| geneid | 51773 |
|---|---|
| ensemblid | ENSG00000048649.14 |
| hgncid | 18118 |
| symbol | RSF1 |
| name | remodeling and spacing factor 1 |
| refseq_nuc | NM_016578.4 |
| refseq_prot | NP_057662.3 |
| ensembl_nuc | ENST00000308488.11 |
| ensembl_prot | ENSP00000311513.6 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 77660009 |
| end | 77820722 |
| strand | - |
| ver | v1.2 |
| region | chr11:77660009-77820722 |
| region5000 | chr11:77655009-77825722 |
| regionname0 | RSF1_chr11_77660009_77820722 |
| regionname5000 | RSF1_chr11_77655009_77825722 |
| 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 | 1/1 | 1441 | 292 | 75 | 43 | 143 | 11 | 18 | 108 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0002 | 0/0 | 1441 | 40 | 3 | 13 | 8 | 4 | 12 | 6 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0003 | 0/0 | 1441 | 5 | 0 | 0 | 5 | 0 | 0 | 2 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0004 | 0/0 | 1441 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0005 | 0/0 | 1441 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0006 | 0/0 | 1441 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0007 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0008 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0009 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0010 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0011 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0012 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0013 | 0/0 | 1441 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| 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 | 1/1 | 4326 | 211 | 50 | 30 | 101 | 10 | 18 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0002 | 0/0 | 4326 | 78 | 24 | 12 | 41 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0003 | 0/0 | 4326 | 40 | 3 | 13 | 8 | 4 | 12 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0004 | 0/0 | 4326 | 5 | 0 | 0 | 5 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0005 | 0/0 | 4326 | 3 | 3 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0006 | 0/0 | 4326 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0007 | 0/0 | 4326 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0008 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0009 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0010 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0011 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0012 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0013 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0014 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0015 | 0/0 | 4326 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0016 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0017 | 0/0 | 4326 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| c0018 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| 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 | 0/1 | 6920 | 75 | 15 | 9 | 44 | 5 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0002 | 0/0 | 6918 | 61 | 16 | 11 | 19 | 3 | 12 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0003 | 0/0 | 6910 | 57 | 15 | 9 | 32 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0004 | 1/0 | 6917 | 50 | 1 | 10 | 22 | 4 | 12 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0005 | 0/0 | 6920 | 10 | 0 | 1 | 9 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0006 | 0/0 | 6918 | 6 | 5 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0007 | 0/0 | 6915 | 6 | 0 | 0 | 6 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0008 | 0/0 | 6920 | 5 | 0 | 3 | 0 | 0 | 2 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0009 | 0/0 | 6918 | 4 | 4 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0010 | 0/0 | 6910 | 3 | 2 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0011 | 0/0 | 6917 | 3 | 0 | 1 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0012 | 0/0 | 6920 | 3 | 2 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0013 | 0/0 | 6920 | 3 | 3 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0014 | 0/0 | 6913 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0015 | 0/0 | 6910 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0016 | 0/0 | 6916 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0017 | 0/0 | 6912 | 2 | 1 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0018 | 0/0 | 6911 | 2 | 0 | 1 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0019 | 0/0 | 6917 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0020 | 0/0 | 6918 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0021 | 0/0 | 6918 | 2 | 0 | 1 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0022 | 0/0 | 6918 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0023 | 0/0 | 6922 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0024 | 0/0 | 6910 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0025 | 0/0 | 6920 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0026 | 0/0 | 6920 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0027 | 0/0 | 6924 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0028 | 0/0 | 6917 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0029 | 0/0 | 6914 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0030 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0031 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0032 | 0/0 | 6915 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0033 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0034 | 0/0 | 6913 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0035 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0036 | 0/0 | 6911 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0037 | 0/0 | 6912 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0038 | 0/0 | 6917 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0039 | 0/0 | 6916 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0040 | 0/0 | 6918 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0041 | 0/0 | 6920 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0042 | 0/0 | 6917 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0043 | 0/0 | 6917 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0044 | 0/0 | 6917 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0045 | 0/0 | 6918 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0046 | 0/0 | 6917 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0047 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0048 | 0/0 | 6917 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0049 | 0/0 | 6917 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0050 | 0/0 | 6918 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0051 | 0/0 | 6917 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0052 | 0/0 | 6918 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0053 | 0/0 | 6917 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0054 | 0/0 | 6918 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0055 | 0/0 | 6917 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0056 | 0/0 | 6917 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0057 | 0/0 | 6920 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0058 | 0/0 | 6917 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0059 | 0/0 | 6920 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0060 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0061 | 0/0 | 6920 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0062 | 0/0 | 6920 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0063 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0064 | 0/0 | 6920 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0065 | 0/0 | 6915 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0066 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0067 | 0/0 | 6917 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| t0068 | 0/0 | 6920 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| 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 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| 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 | 1/1 | 4326 | 211 | 50 | 30 | 101 | 10 | 18 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002 | 0/0 | 4326 | 78 | 24 | 12 | 41 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0009 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0010 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0017 | 0/0 | 4326 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0002c0003 | 0/0 | 4326 | 40 | 3 | 13 | 8 | 4 | 12 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0003c0004 | 0/0 | 4326 | 5 | 0 | 0 | 5 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0004c0005 | 0/0 | 4326 | 3 | 3 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0004c0016 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0005c0006 | 0/0 | 4326 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0006c0007 | 0/0 | 4326 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0007c0018 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0008c0014 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0009c0008 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0010c0013 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0011c0012 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0012c0011 | 0/0 | 4326 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0013c0015 | 0/0 | 4326 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 11245 | 71 | 15 | 8 | 41 | 5 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0002 | 0/0 | 11243 | 21 | 13 | 0 | 7 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0004 | 1/0 | 11242 | 49 | 1 | 10 | 22 | 3 | 12 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0005 | 0/0 | 11245 | 