| geneid | 6239 |
|---|---|
| ensemblid | ENSG00000124782.21 |
| hgncid | 10449 |
| symbol | RREB1 |
| name | ras responsive element binding protein 1 |
| refseq_nuc | NM_001003699.4 |
| refseq_prot | NP_001003699.1 |
| ensembl_nuc | ENST00000379938.7 |
| ensembl_prot | ENSP00000369270.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 7107961 |
| end | 7251980 |
| strand | + |
| ver | v1.2 |
| region | chr6:7107961-7251980 |
| region5000 | chr6:7102961-7256980 |
| regionname0 | RREB1_chr6_7107961_7251980 |
| regionname5000 | RREB1_chr6_7102961_7256980 |
| 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 | 1/0 | 1742 | 43 | 4 | 12 | 19 | 1 | 6 | 14 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002 | 0/0 | 1742 | 43 | 7 | 10 | 20 | 0 | 6 | 12 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003 | 0/0 | 1742 | 35 | 8 | 5 | 13 | 2 | 7 | 8 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004 | 0/1 | 1742 | 33 | 10 | 9 | 4 | 5 | 4 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005 | 0/0 | 1742 | 32 | 18 | 2 | 12 | 0 | 0 | 6 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006 | 0/0 | 1742 | 20 | 0 | 0 | 20 | 0 | 0 | 18 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007 | 0/0 | 1742 | 20 | 9 | 3 | 5 | 3 | 0 | 3 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0008 | 0/0 | 1742 | 10 | 1 | 4 | 1 | 3 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0009 | 0/0 | 1742 | 5 | 2 | 0 | 3 | 0 | 0 | 3 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010 | 0/0 | 1742 | 5 | 1 | 2 | 1 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0011 | 0/0 | 1742 | 5 | 3 | 0 | 0 | 0 | 2 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0012 | 0/0 | 1742 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0013 | 0/0 | 1742 | 4 | 0 | 2 | 1 | 0 | 1 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0014 | 0/0 | 1742 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0015 | 0/0 | 1742 | 3 | 1 | 0 | 1 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0016 | 0/0 | 1742 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0017 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0018 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0019 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0020 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0021 | 0/0 | 1742 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0022 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0023 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0024 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0025 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0026 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0027 | 0/0 | 1742 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0028 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0029 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0030 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0031 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0032 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0033 | 0/0 | 1742 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0034 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0035 | 0/0 | 1742 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0036 | 0/0 | 1742 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0037 | 0/0 | 1742 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0038 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0039 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0040 | 0/0 | 1742 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0041 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| 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 | 1/0 | 5229 | 40 | 4 | 11 | 18 | 1 | 5 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0002 | 0/0 | 5229 | 26 | 4 | 5 | 9 | 2 | 6 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0003 | 0/0 | 5229 | 26 | 17 | 2 | 7 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0004 | 0/0 | 5229 | 25 | 7 | 8 | 6 | 0 | 4 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0005 | 0/0 | 5229 | 17 | 0 | 0 | 17 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0006 | 0/0 | 5229 | 16 | 8 | 6 | 1 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0007 | 0/0 | 5229 | 14 | 0 | 2 | 10 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0008 | 0/1 | 5229 | 13 | 1 | 2 | 1 | 5 | 3 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0009 | 0/0 | 5229 | 11 | 1 | 2 | 5 | 3 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0010 | 0/0 | 5229 | 9 | 1 | 4 | 1 | 2 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0011 | 0/0 | 5229 | 7 | 7 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0012 | 0/0 | 5229 | 4 | 3 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0013 | 0/0 | 5229 | 4 | 4 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0014 | 0/0 | 5229 | 4 | 0 | 0 | 4 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0015 | 0/0 | 5229 | 3 | 1 | 0 | 0 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0016 | 0/0 | 5229 | 3 | 0 | 0 | 3 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0017 | 0/0 | 5229 | 3 | 0 | 1 | 1 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0018 | 0/0 | 5229 | 3 | 0 | 0 | 3 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0019 | 0/0 | 5229 | 3 | 0 | 2 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0020 | 0/0 | 5229 | 3 | 3 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0021 | 0/0 | 5229 | 2 | 0 | 1 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0022 | 0/0 | 5229 | 2 | 1 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0023 | 0/0 | 5229 | 2 | 0 | 0 | 2 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0024 | 0/0 | 5229 | 2 | 1 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0025 | 0/0 | 5229 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0026 | 0/0 | 5229 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0027 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0028 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0029 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0030 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0031 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0032 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0033 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0034 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0035 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0036 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0037 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0038 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0039 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0040 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0041 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0042 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0043 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0044 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0045 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0046 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0047 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0048 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0049 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0050 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0051 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0052 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0053 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0054 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0055 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0056 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0057 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0058 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0059 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0060 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0061 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0062 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0063 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0064 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0065 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0066 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0067 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0068 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0069 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0070 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0071 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| c0072 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| 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 | 3395 | 41 | 2 | 13 | 15 | 5 | 6 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0002 | 1/0 | 3397 | 27 | 2 | 6 | 13 | 0 | 5 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0003 | 0/0 | 3391 | 25 | 5 | 6 | 9 | 3 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0004 | 0/0 | 3386 | 19 | 5 | 1 | 13 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0005 | 0/0 | 3391 | 11 | 1 | 2 | 2 | 3 | 3 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0006 | 0/1 | 3390 | 11 | 5 | 3 | 0 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0007 | 0/0 | 3392 | 11 | 0 | 4 | 7 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0008 | 0/0 | 3393 | 9 | 1 | 3 | 2 | 1 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0009 | 0/0 | 3389 | 8 | 0 | 0 | 8 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0010 | 0/0 | 3399 | 8 | 0 | 3 | 4 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0011 | 0/0 | 3394 | 6 | 0 | 0 | 6 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0012 | 0/0 | 3391 | 5 | 4 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0013 | 0/0 | 3393 | 5 | 5 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0014 | 0/0 | 3394 | 5 | 5 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0015 | 0/0 | 3384 | 4 | 4 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0016 | 0/0 | 3395 | 4 | 0 | 2 | 2 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0017 | 0/0 | 3394 | 4 | 2 | 1 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0018 | 0/0 | 3401 | 4 | 3 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0019 | 0/0 | 3383 | 3 | 2 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0020 | 0/0 | 3387 | 3 | 0 | 0 | 3 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0021 | 0/0 | 3386 | 3 | 3 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0022 | 0/0 | 3391 | 3 | 0 | 2 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0023 | 0/0 | 3405 | 3 | 1 | 0 | 2 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0024 | 0/0 | 3378 | 2 | 1 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0025 | 0/0 | 3383 | 2 | 0 | 0 | 0 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0026 | 0/0 | 3392 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0027 | 0/0 | 3394 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0028 | 0/0 | 3396 | 2 | 0 | 0 | 1 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0029 | 0/0 | 3398 | 2 | 0 | 0 | 0 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0030 | 0/0 | 3399 | 2 | 0 | 0 | 2 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0031 | 0/0 | 3406 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0032 | 0/0 | 3407 | 2 | 1 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0033 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0034 | 0/0 | 3403 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0035 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0036 | 0/0 | 3394 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0037 | 0/0 | 3382 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0038 | 0/0 | 3389 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0039 | 0/0 | 3385 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0040 | 0/0 | 3388 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0041 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0042 | 0/0 | 3385 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0043 | 0/0 | 3388 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0044 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0045 | 0/0 | 3389 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0046 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0047 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0048 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0049 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0050 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0051 | 0/0 | 3397 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0052 | 0/0 | 3397 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0053 | 0/0 | 3393 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0054 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0055 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0056 | 0/0 | 3392 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0057 | 0/0 | 3394 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0058 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0059 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0060 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0061 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0062 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0063 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0064 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0065 | 0/0 | 3401 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0066 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0067 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0068 | 0/0 | 3397 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0069 | 0/0 | 3398 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0070 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0071 | 0/0 | 3399 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0072 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0073 | 0/0 | 3398 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0074 | 0/0 | 3403 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0075 | 0/0 | 3401 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0076 | 0/0 | 3403 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0077 | 0/0 | 3394 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0078 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0079 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0080 | 0/0 | 3394 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0081 | 0/0 | 3396 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| t0082 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| 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 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| 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 | 1/0 | 5229 | 40 | 4 | 11 | 18 | 1 | 5 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0017 | 0/0 | 5229 | 3 | 0 | 1 | 1 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004 | 0/0 | 5229 | 25 | 7 | 8 | 6 | 0 | 4 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0007 | 0/0 | 5229 | 14 | 0 | 2 | 10 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0023 | 0/0 | 5229 | 2 | 0 | 0 | 2 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0042 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0046 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002 | 0/0 | 5229 | 26 | 4 | 5 | 9 | 2 | 6 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0012 | 0/0 | 5229 | 4 | 3 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0032 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0034 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0040 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0044 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0045 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0006 | 0/0 | 5229 | 16 | 8 | 6 | 1 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0008 | 0/1 | 5229 | 13 | 1 | 2 | 1 | 5 | 3 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0050 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0052 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0063 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0068 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003 | 0/0 | 5229 | 26 | 17 | 2 | 7 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0014 | 0/0 | 5229 | 4 | 0 | 0 | 4 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0056 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0059 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0005 | 0/0 | 5229 | 17 | 0 | 0 | 17 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0016 | 0/0 | 5229 | 3 | 0 | 0 | 3 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0009 | 0/0 | 5229 | 11 | 1 | 2 | 5 | 3 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0011 | 0/0 | 5229 | 7 | 7 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0022 | 0/0 | 5229 | 2 | 1 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0008c0010 | 0/0 | 5229 | 9 | 1 | 4 | 1 | 2 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0008c0065 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0009c0018 | 0/0 | 5229 | 3 | 0 | 0 | 3 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0009c0026 | 0/0 | 5229 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010c0021 | 0/0 | 5229 | 2 | 0 | 1 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010c0028 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010c0035 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010c0036 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0011c0015 | 0/0 | 5229 | 3 | 1 | 0 | 0 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0011c0031 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0011c0041 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0012c0013 | 0/0 | 5229 | 4 | 4 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0013c0019 | 0/0 | 5229 | 3 | 0 | 2 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0013c0058 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0014c0020 | 0/0 | 5229 | 3 | 3 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0015c0024 | 0/0 | 5229 | 2 | 1 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0015c0066 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0016c0025 | 0/0 | 5229 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0017c0027 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0018c0071 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0019c0049 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0020c0051 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0021c0064 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0022c0048 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0023c0067 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0024c0061 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0025c0060 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0026c0057 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0027c0055 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0028c0054 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0029c0053 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0030c0047 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0031c0062 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0032c0029 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0033c0038 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0034c0039 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0035c0033 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0036c0030 | 0/0 | 5229 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0037c0037 | 0/0 | 5229 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0038c0043 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0039c0070 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0040c0069 | 0/0 | 5229 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0041c0072 | 0/0 | 5229 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8623 | 21 | 1 | 5 | 11 | 0 | 4 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0001t0002 | 1/0 | 8625 | 8 | 0 | 4 | 2 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0001t0010 | 0/0 | 8627 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0001t0016 | 0/0 | 8623 | 3 | 0 | 1 | 2 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0001t0017 | 0/0 | 8622 | 4 | 2 | 1 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0001t0035 | 0/0 | 8623 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0001t0042 | 0/0 | 8613 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0001t0082 | 0/0 | 8623 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0017t0001 | 0/0 | 8623 | 2 | 0 | 1 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0001c0017t0032 | 0/0 | 8635 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004t0003 | 0/0 | 8619 | 9 | 2 | 3 | 3 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004t0007 | 0/0 | 8620 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004t0008 | 0/0 | 8621 | 5 | 1 | 2 | 0 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004t0011 | 0/0 | 8622 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004t0015 | 0/0 | 8612 | 3 | 3 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004t0016 | 0/0 | 8623 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004t0022 | 0/0 | 8619 | 3 | 0 | 2 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004t0026 | 0/0 | 8620 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0004t0072 | 0/0 | 8628 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0007t0007 | 0/0 | 8620 | 5 | 0 | 1 | 4 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0007t0008 | 0/0 | 8621 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0007t0011 | 0/0 | 8622 | 4 | 0 | 0 | 4 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0007t0028 | 0/0 | 8624 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0007t0063 | 0/0 | 8623 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0007t0064 | 0/0 | 8620 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0007t0069 | 0/0 | 8626 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0023t0044 | 0/0 | 8615 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0023t0048 | 0/0 | 8619 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0042t0060 | 0/0 | 8620 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0002c0046t0003 | 0/0 | 8619 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0001 | 0/0 | 8623 | 2 | 0 | 1 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0002 | 0/0 | 8625 | 9 | 1 | 1 | 5 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0003 | 0/0 | 8619 | 4 | 0 | 2 | 1 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0004 | 0/0 | 8614 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0008 | 0/0 | 8621 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0010 | 0/0 | 8627 | 3 | 0 | 1 | 1 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0023 | 0/0 | 8633 | 2 | 1 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0029 | 0/0 | 8626 | 2 | 0 | 0 | 0 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0071 | 0/0 | 8627 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0002t0074 | 0/0 | 8631 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0012t0003 | 0/0 | 8619 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0012t0004 | 0/0 | 8614 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0012t0011 | 0/0 | 8622 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0012t0013 | 0/0 | 8621 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0032t0057 | 0/0 | 8622 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0034t0008 | 0/0 | 8621 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0040t0001 | 0/0 | 8623 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0044t0066 | 0/0 | 8625 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0003c0045t0002 | 0/0 | 8625 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0006t0006 | 0/0 | 8618 | 4 | 1 | 2 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0006t0007 | 0/0 | 8620 | 4 | 0 | 3 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0006t0018 | 0/0 | 8629 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0006t0021 | 0/0 | 8614 | 3 | 3 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0006t0024 | 0/0 | 8606 | 2 | 1 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0006t0031 | 0/0 | 8634 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0006t0058 | 0/0 | 8624 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0008t0001 | 0/0 | 8623 | 4 | 0 | 2 | 0 | 2 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0008t0002 | 0/0 | 8625 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0008t0003 | 0/0 | 8619 | 3 | 0 | 0 | 0 | 3 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0008t0004 | 0/0 | 8614 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0008t0006 | 0/1 | 8618 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0008t0025 | 0/0 | 8611 | 2 | 0 | 0 | 0 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0008t0037 | 0/0 | 8610 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0050t0006 | 0/0 | 8618 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0052t0020 | 0/0 | 8615 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0063t0003 | 0/0 | 8619 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0004c0068t0073 | 0/0 | 8626 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0004 | 0/0 | 8614 | 7 | 3 | 1 | 3 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0009 | 0/0 | 8617 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0012 | 0/0 | 8619 | 4 | 3 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0013 | 0/0 | 8621 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0018 | 0/0 | 8629 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0020 | 0/0 | 8615 | 2 | 0 | 0 | 2 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0028 | 0/0 | 8624 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0033 | 0/0 | 8621 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0046 | 0/0 | 8620 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0047 | 0/0 | 8619 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0050 | 0/0 | 8619 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0054 | 0/0 | 8621 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0056 | 0/0 | 8620 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0003t0079 | 0/0 | 8621 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0014t0002 | 0/0 | 8625 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0014t0010 | 0/0 | 8627 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0014t0018 | 0/0 | 8629 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0014t0023 | 0/0 | 8633 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0056t0010 | 0/0 | 8627 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0005c0059t0013 | 0/0 | 8621 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0005t0004 | 0/0 | 8614 | 8 | 0 | 0 | 8 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0005t0009 | 0/0 | 8617 | 3 | 0 | 0 | 3 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0005t0030 | 0/0 | 8627 | 2 | 0 | 0 | 2 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0005t0041 | 0/0 | 8615 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0005t0043 | 0/0 | 8616 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0005t0070 | 0/0 | 8625 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0005t0075 | 0/0 | 8629 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0006c0016t0009 | 0/0 | 8617 | 3 | 0 | 0 | 3 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0009t0005 | 0/0 | 8619 | 8 | 1 | 2 | 2 | 3 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0009t0039 | 0/0 | 8613 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0009t0040 | 0/0 | 8616 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0009t0053 | 0/0 | 8621 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0011t0014 | 0/0 | 8622 | 4 | 4 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0011t0051 | 0/0 | 8625 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0011t0052 | 0/0 | 8625 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0011t0061 | 0/0 | 8624 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0007c0022t0019 | 0/0 | 8611 | 2 | 1 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0008c0010t0001 | 0/0 | 8623 | 7 | 1 | 3 | 0 | 2 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0008c0010t0002 | 0/0 | 8625 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0008c0010t0010 | 0/0 | 8627 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0008c0065t0001 | 0/0 | 8623 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0009c0018t0003 | 0/0 | 8619 | 2 | 0 | 0 | 2 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0009c0018t0008 | 0/0 | 8621 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0009c0026t0003 | 0/0 | 8619 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010c0021t0003 | 0/0 | 8619 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010c0021t0006 | 0/0 | 8618 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010c0028t0006 | 0/0 | 8618 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010c0035t0065 | 0/0 | 8629 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0010c0036t0002 | 0/0 | 8625 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0011c0015t0005 | 0/0 | 8619 | 2 | 0 | 0 | 0 | 0 | 2 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0011c0015t0019 | 0/0 | 8611 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0011c0031t0068 | 0/0 | 8625 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0011c0041t0067 | 0/0 | 8628 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0012c0013t0027 | 0/0 | 8622 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0012c0013t0031 | 0/0 | 8634 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0012c0013t0036 | 0/0 | 8622 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0012c0013t0080 | 0/0 | 8622 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0013c0019t0010 | 0/0 | 8627 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0013c0019t0049 | 0/0 | 8619 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0013c0019t0059 | 0/0 | 8621 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0013c0058t0001 | 0/0 | 8623 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0014c0020t0034 | 0/0 | 8631 | 2 | 2 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0014c0020t0076 | 0/0 | 8631 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0015c0024t0006 | 0/0 | 8618 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0015c0024t0055 | 0/0 | 8621 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0015c0066t0003 | 0/0 | 8619 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0016c0025t0013 | 0/0 | 8621 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0016c0025t0018 | 0/0 | 8629 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0017c0027t0077 | 0/0 | 8622 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0018c0071t0002 | 0/0 | 8625 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0019c0049t0002 | 0/0 | 8625 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0020c0051t0006 | 0/0 | 8618 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0021c0064t0001 | 0/0 | 8623 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0022c0048t0006 | 0/0 | 8618 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0023c0067t0002 | 0/0 | 8625 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0024c0061t0015 | 0/0 | 8612 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0025c0060t0012 | 0/0 | 8619 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0026c0057t0014 | 0/0 | 8622 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0027c0055t0002 | 0/0 | 8625 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0028c0054t0007 | 0/0 | 8620 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0029c0053t0062 | 0/0 | 8621 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0030c0047t0027 | 0/0 | 8622 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0031c0062t0004 | 0/0 | 8614 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0032c0029t0038 | 0/0 | 8617 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0033c0038t0005 | 0/0 | 8619 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0034c0039t0026 | 0/0 | 8620 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0035c0033t0081 | 0/0 | 8624 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0036c0030t0045 | 0/0 | 8617 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0037c0037t0001 | 0/0 | 8623 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0038c0043t0032 | 0/0 | 8635 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0039c0070t0009 | 0/0 | 8617 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0040c0069t0002 | 0/0 | 8625 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| a0041c0072t0078 | 0/0 | 8628 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | copy fasta | chr6 | 7102961 | 7256980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0002g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0016g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0016g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0016g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0017g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0017g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0017g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0017g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0035g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0042g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0001t0082g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0017t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0017t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0001c0017t0032g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0008g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0008g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0008g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0008g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0011g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0015g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0015g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0016g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0022g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0022g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0022g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0026g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0004t0072g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0007g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0011g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0011g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0011g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0028g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0063g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0064g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0007t0069g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0023t0044g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0023t0048g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0042t0060g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0002c0046t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0008g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0010g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0010g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0010g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0023g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0023g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0029g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0029g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0071g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0002t0074g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0012t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0012t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0012t0011g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0012t0013g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0032t0057g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0034t0008g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0040t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0044t0066g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0003c0045t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0006g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0006g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0006g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0007g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0007g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0018g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0021g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0021g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0021g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0024g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0024g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0031g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0006t0058g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0006g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0025g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0025g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0008t0037g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0050t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0052t0020g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0063t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0004c0068t0073g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0009g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0012g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0013g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0013g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0018g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0020g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0020g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0028g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0033g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0033g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0046g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0047g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0050g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0054g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0056g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0003t0079g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0014t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0014t0010g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0014t0018g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0014t0023g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0056t0010g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0005c0059t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0009g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0009g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0030g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0030g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0041g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0043g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0070g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0005t0075g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0016t0009g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0016t0009g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0006c0016t0009g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0005g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0039g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0040g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0009t0053g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0011t0014g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0011t0014g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0011t0014g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0011t0014g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0011t0051g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0011t0052g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0011t0061g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0022t0019g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0007c0022t0019g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0010t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0010t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0010t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0010t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0010t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0010t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0010t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0010t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0010t0010g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0008c0065t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0009c0018t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0009c0018t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0009c0018t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0009c0026t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0009c0026t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0010c0021t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0010c0021t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0010c0028t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0010c0035t0065g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0010c0036t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0011c0015t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0011c0015t0005g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0011c0015t0019g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0011c0031t0068g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0011c0041t0067g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0012c0013t0027g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0012c0013t0031g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0012c0013t0036g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0012c0013t0080g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0013c0019t0010g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0013c0019t0049g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0013c0019t0059g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0013c0058t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0014c0020t0034g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0014c0020t0034g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0014c0020t0076g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0015c0024t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0015c0024t0055g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0015c0066t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0016c0025t0013g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0016c0025t0018g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0017c0027t0077g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0018c0071t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0019c0049t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0020c0051t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0021c0064t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0022c0048t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0023c0067t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0024c0061t0015g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0025c0060t0012g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0026c0057t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0027c0055t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0028c0054t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0029c0053t0062g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0030c0047t0027g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0031c0062t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0032c0029t0038g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0033c0038t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0034c0039t0026g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0035c0033t0081g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0036c0030t0045g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0037c0037t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0038c0043t0032g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0039c0070t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0040c0069t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| a0041c0072t0078g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0007 | c0009 | t0005 | g0246 | EUR | GBR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00140 | hp2 | a0003 | c0002 | t0008 | g0128 | EUR | GBR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00280 | hp1 | a0001 | c0001 | t0042 | g0187 | EUR | FIN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00280 | hp2 | a0004 | c0008 | t0001 | g0265 | EUR | FIN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00323 | hp1 | a0004 | c0008 | t0001 | g0266 | EUR | FIN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00323 | hp2 | a0008 | c0010 | t0001 | g0277 | EUR | FIN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00423 | hp1 | a0002 | c0007 | t0064 | g0143 | EAS | CHS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00423 | hp2 | a0028 | c0054 | t0007 | g0029 | EAS | CHS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00438 | hp1 | a0004 | c0052 | t0020 | g0005 | EAS | CHS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00438 | hp2 | a0002 | c0004 | t0072 | g0226 | EAS | CHS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00558 | hp1 | a0007 | c0009 | t0039 | g0002 | EAS | CHS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00558 | hp2 | a0005 | c0014 | t0018 | g0113 | EAS | CHS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00621 | hp1 | a0002 | c0007 | t0007 | g0140 | EAS | CHS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00639 | hp1 | a0004 | c0008 | t0001 | g0267 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00639 | hp2 | a0002 | c0004 | t0022 | g0027 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00642 | hp1 | a0008 | c0010 | t0010 | g0254 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00642 | hp2 | a0004 | c0006 | t0006 | g0072 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00735 | hp1 | a0013 | c0019 | t0010 | g0256 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00735 | hp2 | a0003 | c0002 | t0002 | g0074 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00738 | hp1 | a0003 | c0002 | t0001 | g0129 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00738 | hp2 | a0004 | c0006 | t0007 | g0281 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00741 | hp1 | a0004 | c0006 | t0007 | g0241 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG00741 | hp2 | a0004 | c0008 | t0001 | g0292 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01071 | hp1 | a0027 | c0055 | t0002 | g0068 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01071 | hp2 | a0001 | c0001 | t0017 | g0096 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01074 | hp1 | a0013 | c0019 | t0049 | g0262 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01074 | hp2 | a0010 | c0021 | t0003 | g0011 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01099 | hp2 | a0005 | c0003 | t0004 | g0215 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01109 | hp1 | a0035 | c0033 | t0081 | g0233 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01109 | hp2 | a0008 | c0010 | t0001 | g0278 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01167 | hp1 | a0004 | c0068 | t0073 | g0273 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01167 | hp2 | a0003 | c0002 | t0003 | g0058 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01169 | hp1 | a0004 | c0006 | t0024 | g0290 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01169 | hp2 | a0003 | c0002 | t0003 | g0059 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01175 | hp1 | a0001 | c0001 | t0016 | g0280 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01175 | hp2 | a0004 | c0006 | t0007 | g0245 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01192 | hp1 | a0007 | c0009 | t0005 | g0007 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01243 | hp1 | a0005 | c0003 | t0012 | g0260 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01243 | hp2 | a0002 | c0004 | t0022 | g0136 | AMR | PUR | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01255 | hp1 | a0002 | c0004 | t0008 | g0039 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01255 | hp2 | a0001 | c0017 | t0001 | g0252 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01261 | hp1 | a0002 | c0004 | t0003 | g0151 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01261 | hp2 | a0004 | c0006 | t0006 | g0257 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01361 | hp1 | a0007 | c0022 | t0019 | g0183 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01361 | hp2 | a0002 | c0007 | t0007 | g0110 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01433 | hp1 | a0010 | c0028 | t0006 | g0019 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01433 | hp2 | a0002 | c0004 | t0008 | g0212 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01496 | hp2 | a0002 | c0004 | t0016 | g0211 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01515 | hp1 | a0004 | c0008 | t0003 | g0243 | EUR | IBS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01515 | hp2 | a0007 | c0009 | t0005 | g0270 | EUR | IBS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01517 | hp1 | a0003 | c0002 | t0010 | g0251 | EUR | IBS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01517 | hp2 | a0004 | c0008 | t0003 | g0244 | EUR | IBS | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01884 | hp1 | a0005 | c0003 | t0056 | g0207 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01884 | hp2 | a0003 | c0012 | t0013 | g0239 