003g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3123-910C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614181 | ||||||
| chr2:11614251
|
C | T | 6 | a0007c0058t0024g0125a0010c0035t0060g0126a0010c0035t0064g0128others(3): Show | 6 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.3123-840C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614251 | ||||||
| chr2:11614328
|
T | C | 208 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.3123-763T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614328 | ||||||
| chr2:11614350
|
C | T | 1 | a0051c0086t0008g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3123-741C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614350 | ||||||
| chr2:11614375
|
C | T | 52 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(49): Show | 52 | HG00423.hp1 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.3123-716C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614375 | ||||||
| chr2:11614550
|
TTTG | T | 12 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(9): Show | 12 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.3123-523_3123-521d others(5): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr2 | 11614550 | |||||
| chr2:11614586
|
T | C | 45 | a0001c0001t0002g0274a0001c0001t0002g0276a0001c0001t0002g0286others(42): Show | 45 | HG00423.hp1 HG00621.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.3123-505T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614586 | ||||||
| chr2:11614602
|
C | T | 6 | a0008c0006t0054g0018a0011c0008t0045g0022a0014c0023t0014g0068others(3): Show | 6 | HG01070.hp2 HG01109.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3123-489C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614602 | ||||||
| chr2:11614615
|
T | G | 105 | a0001c0001t0002g0232a0001c0001t0002g0247a0001c0001t0002g0274others(102): Show | 105 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.3123-476T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614615 | ||||||
| chr2:11614633
|
G | A | 1 | a0007c0015t0021g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3123-458G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614633 | ||||||
| chr2:11614640
|
G | T | 1 | a0011c0008t0045g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3123-451G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614640 | ||||||
| chr2:11614641
|
G | T | 14 | a0002c0007t0052g0075a0002c0055t0044g0003a0005c0002t0010g0101others(11): Show | 14 | HG01109.hp1 HG01261.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.3123-450G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614641 | ||||||
| chr2:11614647
|
T | C | 1 | a0011c0008t0045g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3123-444T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614647 | ||||||
| chr2:11614649
|
T | C | 1 | a0011c0008t0045g0022 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3123-442T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614649 | ||||||
| chr2:11614683
|
C | T | 62 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(59): Show | 62 | HG01071.hp1 HG01074.hp1 HG01081.hp1 others(59): Show |
intron_variant | MODIFIER | c.3123-408C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614683 | ||||||
| chr2:11614709
|
G | A | 2 | a0017c0024t0008g0234a0017c0024t0025g0233 | 2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.3123-382G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614709 | ||||||
| chr2:11614713
|
G | A | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3123-378G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614713 | ||||||
| chr2:11614717
|
C | T | 1 | a0053c0083t0008g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3123-374C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614717 | ||||||
| chr2:11614779
|
G | A | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3123-312G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614779 | ||||||
| chr2:11614784
|
C | T | 1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3123-307C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614784 | ||||||
| chr2:11614806
|
G | A | 1 | a0003c0003t0005g0130 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3123-285G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614806 | ||||||
| chr2:11614809
|
C | T | 12 | a0002c0007t0052g0075a0002c0055t0044g0003a0006c0054t0043g0002others(9): Show | 12 | HG01109.hp1 HG01261.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3123-282C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614809 | ||||||
| chr2:11614838
|
C | T | 2 | a0010c0031t0046g0096a0013c0018t0022g0030 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3123-253C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614838 | ||||||
| chr2:11614839
|
C | CT | 93 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(90): Show | 93 | HG00099.hp1 HG00639.hp1 HG00741.hp1 others(90): Show |
intron_variant | MODIFIER | c.3123-246dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | INFO_REALIGN_3_PRIME | chr2 | 11614839 | |||||
| chr2:11614974
|
C | G | 1 | a0002c0005t0001g0066 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3123-117C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11614974 | ||||||
| chr2:11615008
|
C | T | 6 | a0002c0007t0001g0104a0002c0053t0019g0090a0002c0061t0062g0134others(3): Show | 6 | HG01884.hp1 HG02809.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3123-83C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 19/32 | chr2 | 11615008 | ||||||
| chr2:11615317
|
T | G | 255 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(252): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.3322+27T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11615317 | ||||||
| chr2:11615359
|
G | T | 12 | a0002c0007t0052g0075a0002c0055t0044g0003a0006c0054t0043g0002others(9): Show | 12 | HG01109.hp1 HG01261.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3322+69G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11615359 | ||||||
| chr2:11615768
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3322+478G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11615768 | ||||||
| chr2:11615800
|
C | T | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3322+510C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11615800 | ||||||
| chr2:11615801
|
G | A | 12 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(9): Show | 12 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.3322+511G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11615801 | ||||||
| chr2:11615902
|
T | C | 9 | a0008c0006t0054g0018a0010c0031t0038g0029a0011c0008t0045g0022others(6): Show | 9 | HG01070.hp2 HG01109.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.3322+612T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11615902 | ||||||
| chr2:11615916
|
C | T | 12 | a0008c0006t0012g0112a0008c0006t0017g0015a0008c0006t0017g0259others(9): Show | 12 | HG00639.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.3322+626C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11615916 | ||||||
| chr2:11615976
|
C | T | 1 | a0002c0057t0059g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3323-655C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11615976 | ||||||
| chr2:11616035
|
C | T | 1 | a0007c0015t0021g0069 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3323-596C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11616035 | ||||||
| chr2:11616100
|
C | T | 14 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.3323-531C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11616100 | ||||||
| chr2:11616128
|
T | A | 1 | a0001c0001t0002g0287 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3323-503T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11616128 | ||||||
| chr2:11616134
|
T | C | 118 | a0001c0001t0002g0192a0001c0001t0002g0210a0001c0001t0002g0222others(115): Show | 118 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.3323-497T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11616134 | ||||||
| chr2:11616175
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3323-456C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11616175 | ||||||
| chr2:11616303
|
C | T | 93 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.3323-328C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11616303 | ||||||
| chr2:11616345
|
C | G | 1 | a0001c0001t0002g0032 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3323-286C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11616345 | ||||||
| chr2:11616363
|
T | C | 1 | a0002c0005t0011g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3323-268T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11616363 | ||||||
| chr2:11616452
|
C | G | 1 | a0007c0015t0027g0004 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3323-179C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 20/32 | chr2 | 11616452 | ||||||
| chr2:11616859
|
T | G | 1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3412+139T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11616859 | ||||||
| chr2:11616883
|
A | G | 282 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0166others(279): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.3412+163A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11616883 | ||||||
| chr2:11616897
|
C | T | 190 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(187): Show | 190 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.3412+177C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11616897 | ||||||
| chr2:11616950
|
G | C | 190 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(187): Show | 190 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.3412+230G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11616950 | ||||||
| chr2:11616960
|
G | A | 189 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0210others(186): Show | 189 | HG00099.hp1 HG00423.hp1 HG00621.hp2 others(186): Show |
intron_variant | MODIFIER | c.3412+240G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11616960 | ||||||
| chr2:11616987
|
G | T | 3 | a0002c0007t0001g0104a0002c0053t0019g0090a0002c0061t0062g0134 | 3 | HG02809.hp1 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3412+267G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11616987 | ||||||
| chr2:11617014
|
G | A | 19 | a0001c0001t0002g0232a0001c0001t0002g0247a0002c0007t0020g0307others(16): Show | 19 | HG00099.hp1 HG00741.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.3412+294G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617014 | ||||||
| chr2:11617032
|
C | T | 1 | a0004c0026t0004g0290 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3412+312C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617032 | ||||||
| chr2:11617097
|