9 | 0 | 1 | 8 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0006 | 0/0 | 11243 | 6 | 5 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0007 | 0/0 | 11240 | 4 | 0 | 0 | 4 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0008 | 0/0 | 11245 | 4 | 0 | 3 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0009 | 0/0 | 11243 | 4 | 4 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0011 | 0/0 | 11242 | 3 | 0 | 1 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0013 | 0/0 | 11245 | 3 | 3 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0019 | 0/0 | 11242 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0022 | 0/0 | 11243 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0023 | 0/0 | 11247 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0025 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0026 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0027 | 0/0 | 11249 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0028 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0038 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0039 | 0/0 | 11241 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0040 | 0/0 | 11243 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0041 | 0/0 | 11245 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0042 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0043 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0044 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0046 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0047 | 0/0 | 11244 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0048 | 0/0 | 11242 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0051 | 0/0 | 11242 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0052 | 0/0 | 11243 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0053 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0054 | 0/0 | 11243 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0055 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0056 | 0/0 | 11242 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0057 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0058 | 0/0 | 11242 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0059 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0060 | 0/0 | 11247 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0061 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0062 | 0/0 | 11245 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0063 | 0/0 | 11244 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0065 | 0/0 | 11240 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0066 | 0/0 | 11244 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0067 | 0/0 | 11242 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0001t0068 | 0/0 | 11245 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0003 | 0/0 | 11235 | 56 | 14 | 9 | 32 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0010 | 0/0 | 11235 | 3 | 2 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0014 | 0/0 | 11238 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0015 | 0/0 | 11235 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0016 | 0/0 | 11241 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0017 | 0/0 | 11237 | 2 | 1 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0018 | 0/0 | 11236 | 2 | 0 | 1 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0024 | 0/0 | 11235 | 2 | 0 | 0 | 2 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0029 | 0/0 | 11239 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0030 | 0/0 | 11235 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0031 | 0/0 | 11235 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0033 | 0/0 | 11235 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0034 | 0/0 | 11238 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0035 | 0/0 | 11235 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0002t0037 | 0/0 | 11237 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0009t0036 | 0/0 | 11236 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0010t0001 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0001c0017t0001 | 0/0 | 11245 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0002c0003t0002 | 0/0 | 11243 | 35 | 3 | 11 | 7 | 3 | 11 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0002c0003t0008 | 0/0 | 11245 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0002c0003t0012 | 0/0 | 11245 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0002c0003t0021 | 0/0 | 11243 | 2 | 0 | 1 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0002c0003t0050 | 0/0 | 11243 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0003c0004t0002 | 0/0 | 11243 | 5 | 0 | 0 | 5 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0004c0005t0020 | 0/0 | 11243 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0004c0005t0049 | 0/0 | 11242 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0004c0016t0045 | 0/0 | 11243 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0005c0006t0012 | 0/0 | 11245 | 2 | 2 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0006c0007t0001 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0006c0007t0064 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0007c0018t0032 | 0/0 | 11240 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0008c0014t0005 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0009c0008t0003 | 0/0 | 11235 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0010c0013t0007 | 0/0 | 11240 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0011c0012t0001 | 0/0 | 11245 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0012c0011t0007 | 0/0 | 11240 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| a0013c0015t0004 | 0/0 | 11242 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | copy fasta | chr11 | 77655009 | 77825722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0005g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0008g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0008g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0008g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0011g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0011g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0011g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0013g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0013g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0013g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0019g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0019g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0022g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0022g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0023g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0023g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0025g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0026g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0027g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0028g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0038g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0039g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0040g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0041g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0042g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0043g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0044g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0046g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0047g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0048g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0051g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0052g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0053g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0054g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0055g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0056g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0057g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0058g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0059g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0060g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0061g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0062g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0063g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0065g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0066g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0067g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0001t0068g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0010g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0010g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0010g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0014g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0015g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0015g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0016g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0017g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0018g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0018g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0024g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0024g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0029g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0030g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0031g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0033g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0034g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0035g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0002t0037g