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01891 | hp1 | a0011 | c0015 | t0019 | g0182 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01891 | hp2 | a0002 | c0004 | t0003 | g0052 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01928 | hp1 | a0002 | c0004 | t0003 | g0150 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01943 | hp1 | a0003 | c0002 | t0010 | g0067 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01943 | hp2 | a0007 | c0009 | t0005 | g0269 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01978 | hp2 | a0008 | c0010 | t0001 | g0288 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02015 | hp1 | a0008 | c0010 | t0002 | g0106 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02015 | hp2 | a0005 | c0014 | t0010 | g0064 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02027 | hp1 | a0002 | c0004 | t0007 | g0030 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02027 | hp2 | a0005 | c0003 | t0028 | g0018 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02040 | hp1 | a0002 | c0007 | t0011 | g0162 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02040 | hp2 | a0003 | c0012 | t0011 | g0119 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02056 | hp1 | a0005 | c0003 | t0004 | g0132 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02056 | hp2 | a0001 | c0001 | t0010 | g0147 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02074 | hp1 | a0003 | c0034 | t0008 | g0031 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02074 | hp2 | a0006 | c0005 | t0004 | g0041 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02080 | hp1 | a0006 | c0005 | t0004 | g0131 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02080 | hp2 | a0001 | c0017 | t0001 | g0168 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02083 | hp1 | a0015 | c0066 | t0003 | g0276 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02083 | hp2 | a0003 | c0002 | t0002 | g0102 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02129 | hp1 | a0002 | c0007 | t0011 | g0161 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02129 | hp2 | a0005 | c0003 | t0004 | g0081 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02135 | hp1 | a0007 | c0009 | t0040 | g0012 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02135 | hp2 | a0001 | c0001 | t0016 | g0026 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02148 | hp2 | a0002 | c0004 | t0003 | g0225 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02155 | hp1 | a0004 | c0006 | t0007 | g0138 | EAS | CDX | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02155 | hp2 | a0002 | c0007 | t0007 | g0218 | EAS | CDX | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02257 | hp1 | a0011 | c0041 | t0067 | g0055 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02257 | hp2 | a0007 | c0009 | t0005 | g0247 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02258 | hp1 | a0007 | c0011 | t0014 | g0200 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02258 | hp2 | a0001 | c0001 | t0017 | g0180 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02280 | hp1 | a0001 | c0001 | t0017 | g0214 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02280 | hp2 | a0016 | c0025 | t0018 | g0179 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02300 | hp1 | a0002 | c0007 | t0008 | g0036 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02300 | hp2 | a0008 | c0010 | t0001 | g0279 | AMR | PEL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02451 | hp1 | a0041 | c0072 | t0078 | g0242 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02451 | hp2 | a0007 | c0011 | t0051 | g0185 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02523 | hp1 | a0003 | c0002 | t0023 | g0075 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02572 | hp1 | a0012 | c0013 | t0027 | g0228 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02572 | hp2 | a0007 | c0022 | t0019 | g0184 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02615 | hp1 | a0005 | c0003 | t0004 | g0037 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02615 | hp2 | a0004 | c0006 | t0024 | g0289 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02622 | hp1 | a0002 | c0004 | t0008 | g0216 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02622 | hp2 | a0012 | c0013 | t0031 | g0222 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02630 | hp1 | a0005 | c0003 | t0012 | g0172 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02630 | hp2 | a0011 | c0031 | t0068 | g0154 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02647 | hp1 | a0005 | c0003 | t0012 | g0173 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02647 | hp2 | a0010 | c0035 | t0065 | g0208 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02698 | hp1 | a0008 | c0010 | t0001 | g0286 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02698 | hp2 | a0002 | c0004 | t0008 | g0146 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02735 | hp1 | a0011 | c0015 | t0005 | g0013 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02735 | hp2 | a0002 | c0007 | t0028 | g0121 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02809 | hp1 | a0034 | c0039 | t0026 | g0249 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02809 | hp2 | a0003 | c0002 | t0074 | g0190 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02818 | hp1 | a0029 | c0053 | t0062 | g0057 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02818 | hp2 | a0005 | c0003 | t0046 | g0258 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02895 | hp1 | a0014 | c0020 | t0034 | g0236 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02895 | hp2 | a0024 | c0061 | t0015 | g0223 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02896 | hp1 | a0002 | c0004 | t0015 | g0044 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02896 | hp2 | a0005 | c0003 | t0012 | g0087 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02897 | hp1 | a0014 | c0020 | t0034 | g0237 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02897 | hp2 | a0002 | c0004 | t0015 | g0204 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02922 | hp1 | a0004 | c0006 | t0021 | g0117 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02922 | hp2 | a0019 | c0049 | t0002 | g0061 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02965 | hp1 | a0005 | c0003 | t0047 | g0178 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02965 | hp2 | a0003 | c0012 | t0004 | g0219 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02970 | hp1 | a0005 | c0003 | t0050 | g0139 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02970 | hp2 | a0005 | c0003 | t0079 | g0231 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03041 | hp1 | a0004 | c0006 | t0021 | g0105 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03041 | hp2 | a0032 | c0029 | t0038 | g0089 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03098 | hp1 | a0002 | c0004 | t0015 | g0203 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03098 | hp2 | a0015 | c0024 | t0006 | g0153 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03130 | hp1 | a0003 | c0012 | t0003 | g0205 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03130 | hp2 | a0004 | c0006 | t0058 | g0048 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03139 | hp1 | a0009 | c0026 | t0003 | g0088 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03139 | hp2 | a0004 | c0006 | t0006 | g0099 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03195 | hp1 | a0003 | c0002 | t0023 | g0175 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03195 | hp2 | a0007 | c0011 | t0052 | g0213 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03209 | hp1 | a0005 | c0003 | t0018 | g0001 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03209 | hp2 | a0004 | c0050 | t0006 | g0049 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03225 | hp1 | a0012 | c0013 | t0036 | g0181 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03239 | hp1 | a0015 | c0024 | t0055 | g0025 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03239 | hp2 | a0004 | c0006 | t0006 | g0021 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03453 | hp1 | a0002 | c0004 | t0026 | g0261 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03453 | hp2 | a0007 | c0011 | t0061 | g0198 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03486 | hp1 | a0017 | c0027 | t0077 | g0053 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03486 | hp2 | a0038 | c0043 | t0032 | g0206 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03490 | hp1 | a0003 | c0002 | t0029 | g0186 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03491 | hp2 | a0003 | c0002 | t0002 | g0063 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03492 | hp1 | a0003 | c0002 | t0029 | g0062 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03492 | hp2 | a0003 | c0002 | t0002 | g0189 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03516 | hp1 | a0004 | c0006 | t0021 | g0051 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03516 | hp2 | a0005 | c0003 | t0054 | g0152 | AFR | ESN | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03540 | hp1 | a0001 | c0001 | t0082 | g0235 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03540 | hp2 | a0025 | c0060 | t0012 | g0227 | AFR | GWD | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03669 | hp1 | a0021 | c0064 | t0001 | g0271 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03669 | hp2 | a0002 | c0004 | t0008 | g0035 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03688 | hp1 | a0002 | c0004 | t0003 | g0148 | SAS | STU | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03688 | hp2 | a0010 | c0021 | t0006 | g0250 | SAS | STU | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03710 | hp1 | a0004 | c0008 | t0002 | g0112 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03710 | hp2 | a0003 | c0045 | t0002 | g0070 | SAS | PJL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03834 | hp1 | a0002 | c0004 | t0022 | g0066 | SAS | BEB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03834 | hp2 | a0011 | c0015 | t0005 | g0010 | SAS | BEB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03927 | hp1 | a0003 | c0002 | t0003 | g0229 | SAS | BEB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03942 | hp1 | a0033 | c0038 | t0005 | g0127 | SAS | BEB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03942 | hp2 | a0004 | c0008 | t0025 | g0272 | SAS | BEB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG04115 | hp1 | a0036 | c0030 | t0045 | g0046 | SAS | STU | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG04184 | hp1 | a0001 | c0017 | t0032 | g0149 | SAS | BEB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG04184 | hp2 | a0004 | c0008 | t0025 | g0291 | SAS | BEB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG04199 | hp1 | a0002 | c0007 | t0069 | g0022 | SAS | STU | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18522 | hp1 | a0012 | c0013 | t0080 | g0234 | AFR | YRI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18522 | hp2 | a0004 | c0006 | t0018 | g0056 | AFR | YRI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18612 | hp1 | a0010 | c0036 | t0002 | g0004 | EAS | CHB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18612 | hp2 | a0003 | c0002 | t0002 | g0065 | EAS | CHB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18747 | hp1 | a0005 | c0014 | t0002 | g0114 | EAS | CHB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18747 | hp2 | a0002 | c0023 | t0044 | g0095 | EAS | CHB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18906 | hp1 | a0005 | c0003 | t0033 | g0230 | AFR | YRI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18906 | hp2 | a0005 | c0059 | t0013 | g0157 | AFR | YRI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18939 | hp1 | a0013 | c0058 | t0001 | g0134 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18939 | hp2 | a0009 | c0018 | t0003 | g0158 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18941 | hp1 | a0005 | c0003 | t0009 | g0101 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18941 | hp2 | a0002 | c0004 | t0003 | g0118 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18942 | hp1 | a0006 | c0016 | t0009 | g0092 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18945 | hp1 | a0002 | c0042 | t0060 | g0108 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18945 | hp2 | a0031 | c0062 | t0004 | g0107 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18946 | hp1 | a0002 | c0046 | t0003 | g0078 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18946 | hp2 | a0006 | c0005 | t0004 | g0084 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18949 | hp1 | a0006 | c0005 | t0004 | g0085 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18949 | hp2 | a0003 | c0002 | t0010 | g0210 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18951 | hp1 | a0002 | c0004 | t0003 | g0082 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18951 | hp2 | a0003 | c0040 | t0001 | g0103 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18952 | hp2 | a0007 | c0009 | t0005 | g0008 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18960 | hp1 | a0003 | c0002 | t0002 | g0020 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18960 | hp2 | a0002 | c0007 | t0011 | g0160 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18963 | hp2 | a0002 | c0007 | t0063 | g0217 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18964 | hp1 | a0002 | c0007 | t0011 | g0169 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18965 | hp1 | a0005 | c0056 | t0010 | g0196 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18965 | hp2 | a0006 | c0005 | t0070 | g0038 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18970 | hp1 | a0002 | c0023 | t0048 | g0171 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18970 | hp2 | a0006 | c0005 | t0030 | g0193 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18971 | hp1 | a0002 | c0007 | t0007 | g0195 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18971 | hp2 | a0007 | c0009 | t0053 | g0014 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18974 | hp1 | a0006 | c0005 | t0009 | g0090 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18974 | hp2 | a0005 | c0014 | t0023 | g0050 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18979 | hp1 | a0006 | c0005 | t0041 | g0156 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18979 | hp2 | a0009 | c0018 | t0003 | g0077 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18982 | hp1 | a0005 | c0003 | t0020 | g0091 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18982 | hp2 | a0001 | c0001 | t0016 | g0083 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18984 | hp1 | a0001 | c0001 | t0017 | g0166 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18984 | hp2 | a0006 | c0016 | t0009 | g0115 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18987 | hp1 | a0040 | c0069 | t0002 | g0123 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18987 | hp2 | a0039 | c0070 | t0009 | g0016 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18990 | hp1 | a0006 | c0005 | t0004 | g0164 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18990 | hp2 | a0002 | c0004 | t0003 | g0130 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18995 | hp1 | a0004 | c0063 | t0003 | g0141 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18995 | hp2 | a0003 | c0044 | t0066 | g0042 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18998 | hp1 | a0007 | c0009 | t0005 | g0009 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA18998 | hp2 | a0006 | c0005 | t0004 | g0080 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19000 | hp1 | a0005 | c0003 | t0020 | g0137 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19000 | hp2 | a0001 | c0001 | t0035 | g0034 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19004 | hp1 | a0003 | c0002 | t0002 | g0076 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19005 | hp1 | a0005 | c0003 | t0004 | g0047 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19005 | hp2 | a0003 | c0002 | t0002 | g0145 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19009 | hp2 | a0002 | c0007 | t0007 | g0116 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19012 | hp2 | a0018 | c0071 | t0002 | g0167 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19030 | hp1 | a0030 | c0047 | t0027 | g0209 | AFR | LWK | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19030 | hp2 | a0020 | c0051 | t0006 | g0045 | AFR | LWK | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19043 | hp1 | a0003 | c0032 | t0057 | g0176 | AFR | LWK | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19043 | hp2 | a0003 | c0002 | t0004 | g0015 | AFR | LWK | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19056 | hp1 | a0006 | c0005 | t0043 | g0100 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19056 | hp2 | a0002 | c0004 | t0011 | g0163 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19066 | hp1 | a0006 | c0005 | t0004 | g0086 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19068 | hp1 | a0003 | c0002 | t0001 | g0124 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19068 | hp2 | a0006 | c0005 | t0009 | g0144 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19075 | hp1 | a0006 | c0016 | t0009 | g0024 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19075 | hp2 | a0009 | c0018 | t0008 | g0032 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19081 | hp1 | a0006 | c0005 | t0009 | g0133 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19083 | hp1 | a0006 | c0005 | t0075 | g0192 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19084 | hp1 | a0006 | c0005 | t0030 | g0194 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19084 | hp2 | a0023 | c0067 | t0002 | g0135 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19086 | hp1 | a0004 | c0008 | t0004 | g0165 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19088 | hp1 | a0006 | c0005 | t0004 | g0104 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19088 | hp2 | a0003 | c0002 | t0003 | g0120 | EAS | JPT | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19240 | hp1 | a0007 | c0011 | t0014 | g0202 | AFR | YRI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA19240 | hp2 | a0014 | c0020 | t0076 | g0177 | AFR | YRI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20129 | hp1 | a0005 | c0003 | t0004 | g0174 | AFR | ASW | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20129 | hp2 | a0002 | c0004 | t0003 | g0094 | AFR | ASW | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20752 | hp1 | a0008 | c0010 | t0001 | g0191 | EUR | TSI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20752 | hp2 | a0008 | c0065 | t0001 | g0275 | EUR | TSI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20805 | hp1 | a0004 | c0008 | t0003 | g0188 | EUR | TSI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20805 | hp2 | a0007 | c0009 | t0005 | g0006 | EUR | TSI | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20905 | hp1 | a0003 | c0002 | t0071 | g0284 | SAS | GIH | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20905 | hp2 | a0013 | c0019 | t0059 | g0287 | SAS | GIH | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG01123 | hp2 | a0037 | c0037 | t0001 | g0093 | AMR | CLM | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02109 | hp1 | a0026 | c0057 | t0014 | g0221 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02109 | hp2 | a0022 | c0048 | t0006 | g0197 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02486 | hp1 | a0007 | c0011 | t0014 | g0201 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02486 | hp2 | a0016 | c0025 | t0013 | g0238 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02559 | hp1 | a0004 | c0006 | t0031 | g0079 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG02559 | hp2 | a0009 | c0026 | t0003 | g0060 | AFR | ACB | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03471 | hp1 | a0005 | c0003 | t0004 | g0220 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG03471 | hp2 | a0005 | c0003 | t0033 | g0232 | AFR | MSL | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG06807 | hp1 | a0008 | c0010 | t0001 | g0003 | AFR | USA | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| HG06807 | hp2 | a0007 | c0011 | t0014 | g0199 | AFR | USA | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20300 | hp1 | a0005 | c0003 | t0013 | g0240 | AFR | USA | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA20300 | hp2 | a0003 | c0002 | t0002 | g0142 | AFR | USA | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA21309 | hp1 | a0004 | c0008 | t0037 | g0264 | AFR | LWK | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| NA21309 | hp2 | a0005 | c0003 | t0013 | g0159 | AFR | LWK | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| homoSapiens_chm13v2 | hp1 | a0004 | c0008 | t0006 | g0274 | REF | REF | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0071 | REF | REF | RREB1_chr6_7102961_7256980 | RREB1 | chr6 | 7102961 | 7256980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:7181922
|
G | A | 1 | a0017 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.11G>A | p.Ser4Asn | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/13 | 395/8625 | 11/5229 | 4/1742 | chr6 | 7181922 | ||
| chr6:7182047
|
C | T | 1 | a0041 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.136C>T | p.Pro46Ser | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/13 | 520/8625 | 136/5229 | 46/1742 | chr6 | 7182047 | ||
| chr6:7189165
|
A | G | 1 | a0014 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.268A>G | p.Thr90Ala | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/13 | 652/8625 | 268/5229 | 90/1742 | chr6 | 7189165 | ||
| chr6:7210863
|
C | T | 1 | a0018 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.485C>T | p.Pro162Leu | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/13 | 869/8625 | 485/5229 | 162/1742 | chr6 | 7210863 | ||
| chr6:7210937
|
C | T | 2 | a0039a0040 | 2 | NA18987.hp1 NA18987.hp2 |
missense_variant | MODERATE | c.559C>T | p.Pro187Ser | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/13 | 943/8625 | 559/5229 | 187/1742 | chr6 | 7210937 | ||
| chr6:7211585
|
G | A | 14 | a0002a0003a0007others(11): Show | 119 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
missense_variant | MODERATE | c.583G>A | p.Gly195Arg | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/13 | 967/8625 | 583/5229 | 195/1742 | chr6 | 7211585 | ||
| chr6:7229703
|
C | T | 1 | a0032 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1604C>T | p.Pro535Leu | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 1988/8625 | 1604/5229 | 535/1742 | chr6 | 7229703 | ||
| chr6:7229741
|
A | C | 1 | a0031 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.1642A>C | p.Lys548Gln | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 2026/8625 | 1642/5229 | 548/1742 | chr6 | 7229741 | ||
| chr6:7229816
|
G | A | 1 | a0030 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.1717G>A | p.Ala573Thr | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 2101/8625 | 1717/5229 | 573/1742 | chr6 | 7229816 | ||
| chr6:7230447
|
G | T | 26 | a0002a0003a0005others(23): Show | 165 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
missense_variant | MODERATE | c.2348G>T | p.Gly783Val | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 2732/8625 | 2348/5229 | 783/1742 | chr6 | 7230447 | ||
| chr6:7230549
|
C | G | 1 | a0023 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.2450C>G | p.Pro817Arg | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 2834/8625 | 2450/5229 | 817/1742 | chr6 | 7230549 | ||
| chr6:7231004
|
C | T | 1 | a0016 | 2 | HG02280.hp2 HG02486.hp2 |
missense_variant | MODERATE | c.2905C>T | p.Pro969Ser | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3289/8625 | 2905/5229 | 969/1742 | chr6 | 7231004 | ||
| chr6:7231047
|
T | C | 1 | a0022 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2948T>C | p.Leu983Ser | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3332/8625 | 2948/5229 | 983/1742 | chr6 | 7231047 | ||
| chr6:7231248
|
C | T | 1 | a0024 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.3149C>T | p.Pro1050Leu | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3533/8625 | 3149/5229 | 1050/1742 | chr6 | 7231248 | ||
| chr6:7231296
|
C | T | 1 | a0038 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.3197C>T | p.Ala1066Val | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3581/8625 | 3197/5229 | 1066/1742 | chr6 | 7231296 | ||
| chr6:7231433
|
G | A | 1 | a0029 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.3334G>A | p.Ala1112Thr | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3718/8625 | 3334/5229 | 1112/1742 | chr6 | 7231433 | ||
| chr6:7231442
|
G | A | 1 | a0037 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.3343G>A | p.Ala1115Thr | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3727/8625 | 3343/5229 | 1115/1742 | chr6 | 7231442 | ||
| chr6:7231503
|
G | T | 1 | a0022 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3404G>T | p.Ser1135Ile | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3788/8625 | 3404/5229 | 1135/1742 | chr6 | 7231503 | ||
| chr6:7231563
|
G | A | 1 | a0033 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.3464G>A | p.Arg1155Gln | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3848/8625 | 3464/5229 | 1155/1742 | chr6 | 7231563 | ||
| chr6:7231610
|
G | A | 8 | a0006a0008a0027others(5): Show | 36 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(33): Show |
missense_variant | MODERATE | c.3511G>A | p.Asp1171Asn | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3895/8625 | 3511/5229 | 1171/1742 | chr6 | 7231610 | ||
| chr6:7231806
|
G | A | 1 | a0034 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.3707G>A | p.Arg1236Gln | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 4091/8625 | 3707/5229 | 1236/1742 | chr6 | 7231806 | ||
| chr6:7246445
|
C | T | 1 | a0025 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.3995C>T | p.Thr1332Ile | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4379/8625 | 3995/5229 | 1332/1742 | chr6 | 7246445 | ||
| chr6:7246450
|
G | C | 1 | a0040 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.4000G>C | p.Ala1334Pro | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4384/8625 | 4000/5229 | 1334/1742 | chr6 | 7246450 | ||
| chr6:7246502
|
C | G | 1 | a0040 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.4052C>G | p.Ser1351Trp | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4436/8625 | 4052/5229 | 1351/1742 | chr6 | 7246502 | ||
| chr6:7246519
|
C | G | 1 | a0040 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.4069C>G | p.Leu1357Val | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4453/8625 | 4069/5229 | 1357/1742 | chr6 | 7246519 | ||
| chr6:7246765
|
G | A | 7 | a0002a0009a0015others(4): Show | 55 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
missense_variant | MODERATE | c.4315G>A | p.Gly1439Arg | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4699/8625 | 4315/5229 | 1439/1742 | chr6 | 7246765 | ||
| chr6:7246898
|
C | T | 1 | a0021 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.4448C>T | p.Ala1483Val | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4832/8625 | 4448/5229 | 1483/1742 | chr6 | 7246898 | ||
| chr6:7246968
|
G | C | 1 | a0019 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.4518G>C | p.Glu1506Asp | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4902/8625 | 4518/5229 | 1506/1742 | chr6 | 7246968 | ||
| chr6:7246979
|
C | T | 1 | a0035 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.4529C>T | p.Ser1510Leu | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4913/8625 | 4529/5229 | 1510/1742 | chr6 | 7246979 | ||
| chr6:7247015
|
T | C | 34 | a0002a0003a0004others(31): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
missense_variant | MODERATE | c.4565T>C | p.Leu1522Pro | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4949/8625 | 4565/5229 | 1522/1742 | chr6 | 7247015 | ||
| chr6:7247111
|
C | A | 9 | a0007a0011a0012others(6): Show | 35 | HG00140.hp1 HG00558.hp1 HG01192.hp1 others(32): Show |
missense_variant | MODERATE | c.4661C>A | p.Ser1554Tyr | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 5045/8625 | 4661/5229 | 1554/1742 | chr6 | 7247111 | ||
| chr6:7248814
|
C | T | 1 | a0020 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.5075C>T | p.Thr1692Met | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 5459/8625 | 5075/5229 | 1692/1742 | chr6 | 7248814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:7181998
|
G | A | 1 | a0017c0027 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.87G>A | p.Lys29Lys | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/13 | 471/8625 | 87/5229 | 29/1742 | chr6 | 7181998 | ||
| chr6:7229113
|
T | C | 40 | a0003c0032a0003c0034a0004c0006others(37): Show | 124 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(121): Show |
synonymous_variant | LOW | c.1014T>C | p.His338His | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 1398/8625 | 1014/5229 | 338/1742 | chr6 | 7229113 | ||
| chr6:7229236
|
C | T | 1 | a0004c0068 | 1 | HG01167.hp1 | synonymous_variant | LOW | c.1137C>T | p.Pro379Pro | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 1521/8625 | 1137/5229 | 379/1742 | chr6 | 7229236 | ||
| chr6:7229386
|
G | A | 15 | a0004c0006a0004c0050a0007c0009others(12): Show | 49 | HG00140.hp1 HG00558.hp1 HG00642.hp2 others(46): Show |
synonymous_variant | LOW | c.1287G>A | p.Ala429Ala | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 1671/8625 | 1287/5229 | 429/1742 | chr6 | 7229386 | ||
| chr6:7230442
|
C | T | 2 | a0007c0011a0010c0035 | 8 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
synonymous_variant | LOW | c.2343C>T | p.Gly781Gly | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 2727/8625 | 2343/5229 | 781/1742 | chr6 | 7230442 | ||
| chr6:7230496
|
C | T | 1 | a0010c0028 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.2397C>T | p.Phe799Phe | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 2781/8625 | 2397/5229 | 799/1742 | chr6 | 7230496 | ||
| chr6:7230529
|
C | G | 1 | a0002c0046 | 1 | NA18946.hp1 | synonymous_variant | LOW | c.2430C>G | p.Leu810Leu | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 2814/8625 | 2430/5229 | 810/1742 | chr6 | 7230529 | ||
| chr6:7230613
|
C | T | 1 | a0003c0045 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.2514C>T | p.Ala838Ala | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 2898/8625 | 2514/5229 | 838/1742 | chr6 | 7230613 | ||
| chr6:7230673
|
C | G | 1 | a0003c0044 | 1 | NA18995.hp2 | synonymous_variant | LOW | c.2574C>G | p.Pro858Pro | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 2958/8625 | 2574/5229 | 858/1742 | chr6 | 7230673 | ||
| chr6:7231537
|
A | G | 12 | a0001c0017a0002c0007a0002c0042others(9): Show | 32 | HG00423.hp1 HG00621.hp1 HG01123.hp2 others(29): Show |
synonymous_variant | LOW | c.3438A>G | p.Pro1146Pro | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/13 | 3822/8625 | 3438/5229 | 1146/1742 | chr6 | 7231537 | ||
| chr6:7246452
|
C | T | 1 | a0005c0059 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.4002C>T | p.Ala1334Ala | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4386/8625 | 4002/5229 | 1334/1742 | chr6 | 7246452 | ||
| chr6:7246503
|
G | C | 1 | a0040c0069 | 1 | NA18987.hp1 | synonymous_variant | LOW | c.4053G>C | p.Ser1351Ser | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4437/8625 | 4053/5229 | 1351/1742 | chr6 | 7246503 | ||
| chr6:7246545
|
T | C | 1 | a0005c0056 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.4095T>C | p.Pro1365Pro | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4479/8625 | 4095/5229 | 1365/1742 | chr6 | 7246545 | ||
| chr6:7246620
|
G | A | 2 | a0006c0016a0039c0070 | 4 | NA18942.hp1 NA18984.hp2 NA18987.hp2 others(1): Show |
synonymous_variant | LOW | c.4170G>A | p.Pro1390Pro | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4554/8625 | 4170/5229 | 1390/1742 | chr6 | 7246620 | ||
| chr6:7246761
|
C | T | 1 | a0022c0048 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.4311C>T | p.Gly1437Gly | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4695/8625 | 4311/5229 | 1437/1742 | chr6 | 7246761 | ||
| chr6:7246932
|
T | A | 1 | a0003c0040 | 1 | NA18951.hp2 | synonymous_variant | LOW | c.4482T>A | p.Pro1494Pro | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 4866/8625 | 4482/5229 | 1494/1742 | chr6 | 7246932 | ||
| chr6:7247121
|
C | T | 1 | a0002c0042 | 1 | NA18945.hp1 | synonymous_variant | LOW | c.4671C>T | p.Ser1557Ser | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/13 | 5055/8625 | 4671/5229 | 1557/1742 | chr6 | 7247121 | ||
| chr6:7248692
|
C | T | 4 | a0002c0023a0003c0034a0004c0063others(1): Show | 7 | HG02074.hp1 NA18747.hp2 NA18939.hp2 others(4): Show |
synonymous_variant | LOW | c.4953C>T | p.Ala1651Ala | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 5337/8625 | 4953/5229 | 1651/1742 | chr6 | 7248692 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:7108036
|
A | T | 6 | a0001c0001t0082a0005c0003t0033a0005c0003t0079others(3): Show | 8 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-309A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/13 | chr6 | 7108036 | ||||||
| chr6:7176733
|
C | A | 1 | a0001c0001t0035 | 1 | NA19000.hp2 | 5_prime_UTR_variant | MODIFIER | c.-206C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/13 | 5179 | chr6 | 7176733 | |||||
| chr6:7181159
|
G | A | 1 | a0012c0013t0036 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-130G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 3/13 | 753 | chr6 | 7181159 | |||||
| chr6:7181874
|
A | G | 2 | a0017c0027t0077a0041c0072t0078 | 2 | HG02451.hp1 HG03486.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/13 | chr6 | 7181874 | ||||||
| chr6:7249062
|
T | TGA | 13 | a0001c0001t0010a0002c0004t0072a0002c0007t0069others(10): Show | 16 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*135_*136dupGA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 137 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
T | TGAGA | 5 | a0004c0006t0018a0005c0003t0018a0005c0014t0018others(2): Show | 6 | HG00558.hp2 HG02280.hp2 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*136dupGAGA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 137 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
T | TGAGAGA | 6 | a0003c0002t0074a0004c0006t0031a0006c0005t0075others(3): Show | 7 | HG02559.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*131_*136dupGAGAGA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 137 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
T | TGAGAGAG others(1): Show |
2 | a0003c0002t0023a0005c0014t0023 | 3 | HG02523.hp1 HG03195.hp1 NA18974.hp2 |
3_prime_UTR_variant | MODIFIER | c.*129_*136dupGAGAGA others(2): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 137 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
T | TGAGAGAG others(3): Show |
2 | a0001c0017t0032a0038c0043t0032 | 2 | HG03486.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*127_*136dupGAGAGA others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 137 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
TGA | T | 20 | a0001c0001t0001a0001c0001t0016a0001c0001t0017others(17): Show | 59 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*135_*136delGA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 135 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
TGAGA | T | 22 | a0002c0004t0007a0002c0004t0008a0002c0007t0007others(19): Show | 34 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*136delGAGA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 133 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
TGAGAGA | T | 45 | a0002c0004t0003a0002c0004t0022a0002c0004t0026others(42): Show | 80 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*131_*136delGAGAGA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 131 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
TGAGAGAG others(3): Show |
T | 16 | a0002c0023t0044a0003c0002t0004a0003c0012t0004others(13): Show | 36 | HG00438.hp1 HG01099.hp2 HG02056.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*127_*136delGAGAGA others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 127 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
TGAGAGAG others(5): Show |
T | 6 | a0001c0001t0042a0002c0004t0015a0006c0005t0041others(3): Show | 8 | HG00280.hp1 HG00558.hp1 HG02135.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*125_*136delGAGAGA others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 125 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
TGAGAGAG others(7): Show |
T | 5 | a0004c0008t0025a0004c0008t0037a0007c0022t0019others(2): Show | 7 | HG01361.hp1 HG01891.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*123_*136delGAGAGA others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 123 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249062
|
TGAGAGAG others(11): Show |
T | 1 | a0004c0006t0024 | 2 | HG01169.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*119_*136delGAGAGA others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 119 | INFO_REALIGN_3_PRIME | chr6 | 7249062 | ||||
| chr6:7249227
|
G | A | 6 | a0007c0009t0005a0007c0009t0039a0007c0009t0040others(3): Show | 14 | HG00140.hp1 HG00558.hp1 HG01192.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*259G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 259 | chr6 | 7249227 | |||||
| chr6:7249312
|
G | A | 1 | a0011c0031t0068 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 344 | chr6 | 7249312 | |||||
| chr6:7249799
|
A | ATAT | 11 | a0002c0007t0063a0004c0006t0031a0007c0009t0040others(8): Show | 11 | HG02135.hp1 HG02451.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*855_*857dupTTA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 858 | INFO_REALIGN_3_PRIME | chr6 | 7249799 | ||||
| chr6:7249799
|
A | ATGT | 3 | a0012c0013t0027a0012c0013t0080a0030c0047t0027 | 3 | HG02572.hp1 NA18522.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*832_*833insGTT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 833 | INFO_REALIGN_3_PRIME | chr6 | 7249799 | ||||
| chr6:7249799
|
A | T | 2 | a0002c0007t0064a0004c0006t0021 | 4 | HG00423.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*831A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 831 | chr6 | 7249799 | |||||
| chr6:7249918
|
C | T | 1 | a0012c0013t0036 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*950C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 950 | chr6 | 7249918 | |||||
| chr6:7250037
|
G | A | 6 | a0007c0009t0005a0007c0009t0039a0007c0009t0040others(3): Show | 14 | HG00140.hp1 HG00558.hp1 HG01192.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1069G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1069 | chr6 | 7250037 | |||||
| chr6:7250103
|
C | T | 1 | a0001c0001t0082 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1135C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1135 | chr6 | 7250103 | |||||
| chr6:7250241
|
C | T | 6 | a0007c0009t0005a0007c0009t0039a0007c0009t0040others(3): Show | 14 | HG00140.hp1 HG00558.hp1 HG01192.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1273C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1273 | chr6 | 7250241 | |||||
| chr6:7250392
|
C | T | 1 | a0004c0068t0073 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1424C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1424 | chr6 | 7250392 | |||||
| chr6:7250406
|
A | G | 6 | a0007c0009t0005a0007c0009t0039a0007c0009t0040others(3): Show | 14 | HG00140.hp1 HG00558.hp1 HG01192.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1438A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1438 | chr6 | 7250406 | |||||
| chr6:7250521
|
A | G | 3 | a0005c0003t0033a0005c0003t0050a0029c0053t0062 | 4 | HG02818.hp1 HG02970.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1553A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1553 | chr6 | 7250521 | |||||
| chr6:7250681
|
G | A | 8 | a0005c0003t0012a0005c0003t0033a0005c0003t0046others(5): Show | 12 | HG01243.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1713G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1713 | chr6 | 7250681 | |||||
| chr6:7250685
|
A | G | 7 | a0007c0011t0014a0007c0011t0051a0007c0011t0052others(4): Show | 10 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1717A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1717 | chr6 | 7250685 | |||||
| chr6:7250714
|
C | T | 1 | a0002c0042t0060 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1746C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1746 | chr6 | 7250714 | |||||
| chr6:7250727
|
G | A | 54 | a0002c0004t0007a0002c0004t0011a0002c0004t0015others(51): Show | 100 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1759G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1759 | chr6 | 7250727 | |||||
| chr6:7250804
|
C | T | 39 | a0002c0004t0007a0002c0004t0011a0002c0004t0015others(36): Show | 74 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1836C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1836 | chr6 | 7250804 | |||||
| chr6:7250874
|
G | A | 1 | a0002c0004t0022 | 3 | HG00639.hp2 HG01243.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1906G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1906 | chr6 | 7250874 | |||||
| chr6:7250897
|
G | T | 1 | a0004c0006t0024 | 2 | HG01169.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1929G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 1929 | chr6 | 7250897 | |||||
| chr6:7250966
|
T | TTTA | 6 | a0005c0003t0009a0006c0005t0009a0006c0005t0041others(3): Show | 10 | NA18941.hp1 NA18942.hp1 NA18974.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2020_*2022dupTTA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2023 | INFO_REALIGN_3_PRIME | chr6 | 7250966 | ||||
| chr6:7251218
|
C | T | 39 | a0002c0004t0007a0002c0004t0011a0002c0004t0015others(36): Show | 74 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2250C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2250 | chr6 | 7251218 | |||||
| chr6:7251270
|
A | G | 1 | a0011c0031t0068 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2302A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2302 | chr6 | 7251270 | |||||
| chr6:7251291
|
T | G | 1 | a0003c0044t0066 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2323T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2323 | chr6 | 7251291 | |||||
| chr6:7251437
|
A | T | 1 | a0005c0003t0047 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2469A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2469 | chr6 | 7251437 | |||||
| chr6:7251489
|
C | CTTG | 10 | a0004c0006t0058a0007c0011t0014a0007c0011t0051others(7): Show | 13 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2523_*2524insGTT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2524 | INFO_REALIGN_3_PRIME | chr6 | 7251489 | ||||
| chr6:7251489
|
CT | C | 42 | a0001c0001t0017a0002c0004t0007a0002c0004t0011others(39): Show | 81 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2543delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2543 | INFO_REALIGN_3_PRIME | chr6 | 7251489 | ||||
| chr6:7251489
|
CTT | C | 5 | a0006c0005t0030a0006c0005t0043a0006c0005t0070others(2): Show | 6 | HG02630.hp2 NA18965.hp2 NA18970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2542_*2543delTT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2542 | INFO_REALIGN_3_PRIME | chr6 | 7251489 | ||||
| chr6:7251490
|
T | TTG | 5 | a0003c0012t0013a0005c0003t0013a0005c0003t0079others(2): Show | 6 | HG01884.hp2 HG02486.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2523_*2524insGT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2524 | INFO_REALIGN_3_PRIME | chr6 | 7251490 | ||||
| chr6:7251491
|
T | TG | 6 | a0002c0004t0026a0002c0004t0072a0003c0032t0057others(3): Show | 6 | HG00438.hp2 HG01109.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2523_*2524insG | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2524 | chr6 | 7251491 | |||||
| chr6:7251492
|
T | G | 42 | a0001c0001t0016a0002c0004t0003a0002c0004t0008others(39): Show | 79 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2524T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2524 | chr6 | 7251492 | |||||
| chr6:7251493
|
T | G | 39 | a0002c0004t0007a0002c0004t0011a0002c0004t0015others(36): Show | 75 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2525T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2525 | chr6 | 7251493 | |||||
| chr6:7251494
|
T | G | 2 | a0006c0005t0043a0011c0031t0068 | 2 | HG02630.hp2 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2526T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2526 | chr6 | 7251494 | |||||
| chr6:7251497
|
T | G | 1 | a0002c0023t0048 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2529T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2529 | chr6 | 7251497 | |||||
| chr6:7251630
|
C | T | 8 | a0004c0006t0058a0007c0011t0052a0010c0035t0065others(5): Show | 8 | HG02257.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2662C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 13/13 | 2662 | chr6 | 7251630 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:7108260
|
G | C | 1 | a0005c0003t0018g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-285+200G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7108260 | ||||||
| chr6:7108316
|
T | TTCC | 11 | a0001c0001t0082g0235a0003c0002t0003g0229a0005c0003t0033g0230others(8): Show | 11 | HG01109.hp1 HG02572.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-285+278_-285+280d others(5): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7108316 | |||||
| chr6:7108316
|
T | TTCCTCC | 3 | a0003c0012t0013g0239a0005c0003t0013g0240a0016c0025t0013g0238 | 3 | HG01884.hp2 HG02486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-285+275_-285+280d others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7108316 | |||||
| chr6:7108316
|
T | TTCCTCCT others(2): Show |
51 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(48): Show | 51 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.-285+272_-285+280d others(11): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7108316 | |||||
| chr6:7108316
|
T | TTCCTCCT others(5): Show |
2 | a0004c0008t0001g0292a0004c0008t0025g0291 | 2 | HG00741.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-285+269_-285+280d others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7108316 | |||||
| chr6:7108382
|
CCAACCAG others(13): Show |
C | 1 | a0002c0004t0072g0226 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-285+324_-285+343d others(22): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7108382 | |||||
| chr6:7108403
|
C | G | 1 | a0002c0004t0072g0226 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-285+343C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7108403 | ||||||
| chr6:7108565
|
C | T | 2 | a0001c0001t0001g0224a0002c0004t0003g0225 | 2 | HG02148.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-285+505C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7108565 | ||||||
| chr6:7108707
|
CCGGGGGT others(20): Show |
C | 2 | a0004c0006t0024g0289a0004c0006t0024g0290 | 2 | HG01169.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-285+661_-285+687d others(29): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7108707 | |||||
| chr6:7108740
|
G | T | 8 | a0001c0001t0082g0235a0005c0003t0033g0230a0005c0003t0033g0232others(5): Show | 8 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+680G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7108740 | ||||||
| chr6:7108751
|
G | C | 13 | a0004c0052t0020g0005a0007c0009t0005g0006a0007c0009t0005g0007others(10): Show | 13 | HG00438.hp1 HG00558.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-285+691G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7108751 | ||||||
| chr6:7108778
|
G | T | 4 | a0005c0003t0004g0220a0012c0013t0031g0222a0024c0061t0015g0223others(1): Show | 4 | HG02109.hp1 HG02622.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-285+718G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7108778 | ||||||
| chr6:7108803
|
C | T | 1 | a0003c0012t0004g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-285+743C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7108803 | ||||||
| chr6:7108864
|
C | T | 50 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.-285+804C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7108864 | ||||||
| chr6:7108937
|
C | T | 2 | a0002c0007t0007g0218a0002c0007t0063g0217 | 2 | HG02155.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-285+877C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7108937 | ||||||
| chr6:7109004
|
G | A | 1 | a0003c0002t0004g0015 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-285+944G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109004 | ||||||
| chr6:7109024
|
C | CG | 34 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(31): Show | 34 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-285+972dupG | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7109024 | |||||
| chr6:7109033
|
T | G | 1 | a0039c0070t0009g0016 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-285+973T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109033 | ||||||
| chr6:7109059
|
C | T | 1 | a0002c0004t0008g0216 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-285+999C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109059 | ||||||
| chr6:7109146
|
G | T | 1 | a0005c0003t0004g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-285+1086G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109146 | ||||||
| chr6:7109191
|
C | T | 1 | a0001c0001t0017g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-285+1131C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109191 | ||||||
| chr6:7109200
|