G | A | 1 | a0001c0001t0002g0193 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3412+377G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617097 | ||||||
| chr2:11617171
|
C | T | 1 | a0015c0022t0001g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3412+451C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617171 | ||||||
| chr2:11617222
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3412+502G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617222 | ||||||
| chr2:11617332
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3412+612C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617332 | ||||||
| chr2:11617568
|
G | A | 7 | a0007c0058t0024g0125a0008c0006t0024g0143a0010c0035t0060g0126others(4): Show | 7 | HG00639.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3413-720G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617568 | ||||||
| chr2:11617664
|
C | T | 1 | a0009c0019t0074g0284 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3413-624C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617664 | ||||||
| chr2:11617669
|
C | G | 1 | a0004c0025t0008g0279 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3413-619C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617669 | ||||||
| chr2:11617677
|
G | A | 1 | a0021c0040t0036g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3413-611G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617677 | ||||||
| chr2:11617686
|
C | T | 1 | a0002c0007t0007g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3413-602C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617686 | ||||||
| chr2:11617709
|
C | T | 5 | a0001c0001t0006g0217a0001c0013t0011g0200a0002c0020t0026g0219others(2): Show | 5 | HG00673.hp2 HG02056.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.3413-579C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617709 | ||||||
| chr2:11617751
|
G | A | 2 | a0008c0006t0024g0143a0033c0047t0031g0107 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3413-537G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617751 | ||||||
| chr2:11617792
|
C | T | 3 | a0005c0002t0003g0133a0007c0016t0015g0017a0008c0060t0061g0305 | 3 | HG02559.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3413-496C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617792 | ||||||
| chr2:11617926
|
C | G | 1 | a0006c0033t0034g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3413-362C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11617926 | ||||||
| chr2:11618092
|
T | TCTGGGAC others(137): Show |
1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3413-186_3413-43du others(145): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618092 | |||||
| chr2:11618092
|
T | TCTGGGAC others(169): Show |
3 | a0004c0004t0004g0239a0004c0004t0004g0242a0004c0088t0025g0223 | 3 | HG01168.hp2 HG01169.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(176): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618092 | |||||
| chr2:11618104
|
C | CACTCCTG others(169): Show |
1 | a0005c0002t0010g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(176): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618104 | |||||
| chr2:11618115
|
C | CAGGTCAC others(118): Show |
1 | a0020c0039t0004g0283 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3413-173_3413-172i others(127): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11618115 | ||||||
| chr2:11618121
|
G | A | 1 | a0020c0039t0004g0283 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3413-167G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11618121 | ||||||
| chr2:11618123
|
C | T | 1 | a0020c0039t0004g0283 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3413-165C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11618123 | ||||||
| chr2:11618128
|
A | AGATGGGC others(25): Show |
2 | a0001c0001t0073g0253a0004c0004t0004g0289 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3413-153_3413-122d others(34): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618128 | |||||
| chr2:11618128
|
A | AGATGGGC others(121): Show |
1 | a0002c0005t0001g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3413-122_3413-121i others(130): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618128 | |||||
| chr2:11618128
|
A | AGATGGGC others(89): Show |
1 | a0006c0033t0034g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3413-122_3413-121i others(98): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618128 | |||||
| chr2:11618128
|
A | AGATGGGC others(217): Show |
1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3413-122_3413-121i others(226): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618128 | |||||
| chr2:11618128
|
A | AGATGGGC others(121): Show |
1 | a0002c0005t0051g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3413-122_3413-121i others(130): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618128 | |||||
| chr2:11618128
|
A | AGATGGGC others(89): Show |
1 | a0026c0092t0018g0249 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3413-153_3413-58du others(97): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618128 | |||||
| chr2:11618128
|
A | AGATGGGC others(185): Show |
1 | a0034c0046t0012g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(192): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618128 | |||||
| chr2:11618128
|
A | AGATGGGC others(377): Show |
1 | a0015c0022t0001g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(384): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618128 | |||||
| chr2:11618128
|
A | G | 1 | a0020c0039t0004g0283 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3413-160A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11618128 | ||||||
| chr2:11618136
|
C | CACTCCTG others(185): Show |
1 | a0054c0084t0002g0208 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3413-122_3413-121i others(194): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(57): Show |
1 | a0002c0005t0006g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3413-122_3413-121i others(66): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(185): Show |
1 | a0004c0026t0013g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3413-122_3413-121i others(194): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(89): Show |
1 | a0013c0052t0049g0261 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3413-122_3413-121i others(98): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(121): Show |
2 | a0001c0001t0007g0062a0005c0002t0010g0123 | 2 | HG01071.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.3413-122_3413-121i others(130): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(217): Show |
1 | a0049c0081t0002g0199 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3413-122_3413-121i others(226): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(89): Show |
1 | a0001c0001t0011g0205 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3413-122_3413-121i others(98): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(25): Show |
19 | a0001c0001t0002g0207a0001c0001t0002g0252a0001c0001t0069g0288others(16): Show | 19 | HG00408.hp1 HG00408.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.3413-72_3413-41dup others(32): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(265): Show |
1 | a0015c0022t0010g0132 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3413-97_3413-96ins others(272): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(89): Show |
1 | a0001c0001t0004g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3413-90_3413-89ins others(96): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(185): Show |
1 | a0001c0001t0002g0247 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3413-90_3413-89ins others(192): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(57): Show |
27 | a0001c0001t0002g0192a0001c0001t0018g0235a0002c0007t0001g0262others(24): Show | 27 | HG00639.hp2 HG00741.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.3413-104_3413-41du others(65): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(105): Show |
1 | a0004c0004t0008g0173 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3413-62_3413-61ins others(112): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(137): Show |
1 | a0003c0009t0015g0105 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3413-62_3413-61ins others(144): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(169): Show |
1 | a0006c0033t0003g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3413-62_3413-61ins others(176): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(89): Show |
13 | a0001c0001t0002g0232a0001c0013t0006g0181a0002c0005t0001g0057others(10): Show | 13 | HG00621.hp2 HG01074.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.3413-136_3413-41du others(97): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(137): Show |
1 | a0003c0003t0057g0059 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(144): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(217): Show |
3 | a0001c0001t0005g0047a0002c0005t0007g0064a0027c0096t0005g0074 | 3 | NA18962.hp1 NA19056.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(224): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(169): Show |
2 | a0001c0001t0018g0258a0047c0077t0002g0174 | 2 | HG01099.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(176): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(201): Show |
4 | a0001c0001t0030g0087a0003c0003t0001g0267a0005c0002t0013g0187others(1): Show | 4 | HG02698.hp1 HG03669.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(208): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(233): Show |
1 | a0005c0002t0013g0188 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(240): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(585): Show |
1 | a0001c0001t0001g0042 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(592): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(265): Show |
8 | a0002c0005t0001g0035a0002c0005t0001g0036a0003c0003t0001g0268others(5): Show | 8 | HG00733.hp2 HG01167.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(272): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(441): Show |
2 | a0017c0024t0008g0234a0017c0024t0025g0233 | 2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(448): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(601): Show |
1 | a0009c0030t0016g0077 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(608): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(329): Show |
1 | a0003c0003t0001g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(336): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(393): Show |
1 | a0005c0002t0071g0185 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(400): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(441): Show |
1 | a0004c0004t0008g0246 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(448): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(345): Show |