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0009t0036g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0010t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0001c0017t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0008g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0012g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0021g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0021g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0002c0003t0050g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0003c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0003c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0003c0004t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0003c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0003c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0004c0005t0020g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0004c0005t0020g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0004c0005t0049g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0004c0016t0045g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0005c0006t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0005c0006t0012g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0006c0007t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0006c0007t0064g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0007c0018t0032g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0008c0014t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0009c0008t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0010c0013t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0011c0012t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0012c0011t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| a0013c0015t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0038 | g0170 | EUR | GBR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0204 | EUR | GBR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00140 | hp1 | a0002 | c0003 | t0021 | g0212 | EUR | GBR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0326 | EUR | GBR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00280 | hp1 | a0013 | c0015 | t0004 | g0190 | EUR | FIN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0059 | EUR | FIN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0152 | EUR | FIN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0064 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00423 | hp2 | a0001 | c0002 | t0037 | g0060 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0155 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00558 | hp1 | a0011 | c0012 | t0001 | g0281 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00558 | hp2 | a0002 | c0003 | t0002 | g0301 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0063 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0178 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00639 | hp1 | a0002 | c0003 | t0002 | g0205 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0118 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00673 | hp1 | a0001 | c0002 | t0030 | g0085 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00673 | hp2 | a0003 | c0004 | t0002 | g0232 | EAS | CHS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00733 | hp1 | a0002 | c0003 | t0002 | g0235 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0055 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01069 | hp1 | a0001 | c0001 | t0039 | g0166 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0078 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0229 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0079 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01074 | hp1 | a0001 | c0002 | t0010 | g0013 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0268 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01081 | hp1 | a0001 | c0002 | t0018 | g0046 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0147 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01109 | hp1 | a0002 | c0003 | t0002 | g0211 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01167 | hp2 | a0002 | c0003 | t0002 | g0238 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01168 | hp1 | a0001 | c0001 | t0053 | g0191 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01168 | hp2 | a0002 | c0003 | t0002 | g0218 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01175 | hp2 | a0001 | c0017 | t0001 | g0095 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01192 | hp1 | a0001 | c0001 | t0056 | g0141 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0052 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01243 | hp2 | a0001 | c0002 | t0017 | g0006 | AMR | PUR | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01255 | hp2 | a0002 | c0003 | t0012 | g0222 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0136 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0058 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0134 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01358 | hp1 | a0001 | c0001 | t0043 | g0157 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01358 | hp2 | a0002 | c0003 | t0002 | g0228 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0056 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01361 | hp2 | a0002 | c0003 | t0002 | g0236 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0269 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0080 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01515 | hp1 | a0002 | c0003 | t0002 | g0221 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0167 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01516 | hp1 | a0002 | c0003 | t0002 | g0206 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0160 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | IBS | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01884 | hp1 | a0001 | c0002 | t0014 | g0009 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0348 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01928 | hp1 | a0001 | c0001 | t0046 | g0171 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01928 | hp2 | a0002 | c0003 | t0002 | g0207 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0253 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01993 | hp1 | a0001 | c0001 | t0044 | g0138 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0048 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02015 | hp2 | a0003 | c0004 | t0002 | g0234 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02027 | hp1 | a0002 | c0003 | t0002 | g0240 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02027 | hp2 | a0001 | c0001 | t0061 | g0304 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02040 | hp1 | a0001 | c0001 | t0067 | g0158 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02055 | hp2 | a0001 | c0002 | t0010 | g0351 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02056 | hp1 | a0001 | c0001 | t0063 | g0289 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02056 | hp2 | a0001 | c0001 | t0026 | g0256 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0054 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02074 | hp2 | a0003 | c0004 | t0002 | g0225 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0164 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0068 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02135 | hp1 | a0012 | c0011 | t0007 | g0179 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02145 | hp1 | a0001 | c0002 | t0014 | g0011 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02145 | hp2 | a0001 | c0001 | t0068 | g0352 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02148 | hp1 | a0001 | c0001 | t0011 | g0143 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0270 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02165 | hp2 | a0001 | c0001 | t0007 | g0181 | EAS | CDX | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0040 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0050 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02273 | hp2 | a0002 | c0003 | t0002 | g0216 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02280 | hp1 | a0001 | c0002 | t0034 | g0010 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0140 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02293 | hp2 | a0002 | c0003 | t0002 | g0220 | AMR | PEL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02451 | hp2 | a0004 | c0005 | t0020 | g0199 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | KHV | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0273 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02572 | hp2 | a0001 | c0002 | t0003 | g0033 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0135 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02602 | hp2 | a0001 | c0001 | t0040 | g0117 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02615 | hp1 | a0001 | c0001 | t0054 | g0146 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0044 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02630 | hp1 | a0001 | c0001 | t0023 | g0251 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02630 | hp2 | a0001 | c0002 | t0033 | g0012 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0045 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02717 | hp2 | a0001 | c0001 | t0041 | g0249 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02809 | hp2 | a0001 | c0001 | t0052 | g0265 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02818 | hp1 | a0005 | c0006 | t0012 | g0002 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02818 | hp2 | a0004 | c0005 | t0049 | g0202 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0042 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02895 | hp1 | a0001 | c0002 | t0029 | g0017 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0242 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0121 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0217 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03041 | hp1 | a0004 | c0005 | t0020 | g0200 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0122 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0037 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03130 | hp2 | a0001 | c0001 | t0022 | g0145 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03139 | hp1 | a0001 | c0002 | t0016 | g0008 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03195 | hp1 | a0001 | c0001 | t0023 | g0275 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03195 | hp2 | a0004 | c0016 | t0045 | g0201 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0245 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03225 | hp1 | a0001 | c0001 | t0022 | g0144 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03225 | hp2 | a0001 | c0001 | t0062 | g0284 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03239 | hp2 | a0001 | c0001 | t0028 | g0149 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03453 | hp1 | a0001 | c0009 | t0036 | g0015 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0035 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0186 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03490 | hp2 | a0002 | c0003 | t0002 | g0347 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0105 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03491 | hp2 | a0002 | c0003 | t0002 | g0224 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0106 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03492 | hp2 | a0002 | c0003 | t0002 | g0345 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0244 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0081 | AFR | ESN | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0036 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03654 | hp1 | a0002 | c0003 | t0002 | g0223 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03669 | hp2 | a0002 | c0003 | t0002 | g0233 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0187 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03688 | hp2 | a0002 | c0003 | t0002 | g0208 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03704 | hp1 | a0002 | c0003 | t0002 | g0219 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0168 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03710 | hp1 | a0001 | c0001 | t0008 | g0267 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03710 | hp2 | a0002 | c0003 | t0002 | g0215 | SAS | PJL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03927 | hp1 | a0002 | c0003 | t0002 | g0210 | SAS | BEB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0250 | SAS | BEB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03942 | hp1 | a0002 | c0003 | t0002 | g0346 | SAS | BEB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | BEB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0246 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0142 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG04228 | hp1 | a0002 | c0003 | t0008 | g0266 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG04228 | hp2 | a0001 | c0001 | t0055 | g0148 | SAS | STU | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0067 | EAS | CHB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | CHB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | CHB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | CHB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0271 | AFR | YRI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | YRI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18942 | hp1 | a0008 | c0014 | t0005 | g0258 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18946 | hp2 | a0001 | c0001 | t0027 | g0260 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0263 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18953 | hp2 | a0001 | c0001 | t0005 | g0261 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18954 | hp2 | a0001 | c0001 | t0051 | g0183 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18957 | hp1 | a0001 | c0001 | t0065 | g0150 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18957 | hp2 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18963 | hp2 | a0001 | c0001 | t0019 | g0161 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18964 | hp2 | a0002 | c0003 | t0002 | g0241 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0066 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18966 | hp2 | a0001 | c0001 | t0060 | g0257 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18967 | hp1 | a0001 | c0001 | t0047 | g0102 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0053 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18971 | hp1 | a0002 | c0003 | t0002 | g0239 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18971 | hp2 | a0001 | c0001 | t0011 | g0163 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18972 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18972 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18977 | hp1 | a0001 | c0001 | t0057 | g0278 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0254 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18979 | hp1 | a0003 | c0004 | t0002 | g0237 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18981 | hp2 | a0001 | c0002 | t0015 | g0051 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18983 | hp2 | a0001 | c0001 | t0011 | g0162 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0022 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18988 | hp2 | a0006 | c0007 | t0001 | g0349 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18990 | hp1 | a0002 | c0003 | t0002 | g0214 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18991 | hp1 | a0001 | c0002 | t0035 | g0057 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18993 | hp1 | a0001 | c0001 | t0048 | g0159 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18994 | hp2 | a0002 | c0003 | t0002 | g0230 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18998 | hp2 | a0001 | c0001 | t0066 | g0172 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19005 | hp2 | a0001 | c0002 | t0024 | g0026 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | LWK | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | LWK | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0272 | AFR | LWK | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19056 | hp1 | a0001 | c0002 | t0024 | g0031 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19056 | hp2 | a0006 | c0007 | t0064 | g0321 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19057 | hp1 | a0001 | c0002 | t0018 | g0065 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19062 | hp1 | a0001 | c0010 | t0001 | g0337 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19063 | hp1 | a0010 | c0013 | t0007 | g0262 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19063 | hp2 | a0001 | c0001 | t0058 | g0331 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19068 | hp2 | a0001 | c0002 | t0031 | g0075 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19074 | hp2 | a0003 | c0004 | t0002 | g0231 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19078 | hp2 | a0001 | c0002 | t0015 | g0074 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19083 | hp1 | a0001 | c0001 | t0059 | g0310 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19083 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0069 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19088 | hp1 | a0001 | c0001 | t0025 | g0259 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19088 | hp2 | a0002 | c0003 | t0050 | g0213 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0252 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19090 | hp2 | a0001 | c0001 | t0019 | g0176 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19240 | hp1 | a0001 | c0002 | t0010 | g0350 | AFR | YRI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA19240 | hp2 | a0007 | c0018 | t0032 | g0014 | AFR | YRI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA20129 | hp1 | a0009 | c0008 | t0003 | g0034 | AFR | ASW | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA20129 | hp2 | a0002 | c0003 | t0002 | g0099 | AFR | ASW | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA20805 | hp1 | a0001 | c0001 | t0042 | g0173 | EUR | TSI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01123 | hp1 | a0002 | c0003 | t0021 | g0209 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02486 | hp1 | a0002 | c0003 | t0002 | g0227 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0125 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG02559 | hp2 | a0001 | c0002 | t0016 | g0005 | AFR | ACB | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0043 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG06807 | hp1 | a0005 | c0006 | t0012 | g0001 | AFR | USA | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| HG06807 | hp2 | a0001 | c0002 | t0017 | g0007 | AFR | USA | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18955 | hp1 | a0002 | c0003 | t0002 | g0203 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0096 | REF | REF | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0226 | REF | REF | RSF1_chr11_77655009_77825722 | RSF1 | chr11 | 77655009 | 77825722 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77667286
|
A | C | 1 | a0012 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.3957T>G | p.Asn1319Lys | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3965/11242 | 3957/4326 | 1319/1441 | chr11 | 77667286 | ||