C | T | 41 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0283others(38): Show | 41 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-285+1140C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109200 | ||||||
| chr6:7109251
|
G | GC | 23 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0043others(20): Show | 23 | HG01109.hp1 HG01192.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.-285+1199dupC | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7109251 | |||||
| chr6:7109311
|
C | T | 1 | a0001c0001t0082g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-285+1251C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109311 | ||||||
| chr6:7109402
|
C | T | 1 | a0005c0003t0004g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-285+1342C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109402 | ||||||
| chr6:7109403
|
G | A | 1 | a0005c0003t0004g0047 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-285+1343G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109403 | ||||||
| chr6:7109432
|
C | G | 56 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.-285+1372C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109432 | ||||||
| chr6:7109448
|
T | C | 1 | a0004c0006t0024g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-285+1388T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109448 | ||||||
| chr6:7109507
|
C | T | 1 | a0026c0057t0014g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-285+1447C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109507 | ||||||
| chr6:7109513
|
C | T | 1 | a0001c0001t0035g0034 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-285+1453C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109513 | ||||||
| chr6:7109631
|
A | G | 1 | a0007c0011t0052g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-285+1571A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109631 | ||||||
| chr6:7109725
|
C | G | 1 | a0036c0030t0045g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-285+1665C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7109725 | ||||||
| chr6:7110053
|
A | AGACTT | 8 | a0001c0001t0082g0235a0005c0003t0033g0230a0005c0003t0033g0232others(5): Show | 8 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+1995_-285+199 others(9): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110053 | |||||
| chr6:7110117
|
C | G | 2 | a0002c0004t0026g0261a0034c0039t0026g0249 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-285+2057C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7110117 | ||||||
| chr6:7110138
|
C | T | 2 | a0002c0004t0008g0212a0002c0004t0016g0211 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-285+2078C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7110138 | ||||||
| chr6:7110258
|
C | T | 1 | a0003c0002t0010g0210 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-285+2198C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7110258 | ||||||
| chr6:7110326
|
TTAGA | T | 4 | a0005c0003t0033g0230a0005c0003t0033g0232a0005c0003t0079g0231others(1): Show | 4 | HG01109.hp1 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-285+2271_-285+227 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110326 | |||||
| chr6:7110479
|
G | GGT | 6 | a0001c0001t0082g0235a0002c0023t0048g0171a0005c0003t0033g0230others(3): Show | 6 | HG01109.hp1 HG02970.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-285+2436_-285+243 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110479 | |||||
| chr6:7110479
|
G | GGTGT | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-285+2434_-285+243 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110479 | |||||
| chr6:7110479
|
G | GGTGTGTG others(1): Show |
6 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+2430_-285+243 others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110479 | |||||
| chr6:7110479
|
G | GGTGTGTG others(3): Show |
40 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0035g0034others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-285+2428_-285+243 others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110479 | |||||
| chr6:7110479
|
G | GGTGTGTG others(5): Show |
16 | a0001c0001t0017g0214a0002c0004t0015g0044a0002c0004t0015g0203others(13): Show | 16 | HG01074.hp1 HG01884.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-285+2426_-285+243 others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110479 | |||||
| chr6:7110479
|
G | GGTGTGTG others(7): Show |
49 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(46): Show | 49 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.-285+2424_-285+243 others(18): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110479 | |||||
| chr6:7110479
|
G | GGTGTGTG others(9): Show |
7 | a0002c0004t0026g0261a0004c0006t0006g0257a0004c0008t0001g0292others(4): Show | 7 | HG00140.hp1 HG00741.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-285+2422_-285+243 others(20): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110479 | |||||
| chr6:7110479
|
G | GGTGTGTG others(11): Show |
2 | a0030c0047t0027g0209a0034c0039t0026g0249 | 2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-285+2420_-285+243 others(22): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110479 | |||||
| chr6:7110494
|
G | GTGTGTGT others(7): Show |
3 | a0001c0001t0017g0180a0005c0003t0047g0178a0016c0025t0018g0179 | 3 | HG02258.hp2 HG02280.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-285+2437_-285+243 others(18): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7110494 | |||||
| chr6:7110780
|
T | C | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-285+2720T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7110780 | ||||||
| chr6:7110897
|
A | G | 1 | a0005c0003t0056g0207 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-285+2837A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7110897 | ||||||
| chr6:7110983
|
A | G | 8 | a0001c0001t0082g0235a0005c0003t0033g0230a0005c0003t0033g0232others(5): Show | 8 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+2923A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7110983 | ||||||
| chr6:7111096
|
C | G | 8 | a0001c0001t0082g0235a0005c0003t0033g0230a0005c0003t0033g0232others(5): Show | 8 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+3036C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7111096 | ||||||
| chr6:7111431
|
T | C | 8 | a0001c0001t0082g0235a0005c0003t0033g0230a0005c0003t0033g0232others(5): Show | 8 | HG01109.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+3371T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7111431 | ||||||
| chr6:7111818
|
A | G | 39 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0017g0180others(36): Show | 39 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.-285+3758A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7111818 | ||||||
| chr6:7111990
|
T | C | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-285+3930T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7111990 | ||||||
| chr6:7112275
|
A | C | 8 | a0001c0001t0002g0170a0001c0001t0017g0166a0001c0017t0001g0168others(5): Show | 8 | HG00438.hp2 HG02080.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+4215A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7112275 | ||||||
| chr6:7112489
|
A | G | 10 | a0001c0001t0082g0235a0003c0002t0023g0175a0003c0032t0057g0176others(7): Show | 10 | HG02630.hp1 HG02647.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-285+4429A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7112489 | ||||||
| chr6:7112517
|
G | A | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-285+4457G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7112517 | ||||||
| chr6:7112558
|
G | C | 4 | a0001c0001t0082g0235a0012c0013t0080g0234a0014c0020t0034g0236others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-285+4498G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7112558 | ||||||
| chr6:7112586
|
A | G | 56 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.-285+4526A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7112586 | ||||||
| chr6:7112791
|
CTGTCGGC others(14): Show |
C | 13 | a0004c0052t0020g0005a0007c0009t0005g0006a0007c0009t0005g0007others(10): Show | 13 | HG00438.hp1 HG00558.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-285+4734_-285+475 others(25): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7112791 | |||||
| chr6:7112807
|
C | T | 4 | a0002c0004t0011g0163a0002c0007t0011g0160a0002c0007t0011g0161others(1): Show | 4 | HG02040.hp1 HG02129.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-285+4747C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7112807 | ||||||
| chr6:7112910
|
G | A | 2 | a0004c0006t0058g0048a0004c0050t0006g0049 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-285+4850G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7112910 | ||||||
| chr6:7112991
|
T | G | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-285+4931T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7112991 | ||||||
| chr6:7113027
|
G | A | 1 | a0005c0003t0028g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-285+4967G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7113027 | ||||||
| chr6:7113135
|
CGGGGACT | C | 66 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.-285+5086_-285+509 others(11): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7113135 | |||||
| chr6:7113368
|
G | A | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-285+5308G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7113368 | ||||||
| chr6:7113524
|
A | T | 1 | a0008c0010t0001g0288 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-285+5464A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7113524 | ||||||
| chr6:7113542
|
G | A | 1 | a0005c0014t0023g0050 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-285+5482G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7113542 | ||||||
| chr6:7113612
|
A | G | 2 | a0009c0018t0003g0158a0009c0018t0008g0032 | 2 | NA18939.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-285+5552A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7113612 | ||||||
| chr6:7113718
|
T | C | 2 | a0007c0022t0019g0183a0007c0022t0019g0184 | 2 | HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-285+5658T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7113718 | ||||||
| chr6:7113816
|
C | G | 1 | a0005c0003t0056g0207 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-285+5756C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7113816 | ||||||
| chr6:7114063
|
A | G | 4 | a0003c0012t0013g0239a0005c0003t0013g0159a0005c0003t0013g0240others(1): Show | 4 | HG01884.hp2 HG02486.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-285+6003A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114063 | ||||||
| chr6:7114128
|
TGGTTCAC others(3): Show |
T | 1 | a0001c0001t0002g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-285+6072_-285+608 others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7114128 | |||||
| chr6:7114205
|
T | C | 44 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0017g0180others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.-285+6145T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114205 | ||||||
| chr6:7114254
|
T | G | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-285+6194T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114254 | ||||||
| chr6:7114279
|
G | A | 1 | a0002c0007t0011g0160 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-285+6219G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114279 | ||||||
| chr6:7114280
|
C | T | 1 | a0005c0059t0013g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-285+6220C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114280 | ||||||
| chr6:7114468
|
T | TG | 76 | a0001c0001t0001g0017a0001c0001t0001g0033a0001c0001t0001g0040others(73): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.-285+6419dupG | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7114468 | |||||
| chr6:7114468
|
T | TGG | 32 | a0001c0001t0001g0043a0001c0001t0017g0180a0001c0001t0035g0034others(29): Show | 32 | HG00741.hp1 HG01109.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.-285+6418_-285+641 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7114468 | |||||
| chr6:7114468
|
TG | T | 67 | a0001c0001t0001g0054a0001c0001t0001g0259a0001c0001t0002g0248others(64): Show | 67 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.-285+6419delG | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7114468 | |||||
| chr6:7114544
|
G | A | 1 | a0010c0035t0065g0208 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-285+6484G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114544 | ||||||
| chr6:7114609
|
A | G | 269 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-285+6549A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114609 | ||||||
| chr6:7114634
|
A | G | 1 | a0002c0004t0072g0226 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-285+6574A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114634 | ||||||
| chr6:7114651
|
G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0126a0002c0046t0003g0078 | 3 | HG00621.hp2 NA18946.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-285+6591G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114651 | ||||||
| chr6:7114811
|
C | T | 2 | a0002c0004t0008g0212a0002c0004t0016g0211 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-285+6751C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114811 | ||||||
| chr6:7114883
|
G | C | 269 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(266): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-285+6823G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114883 | ||||||
| chr6:7114918
|
A | G | 9 | a0001c0001t0017g0214a0007c0011t0014g0199a0007c0011t0014g0200others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-285+6858A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114918 | ||||||
| chr6:7114963
|
T | G | 2 | a0001c0001t0001g0054a0011c0041t0067g0055 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-285+6903T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7114963 | ||||||
| chr6:7114990
|
C | CT | 127 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(124): Show | 127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.-285+6943dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7114990 | |||||
| chr6:7115105
|
C | T | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-285+7045C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7115105 | ||||||
| chr6:7115267
|
C | T | 1 | a0022c0048t0006g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-285+7207C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7115267 | ||||||
| chr6:7115300
|
T | A | 127 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(124): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-285+7240T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7115300 | ||||||
| chr6:7115694
|
G | C | 122 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-285+7634G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7115694 | ||||||
| chr6:7115741
|
A | C | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-285+7681A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7115741 | ||||||
| chr6:7115755
|
T | G | 1 | a0004c0008t0037g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-285+7695T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7115755 | ||||||
| chr6:7115861
|
G | C | 1 | a0039c0070t0009g0016 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-285+7801G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7115861 | ||||||
| chr6:7115862
|
C | G | 1 | a0039c0070t0009g0016 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-285+7802C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7115862 | ||||||
| chr6:7115980
|
C | G | 2 | a0001c0001t0001g0224a0002c0004t0003g0225 | 2 | HG02148.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-285+7920C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7115980 | ||||||
| chr6:7116412
|
G | A | 9 | a0001c0001t0017g0214a0007c0011t0014g0199a0007c0011t0014g0200others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-285+8352G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7116412 | ||||||
| chr6:7116698
|
G | A | 13 | a0004c0052t0020g0005a0007c0009t0005g0006a0007c0009t0005g0007others(10): Show | 13 | HG00438.hp1 HG00558.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-285+8638G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7116698 | ||||||
| chr6:7116829
|
G | A | 5 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-285+8769G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7116829 | ||||||
| chr6:7117220
|
A | T | 1 | a0004c0006t0031g0079 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-285+9160A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117220 | ||||||
| chr6:7117264
|
A | G | 6 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+9204A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117264 | ||||||
| chr6:7117388
|
G | GT | 44 | a0001c0001t0001g0023a0001c0001t0001g0054a0001c0001t0001g0109others(41): Show | 44 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.-285+9365dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTT | 26 | a0001c0001t0001g0040a0001c0001t0002g0028a0001c0001t0010g0147others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-285+9364_-285+936 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTT | 12 | a0001c0001t0001g0017a0001c0001t0002g0170a0002c0004t0003g0150others(9): Show | 12 | HG01261.hp1 HG01928.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.-285+9363_-285+936 others(7): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0122a0004c0006t0021g0051 | 2 | HG03516.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-285+9356_-285+936 others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTTTTTT others(4): Show |
2 | a0007c0009t0005g0006a0007c0009t0005g0007 | 2 | HG01192.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-285+9355_-285+936 others(15): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTTTTTT others(5): Show |
2 | a0007c0009t0005g0008a0011c0015t0005g0013 | 2 | HG02735.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.-285+9354_-285+936 others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTTTTTT others(6): Show |
1 | a0007c0009t0005g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-285+9353_-285+936 others(17): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTTTTTT others(7): Show |
1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-285+9352_-285+936 others(18): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTTTTTT others(11): Show |
1 | a0007c0009t0053g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-285+9348_-285+936 others(22): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTTTTTT others(17): Show |
1 | a0011c0015t0005g0010 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-285+9342_-285+936 others(28): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTTTTTT others(19): Show |
1 | a0001c0001t0001g0155 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-285+9340_-285+936 others(30): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
G | GTTTTTTT others(21): Show |
1 | a0010c0021t0003g0011 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-285+9338_-285+936 others(32): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GT | G | 26 | a0001c0001t0001g0125a0001c0001t0002g0069a0001c0001t0017g0214others(23): Show | 26 | HG01071.hp1 HG01943.hp1 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.-285+9365delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTT | G | 6 | a0003c0002t0002g0063a0003c0002t0029g0062a0004c0050t0006g0049others(3): Show | 6 | HG01109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-285+9364_-285+936 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTT | G | 7 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(4): Show | 7 | HG01891.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-285+9363_-285+936 others(7): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTTTTTT others(3): Show |
G | 1 | a0002c0004t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-285+9356_-285+936 others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTTTTTT others(4): Show |
G | 1 | a0007c0009t0040g0012 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-285+9355_-285+936 others(15): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTTTTTT others(5): Show |
G | 1 | a0007c0009t0039g0002 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-285+9354_-285+936 others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTTTTTT others(6): Show |
G | 8 | a0001c0001t0001g0043a0002c0004t0015g0044a0003c0002t0003g0229others(5): Show | 8 | HG00140.hp2 HG01978.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+9353_-285+936 others(17): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTTTTTT others(7): Show |
G | 75 | a0001c0001t0001g0033a0001c0001t0001g0253a0001c0001t0001g0255others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-285+9352_-285+936 others(18): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTTTTTT others(8): Show |
G | 14 | a0002c0004t0026g0261a0003c0002t0010g0251a0003c0012t0013g0239others(11): Show | 14 | HG00140.hp1 HG00741.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-285+9351_-285+936 others(19): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTTTTTT others(9): Show |
G | 2 | a0006c0005t0004g0085a0041c0072t0078g0242 | 2 | HG02451.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.-285+9350_-285+936 others(20): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTTTTTT others(10): Show |
G | 1 | a0006c0005t0004g0084 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-285+9349_-285+936 others(21): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117388
|
GTTTTTTT others(13): Show |
G | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-285+9346_-285+936 others(24): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7117388 | |||||
| chr6:7117395
|
T | G | 6 | a0001c0001t0016g0083a0002c0004t0003g0082a0002c0004t0003g0130others(3): Show | 6 | HG02080.hp1 HG02129.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+9335T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117395 | ||||||
| chr6:7117396
|
T | G | 1 | a0014c0020t0076g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-285+9336T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117396 | ||||||
| chr6:7117398
|
T | G | 5 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(2): Show | 5 | HG02630.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-285+9338T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117398 | ||||||
| chr6:7117466
|
A | G | 2 | a0004c0006t0058g0048a0004c0050t0006g0049 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-285+9406A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117466 | ||||||
| chr6:7117472
|
G | A | 1 | a0004c0006t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-285+9412G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117472 | ||||||
| chr6:7117485
|
A | G | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-285+9425A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117485 | ||||||
| chr6:7117512
|
G | T | 1 | a0004c0006t0007g0138 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-285+9452G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117512 | ||||||
| chr6:7117601
|
G | T | 26 | a0002c0007t0007g0116a0002c0007t0028g0121a0002c0007t0069g0022others(23): Show | 26 | HG00558.hp2 HG01099.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.-285+9541G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117601 | ||||||
| chr6:7117825
|
C | T | 6 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+9765C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7117825 | ||||||
| chr6:7118068
|
G | A | 264 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(261): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-285+10008G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7118068 | ||||||
| chr6:7118261
|
C | G | 1 | a0001c0001t0016g0083 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-285+10201C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7118261 | ||||||
| chr6:7118346
|
C | A | 1 | a0007c0009t0053g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-285+10286C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7118346 | ||||||
| chr6:7118368
|
G | A | 6 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+10308G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7118368 | ||||||
| chr6:7118497
|
A | G | 1 | a0003c0002t0002g0074 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-285+10437A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7118497 | ||||||
| chr6:7118549
|
T | A | 1 | a0015c0024t0055g0025 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-285+10489T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7118549 | ||||||
| chr6:7118723
|
C | A | 1 | a0001c0001t0002g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-285+10663C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7118723 | ||||||
| chr6:7118757
|
A | G | 63 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(60): Show | 63 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-285+10697A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7118757 | ||||||
| chr6:7118801
|
A | AT | 6 | a0001c0001t0002g0069a0002c0004t0003g0052a0003c0002t0002g0020others(3): Show | 6 | HG00423.hp2 HG00735.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-285+10771dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7118801 | |||||
| chr6:7118801
|
AT | A | 22 | a0001c0001t0001g0224a0002c0004t0003g0082a0002c0004t0008g0212others(19): Show | 22 | HG00639.hp2 HG00738.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.-285+10771delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7118801 | |||||
| chr6:7118801
|
ATT | A | 122 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(119): Show | 122 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-285+10770_-285+10 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7118801 | |||||
| chr6:7118801
|
ATTT | A | 72 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(69): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.-285+10769_-285+10 others(9): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7118801 | |||||
| chr6:7118801
|
ATTTT | A | 39 | a0001c0001t0017g0180a0001c0001t0035g0034a0001c0001t0042g0187others(36): Show | 39 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-285+10768_-285+10 others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7118801 | |||||
| chr6:7118901
|
G | A | 58 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-285+10841G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7118901 | ||||||
| chr6:7119002
|
A | G | 2 | a0002c0004t0008g0212a0002c0004t0016g0211 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-285+10942A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7119002 | ||||||
| chr6:7119273
|
C | A | 6 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+11213C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7119273 | ||||||
| chr6:7119288
|
T | C | 1 | a0011c0015t0019g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-285+11228T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7119288 | ||||||
| chr6:7119302
|
A | G | 1 | a0011c0015t0019g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-285+11242A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7119302 | ||||||
| chr6:7119347
|
C | G | 1 | a0007c0009t0005g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-285+11287C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7119347 | ||||||
| chr6:7119469
|
G | A | 1 | a0006c0016t0009g0024 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-285+11409G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7119469 | ||||||
| chr6:7120051
|
G | A | 1 | a0004c0008t0002g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-285+11991G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120051 | ||||||
| chr6:7120110
|
C | G | 4 | a0004c0006t0007g0281a0013c0019t0010g0256a0013c0019t0049g0262others(1): Show | 4 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-285+12050C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120110 | ||||||
| chr6:7120138
|
G | A | 1 | a0022c0048t0006g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-285+12078G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120138 | ||||||
| chr6:7120217
|
G | A | 6 | a0001c0001t0017g0214a0007c0011t0014g0199a0007c0011t0014g0200others(3): Show | 6 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+12157G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120217 | ||||||
| chr6:7120224
|
G | A | 61 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(58): Show | 61 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-285+12164G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120224 | ||||||
| chr6:7120279
|
C | T | 1 | a0019c0049t0002g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-285+12219C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120279 | ||||||
| chr6:7120318
|
G | A | 2 | a0005c0003t0020g0091a0005c0003t0020g0137 | 2 | NA18982.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-285+12258G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120318 | ||||||
| chr6:7120416
|
T | A | 6 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+12356T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120416 | ||||||
| chr6:7120675
|
AT | A | 116 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(113): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-285+12629delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7120675 | |||||
| chr6:7120693
|
A | G | 87 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(84): Show | 87 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.-285+12633A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120693 | ||||||
| chr6:7120698
|
G | A | 1 | a0018c0071t0002g0167 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-285+12638G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120698 | ||||||
| chr6:7120705
|
T | A | 1 | a0004c0008t0002g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-285+12645T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120705 | ||||||
| chr6:7120723
|
T | C | 1 | a0002c0004t0003g0118 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-285+12663T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120723 | ||||||
| chr6:7120728
|
C | A | 2 | a0007c0022t0019g0183a0007c0022t0019g0184 | 2 | HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-285+12668C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120728 | ||||||
| chr6:7120737
|
C | G | 4 | a0001c0001t0082g0235a0007c0022t0019g0183a0007c0022t0019g0184others(1): Show | 4 | HG01361.hp1 HG02572.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-285+12677C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120737 | ||||||
| chr6:7120813
|
A | AT | 54 | a0001c0001t0001g0043a0001c0001t0001g0073a0001c0001t0001g0098others(51): Show | 54 | HG00423.hp1 HG00438.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.-285+12777dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7120813 | |||||
| chr6:7120813
|
AT | A | 13 | a0001c0001t0082g0235a0003c0045t0002g0070a0006c0005t0043g0100others(10): Show | 13 | HG01123.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-285+12777delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7120813 | |||||
| chr6:7120882
|
C | T | 2 | a0016c0025t0018g0179a0017c0027t0077g0053 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-285+12822C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7120882 | ||||||
| chr6:7121371
|
C | A | 1 | a0003c0002t0002g0076 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-285+13311C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7121371 | ||||||
| chr6:7121839
|
C | T | 6 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+13779C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7121839 | ||||||
| chr6:7122059
|
C | T | 34 | a0001c0001t0017g0180a0001c0001t0035g0034a0001c0001t0042g0187others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.-285+13999C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7122059 | ||||||
| chr6:7122115
|
C | T | 6 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+14055C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7122115 | ||||||
| chr6:7122133
|
C | T | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-285+14073C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7122133 | ||||||
| chr6:7122382
|
C | T | 1 | a0002c0004t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-285+14322C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7122382 | ||||||
| chr6:7122383
|
A | G | 3 | a0003c0002t0023g0175a0005c0003t0004g0174a0014c0020t0076g0177 | 3 | HG03195.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-285+14323A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7122383 | ||||||
| chr6:7122414
|
C | T | 8 | a0001c0001t0017g0214a0007c0011t0014g0199a0007c0011t0014g0200others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+14354C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7122414 | ||||||
| chr6:7122703
|
G | A | 34 | a0001c0001t0017g0180a0001c0001t0035g0034a0001c0001t0042g0187others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.-285+14643G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7122703 | ||||||
| chr6:7122927
|
C | G | 4 | a0003c0012t0013g0239a0005c0003t0013g0159a0005c0003t0013g0240others(1): Show | 4 | HG01884.hp2 HG02486.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-285+14867C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7122927 | ||||||
| chr6:7123102
|
C | T | 2 | a0009c0018t0003g0158a0009c0018t0008g0032 | 2 | NA18939.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-285+15042C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123102 | ||||||
| chr6:7123181
|
A | G | 1 | a0005c0003t0050g0139 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-285+15121A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123181 | ||||||
| chr6:7123214
|
A | G | 1 | a0007c0022t0019g0183 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-285+15154A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123214 | ||||||
| chr6:7123226
|
C | T | 1 | a0005c0003t0046g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-285+15166C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123226 | ||||||
| chr6:7123227
|
G | A | 1 | a0031c0062t0004g0107 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-285+15167G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123227 | ||||||
| chr6:7123243
|
C | T | 1 | a0002c0004t0003g0148 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-285+15183C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123243 | ||||||
| chr6:7123302
|
C | T | 3 | a0009c0018t0003g0077a0009c0018t0003g0158a0009c0018t0008g0032 | 3 | NA18939.hp2 NA18979.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-285+15242C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123302 | ||||||
| chr6:7123331
|
T | C | 13 | a0004c0052t0020g0005a0007c0009t0005g0006a0007c0009t0005g0007others(10): Show | 13 | HG00438.hp1 HG00558.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-285+15271T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123331 | ||||||
| chr6:7123408
|
C | T | 3 | a0005c0003t0012g0172a0005c0003t0012g0173a0041c0072t0078g0242 | 3 | HG02451.hp1 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-285+15348C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123408 | ||||||
| chr6:7123422
|
G | A | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-285+15362G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123422 | ||||||
| chr6:7123610
|
C | CT | 102 | a0001c0001t0001g0097a0001c0001t0001g0253a0001c0001t0001g0255others(99): Show | 102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-285+15568dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7123610 | |||||
| chr6:7123756
|
G | A | 3 | a0005c0003t0012g0260a0005c0003t0018g0001a0005c0003t0046g0258 | 3 | HG01243.hp1 HG02818.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-285+15696G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123756 | ||||||
| chr6:7123908
|
G | A | 2 | a0002c0004t0008g0216a0017c0027t0077g0053 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-285+15848G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123908 | ||||||
| chr6:7123976
|
C | G | 1 | a0007c0011t0052g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-285+15916C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7123976 | ||||||
| chr6:7124058
|
A | T | 2 | a0001c0001t0001g0073a0040c0069t0002g0123 | 2 | NA18987.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.-285+15998A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124058 | ||||||
| chr6:7124277
|
T | C | 2 | a0001c0001t0017g0180a0005c0003t0047g0178 | 2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-285+16217T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124277 | ||||||
| chr6:7124307
|
G | A | 2 | a0002c0007t0007g0218a0002c0007t0063g0217 | 2 | HG02155.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-285+16247G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124307 | ||||||
| chr6:7124449
|
C | T | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-285+16389C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124449 | ||||||
| chr6:7124472
|
G | T | 2 | a0001c0001t0082g0235a0012c0013t0027g0228 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-285+16412G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124472 | ||||||
| chr6:7124593
|
A | G | 1 | a0006c0005t0009g0090 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-285+16533A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124593 | ||||||
| chr6:7124638
|
T | G | 3 | a0004c0052t0020g0005a0007c0009t0053g0014a0010c0036t0002g0004 | 3 | HG00438.hp1 NA18612.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-285+16578T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124638 | ||||||
| chr6:7124677
|
A | T | 1 | a0005c0003t0050g0139 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-285+16617A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124677 | ||||||
| chr6:7124706
|
A | G | 2 | a0002c0004t0022g0027a0002c0004t0022g0136 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-285+16646A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124706 | ||||||
| chr6:7124998
|
T | C | 9 | a0001c0001t0017g0214a0003c0002t0074g0190a0003c0012t0004g0219others(6): Show | 9 | HG02280.hp1 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-285+16938T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7124998 | ||||||
| chr6:7125045
|
G | C | 2 | a0007c0022t0019g0183a0007c0022t0019g0184 | 2 | HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-285+16985G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7125045 | ||||||
| chr6:7125138
|
G | T | 6 | a0001c0001t0017g0214a0007c0011t0014g0199a0007c0011t0014g0201others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-285+17078G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7125138 | ||||||
| chr6:7125296
|
A | G | 6 | a0003c0002t0010g0251a0008c0010t0001g0277a0008c0010t0001g0278others(3): Show | 6 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-285+17236A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7125296 | ||||||
| chr6:7125476
|
T | C | 82 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-285+17416T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7125476 | ||||||
| chr6:7125672
|
A | G | 7 | a0001c0001t0017g0214a0007c0011t0014g0199a0007c0011t0014g0201others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-285+17612A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7125672 | ||||||
| chr6:7125736
|
A | T | 1 | a0002c0004t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-285+17676A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7125736 | ||||||
| chr6:7125799
|
G | T | 3 | a0001c0001t0017g0214a0007c0011t0052g0213a0010c0035t0065g0208 | 3 | HG02280.hp1 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-285+17739G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7125799 | ||||||
| chr6:7125987
|
T | TTTTG | 21 | a0001c0001t0042g0187a0002c0004t0026g0261a0003c0002t0023g0175others(18): Show | 21 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-285+17955_-285+17 others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7125987 | |||||
| chr6:7125987
|
T | TTTTGTTT others(1): Show |
46 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(43): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.-285+17951_-285+17 others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7125987 | |||||
| chr6:7125987
|
T | TTTTGTTT others(5): Show |
3 | a0001c0001t0001g0283a0001c0001t0002g0282a0001c0001t0016g0280 | 3 | HG01175.hp1 HG01496.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-285+17947_-285+17 others(18): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7125987 | |||||
| chr6:7125987
|
TTTTG | T | 5 | a0007c0009t0053g0014a0012c0013t0080g0234a0014c0020t0034g0236others(2): Show | 5 | HG02895.hp1 HG02897.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.-285+17955_-285+17 others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7125987 | |||||
| chr6:7125991
|
G | T | 11 | a0002c0004t0015g0044a0002c0004t0015g0203a0002c0004t0015g0204others(8): Show | 11 | HG02109.hp2 HG02280.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-285+17931G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7125991 | ||||||
| chr6:7126057
|
A | C | 4 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237others(1): Show | 4 | HG02895.hp1 HG02897.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-285+17997A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126057 | ||||||
| chr6:7126087
|
C | T | 1 | a0011c0015t0019g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-285+18027C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126087 | ||||||
| chr6:7126091
|
T | C | 5 | a0002c0004t0015g0044a0002c0004t0015g0203a0002c0004t0015g0204others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-285+18031T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126091 | ||||||
| chr6:7126146
|
T | C | 1 | a0007c0022t0019g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-285+18086T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126146 | ||||||
| chr6:7126147
|
G | A | 1 | a0007c0022t0019g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-285+18087G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126147 | ||||||
| chr6:7126149
|
G | A | 1 | a0004c0006t0021g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-285+18089G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126149 | ||||||
| chr6:7126149
|
G | C | 1 | a0004c0006t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-285+18089G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126149 | ||||||
| chr6:7126150
|
C | A | 1 | a0004c0006t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-285+18090C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126150 | ||||||
| chr6:7126151
|
A | G | 1 | a0004c0006t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-285+18091A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126151 | ||||||
| chr6:7126189
|
G | A | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-285+18129G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126189 | ||||||
| chr6:7126191
|
T | A | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-285+18131T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126191 | ||||||
| chr6:7126201
|
T | C | 8 | a0001c0001t0082g0235a0004c0008t0001g0265a0004c0008t0001g0266others(5): Show | 8 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+18141T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126201 | ||||||
| chr6:7126280
|
G | A | 1 | a0008c0010t0001g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-285+18220G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126280 | ||||||
| chr6:7126283
|
A | C | 1 | a0020c0051t0006g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-285+18223A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126283 | ||||||
| chr6:7126289
|
T | C | 180 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(177): Show | 180 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.-285+18229T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126289 | ||||||
| chr6:7126289
|
T | TGCGCCCG others(262): Show |
1 | a0020c0051t0006g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-285+18488_-285+18 others(275): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7126289 | |||||
| chr6:7126290
|
G | A | 2 | a0002c0004t0003g0150a0007c0009t0005g0007 | 2 | HG01192.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.-285+18230G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126290 | ||||||
| chr6:7126291
|
C | T | 1 | a0002c0004t0003g0150 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-285+18231C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126291 | ||||||
| chr6:7126292
|
G | A | 3 | a0005c0003t0033g0230a0005c0003t0033g0232a0029c0053t0062g0057 | 3 | HG02818.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-285+18232G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126292 | ||||||
| chr6:7126293
|
C | T | 1 | a0007c0009t0005g0007 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-285+18233C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126293 | ||||||
| chr6:7126301
|
C | T | 9 | a0007c0009t0005g0006a0007c0009t0005g0008a0007c0009t0005g0009others(6): Show | 9 | HG00558.hp1 HG02135.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-285+18241C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126301 | ||||||
| chr6:7126313
|
G | A | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-285+18253G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126313 | ||||||
| chr6:7126317
|
C | T | 2 | a0003c0002t0002g0189a0003c0002t0029g0186 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-285+18257C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126317 | ||||||
| chr6:7126372
|
G | A | 1 | a0005c0003t0046g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-285+18312G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7126372 | ||||||
| chr6:7127031
|
A | C | 3 | a0004c0006t0058g0048a0004c0050t0006g0049a0026c0057t0014g0221 | 3 | HG02109.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-285+18971A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127031 | ||||||
| chr6:7127076
|
A | G | 1 | a0001c0001t0082g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-285+19016A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127076 | ||||||
| chr6:7127327
|
C | G | 1 | a0015c0066t0003g0276 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-285+19267C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127327 | ||||||
| chr6:7127354
|
A | C | 1 | a0036c0030t0045g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-285+19294A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127354 | ||||||
| chr6:7127451
|
C | T | 1 | a0004c0006t0018g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-285+19391C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127451 | ||||||
| chr6:7127583
|
A | G | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-285+19523A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127583 | ||||||
| chr6:7127754
|
A | G | 60 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-285+19694A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127754 | ||||||
| chr6:7127789
|
G | T | 2 | a0001c0001t0082g0235a0012c0013t0027g0228 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-285+19729G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127789 | ||||||
| chr6:7127841
|
C | T | 1 | a0005c0003t0004g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-285+19781C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127841 | ||||||
| chr6:7127843
|
A | G | 136 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-285+19783A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127843 | ||||||
| chr6:7127948
|
G | A | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-285+19888G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127948 | ||||||
| chr6:7127965
|
G | T | 60 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-285+19905G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7127965 | ||||||
| chr6:7128160
|
G | A | 12 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(9): Show | 12 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.-285+20100G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7128160 | ||||||
| chr6:7128662
|
A | G | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-285+20602A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7128662 | ||||||
| chr6:7128810
|
A | G | 2 | a0003c0002t0002g0189a0003c0002t0029g0186 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-285+20750A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7128810 | ||||||
| chr6:7128886
|
G | A | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-285+20826G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7128886 | ||||||
| chr6:7128901
|
G | A | 1 | a0004c0006t0024g0290 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-285+20841G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7128901 | ||||||
| chr6:7129199
|
C | T | 5 | a0002c0004t0015g0044a0002c0004t0015g0203a0002c0004t0015g0204others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-285+21139C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7129199 | ||||||
| chr6:7129330
|
A | G | 39 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0035g0034others(36): Show | 39 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.-285+21270A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7129330 | ||||||
| chr6:7129384
|
G | A | 13 | a0003c0002t0023g0175a0005c0003t0004g0174a0005c0003t0012g0172others(10): Show | 13 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.-285+21324G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7129384 | ||||||