1 | a0056c0091t0002g0209 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(352): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(121): Show |
11 | a0002c0007t0020g0307a0002c0012t0065g0103a0002c0057t0059g0021others(8): Show | 11 | HG01106.hp2 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(128): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(153): Show |
5 | a0001c0001t0004g0175a0002c0007t0001g0104a0003c0003t0002g0225others(2): Show | 5 | HG00673.hp1 HG01074.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(160): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(185): Show |
6 | a0001c0089t0002g0189a0002c0053t0019g0090a0005c0002t0003g0139others(3): Show | 6 | HG01081.hp1 HG01433.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(192): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(217): Show |
2 | a0004c0004t0025g0248a0015c0022t0010g0140 | 2 | HG01257.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(224): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(457): Show |
1 | a0053c0083t0008g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(464): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(249): Show |
1 | a0008c0006t0017g0259 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(256): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(1017): Show |
1 | a0003c0003t0022g0120 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(1024): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(313): Show |
1 | a0008c0006t0019g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(320): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(633): Show |
1 | a0002c0012t0024g0127 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(640): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
C | CACTCCTG others(793): Show |
1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3413-77_3413-76ins others(800): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
CACTCCTG others(25): Show |
C | 68 | a0001c0001t0001g0166a0001c0001t0002g0032a0001c0001t0002g0193others(65): Show | 68 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.3413-72_3413-41del others(32): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618136
|
CACTCCTG others(57): Show |
C | 28 | a0002c0005t0007g0031a0002c0005t0007g0061a0002c0007t0007g0150others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.3413-104_3413-41de others(65): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618136 | |||||
| chr2:11618155
|
T | TCCTGGGA others(105): Show |
1 | a0001c0001t0006g0212 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3413-90_3413-89ins others(112): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618155 | |||||
| chr2:11618160
|
G | GGATGGGC others(25): Show |
1 | a0004c0004t0008g0273 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3413-122_3413-121i others(34): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618160 | |||||
| chr2:11618167
|
T | C | 9 | a0001c0001t0006g0255a0001c0013t0011g0218a0002c0005t0001g0034others(6): Show | 9 | HG02083.hp1 HG03669.hp2 HG03710.hp1 others(6): Show |
intron_variant | MODIFIER | c.3413-121T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11618167 | ||||||
| chr2:11618167
|
T | TGACTCCT others(25): Show |
1 | a0002c0005t0011g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3413-90_3413-89ins others(32): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618167 | |||||
| chr2:11618168
|
G | C | 8 | a0001c0001t0006g0255a0001c0013t0011g0218a0002c0005t0001g0034others(5): Show | 8 | HG02083.hp1 HG03669.hp2 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.3413-120G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11618168 | ||||||
| chr2:11618168
|
G | GACTCCTG others(57): Show |
1 | a0011c0008t0003g0297 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3413-90_3413-89ins others(64): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618168 | |||||
| chr2:11618168
|
G | GACTCCTG others(57): Show |
1 | a0044c0068t0009g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3413-65_3413-64ins others(64): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618168 | |||||
| chr2:11618168
|
G | GACTCCTG others(89): Show |
1 | a0011c0008t0003g0027 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3413-58_3413-57ins others(96): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618168 | |||||
| chr2:11618168
|
G | GACTCCTG others(377): Show |
2 | a0003c0038t0001g0083a0003c0038t0001g0088 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(384): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618168 | |||||
| chr2:11618168
|
G | GACTCCTG others(137): Show |
1 | a0051c0086t0008g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(144): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618168 | |||||
| chr2:11618168
|
G | GACTCCTG others(345): Show |
1 | a0004c0004t0004g0244 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(352): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618168 | |||||
| chr2:11618168
|
G | GACTCCTG others(121): Show |
1 | a0002c0055t0044g0003 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(128): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618168 | |||||
| chr2:11618168
|
G | GACTCCTG others(217): Show |
1 | a0007c0043t0035g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(224): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618168 | |||||
| chr2:11618168
|
G | GACTCCTG others(25): Show |
1 | a0008c0006t0005g0121 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3413-109_3413-108i others(34): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618168 | |||||
| chr2:11618187
|
T | TCCTGGGA others(137): Show |
1 | a0025c0093t0002g0178 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(144): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618187 | |||||
| chr2:11618192
|
G | A | 2 | a0002c0005t0005g0065a0004c0004t0008g0273 | 2 | HG02083.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.3413-96G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11618192 | ||||||
| chr2:11618192
|
G | GGATGGGC others(25): Show |
1 | a0001c0001t0007g0138 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3413-90_3413-89ins others(32): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618192 | |||||
| chr2:11618192
|
G | GGATGGGC others(121): Show |
1 | a0001c0001t0072g0254 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3413-90_3413-89ins others(128): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618192 | |||||
| chr2:11618199
|
T | C | 32 | a0001c0001t0001g0166a0001c0001t0002g0032a0001c0001t0002g0203others(29): Show | 32 | HG00140.hp1 HG02056.hp1 HG02083.hp1 others(29): Show |
intron_variant | MODIFIER | c.3413-89T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11618199 | ||||||
| chr2:11618200
|
G | C | 31 | a0001c0001t0001g0166a0001c0001t0002g0032a0001c0001t0002g0203others(28): Show | 31 | HG00140.hp1 HG02056.hp1 HG02083.hp1 others(28): Show |
intron_variant | MODIFIER | c.3413-88G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | chr2 | 11618200 | ||||||
| chr2:11618200
|
G | GACTCCTG others(73): Show |
1 | a0001c0001t0002g0182 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3413-62_3413-61ins others(80): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618200
|
G | GACTCCTG others(313): Show |
1 | a0001c0001t0002g0274 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3413-58_3413-57ins others(320): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618200
|
G | GACTCCTG others(217): Show |
1 | a0010c0031t0046g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3413-58_3413-57ins others(224): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618200
|
G | GACTCCTG others(201): Show |
1 | a0001c0001t0006g0214 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(208): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618200
|
G | GACTCCTG others(233): Show |
1 | a0001c0001t0006g0217 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(240): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618200
|
G | GACTCCTG others(297): Show |
2 | a0004c0004t0002g0215a0004c0082t0002g0216 | 2 | NA18952.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(304): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618200
|
G | GACTCCTG others(57): Show |
2 | a0004c0004t0002g0237a0013c0018t0047g0303 | 2 | HG02602.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(64): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618200
|
G | GACTCCTG others(153): Show |
1 | a0024c0094t0001g0048 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(160): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618200
|
G | GACTCCTG others(89): Show |
2 | a0003c0076t0007g0102a0004c0026t0004g0290 | 2 | NA18995.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.3413-41_3413-40ins others(96): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618200
|
G | GACTCCTG others(153): Show |
1 | a0004c0004t0002g0281 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(160): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618200 | |||||
| chr2:11618232
|
G | GACTCCTG others(297): Show |
1 | a0003c0003t0001g0141 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3413-41_3413-40ins others(304): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr2 | 11618232 | |||||
| chr2:11618996
|
G | A | 1 | a0037c0067t0021g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4044+77G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11618996 | ||||||
| chr2:11619069
|
G | A | 4 | a0002c0034t0019g0026a0009c0028t0003g0260a0019c0036t0001g0299others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.4044+150G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11619069 | ||||||
| chr2:11619267
|
G | A | 3 | a0002c0007t0001g0104a0002c0061t0062g0134a0010c0031t0046g0096 | 3 | HG01884.hp1 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4044+348G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11619267 | ||||||
| chr2:11619319
|
T | C | 1 | a0042c0070t0015g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4044+400T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11619319 | ||||||
| chr2:11619367
|
A | G | 2 | a0003c0003t0001g0160a0003c0003t0005g0158 | 2 | HG00558.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.4044+448A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11619367 | ||||||
| chr2:11619910
|
G | T | 1 | a0008c0006t0012g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4044+991G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11619910 | ||||||
| chr2:11619974
|
G | A | 251 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(248): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.4045-931G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11619974 | ||||||
| chr2:11620040
|