| chr11:77667329
|
G | A | 1 | a0011 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.3914C>T | p.Thr1305Met | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3922/11242 | 3914/4326 | 1305/1441 | chr11 | 77667329 | ||
| chr11:77675080
|
T | G | 1 | a0010 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.3518A>C | p.Asp1173Ala | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/16 | 3526/11242 | 3518/4326 | 1173/1441 | chr11 | 77675080 | ||
| chr11:77676888
|
G | C | 1 | a0009 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.3245C>G | p.Ala1082Gly | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/16 | 3253/11242 | 3245/4326 | 1082/1441 | chr11 | 77676888 | ||
| chr11:77701117
|
G | T | 1 | a0009 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.2112C>A | p.Ser704Arg | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 2120/11242 | 2112/4326 | 704/1441 | chr11 | 77701117 | ||
| chr11:77701134
|
C | G | 1 | a0006 | 2 | NA18988.hp2 NA19056.hp2 |
missense_variant | MODERATE | c.2095G>C | p.Gly699Arg | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 2103/11242 | 2095/4326 | 699/1441 | chr11 | 77701134 | ||
| chr11:77701197
|
C | A | 1 | a0008 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2032G>T | p.Val678Leu | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 2040/11242 | 2032/4326 | 678/1441 | chr11 | 77701197 | ||
| chr11:77701411
|
T | C | 1 | a0013 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.1818A>G | p.Ile606Met | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 1826/11242 | 1818/4326 | 606/1441 | chr11 | 77701411 | ||
| chr11:77701806
|
A | C | 1 | a0003 | 5 | HG00673.hp2 HG02015.hp2 HG02074.hp2 others(2): Show |
missense_variant | MODERATE | c.1423T>G | p.Ser475Ala | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 1431/11242 | 1423/4326 | 475/1441 | chr11 | 77701806 | ||
| chr11:77701806
|
A | G | 1 | a0002 | 40 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(37): Show |
missense_variant | MODERATE | c.1423T>C | p.Ser475Pro | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 1431/11242 | 1423/4326 | 475/1441 | chr11 | 77701806 | ||
| chr11:77702178
|
T | C | 1 | a0004 | 4 | HG02451.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.1051A>G | p.Ile351Val | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 1059/11242 | 1051/4326 | 351/1441 | chr11 | 77702178 | ||
| chr11:77702317
|
T | G | 1 | a0007 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.912A>C | p.Glu304Asp | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 920/11242 | 912/4326 | 304/1441 | chr11 | 77702317 | ||
| chr11:77820687
|
C | G | 1 | a0005 | 2 | HG02818.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.28G>C | p.Val10Leu | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/16 | 36/11242 | 28/4326 | 10/1441 | chr11 | 77820687 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77667343
|
T | C | 4 | a0001c0002a0001c0009a0007c0018others(1): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
synonymous_variant | LOW | c.3900A>G | p.Leu1300Leu | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3908/11242 | 3900/4326 | 1300/1441 | chr11 | 77667343 | ||
| chr11:77667460
|
A | G | 4 | a0001c0002a0001c0009a0007c0018others(1): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
synonymous_variant | LOW | c.3783T>C | p.Asp1261Asp | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3791/11242 | 3783/4326 | 1261/1441 | chr11 | 77667460 | ||
| chr11:77672205
|
A | G | 1 | a0004c0016 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.3588T>C | p.Ser1196Ser | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/16 | 3596/11242 | 3588/4326 | 1196/1441 | chr11 | 77672205 | ||
| chr11:77698523
|
T | C | 4 | a0001c0002a0001c0009a0007c0018others(1): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
synonymous_variant | LOW | c.2679A>G | p.Pro893Pro | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/16 | 2687/11242 | 2679/4326 | 893/1441 | chr11 | 77698523 | ||
| chr11:77698622
|
A | G | 1 | a0001c0010 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.2580T>C | p.Asp860Asp | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/16 | 2588/11242 | 2580/4326 | 860/1441 | chr11 | 77698622 | ||
| chr11:77700931
|
C | T | 1 | a0001c0009 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.2298G>A | p.Glu766Glu | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 2306/11242 | 2298/4326 | 766/1441 | chr11 | 77700931 | ||
| chr11:77702266
|
G | C | 1 | a0001c0017 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.963C>G | p.Pro321Pro | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/16 | 971/11242 | 963/4326 | 321/1441 | chr11 | 77702266 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77660021
|
T | C | 1 | a0001c0002t0017 | 2 | HG01243.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6896A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6896 | chr11 | 77660021 | |||||
| chr11:77660030
|
T | C | 2 | a0001c0001t0059a0001c0001t0060 | 2 | NA18966.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6887A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6887 | chr11 | 77660030 | |||||
| chr11:77660169
|
G | C | 1 | a0001c0002t0033 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6748C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6748 | chr11 | 77660169 | |||||
| chr11:77660386
|
T | C | 1 | a0001c0001t0046 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6531A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6531 | chr11 | 77660386 | |||||
| chr11:77660449
|
G | C | 18 | a0001c0002t0003a0001c0002t0010a0001c0002t0014others(15): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*6468C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6468 | chr11 | 77660449 | |||||
| chr11:77660581
|
T | C | 2 | a0001c0001t0059a0001c0001t0060 | 2 | NA18966.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6336A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6336 | chr11 | 77660581 | |||||
| chr11:77660708
|
C | G | 1 | a0007c0018t0032 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6209G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6209 | chr11 | 77660708 | |||||
| chr11:77660749
|
G | T | 1 | a0004c0005t0049 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6168C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6168 | chr11 | 77660749 | |||||
| chr11:77660775
|
T | C | 1 | a0001c0002t0035 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6142A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6142 | chr11 | 77660775 | |||||
| chr11:77660800
|
AC | A | 17 | a0001c0002t0003a0001c0002t0010a0001c0002t0014others(14): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*6116delG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 6116 | chr11 | 77660800 | |||||
| chr11:77661120
|
A | C | 10 | a0001c0001t0005a0001c0001t0008a0001c0001t0013others(7): Show | 23 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5797T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5797 | chr11 | 77661120 | |||||
| chr11:77661187
|
C | G | 2 | a0001c0002t0014a0001c0002t0034 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5730G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5730 | chr11 | 77661187 | |||||
| chr11:77661204
|
T | C | 1 | a0007c0018t0032 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5713A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5713 | chr11 | 77661204 | |||||
| chr11:77661311
|
T | A | 1 | a0002c0003t0050 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5606A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5606 | chr11 | 77661311 | |||||
| chr11:77661376
|
GC | G | 9 | a0001c0002t0003a0001c0002t0015a0001c0002t0018others(6): Show | 67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*5540delG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5540 | chr11 | 77661376 | |||||
| chr11:77661437
|
A | ATG | 11 | a0001c0001t0023a0001c0001t0041a0001c0001t0047others(8): Show | 14 | HG01255.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*5478_*5479dupCA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5479 | chr11 | 77661437 | |||||
| chr11:77661437
|
A | ATGTG | 2 | a0001c0001t0027a0001c0002t0016 | 3 | HG02559.hp2 HG03139.hp1 NA18946.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5476_*5479dupCACA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5479 | chr11 | 77661437 | |||||
| chr11:77661437
|
ATG | A | 3 | a0001c0001t0052a0001c0002t0010a0001c0002t0033 | 5 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5478_*5479delCA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5478 | chr11 | 77661437 | |||||
| chr11:77661464
|
C | T | 1 | a0001c0001t0025 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5453G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5453 | chr11 | 77661464 | |||||
| chr11:77661638
|
T | C | 1 | a0001c0001t0062 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5279A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5279 | chr11 | 77661638 | |||||
| chr11:77661673
|
T | C | 1 | a0001c0001t0048 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5244A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5244 | chr11 | 77661673 | |||||
| chr11:77661727
|
T | G | 1 | a0001c0001t0026 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5190A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5190 | chr11 | 77661727 | |||||
| chr11:77661733
|
A | T | 2 | a0001c0001t0019a0007c0018t0032 | 3 | NA18963.hp2 NA19090.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5184T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5184 | chr11 | 77661733 | |||||
| chr11:77661762