| chr6:7129554
|
C | T | 2 | a0004c0006t0058g0048a0004c0050t0006g0049 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-285+21494C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7129554 | ||||||
| chr6:7129570
|
A | G | 1 | a0005c0059t0013g0157 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-285+21510A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7129570 | ||||||
| chr6:7129742
|
C | T | 1 | a0012c0013t0031g0222 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-285+21682C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7129742 | ||||||
| chr6:7129854
|
G | A | 2 | a0001c0001t0082g0235a0012c0013t0027g0228 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-285+21794G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7129854 | ||||||
| chr6:7129889
|
G | A | 1 | a0007c0011t0052g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-285+21829G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7129889 | ||||||
| chr6:7130062
|
C | T | 1 | a0007c0009t0005g0246 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-285+22002C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130062 | ||||||
| chr6:7130200
|
T | C | 2 | a0004c0006t0007g0241a0004c0006t0007g0245 | 2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-285+22140T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130200 | ||||||
| chr6:7130363
|
A | G | 138 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(135): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.-285+22303A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130363 | ||||||
| chr6:7130412
|
A | G | 6 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237others(3): Show | 6 | HG01109.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-285+22352A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130412 | ||||||
| chr6:7130512
|
T | C | 8 | a0001c0001t0001g0097a0002c0004t0003g0130a0003c0012t0011g0119others(5): Show | 8 | HG02040.hp2 HG02056.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-285+22452T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130512 | ||||||
| chr6:7130520
|
A | G | 1 | a0004c0006t0007g0138 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-285+22460A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130520 | ||||||
| chr6:7130642
|
A | G | 1 | a0002c0007t0028g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-285+22582A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130642 | ||||||
| chr6:7130726
|
T | C | 137 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.-285+22666T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130726 | ||||||
| chr6:7130836
|
C | G | 2 | a0001c0001t0082g0235a0012c0013t0027g0228 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-285+22776C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130836 | ||||||
| chr6:7130881
|
T | C | 290 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(287): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.-285+22821T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130881 | ||||||
| chr6:7130895
|
G | A | 47 | a0001c0001t0001g0097a0002c0004t0003g0130a0002c0007t0028g0121others(44): Show | 47 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.-285+22835G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130895 | ||||||
| chr6:7130909
|
C | T | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-285+22849C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130909 | ||||||
| chr6:7130929
|
C | CT | 26 | a0001c0001t0001g0283a0001c0001t0002g0248a0001c0001t0016g0280others(23): Show | 26 | HG00735.hp1 HG00741.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-285+22896dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7130929 | |||||
| chr6:7130929
|
CT | C | 139 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(136): Show | 139 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-285+22896delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7130929 | |||||
| chr6:7130929
|
CTT | C | 8 | a0001c0001t0001g0054a0007c0011t0014g0199a0007c0011t0014g0200others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-285+22895_-285+22 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7130929 | |||||
| chr6:7130959
|
G | T | 1 | a0015c0024t0055g0025 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-285+22899G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7130959 | ||||||
| chr6:7131061
|
C | T | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-285+23001C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7131061 | ||||||
| chr6:7131063
|
G | A | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-285+23003G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7131063 | ||||||
| chr6:7131129
|
G | A | 1 | a0002c0004t0026g0261 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-285+23069G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7131129 | ||||||
| chr6:7131203
|
G | A | 60 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-285+23143G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7131203 | ||||||
| chr6:7131227
|
A | G | 41 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0035g0034others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-285+23167A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7131227 | ||||||
| chr6:7131259
|
C | T | 1 | a0004c0008t0002g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-285+23199C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7131259 | ||||||
| chr6:7131291
|
A | G | 41 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0035g0034others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.-285+23231A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7131291 | ||||||
| chr6:7131774
|
T | C | 4 | a0005c0003t0004g0220a0009c0026t0003g0060a0009c0026t0003g0088others(1): Show | 4 | HG02559.hp2 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-285+23714T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7131774 | ||||||
| chr6:7132062
|
T | G | 12 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(9): Show | 12 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.-285+24002T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7132062 | ||||||
| chr6:7132110
|
A | G | 1 | a0002c0004t0022g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-285+24050A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7132110 | ||||||
| chr6:7132136
|
C | T | 2 | a0005c0003t0004g0220a0024c0061t0015g0223 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-285+24076C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7132136 | ||||||
| chr6:7132307
|
G | A | 2 | a0003c0032t0057g0176a0005c0003t0004g0220 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-285+24247G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7132307 | ||||||
| chr6:7132316
|
A | G | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-285+24256A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7132316 | ||||||
| chr6:7132369
|
C | CT | 60 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(57): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-285+24310dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7132369 | |||||
| chr6:7132542
|
G | A | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-285+24482G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7132542 | ||||||
| chr6:7132603
|
T | G | 1 | a0040c0069t0002g0123 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-285+24543T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7132603 | ||||||
| chr6:7132794
|
G | T | 2 | a0004c0006t0058g0048a0004c0050t0006g0049 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-285+24734G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7132794 | ||||||
| chr6:7132825
|
GTGAC | G | 81 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(78): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-285+24768_-285+24 others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7132825 | |||||
| chr6:7133005
|
A | G | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-285+24945A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7133005 | ||||||
| chr6:7133209
|
A | C | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-285+25149A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7133209 | ||||||
| chr6:7133476
|
A | G | 30 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(27): Show | 30 | HG00621.hp2 HG01934.hp2 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.-285+25416A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7133476 | ||||||
| chr6:7133558
|
A | T | 2 | a0004c0006t0006g0072a0027c0055t0002g0068 | 2 | HG00642.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-285+25498A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7133558 | ||||||
| chr6:7133605
|
A | G | 3 | a0005c0003t0033g0230a0005c0003t0033g0232a0005c0003t0079g0231 | 3 | HG02970.hp2 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-285+25545A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7133605 | ||||||
| chr6:7133720
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0017g0214 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-285+25660A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7133720 | ||||||
| chr6:7133969
|
A | G | 4 | a0004c0008t0001g0265a0004c0008t0001g0266a0004c0008t0001g0267others(1): Show | 4 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.-285+25909A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7133969 | ||||||
| chr6:7134061
|
T | C | 1 | a0002c0004t0003g0150 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-285+26001T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7134061 | ||||||
| chr6:7134093
|
G | T | 1 | a0014c0020t0076g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-285+26033G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7134093 | ||||||
| chr6:7134168
|
T | C | 134 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(131): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-285+26108T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7134168 | ||||||
| chr6:7134635
|
A | T | 1 | a0040c0069t0002g0123 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-285+26575A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7134635 | ||||||
| chr6:7134856
|
A | T | 3 | a0004c0006t0006g0099a0010c0028t0006g0019a0015c0024t0006g0153 | 3 | HG01433.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-285+26796A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7134856 | ||||||
| chr6:7134914
|
C | G | 1 | a0005c0003t0050g0139 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-285+26854C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7134914 | ||||||
| chr6:7135001
|
A | G | 1 | a0004c0006t0021g0051 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-285+26941A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7135001 | ||||||
| chr6:7135289
|
C | T | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-285+27229C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7135289 | ||||||
| chr6:7135335
|
T | C | 3 | a0005c0003t0033g0230a0005c0003t0033g0232a0005c0003t0079g0231 | 3 | HG02970.hp2 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-285+27275T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7135335 | ||||||
| chr6:7135464
|
T | C | 1 | a0023c0067t0002g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-285+27404T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7135464 | ||||||
| chr6:7136033
|
C | T | 2 | a0030c0047t0027g0209a0035c0033t0081g0233 | 2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-285+27973C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7136033 | ||||||
| chr6:7136203
|
A | C | 3 | a0005c0003t0033g0230a0005c0003t0033g0232a0005c0003t0079g0231 | 3 | HG02970.hp2 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-285+28143A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7136203 | ||||||
| chr6:7136435
|
T | C | 7 | a0005c0003t0009g0101a0006c0005t0009g0090a0006c0005t0009g0133others(4): Show | 7 | NA18941.hp1 NA18974.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.-285+28375T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7136435 | ||||||
| chr6:7136489
|
C | T | 1 | a0010c0035t0065g0208 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-285+28429C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7136489 | ||||||
| chr6:7136539
|
A | G | 136 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-285+28479A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7136539 | ||||||
| chr6:7136821
|
G | T | 1 | a0005c0003t0046g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-285+28761G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7136821 | ||||||
| chr6:7137130
|
T | C | 133 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0253others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-285+29070T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7137130 | ||||||
| chr6:7137301
|
G | C | 1 | a0039c0070t0009g0016 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-285+29241G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7137301 | ||||||
| chr6:7137388
|
G | C | 12 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(9): Show | 12 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.-285+29328G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7137388 | ||||||
| chr6:7137525
|
C | A | 1 | a0006c0016t0009g0115 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-285+29465C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7137525 | ||||||
| chr6:7137535
|
G | A | 1 | a0004c0008t0002g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-285+29475G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7137535 | ||||||
| chr6:7137563
|
T | C | 1 | a0006c0005t0043g0100 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-285+29503T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7137563 | ||||||
| chr6:7137725
|
C | G | 1 | a0006c0005t0004g0104 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-285+29665C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7137725 | ||||||
| chr6:7137802
|
C | T | 1 | a0003c0002t0002g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-285+29742C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7137802 | ||||||
| chr6:7137985
|
C | T | 14 | a0001c0001t0035g0034a0001c0001t0042g0187a0003c0002t0008g0128others(11): Show | 14 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-285+29925C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7137985 | ||||||
| chr6:7138061
|
C | G | 1 | a0003c0002t0010g0067 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-285+30001C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7138061 | ||||||
| chr6:7138093
|
C | T | 2 | a0003c0002t0002g0189a0003c0002t0029g0186 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-285+30033C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7138093 | ||||||
| chr6:7138140
|
A | T | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-285+30080A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7138140 | ||||||
| chr6:7138520
|
A | G | 1 | a0033c0038t0005g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-285+30460A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7138520 | ||||||
| chr6:7138692
|
G | A | 1 | a0001c0001t0002g0268 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-285+30632G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7138692 | ||||||
| chr6:7138792
|
T | G | 1 | a0004c0006t0007g0138 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-285+30732T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7138792 | ||||||
| chr6:7138794
|
T | C | 1 | a0039c0070t0009g0016 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-285+30734T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7138794 | ||||||
| chr6:7138831
|
C | T | 130 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-285+30771C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7138831 | ||||||
| chr6:7138927
|
CT | C | 130 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.-285+30869delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7138927 | |||||
| chr6:7139021
|
G | C | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-285+30961G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7139021 | ||||||
| chr6:7139060
|
T | C | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-285+31000T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7139060 | ||||||
| chr6:7139568
|
T | G | 1 | a0003c0002t0071g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-285+31508T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7139568 | ||||||
| chr6:7139583
|
A | G | 88 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(85): Show | 88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-285+31523A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7139583 | ||||||
| chr6:7139583
|
A | T | 2 | a0030c0047t0027g0209a0035c0033t0081g0233 | 2 | HG01109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-285+31523A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7139583 | ||||||
| chr6:7139584
|
A | G | 1 | a0002c0004t0003g0148 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-285+31524A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7139584 | ||||||
| chr6:7139665
|
T | G | 1 | a0001c0001t0082g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-285+31605T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7139665 | ||||||
| chr6:7139722
|
G | A | 1 | a0007c0011t0052g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-285+31662G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7139722 | ||||||
| chr6:7140147
|
C | T | 4 | a0004c0006t0007g0281a0013c0019t0010g0256a0013c0019t0049g0262others(1): Show | 4 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-285+32087C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7140147 | ||||||
| chr6:7140153
|
G | A | 11 | a0005c0003t0012g0172a0005c0003t0012g0173a0007c0009t0005g0006others(8): Show | 11 | HG01074.hp2 HG01192.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-285+32093G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7140153 | ||||||
| chr6:7140237
|
G | T | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-285+32177G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7140237 | ||||||
| chr6:7140598
|
G | A | 87 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.-285+32538G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7140598 | ||||||
| chr6:7140690
|
A | G | 1 | a0002c0004t0022g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-285+32630A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7140690 | ||||||
| chr6:7140758
|
T | C | 2 | a0011c0041t0067g0055a0014c0020t0076g0177 | 2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-285+32698T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7140758 | ||||||
| chr6:7140861
|
G | A | 1 | a0002c0004t0022g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-285+32801G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7140861 | ||||||
| chr6:7140861
|
G | C | 1 | a0003c0034t0008g0031 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-285+32801G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7140861 | ||||||
| chr6:7140958
|
C | T | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-285+32898C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7140958 | ||||||
| chr6:7141167
|
C | T | 1 | a0005c0003t0004g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-285+33107C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141167 | ||||||
| chr6:7141171
|
G | T | 2 | a0004c0008t0003g0243a0004c0008t0003g0244 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-285+33111G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141171 | ||||||
| chr6:7141206
|
C | CGCCGATT others(19): Show |
4 | a0002c0046t0003g0078a0006c0005t0004g0084a0006c0005t0004g0085others(1): Show | 4 | NA18946.hp1 NA18946.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.-285+33151_-285+33 others(32): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7141206 | |||||
| chr6:7141255
|
G | A | 34 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(31): Show | 34 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-285+33195G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141255 | ||||||
| chr6:7141395
|
A | G | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-285+33335A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141395 | ||||||
| chr6:7141396
|
A | G | 1 | a0019c0049t0002g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-285+33336A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141396 | ||||||
| chr6:7141422
|
C | T | 4 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(1): Show | 4 | HG02258.hp1 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-285+33362C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141422 | ||||||
| chr6:7141495
|
G | C | 1 | a0001c0001t0001g0043 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-285+33435G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141495 | ||||||
| chr6:7141566
|
T | G | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-285+33506T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141566 | ||||||
| chr6:7141640
|
A | G | 3 | a0005c0003t0033g0230a0005c0003t0033g0232a0005c0003t0079g0231 | 3 | HG02970.hp2 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-285+33580A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141640 | ||||||
| chr6:7141674
|
A | G | 1 | a0005c0003t0004g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-285+33614A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141674 | ||||||
| chr6:7141827
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-285+33767G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141827 | ||||||
| chr6:7141943
|
G | T | 1 | a0003c0002t0074g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-285+33883G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7141943 | ||||||
| chr6:7142034
|
A | G | 1 | a0005c0003t0054g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-285+33974A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142034 | ||||||
| chr6:7142049
|
T | TA | 18 | a0002c0004t0026g0261a0003c0002t0010g0251a0003c0012t0013g0239others(15): Show | 18 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-285+33997dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7142049 | |||||
| chr6:7142220
|
T | TA | 81 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(78): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.-285+34174dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7142220 | |||||
| chr6:7142255
|
G | A | 16 | a0002c0004t0026g0261a0003c0002t0010g0251a0003c0012t0013g0239others(13): Show | 16 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-285+34195G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142255 | ||||||
| chr6:7142369
|
C | T | 1 | a0001c0001t0042g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-284-34286C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142369 | ||||||
| chr6:7142523
|
G | A | 1 | a0005c0003t0004g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-284-34132G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142523 | ||||||
| chr6:7142589
|
G | T | 1 | a0022c0048t0006g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-284-34066G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142589 | ||||||
| chr6:7142629
|
G | A | 1 | a0011c0015t0019g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-284-34026G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142629 | ||||||
| chr6:7142658
|
G | A | 70 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-284-33997G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142658 | ||||||
| chr6:7142781
|
CT | C | 4 | a0002c0007t0028g0121a0002c0007t0069g0022a0004c0006t0007g0138others(1): Show | 4 | HG02155.hp1 HG02735.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-33873delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142781 | ||||||
| chr6:7142842
|
T | C | 50 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(47): Show | 50 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-284-33813T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142842 | ||||||
| chr6:7142938
|
T | C | 11 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(8): Show | 11 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-284-33717T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7142938 | ||||||
| chr6:7143091
|
A | T | 1 | a0002c0004t0003g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-284-33564A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7143091 | ||||||
| chr6:7143371
|
A | G | 42 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-284-33284A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7143371 | ||||||
| chr6:7143499
|
C | T | 4 | a0002c0004t0011g0163a0002c0007t0011g0160a0002c0007t0011g0161others(1): Show | 4 | HG02040.hp1 HG02129.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284-33156C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7143499 | ||||||
| chr6:7143626
|
C | A | 2 | a0003c0002t0003g0058a0003c0002t0003g0059 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-284-33029C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7143626 | ||||||
| chr6:7143693
|
A | G | 1 | a0006c0005t0009g0144 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-284-32962A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7143693 | ||||||
| chr6:7143795
|
C | G | 3 | a0003c0002t0023g0175a0005c0003t0004g0174a0014c0020t0076g0177 | 3 | HG03195.hp1 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-284-32860C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7143795 | ||||||
| chr6:7143851
|
C | CT | 37 | a0001c0001t0042g0187a0001c0001t0082g0235a0002c0004t0015g0044others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.-284-32785dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7143851 | |||||
| chr6:7143851
|
CT | C | 239 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(236): Show | 239 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.-284-32785delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7143851 | |||||
| chr6:7143855
|
T | C | 3 | a0002c0004t0003g0148a0002c0007t0063g0217a0034c0039t0026g0249 | 3 | HG02809.hp1 HG03688.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-284-32800T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7143855 | ||||||
| chr6:7143856
|
T | C | 15 | a0002c0004t0026g0261a0002c0007t0007g0218a0003c0002t0010g0251others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-284-32799T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7143856 | ||||||
| chr6:7143916
|
T | C | 1 | a0003c0002t0001g0124 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-284-32739T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7143916 | ||||||
| chr6:7144069
|
CT | C | 41 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.-284-32576delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7144069 | |||||
| chr6:7144282
|
T | A | 1 | a0004c0006t0018g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-284-32373T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7144282 | ||||||
| chr6:7144315
|
T | C | 11 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(8): Show | 11 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-284-32340T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7144315 | ||||||
| chr6:7144474
|
T | A | 2 | a0009c0026t0003g0060a0009c0026t0003g0088 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-284-32181T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7144474 | ||||||
| chr6:7144614
|
C | CT | 14 | a0002c0004t0026g0261a0003c0012t0013g0239a0005c0003t0012g0260others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-284-32029dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7144614 | |||||
| chr6:7144614
|
CT | C | 50 | a0001c0001t0001g0054a0001c0001t0017g0096a0001c0001t0035g0034others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.-284-32029delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7144614 | |||||
| chr6:7144940
|
G | A | 12 | a0003c0002t0023g0175a0003c0032t0057g0176a0005c0003t0004g0174others(9): Show | 12 | HG02258.hp1 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.-284-31715G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7144940 | ||||||
| chr6:7144958
|
T | G | 82 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(79): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-284-31697T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7144958 | ||||||
| chr6:7145095
|
C | T | 2 | a0009c0026t0003g0060a0009c0026t0003g0088 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-284-31560C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7145095 | ||||||
| chr6:7145286
|
G | A | 3 | a0002c0004t0003g0052a0003c0002t0004g0015a0004c0006t0021g0051 | 3 | HG01891.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-284-31369G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7145286 | ||||||
| chr6:7145351
|
G | A | 67 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(64): Show | 67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.-284-31304G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7145351 | ||||||
| chr6:7145420
|
C | T | 2 | a0003c0002t0002g0063a0003c0002t0029g0062 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-284-31235C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7145420 | ||||||
| chr6:7145433
|
A | G | 3 | a0003c0002t0002g0063a0003c0002t0029g0062a0003c0045t0002g0070 | 3 | HG03491.hp2 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-284-31222A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7145433 | ||||||
| chr6:7145536
|
A | G | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-284-31119A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7145536 | ||||||
| chr6:7145860
|
G | T | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-284-30795G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7145860 | ||||||
| chr6:7145880
|
G | A | 12 | a0002c0004t0026g0261a0003c0012t0013g0239a0005c0003t0012g0260others(9): Show | 12 | HG01243.hp1 HG01361.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-284-30775G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7145880 | ||||||
| chr6:7145960
|
T | TGATGAA | 67 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(64): Show | 67 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-284-30694_-284-30 others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7145960 | |||||
| chr6:7145987
|
CTT | C | 39 | a0002c0004t0026g0261a0003c0002t0023g0175a0003c0012t0013g0239others(36): Show | 39 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.-284-30666_-284-30 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7145987 | |||||
| chr6:7146014
|
C | T | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-284-30641C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7146014 | ||||||
| chr6:7146117
|
A | G | 62 | a0001c0001t0001g0054a0001c0001t0001g0253a0001c0001t0001g0255others(59): Show | 62 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.-284-30538A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7146117 | ||||||
| chr6:7146179
|
T | C | 1 | a0003c0002t0010g0067 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-284-30476T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7146179 | ||||||
| chr6:7146592
|
A | G | 14 | a0001c0017t0032g0149a0005c0003t0012g0172a0005c0003t0012g0173others(11): Show | 14 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.-284-30063A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7146592 | ||||||
| chr6:7146758
|
CTTCT | C | 5 | a0001c0001t0001g0098a0001c0001t0017g0166a0002c0007t0011g0169others(2): Show | 5 | NA18964.hp1 NA18964.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.-284-29890_-284-29 others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7146758 | |||||
| chr6:7146858
|
C | T | 1 | a0028c0054t0007g0029 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-284-29797C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7146858 | ||||||
| chr6:7146998
|
T | C | 1 | a0002c0042t0060g0108 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-284-29657T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7146998 | ||||||
| chr6:7147267
|
G | A | 1 | a0004c0006t0007g0138 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-284-29388G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7147267 | ||||||
| chr6:7147315
|
C | T | 21 | a0001c0001t0001g0122a0001c0001t0001g0224a0002c0004t0003g0094others(18): Show | 21 | HG00438.hp2 HG00639.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-284-29340C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7147315 | ||||||
| chr6:7147332
|
C | T | 1 | a0025c0060t0012g0227 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-284-29323C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7147332 | ||||||
| chr6:7147448
|
G | A | 2 | a0007c0022t0019g0183a0007c0022t0019g0184 | 2 | HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-284-29207G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7147448 | ||||||
| chr6:7147540
|
T | G | 1 | a0008c0010t0001g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-284-29115T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7147540 | ||||||
| chr6:7147558
|
A | C | 1 | a0002c0004t0007g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-284-29097A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7147558 | ||||||
| chr6:7147962
|
A | G | 1 | a0006c0005t0070g0038 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-284-28693A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7147962 | ||||||
| chr6:7148089
|
G | A | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-284-28566G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7148089 | ||||||
| chr6:7148106
|
G | C | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-284-28549G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7148106 | ||||||
| chr6:7148451
|
C | T | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-284-28204C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7148451 | ||||||
| chr6:7148522
|
G | A | 11 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(8): Show | 11 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-284-28133G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7148522 | ||||||
| chr6:7148542
|
T | TG | 33 | a0003c0002t0003g0229a0004c0006t0007g0245a0004c0006t0021g0105others(30): Show | 33 | HG00558.hp1 HG01074.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-284-28104dupG | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7148542 | |||||
| chr6:7148640
|
C | T | 8 | a0003c0012t0013g0239a0005c0003t0012g0260a0005c0003t0013g0159others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-284-28015C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7148640 | ||||||
| chr6:7148725
|
T | G | 2 | a0002c0004t0015g0044a0002c0004t0015g0204 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-284-27930T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7148725 | ||||||
| chr6:7148875
|
A | G | 2 | a0001c0001t0001g0043a0003c0044t0066g0042 | 2 | NA18995.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-284-27780A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7148875 | ||||||
| chr6:7149069
|
C | T | 3 | a0004c0052t0020g0005a0005c0003t0020g0091a0005c0003t0020g0137 | 3 | HG00438.hp1 NA18982.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-284-27586C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7149069 | ||||||
| chr6:7149095
|
G | T | 11 | a0005c0003t0012g0172a0005c0003t0012g0173a0007c0009t0005g0006others(8): Show | 11 | HG01074.hp2 HG01192.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-284-27560G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7149095 | ||||||
| chr6:7149345
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-284-27310C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7149345 | ||||||
| chr6:7149774
|
C | T | 4 | a0007c0009t0005g0008a0007c0009t0005g0009a0007c0009t0053g0014others(1): Show | 4 | NA18612.hp1 NA18952.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284-26881C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7149774 | ||||||
| chr6:7149937
|
C | A | 3 | a0005c0003t0033g0230a0005c0003t0033g0232a0005c0003t0079g0231 | 3 | HG02970.hp2 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-284-26718C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7149937 | ||||||
| chr6:7149939
|
T | C | 1 | a0004c0050t0006g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-284-26716T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7149939 | ||||||
| chr6:7149968
|
C | T | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-284-26687C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7149968 | ||||||
| chr6:7149995
|
G | GT | 78 | a0001c0001t0001g0033a0001c0001t0001g0073a0001c0001t0001g0097others(75): Show | 78 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-284-26645dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7149995 | |||||
| chr6:7150271
|
A | G | 3 | a0004c0006t0006g0099a0010c0028t0006g0019a0015c0024t0006g0153 | 3 | HG01433.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-284-26384A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7150271 | ||||||
| chr6:7150545
|
C | T | 1 | a0003c0002t0010g0251 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-284-26110C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7150545 | ||||||
| chr6:7150558
|
CAT | C | 16 | a0002c0007t0028g0121a0002c0007t0069g0022a0004c0006t0006g0099others(13): Show | 16 | HG01167.hp1 HG01261.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.-284-26096_-284-26 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7150558 | ||||||
| chr6:7150632
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0122others(1): Show | 4 | HG02056.hp2 HG02523.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284-26023C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7150632 | ||||||
| chr6:7150776
|
G | A | 3 | a0001c0001t0016g0026a0001c0001t0016g0083a0002c0004t0003g0082 | 3 | HG02135.hp2 NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-284-25879G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7150776 | ||||||
| chr6:7150936
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-284-25719C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7150936 | ||||||
| chr6:7150973
|
G | T | 1 | a0006c0005t0004g0086 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-284-25682G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7150973 | ||||||
| chr6:7151136
|
A | G | 4 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0031t0068g0154others(1): Show | 4 | HG01109.hp1 HG01361.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284-25519A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7151136 | ||||||
| chr6:7151263
|
G | GAGCTGAG others(4): Show |
1 | a0006c0016t0009g0024 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-284-25390_-284-25 others(17): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7151263 | |||||
| chr6:7151276
|
A | G | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-284-25379A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7151276 | ||||||
| chr6:7151417
|
A | G | 1 | a0023c0067t0002g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-284-25238A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7151417 | ||||||
| chr6:7151669
|
A | G | 2 | a0005c0003t0004g0037a0029c0053t0062g0057 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-284-24986A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7151669 | ||||||
| chr6:7151791
|
C | T | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-284-24864C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7151791 | ||||||
| chr6:7151822
|
A | G | 4 | a0001c0001t0001g0073a0003c0002t0002g0020a0003c0002t0002g0065others(1): Show | 4 | NA18612.hp2 NA18960.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-24833A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7151822 | ||||||
| chr6:7151943
|
G | A | 4 | a0004c0008t0001g0265a0004c0008t0001g0266a0004c0008t0001g0267others(1): Show | 4 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-24712G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7151943 | ||||||
| chr6:7151984
|
C | A | 1 | a0004c0052t0020g0005 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-284-24671C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7151984 | ||||||
| chr6:7151984
|
C | T | 6 | a0001c0001t0001g0073a0003c0002t0001g0124a0003c0002t0002g0020others(3): Show | 6 | NA18612.hp2 NA18951.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-284-24671C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7151984 | ||||||
| chr6:7152010
|
C | T | 83 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-284-24645C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7152010 | ||||||
| chr6:7152311
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0017g0214 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-284-24344T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7152311 | ||||||
| chr6:7152377
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-284-24278T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7152377 | ||||||
| chr6:7152545
|
T | C | 1 | a0005c0003t0013g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-284-24110T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7152545 | ||||||
| chr6:7152587
|
T | C | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-284-24068T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7152587 | ||||||
| chr6:7152898
|
C | G | 2 | a0006c0005t0004g0084a0006c0005t0004g0085 | 2 | NA18946.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.-284-23757C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7152898 | ||||||
| chr6:7152919
|
C | T | 45 | a0001c0001t0001g0054a0001c0001t0001g0253a0001c0001t0001g0255others(42): Show | 45 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.-284-23736C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7152919 | ||||||
| chr6:7153029
|
A | G | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-284-23626A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153029 | ||||||
| chr6:7153105
|
G | GT | 24 | a0001c0001t0001g0285a0001c0001t0002g0268a0001c0017t0032g0149others(21): Show | 24 | HG00438.hp2 HG01109.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.-284-23529dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153105 | |||||
| chr6:7153105
|
GT | G | 13 | a0002c0004t0015g0044a0002c0004t0022g0066a0003c0002t0008g0128others(10): Show | 13 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.-284-23529delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153105 | |||||
| chr6:7153246
|
T | A | 13 | a0003c0002t0023g0175a0005c0003t0033g0230a0005c0003t0033g0232others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-284-23409T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153246 | ||||||
| chr6:7153246
|
T | TTA | 11 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(8): Show | 11 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-284-23409_-284-23 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153246 | ||||||
| chr6:7153247
|
A | T | 1 | a0003c0002t0010g0251 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-284-23408A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153247 | ||||||
| chr6:7153303
|
G | A | 83 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-284-23352G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153303 | ||||||
| chr6:7153333
|
G | A | 2 | a0001c0001t0016g0026a0001c0001t0016g0083 | 2 | HG02135.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-284-23322G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153333 | ||||||
| chr6:7153392
|
C | A | 22 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0172others(19): Show | 22 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-284-23263C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153392 | ||||||
| chr6:7153413
|
T | C | 1 | a0004c0008t0006g0274 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-284-23242T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153413 | ||||||
| chr6:7153413
|
T | TAC | 36 | a0001c0001t0001g0255a0001c0001t0001g0259a0001c0001t0001g0285others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.-284-23212_-284-23 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153413
|
T | TACAC | 13 | a0002c0004t0011g0163a0002c0007t0011g0160a0002c0007t0011g0161others(10): Show | 13 | HG02040.hp1 HG02040.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.-284-23214_-284-23 others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153413
|
T | TACACACA others(1): Show |
17 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(14): Show | 17 | HG00558.hp1 HG01192.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-284-23218_-284-23 others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153413
|
T | TACACACA others(3): Show |
5 | a0005c0003t0033g0230a0005c0003t0033g0232a0005c0003t0079g0231others(2): Show | 5 | HG01074.hp2 HG02135.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-284-23220_-284-23 others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153413
|
T | TACACACA others(5): Show |
12 | a0001c0001t0082g0235a0003c0002t0002g0189a0003c0002t0010g0251others(9): Show | 12 | HG00741.hp1 HG01517.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-284-23222_-284-23 others(18): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153413
|
T | TACACACA others(7): Show |
24 | a0002c0004t0008g0212a0002c0004t0016g0211a0003c0002t0008g0128others(21): Show | 24 | HG00140.hp2 HG00642.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-284-23224_-284-23 others(20): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153413
|
T | TACACACA others(9): Show |
4 | a0001c0001t0035g0034a0005c0003t0047g0178a0006c0005t0004g0041others(1): Show | 4 | HG02074.hp2 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-23226_-284-23 others(22): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153413
|
T | TACACACA others(11): Show |
6 | a0004c0006t0058g0048a0005c0003t0012g0260a0005c0003t0018g0001others(3): Show | 6 | HG01243.hp1 HG01891.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-284-23228_-284-23 others(24): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153413
|
T | TACACACA others(13): Show |
2 | a0014c0020t0034g0236a0014c0020t0034g0237 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-284-23230_-284-23 others(26): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153413
|
TAC | T | 20 | a0001c0001t0017g0096a0001c0001t0042g0187a0002c0004t0003g0118others(17): Show | 20 | HG00280.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-284-23212_-284-23 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7153413 | |||||
| chr6:7153436
|
A | G | 1 | a0007c0022t0019g0183 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-284-23219A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153436 | ||||||
| chr6:7153446
|
A | G | 2 | a0004c0006t0007g0241a0004c0006t0007g0245 | 2 | HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-284-23209A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153446 | ||||||
| chr6:7153489
|
C | T | 1 | a0001c0001t0082g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-284-23166C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153489 | ||||||
| chr6:7153663
|
T | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(5): Show | 8 | HG01255.hp2 HG01934.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-284-22992T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153663 | ||||||
| chr6:7153811
|
T | C | 1 | a0011c0041t0067g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-284-22844T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153811 | ||||||
| chr6:7153875
|
C | T | 2 | a0005c0003t0004g0220a0024c0061t0015g0223 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-284-22780C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7153875 | ||||||
| chr6:7154444
|
G | A | 2 | a0005c0003t0012g0260a0005c0003t0046g0258 | 2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-284-22211G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7154444 | ||||||
| chr6:7154471
|
G | A | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-284-22184G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7154471 | ||||||
| chr6:7154756
|
G | A | 13 | a0003c0002t0023g0175a0005c0003t0033g0230a0005c0003t0033g0232others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-284-21899G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7154756 | ||||||
| chr6:7154849
|
G | A | 1 | a0002c0004t0007g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-284-21806G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7154849 | ||||||
| chr6:7154957
|
G | T | 4 | a0004c0006t0007g0281a0013c0019t0010g0256a0013c0019t0049g0262others(1): Show | 4 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-21698G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7154957 | ||||||
| chr6:7155045
|
G | A | 8 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-284-21610G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7155045 | ||||||
| chr6:7155194
|
C | G | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-284-21461C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7155194 | ||||||
| chr6:7155368
|
A | G | 83 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(80): Show | 83 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-284-21287A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7155368 | ||||||
| chr6:7155393
|
G | A | 22 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0172others(19): Show | 22 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-284-21262G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7155393 | ||||||
| chr6:7155506
|
T | G | 2 | a0005c0003t0012g0087a0032c0029t0038g0089 | 2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-284-21149T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7155506 | ||||||
| chr6:7155528
|
C | G | 1 | a0002c0042t0060g0108 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-284-21127C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7155528 | ||||||