G | A | 1 | a0003c0003t0022g0120 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4045-865G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11620040 | ||||||
| chr2:11620054
|
G | A | 3 | a0008c0006t0017g0015a0008c0006t0017g0259a0008c0006t0024g0143 | 3 | HG02647.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4045-851G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11620054 | ||||||
| chr2:11620101
|
C | T | 4 | a0001c0001t0002g0232a0005c0002t0010g0119a0015c0022t0010g0140others(1): Show | 4 | HG00099.hp1 HG01074.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.4045-804C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11620101 | ||||||
| chr2:11620293
|
C | A | 8 | a0004c0004t0004g0240a0005c0002t0003g0133a0006c0033t0003g0266others(5): Show | 8 | HG02572.hp1 HG02615.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.4045-612C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11620293 | ||||||
| chr2:11620450
|
A | G | 6 | a0007c0058t0024g0125a0014c0023t0014g0068a0014c0023t0014g0071others(3): Show | 6 | HG01070.hp2 HG02922.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.4045-455A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11620450 | ||||||
| chr2:11620698
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4045-207A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11620698 | ||||||
| chr2:11620858
|
C | T | 12 | a0002c0007t0052g0075a0002c0034t0019g0026a0002c0034t0031g0263others(9): Show | 12 | HG00639.hp1 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.4045-47C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 22/32 | chr2 | 11620858 | ||||||
| chr2:11621051
|
A | G | 1 | a0002c0005t0001g0045 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4147+44A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621051 | ||||||
| chr2:11621064
|
G | A | 1 | a0019c0036t0001g0299 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4147+57G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621064 | ||||||
| chr2:11621131
|
G | T | 2 | a0009c0019t0012g0161a0009c0019t0074g0284 | 2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4147+124G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621131 | ||||||
| chr2:11621183
|
T | C | 274 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.4147+176T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621183 | ||||||
| chr2:11621214
|
GCTGA | G | 119 | a0001c0001t0002g0203a0001c0001t0002g0207a0001c0001t0002g0210others(116): Show | 119 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.4147+211_4147+214d others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr2 | 11621214 | |||||
| chr2:11621296
|
C | G | 119 | a0001c0001t0002g0203a0001c0001t0002g0207a0001c0001t0002g0210others(116): Show | 119 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.4147+289C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621296 | ||||||
| chr2:11621454
|
G | A | 1 | a0003c0003t0001g0141 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4147+447G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621454 | ||||||
| chr2:11621469
|
C | A | 1 | a0003c0003t0057g0059 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4147+462C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621469 | ||||||
| chr2:11621665
|
G | C | 1 | a0004c0026t0004g0290 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4147+658G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621665 | ||||||
| chr2:11621676
|
A | T | 1 | a0049c0081t0002g0199 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4147+669A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621676 | ||||||
| chr2:11621677
|
C | T | 5 | a0002c0007t0001g0104a0002c0061t0062g0134a0003c0009t0021g0308others(2): Show | 5 | HG01884.hp1 HG02809.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.4147+670C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621677 | ||||||
| chr2:11621812
|
C | T | 1 | a0010c0031t0038g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4147+805C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11621812 | ||||||
| chr2:11622001
|
T | A | 1 | a0004c0004t0004g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4147+994T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622001 | ||||||
| chr2:11622091
|
GT | G | 12 | a0002c0007t0052g0075a0002c0034t0019g0026a0002c0034t0031g0263others(9): Show | 12 | HG00639.hp1 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.4147+1092delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr2 | 11622091 | |||||
| chr2:11622244
|
C | A | 4 | a0001c0001t0002g0232a0005c0002t0010g0119a0015c0022t0010g0140others(1): Show | 4 | HG00099.hp1 HG01074.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.4147+1237C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622244 | ||||||
| chr2:11622292
|
G | C | 1 | a0016c0021t0017g0092 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4147+1285G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622292 | ||||||
| chr2:11622293
|
C | G | 3 | a0010c0031t0038g0029a0010c0035t0060g0126a0033c0047t0031g0107 | 3 | HG02451.hp1 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4147+1286C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622293 | ||||||
| chr2:11622424
|
A | G | 126 | a0001c0001t0002g0193a0001c0001t0002g0203a0001c0001t0002g0207others(123): Show | 126 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.4147+1417A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622424 | ||||||
| chr2:11622579
|
T | C | 1 | a0004c0082t0002g0216 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4147+1572T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622579 | ||||||
| chr2:11622837
|
G | T | 1 | a0001c0001t0011g0205 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4147+1830G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622837 | ||||||
| chr2:11622862
|
G | A | 12 | a0002c0007t0052g0075a0002c0034t0019g0026a0002c0034t0031g0263others(9): Show | 12 | HG00639.hp1 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.4147+1855G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622862 | ||||||
| chr2:11622889
|
C | G | 6 | a0002c0007t0020g0307a0002c0053t0019g0090a0008c0006t0019g0076others(3): Show | 6 | HG02451.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.4147+1882C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622889 | ||||||
| chr2:11622965
|
G | A | 1 | a0005c0002t0016g0164 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4147+1958G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11622965 | ||||||
| chr2:11623103
|
G | A | 1 | a0008c0006t0019g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4148-2051G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11623103 | ||||||
| chr2:11623118
|
C | T | 2 | a0003c0003t0001g0145a0011c0008t0045g0022 | 2 | NA18952.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4148-2036C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11623118 | ||||||
| chr2:11623155
|
C | A | 1 | a0009c0019t0066g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4148-1999C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11623155 | ||||||
| chr2:11623292
|
A | G | 1 | a0007c0016t0015g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4148-1862A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11623292 | ||||||
| chr2:11623629
|
G | A | 1 | a0004c0004t0008g0173 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4148-1525G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11623629 | ||||||
| chr2:11623853
|
C | A | 3 | a0001c0001t0005g0131a0002c0005t0005g0063a0003c0003t0007g0159 | 3 | HG02129.hp1 NA18940.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.4148-1301C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11623853 | ||||||
| chr2:11623970
|
CAAGA | C | 12 | a0002c0007t0052g0075a0002c0034t0019g0026a0002c0034t0031g0263others(9): Show | 12 | HG00639.hp1 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.4148-1178_4148-117 others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr2 | 11623970 | |||||
| chr2:11624091
|
A | G | 1 | a0003c0003t0001g0146 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4148-1063A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11624091 | ||||||
| chr2:11624204
|
G | A | 88 | a0001c0001t0002g0203a0001c0001t0002g0207a0001c0001t0002g0210others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.4148-950G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11624204 | ||||||
| chr2:11624308
|
C | G | 128 | a0001c0001t0002g0193a0001c0001t0002g0203a0001c0001t0002g0207others(125): Show | 128 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.4148-846C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11624308 | ||||||
| chr2:11624341
|
C | CT | 17 | a0002c0007t0001g0104a0002c0007t0001g0262a0002c0012t0023g0085others(14): Show | 17 | HG01175.hp2 HG01884.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.4148-793dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr2 | 11624341 | |||||
| chr2:11624341
|
CT | C | 7 | a0001c0001t0006g0278a0001c0001t0069g0288a0002c0005t0001g0036others(4): Show | 7 | HG01168.hp2 HG02486.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.4148-793delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr2 | 11624341 | |||||
| chr2:11624341
|
CTT | C | 107 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0002g0032others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.4148-794_4148-793d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr2 | 11624341 | |||||
| chr2:11624341
|
CTTT | C | 7 | a0001c0001t0002g0287a0001c0001t0007g0062a0001c0001t0032g0201others(4): Show | 7 | HG01168.hp1 HG03669.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.4148-795_4148-793d others(5): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr2 | 11624341 | |||||
| chr2:11624640
|
C | T | 1 | a0002c0012t0065g0103 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4148-514C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11624640 | ||||||
| chr2:11624804
|
C | A | 1 | a0006c0098t0068g0052 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4148-350C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11624804 | ||||||
| chr2:11624820
|
AT | A | 126 | a0001c0001t0002g0203a0001c0001t0002g0207a0001c0001t0002g0210others(123): Show | 126 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.4148-324delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | INFO_REALIGN_3_PRIME | chr2 | 11624820 | |||||
| chr2:11624847
|
A | G | 2 | a0010c0035t0060g0126a0033c0047t0031g0107 | 2 | HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4148-307A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11624847 | ||||||
| chr2:11624908
|
C | T | 4 | a0002c0005t0011g0250a0004c0004t0002g0230a0004c0004t0002g0281others(1): Show | 4 | HG03017.hp2 HG04199.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.4148-246C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11624908 | ||||||
| chr2:11624931
|