|
CT | C | 10 | a0001c0001t0039a0001c0001t0063a0001c0002t0010others(7): Show | 15 | HG01069.hp1 HG01074.hp1 HG01081.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5154delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5154 | chr11 | 77661762 | |||||
| chr11:77661762
|
CTT | C | 11 | a0001c0002t0003a0001c0002t0014a0001c0002t0015others(8): Show | 69 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*5153_*5154delAA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 5153 | chr11 | 77661762 | |||||
| chr11:77662028
|
C | T | 1 | a0001c0001t0059 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4889G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4889 | chr11 | 77662028 | |||||
| chr11:77662037
|
T | G | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4880A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4880 | chr11 | 77662037 | |||||
| chr11:77662157
|
C | T | 1 | a0001c0001t0022 | 2 | HG03130.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4760G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4760 | chr11 | 77662157 | |||||
| chr11:77662205
|
T | C | 2 | a0001c0001t0013a0001c0001t0052 | 4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4712A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4712 | chr11 | 77662205 | |||||
| chr11:77662327
|
G | T | 3 | a0001c0001t0011a0001c0001t0046a0001c0001t0056 | 5 | HG01192.hp1 HG01928.hp1 HG02148.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4590C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4590 | chr11 | 77662327 | |||||
| chr11:77662369
|
T | G | 12 | a0001c0002t0003a0001c0002t0014a0001c0002t0015others(9): Show | 71 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*4548A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4548 | chr11 | 77662369 | |||||
| chr11:77662426
|
C | A | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(49): Show | 267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*4491G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4491 | chr11 | 77662426 | |||||
| chr11:77662543
|
A | G | 2 | a0001c0002t0016a0001c0002t0017 | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4374T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4374 | chr11 | 77662543 | |||||
| chr11:77662584
|
T | TA | 57 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(54): Show | 274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*4332dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4332 | chr11 | 77662584 | |||||
| chr11:77662685
|
C | A | 1 | a0001c0001t0065 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4232G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4232 | chr11 | 77662685 | |||||
| chr11:77662864
|
T | C | 1 | a0002c0003t0021 | 2 | HG00140.hp1 HG01123.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4053A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4053 | chr11 | 77662864 | |||||
| chr11:77662888
|
G | A | 7 | a0001c0001t0005a0001c0001t0008a0001c0001t0025others(4): Show | 18 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4029C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 4029 | chr11 | 77662888 | |||||
| chr11:77663004
|
G | A | 1 | a0001c0001t0051 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3913C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3913 | chr11 | 77663004 | |||||
| chr11:77663017
|
G | T | 1 | a0001c0002t0015 | 2 | NA18981.hp2 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3900C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3900 | chr11 | 77663017 | |||||
| chr11:77663019
|
G | GCA | 24 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(21): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3896_*3897dupTG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3897 | chr11 | 77663019 | |||||
| chr11:77663097
|
A | G | 1 | a0004c0016t0045 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3820T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3820 | chr11 | 77663097 | |||||
| chr11:77663164
|
A | G | 1 | a0001c0001t0044 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3753T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3753 | chr11 | 77663164 | |||||
| chr11:77663356
|
A | C | 2 | a0001c0001t0028a0001c0001t0043 | 2 | HG01358.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3561T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3561 | chr11 | 77663356 | |||||
| chr11:77663385
|
T | A | 1 | a0001c0001t0009 | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3532A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3532 | chr11 | 77663385 | |||||
| chr11:77663406
|
A | G | 1 | a0001c0001t0042 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3511T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3511 | chr11 | 77663406 | |||||
| chr11:77663626
|
T | A | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3291A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3291 | chr11 | 77663626 | |||||
| chr11:77663709
|
A | T | 1 | a0001c0001t0058 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3208T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 3208 | chr11 | 77663709 | |||||
| chr11:77663989
|
T | C | 1 | a0001c0001t0053 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2928A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2928 | chr11 | 77663989 | |||||
| chr11:77664037
|
C | T | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2880G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2880 | chr11 | 77664037 | |||||
| chr11:77664181
|
A | G | 1 | a0001c0002t0031 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2736T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2736 | chr11 | 77664181 | |||||
| chr11:77664316
|
G | A | 1 | a0001c0001t0027 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2601C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2601 | chr11 | 77664316 | |||||
| chr11:77664525
|
C | T | 1 | a0001c0002t0030 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2392G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2392 | chr11 | 77664525 | |||||
| chr11:77664738
|
T | C | 2 | a0001c0001t0022a0001c0001t0054 | 3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2179A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2179 | chr11 | 77664738 | |||||
| chr11:77664752
|
T | C | 1 | a0001c0001t0055 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2165A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2165 | chr11 | 77664752 | |||||
| chr11:77664886
|
T | G | 1 | a0001c0001t0056 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2031A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 2031 | chr11 | 77664886 | |||||
| chr11:77665060
|
A | G | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1857T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1857 | chr11 | 77665060 | |||||
| chr11:77665065
|
A | G | 1 | a0001c0002t0029 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1852T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1852 | chr11 | 77665065 | |||||
| chr11:77665078
|
A | G | 1 | a0001c0001t0057 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1839T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1839 | chr11 | 77665078 | |||||
| chr11:77665163
|
G | T | 2 | a0001c0001t0006a0001c0001t0041 | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1754C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1754 | chr11 | 77665163 | |||||
| chr11:77665202
|
C | T | 18 | a0001c0002t0003a0001c0002t0010a0001c0002t0014others(15): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1715G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1715 | chr11 | 77665202 | |||||
| chr11:77665369
|
A | G | 1 | a0001c0001t0040 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1548T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1548 | chr11 | 77665369 | |||||
| chr11:77665432
|
T | C | 1 | a0006c0007t0064 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1485A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1485 | chr11 | 77665432 | |||||
| chr11:77665733
|
A | G | 2 | a0001c0001t0038a0001c0001t0039 | 2 | HG00099.hp1 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1184T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1184 | chr11 | 77665733 | |||||
| chr11:77665761
|
C | A | 15 | a0001c0001t0001a0001c0001t0023a0001c0001t0057others(12): Show | 86 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1156G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1156 | chr11 | 77665761 | |||||
| chr11:77665776
|
GCACA | G | 18 | a0001c0002t0003a0001c0002t0010a0001c0002t0014others(15): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1137_*1140delTGTG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1137 | chr11 | 77665776 | |||||
| chr11:77665787
|
AAC | A | 4 | a0001c0001t0007a0001c0001t0065a0010c0013t0007others(1): Show | 7 | HG00544.hp1 HG00597.hp2 HG02080.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1128_*1129delGT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1128 | chr11 | 77665787 | |||||
| chr11:77665799
|
C | T | 1 | a0001c0002t0014 | 2 | HG01884.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1118G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1118 | chr11 | 77665799 | |||||
| chr11:77665873
|
G | A | 1 | a0001c0002t0024 | 2 | NA19005.hp2 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1044C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 1044 | chr11 | 77665873 | |||||
| chr11:77666247
|
A | T | 1 | a0001c0001t0028 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 670 | chr11 | 77666247 | |||||
| chr11:77666373
|
G | C | 2 | a0001c0001t0066a0001c0001t0067 | 2 | HG02040.hp1 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*544C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 544 | chr11 | 77666373 | |||||