| chr6:7155665
|
A | T | 1 | a0001c0001t0016g0026 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-284-20990A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7155665 | ||||||
| chr6:7155792
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-284-20863T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7155792 | ||||||
| chr6:7155967
|
A | G | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-284-20688A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7155967 | ||||||
| chr6:7156255
|
C | G | 2 | a0006c0005t0004g0084a0006c0005t0004g0085 | 2 | NA18946.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.-284-20400C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156255 | ||||||
| chr6:7156317
|
G | A | 1 | a0002c0007t0064g0143 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-284-20338G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156317 | ||||||
| chr6:7156503
|
C | T | 50 | a0001c0001t0001g0097a0002c0007t0028g0121a0002c0007t0069g0022others(47): Show | 50 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.-284-20152C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156503 | ||||||
| chr6:7156516
|
C | T | 10 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0260others(7): Show | 10 | HG01243.hp1 HG01517.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-284-20139C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156516 | ||||||
| chr6:7156526
|
C | T | 4 | a0004c0006t0007g0281a0013c0019t0010g0256a0013c0019t0049g0262others(1): Show | 4 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-20129C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156526 | ||||||
| chr6:7156574
|
C | T | 1 | a0004c0006t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-284-20081C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156574 | ||||||
| chr6:7156668
|
T | C | 79 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(76): Show | 79 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-284-19987T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156668 | ||||||
| chr6:7156703
|
G | A | 1 | a0007c0011t0052g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-284-19952G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156703 | ||||||
| chr6:7156791
|
T | C | 38 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(35): Show | 38 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.-284-19864T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156791 | ||||||
| chr6:7156797
|
G | C | 13 | a0005c0003t0012g0172a0005c0003t0012g0173a0007c0009t0005g0006others(10): Show | 13 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-284-19858G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156797 | ||||||
| chr6:7156807
|
C | T | 40 | a0001c0001t0001g0054a0001c0001t0001g0253a0001c0001t0001g0255others(37): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.-284-19848C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156807 | ||||||
| chr6:7156834
|
G | A | 9 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0260others(6): Show | 9 | HG01243.hp1 HG01517.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-19821G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7156834 | ||||||
| chr6:7157128
|
C | G | 1 | a0005c0003t0013g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-284-19527C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7157128 | ||||||
| chr6:7157402
|
C | T | 1 | a0002c0004t0022g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-284-19253C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7157402 | ||||||
| chr6:7157433
|
CA | C | 39 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(36): Show | 39 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.-284-19208delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7157433 | |||||
| chr6:7157747
|
ACT | A | 6 | a0004c0006t0021g0051a0005c0003t0012g0087a0005c0003t0050g0139others(3): Show | 6 | HG02896.hp2 HG02970.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-284-18905_-284-18 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7157747 | |||||
| chr6:7157767
|
A | G | 1 | a0003c0002t0002g0142 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-284-18888A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7157767 | ||||||
| chr6:7157818
|
C | G | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-284-18837C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7157818 | ||||||
| chr6:7157867
|
C | A | 1 | a0005c0003t0004g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-284-18788C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7157867 | ||||||
| chr6:7157992
|
G | T | 77 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(74): Show | 77 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-284-18663G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7157992 | ||||||
| chr6:7158006
|
C | T | 3 | a0007c0022t0019g0183a0007c0022t0019g0184a0035c0033t0081g0233 | 3 | HG01109.hp1 HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-284-18649C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158006 | ||||||
| chr6:7158271
|
G | C | 1 | a0002c0004t0003g0225 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-284-18384G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158271 | ||||||
| chr6:7158296
|
C | G | 1 | a0019c0049t0002g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-284-18359C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158296 | ||||||
| chr6:7158386
|
A | G | 2 | a0003c0002t0023g0175a0014c0020t0076g0177 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-284-18269A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158386 | ||||||
| chr6:7158386
|
A | T | 3 | a0002c0023t0044g0095a0002c0023t0048g0171a0003c0034t0008g0031 | 3 | HG02074.hp1 NA18747.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-284-18269A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158386 | ||||||
| chr6:7158390
|
C | G | 8 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-284-18265C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158390 | ||||||
| chr6:7158409
|
C | T | 2 | a0005c0003t0004g0220a0024c0061t0015g0223 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-284-18246C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158409 | ||||||
| chr6:7158685
|
C | G | 37 | a0001c0001t0035g0034a0001c0001t0042g0187a0001c0001t0082g0235others(34): Show | 37 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-284-17970C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158685 | ||||||
| chr6:7158718
|
C | T | 22 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0172others(19): Show | 22 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-284-17937C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158718 | ||||||
| chr6:7158758
|
A | T | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-284-17897A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158758 | ||||||
| chr6:7158865
|
C | CT | 10 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(7): Show | 10 | HG00558.hp1 HG01192.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.-284-17780dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7158865 | |||||
| chr6:7158894
|
G | C | 5 | a0001c0001t0017g0180a0004c0006t0018g0056a0016c0025t0018g0179others(2): Show | 5 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-284-17761G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7158894 | ||||||
| chr6:7159117
|
A | G | 12 | a0002c0004t0003g0052a0003c0002t0004g0015a0003c0012t0003g0205others(9): Show | 12 | HG01361.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-284-17538A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7159117 | ||||||
| chr6:7159233
|
G | T | 1 | a0004c0063t0003g0141 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-284-17422G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7159233 | ||||||
| chr6:7159297
|
C | T | 1 | a0010c0021t0003g0011 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-284-17358C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7159297 | ||||||
| chr6:7159415
|
C | T | 9 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0260others(6): Show | 9 | HG01243.hp1 HG01517.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-17240C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7159415 | ||||||
| chr6:7159781
|
G | A | 41 | a0001c0001t0001g0054a0001c0001t0001g0253a0001c0001t0001g0255others(38): Show | 41 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.-284-16874G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7159781 | ||||||
| chr6:7160122
|
A | AT | 117 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-284-16521dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7160122 | |||||
| chr6:7160210
|
A | T | 13 | a0005c0003t0012g0172a0005c0003t0012g0173a0007c0009t0005g0006others(10): Show | 13 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-284-16445A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160210 | ||||||
| chr6:7160249
|
A | G | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-284-16406A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160249 | ||||||
| chr6:7160335
|
T | A | 2 | a0005c0003t0004g0220a0024c0061t0015g0223 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-284-16320T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160335 | ||||||
| chr6:7160336
|
A | T | 1 | a0006c0005t0004g0041 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-284-16319A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160336 | ||||||
| chr6:7160340
|
A | C | 1 | a0002c0023t0044g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-284-16315A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160340 | ||||||
| chr6:7160535
|
G | A | 3 | a0002c0004t0003g0094a0002c0004t0003g0151a0002c0004t0008g0039 | 3 | HG01255.hp1 HG01261.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-284-16120G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160535 | ||||||
| chr6:7160588
|
C | G | 6 | a0005c0003t0009g0101a0006c0005t0009g0090a0006c0005t0009g0133others(3): Show | 6 | NA18941.hp1 NA18974.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-284-16067C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160588 | ||||||
| chr6:7160660
|
A | G | 6 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-284-15995A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160660 | ||||||
| chr6:7160689
|
CTT | C | 7 | a0001c0001t0001g0122a0002c0004t0003g0094a0002c0004t0003g0118others(4): Show | 7 | HG01255.hp1 HG01261.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-284-15957_-284-15 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7160689 | |||||
| chr6:7160815
|
T | TAGCTGGG others(7): Show |
117 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-284-15839_-284-15 others(20): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7160815 | |||||
| chr6:7160828
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-284-15827A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160828 | ||||||
| chr6:7160920
|
G | A | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-284-15735G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7160920 | ||||||
| chr6:7161018
|
A | T | 1 | a0005c0003t0013g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-284-15637A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7161018 | ||||||
| chr6:7161054
|
C | T | 3 | a0005c0003t0033g0230a0005c0003t0033g0232a0005c0003t0079g0231 | 3 | HG02970.hp2 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-284-15601C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7161054 | ||||||
| chr6:7161122
|
T | C | 5 | a0001c0001t0035g0034a0005c0056t0010g0196a0006c0005t0030g0193others(2): Show | 5 | NA18965.hp1 NA18970.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.-284-15533T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7161122 | ||||||
| chr6:7161238
|
T | C | 90 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-284-15417T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7161238 | ||||||
| chr6:7161299
|
A | G | 1 | a0003c0002t0002g0076 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-284-15356A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7161299 | ||||||
| chr6:7161557
|
C | T | 1 | a0013c0058t0001g0134 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-284-15098C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7161557 | ||||||
| chr6:7161598
|
T | C | 291 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-284-15057T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7161598 | ||||||
| chr6:7161691
|
A | G | 1 | a0002c0004t0003g0148 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-284-14964A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7161691 | ||||||
| chr6:7161944
|
G | C | 1 | a0007c0009t0005g0009 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-284-14711G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7161944 | ||||||
| chr6:7162017
|
A | G | 1 | a0009c0018t0003g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-284-14638A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7162017 | ||||||
| chr6:7162048
|
C | T | 1 | a0007c0022t0019g0183 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-284-14607C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7162048 | ||||||
| chr6:7162273
|
T | A | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-284-14382T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7162273 | ||||||
| chr6:7162337
|
C | T | 90 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-284-14318C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7162337 | ||||||
| chr6:7162373
|
C | T | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-284-14282C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7162373 | ||||||
| chr6:7162718
|
T | C | 1 | a0001c0001t0042g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-284-13937T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7162718 | ||||||
| chr6:7162745
|
G | A | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-284-13910G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7162745 | ||||||
| chr6:7162912
|
G | A | 22 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0172others(19): Show | 22 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-284-13743G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7162912 | ||||||
| chr6:7163266
|
G | C | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-284-13389G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163266 | ||||||
| chr6:7163274
|
A | G | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-284-13381A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163274 | ||||||
| chr6:7163315
|
C | A | 2 | a0006c0005t0004g0084a0006c0005t0004g0085 | 2 | NA18946.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.-284-13340C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163315 | ||||||
| chr6:7163456
|
A | G | 3 | a0006c0005t0030g0193a0006c0005t0030g0194a0006c0005t0075g0192 | 3 | NA18970.hp2 NA19083.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-284-13199A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163456 | ||||||
| chr6:7163540
|
C | T | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-284-13115C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163540 | ||||||
| chr6:7163595
|
C | T | 1 | a0009c0018t0003g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-284-13060C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163595 | ||||||
| chr6:7163624
|
G | A | 1 | a0003c0034t0008g0031 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-284-13031G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163624 | ||||||
| chr6:7163640
|
C | T | 90 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(87): Show | 90 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-284-13015C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163640 | ||||||
| chr6:7163733
|
T | C | 5 | a0001c0001t0017g0096a0002c0007t0007g0110a0002c0007t0007g0116others(2): Show | 5 | HG01071.hp2 HG01123.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-284-12922T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163733 | ||||||
| chr6:7163974
|
C | T | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-284-12681C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7163974 | ||||||
| chr6:7164029
|
C | T | 1 | a0002c0004t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-284-12626C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164029 | ||||||
| chr6:7164073
|
G | T | 1 | a0003c0002t0002g0020 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-284-12582G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164073 | ||||||
| chr6:7164186
|
C | T | 4 | a0004c0008t0001g0265a0004c0008t0001g0266a0004c0008t0001g0267others(1): Show | 4 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-12469C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164186 | ||||||
| chr6:7164286
|
C | T | 3 | a0004c0052t0020g0005a0005c0003t0020g0091a0005c0003t0020g0137 | 3 | HG00438.hp1 NA18982.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-284-12369C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164286 | ||||||
| chr6:7164544
|
C | G | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-12111C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164544 | ||||||
| chr6:7164577
|
C | T | 4 | a0003c0012t0013g0239a0005c0003t0013g0159a0005c0003t0013g0240others(1): Show | 4 | HG01884.hp2 HG02486.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-12078C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164577 | ||||||
| chr6:7164619
|
T | C | 1 | a0004c0006t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-284-12036T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164619 | ||||||
| chr6:7164646
|
G | T | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-284-12009G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164646 | ||||||
| chr6:7164840
|
C | G | 4 | a0007c0009t0005g0008a0007c0009t0005g0009a0007c0009t0053g0014others(1): Show | 4 | NA18612.hp1 NA18952.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284-11815C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164840 | ||||||
| chr6:7164940
|
A | G | 8 | a0001c0001t0001g0122a0001c0001t0016g0280a0002c0004t0003g0094others(5): Show | 8 | HG01175.hp1 HG01255.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-284-11715A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7164940 | ||||||
| chr6:7165143
|
A | G | 75 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-284-11512A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165143 | ||||||
| chr6:7165153
|
G | A | 13 | a0005c0003t0012g0172a0005c0003t0012g0173a0007c0009t0005g0006others(10): Show | 13 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-284-11502G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165153 | ||||||
| chr6:7165207
|
C | G | 1 | a0023c0067t0002g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-284-11448C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165207 | ||||||
| chr6:7165215
|
A | G | 2 | a0003c0002t0002g0189a0003c0002t0029g0186 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-284-11440A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165215 | ||||||
| chr6:7165230
|
G | A | 1 | a0008c0010t0001g0279 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-284-11425G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165230 | ||||||
| chr6:7165566
|
C | CA | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-11088dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7165566 | |||||
| chr6:7165606
|
A | G | 1 | a0004c0068t0073g0273 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-284-11049A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165606 | ||||||
| chr6:7165693
|
G | T | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-284-10962G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165693 | ||||||
| chr6:7165781
|
G | A | 1 | a0002c0004t0007g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-284-10874G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165781 | ||||||
| chr6:7165803
|
A | G | 2 | a0003c0002t0002g0063a0003c0002t0029g0062 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-284-10852A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165803 | ||||||
| chr6:7165831
|
C | T | 1 | a0003c0002t0071g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-284-10824C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165831 | ||||||
| chr6:7165922
|
A | G | 1 | a0021c0064t0001g0271 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-284-10733A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7165922 | ||||||
| chr6:7166005
|
A | G | 117 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-284-10650A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166005 | ||||||
| chr6:7166049
|
C | T | 6 | a0001c0001t0001g0122a0002c0004t0003g0118a0002c0004t0003g0150others(3): Show | 6 | HG01255.hp1 HG01261.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-284-10606C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166049 | ||||||
| chr6:7166063
|
G | A | 1 | a0002c0007t0007g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-284-10592G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166063 | ||||||
| chr6:7166098
|
A | G | 2 | a0005c0003t0050g0139a0005c0059t0013g0157 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-284-10557A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166098 | ||||||
| chr6:7166123
|
C | T | 13 | a0005c0003t0012g0172a0005c0003t0012g0173a0007c0009t0005g0006others(10): Show | 13 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-284-10532C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166123 | ||||||
| chr6:7166563
|
G | A | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-284-10092G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166563 | ||||||
| chr6:7166572
|
C | T | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-284-10083C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166572 | ||||||
| chr6:7166596
|
C | G | 2 | a0001c0001t0042g0187a0008c0010t0001g0191 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-284-10059C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166596 | ||||||
| chr6:7166610
|
A | T | 9 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0260others(6): Show | 9 | HG01243.hp1 HG01517.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-10045A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166610 | ||||||
| chr6:7166901
|
T | C | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-284-9754T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166901 | ||||||
| chr6:7166937
|
A | G | 91 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-284-9718A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7166937 | ||||||
| chr6:7167168
|
C | T | 20 | a0004c0006t0058g0048a0005c0003t0033g0230a0005c0003t0033g0232others(17): Show | 20 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-284-9487C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7167168 | ||||||
| chr6:7167349
|
A | AT | 33 | a0001c0001t0001g0033a0001c0001t0001g0253a0001c0001t0001g0283others(30): Show | 33 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.-284-9285dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7167349 | |||||
| chr6:7167349
|
AT | A | 10 | a0001c0017t0001g0252a0004c0006t0031g0079a0004c0068t0073g0273others(7): Show | 10 | HG01167.hp1 HG01255.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-284-9285delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7167349 | |||||
| chr6:7167403
|
G | C | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-9252G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7167403 | ||||||
| chr6:7167521
|
T | A | 2 | a0003c0002t0001g0124a0003c0040t0001g0103 | 2 | NA18951.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-284-9134T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7167521 | ||||||
| chr6:7167765
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0155 | 2 | HG02148.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-284-8890G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7167765 | ||||||
| chr6:7167790
|
C | T | 4 | a0002c0004t0022g0027a0002c0004t0022g0136a0003c0002t0010g0251others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-8865C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7167790 | ||||||
| chr6:7167909
|
G | A | 24 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(21): Show | 24 | HG00621.hp2 HG01255.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.-284-8746G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7167909 | ||||||
| chr6:7167929
|
A | G | 22 | a0003c0002t0023g0175a0004c0006t0058g0048a0005c0003t0033g0230others(19): Show | 22 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-284-8726A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7167929 | ||||||
| chr6:7167947
|
T | A | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-284-8708T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7167947 | ||||||
| chr6:7167973
|
A | ATG | 11 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(8): Show | 11 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.-284-8680_-284-867 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7167973 | |||||
| chr6:7168035
|
A | T | 2 | a0002c0004t0022g0027a0002c0004t0022g0136 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-284-8620A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7168035 | ||||||
| chr6:7168156
|
G | A | 1 | a0004c0006t0006g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-284-8499G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7168156 | ||||||
| chr6:7168239
|
A | G | 1 | a0003c0002t0002g0076 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-284-8416A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7168239 | ||||||
| chr6:7168241
|
T | C | 39 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0001g0259others(36): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.-284-8414T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7168241 | ||||||
| chr6:7168254
|
G | GA | 14 | a0001c0001t0001g0126a0002c0004t0026g0261a0002c0004t0072g0226others(11): Show | 14 | HG00438.hp2 HG00621.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-284-8379dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7168254 | |||||
| chr6:7168254
|
G | GAA | 25 | a0001c0001t0042g0187a0002c0004t0016g0211a0003c0002t0002g0189others(22): Show | 25 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-284-8380_-284-837 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7168254 | |||||
| chr6:7168254
|
G | GAAA | 48 | a0001c0001t0001g0097a0001c0001t0035g0034a0002c0004t0015g0044others(45): Show | 48 | HG00423.hp2 HG01099.hp2 HG01517.hp1 others(45): Show |
intron_variant | MODIFIER | c.-284-8381_-284-837 others(7): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7168254 | |||||
| chr6:7168254
|
G | GAAAA | 6 | a0003c0012t0004g0219a0004c0052t0020g0005a0005c0003t0012g0260others(3): Show | 6 | HG00438.hp1 HG00558.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-284-8382_-284-837 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7168254 | |||||
| chr6:7168254
|
GA | G | 28 | a0001c0001t0001g0043a0001c0001t0001g0259a0001c0001t0002g0170others(25): Show | 28 | HG01074.hp1 HG01891.hp1 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.-284-8379delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7168254 | |||||
| chr6:7168438
|
G | T | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-284-8217G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7168438 | ||||||
| chr6:7168713
|
A | G | 2 | a0001c0001t0042g0187a0008c0010t0001g0191 | 2 | HG00280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-284-7942A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7168713 | ||||||
| chr6:7168873
|
C | T | 1 | a0001c0001t0016g0026 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-284-7782C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7168873 | ||||||
| chr6:7168955
|
A | AGTGCCTA others(29): Show |
2 | a0003c0002t0003g0058a0003c0002t0003g0059 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-284-7699_-284-766 others(40): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7168955 | |||||
| chr6:7168978
|
A | G | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-7677A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7168978 | ||||||
| chr6:7169187
|
A | G | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-284-7468A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7169187 | ||||||
| chr6:7169509
|
C | A | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-284-7146C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7169509 | ||||||
| chr6:7169514
|
A | G | 1 | a0004c0006t0024g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-284-7141A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7169514 | ||||||
| chr6:7169645
|
T | C | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-284-7010T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7169645 | ||||||
| chr6:7169647
|
G | A | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-284-7008G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7169647 | ||||||
| chr6:7169654
|
G | A | 1 | a0003c0002t0071g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-284-7001G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7169654 | ||||||
| chr6:7169851
|
T | A | 3 | a0002c0004t0008g0216a0003c0002t0003g0058a0003c0002t0003g0059 | 3 | HG01167.hp2 HG01169.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-284-6804T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7169851 | ||||||
| chr6:7169959
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-284-6696A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7169959 | ||||||
| chr6:7170060
|
T | G | 6 | a0002c0004t0015g0044a0002c0004t0015g0203a0002c0004t0015g0204others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-284-6595T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7170060 | ||||||
| chr6:7170318
|
A | G | 5 | a0001c0001t0035g0034a0005c0056t0010g0196a0006c0005t0030g0193others(2): Show | 5 | NA18965.hp1 NA18970.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.-284-6337A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7170318 | ||||||
| chr6:7170430
|
C | T | 20 | a0004c0006t0058g0048a0005c0003t0033g0230a0005c0003t0033g0232others(17): Show | 20 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-284-6225C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7170430 | ||||||
| chr6:7170496
|
G | A | 1 | a0001c0001t0017g0096 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-284-6159G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7170496 | ||||||
| chr6:7170563
|
G | A | 20 | a0004c0006t0058g0048a0005c0003t0033g0230a0005c0003t0033g0232others(17): Show | 20 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-284-6092G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7170563 | ||||||
| chr6:7170567
|
C | T | 1 | a0020c0051t0006g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-284-6088C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7170567 | ||||||
| chr6:7170857
|
T | G | 6 | a0005c0003t0009g0101a0006c0005t0009g0090a0006c0005t0009g0133others(3): Show | 6 | NA18941.hp1 NA18974.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-284-5798T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7170857 | ||||||
| chr6:7170884
|
A | G | 1 | a0039c0070t0009g0016 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-284-5771A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7170884 | ||||||
| chr6:7171067
|
G | A | 1 | a0003c0002t0001g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-284-5588G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7171067 | ||||||
| chr6:7171112
|
A | C | 1 | a0003c0002t0010g0251 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-284-5543A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7171112 | ||||||
| chr6:7171174
|
T | G | 118 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(115): Show | 118 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-284-5481T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7171174 | ||||||
| chr6:7171460
|
C | G | 4 | a0005c0003t0012g0260a0005c0003t0018g0001a0005c0003t0046g0258others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-284-5195C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7171460 | ||||||
| chr6:7171589
|
T | C | 1 | a0007c0022t0019g0183 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-284-5066T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7171589 | ||||||
| chr6:7171688
|
G | A | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-4967G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7171688 | ||||||
| chr6:7171847
|
A | T | 2 | a0007c0009t0039g0002a0007c0009t0040g0012 | 2 | HG00558.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-284-4808A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7171847 | ||||||
| chr6:7171872
|
G | A | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-4783G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7171872 | ||||||
| chr6:7171947
|
C | CT | 6 | a0002c0007t0063g0217a0004c0006t0006g0099a0010c0035t0065g0208others(3): Show | 6 | HG02647.hp2 HG03098.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-284-4693dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7171947 | |||||
| chr6:7171988
|
C | G | 73 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(70): Show | 73 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-284-4667C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7171988 | ||||||
| chr6:7172143
|
A | G | 2 | a0002c0007t0007g0218a0002c0007t0063g0217 | 2 | HG02155.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-284-4512A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7172143 | ||||||
| chr6:7172458
|
G | T | 2 | a0004c0006t0058g0048a0011c0015t0019g0182 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-284-4197G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7172458 | ||||||
| chr6:7172639
|
G | A | 1 | a0002c0007t0011g0160 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-284-4016G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7172639 | ||||||
| chr6:7172691
|
T | TG | 25 | a0001c0001t0001g0017a0001c0001t0001g0073a0003c0002t0002g0145others(22): Show | 25 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.-284-3957dupG | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7172691 | |||||
| chr6:7172692
|
G | C | 3 | a0005c0003t0033g0230a0005c0003t0033g0232a0005c0003t0079g0231 | 3 | HG02970.hp2 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-284-3963G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7172692 | ||||||
| chr6:7172693
|
G | T | 2 | a0004c0006t0058g0048a0011c0015t0019g0182 | 2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-284-3962G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7172693 | ||||||
| chr6:7172698
|
GT | G | 31 | a0001c0001t0042g0187a0003c0002t0008g0128a0003c0002t0010g0251others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-284-3956delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7172698 | ||||||
| chr6:7172699
|
T | G | 72 | a0001c0001t0001g0097a0001c0001t0035g0034a0002c0004t0015g0044others(69): Show | 72 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.-284-3956T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7172699 | ||||||
| chr6:7172713
|
T | G | 119 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(116): Show | 119 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-284-3942T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7172713 | ||||||
| chr6:7172913
|
C | T | 1 | a0001c0001t0016g0280 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-284-3742C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7172913 | ||||||
| chr6:7173447
|
C | T | 1 | a0011c0041t0067g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-284-3208C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7173447 | ||||||
| chr6:7173504
|
GA | G | 9 | a0002c0007t0064g0143a0007c0011t0014g0199a0007c0011t0014g0200others(6): Show | 9 | HG00423.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-3137delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7173504 | |||||
| chr6:7173572
|
A | G | 285 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(282): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-284-3083A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7173572 | ||||||
| chr6:7173757
|
G | A | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-284-2898G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7173757 | ||||||
| chr6:7173765
|
CTTTCAGC others(13): Show |
C | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-284-2889_-284-287 others(24): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7173765 | ||||||
| chr6:7173815
|
G | A | 2 | a0004c0006t0031g0079a0012c0013t0031g0222 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-284-2840G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7173815 | ||||||
| chr6:7173828
|
G | A | 5 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0031t0068g0154others(2): Show | 5 | HG01109.hp1 HG01361.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-284-2827G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7173828 | ||||||
| chr6:7173915
|
T | C | 2 | a0007c0022t0019g0183a0007c0022t0019g0184 | 2 | HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-284-2740T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7173915 | ||||||
| chr6:7174093
|
C | A | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-284-2562C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7174093 | ||||||
| chr6:7174151
|
C | CTTT | 7 | a0001c0001t0042g0187a0003c0002t0002g0145a0003c0012t0004g0219others(4): Show | 7 | HG00280.hp1 HG00558.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.-284-2489_-284-248 others(7): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7174151 | |||||
| chr6:7174151
|
C | CTTTT | 77 | a0001c0001t0001g0097a0002c0004t0015g0044a0002c0004t0015g0203others(74): Show | 77 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-284-2490_-284-248 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7174151 | |||||
| chr6:7174151
|
C | CTTTTT | 6 | a0001c0001t0035g0034a0004c0006t0058g0048a0005c0003t0020g0137others(3): Show | 6 | HG01891.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-284-2491_-284-248 others(9): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7174151 | |||||
| chr6:7174151
|
CTT | C | 8 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0260others(5): Show | 8 | HG01243.hp1 HG01517.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-284-2488_-284-248 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr6 | 7174151 | |||||
| chr6:7174419
|
C | G | 88 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-284-2236C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7174419 | ||||||
| chr6:7174489
|
G | A | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-2166G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7174489 | ||||||
| chr6:7174575
|
T | C | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-284-2080T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7174575 | ||||||
| chr6:7175056
|
A | G | 1 | a0004c0052t0020g0005 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-284-1599A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7175056 | ||||||
| chr6:7175375
|
G | A | 1 | a0007c0011t0052g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-284-1280G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7175375 | ||||||
| chr6:7175378
|
G | C | 1 | a0005c0003t0012g0087 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-284-1277G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7175378 | ||||||
| chr6:7175496
|
G | A | 2 | a0002c0004t0022g0027a0002c0004t0022g0136 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-284-1159G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7175496 | ||||||
| chr6:7175549
|
C | T | 1 | a0006c0005t0004g0164 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-284-1106C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7175549 | ||||||
| chr6:7175557
|
G | C | 4 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0031t0068g0154others(1): Show | 4 | HG01109.hp1 HG01361.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284-1098G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7175557 | ||||||
| chr6:7175566
|
G | A | 2 | a0011c0015t0005g0010a0011c0015t0005g0013 | 2 | HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-284-1089G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7175566 | ||||||
| chr6:7175725
|
A | T | 4 | a0004c0006t0058g0048a0011c0015t0019g0182a0012c0013t0027g0228others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-284-930A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7175725 | ||||||
| chr6:7175982
|
A | G | 7 | a0004c0006t0058g0048a0005c0003t0033g0230a0005c0003t0033g0232others(4): Show | 7 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-284-673A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7175982 | ||||||
| chr6:7176062
|
G | A | 1 | a0005c0003t0054g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-284-593G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7176062 | ||||||
| chr6:7176142
|
C | G | 88 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-284-513C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7176142 | ||||||
| chr6:7176235
|
A | T | 2 | a0008c0010t0001g0003a0008c0010t0001g0288 | 2 | HG01978.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-284-420A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7176235 | ||||||
| chr6:7176361
|
G | C | 1 | a0003c0002t0002g0145 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-284-294G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7176361 | ||||||
| chr6:7176511
|
C | T | 68 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(65): Show | 68 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.-284-144C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7176511 | ||||||
| chr6:7176587
|
T | A | 1 | a0003c0002t0071g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-284-68T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7176587 | ||||||
| chr6:7176591
|
G | A | 9 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0260others(6): Show | 9 | HG01243.hp1 HG01517.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-284-64G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7176591 | ||||||
| chr6:7176603
|
A | G | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-284-52A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 1/12 | chr6 | 7176603 | ||||||
| chr6:7176795
|
C | T | 29 | a0001c0001t0001g0122a0001c0001t0001g0224a0002c0004t0003g0118others(26): Show | 29 | HG00438.hp2 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-166+22C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7176795 | ||||||
| chr6:7176796
|
G | A | 5 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0031t0068g0154others(2): Show | 5 | HG01109.hp1 HG01361.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.-166+23G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7176796 | ||||||
| chr6:7176907
|
T | G | 113 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(110): Show | 113 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-166+134T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7176907 | ||||||
| chr6:7176964
|
T | C | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-166+191T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7176964 | ||||||
| chr6:7177000
|
T | G | 1 | a0005c0014t0002g0114 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-166+227T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7177000 | ||||||
| chr6:7177014
|
C | T | 2 | a0004c0006t0031g0079a0012c0013t0031g0222 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-166+241C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7177014 | ||||||
| chr6:7177218
|
C | CA | 40 | a0001c0001t0001g0040a0001c0001t0001g0097a0001c0001t0001g0122others(37): Show | 40 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-166+469dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 7177218 | |||||
| chr6:7177218
|
C | CAA | 9 | a0002c0004t0022g0066a0006c0005t0004g0080a0006c0005t0004g0131others(6): Show | 9 | HG02080.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-166+468_-166+469d others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 7177218 | |||||
| chr6:7177218
|
CA | C | 17 | a0001c0001t0010g0147a0001c0001t0017g0166a0003c0002t0001g0124others(14): Show | 17 | HG01243.hp1 HG01517.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-166+469delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 7177218 | |||||
| chr6:7177326
|
C | T | 1 | a0008c0010t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-166+553C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7177326 | ||||||
| chr6:7177393
|
C | T | 3 | a0004c0006t0021g0051a0004c0006t0021g0105a0004c0006t0021g0117 | 3 | HG02922.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-166+620C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7177393 | ||||||
| chr6:7177574
|
G | T | 3 | a0007c0022t0019g0183a0007c0022t0019g0184a0035c0033t0081g0233 | 3 | HG01109.hp1 HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-166+801G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7177574 | ||||||
| chr6:7177591
|
A | G | 2 | a0002c0007t0007g0195a0003c0002t0010g0210 | 2 | NA18949.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-166+818A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7177591 | ||||||
| chr6:7177625
|
C | T | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-166+852C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7177625 | ||||||
| chr6:7177651
|
A | G | 87 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(84): Show | 87 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-166+878A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7177651 | ||||||
| chr6:7177843
|
C | G | 4 | a0001c0001t0001g0073a0003c0002t0002g0065a0003c0002t0002g0145others(1): Show | 4 | NA18612.hp2 NA18987.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-166+1070C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7177843 | ||||||
| chr6:7178043
|
A | G | 1 | a0011c0015t0019g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-166+1270A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7178043 | ||||||
| chr6:7178306
|
T | A | 109 | a0001c0001t0001g0097a0001c0001t0035g0034a0001c0001t0042g0187others(106): Show | 109 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-166+1533T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7178306 | ||||||
| chr6:7178415
|
T | A | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-166+1642T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7178415 | ||||||
| chr6:7178622
|
G | T | 9 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0260others(6): Show | 9 | HG01243.hp1 HG01517.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-166+1849G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7178622 | ||||||
| chr6:7178676
|
C | CT | 4 | a0004c0006t0058g0048a0011c0015t0019g0182a0012c0013t0027g0228others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-166+1910dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 7178676 | |||||
| chr6:7179051
|
T | C | 14 | a0001c0001t0017g0180a0003c0002t0010g0251a0003c0012t0013g0239others(11): Show | 14 | HG01243.hp1 HG01361.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.-165-2073T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7179051 | ||||||
| chr6:7179315
|
G | A | 9 | a0003c0002t0010g0251a0003c0012t0013g0239a0005c0003t0012g0260others(6): Show | 9 | HG01243.hp1 HG01517.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-165-1809G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7179315 | ||||||
| chr6:7179518
|
G | A | 88 | a0001c0001t0001g0097a0001c0001t0042g0187a0002c0004t0015g0044others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-165-1606G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7179518 | ||||||
| chr6:7179574
|
T | C | 65 | a0001c0001t0001g0097a0001c0001t0042g0187a0002c0004t0015g0044others(62): Show | 65 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-165-1550T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7179574 | ||||||
| chr6:7179742
|
A | T | 1 | a0005c0003t0056g0207 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-165-1382A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7179742 | ||||||
| chr6:7179796
|
G | GT | 106 | a0001c0001t0001g0097a0001c0001t0001g0224a0001c0001t0042g0187others(103): Show | 106 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-165-1316dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 7179796 | |||||
| chr6:7179808
|
T | TC | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-165-1315dupC | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr6 | 7179808 | |||||
| chr6:7179830
|
T | C | 5 | a0003c0002t0010g0251a0005c0003t0012g0260a0005c0003t0018g0001others(2): Show | 5 | HG01243.hp1 HG01517.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-165-1294T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7179830 | ||||||
| chr6:7179941
|
T | G | 1 | a0005c0003t0004g0047 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-165-1183T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7179941 | ||||||
| chr6:7179946
|
C | T | 89 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(86): Show | 89 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.-165-1178C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7179946 | ||||||
| chr6:7180122
|
C | T | 3 | a0009c0018t0003g0077a0009c0018t0003g0158a0009c0018t0008g0032 | 3 | NA18939.hp2 NA18979.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-165-1002C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7180122 | ||||||
| chr6:7180579
|
G | A | 1 | a0010c0035t0065g0208 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-165-545G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7180579 | ||||||
| chr6:7180819
|