C | T | 1 | a0005c0002t0003g0082 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4148-223C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11624931 | ||||||
| chr2:11624995
|
G | A | 2 | a0002c0005t0006g0293a0003c0003t0002g0257 | 2 | HG01167.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.4148-159G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11624995 | ||||||
| chr2:11625069
|
G | A | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4148-85G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 23/32 | chr2 | 11625069 | ||||||
| chr2:11625531
|
G | A | 2 | a0008c0060t0061g0305a0042c0070t0015g0010 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4306+219G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625531 | ||||||
| chr2:11625620
|
G | A | 7 | a0008c0006t0054g0018a0014c0023t0014g0068a0014c0023t0014g0071others(4): Show | 7 | HG01070.hp2 HG01109.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.4306+308G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625620 | ||||||
| chr2:11625739
|
G | A | 1 | a0004c0004t0013g0296 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4306+427G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625739 | ||||||
| chr2:11625775
|
C | T | 1 | a0002c0007t0007g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4306+463C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625775 | ||||||
| chr2:11625810
|
C | T | 3 | a0005c0002t0010g0124a0005c0002t0013g0187a0005c0002t0013g0188 | 3 | HG00733.hp2 HG01081.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.4306+498C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625810 | ||||||
| chr2:11625849
|
A | G | 5 | a0007c0016t0015g0017a0007c0058t0024g0125a0008c0006t0015g0005others(2): Show | 5 | HG02145.hp2 HG02647.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.4306+537A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625849 | ||||||
| chr2:11625878
|
T | C | 37 | a0001c0001t0002g0232a0002c0011t0009g0043a0002c0012t0023g0085others(34): Show | 37 | HG00099.hp1 HG01074.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.4306+566T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625878 | ||||||
| chr2:11625906
|
C | T | 1 | a0001c0001t0007g0037 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4306+594C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625906 | ||||||
| chr2:11625927
|
C | T | 17 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(14): Show | 17 | HG01175.hp2 HG01261.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.4306+615C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625927 | ||||||
| chr2:11625994
|
T | C | 63 | a0001c0001t0004g0291a0001c0001t0005g0047a0001c0001t0005g0168others(60): Show | 63 | HG00408.hp2 HG00673.hp2 HG01175.hp2 others(60): Show |
intron_variant | MODIFIER | c.4306+682T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11625994 | ||||||
| chr2:11626064
|
C | T | 8 | a0004c0004t0004g0239a0004c0004t0004g0242a0004c0004t0004g0244others(5): Show | 8 | HG00099.hp1 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.4306+752C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626064 | ||||||
| chr2:11626236
|
G | A | 19 | a0001c0001t0001g0166a0001c0001t0006g0214a0001c0001t0006g0278others(16): Show | 19 | HG01106.hp1 HG02040.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.4307-726G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626236 | ||||||
| chr2:11626279
|
G | A | 3 | a0003c0003t0002g0225a0003c0003t0022g0120a0053c0083t0008g0256 | 3 | HG00735.hp1 HG01074.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.4307-683G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626279 | ||||||
| chr2:11626480
|
C | T | 32 | a0001c0001t0004g0186a0004c0004t0004g0239a0004c0004t0004g0242others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.4307-482C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626480 | ||||||
| chr2:11626483
|
G | T | 27 | a0002c0012t0023g0085a0002c0012t0023g0086a0002c0012t0024g0127others(24): Show | 27 | HG01175.hp2 HG02145.hp2 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.4307-479G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626483 | ||||||
| chr2:11626514
|
C | T | 33 | a0001c0001t0004g0186a0004c0004t0004g0239a0004c0004t0004g0242others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(30): Show |
intron_variant | MODIFIER | c.4307-448C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626514 | ||||||
| chr2:11626520
|
G | A | 1 | a0001c0013t0002g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4307-442G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626520 | ||||||
| chr2:11626551
|
G | A | 1 | a0013c0018t0022g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4307-411G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626551 | ||||||
| chr2:11626677
|
A | G | 1 | a0001c0001t0004g0291 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.4307-285A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626677 | ||||||
| chr2:11626891
|
T | C | 1 | a0013c0018t0022g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4307-71T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 24/32 | chr2 | 11626891 | ||||||
| chr2:11627149
|
A | G | 2 | a0006c0064t0012g0078a0010c0031t0038g0029 | 2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.4449+45A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627149 | ||||||
| chr2:11627156
|
G | A | 21 | a0002c0007t0001g0104a0002c0007t0052g0075a0002c0034t0019g0026others(18): Show | 21 | HG01070.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.4449+52G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627156 | ||||||
| chr2:11627169
|
C | G | 22 | a0001c0001t0004g0291a0001c0001t0005g0131a0001c0001t0005g0168others(19): Show | 22 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.4449+65C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627169 | ||||||
| chr2:11627173
|
C | T | 1 | a0039c0074t0014g0301 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.4449+69C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627173 | ||||||
| chr2:11627196
|
T | C | 1 | a0001c0013t0011g0218 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4449+92T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627196 | ||||||
| chr2:11627256
|
T | G | 37 | a0001c0001t0004g0186a0002c0005t0001g0034a0004c0004t0004g0239others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.4449+152T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627256 | ||||||
| chr2:11627335
|
G | A | 2 | a0013c0018t0022g0030a0021c0040t0036g0089 | 2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4449+231G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627335 | ||||||
| chr2:11627579
|
A | G | 2 | a0008c0060t0061g0305a0042c0070t0015g0010 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4449+475A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627579 | ||||||
| chr2:11627628
|
A | G | 2 | a0002c0005t0001g0045a0002c0005t0001g0066 | 2 | NA18966.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.4449+524A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627628 | ||||||
| chr2:11627751
|
C | T | 1 | a0009c0029t0020g0016 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4449+647C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627751 | ||||||
| chr2:11627770
|
G | A | 1 | a0003c0009t0015g0105 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4449+666G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627770 | ||||||
| chr2:11627968
|
G | A | 1 | a0003c0009t0015g0105 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4449+864G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11627968 | ||||||
| chr2:11628048
|
G | A | 8 | a0001c0001t0004g0291a0001c0001t0073g0253a0002c0005t0005g0046others(5): Show | 8 | HG00558.hp1 NA18960.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.4449+944G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11628048 | ||||||
| chr2:11628056
|
G | A | 1 | a0001c0001t0032g0251 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4449+952G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11628056 | ||||||
| chr2:11628057
|
A | G | 1 | a0001c0001t0032g0251 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4449+953A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11628057 | ||||||
| chr2:11628519
|
G | A | 1 | a0005c0002t0010g0124 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4449+1415G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11628519 | ||||||
| chr2:11628672
|
A | ATT | 3 | a0006c0064t0012g0078a0010c0031t0038g0029a0013c0018t0022g0030 | 3 | HG02451.hp2 HG02615.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4450-1273_4450-127 others(6): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | INFO_REALIGN_3_PRIME | chr2 | 11628672 | |||||
| chr2:11628746
|
G | T | 40 | a0001c0001t0011g0205a0002c0007t0001g0104a0002c0007t0052g0075others(37): Show | 40 | HG00408.hp2 HG00558.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.4450-1202G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11628746 | ||||||
| chr2:11628815
|
C | T | 1 | a0013c0052t0049g0261 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4450-1133C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11628815 | ||||||
| chr2:11628918
|
C | T | 1 | a0005c0002t0003g0114 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4450-1030C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11628918 | ||||||
| chr2:11628928
|
G | A | 3 | a0008c0060t0061g0305a0030c0051t0042g0306a0042c0070t0015g0010 | 3 | HG02559.hp1 HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4450-1020G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11628928 | ||||||
| chr2:11628966
|
G | A | 1 | a0033c0047t0031g0107 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4450-982G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11628966 | ||||||
| chr2:11629160
|
T | C | 50 | a0001c0001t0073g0253a0003c0003t0001g0155a0004c0004t0002g0183others(47): Show | 50 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.4450-788T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629160 | ||||||
| chr2:11629181
|
T | TG | 164 | a0001c0001t0002g0182a0001c0001t0004g0186a0001c0001t0004g0291others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.4450-765dupG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | INFO_REALIGN_3_PRIME | chr2 | 11629181 | |||||
| chr2:11629246
|
G | A | 1 | a0004c0026t0004g0290 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4450-702G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629246 | ||||||
| chr2:11629321
|
T | C | 90 | a0001c0001t0002g0182a0001c0001t0004g0186a0001c0001t0004g0291others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.4450-627T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629321 | ||||||
| chr2:11629410
|
A | C | 1 | a0003c0009t0015g0105 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4450-538A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629410 | ||||||