| chr11:77666756
|
C | A | 1 | a0001c0001t0068 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*161G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 161 | chr11 | 77666756 | |||||
| chr11:77666823
|
A | T | 5 | a0001c0001t0005a0001c0001t0025a0001c0001t0026others(2): Show | 13 | HG01975.hp2 HG02056.hp2 NA18942.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*94T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 16/16 | 94 | chr11 | 77666823 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77667518
|
T | C | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.3752-27A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667518 | ||||||
| chr11:77667636
|
T | C | 1 | a0006c0007t0001g0349 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3752-145A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667636 | ||||||
| chr11:77667760
|
A | G | 76 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.3752-269T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667760 | ||||||
| chr11:77667841
|
T | A | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3752-350A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667841 | ||||||
| chr11:77667849
|
G | A | 45 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3752-358C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667849 | ||||||
| chr11:77667862
|
C | A | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3752-371G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77667862 | ||||||
| chr11:77668054
|
A | G | 273 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(270): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.3752-563T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668054 | ||||||
| chr11:77668160
|
C | T | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3752-669G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668160 | ||||||
| chr11:77668255
|
G | A | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3752-764C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668255 | ||||||
| chr11:77668262
|
A | G | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3752-771T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668262 | ||||||
| chr11:77668311
|
T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3752-820A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668311 | ||||||
| chr11:77668370
|
T | G | 1 | a0001c0001t0001g0336 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3752-879A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668370 | ||||||
| chr11:77668517
|
T | C | 1 | a0001c0002t0003g0049 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3752-1026A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668517 | ||||||
| chr11:77668543
|
T | G | 67 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(64): Show | 67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.3752-1052A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668543 | ||||||
| chr11:77668595
|
A | G | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3752-1104T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668595 | ||||||
| chr11:77668713
|
G | T | 13 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(10): Show | 13 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.3752-1222C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668713 | ||||||
| chr11:77668807
|
C | A | 1 | a0001c0001t0004g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3752-1316G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668807 | ||||||
| chr11:77668921
|
C | CAT | 350 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.3752-1432_3752-143 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77668921 | ||||||
| chr11:77669033
|
C | T | 2 | a0001c0001t0004g0105a0001c0001t0004g0106 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3752-1542G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669033 | ||||||
| chr11:77669103
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3752-1612G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669103 | ||||||
| chr11:77669183
|
T | C | 1 | a0002c0003t0002g0208 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3752-1692A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669183 | ||||||
| chr11:77669189
|
C | T | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3752-1698G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669189 | ||||||
| chr11:77669448
|
T | C | 67 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(64): Show | 67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.3752-1957A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669448 | ||||||
| chr11:77669820
|
A | G | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3751+2222T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669820 | ||||||
| chr11:77669989
|
T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3751+2053A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77669989 | ||||||
| chr11:77670092
|
C | T | 31 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(28): Show | 31 | HG00639.hp2 HG02055.hp1 HG02451.hp1 others(28): Show |
intron_variant | MODIFIER | c.3751+1950G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670092 | ||||||
| chr11:77670350
|
C | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0307a0001c0001t0001g0308 | 3 | HG01891.hp2 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3751+1692G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670350 | ||||||
| chr11:77670427
|
G | A | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3751+1615C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670427 | ||||||
| chr11:77670539
|
C | T | 3 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0126 | 3 | NA18963.hp1 NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.3751+1503G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670539 | ||||||
| chr11:77670706
|
T | C | 161 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(158): Show | 161 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.3751+1336A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670706 | ||||||
| chr11:77670721
|
T | A | 3 | a0001c0001t0002g0110a0001c0001t0002g0112a0001c0001t0002g0113 | 3 | HG02055.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3751+1321A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670721 | ||||||
| chr11:77670844
|
C | T | 3 | a0001c0001t0004g0101a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG02083.hp2 NA18612.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.3751+1198G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670844 | ||||||
| chr11:77670913
|
C | T | 108 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(105): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.3751+1129G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77670913 | ||||||
| chr11:77671021
|
G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3751+1021C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671021 | ||||||
| chr11:77671106
|
C | CA | 8 | a0001c0001t0001g0309a0001c0001t0001g0323a0001c0001t0001g0324others(5): Show | 8 | HG00280.hp1 HG02145.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.3751+935dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671106 | ||||||
| chr11:77671106
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0008g0267a0001c0001t0008g0270 | 2 | HG02148.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.3751+921_3751+935d others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671106 | ||||||
| chr11:77671122
|
AAAAAAAA others(25): Show |
A | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3751+888_3751+919d others(34): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671122 | ||||||
| chr11:77671122
|
AAAAAAAA others(27): Show |
A | 11 | a0001c0002t0003g0018a0001c0002t0003g0022a0001c0002t0003g0023others(8): Show | 11 | HG01243.hp2 HG02132.hp1 HG06807.hp2 others(8): Show |
intron_variant | MODIFIER | c.3751+886_3751+919d others(36): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671122 | ||||||
| chr11:77671123
|
AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0002g0115 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3751+894_3751+918d others(27): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671123 | ||||||
| chr11:77671123
|
AAAAAAAA others(26): Show |
A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3751+886_3751+918d others(35): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671123 | ||||||
| chr11:77671123
|
AAAAAAAA others(28): Show |
A | 1 | a0001c0002t0003g0048 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3751+884_3751+918d others(37): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671123 | ||||||
| chr11:77671124
|
AAAAAAAA others(23): Show |
A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3751+888_3751+917d others(32): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671124 | ||||||
| chr11:77671124
|
AAAAAAAA others(25): Show |
A | 2 | a0001c0002t0003g0030a0001c0002t0003g0072 | 2 | NA18967.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.3751+886_3751+917d others(34): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671124 | ||||||
| chr11:77671124
|
AAAAAAAA others(27): Show |
A | 34 | a0001c0002t0003g0019a0001c0002t0003g0020a0001c0002t0003g0021others(31): Show | 34 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.3751+884_3751+917d others(36): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671124 | ||||||
| chr11:77671125
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0008g0269 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3751+900_3751+916d others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671125 | ||||||