G | A | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-165-305G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7180819 | ||||||
| chr6:7180947
|
G | A | 18 | a0003c0002t0010g0251a0005c0003t0012g0172a0005c0003t0012g0173others(15): Show | 18 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.-165-177G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7180947 | ||||||
| chr6:7180957
|
A | T | 1 | a0018c0071t0002g0167 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-165-167A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7180957 | ||||||
| chr6:7181049
|
T | C | 1 | a0007c0009t0005g0007 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-165-75T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 2/12 | chr6 | 7181049 | ||||||
| chr6:7181389
|
T | G | 1 | a0012c0013t0031g0222 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-43+143T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 3/12 | chr6 | 7181389 | ||||||
| chr6:7181502
|
A | G | 96 | a0001c0001t0001g0097a0001c0001t0042g0187a0002c0004t0015g0044others(93): Show | 96 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.-43+256A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 3/12 | chr6 | 7181502 | ||||||
| chr6:7181610
|
A | G | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-42-260A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 3/12 | chr6 | 7181610 | ||||||
| chr6:7181760
|
T | C | 69 | a0001c0001t0001g0097a0001c0001t0042g0187a0002c0004t0015g0044others(66): Show | 69 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-42-110T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 3/12 | chr6 | 7181760 | ||||||
| chr6:7181777
|
G | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0017t0001g0252 | 3 | HG01255.hp2 HG01934.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-42-93G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 3/12 | chr6 | 7181777 | ||||||
| chr6:7181782
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-42-88A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 3/12 | chr6 | 7181782 | ||||||
| chr6:7182137
|
G | A | 13 | a0005c0003t0012g0172a0005c0003t0012g0173a0007c0009t0005g0006others(10): Show | 13 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.171+55G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7182137 | ||||||
| chr6:7182390
|
A | G | 1 | a0008c0010t0001g0003 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.171+308A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7182390 | ||||||
| chr6:7182509
|
G | A | 2 | a0007c0009t0005g0008a0007c0009t0005g0009 | 2 | NA18952.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.171+427G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7182509 | ||||||
| chr6:7182565
|
T | C | 1 | a0002c0023t0048g0171 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.171+483T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7182565 | ||||||
| chr6:7182606
|
T | C | 1 | a0039c0070t0009g0016 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.171+524T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7182606 | ||||||
| chr6:7183290
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0010g0147 | 3 | HG02056.hp2 HG02523.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.171+1208G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7183290 | ||||||
| chr6:7183377
|
T | C | 1 | a0005c0003t0056g0207 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.171+1295T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7183377 | ||||||
| chr6:7183393
|
C | G | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.171+1311C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7183393 | ||||||
| chr6:7183465
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.171+1383C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7183465 | ||||||
| chr6:7183530
|
T | A | 1 | a0001c0001t0082g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.171+1448T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7183530 | ||||||
| chr6:7183617
|
T | C | 1 | a0004c0063t0003g0141 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.171+1535T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7183617 | ||||||
| chr6:7183686
|
C | T | 1 | a0006c0005t0004g0086 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.171+1604C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7183686 | ||||||
| chr6:7183696
|
T | G | 1 | a0003c0002t0023g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.171+1614T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7183696 | ||||||
| chr6:7183701
|
A | G | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.171+1619A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7183701 | ||||||
| chr6:7184002
|
A | C | 1 | a0003c0002t0001g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.171+1920A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184002 | ||||||
| chr6:7184039
|
A | C | 4 | a0005c0014t0002g0114a0005c0014t0010g0064a0005c0014t0018g0113others(1): Show | 4 | HG00558.hp2 HG02015.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+1957A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184039 | ||||||
| chr6:7184051
|
C | G | 1 | a0001c0001t0010g0147 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.171+1969C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184051 | ||||||
| chr6:7184210
|
C | T | 1 | a0008c0010t0001g0277 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.171+2128C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184210 | ||||||
| chr6:7184271
|
A | T | 5 | a0003c0002t0010g0251a0005c0003t0012g0260a0005c0003t0018g0001others(2): Show | 5 | HG01243.hp1 HG01517.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+2189A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184271 | ||||||
| chr6:7184274
|
A | AT | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+2200dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 7184274 | |||||
| chr6:7184274
|
A | T | 5 | a0003c0002t0010g0251a0005c0003t0012g0260a0005c0003t0018g0001others(2): Show | 5 | HG01243.hp1 HG01517.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+2192A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184274 | ||||||
| chr6:7184282
|
T | A | 3 | a0012c0013t0080g0234a0014c0020t0034g0236a0014c0020t0034g0237 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.171+2200T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184282 | ||||||
| chr6:7184371
|
T | A | 1 | a0005c0003t0012g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.171+2289T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184371 | ||||||
| chr6:7184373
|
T | G | 9 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0039g0002others(6): Show | 9 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+2291T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184373 | ||||||
| chr6:7184406
|
C | CT | 75 | a0001c0001t0001g0097a0001c0001t0017g0214a0001c0001t0042g0187others(72): Show | 75 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.171+2337dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 7184406 | |||||
| chr6:7184406
|
CT | C | 22 | a0001c0001t0001g0073a0003c0002t0023g0175a0004c0006t0058g0048others(19): Show | 22 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.171+2337delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 7184406 | |||||
| chr6:7184496
|
C | T | 2 | a0007c0022t0019g0183a0007c0022t0019g0184 | 2 | HG01361.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.171+2414C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184496 | ||||||
| chr6:7184580
|
A | T | 21 | a0003c0002t0023g0175a0004c0006t0058g0048a0005c0003t0033g0230others(18): Show | 21 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.171+2498A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184580 | ||||||
| chr6:7184747
|
T | C | 9 | a0003c0002t0023g0175a0004c0006t0058g0048a0005c0003t0033g0230others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+2665T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184747 | ||||||
| chr6:7184826
|
T | A | 1 | a0028c0054t0007g0029 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.172-2608T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184826 | ||||||
| chr6:7184827
|
A | T | 1 | a0002c0007t0007g0116 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.172-2607A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184827 | ||||||
| chr6:7184903
|
C | T | 1 | a0005c0003t0012g0087 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.172-2531C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184903 | ||||||
| chr6:7184924
|
A | G | 9 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0039g0002others(6): Show | 9 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.172-2510A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7184924 | ||||||
| chr6:7185029
|
A | G | 291 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.172-2405A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7185029 | ||||||
| chr6:7185328
|
G | A | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.172-2106G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7185328 | ||||||
| chr6:7185340
|
C | T | 4 | a0004c0008t0001g0265a0004c0008t0001g0266a0004c0008t0001g0267others(1): Show | 4 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-2094C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7185340 | ||||||
| chr6:7185378
|
T | C | 2 | a0005c0003t0004g0037a0029c0053t0062g0057 | 2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.172-2056T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7185378 | ||||||
| chr6:7185581
|
A | G | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.172-1853A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7185581 | ||||||
| chr6:7185724
|
C | T | 4 | a0005c0003t0012g0260a0005c0003t0018g0001a0005c0003t0046g0258others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1710C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7185724 | ||||||
| chr6:7185828
|
G | A | 1 | a0003c0002t0071g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.172-1606G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7185828 | ||||||
| chr6:7186025
|
G | T | 1 | a0003c0032t0057g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.172-1409G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186025 | ||||||
| chr6:7186060
|
C | T | 1 | a0002c0004t0003g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.172-1374C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186060 | ||||||
| chr6:7186123
|
C | T | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.172-1311C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186123 | ||||||
| chr6:7186141
|
A | G | 2 | a0014c0020t0034g0236a0014c0020t0034g0237 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.172-1293A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186141 | ||||||
| chr6:7186471
|
C | T | 1 | a0005c0003t0004g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.172-963C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186471 | ||||||
| chr6:7186567
|
C | T | 1 | a0017c0027t0077g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.172-867C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186567 | ||||||
| chr6:7186568
|
G | A | 9 | a0004c0006t0006g0257a0004c0008t0001g0265a0004c0008t0001g0266others(6): Show | 9 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.172-866G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186568 | ||||||
| chr6:7186649
|
T | C | 1 | a0002c0007t0064g0143 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.172-785T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186649 | ||||||
| chr6:7186665
|
T | C | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.172-769T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186665 | ||||||
| chr6:7186670
|
G | A | 2 | a0004c0006t0031g0079a0012c0013t0031g0222 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.172-764G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186670 | ||||||
| chr6:7186700
|
A | G | 2 | a0006c0005t0009g0144a0006c0016t0009g0115 | 2 | NA18984.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.172-734A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186700 | ||||||
| chr6:7186782
|
G | T | 1 | a0005c0003t0004g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.172-652G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186782 | ||||||
| chr6:7186828
|
A | T | 1 | a0007c0011t0052g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.172-606A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7186828 | ||||||
| chr6:7187013
|
T | C | 21 | a0003c0002t0023g0175a0004c0006t0058g0048a0005c0003t0033g0230others(18): Show | 21 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.172-421T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7187013 | ||||||
| chr6:7187045
|
T | G | 1 | a0006c0005t0043g0100 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.172-389T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7187045 | ||||||
| chr6:7187078
|
G | A | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.172-356G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | chr6 | 7187078 | ||||||
| chr6:7187109
|
GATT | G | 14 | a0003c0002t0010g0251a0005c0003t0012g0260a0005c0003t0018g0001others(11): Show | 14 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.172-320_172-318del others(3): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr6 | 7187109 | |||||
| chr6:7187528
|
A | C | 1 | a0009c0026t0003g0088 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.261+5A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7187528 | ||||||
| chr6:7187540
|
C | CTTTTA | 86 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0054others(83): Show | 86 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.261+63_261+67dupTT others(3): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7187540 | |||||
| chr6:7187540
|
C | CTTTTATT others(3): Show |
16 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0001t0002g0268others(13): Show | 16 | HG01099.hp1 HG01496.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.261+58_261+67dupTT others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7187540 | |||||
| chr6:7187540
|
C | CTTTTATT others(8): Show |
3 | a0003c0044t0066g0042a0006c0005t0009g0144a0006c0016t0009g0115 | 3 | NA18984.hp2 NA18995.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.261+53_261+67dupTT others(13): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7187540 | |||||
| chr6:7187540
|
CTTTTA | C | 34 | a0001c0001t0010g0147a0001c0001t0016g0280a0002c0004t0003g0130others(31): Show | 34 | HG00639.hp2 HG01099.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.261+63_261+67delTT others(3): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7187540 | |||||
| chr6:7187540
|
CTTTTATT others(3): Show |
C | 9 | a0003c0002t0001g0129a0005c0003t0012g0172a0005c0003t0012g0173others(6): Show | 9 | HG00738.hp1 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+58_261+67delTT others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7187540 | |||||
| chr6:7187540
|
CTTTTATT others(8): Show |
C | 1 | a0006c0005t0004g0041 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.261+53_261+67delTT others(13): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7187540 | |||||
| chr6:7187540
|
CTTTTATT others(13): Show |
C | 2 | a0022c0048t0006g0197a0035c0033t0081g0233 | 2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.261+48_261+67delTT others(18): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7187540 | |||||
| chr6:7187642
|
C | G | 2 | a0004c0006t0031g0079a0012c0013t0031g0222 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.261+119C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7187642 | ||||||
| chr6:7187759
|
G | C | 1 | a0003c0012t0003g0205 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.261+236G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7187759 | ||||||
| chr6:7187788
|
A | T | 1 | a0006c0016t0009g0024 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.261+265A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7187788 | ||||||
| chr6:7187941
|
A | G | 2 | a0003c0002t0001g0124a0003c0040t0001g0103 | 2 | NA18951.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.261+418A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7187941 | ||||||
| chr6:7188094
|
G | A | 59 | a0001c0001t0001g0097a0001c0001t0042g0187a0002c0004t0015g0044others(56): Show | 59 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.261+571G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188094 | ||||||
| chr6:7188226
|
C | CGT | 22 | a0001c0001t0001g0033a0001c0001t0016g0280a0001c0001t0017g0214others(19): Show | 22 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+729_261+730dup others(2): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188226 | |||||
| chr6:7188226
|
C | CGTGT | 99 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(96): Show | 99 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.261+727_261+730dup others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188226 | |||||
| chr6:7188226
|
C | CGTGTGT | 23 | a0001c0001t0001g0111a0001c0001t0001g0255a0001c0001t0002g0248others(20): Show | 23 | HG00423.hp1 HG01099.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.261+725_261+730dup others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188226 | |||||
| chr6:7188226
|
C | CGTGTGTG others(1): Show |
17 | a0001c0001t0001g0253a0001c0001t0001g0283a0001c0001t0002g0069others(14): Show | 17 | HG00140.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.261+723_261+730dup others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188226 | |||||
| chr6:7188226
|
C | CGTGTGTG others(3): Show |
1 | a0005c0003t0054g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.261+721_261+730dup others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188226 | |||||
| chr6:7188226
|
CGT | C | 4 | a0002c0004t0003g0052a0003c0002t0004g0015a0005c0003t0079g0231others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+729_261+730del others(2): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188226 | |||||
| chr6:7188226
|
CGTGT | C | 12 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(9): Show | 12 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+727_261+730del others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188226 | |||||
| chr6:7188226
|
CGTGTGTG others(1): Show |
C | 64 | a0001c0001t0001g0097a0001c0001t0042g0187a0002c0004t0015g0044others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.261+723_261+730del others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188226 | |||||
| chr6:7188226
|
CGTGTGTG others(3): Show |
C | 1 | a0026c0057t0014g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.261+721_261+730del others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188226 | |||||
| chr6:7188252
|
T | C | 6 | a0003c0002t0010g0251a0004c0052t0020g0005a0005c0003t0012g0260others(3): Show | 6 | HG00438.hp1 HG01243.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+729T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188252 | ||||||
| chr6:7188252
|
T | TGTGTGTG others(3): Show |
1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.261+730_261+731ins others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188252 | |||||
| chr6:7188252
|
T | TGTGTGTG others(7): Show |
1 | a0007c0022t0019g0184 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.261+730_261+731ins others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188252 | |||||
| chr6:7188252
|
T | TGTGTGTG others(9): Show |
1 | a0007c0022t0019g0183 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.261+730_261+731ins others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188252 | |||||
| chr6:7188252
|
TGC | T | 3 | a0004c0006t0007g0281a0013c0019t0010g0256a0013c0019t0049g0262 | 3 | HG00735.hp1 HG00738.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.261+738_261+739del others(2): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188252 | |||||
| chr6:7188254
|
C | T | 136 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(133): Show | 136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.261+731C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188254 | ||||||
| chr6:7188255
|
G | A | 1 | a0010c0035t0065g0208 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.261+732G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188255 | ||||||
| chr6:7188258
|
C | T | 1 | a0010c0021t0006g0250 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.261+735C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188258 | ||||||
| chr6:7188271
|
G | C | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.261+748G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188271 | ||||||
| chr6:7188273
|
C | T | 2 | a0002c0004t0026g0261a0034c0039t0026g0249 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.261+750C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188273 | ||||||
| chr6:7188295
|
G | A | 2 | a0002c0007t0007g0218a0002c0007t0063g0217 | 2 | HG02155.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.261+772G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188295 | ||||||
| chr6:7188313
|
C | T | 66 | a0001c0001t0001g0097a0001c0001t0042g0187a0002c0004t0015g0044others(63): Show | 66 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.261+790C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188313 | ||||||
| chr6:7188375
|
C | T | 1 | a0004c0063t0003g0141 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.262-784C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188375 | ||||||
| chr6:7188400
|
A | G | 266 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0040others(263): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.262-759A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188400 | ||||||
| chr6:7188429
|
T | G | 1 | a0007c0009t0005g0008 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.262-730T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188429 | ||||||
| chr6:7188545
|
CCTT | C | 11 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(8): Show | 11 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.262-608_262-606del others(3): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr6 | 7188545 | |||||
| chr6:7188581
|
A | G | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.262-578A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188581 | ||||||
| chr6:7188614
|
C | T | 1 | a0004c0068t0073g0273 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.262-545C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188614 | ||||||
| chr6:7188697
|
G | A | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.262-462G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188697 | ||||||
| chr6:7188706
|
A | G | 1 | a0003c0002t0010g0251 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.262-453A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188706 | ||||||
| chr6:7188761
|
G | A | 1 | a0003c0032t0057g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262-398G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188761 | ||||||
| chr6:7188836
|
C | T | 2 | a0002c0004t0003g0052a0011c0041t0067g0055 | 2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.262-323C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188836 | ||||||
| chr6:7188888
|
C | A | 6 | a0003c0002t0023g0175a0005c0003t0004g0037a0005c0003t0033g0230others(3): Show | 6 | HG02615.hp1 HG02818.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-271C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188888 | ||||||
| chr6:7188968
|
C | T | 2 | a0003c0002t0001g0124a0003c0040t0001g0103 | 2 | NA18951.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.262-191C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7188968 | ||||||
| chr6:7189064
|
T | G | 1 | a0002c0004t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.262-95T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7189064 | ||||||
| chr6:7189136
|
G | A | 1 | a0002c0004t0003g0148 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.262-23G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 5/12 | chr6 | 7189136 | ||||||
| chr6:7189334
|
C | T | 11 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0039g0002others(8): Show | 11 | HG00558.hp1 HG01074.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.425+12C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7189334 | ||||||
| chr6:7189499
|
G | A | 15 | a0003c0002t0023g0175a0004c0006t0058g0048a0007c0011t0014g0199others(12): Show | 15 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.425+177G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7189499 | ||||||
| chr6:7189537
|
A | G | 1 | a0003c0002t0071g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.425+215A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7189537 | ||||||
| chr6:7189568
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.425+246T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7189568 | ||||||
| chr6:7189625
|
G | A | 96 | a0001c0001t0017g0180a0001c0001t0017g0214a0002c0004t0003g0052others(93): Show | 96 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.425+303G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7189625 | ||||||
| chr6:7189648
|
A | G | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.425+326A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7189648 | ||||||
| chr6:7190152
|
C | G | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.425+830C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7190152 | ||||||
| chr6:7190281
|
A | AT | 14 | a0001c0001t0001g0098a0001c0001t0017g0166a0004c0006t0058g0048others(11): Show | 14 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.425+967dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7190281 | |||||
| chr6:7190295
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.425+973A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7190295 | ||||||
| chr6:7190344
|
G | A | 1 | a0027c0055t0002g0068 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.425+1022G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7190344 | ||||||
| chr6:7190424
|
G | A | 12 | a0004c0006t0058g0048a0007c0011t0014g0199a0007c0011t0014g0200others(9): Show | 12 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.425+1102G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7190424 | ||||||
| chr6:7190474
|
A | T | 12 | a0004c0006t0058g0048a0007c0011t0014g0199a0007c0011t0014g0200others(9): Show | 12 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.425+1152A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7190474 | ||||||
| chr6:7190554
|
G | A | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.425+1232G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7190554 | ||||||
| chr6:7190587
|
T | C | 1 | a0001c0001t0042g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.425+1265T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7190587 | ||||||
| chr6:7190707
|
T | TA | 12 | a0004c0006t0058g0048a0007c0011t0014g0199a0007c0011t0014g0200others(9): Show | 12 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.425+1386dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7190707 | |||||
| chr6:7190803
|
A | T | 3 | a0004c0006t0021g0051a0004c0006t0021g0105a0004c0006t0021g0117 | 3 | HG02922.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.425+1481A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7190803 | ||||||
| chr6:7191221
|
AT | A | 15 | a0004c0006t0058g0048a0007c0011t0014g0199a0007c0011t0014g0200others(12): Show | 15 | HG01433.hp1 HG02258.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.425+1911delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7191221 | |||||
| chr6:7191291
|
G | C | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.425+1969G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7191291 | ||||||
| chr6:7191302
|
G | T | 6 | a0003c0002t0023g0175a0003c0002t0074g0190a0011c0041t0067g0055others(3): Show | 6 | HG02257.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.425+1980G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7191302 | ||||||
| chr6:7191438
|
C | T | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.425+2116C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7191438 | ||||||
| chr6:7191507
|
A | C | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.425+2185A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7191507 | ||||||
| chr6:7191528
|
C | T | 4 | a0005c0003t0012g0260a0005c0003t0018g0001a0005c0003t0046g0258others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.425+2206C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7191528 | ||||||
| chr6:7191707
|
T | G | 1 | a0001c0001t0002g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.425+2385T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7191707 | ||||||
| chr6:7192116
|
A | ATT | 6 | a0003c0002t0023g0175a0003c0002t0074g0190a0011c0041t0067g0055others(3): Show | 6 | HG02257.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.425+2820_425+2821d others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7192116 | |||||
| chr6:7192116
|
A | ATTTTT | 28 | a0003c0012t0011g0119a0004c0050t0006g0049a0004c0052t0020g0005others(25): Show | 28 | HG00438.hp1 HG01071.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.425+2817_425+2821d others(7): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7192116 | |||||
| chr6:7192116
|
A | ATTTTTT | 24 | a0004c0006t0058g0048a0005c0003t0004g0047a0005c0003t0004g0220others(21): Show | 24 | HG00423.hp2 HG00558.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.425+2816_425+2821d others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7192116 | |||||
| chr6:7192116
|
AT | A | 96 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0040others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.425+2821delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7192116 | |||||
| chr6:7192116
|
ATT | A | 96 | a0001c0001t0001g0098a0001c0001t0001g0224a0001c0001t0001g0253others(93): Show | 96 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.425+2820_425+2821d others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7192116 | |||||
| chr6:7192116
|
ATTTTTTT others(3): Show |
A | 1 | a0002c0004t0008g0039 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.425+2812_425+2821d others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7192116 | |||||
| chr6:7192237
|
G | C | 4 | a0005c0003t0012g0260a0005c0003t0018g0001a0005c0003t0046g0258others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.425+2915G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192237 | ||||||
| chr6:7192268
|
C | T | 23 | a0001c0001t0042g0187a0004c0006t0006g0021a0004c0006t0006g0072others(20): Show | 23 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.425+2946C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192268 | ||||||
| chr6:7192393
|
A | G | 2 | a0005c0003t0012g0087a0025c0060t0012g0227 | 2 | HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.425+3071A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192393 | ||||||
| chr6:7192401
|
C | T | 49 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(46): Show | 49 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.425+3079C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192401 | ||||||
| chr6:7192405
|
C | T | 4 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.425+3083C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192405 | ||||||
| chr6:7192553
|
T | C | 165 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(162): Show | 165 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.425+3231T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192553 | ||||||
| chr6:7192653
|
T | C | 1 | a0002c0007t0063g0217 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.425+3331T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192653 | ||||||
| chr6:7192736
|
T | G | 165 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(162): Show | 165 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.425+3414T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192736 | ||||||
| chr6:7192933
|
C | T | 1 | a0005c0003t0054g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.425+3611C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192933 | ||||||
| chr6:7192940
|
G | A | 1 | a0027c0055t0002g0068 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.425+3618G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192940 | ||||||
| chr6:7192961
|
A | G | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.425+3639A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7192961 | ||||||
| chr6:7193100
|
T | A | 1 | a0002c0004t0022g0066 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.425+3778T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7193100 | ||||||
| chr6:7193272
|
T | C | 1 | a0003c0002t0003g0229 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.425+3950T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7193272 | ||||||
| chr6:7193327
|
G | A | 4 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.425+4005G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7193327 | ||||||
| chr6:7193710
|
C | T | 1 | a0003c0012t0004g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.425+4388C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7193710 | ||||||
| chr6:7193733
|
A | G | 4 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.425+4411A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7193733 | ||||||
| chr6:7193949
|
A | G | 73 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(70): Show | 73 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.425+4627A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7193949 | ||||||
| chr6:7193953
|
GA | G | 68 | a0003c0012t0013g0239a0004c0050t0006g0049a0004c0052t0020g0005others(65): Show | 68 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.425+4638delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7193953 | |||||
| chr6:7194008
|
A | T | 1 | a0006c0005t0009g0133 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.425+4686A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194008 | ||||||
| chr6:7194062
|
A | G | 1 | a0004c0006t0058g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.425+4740A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194062 | ||||||
| chr6:7194097
|
C | G | 1 | a0005c0003t0046g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.425+4775C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194097 | ||||||
| chr6:7194120
|
C | G | 1 | a0001c0001t0001g0033 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.425+4798C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194120 | ||||||
| chr6:7194178
|
T | C | 89 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(86): Show | 89 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.425+4856T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194178 | ||||||
| chr6:7194265
|
A | G | 1 | a0011c0041t0067g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.425+4943A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194265 | ||||||
| chr6:7194365
|
C | T | 72 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(69): Show | 72 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.425+5043C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194365 | ||||||
| chr6:7194524
|
G | C | 4 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.425+5202G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194524 | ||||||
| chr6:7194650
|
C | T | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425+5328C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194650 | ||||||
| chr6:7194685
|
T | C | 1 | a0010c0036t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.425+5363T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194685 | ||||||
| chr6:7194776
|
G | A | 50 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(47): Show | 50 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.425+5454G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194776 | ||||||
| chr6:7194924
|
T | G | 1 | a0005c0003t0004g0132 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.425+5602T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7194924 | ||||||
| chr6:7195451
|
C | T | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.425+6129C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7195451 | ||||||
| chr6:7195483
|
T | C | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.425+6161T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7195483 | ||||||
| chr6:7195503
|
G | A | 1 | a0007c0009t0053g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.425+6181G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7195503 | ||||||
| chr6:7195503
|
G | T | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425+6181G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7195503 | ||||||
| chr6:7195786
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.425+6464A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7195786 | ||||||
| chr6:7195823
|
G | A | 66 | a0003c0012t0013g0239a0004c0050t0006g0049a0004c0052t0020g0005others(63): Show | 66 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.425+6501G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7195823 | ||||||
| chr6:7195837
|
C | T | 1 | a0002c0004t0003g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.425+6515C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7195837 | ||||||
| chr6:7195964
|
A | G | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425+6642A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7195964 | ||||||
| chr6:7196026
|
A | G | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.425+6704A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196026 | ||||||
| chr6:7196084
|
C | A | 3 | a0004c0006t0058g0048a0012c0013t0027g0228a0030c0047t0027g0209 | 3 | HG02572.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.425+6762C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196084 | ||||||
| chr6:7196090
|
G | T | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.425+6768G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196090 | ||||||
| chr6:7196091
|
C | T | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.425+6769C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196091 | ||||||
| chr6:7196112
|
C | T | 1 | a0003c0002t0074g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.425+6790C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196112 | ||||||
| chr6:7196170
|
A | C | 2 | a0004c0006t0007g0138a0015c0024t0055g0025 | 2 | HG02155.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.425+6848A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196170 | ||||||
| chr6:7196207
|
T | G | 13 | a0001c0001t0001g0111a0001c0001t0001g0155a0001c0001t0017g0096others(10): Show | 13 | HG00735.hp1 HG01071.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.425+6885T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196207 | ||||||
| chr6:7196217
|
C | T | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.425+6895C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196217 | ||||||
| chr6:7196218
|
GT | G | 168 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(165): Show | 168 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.425+6908delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7196218 | |||||
| chr6:7196218
|
GTTTTTTT others(8): Show |
G | 2 | a0006c0005t0004g0080a0006c0005t0004g0164 | 2 | NA18990.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.425+6909_425+6923d others(17): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7196218 | |||||
| chr6:7196220
|
TTTTTTTT others(4): Show |
T | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.425+6909_425+6919d others(13): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7196220 | |||||
| chr6:7196230
|
T | G | 24 | a0001c0001t0001g0040a0001c0001t0001g0122a0001c0001t0001g0285others(21): Show | 24 | HG01169.hp1 HG01433.hp1 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.425+6908T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196230 | ||||||
| chr6:7196231
|
G | T | 26 | a0001c0001t0001g0040a0001c0001t0001g0122a0001c0001t0001g0285others(23): Show | 26 | HG01169.hp1 HG01433.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.425+6909G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196231 | ||||||
| chr6:7196232
|
T | G | 1 | a0004c0006t0018g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.425+6910T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196232 | ||||||
| chr6:7196236
|
T | G | 1 | a0006c0005t0009g0144 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.425+6914T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196236 | ||||||
| chr6:7196410
|
C | G | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.425+7088C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196410 | ||||||
| chr6:7196552
|
G | A | 1 | a0002c0007t0064g0143 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.425+7230G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196552 | ||||||
| chr6:7196606
|
G | C | 3 | a0006c0005t0004g0084a0006c0005t0004g0085a0006c0005t0004g0086 | 3 | NA18946.hp2 NA18949.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.425+7284G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7196606 | ||||||
| chr6:7197113
|
G | A | 141 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(138): Show | 141 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.425+7791G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7197113 | ||||||
| chr6:7197321
|
A | C | 3 | a0004c0006t0058g0048a0012c0013t0027g0228a0030c0047t0027g0209 | 3 | HG02572.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.425+7999A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7197321 | ||||||
| chr6:7197501
|
A | G | 4 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.425+8179A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7197501 | ||||||
| chr6:7197713
|
A | G | 1 | a0003c0032t0057g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.425+8391A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7197713 | ||||||
| chr6:7198056
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.425+8734A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7198056 | ||||||
| chr6:7198486
|
C | G | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.425+9164C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7198486 | ||||||
| chr6:7198740
|
A | C | 78 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(75): Show | 78 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.425+9418A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7198740 | ||||||
| chr6:7198956
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.425+9634T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7198956 | ||||||
| chr6:7199106
|
T | C | 4 | a0002c0004t0015g0044a0002c0004t0015g0203a0002c0004t0015g0204others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.425+9784T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7199106 | ||||||
| chr6:7199299
|
A | T | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.425+9977A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7199299 | ||||||
| chr6:7199519
|
G | T | 2 | a0003c0002t0002g0189a0003c0002t0029g0186 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.425+10197G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7199519 | ||||||
| chr6:7199766
|
C | T | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.425+10444C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7199766 | ||||||
| chr6:7199950
|
C | G | 1 | a0001c0001t0017g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.425+10628C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7199950 | ||||||
| chr6:7200098
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.426-10706G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200098 | ||||||
| chr6:7200099
|
A | G | 1 | a0008c0065t0001g0275 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.426-10705A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200099 | ||||||
| chr6:7200114
|
T | C | 71 | a0003c0012t0011g0119a0003c0012t0013g0239a0004c0050t0006g0049others(68): Show | 71 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.426-10690T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200114 | ||||||
| chr6:7200117
|
T | C | 1 | a0005c0003t0004g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.426-10687T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200117 | ||||||
| chr6:7200218
|
G | GTA | 6 | a0005c0003t0013g0159a0006c0005t0009g0144a0006c0016t0009g0024others(3): Show | 6 | NA18942.hp1 NA18984.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.426-10574_426-1057 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200218 | |||||
| chr6:7200218
|
GTA | G | 4 | a0002c0007t0007g0218a0007c0022t0019g0183a0007c0022t0019g0184others(1): Show | 4 | HG01361.hp1 HG01891.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-10574_426-1057 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200218 | |||||
| chr6:7200220
|
A | G | 10 | a0002c0004t0007g0030a0002c0007t0007g0110a0002c0007t0007g0116others(7): Show | 10 | HG00621.hp1 HG01123.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.426-10584A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200220 | ||||||
| chr6:7200242
|
A | ATGTGTGT others(5): Show |
1 | a0003c0040t0001g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.426-10561_426-1056 others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200242 | |||||
| chr6:7200242
|
A | G | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.426-10562A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200242 | ||||||
| chr6:7200242
|
ATATGTGT others(5): Show |
A | 1 | a0006c0005t0041g0156 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.426-10560_426-1054 others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200242 | |||||
| chr6:7200244
|
A | ATG | 18 | a0001c0001t0001g0224a0001c0001t0002g0069a0002c0004t0003g0052others(15): Show | 18 | HG00423.hp1 HG00639.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.426-10524_426-1052 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
A | ATGTG | 12 | a0002c0046t0003g0078a0003c0002t0002g0189a0003c0002t0029g0186others(9): Show | 12 | HG01515.hp2 HG02735.hp1 HG03490.hp1 others(9): Show |
intron_variant | MODIFIER | c.426-10526_426-1052 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
A | ATGTGTG | 4 | a0003c0002t0002g0074a0007c0009t0005g0246a0007c0009t0005g0247others(1): Show | 4 | HG00140.hp1 HG00735.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-10528_426-1052 others(10): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
A | ATGTGTGT others(1): Show |
14 | a0003c0002t0001g0124a0003c0002t0002g0020a0003c0002t0002g0145others(11): Show | 14 | HG00558.hp1 HG00735.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.426-10530_426-1052 others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
A | ATGTGTGT others(3): Show |
5 | a0003c0002t0002g0102a0003c0002t0002g0142a0003c0002t0010g0067others(2): Show | 5 | HG01943.hp1 HG02083.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-10532_426-1052 others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
A | ATGTGTGT others(5): Show |
4 | a0003c0002t0002g0065a0003c0002t0002g0076a0004c0068t0073g0273others(1): Show | 4 | HG01167.hp1 NA18612.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.426-10534_426-1052 others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
A | ATGTGTGT others(7): Show |
4 | a0003c0002t0002g0063a0003c0002t0029g0062a0003c0045t0002g0070others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-10536_426-1052 others(18): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
A | G | 2 | a0003c0040t0001g0103a0010c0028t0006g0019 | 2 | HG01433.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.426-10560A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200244 | ||||||
| chr6:7200244
|
ATG | A | 16 | a0002c0004t0026g0261a0002c0007t0007g0110a0002c0007t0007g0116others(13): Show | 16 | HG00741.hp2 HG01109.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.426-10524_426-1052 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
ATGTGTGT others(1): Show |
A | 12 | a0005c0056t0010g0196a0007c0011t0014g0199a0007c0011t0014g0200others(9): Show | 12 | HG01074.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.426-10530_426-1052 others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
ATGTGTGT others(3): Show |
A | 3 | a0006c0005t0030g0193a0006c0005t0030g0194a0006c0005t0075g0192 | 3 | NA18970.hp2 NA19083.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.426-10532_426-1052 others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200244
|
ATGTGTGT others(5): Show |
A | 2 | a0006c0005t0004g0041a0027c0055t0002g0068 | 2 | HG01071.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.426-10534_426-1052 others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200244 | |||||
| chr6:7200270
|
GTGTGTGT others(5): Show |
G | 2 | a0005c0003t0020g0091a0005c0003t0020g0137 | 2 | NA18982.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.426-10532_426-1052 others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200270 | |||||
| chr6:7200271
|
TGTGTGTG others(4): Show |
T | 56 | a0003c0012t0011g0119a0003c0012t0013g0239a0004c0050t0006g0049others(53): Show | 56 | HG00423.hp2 HG00438.hp1 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.426-10532_426-1052 others(15): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200271 | ||||||
| chr6:7200273
|
TGTGTGTG others(2): Show |
T | 11 | a0003c0002t0023g0175a0003c0002t0074g0190a0005c0003t0013g0240others(8): Show | 11 | HG00558.hp2 HG02015.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.426-10530_426-1052 others(13): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200273 | ||||||
| chr6:7200280
|
G | A | 56 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0040others(53): Show | 56 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.426-10524G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200280 | ||||||
| chr6:7200280
|