| chr2:11629491
|
C | T | 1 | a0009c0019t0012g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4450-457C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629491 | ||||||
| chr2:11629648
|
G | A | 47 | a0003c0003t0001g0155a0004c0004t0002g0183a0004c0004t0002g0215others(44): Show | 47 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.4450-300G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629648 | ||||||
| chr2:11629741
|
C | T | 6 | a0002c0007t0020g0307a0002c0034t0031g0263a0007c0016t0015g0017others(3): Show | 6 | HG02647.hp2 HG02723.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.4450-207C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629741 | ||||||
| chr2:11629753
|
G | C | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4450-195G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629753 | ||||||
| chr2:11629765
|
G | A | 1 | a0002c0005t0051g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4450-183G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629765 | ||||||
| chr2:11629838
|
G | A | 1 | a0009c0028t0020g0304 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4450-110G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629838 | ||||||
| chr2:11629916
|
C | T | 2 | a0004c0004t0002g0202a0043c0069t0003g0154 | 2 | HG01243.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.4450-32C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 25/32 | chr2 | 11629916 | ||||||
| chr2:11630167
|
C | T | 3 | a0005c0002t0055g0014a0006c0064t0012g0078a0013c0018t0047g0303 | 3 | HG02615.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4611+58C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630167 | ||||||
| chr2:11630389
|
T | C | 1 | a0053c0083t0008g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4611+280T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630389 | ||||||
| chr2:11630453
|
G | A | 3 | a0002c0007t0020g0307a0008c0006t0012g0112a0018c0037t0003g0298 | 3 | HG02723.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4611+344G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630453 | ||||||
| chr2:11630463
|
C | T | 12 | a0005c0002t0010g0101a0005c0002t0010g0119a0005c0002t0050g0084others(9): Show | 12 | HG00099.hp1 HG01109.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.4611+354C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630463 | ||||||
| chr2:11630485
|
T | C | 2 | a0004c0004t0008g0292a0005c0002t0016g0164 | 2 | NA18941.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.4611+376T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630485 | ||||||
| chr2:11630515
|
G | A | 1 | a0036c0041t0003g0091 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4611+406G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630515 | ||||||
| chr2:11630559
|
A | G | 52 | a0002c0005t0001g0034a0004c0004t0002g0196a0004c0004t0002g0202others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.4611+450A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630559 | ||||||
| chr2:11630607
|
G | A | 1 | a0002c0011t0009g0043 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.4611+498G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630607 | ||||||
| chr2:11630672
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4611+563A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630672 | ||||||
| chr2:11630768
|
C | T | 2 | a0008c0006t0054g0018a0028c0062t0040g0025 | 2 | HG01109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4611+659C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630768 | ||||||
| chr2:11630803
|
T | A | 11 | a0005c0002t0010g0101a0005c0002t0010g0119a0005c0002t0050g0084others(8): Show | 11 | HG00099.hp1 HG01109.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.4611+694T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630803 | ||||||
| chr2:11630878
|
G | A | 1 | a0002c0005t0007g0031 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.4611+769G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11630878 | ||||||
| chr2:11631262
|
T | C | 1 | a0005c0002t0055g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4612-647T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631262 | ||||||
| chr2:11631370
|
A | G | 3 | a0003c0003t0001g0268a0003c0003t0002g0225a0003c0003t0022g0120 | 3 | HG01074.hp1 HG01516.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4612-539A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631370 | ||||||
| chr2:11631382
|
G | C | 1 | a0005c0002t0055g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4612-527G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631382 | ||||||
| chr2:11631451
|
G | A | 1 | a0021c0040t0036g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4612-458G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631451 | ||||||
| chr2:11631590
|
G | A | 29 | a0002c0007t0020g0307a0002c0007t0037g0023a0002c0012t0023g0085others(26): Show | 29 | HG01175.hp2 HG02559.hp2 HG02572.hp2 others(26): Show |
intron_variant | MODIFIER | c.4612-319G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631590 | ||||||
| chr2:11631642
|
A | G | 2 | a0005c0002t0055g0014a0006c0064t0012g0078 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4612-267A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631642 | ||||||
| chr2:11631662
|
G | A | 1 | a0051c0086t0008g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4612-247G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631662 | ||||||
| chr2:11631813
|
C | T | 1 | a0021c0040t0036g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4612-96C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631813 | ||||||
| chr2:11631824
|
G | A | 25 | a0001c0001t0005g0131a0001c0001t0005g0168a0001c0001t0011g0205others(22): Show | 25 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.4612-85G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631824 | ||||||
| chr2:11631888
|
C | A | 1 | a0003c0003t0001g0155 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4612-21C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 26/32 | chr2 | 11631888 | ||||||
| chr2:11632128
|
A | G | 1 | a0006c0064t0012g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4816+15A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | chr2 | 11632128 | ||||||
| chr2:11632282
|
G | A | 2 | a0005c0002t0055g0014a0006c0064t0012g0078 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4816+169G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | chr2 | 11632282 | ||||||
| chr2:11632335
|
C | CT | 63 | a0001c0001t0004g0291a0002c0005t0001g0034a0004c0004t0002g0196others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.4816+243dupT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr2 | 11632335 | |||||
| chr2:11632335
|
CT | C | 33 | a0001c0001t0002g0192a0001c0001t0002g0247a0001c0001t0002g0252others(30): Show | 33 | HG01070.hp1 HG01168.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.4816+243delT | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr2 | 11632335 | |||||
| chr2:11632335
|
CTTT | C | 8 | a0002c0012t0024g0127a0007c0058t0024g0125a0008c0006t0017g0015others(5): Show | 8 | HG02647.hp1 HG02895.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.4816+241_4816+243d others(5): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | INFO_REALIGN_3_PRIME | chr2 | 11632335 | |||||
| chr2:11632432
|
G | A | 1 | a0001c0001t0018g0258 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4816+319G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | chr2 | 11632432 | ||||||
| chr2:11632484
|
G | A | 116 | a0002c0005t0001g0034a0004c0004t0002g0183a0004c0004t0002g0196others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.4816+371G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | chr2 | 11632484 | ||||||
| chr2:11632563
|
C | T | 1 | a0046c0078t0011g0176 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.4817-326C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | chr2 | 11632563 | ||||||
| chr2:11632594
|
C | T | 1 | a0017c0024t0013g0228 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4817-295C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | chr2 | 11632594 | ||||||
| chr2:11632850
|
G | A | 1 | a0004c0004t0004g0289 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4817-39G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 27/32 | chr2 | 11632850 | ||||||
| chr2:11633209
|
A | C | 1 | a0003c0003t0007g0159 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4991+146A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11633209 | ||||||
| chr2:11633284
|
C | T | 20 | a0004c0004t0008g0173a0004c0004t0008g0246a0004c0004t0008g0273others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.4991+221C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11633284 | ||||||
| chr2:11633285
|
G | A | 2 | a0008c0006t0054g0018a0028c0062t0040g0025 | 2 | HG01109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.4991+222G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11633285 | ||||||
| chr2:11633358
|
C | G | 48 | a0001c0001t0004g0291a0004c0004t0002g0196a0004c0004t0002g0202others(45): Show | 48 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.4991+295C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11633358 | ||||||
| chr2:11633488
|
C | T | 1 | a0030c0051t0042g0306 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4991+425C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11633488 | ||||||
| chr2:11633541
|
C | G | 122 | a0001c0001t0004g0291a0004c0004t0002g0183a0004c0004t0002g0196others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.4991+478C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11633541 | ||||||
| chr2:11633562
|
T | TA | 45 | a0001c0001t0004g0291a0004c0004t0002g0196a0004c0004t0002g0202others(42): Show | 45 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.4991+513dupA | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr2 | 11633562 | |||||
| chr2:11633645
|
C | T | 1 | a0002c0005t0051g0055 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4992-486C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11633645 | ||||||
| chr2:11633918
|
A | T | 1 | a0050c0087t0004g0172 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4992-213A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11633918 | ||||||
| chr2:11633974
|
G | A | 8 | a0002c0007t0037g0023a0002c0012t0024g0127a0007c0058t0024g0125others(5): Show | 8 | HG02647.hp1 HG02895.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.4992-157G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11633974 | ||||||
| chr2:11634016
|
C | T | 1 | a0001c0001t0007g0138 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4992-115C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11634016 | ||||||
| chr2:11634021
|
C | G | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4992-110C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11634021 | ||||||
| chr2:11634035
|
C | T | 1 | a0012c0010t0006g0227 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4992-96C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11634035 | ||||||
| chr2:11634051
|
G | A | 2 | a0007c0043t0035g0095a0033c0047t0031g0107 | 2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4992-80G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11634051 | ||||||
| chr2:11634088
|
C | T | 1 | a0003c0003t0007g0159 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4992-43C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 28/32 | chr2 | 11634088 | ||||||
| chr2:11634361
|
C | T | 1 | a0006c0033t0034g0302 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5210+12C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634361 | ||||||
| chr2:11634395
|
G | A | 1 | a0003c0003t0002g0257 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.5210+46G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634395 | ||||||
| chr2:11634597
|
T | A | 105 | a0001c0001t0004g0291a0001c0001t0005g0047a0001c0001t0005g0131others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.5210+248T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634597 | ||||||
| chr2:11634697
|
C | T | 2 | a0011c0008t0003g0027a0011c0008t0003g0297 | 2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.5210+348C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634697 | ||||||
| chr2:11634787
|
C | T | 45 | a0004c0004t0002g0183a0004c0004t0002g0215a0004c0004t0002g0230others(42): Show | 45 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.5210+438C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634787 | ||||||
| chr2:11634798
|
G | A | 1 | a0001c0001t0004g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5210+449G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634798 | ||||||
| chr2:11634808
|
G | A | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5210+459G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634808 | ||||||
| chr2:11634872
|
A | C | 1 | a0013c0018t0022g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5211-398A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634872 | ||||||
| chr2:11634906
|
C | T | 52 | a0001c0001t0004g0291a0004c0004t0002g0196a0004c0004t0002g0202others(49): Show | 52 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.5211-364C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634906 | ||||||
| chr2:11634946
|
C | A | 1 | a0008c0006t0024g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5211-324C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634946 | ||||||
| chr2:11634983
|
G | A | 2 | a0006c0033t0034g0302a0021c0040t0036g0089 | 2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.5211-287G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11634983 | ||||||
| chr2:11635011
|
C | T | 44 | a0004c0004t0002g0183a0004c0004t0002g0215a0004c0004t0002g0230others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.5211-259C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11635011 | ||||||
| chr2:11635170
|
AG | A | 12 | a0005c0002t0010g0101a0005c0002t0010g0119a0005c0002t0050g0084others(9): Show | 12 | HG00099.hp1 HG01109.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5211-99delG | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11635170 | ||||||
| chr2:11635172
|
C | T | 12 | a0005c0002t0010g0101a0005c0002t0010g0119a0005c0002t0050g0084others(9): Show | 12 | HG00099.hp1 HG01109.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5211-98C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11635172 | ||||||
| chr2:11635249
|
C | A | 1 | a0013c0018t0022g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5211-21C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 29/32 | chr2 | 11635249 | ||||||
| chr2:11635485
|
T | C | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5346+80T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11635485 | ||||||
| chr2:11635557
|
C | T | 2 | a0008c0060t0061g0305a0010c0031t0038g0029 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.5346+152C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11635557 | ||||||
| chr2:11635583
|
G | A | 3 | a0002c0034t0031g0263a0007c0016t0015g0017a0008c0006t0015g0005 | 3 | HG02647.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5346+178G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11635583 | ||||||
| chr2:11635640
|
G | A | 1 | a0001c0001t0004g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5346+235G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11635640 | ||||||
| chr2:11635701
|
C | T | 1 | a0020c0039t0009g0050 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.5346+296C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11635701 | ||||||
| chr2:11635712
|
G | C | 2 | a0011c0008t0045g0022a0013c0018t0047g0303 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.5346+307G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11635712 | ||||||
| chr2:11636122
|
G | T | 72 | a0001c0001t0004g0291a0004c0004t0002g0196a0004c0004t0002g0202others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.5346+717G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636122 | ||||||
| chr2:11636152
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0002g0203a0001c0001t0002g0252others(4): Show | 7 | HG00621.hp2 HG02083.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.5346+747C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636152 | ||||||
| chr2:11636153
|
G | A | 44 | a0004c0004t0002g0183a0004c0004t0002g0215a0004c0004t0002g0230others(41): Show | 44 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.5346+748G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636153 | ||||||
| chr2:11636424
|
T | C | 83 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(80): Show | 83 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.5346+1019T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636424 | ||||||
| chr2:11636513
|
A | G | 5 | a0004c0004t0002g0202a0004c0004t0002g0295a0005c0002t0003g0139others(2): Show | 5 | HG01243.hp1 HG01243.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.5346+1108A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636513 | ||||||
| chr2:11636549
|
C | A | 81 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.5346+1144C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636549 | ||||||
| chr2:11636561
|
C | T | 5 | a0004c0025t0008g0277a0004c0025t0008g0279a0004c0025t0008g0285others(2): Show | 5 | HG00673.hp1 NA18942.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.5347-1155C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636561 | ||||||
| chr2:11636663
|
A | G | 85 | a0001c0001t0004g0291a0001c0001t0005g0047a0001c0001t0005g0131others(82): Show | 85 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.5347-1053A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636663 | ||||||
| chr2:11636698
|
A | C | 47 | a0003c0003t0001g0155a0004c0004t0002g0183a0004c0004t0002g0215others(44): Show | 47 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.5347-1018A>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636698 | ||||||
| chr2:11636722
|
G | A | 1 | a0005c0002t0003g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5347-994G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636722 | ||||||
| chr2:11636737
|
AGGGCAT | A | 82 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(79): Show | 82 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.5347-967_5347-962d others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11636737 | |||||
| chr2:11636761
|
A | G | 1 | a0003c0009t0015g0105 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.5347-955A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636761 | ||||||
| chr2:11636761
|
AGGGCAG | A | 81 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.5347-937_5347-932d others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11636761 | |||||
| chr2:11636791
|
TGGGCAG | T | 81 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.5347-918_5347-913d others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11636791 | |||||
| chr2:11636803
|
G | A | 21 | a0004c0004t0008g0173a0004c0004t0008g0246a0004c0004t0008g0273others(18): Show | 21 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.5347-913G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636803 | ||||||
| chr2:11636804
|
A | G | 21 | a0004c0004t0008g0173a0004c0004t0008g0246a0004c0004t0008g0273others(18): Show | 21 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.5347-912A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636804 | ||||||
| chr2:11636812
|
A | G | 21 | a0004c0004t0008g0173a0004c0004t0008g0246a0004c0004t0008g0273others(18): Show | 21 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.5347-904A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636812 | ||||||
| chr2:11636816
|
A | G | 21 | a0004c0004t0008g0173a0004c0004t0008g0246a0004c0004t0008g0273others(18): Show | 21 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.5347-900A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636816 | ||||||
| chr2:11636822
|
G | GGATAGA | 21 | a0004c0004t0008g0173a0004c0004t0008g0246a0004c0004t0008g0273others(18): Show | 21 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.5347-893_5347-892i others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11636822 | |||||
| chr2:11636887
|
T | G | 81 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.5347-829T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636887 | ||||||
| chr2:11636935
|
G | GGGGTAT | 76 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.5347-779_5347-778i others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11636935 | |||||
| chr2:11636936
|
G | GGGTATGG others(17): Show |
5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5347-779_5347-778i others(26): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11636936 | |||||
| chr2:11636938
|
T | G | 82 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(79): Show | 82 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.5347-778T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636938 | ||||||
| chr2:11636941
|
T | G | 81 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.5347-775T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636941 | ||||||
| chr2:11636963
|
C | T | 26 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(23): Show | 26 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.5347-753C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636963 | ||||||
| chr2:11636983
|
T | G | 1 | a0021c0040t0036g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5347-733T>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636983 | ||||||
| chr2:11636986
|
G | A | 1 | a0021c0040t0036g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5347-730G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636986 | ||||||