G | GTGTA | 4 | a0004c0006t0021g0051a0004c0006t0021g0105a0004c0006t0021g0117others(1): Show | 4 | HG02922.hp1 HG03041.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.426-10523_426-1052 others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200280 | |||||
| chr6:7200280
|
G | T | 2 | a0004c0006t0007g0245a0015c0066t0003g0276 | 2 | HG01175.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.426-10524G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200280 | ||||||
| chr6:7200282
|
A | ATT | 10 | a0001c0001t0001g0017a0001c0001t0001g0054a0001c0001t0002g0248others(7): Show | 10 | HG01192.hp2 HG01255.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.426-10510_426-1050 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7200282 | |||||
| chr6:7200282
|
A | G | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.426-10522A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200282 | ||||||
| chr6:7200282
|
A | T | 61 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0040others(58): Show | 61 | HG00280.hp1 HG00621.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.426-10522A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200282 | ||||||
| chr6:7200283
|
T | A | 67 | a0003c0002t0023g0175a0003c0002t0074g0190a0003c0012t0011g0119others(64): Show | 67 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.426-10521T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200283 | ||||||
| chr6:7200284
|
T | A | 2 | a0005c0003t0020g0091a0005c0003t0020g0137 | 2 | NA18982.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.426-10520T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200284 | ||||||
| chr6:7200285
|
T | A | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.426-10519T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200285 | ||||||
| chr6:7200317
|
C | G | 1 | a0025c0060t0012g0227 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.426-10487C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200317 | ||||||
| chr6:7200338
|
C | T | 1 | a0002c0007t0007g0218 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.426-10466C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7200338 | ||||||
| chr6:7201063
|
G | T | 1 | a0011c0015t0005g0013 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.426-9741G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201063 | ||||||
| chr6:7201170
|
A | G | 7 | a0003c0012t0011g0119a0005c0003t0004g0047a0005c0003t0004g0081others(4): Show | 7 | HG02040.hp2 HG02056.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.426-9634A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201170 | ||||||
| chr6:7201190
|
T | C | 1 | a0003c0002t0002g0076 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.426-9614T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201190 | ||||||
| chr6:7201427
|
T | C | 222 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(219): Show | 222 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.426-9377T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201427 | ||||||
| chr6:7201494
|
T | TC | 53 | a0001c0001t0001g0023a0001c0001t0001g0253a0001c0001t0001g0283others(50): Show | 53 | HG00558.hp1 HG00621.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.426-9299dupC | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7201494 | |||||
| chr6:7201494
|
TC | T | 15 | a0001c0001t0001g0054a0003c0002t0023g0175a0003c0002t0074g0190others(12): Show | 15 | HG01433.hp1 HG02074.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.426-9299delC | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7201494 | |||||
| chr6:7201495
|
C | T | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.426-9309C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201495 | ||||||
| chr6:7201499
|
C | G | 1 | a0005c0003t0046g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.426-9305C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201499 | ||||||
| chr6:7201499
|
C | T | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.426-9305C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201499 | ||||||
| chr6:7201502
|
C | A | 1 | a0005c0014t0002g0114 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.426-9302C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201502 | ||||||
| chr6:7201504
|
C | G | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.426-9300C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201504 | ||||||
| chr6:7201506
|
A | C | 2 | a0012c0013t0027g0228a0030c0047t0027g0209 | 2 | HG02572.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.426-9298A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201506 | ||||||
| chr6:7201579
|
G | A | 1 | a0006c0005t0004g0131 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.426-9225G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7201579 | ||||||
| chr6:7201991
|
T | TA | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.426-8812dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7201991 | |||||
| chr6:7202045
|
T | C | 2 | a0007c0009t0005g0246a0007c0009t0005g0247 | 2 | HG00140.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.426-8759T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7202045 | ||||||
| chr6:7202086
|
C | G | 73 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(70): Show | 73 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.426-8718C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7202086 | ||||||
| chr6:7202086
|
C | T | 1 | a0002c0004t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.426-8718C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7202086 | ||||||
| chr6:7202164
|
C | T | 1 | a0004c0006t0058g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.426-8640C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7202164 | ||||||
| chr6:7202211
|
C | T | 3 | a0004c0006t0018g0056a0016c0025t0018g0179a0019c0049t0002g0061 | 3 | HG02280.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.426-8593C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7202211 | ||||||
| chr6:7202771
|
C | T | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.426-8033C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7202771 | ||||||
| chr6:7202893
|
C | T | 1 | a0005c0003t0004g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.426-7911C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7202893 | ||||||
| chr6:7202924
|
G | A | 1 | a0003c0002t0003g0120 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.426-7880G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7202924 | ||||||
| chr6:7203049
|
G | A | 2 | a0011c0015t0005g0010a0011c0015t0005g0013 | 2 | HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.426-7755G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203049 | ||||||
| chr6:7203097
|
G | A | 1 | a0002c0004t0008g0216 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.426-7707G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203097 | ||||||
| chr6:7203174
|
T | C | 3 | a0003c0002t0002g0020a0003c0002t0002g0145a0040c0069t0002g0123 | 3 | NA18960.hp1 NA18987.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.426-7630T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203174 | ||||||
| chr6:7203321
|
C | T | 1 | a0002c0004t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.426-7483C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203321 | ||||||
| chr6:7203352
|
A | G | 1 | a0005c0003t0018g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.426-7452A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203352 | ||||||
| chr6:7203480
|
T | C | 6 | a0005c0056t0010g0196a0006c0005t0004g0041a0006c0005t0030g0193others(3): Show | 6 | HG01071.hp1 HG02074.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.426-7324T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203480 | ||||||
| chr6:7203481
|
C | G | 178 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(175): Show | 178 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.426-7323C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203481 | ||||||
| chr6:7203546
|
A | G | 83 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(80): Show | 83 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.426-7258A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203546 | ||||||
| chr6:7203600
|
T | C | 1 | a0005c0003t0004g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.426-7204T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203600 | ||||||
| chr6:7203762
|
A | C | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.426-7042A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203762 | ||||||
| chr6:7203762
|
A | G | 4 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.426-7042A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203762 | ||||||
| chr6:7203920
|
T | C | 152 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(149): Show | 152 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.426-6884T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203920 | ||||||
| chr6:7203929
|
T | C | 5 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(2): Show | 5 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-6875T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203929 | ||||||
| chr6:7203988
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.426-6816G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7203988 | ||||||
| chr6:7204243
|
C | T | 5 | a0005c0003t0004g0174a0005c0003t0004g0220a0017c0027t0077g0053others(2): Show | 5 | HG02109.hp1 HG02895.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-6561C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204243 | ||||||
| chr6:7204301
|
T | TC | 7 | a0001c0001t0002g0028a0001c0001t0002g0069a0001c0001t0035g0034others(4): Show | 7 | HG02135.hp1 HG03098.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.426-6497dupC | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7204301 | |||||
| chr6:7204307
|
C | T | 2 | a0002c0007t0007g0218a0002c0007t0063g0217 | 2 | HG02155.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.426-6497C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204307 | ||||||
| chr6:7204311
|
C | T | 1 | a0004c0008t0006g0274 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.426-6493C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204311 | ||||||
| chr6:7204354
|
T | C | 3 | a0004c0052t0020g0005a0005c0003t0020g0091a0005c0003t0020g0137 | 3 | HG00438.hp1 NA18982.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.426-6450T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204354 | ||||||
| chr6:7204430
|
C | T | 3 | a0003c0002t0002g0142a0003c0002t0010g0067a0003c0002t0010g0210 | 3 | HG01943.hp1 NA18949.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.426-6374C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204430 | ||||||
| chr6:7204503
|
G | A | 175 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(172): Show | 175 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.426-6301G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204503 | ||||||
| chr6:7204529
|
T | A | 3 | a0004c0006t0018g0056a0016c0025t0018g0179a0019c0049t0002g0061 | 3 | HG02280.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.426-6275T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204529 | ||||||
| chr6:7204589
|
C | T | 5 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(2): Show | 5 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-6215C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204589 | ||||||
| chr6:7204637
|
G | A | 6 | a0003c0002t0023g0175a0003c0002t0074g0190a0011c0041t0067g0055others(3): Show | 6 | HG02257.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.426-6167G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204637 | ||||||
| chr6:7204729
|
C | T | 1 | a0006c0005t0004g0104 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.426-6075C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204729 | ||||||
| chr6:7204832
|
C | T | 1 | a0013c0058t0001g0134 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.426-5972C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204832 | ||||||
| chr6:7204871
|
A | G | 3 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0015t0019g0182 | 3 | HG01361.hp1 HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.426-5933A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204871 | ||||||
| chr6:7204875
|
A | G | 1 | a0002c0004t0008g0216 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.426-5929A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7204875 | ||||||
| chr6:7205038
|
A | G | 5 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(2): Show | 5 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-5766A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7205038 | ||||||
| chr6:7205049
|
T | G | 1 | a0002c0023t0048g0171 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.426-5755T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7205049 | ||||||
| chr6:7205074
|
G | C | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.426-5730G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7205074 | ||||||
| chr6:7205511
|
A | G | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.426-5293A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7205511 | ||||||
| chr6:7205563
|
G | A | 198 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.426-5241G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7205563 | ||||||
| chr6:7205580
|
C | T | 2 | a0004c0008t0001g0265a0004c0008t0001g0266 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.426-5224C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7205580 | ||||||
| chr6:7205813
|
A | G | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.426-4991A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7205813 | ||||||
| chr6:7205949
|
A | G | 1 | a0036c0030t0045g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.426-4855A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7205949 | ||||||
| chr6:7206094
|
G | A | 2 | a0012c0013t0036g0181a0012c0013t0080g0234 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.426-4710G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7206094 | ||||||
| chr6:7206150
|
C | A | 196 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.426-4654C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7206150 | ||||||
| chr6:7206313
|
C | T | 6 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.426-4491C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7206313 | ||||||
| chr6:7206464
|
T | C | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.426-4340T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7206464 | ||||||
| chr6:7206530
|
A | G | 1 | a0005c0003t0018g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.426-4274A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7206530 | ||||||
| chr6:7206631
|
T | TA | 202 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.426-4172dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7206631 | |||||
| chr6:7206750
|
G | A | 1 | a0003c0002t0023g0075 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.426-4054G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7206750 | ||||||
| chr6:7206769
|
G | T | 1 | a0001c0001t0002g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.426-4035G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7206769 | ||||||
| chr6:7206828
|
CT | C | 202 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.426-3974delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7206828 | |||||
| chr6:7206862
|
T | C | 1 | a0003c0002t0003g0120 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.426-3942T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7206862 | ||||||
| chr6:7207012
|
T | G | 2 | a0012c0013t0036g0181a0012c0013t0080g0234 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.426-3792T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207012 | ||||||
| chr6:7207104
|
C | T | 2 | a0012c0013t0036g0181a0012c0013t0080g0234 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.426-3700C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207104 | ||||||
| chr6:7207130
|
G | A | 1 | a0005c0003t0054g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.426-3674G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207130 | ||||||
| chr6:7207312
|
A | C | 202 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.426-3492A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207312 | ||||||
| chr6:7207341
|
C | T | 2 | a0012c0013t0036g0181a0012c0013t0080g0234 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.426-3463C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207341 | ||||||
| chr6:7207438
|
C | T | 2 | a0007c0009t0053g0014a0010c0036t0002g0004 | 2 | NA18612.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.426-3366C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207438 | ||||||
| chr6:7207465
|
T | C | 3 | a0004c0006t0058g0048a0012c0013t0027g0228a0030c0047t0027g0209 | 3 | HG02572.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.426-3339T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207465 | ||||||
| chr6:7207488
|
G | T | 2 | a0012c0013t0036g0181a0012c0013t0080g0234 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.426-3316G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207488 | ||||||
| chr6:7207521
|
G | C | 5 | a0003c0002t0023g0175a0003c0002t0074g0190a0014c0020t0034g0236others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-3283G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207521 | ||||||
| chr6:7207622
|
A | G | 3 | a0002c0004t0015g0044a0002c0004t0015g0203a0002c0004t0015g0204 | 3 | HG02896.hp1 HG02897.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.426-3182A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207622 | ||||||
| chr6:7207629
|
C | G | 1 | a0004c0006t0024g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.426-3175C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207629 | ||||||
| chr6:7207757
|
A | G | 205 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(202): Show | 205 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.426-3047A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207757 | ||||||
| chr6:7207774
|
G | A | 202 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.426-3030G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207774 | ||||||
| chr6:7207776
|
A | T | 1 | a0002c0004t0003g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.426-3028A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207776 | ||||||
| chr6:7207779
|
A | G | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.426-3025A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7207779 | ||||||
| chr6:7208075
|
G | A | 2 | a0014c0020t0034g0236a0014c0020t0034g0237 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.426-2729G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7208075 | ||||||
| chr6:7208098
|
C | T | 9 | a0003c0002t0023g0175a0003c0002t0074g0190a0004c0006t0058g0048others(6): Show | 9 | HG02257.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.426-2706C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7208098 | ||||||
| chr6:7208396
|
G | A | 1 | a0003c0002t0002g0020 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.426-2408G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7208396 | ||||||
| chr6:7208405
|
C | T | 1 | a0003c0002t0002g0065 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.426-2399C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7208405 | ||||||
| chr6:7208561
|
G | A | 3 | a0004c0006t0021g0051a0004c0006t0021g0105a0004c0006t0021g0117 | 3 | HG02922.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.426-2243G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7208561 | ||||||
| chr6:7208565
|
C | T | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.426-2239C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7208565 | ||||||
| chr6:7208588
|
G | A | 1 | a0006c0005t0004g0086 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.426-2216G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7208588 | ||||||
| chr6:7208607
|
A | T | 93 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(90): Show | 93 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.426-2197A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7208607 | ||||||
| chr6:7208899
|
C | T | 135 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(132): Show | 135 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.426-1905C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7208899 | ||||||
| chr6:7209007
|
A | G | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.426-1797A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209007 | ||||||
| chr6:7209018
|
A | G | 133 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(130): Show | 133 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.426-1786A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209018 | ||||||
| chr6:7209100
|
A | G | 1 | a0007c0009t0005g0247 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.426-1704A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209100 | ||||||
| chr6:7209184
|
A | G | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.426-1620A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209184 | ||||||
| chr6:7209260
|
A | G | 1 | a0004c0006t0024g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.426-1544A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209260 | ||||||
| chr6:7209279
|
T | C | 5 | a0005c0003t0009g0101a0006c0005t0009g0090a0006c0005t0009g0133others(2): Show | 5 | NA18941.hp1 NA18974.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-1525T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209279 | ||||||
| chr6:7209334
|
C | T | 1 | a0003c0012t0004g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.426-1470C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209334 | ||||||
| chr6:7209492
|
A | G | 4 | a0007c0009t0005g0008a0007c0009t0005g0009a0007c0009t0053g0014others(1): Show | 4 | NA18612.hp1 NA18952.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-1312A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209492 | ||||||
| chr6:7209572
|
C | CT | 10 | a0001c0001t0001g0109a0001c0001t0082g0235a0002c0004t0011g0163others(7): Show | 10 | HG02040.hp2 HG02922.hp1 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.426-1213dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7209572 | |||||
| chr6:7209572
|
CT | C | 68 | a0002c0004t0015g0204a0002c0004t0016g0211a0004c0050t0006g0049others(65): Show | 68 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.426-1213delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr6 | 7209572 | |||||
| chr6:7209606
|
G | C | 201 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.426-1198G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209606 | ||||||
| chr6:7209700
|
G | A | 2 | a0003c0002t0003g0058a0003c0002t0003g0059 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.426-1104G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209700 | ||||||
| chr6:7209778
|
G | A | 1 | a0005c0003t0054g0152 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.426-1026G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7209778 | ||||||
| chr6:7210175
|
A | G | 1 | a0004c0006t0007g0281 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.426-629A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7210175 | ||||||
| chr6:7210216
|
G | A | 1 | a0025c0060t0012g0227 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.426-588G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7210216 | ||||||
| chr6:7210258
|
C | T | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.426-546C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 6/12 | chr6 | 7210258 | ||||||
| chr6:7211213
|
G | A | 10 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(7): Show | 10 | HG01433.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.570+265G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211213 | ||||||
| chr6:7211320
|
GTGGATGG others(13): Show |
G | 1 | a0004c0008t0003g0188 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.571-236_571-217del others(20): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211320 | |||||
| chr6:7211333
|
T | TGGAC | 4 | a0002c0007t0007g0110a0002c0007t0007g0116a0002c0007t0008g0036others(1): Show | 4 | HG01123.hp2 HG01361.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-239_571-236dup others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211333 | |||||
| chr6:7211337
|
C | CGGAT | 3 | a0002c0007t0007g0195a0002c0007t0011g0169a0002c0042t0060g0108 | 3 | NA18945.hp1 NA18964.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.571-236_571-235ins others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211337 | ||||||
| chr6:7211337
|
C | CGGATGGA others(5): Show |
1 | a0002c0004t0007g0030 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.571-236_571-235ins others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211337 | ||||||
| chr6:7211337
|
CAGAT | C | 6 | a0002c0004t0011g0163a0002c0007t0007g0218a0002c0007t0011g0160others(3): Show | 6 | HG02040.hp1 HG02040.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-235_571-232del others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211337 | ||||||
| chr6:7211338
|
A | AGATG | 86 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(83): Show | 86 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.571-185_571-182dup others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211338 | |||||
| chr6:7211338
|
A | AGATGGAT others(1): Show |
77 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0285others(74): Show | 77 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.571-189_571-182dup others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211338 | |||||
| chr6:7211338
|
A | AGATGGAT others(5): Show |
50 | a0001c0017t0032g0149a0002c0004t0003g0150a0002c0004t0008g0216others(47): Show | 50 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.571-193_571-182dup others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211338 | |||||
| chr6:7211338
|
A | AGATGGAT others(9): Show |
13 | a0002c0004t0022g0066a0003c0002t0003g0058a0003c0002t0003g0059others(10): Show | 13 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.571-197_571-182dup others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211338 | |||||
| chr6:7211338
|
A | AGATGGAT others(13): Show |
1 | a0010c0036t0002g0004 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.571-201_571-182dup others(20): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211338 | |||||
| chr6:7211338
|
A | AGATGGAT others(17): Show |
1 | a0005c0003t0004g0081 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.571-205_571-182dup others(24): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211338 | |||||
| chr6:7211338
|
A | G | 13 | a0002c0004t0007g0030a0002c0007t0007g0110a0002c0007t0007g0116others(10): Show | 13 | HG00423.hp1 HG00621.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.571-235A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211338 | ||||||
| chr6:7211338
|
AGATG | A | 4 | a0001c0001t0001g0255a0001c0001t0082g0235a0004c0006t0031g0079others(1): Show | 4 | HG01099.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-185_571-182del others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211338 | |||||
| chr6:7211338
|
AGATGGAT others(5): Show |
A | 7 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(4): Show | 7 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-193_571-182del others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211338 | |||||
| chr6:7211338
|
AGATGGAT others(9): Show |
A | 6 | a0003c0002t0010g0210a0004c0006t0058g0048a0012c0013t0027g0228others(3): Show | 6 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-197_571-182del others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr6 | 7211338 | |||||
| chr6:7211364
|
A | G | 4 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-209A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211364 | ||||||
| chr6:7211405
|
G | A | 1 | a0002c0004t0008g0216 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.571-168G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211405 | ||||||
| chr6:7211479
|
T | A | 1 | a0003c0002t0004g0015 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571-94T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211479 | ||||||
| chr6:7211517
|
C | T | 1 | a0008c0010t0001g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.571-56C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211517 | ||||||
| chr6:7211518
|
G | A | 86 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(83): Show | 86 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.571-55G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 7/12 | chr6 | 7211518 | ||||||
| chr6:7211851
|
C | T | 197 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.707+142C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7211851 | ||||||
| chr6:7211857
|
G | A | 1 | a0004c0006t0021g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.707+148G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7211857 | ||||||
| chr6:7211968
|
G | C | 6 | a0003c0002t0023g0175a0003c0002t0074g0190a0011c0041t0067g0055others(3): Show | 6 | HG02257.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.707+259G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7211968 | ||||||
| chr6:7211993
|
A | G | 2 | a0003c0012t0003g0205a0003c0012t0013g0239 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.707+284A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7211993 | ||||||
| chr6:7212046
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.707+337C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212046 | ||||||
| chr6:7212110
|
C | A | 1 | a0002c0007t0069g0022 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.707+401C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212110 | ||||||
| chr6:7212184
|
C | G | 1 | a0002c0007t0011g0162 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.707+475C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212184 | ||||||
| chr6:7212236
|
G | A | 1 | a0007c0009t0039g0002 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.707+527G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212236 | ||||||
| chr6:7212362
|
C | T | 1 | a0004c0006t0006g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.707+653C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212362 | ||||||
| chr6:7212511
|
C | A | 196 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.707+802C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212511 | ||||||
| chr6:7212783
|
G | A | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.707+1074G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212783 | ||||||
| chr6:7212809
|
T | C | 1 | a0004c0006t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.707+1100T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212809 | ||||||
| chr6:7212919
|
C | A | 1 | a0001c0001t0001g0033 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.707+1210C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212919 | ||||||
| chr6:7212967
|
C | T | 86 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(83): Show | 86 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.707+1258C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7212967 | ||||||
| chr6:7213046
|
C | T | 200 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.707+1337C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7213046 | ||||||
| chr6:7213076
|
C | T | 1 | a0025c0060t0012g0227 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.707+1367C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7213076 | ||||||
| chr6:7213538
|
G | T | 1 | a0007c0011t0052g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.707+1829G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7213538 | ||||||
| chr6:7213549
|
C | T | 2 | a0008c0010t0001g0003a0008c0010t0001g0288 | 2 | HG01978.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.707+1840C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7213549 | ||||||
| chr6:7213578
|
A | G | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.707+1869A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7213578 | ||||||
| chr6:7213674
|
A | C | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.707+1965A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7213674 | ||||||
| chr6:7213974
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0283a0001c0001t0002g0282 | 3 | HG01496.hp1 HG01934.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.707+2265G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7213974 | ||||||
| chr6:7213985
|
A | C | 5 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(2): Show | 5 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.707+2276A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7213985 | ||||||
| chr6:7214226
|
A | C | 3 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0015t0019g0182 | 3 | HG01361.hp1 HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.707+2517A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7214226 | ||||||
| chr6:7214235
|
C | T | 10 | a0001c0001t0001g0043a0001c0001t0001g0073a0001c0001t0001g0097others(7): Show | 10 | HG00621.hp2 NA18942.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.707+2526C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7214235 | ||||||
| chr6:7214266
|
C | T | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.707+2557C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7214266 | ||||||
| chr6:7214323
|
A | G | 5 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(2): Show | 5 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.707+2614A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7214323 | ||||||
| chr6:7214443
|
C | T | 86 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(83): Show | 86 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.707+2734C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7214443 | ||||||
| chr6:7214647
|
C | T | 1 | a0004c0006t0058g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.707+2938C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7214647 | ||||||
| chr6:7214690
|
C | T | 196 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.707+2981C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7214690 | ||||||
| chr6:7214755
|
G | A | 1 | a0011c0041t0067g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.707+3046G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7214755 | ||||||
| chr6:7214800
|
A | G | 195 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.707+3091A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7214800 | ||||||
| chr6:7215077
|
G | A | 14 | a0003c0002t0023g0175a0003c0002t0074g0190a0007c0011t0014g0199others(11): Show | 14 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.707+3368G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215077 | ||||||
| chr6:7215110
|
T | C | 73 | a0004c0050t0006g0049a0004c0052t0020g0005a0005c0003t0004g0037others(70): Show | 73 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.707+3401T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215110 | ||||||
| chr6:7215138
|
T | C | 1 | a0003c0002t0071g0284 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.707+3429T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215138 | ||||||
| chr6:7215305
|
G | A | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.707+3596G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215305 | ||||||
| chr6:7215308
|
C | T | 196 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.707+3599C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215308 | ||||||
| chr6:7215332
|
G | A | 196 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.707+3623G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215332 | ||||||
| chr6:7215619
|
C | T | 1 | a0004c0006t0006g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.707+3910C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215619 | ||||||
| chr6:7215663
|
A | G | 3 | a0003c0002t0002g0063a0003c0002t0029g0062a0003c0045t0002g0070 | 3 | HG03491.hp2 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.707+3954A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215663 | ||||||
| chr6:7215740
|
A | G | 3 | a0009c0018t0003g0077a0009c0018t0003g0158a0009c0018t0008g0032 | 3 | NA18939.hp2 NA18979.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.707+4031A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215740 | ||||||
| chr6:7215759
|
T | A | 1 | a0005c0003t0028g0018 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.707+4050T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215759 | ||||||
| chr6:7215828
|
G | A | 1 | a0005c0003t0047g0178 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.707+4119G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215828 | ||||||
| chr6:7215845
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.707+4136C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215845 | ||||||
| chr6:7215897
|
C | T | 1 | a0008c0010t0001g0279 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.707+4188C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215897 | ||||||
| chr6:7215934
|
A | G | 195 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.707+4225A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7215934 | ||||||
| chr6:7215946
|
TGAA | T | 196 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.707+4242_707+4244d others(5): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7215946 | |||||
| chr6:7216014
|
C | T | 196 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.707+4305C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216014 | ||||||
| chr6:7216077
|
C | T | 1 | a0011c0041t0067g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.707+4368C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216077 | ||||||
| chr6:7216185
|
G | A | 2 | a0009c0026t0003g0060a0009c0026t0003g0088 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.707+4476G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216185 | ||||||
| chr6:7216251
|
G | C | 91 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.707+4542G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216251 | ||||||
| chr6:7216364
|
G | A | 2 | a0007c0009t0005g0008a0007c0009t0005g0009 | 2 | NA18952.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.707+4655G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216364 | ||||||
| chr6:7216370
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.707+4661A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216370 | ||||||
| chr6:7216615
|
C | T | 1 | a0002c0004t0003g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.707+4906C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216615 | ||||||
| chr6:7216672
|
T | C | 8 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.707+4963T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216672 | ||||||
| chr6:7216810
|
A | G | 1 | a0006c0005t0004g0041 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.707+5101A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216810 | ||||||
| chr6:7216820
|
A | G | 9 | a0001c0001t0042g0187a0004c0006t0006g0072a0004c0006t0006g0257others(6): Show | 9 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.707+5111A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216820 | ||||||
| chr6:7216837
|
C | T | 1 | a0004c0006t0007g0281 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.707+5128C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216837 | ||||||
| chr6:7216850
|
C | T | 1 | a0005c0003t0004g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.707+5141C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216850 | ||||||
| chr6:7216987
|
G | C | 26 | a0001c0001t0042g0187a0004c0006t0006g0021a0004c0006t0006g0072others(23): Show | 26 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.707+5278G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7216987 | ||||||
| chr6:7217060
|
G | T | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.707+5351G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217060 | ||||||
| chr6:7217122
|
T | A | 1 | a0005c0003t0012g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.707+5413T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217122 | ||||||
| chr6:7217284
|
C | T | 65 | a0004c0050t0006g0049a0004c0052t0020g0005a0005c0003t0004g0037others(62): Show | 65 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.707+5575C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217284 | ||||||
| chr6:7217305
|
G | T | 1 | a0001c0001t0002g0248 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.707+5596G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217305 | ||||||
| chr6:7217431
|
T | C | 26 | a0001c0001t0042g0187a0004c0006t0006g0021a0004c0006t0006g0072others(23): Show | 26 | HG00280.hp1 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.707+5722T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217431 | ||||||
| chr6:7217469
|
C | T | 3 | a0006c0005t0030g0193a0006c0005t0070g0038a0006c0005t0075g0192 | 3 | NA18965.hp2 NA18970.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.707+5760C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217469 | ||||||
| chr6:7217494
|
A | T | 2 | a0005c0014t0010g0064a0005c0014t0023g0050 | 2 | HG02015.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.707+5785A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217494 | ||||||
| chr6:7217585
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.707+5876G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217585 | ||||||
| chr6:7217864
|
G | T | 1 | a0003c0002t0010g0251 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.707+6155G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217864 | ||||||
| chr6:7217882
|
G | A | 5 | a0004c0006t0058g0048a0012c0013t0027g0228a0012c0013t0036g0181others(2): Show | 5 | HG02572.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.707+6173G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217882 | ||||||
| chr6:7217954
|
G | A | 66 | a0004c0050t0006g0049a0004c0052t0020g0005a0005c0003t0004g0037others(63): Show | 66 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.707+6245G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217954 | ||||||
| chr6:7217962
|
A | G | 3 | a0003c0002t0002g0063a0003c0002t0029g0062a0003c0045t0002g0070 | 3 | HG03491.hp2 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.707+6253A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7217962 | ||||||
| chr6:7218104
|
T | C | 4 | a0004c0008t0025g0272a0004c0008t0025g0291a0004c0008t0037g0264others(1): Show | 4 | HG01167.hp1 HG03942.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.707+6395T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7218104 | ||||||
| chr6:7218432
|
TAGTG | T | 66 | a0004c0050t0006g0049a0004c0052t0020g0005a0005c0003t0004g0037others(63): Show | 66 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.707+6726_707+6729d others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7218432 | |||||
| chr6:7218487
|
TA | T | 7 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(4): Show | 7 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.707+6790delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7218487 | |||||
| chr6:7218825
|
T | TA | 13 | a0001c0001t0001g0125a0001c0001t0001g0285a0004c0006t0007g0245others(10): Show | 13 | HG00642.hp1 HG01175.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.707+7138dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7218825 | |||||
| chr6:7218825
|
TA | T | 103 | a0001c0001t0001g0043a0001c0001t0001g0073a0001c0001t0001g0097others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.707+7138delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7218825 | |||||
| chr6:7218825
|
TAA | T | 17 | a0002c0004t0011g0163a0002c0007t0007g0218a0002c0007t0011g0160others(14): Show | 17 | HG00423.hp1 HG01433.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.707+7137_707+7138d others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7218825 | |||||
| chr6:7218872
|
C | G | 1 | a0005c0014t0023g0050 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.707+7163C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7218872 | ||||||
| chr6:7219028
|
G | A | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.707+7319G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7219028 | ||||||
| chr6:7219092
|
C | CA | 6 | a0001c0001t0001g0253a0001c0001t0002g0268a0021c0064t0001g0271others(3): Show | 6 | HG01928.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.708-7344dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219092
|
CA | C | 78 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0043others(75): Show | 78 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.708-7344delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219092
|
CAA | C | 21 | a0001c0001t0001g0073a0001c0001t0001g0255a0001c0001t0002g0170others(18): Show | 21 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.708-7345_708-7344d others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219092
|
CAAA | C | 18 | a0002c0004t0007g0030a0004c0006t0006g0072a0004c0006t0006g0099others(15): Show | 18 | HG00642.hp2 HG00741.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.708-7346_708-7344d others(5): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219092
|
CAAAA | C | 19 | a0002c0004t0015g0044a0002c0004t0015g0204a0002c0004t0026g0261others(16): Show | 19 | HG00423.hp1 HG00735.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.708-7347_708-7344d others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219092
|
CAAAAA | C | 87 | a0002c0004t0003g0052a0002c0004t0003g0082a0002c0004t0003g0094others(84): Show | 87 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.708-7348_708-7344d others(7): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219092
|
CAAAAAA | C | 14 | a0002c0007t0011g0160a0007c0009t0005g0007a0007c0009t0005g0008others(11): Show | 14 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.708-7349_708-7344d others(8): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219092
|
CAAAAAAA others(3): Show |
C | 1 | a0003c0002t0029g0186 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.708-7353_708-7344d others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219092
|
CAAAAAAA others(5): Show |
C | 1 | a0008c0010t0010g0254 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.708-7355_708-7344d others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219092
|
CAAAAAAA others(8): Show |
C | 1 | a0005c0014t0023g0050 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.708-7358_708-7344d others(17): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7219092 | |||||
| chr6:7219133
|
G | A | 16 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(13): Show | 16 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.708-7334G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7219133 | ||||||
| chr6:7219230
|
A | G | 1 | a0029c0053t0062g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.708-7237A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7219230 | ||||||
| chr6:7219537
|
C | T | 1 | a0035c0033t0081g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.708-6930C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7219537 | ||||||
| chr6:7219640
|
G | T | 67 | a0004c0050t0006g0049a0004c0052t0020g0005a0005c0003t0004g0037others(64): Show | 67 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.708-6827G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7219640 | ||||||
| chr6:7219815
|
G | A | 1 | a0001c0001t0082g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.708-6652G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7219815 | ||||||
| chr6:7219919
|
T | A | 2 | a0002c0004t0026g0261a0034c0039t0026g0249 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.708-6548T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7219919 | ||||||
| chr6:7220146
|
A | G | 59 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(56): Show | 59 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.708-6321A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7220146 | ||||||
| chr6:7220469
|
A | G | 18 | a0003c0002t0023g0175a0003c0002t0074g0190a0004c0006t0058g0048others(15): Show | 18 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.708-5998A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7220469 | ||||||
| chr6:7220547
|
A | C | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.708-5920A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7220547 | ||||||
| chr6:7220597
|
T | C | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.708-5870T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7220597 | ||||||
| chr6:7220727
|
T | C | 66 | a0004c0050t0006g0049a0004c0052t0020g0005a0005c0003t0004g0037others(63): Show | 66 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.708-5740T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7220727 | ||||||
| chr6:7220728
|
C | T | 5 | a0003c0002t0023g0175a0003c0002t0074g0190a0014c0020t0034g0236others(2): Show | 5 | HG02809.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.708-5739C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7220728 | ||||||
| chr6:7220824
|
C | T | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.708-5643C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7220824 | ||||||
| chr6:7220842
|
G | A | 1 | a0011c0015t0019g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.708-5625G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7220842 | ||||||
| chr6:7221037
|
C | T | 1 | a0006c0016t0009g0024 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.708-5430C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221037 | ||||||
| chr6:7221166
|
C | CT | 10 | a0001c0001t0010g0147a0004c0006t0058g0048a0007c0011t0014g0199others(7): Show | 10 | HG02056.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.708-5288dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7221166 | |||||
| chr6:7221209
|
C | A | 2 | a0004c0006t0018g0056a0019c0049t0002g0061 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.708-5258C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221209 | ||||||