| chr2:11636987
|
CAGAGGT | C | 75 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(72): Show | 75 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.5347-726_5347-721d others(8): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11636987 | |||||
| chr2:11636990
|
A | AGGCAGGG others(5): Show |
1 | a0021c0040t0036g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5347-724_5347-723i others(14): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11636990 | |||||
| chr2:11636993
|
T | C | 1 | a0021c0040t0036g0089 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5347-723T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11636993 | ||||||
| chr2:11636999
|
CAG | C | 14 | a0001c0001t0002g0207a0001c0001t0002g0210a0001c0001t0002g0222others(11): Show | 14 | HG00423.hp1 HG00621.hp1 NA18960.hp1 others(11): Show |
intron_variant | MODIFIER | c.5347-714_5347-713d others(4): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11636999 | |||||
| chr2:11637028
|
G | GCGGGGCA others(88): Show |
5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5347-687_5347-686i others(97): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637028 | |||||
| chr2:11637041
|
T | C | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5347-675T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637041 | ||||||
| chr2:11637046
|
A | G | 1 | a0002c0007t0001g0262 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5347-670A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637046 | ||||||
| chr2:11637064
|
A | ACAGAGGC others(11): Show |
1 | a0001c0001t0004g0291 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.5347-634_5347-617d others(20): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637064 | |||||
| chr2:11637073
|
G | GGGGCAGG others(670): Show |
1 | a0006c0014t0003g0060 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.5347-623_5347-622i others(679): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(665): Show |
1 | a0005c0002t0001g0142 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.5347-623_5347-622i others(674): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(671): Show |
40 | a0004c0004t0002g0183a0004c0004t0002g0230a0004c0004t0002g0237others(37): Show | 40 | HG00408.hp1 HG00423.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.5347-623_5347-622i others(680): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(671): Show |
2 | a0003c0003t0001g0155a0049c0081t0002g0199 | 2 | NA18939.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.5347-623_5347-622i others(680): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(671): Show |
1 | a0004c0004t0002g0215 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.5347-623_5347-622i others(680): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(665): Show |
1 | a0020c0039t0009g0050 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.5347-623_5347-622i others(674): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(689): Show |
2 | a0001c0001t0005g0047a0027c0096t0005g0074 | 2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.5347-623_5347-622i others(698): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(689): Show |
26 | a0001c0001t0005g0131a0001c0001t0005g0168a0001c0001t0011g0205others(23): Show | 26 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.5347-623_5347-622i others(698): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(665): Show |
1 | a0002c0005t0005g0063 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.5347-623_5347-622i others(674): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(683): Show |
1 | a0002c0005t0011g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5347-623_5347-622i others(692): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637073
|
G | GGGGCAGG others(545): Show |
5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5347-623_5347-622i others(554): Show |
GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | INFO_REALIGN_3_PRIME | chr2 | 11637073 | |||||
| chr2:11637168
|
G | T | 1 | a0026c0092t0018g0249 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5347-548G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637168 | ||||||
| chr2:11637178
|
G | A | 81 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.5347-538G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637178 | ||||||
| chr2:11637229
|
G | C | 1 | a0006c0064t0012g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5347-487G>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637229 | ||||||
| chr2:11637291
|
T | C | 29 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(26): Show | 29 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.5347-425T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637291 | ||||||
| chr2:11637350
|
G | A | 22 | a0002c0007t0020g0307a0002c0012t0023g0085a0002c0012t0023g0086others(19): Show | 22 | HG01175.hp2 HG02559.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.5347-366G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637350 | ||||||
| chr2:11637358
|
G | T | 76 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.5347-358G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637358 | ||||||
| chr2:11637564
|
A | T | 25 | a0004c0004t0008g0173a0004c0004t0008g0246a0004c0004t0008g0273others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.5347-152A>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637564 | ||||||
| chr2:11637631
|
T | C | 81 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.5347-85T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637631 | ||||||
| chr2:11637689
|
T | C | 2 | a0008c0060t0061g0305a0010c0031t0038g0029 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.5347-27T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 30/32 | chr2 | 11637689 | ||||||
| chr2:11637966
|
A | G | 1 | a0006c0097t0016g0058 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.5547+50A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 31/32 | chr2 | 11637966 | ||||||
| chr2:11638058
|
G | A | 68 | a0003c0003t0001g0155a0004c0004t0002g0183a0004c0004t0002g0215others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.5547+142G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 31/32 | chr2 | 11638058 | ||||||
| chr2:11638180
|
G | A | 4 | a0005c0066t0022g0072a0009c0019t0066g0108a0009c0029t0041g0028others(1): Show | 4 | HG02258.hp1 HG02486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.5547+264G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 31/32 | chr2 | 11638180 | ||||||
| chr2:11638331
|
G | A | 68 | a0003c0003t0001g0155a0004c0004t0002g0183a0004c0004t0002g0215others(65): Show | 68 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.5548-340G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 31/32 | chr2 | 11638331 | ||||||
| chr2:11638387
|
C | T | 2 | a0004c0026t0016g0041a0017c0024t0008g0234 | 2 | HG01361.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.5548-284C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 31/32 | chr2 | 11638387 | ||||||
| chr2:11638392
|
C | T | 84 | a0001c0001t0004g0291a0001c0001t0005g0047a0001c0001t0005g0131others(81): Show | 84 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.5548-279C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 31/32 | chr2 | 11638392 | ||||||
| chr2:11638552
|
C | T | 1 | a0005c0002t0010g0124 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.5548-119C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 31/32 | chr2 | 11638552 | ||||||
| chr2:11638975
|
G | A | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5686+166G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11638975 | ||||||
| chr2:11639036
|
C | G | 57 | a0001c0001t0004g0291a0004c0004t0002g0196a0004c0004t0002g0202others(54): Show | 57 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.5686+227C>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639036 | ||||||
| chr2:11639040
|
T | A | 1 | a0040c0072t0058g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5686+231T>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639040 | ||||||
| chr2:11639084
|
T | C | 8 | a0002c0007t0020g0307a0002c0034t0031g0263a0007c0016t0015g0017others(5): Show | 8 | HG02630.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.5686+275T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639084 | ||||||
| chr2:11639171
|
C | T | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5686+362C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639171 | ||||||
| chr2:11639238
|
C | T | 1 | a0013c0018t0047g0303 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.5686+429C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639238 | ||||||
| chr2:11639285
|
T | C | 68 | a0003c0003t0001g0155a0004c0004t0002g0183a0004c0004t0002g0215others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.5686+476T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639285 | ||||||
| chr2:11639290
|
T | C | 3 | a0008c0006t0054g0018a0028c0062t0040g0025a0030c0051t0042g0306 | 3 | HG01109.hp2 HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5686+481T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639290 | ||||||
| chr2:11639368
|
C | T | 26 | a0001c0001t0005g0047a0001c0001t0005g0131a0001c0001t0005g0168others(23): Show | 26 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.5686+559C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639368 | ||||||
| chr2:11639397
|
C | T | 1 | a0040c0072t0058g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5686+588C>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639397 | ||||||
| chr2:11639452
|
T | C | 1 | a0040c0072t0058g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5686+643T>C | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639452 | ||||||
| chr2:11639477
|
A | G | 152 | a0001c0001t0004g0291a0001c0001t0005g0047a0001c0001t0005g0131others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.5686+668A>G | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639477 | ||||||
| chr2:11639783
|
G | A | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5687-508G>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639783 | ||||||
| chr2:11639806
|
C | A | 5 | a0014c0023t0014g0068a0014c0023t0014g0071a0014c0023t0014g0073others(2): Show | 5 | HG01070.hp2 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5687-485C>A | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639806 | ||||||
| chr2:11639959
|
G | T | 1 | a0040c0072t0058g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5687-332G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639959 | ||||||
| chr2:11639982
|
G | T | 1 | a0040c0072t0058g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5687-309G>T | GREB1 | ENSG00000196208.14 | transcript | ENST00000381486.7 | protein_coding | 32/32 | chr2 | 11639982 |