| chr6:7221210
|
G | A | 106 | a0003c0002t0023g0175a0003c0002t0074g0190a0004c0006t0058g0048others(103): Show | 106 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.708-5257G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221210 | ||||||
| chr6:7221257
|
T | C | 19 | a0003c0002t0023g0175a0003c0002t0074g0190a0004c0006t0058g0048others(16): Show | 19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.708-5210T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221257 | ||||||
| chr6:7221259
|
C | T | 1 | a0010c0028t0006g0019 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.708-5208C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221259 | ||||||
| chr6:7221341
|
T | A | 1 | a0001c0001t0001g0285 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.708-5126T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221341 | ||||||
| chr6:7221375
|
T | C | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.708-5092T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221375 | ||||||
| chr6:7221408
|
A | G | 1 | a0012c0013t0080g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.708-5059A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221408 | ||||||
| chr6:7221510
|
G | A | 196 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.708-4957G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221510 | ||||||
| chr6:7221584
|
A | G | 1 | a0015c0024t0006g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.708-4883A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221584 | ||||||
| chr6:7221860
|
G | T | 194 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(191): Show | 194 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.708-4607G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221860 | ||||||
| chr6:7221979
|
A | G | 74 | a0001c0001t0001g0043a0001c0001t0001g0111a0001c0001t0001g0126others(71): Show | 74 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.708-4488A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7221979 | ||||||
| chr6:7222228
|
T | C | 1 | a0001c0001t0017g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.708-4239T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222228 | ||||||
| chr6:7222386
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.708-4081T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222386 | ||||||
| chr6:7222477
|
C | G | 1 | a0010c0021t0003g0011 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.708-3990C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222477 | ||||||
| chr6:7222541
|
T | C | 1 | a0005c0056t0010g0196 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.708-3926T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222541 | ||||||
| chr6:7222572
|
G | A | 3 | a0009c0018t0003g0077a0009c0018t0003g0158a0009c0018t0008g0032 | 3 | NA18939.hp2 NA18979.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.708-3895G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222572 | ||||||
| chr6:7222580
|
G | C | 125 | a0003c0012t0013g0239a0003c0032t0057g0176a0004c0006t0006g0021others(122): Show | 125 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.708-3887G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222580 | ||||||
| chr6:7222584
|
C | T | 2 | a0002c0004t0022g0027a0002c0004t0022g0136 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.708-3883C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222584 | ||||||
| chr6:7222597
|
G | A | 23 | a0004c0006t0006g0021a0004c0006t0006g0072a0004c0006t0006g0099others(20): Show | 23 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.708-3870G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222597 | ||||||
| chr6:7222727
|
T | G | 1 | a0004c0006t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.708-3740T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222727 | ||||||
| chr6:7222800
|
G | GA | 17 | a0005c0014t0023g0050a0007c0009t0005g0006a0007c0009t0005g0007others(14): Show | 17 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.708-3658dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7222800 | |||||
| chr6:7222875
|
C | T | 2 | a0002c0004t0003g0225a0004c0008t0003g0188 | 2 | HG02148.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.708-3592C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7222875 | ||||||
| chr6:7223142
|
G | T | 1 | a0003c0012t0004g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.708-3325G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223142 | ||||||
| chr6:7223173
|
C | T | 1 | a0011c0041t0067g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.708-3294C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223173 | ||||||
| chr6:7223257
|
T | A | 1 | a0006c0005t0070g0038 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.708-3210T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223257 | ||||||
| chr6:7223257
|
T | TA | 93 | a0001c0001t0001g0040a0001c0001t0001g0111a0001c0001t0001g0126others(90): Show | 93 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.708-3188dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223257 | |||||
| chr6:7223257
|
T | TAA | 10 | a0004c0006t0058g0048a0006c0005t0004g0085a0007c0009t0005g0007others(7): Show | 10 | HG01192.hp1 HG02572.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.708-3189_708-3188d others(4): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223257 | |||||
| chr6:7223257
|
T | TAAAA | 13 | a0004c0006t0006g0021a0004c0006t0006g0072a0004c0006t0006g0099others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.708-3191_708-3188d others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223257 | |||||
| chr6:7223257
|
T | TAAAAA | 9 | a0004c0006t0007g0245a0004c0006t0018g0056a0004c0006t0021g0105others(6): Show | 9 | HG01175.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.708-3192_708-3188d others(7): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223257 | |||||
| chr6:7223257
|
TA | T | 7 | a0002c0004t0011g0163a0002c0007t0063g0217a0002c0007t0069g0022others(4): Show | 7 | HG00323.hp2 HG02895.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.708-3188delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223257 | |||||
| chr6:7223257
|
TAAAAAAA others(5): Show |
T | 2 | a0005c0003t0012g0260a0005c0003t0046g0258 | 2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.708-3199_708-3188d others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223257 | |||||
| chr6:7223258
|
A | T | 1 | a0001c0001t0016g0026 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.708-3209A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223258 | ||||||
| chr6:7223304
|
G | C | 1 | a0004c0006t0018g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.708-3163G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223304 | ||||||
| chr6:7223333
|
G | A | 6 | a0008c0010t0001g0191a0008c0010t0001g0277a0008c0010t0001g0278others(3): Show | 6 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.708-3134G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223333 | ||||||
| chr6:7223430
|
G | A | 121 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0006t0006g0021others(118): Show | 121 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.708-3037G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223430 | ||||||
| chr6:7223518
|
G | A | 6 | a0002c0004t0003g0094a0002c0004t0003g0118a0002c0004t0003g0150others(3): Show | 6 | HG01255.hp1 HG01261.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.708-2949G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223518 | ||||||
| chr6:7223561
|
C | CAAAAAAA others(3): Show |
8 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.708-2901_708-2892d others(12): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223561 | |||||
| chr6:7223561
|
C | CAAAAAAA others(4): Show |
12 | a0003c0032t0057g0176a0004c0006t0018g0056a0006c0005t0009g0090others(9): Show | 12 | HG01109.hp1 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.708-2902_708-2892d others(13): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223561 | |||||
| chr6:7223561
|
C | CAAAAAAA others(5): Show |
55 | a0004c0006t0007g0138a0004c0006t0058g0048a0004c0052t0020g0005others(52): Show | 55 | HG00423.hp2 HG00438.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.708-2903_708-2892d others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223561 | |||||
| chr6:7223561
|
C | CAAAAAAA others(6): Show |
38 | a0004c0006t0006g0021a0004c0006t0006g0072a0004c0006t0006g0099others(35): Show | 38 | HG00558.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.708-2904_708-2892d others(15): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223561 | |||||
| chr6:7223561
|
C | CAAAAAAA others(7): Show |
10 | a0003c0034t0008g0031a0004c0006t0021g0051a0007c0009t0005g0006others(7): Show | 10 | HG00140.hp1 HG01192.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.708-2905_708-2892d others(16): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7223561 | |||||
| chr6:7223625
|
T | G | 2 | a0002c0004t0008g0212a0002c0004t0016g0211 | 2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.708-2842T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223625 | ||||||
| chr6:7223792
|
C | T | 1 | a0030c0047t0027g0209 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.708-2675C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223792 | ||||||
| chr6:7223904
|
C | T | 4 | a0005c0003t0012g0260a0005c0003t0018g0001a0005c0003t0046g0258others(1): Show | 4 | HG01243.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.708-2563C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223904 | ||||||
| chr6:7223917
|
C | A | 119 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0006t0006g0021others(116): Show | 119 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.708-2550C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7223917 | ||||||
| chr6:7224036
|
A | AT | 123 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0006t0006g0021others(120): Show | 123 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.708-2421dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr6 | 7224036 | |||||
| chr6:7224215
|
T | C | 2 | a0016c0025t0013g0238a0016c0025t0018g0179 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.708-2252T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7224215 | ||||||
| chr6:7224477
|
C | T | 118 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0006t0006g0021others(115): Show | 118 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.708-1990C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7224477 | ||||||
| chr6:7224650
|
A | G | 2 | a0002c0004t0003g0052a0007c0009t0005g0270 | 2 | HG01515.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.708-1817A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7224650 | ||||||
| chr6:7225075
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.708-1392G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7225075 | ||||||
| chr6:7225441
|
A | C | 66 | a0003c0032t0057g0176a0004c0052t0020g0005a0005c0003t0004g0037others(63): Show | 66 | HG00423.hp2 HG00438.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.708-1026A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7225441 | ||||||
| chr6:7225478
|
C | T | 8 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.708-989C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7225478 | ||||||
| chr6:7225762
|
G | T | 115 | a0003c0032t0057g0176a0004c0006t0006g0021a0004c0006t0006g0072others(112): Show | 115 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.708-705G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7225762 | ||||||
| chr6:7225764
|
G | A | 1 | a0006c0016t0009g0024 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.708-703G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7225764 | ||||||
| chr6:7225948
|
A | G | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.708-519A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7225948 | ||||||
| chr6:7226356
|
A | G | 2 | a0003c0002t0003g0058a0003c0002t0003g0059 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.708-111A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 8/12 | chr6 | 7226356 | ||||||
| chr6:7226726
|
C | T | 64 | a0003c0032t0057g0176a0004c0052t0020g0005a0005c0003t0004g0037others(61): Show | 64 | HG00423.hp2 HG00438.hp1 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.897+70C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7226726 | ||||||
| chr6:7226922
|
G | A | 3 | a0004c0006t0007g0241a0004c0006t0007g0245a0004c0006t0007g0281 | 3 | HG00738.hp2 HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.897+266G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7226922 | ||||||
| chr6:7226939
|
G | T | 14 | a0005c0003t0004g0037a0005c0003t0012g0087a0005c0003t0012g0172others(11): Show | 14 | HG02615.hp1 HG02630.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.897+283G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7226939 | ||||||
| chr6:7227036
|
G | A | 8 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.897+380G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7227036 | ||||||
| chr6:7227278
|
C | T | 65 | a0003c0032t0057g0176a0004c0052t0020g0005a0005c0003t0004g0037others(62): Show | 65 | HG00423.hp2 HG00438.hp1 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.897+622C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7227278 | ||||||
| chr6:7227430
|
A | C | 1 | a0011c0015t0019g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.897+774A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7227430 | ||||||
| chr6:7227529
|
A | T | 3 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0015t0019g0182 | 3 | HG01361.hp1 HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.897+873A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7227529 | ||||||
| chr6:7227542
|
G | GA | 123 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0006t0006g0021others(120): Show | 123 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.897+896dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 7227542 | |||||
| chr6:7227553
|
T | A | 122 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0006t0006g0021others(119): Show | 122 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.897+897T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7227553 | ||||||
| chr6:7227629
|
T | A | 2 | a0012c0013t0027g0228a0012c0013t0080g0234 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.897+973T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7227629 | ||||||
| chr6:7227696
|
A | T | 1 | a0006c0016t0009g0024 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.897+1040A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7227696 | ||||||
| chr6:7227813
|
T | C | 124 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0006t0006g0021others(121): Show | 124 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.897+1157T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7227813 | ||||||
| chr6:7228077
|
C | CT | 4 | a0001c0001t0001g0259a0001c0001t0002g0248a0004c0008t0003g0243others(1): Show | 4 | HG01192.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-919dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 7228077 | |||||
| chr6:7228229
|
A | C | 122 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0006t0006g0021others(119): Show | 122 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.898-768A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228229 | ||||||
| chr6:7228350
|
T | G | 1 | a0036c0030t0045g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.898-647T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228350 | ||||||
| chr6:7228409
|
A | G | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.898-588A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228409 | ||||||
| chr6:7228495
|
C | CT | 27 | a0001c0001t0001g0033a0002c0004t0003g0082a0004c0006t0058g0048others(24): Show | 27 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.898-476dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 7228495 | |||||
| chr6:7228495
|
C | CTT | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-477_898-476dup others(2): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 7228495 | |||||
| chr6:7228495
|
CT | C | 39 | a0002c0004t0008g0146a0002c0004t0015g0044a0002c0007t0007g0218others(36): Show | 39 | HG00642.hp2 HG00738.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.898-476delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr6 | 7228495 | |||||
| chr6:7228577
|
G | C | 123 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0006t0006g0021others(120): Show | 123 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.898-420G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228577 | ||||||
| chr6:7228583
|
T | G | 67 | a0003c0032t0057g0176a0003c0034t0008g0031a0004c0052t0020g0005others(64): Show | 67 | HG00423.hp2 HG00438.hp1 HG01071.hp1 others(64): Show |
intron_variant | MODIFIER | c.898-414T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228583 | ||||||
| chr6:7228640
|
G | C | 2 | a0009c0026t0003g0060a0009c0026t0003g0088 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.898-357G>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228640 | ||||||
| chr6:7228656
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0073a0001c0001t0001g0097others(4): Show | 7 | NA18952.hp1 NA18964.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-341C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228656 | ||||||
| chr6:7228761
|
G | A | 1 | a0036c0030t0045g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.898-236G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228761 | ||||||
| chr6:7228801
|
C | T | 1 | a0006c0005t0004g0041 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.898-196C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228801 | ||||||
| chr6:7228874
|
G | A | 1 | a0004c0063t0003g0141 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.898-123G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228874 | ||||||
| chr6:7228921
|
T | C | 1 | a0011c0015t0019g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.898-76T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228921 | ||||||
| chr6:7228957
|
C | G | 18 | a0005c0003t0004g0037a0005c0003t0012g0087a0005c0003t0012g0172others(15): Show | 18 | HG01243.hp1 HG02615.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.898-40C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 9/12 | chr6 | 7228957 | ||||||
| chr6:7231939
|
G | A | 1 | a0001c0001t0035g0034 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3808+32G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7231939 | ||||||
| chr6:7231953
|
T | C | 114 | a0001c0001t0001g0054a0001c0001t0016g0280a0001c0001t0017g0180others(111): Show | 114 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.3808+46T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7231953 | ||||||
| chr6:7231965
|
C | T | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3808+58C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7231965 | ||||||
| chr6:7231966
|
G | A | 7 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3808+59G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7231966 | ||||||
| chr6:7232075
|
A | G | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3808+168A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232075 | ||||||
| chr6:7232156
|
C | T | 15 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(12): Show | 15 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.3808+249C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232156 | ||||||
| chr6:7232201
|
G | A | 3 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0015t0019g0182 | 3 | HG01361.hp1 HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.3808+294G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232201 | ||||||
| chr6:7232401
|
A | T | 1 | a0004c0006t0058g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3808+494A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232401 | ||||||
| chr6:7232412
|
G | A | 1 | a0008c0065t0001g0275 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3808+505G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232412 | ||||||
| chr6:7232543
|
C | G | 7 | a0002c0004t0022g0027a0002c0004t0022g0066a0002c0004t0022g0136others(4): Show | 7 | HG00140.hp2 HG00639.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.3808+636C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232543 | ||||||
| chr6:7232564
|
G | A | 1 | a0004c0006t0058g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3808+657G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232564 | ||||||
| chr6:7232717
|
A | G | 15 | a0003c0002t0023g0175a0003c0002t0074g0190a0005c0003t0018g0001others(12): Show | 15 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.3808+810A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232717 | ||||||
| chr6:7232724
|
C | G | 1 | a0003c0045t0002g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3808+817C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232724 | ||||||
| chr6:7232763
|
C | CT | 145 | a0001c0001t0016g0280a0001c0001t0042g0187a0002c0004t0003g0052others(142): Show | 145 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.3808+874dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 7232763 | |||||
| chr6:7232763
|
C | T | 1 | a0020c0051t0006g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3808+856C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7232763 | ||||||
| chr6:7233620
|
G | A | 1 | a0005c0003t0012g0260 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3808+1713G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7233620 | ||||||
| chr6:7233724
|
T | C | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3808+1817T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7233724 | ||||||
| chr6:7233939
|
G | A | 11 | a0004c0006t0006g0021a0004c0006t0006g0072a0004c0006t0006g0099others(8): Show | 11 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.3808+2032G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7233939 | ||||||
| chr6:7233981
|
T | A | 1 | a0009c0018t0008g0032 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3808+2074T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7233981 | ||||||
| chr6:7234030
|
AG | A | 11 | a0003c0012t0004g0219a0007c0011t0014g0199a0007c0011t0014g0200others(8): Show | 11 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.3808+2124delG | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7234030 | ||||||
| chr6:7234178
|
C | T | 10 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(7): Show | 10 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3808+2271C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7234178 | ||||||
| chr6:7234487
|
A | G | 16 | a0003c0002t0023g0175a0003c0002t0074g0190a0004c0006t0058g0048others(13): Show | 16 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.3808+2580A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7234487 | ||||||
| chr6:7234918
|
C | T | 1 | a0006c0016t0009g0024 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3808+3011C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7234918 | ||||||
| chr6:7235298
|
T | C | 3 | a0001c0001t0001g0283a0001c0001t0002g0282a0001c0001t0016g0280 | 3 | HG01175.hp1 HG01496.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.3808+3391T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7235298 | ||||||
| chr6:7235504
|
C | T | 55 | a0003c0032t0057g0176a0005c0003t0004g0037a0005c0003t0004g0047others(52): Show | 55 | HG00423.hp2 HG01099.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.3808+3597C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7235504 | ||||||
| chr6:7235754
|
T | C | 2 | a0007c0009t0005g0008a0007c0009t0005g0009 | 2 | NA18952.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.3808+3847T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7235754 | ||||||
| chr6:7236115
|
C | T | 1 | a0028c0054t0007g0029 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3808+4208C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236115 | ||||||
| chr6:7236135
|
C | T | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3808+4228C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236135 | ||||||
| chr6:7236258
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3809-4180A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236258 | ||||||
| chr6:7236368
|
A | G | 1 | a0005c0003t0004g0220 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3809-4070A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236368 | ||||||
| chr6:7236387
|
T | C | 284 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(281): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.3809-4051T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236387 | ||||||
| chr6:7236430
|
C | T | 14 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(11): Show | 14 | HG00140.hp1 HG00558.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.3809-4008C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236430 | ||||||
| chr6:7236721
|
G | A | 1 | a0004c0008t0002g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3809-3717G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236721 | ||||||
| chr6:7236733
|
G | GT | 20 | a0001c0001t0001g0111a0001c0001t0016g0280a0002c0004t0003g0052others(17): Show | 20 | HG01175.hp1 HG01891.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.3809-3690dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 7236733 | |||||
| chr6:7236827
|
C | T | 6 | a0002c0007t0028g0121a0002c0007t0069g0022a0012c0013t0027g0228others(3): Show | 6 | HG02572.hp1 HG02735.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.3809-3611C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236827 | ||||||
| chr6:7236842
|
C | G | 1 | a0003c0012t0004g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3809-3596C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236842 | ||||||
| chr6:7236861
|
C | A | 1 | a0003c0012t0004g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3809-3577C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236861 | ||||||
| chr6:7236887
|
G | GT | 55 | a0001c0001t0001g0040a0001c0001t0001g0125a0001c0001t0001g0126others(52): Show | 55 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.3809-3526dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 7236887 | |||||
| chr6:7236887
|
G | GTT | 81 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(78): Show | 81 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.3809-3527_3809-352 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 7236887 | |||||
| chr6:7236887
|
G | GTTT | 18 | a0002c0004t0003g0130a0002c0004t0003g0151a0002c0004t0007g0030others(15): Show | 18 | HG01243.hp2 HG01261.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.3809-3528_3809-352 others(7): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 7236887 | |||||
| chr6:7236887
|
G | GTTTTT | 8 | a0003c0002t0023g0175a0003c0002t0074g0190a0011c0015t0019g0182others(5): Show | 8 | HG01891.hp1 HG02257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.3809-3530_3809-352 others(9): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 7236887 | |||||
| chr6:7236887
|
GT | G | 26 | a0001c0001t0001g0054a0001c0001t0017g0180a0001c0001t0017g0214others(23): Show | 26 | HG00558.hp2 HG00735.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.3809-3526delT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr6 | 7236887 | |||||
| chr6:7236952
|
G | T | 2 | a0006c0005t0004g0041a0031c0062t0004g0107 | 2 | HG02074.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.3809-3486G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7236952 | ||||||
| chr6:7237073
|
T | C | 14 | a0003c0002t0023g0175a0003c0002t0074g0190a0007c0022t0019g0183others(11): Show | 14 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3809-3365T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237073 | ||||||
| chr6:7237112
|
T | C | 15 | a0003c0002t0023g0175a0003c0002t0074g0190a0004c0006t0058g0048others(12): Show | 15 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.3809-3326T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237112 | ||||||
| chr6:7237224
|
T | A | 10 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(7): Show | 10 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3809-3214T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237224 | ||||||
| chr6:7237230
|
T | C | 291 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0033others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.3809-3208T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237230 | ||||||
| chr6:7237235
|
G | A | 1 | a0019c0049t0002g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3809-3203G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237235 | ||||||
| chr6:7237246
|
C | A | 1 | a0009c0018t0008g0032 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3809-3192C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237246 | ||||||
| chr6:7237393
|
T | A | 2 | a0005c0003t0079g0231a0041c0072t0078g0242 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3809-3045T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237393 | ||||||
| chr6:7237395
|
TA | T | 10 | a0003c0002t0074g0190a0007c0022t0019g0183a0007c0022t0019g0184others(7): Show | 10 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3809-3042delA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237395 | ||||||
| chr6:7237396
|
A | T | 120 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(117): Show | 120 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.3809-3042A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237396 | ||||||
| chr6:7237399
|
A | T | 14 | a0003c0002t0023g0175a0003c0002t0074g0190a0007c0022t0019g0183others(11): Show | 14 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3809-3039A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237399 | ||||||
| chr6:7237421
|
T | C | 1 | a0004c0006t0006g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3809-3017T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237421 | ||||||
| chr6:7237424
|
C | T | 1 | a0005c0003t0018g0001 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3809-3014C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237424 | ||||||
| chr6:7237446
|
T | C | 1 | a0009c0018t0008g0032 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3809-2992T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237446 | ||||||
| chr6:7237448
|
A | T | 1 | a0009c0018t0008g0032 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3809-2990A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237448 | ||||||
| chr6:7237465
|
C | T | 1 | a0005c0003t0012g0260 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3809-2973C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237465 | ||||||
| chr6:7237551
|
T | A | 3 | a0002c0004t0003g0094a0002c0004t0003g0151a0002c0004t0008g0039 | 3 | HG01255.hp1 HG01261.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3809-2887T>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237551 | ||||||
| chr6:7237568
|
C | A | 3 | a0002c0004t0003g0094a0002c0004t0003g0151a0002c0004t0008g0039 | 3 | HG01255.hp1 HG01261.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3809-2870C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237568 | ||||||
| chr6:7237675
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3809-2763C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237675 | ||||||
| chr6:7237685
|
T | C | 1 | a0015c0024t0006g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3809-2753T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237685 | ||||||
| chr6:7237733
|
ATACTAAA others(20): Show |
A | 1 | a0009c0018t0008g0032 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3809-2704_3809-267 others(31): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237733 | ||||||
| chr6:7237836
|
T | C | 224 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(221): Show | 224 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.3809-2602T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237836 | ||||||
| chr6:7237981
|
C | G | 16 | a0004c0052t0020g0005a0005c0003t0009g0101a0005c0003t0020g0091others(13): Show | 16 | HG00423.hp2 HG00438.hp1 NA18941.hp1 others(13): Show |
intron_variant | MODIFIER | c.3809-2457C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7237981 | ||||||
| chr6:7238011
|
A | G | 16 | a0003c0002t0023g0175a0003c0002t0074g0190a0004c0006t0058g0048others(13): Show | 16 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.3809-2427A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7238011 | ||||||
| chr6:7238027
|
C | T | 6 | a0006c0005t0009g0144a0006c0016t0009g0024a0006c0016t0009g0092others(3): Show | 6 | NA18942.hp1 NA18984.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.3809-2411C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7238027 | ||||||
| chr6:7238287
|
G | A | 1 | a0002c0004t0003g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3809-2151G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7238287 | ||||||
| chr6:7238324
|
G | A | 2 | a0002c0004t0022g0027a0002c0004t0022g0136 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.3809-2114G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7238324 | ||||||
| chr6:7238342
|
A | G | 91 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(88): Show | 91 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.3809-2096A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7238342 | ||||||
| chr6:7238740
|
G | A | 5 | a0003c0002t0001g0129a0004c0008t0001g0265a0004c0008t0001g0266others(2): Show | 5 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(2): Show |
intron_variant | MODIFIER | c.3809-1698G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7238740 | ||||||
| chr6:7238878
|
A | G | 4 | a0002c0004t0011g0163a0002c0007t0011g0160a0002c0007t0011g0162others(1): Show | 4 | HG02040.hp1 NA18522.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.3809-1560A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7238878 | ||||||
| chr6:7238966
|
G | T | 1 | a0002c0004t0008g0216 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3809-1472G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7238966 | ||||||
| chr6:7238968
|
A | G | 3 | a0005c0003t0012g0260a0005c0003t0046g0258a0005c0003t0047g0178 | 3 | HG01243.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3809-1470A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7238968 | ||||||
| chr6:7239139
|
A | G | 1 | a0001c0001t0082g0235 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3809-1299A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239139 | ||||||
| chr6:7239149
|
A | G | 1 | a0012c0013t0027g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3809-1289A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239149 | ||||||
| chr6:7239172
|
A | G | 14 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(11): Show | 14 | HG00140.hp1 HG00558.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.3809-1266A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239172 | ||||||
| chr6:7239235
|
G | A | 7 | a0002c0004t0007g0030a0002c0007t0007g0110a0002c0007t0007g0116others(4): Show | 7 | HG00621.hp1 HG01361.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.3809-1203G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239235 | ||||||
| chr6:7239293
|
A | C | 4 | a0005c0003t0004g0174a0005c0003t0004g0220a0009c0026t0003g0060others(1): Show | 4 | HG02559.hp2 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3809-1145A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239293 | ||||||
| chr6:7239382
|
A | T | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3809-1056A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239382 | ||||||
| chr6:7239426
|
T | G | 29 | a0003c0002t0023g0175a0003c0002t0074g0190a0005c0003t0004g0037others(26): Show | 29 | HG01243.hp1 HG01361.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.3809-1012T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239426 | ||||||
| chr6:7239503
|
T | G | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3809-935T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239503 | ||||||
| chr6:7239616
|
G | A | 17 | a0002c0004t0007g0030a0002c0004t0011g0163a0002c0007t0007g0110others(14): Show | 17 | HG00423.hp1 HG00621.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.3809-822G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239616 | ||||||
| chr6:7239742
|
T | G | 1 | a0013c0058t0001g0134 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3809-696T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239742 | ||||||
| chr6:7239820
|
A | T | 14 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(11): Show | 14 | HG00140.hp1 HG00558.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.3809-618A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7239820 | ||||||
| chr6:7240344
|
A | T | 88 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.3809-94A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 10/12 | chr6 | 7240344 | ||||||
| chr6:7240643
|
G | A | 8 | a0008c0010t0001g0003a0008c0010t0001g0191a0008c0010t0001g0277others(5): Show | 8 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3973+41G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7240643 | ||||||
| chr6:7240714
|
G | A | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3973+112G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7240714 | ||||||
| chr6:7240834
|
C | T | 1 | a0004c0008t0001g0292 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3973+232C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7240834 | ||||||
| chr6:7241194
|
G | A | 1 | a0012c0013t0036g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3973+592G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7241194 | ||||||
| chr6:7241248
|
G | A | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3973+646G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7241248 | ||||||
| chr6:7241483
|
T | C | 13 | a0003c0002t0023g0175a0003c0002t0074g0190a0004c0006t0058g0048others(10): Show | 13 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3973+881T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7241483 | ||||||
| chr6:7241505
|
C | G | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3973+903C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7241505 | ||||||
| chr6:7241798
|
G | T | 1 | a0005c0003t0046g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3973+1196G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7241798 | ||||||
| chr6:7241944
|
TCAGCCCA others(4): Show |
T | 14 | a0007c0009t0005g0006a0007c0009t0005g0007a0007c0009t0005g0008others(11): Show | 14 | HG00140.hp1 HG00558.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.3973+1343_3973+135 others(15): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7241944 | ||||||
| chr6:7242035
|
T | G | 1 | a0011c0015t0019g0182 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3973+1433T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242035 | ||||||
| chr6:7242188
|
G | A | 1 | a0003c0012t0004g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3973+1586G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242188 | ||||||
| chr6:7242372
|
T | C | 8 | a0008c0010t0001g0003a0008c0010t0001g0191a0008c0010t0001g0277others(5): Show | 8 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3973+1770T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242372 | ||||||
| chr6:7242640
|
G | GT | 20 | a0002c0004t0008g0216a0003c0012t0003g0205a0005c0003t0004g0037others(17): Show | 20 | HG01243.hp1 HG02615.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.3973+2040dupT | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 7242640 | |||||
| chr6:7242642
|
T | TC | 16 | a0001c0001t0001g0111a0001c0001t0001g0155a0001c0001t0017g0096others(13): Show | 16 | HG00558.hp1 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.3973+2050dupC | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 7242642 | |||||
| chr6:7242642
|
T | TTC | 84 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(81): Show | 84 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.3973+2040_3973+204 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242642 | ||||||
| chr6:7242649
|
C | A | 2 | a0001c0001t0016g0026a0001c0001t0016g0083 | 2 | HG02135.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.3973+2047C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242649 | ||||||
| chr6:7242649
|
C | G | 1 | a0002c0007t0011g0160 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3973+2047C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242649 | ||||||
| chr6:7242650
|
C | G | 1 | a0004c0050t0006g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3973+2048C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242650 | ||||||
| chr6:7242651
|
C | A | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3973+2049C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242651 | ||||||
| chr6:7242700
|
A | AG | 123 | a0001c0001t0001g0155a0001c0001t0001g0285a0001c0001t0002g0248others(120): Show | 123 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.3973+2109dupG | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 7242700 | |||||
| chr6:7242700
|
A | AGG | 53 | a0002c0004t0003g0148a0002c0004t0003g0151a0002c0004t0008g0212others(50): Show | 53 | HG01167.hp1 HG01192.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.3973+2108_3973+210 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 7242700 | |||||
| chr6:7242700
|
A | G | 2 | a0003c0045t0002g0070a0041c0072t0078g0242 | 2 | HG02451.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.3973+2098A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242700 | ||||||
| chr6:7242708
|
G | GC | 3 | a0007c0009t0005g0269a0007c0009t0005g0270a0010c0021t0006g0250 | 3 | HG01515.hp2 HG01943.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.3973+2106_3973+210 others(5): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242708 | ||||||
| chr6:7242712
|
A | G | 2 | a0011c0041t0067g0055a0032c0029t0038g0089 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3973+2110A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242712 | ||||||
| chr6:7242841
|
A | C | 2 | a0002c0004t0026g0261a0034c0039t0026g0249 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3973+2239A>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242841 | ||||||
| chr6:7242860
|
A | T | 2 | a0011c0041t0067g0055a0032c0029t0038g0089 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3973+2258A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242860 | ||||||
| chr6:7242993
|
C | T | 1 | a0003c0002t0002g0065 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3973+2391C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7242993 | ||||||
| chr6:7243090
|
G | A | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3973+2488G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7243090 | ||||||
| chr6:7243209
|
T | C | 1 | a0005c0003t0012g0260 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3973+2607T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7243209 | ||||||
| chr6:7243571
|
G | A | 1 | a0011c0031t0068g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3974-2853G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7243571 | ||||||
| chr6:7243810
|
G | A | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3974-2614G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7243810 | ||||||
| chr6:7243893
|
G | GA | 11 | a0004c0006t0058g0048a0006c0005t0030g0193a0006c0005t0030g0194others(8): Show | 11 | HG00140.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.3974-2519dupA | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 7243893 | |||||
| chr6:7243968
|
T | C | 2 | a0005c0003t0012g0172a0005c0003t0012g0173 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.3974-2456T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7243968 | ||||||
| chr6:7244262
|
C | CAA | 8 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0015t0019g0182others(5): Show | 8 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3974-2146_3974-214 others(6): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 7244262 | |||||
| chr6:7244299
|
A | G | 1 | a0010c0021t0003g0011 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3974-2125A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7244299 | ||||||
| chr6:7244339
|
A | G | 1 | a0006c0005t0004g0104 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3974-2085A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7244339 | ||||||
| chr6:7244793
|
T | G | 10 | a0004c0006t0058g0048a0007c0022t0019g0183a0007c0022t0019g0184others(7): Show | 10 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3974-1631T>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7244793 | ||||||
| chr6:7244947
|
C | A | 1 | a0041c0072t0078g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3974-1477C>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7244947 | ||||||
| chr6:7244996
|
T | C | 11 | a0004c0006t0058g0048a0005c0003t0004g0220a0007c0022t0019g0183others(8): Show | 11 | HG01361.hp1 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3974-1428T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7244996 | ||||||
| chr6:7245123
|
C | T | 3 | a0007c0022t0019g0183a0007c0022t0019g0184a0011c0015t0019g0182 | 3 | HG01361.hp1 HG01891.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.3974-1301C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7245123 | ||||||
| chr6:7245225
|
A | G | 131 | a0001c0001t0016g0280a0002c0004t0003g0052a0002c0004t0003g0082others(128): Show | 131 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.3974-1199A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7245225 | ||||||
| chr6:7245463
|
T | C | 1 | a0003c0012t0004g0219 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3974-961T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7245463 | ||||||
| chr6:7245738
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3974-686C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7245738 | ||||||
| chr6:7245864
|
C | T | 1 | a0004c0006t0006g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3974-560C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7245864 | ||||||
| chr6:7246017
|
T | C | 1 | a0006c0005t0004g0086 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3974-407T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7246017 | ||||||
| chr6:7246036
|
T | C | 1 | a0008c0010t0001g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3974-388T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7246036 | ||||||
| chr6:7246055
|
A | G | 2 | a0012c0013t0027g0228a0012c0013t0080g0234 | 2 | HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3974-369A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7246055 | ||||||
| chr6:7246220
|
G | A | 3 | a0003c0002t0002g0063a0003c0002t0002g0189a0003c0045t0002g0070 | 3 | HG03491.hp2 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3974-204G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7246220 | ||||||
| chr6:7246295
|
C | T | 2 | a0021c0064t0001g0271a0037c0037t0001g0093 | 2 | HG01123.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.3974-129C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | chr6 | 7246295 | ||||||
| chr6:7246372
|
GGCGTACC others(7): Show |
G | 1 | a0040c0069t0002g0123 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3974-49_3974-36del others(14): Show |
RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr6 | 7246372 | |||||
| chr6:7247604
|
T | C | 4 | a0006c0005t0030g0193a0006c0005t0030g0194a0006c0005t0070g0038others(1): Show | 4 | NA18965.hp2 NA18970.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.4771+383T>C | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7247604 | ||||||
| chr6:7247630
|
C | T | 1 | a0007c0009t0005g0008 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4771+409C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7247630 | ||||||
| chr6:7247679
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4771+458C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7247679 | ||||||
| chr6:7247892
|
C | T | 1 | a0032c0029t0038g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4772-619C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7247892 | ||||||
| chr6:7247945
|
A | G | 10 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(7): Show | 10 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.4772-566A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7247945 | ||||||
| chr6:7247946
|
C | G | 2 | a0001c0001t0002g0248a0008c0010t0001g0191 | 2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4772-565C>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7247946 | ||||||
| chr6:7247979
|
G | A | 26 | a0003c0002t0001g0124a0003c0002t0002g0020a0003c0002t0002g0063others(23): Show | 26 | HG00558.hp2 HG01167.hp1 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.4772-532G>A | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7247979 | ||||||
| chr6:7248032
|
A | G | 1 | a0011c0041t0067g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4772-479A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7248032 | ||||||
| chr6:7248089
|
G | T | 3 | a0004c0006t0021g0051a0004c0006t0021g0105a0004c0006t0021g0117 | 3 | HG02922.hp1 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4772-422G>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7248089 | ||||||
| chr6:7248170
|
A | G | 1 | a0004c0006t0006g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4772-341A>G | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7248170 | ||||||
| chr6:7248226
|
C | T | 9 | a0007c0011t0014g0199a0007c0011t0014g0200a0007c0011t0014g0201others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.4772-285C>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7248226 | ||||||
| chr6:7248356
|
A | T | 1 | a0001c0001t0001g0285 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4772-155A>T | RREB1 | ENSG00000124782.21 | transcript | ENST00000379938.7 | protein_coding | 12/12 | chr6 | 7248356 |