| chr11:77671125
|
AAAAAAAA others(26): Show |
A | 3 | a0001c0002t0003g0052a0001c0002t0003g0061a0001c0002t0003g0063 | 3 | HG00597.hp1 HG01192.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.3751+884_3751+916d others(35): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671125 | ||||||
| chr11:77671125
|
AAAAAAAA others(28): Show |
A | 3 | a0001c0002t0010g0013a0001c0002t0010g0350a0001c0002t0018g0046 | 3 | HG01074.hp1 HG01081.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3751+882_3751+916d others(37): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671125 | ||||||
| chr11:77671126
|
AAAAAAAA others(25): Show |
A | 1 | a0001c0002t0003g0073 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3751+884_3751+915d others(34): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671126 | ||||||
| chr11:77671126
|
AAAAAAAA others(27): Show |
A | 18 | a0001c0002t0003g0033a0001c0002t0003g0037a0001c0002t0003g0039others(15): Show | 18 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.3751+882_3751+915d others(36): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671126 | ||||||
| chr11:77671127
|
AAAAAAAA others(26): Show |
A | 3 | a0001c0002t0003g0032a0001c0002t0003g0036a0001c0002t0003g0070 | 3 | HG02809.hp1 HG03579.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.3751+882_3751+914d others(35): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671127 | ||||||
| chr11:77671127
|
AAAAAAAA others(28): Show |
A | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3751+880_3751+914d others(37): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671127 | ||||||
| chr11:77671129
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0004g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3751+898_3751+912d others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671129 | ||||||
| chr11:77671134
|
AAAAAATA others(3): Show |
A | 1 | a0004c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3751+898_3751+907d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671134 | ||||||
| chr11:77671136
|
A | T | 6 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315others(3): Show | 6 | HG02818.hp1 HG03516.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.3751+906T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671136 | ||||||
| chr11:77671136
|
AAAATATA others(9): Show |
A | 1 | a0001c0001t0001g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3751+890_3751+905d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671136 | ||||||
| chr11:77671137
|
AAATATAT others(4): Show |
A | 2 | a0001c0001t0022g0145a0001c0001t0054g0146 | 2 | HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3751+894_3751+904d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671137 | ||||||
| chr11:77671137
|
AAATATAT others(16): Show |
A | 2 | a0001c0001t0053g0191a0010c0013t0007g0262 | 2 | HG01168.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3751+882_3751+904d others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671137 | ||||||
| chr11:77671138
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3751+903_3751+904i others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
A | AT | 3 | a0001c0001t0005g0253a0001c0001t0038g0170a0008c0014t0005g0258 | 3 | HG00099.hp1 HG01975.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.3751+903_3751+904i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
A | T | 20 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0093others(17): Show | 20 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3751+904T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AAT | A | 17 | a0001c0001t0001g0292a0001c0001t0001g0297a0001c0001t0002g0129others(14): Show | 17 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.3751+902_3751+903d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AATAT | A | 17 | a0001c0001t0001g0094a0001c0001t0001g0299a0001c0001t0002g0124others(14): Show | 17 | HG00558.hp2 HG00639.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.3751+900_3751+903d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AATATAT | A | 18 | a0001c0001t0001g0280a0001c0001t0001g0312a0001c0001t0001g0334others(15): Show | 18 | HG00099.hp2 HG00673.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.3751+898_3751+903d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AATATATA others(1): Show |
A | 16 | a0001c0001t0001g0290a0001c0001t0001g0305a0001c0001t0001g0311others(13): Show | 16 | HG00408.hp1 HG00609.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.3751+896_3751+903d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AATATATA others(3): Show |
A | 11 | a0001c0001t0001g0279a0001c0001t0001g0293a0001c0001t0001g0294others(8): Show | 11 | HG00423.hp1 HG00544.hp2 HG03225.hp1 others(8): Show |
intron_variant | MODIFIER | c.3751+894_3751+903d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AATATATA others(5): Show |
A | 2 | a0004c0005t0020g0200a0012c0011t0007g0179 | 2 | HG02135.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3751+892_3751+903d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AATATATA others(7): Show |
A | 1 | a0001c0001t0002g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3751+890_3751+903d others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AATATATA others(9): Show |
A | 1 | a0001c0001t0002g0112 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3751+888_3751+903d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AATATATA others(13): Show |
A | 1 | a0001c0001t0001g0330 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3751+884_3751+903d others(22): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671138
|
AATATATA others(15): Show |
A | 1 | a0001c0001t0004g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3751+882_3751+903d others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671138 | ||||||
| chr11:77671139
|
AT | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0285a0001c0001t0002g0003others(6): Show | 9 | HG00323.hp2 HG01109.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3751+902delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | ||||||
| chr11:77671139
|
ATAT | A | 17 | a0001c0001t0002g0132a0001c0001t0004g0137a0001c0001t0004g0154others(14): Show | 17 | HG00733.hp1 HG01167.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.3751+900_3751+902d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | ||||||
| chr11:77671139
|
ATATAT | A | 18 | a0001c0001t0001g0089a0001c0001t0001g0092a0001c0001t0002g0108others(15): Show | 18 | HG00741.hp2 HG01070.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.3751+898_3751+902d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | ||||||
| chr11:77671139
|
ATATATAT | A | 8 | a0001c0001t0001g0282a0001c0001t0001g0286a0001c0001t0001g0288others(5): Show | 8 | HG00140.hp2 HG02132.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.3751+896_3751+902d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | ||||||
| chr11:77671139
|
ATATATAT others(2): Show |
A | 8 | a0001c0001t0001g0274a0001c0001t0001g0287a0001c0001t0001g0307others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.3751+894_3751+902d others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | ||||||
| chr11:77671139
|
ATATATAT others(4): Show |
A | 5 | a0001c0001t0001g0276a0001c0001t0058g0331a0001c0001t0063g0289others(2): Show | 5 | HG00558.hp1 HG02056.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3751+892_3751+902d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | ||||||
| chr11:77671139
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3751+884_3751+902d others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671139 | ||||||
| chr11:77671140
|
T | A | 12 | a0001c0001t0001g0296a0001c0001t0001g0317a0001c0001t0001g0324others(9): Show | 12 | HG00280.hp1 HG01123.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.3751+902A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671140 | ||||||
| chr11:77671142
|
T | A | 21 | a0001c0001t0001g0292a0001c0001t0001g0297a0001c0001t0002g0003others(18): Show | 21 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.3751+900A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671142 | ||||||
| chr11:77671144
|
T | A | 34 | a0001c0001t0001g0094a0001c0001t0001g0299a0001c0001t0002g0129others(31): Show | 34 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.3751+898A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671144 | ||||||
| chr11:77671146
|
T | A | 35 | a0001c0001t0001g0280a0001c0001t0001g0312a0001c0001t0001g0334others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.3751+896A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671146 | ||||||
| chr11:77671148
|
T | A | 29 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0286others(26): Show | 29 | HG00408.hp1 HG00609.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.3751+894A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671148 | ||||||
| chr11:77671150
|
T | A | 24 | a0001c0001t0001g0279a0001c0001t0001g0293a0001c0001t0001g0294others(21): Show | 24 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.3751+892A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671150 | ||||||
| chr11:77671152
|
T | A | 8 | a0001c0001t0001g0276a0001c0001t0001g0307a0001c0001t0006g0123others(5): Show | 8 | HG01891.hp2 HG02056.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3751+890A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671152 | ||||||
| chr11:77671154
|
T | A | 2 | a0001c0001t0002g0110a0001c0001t0041g0249 | 2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.3751+888A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671154 | ||||||
| chr11:77671156
|
T | A | 1 | a0001c0001t0002g0112 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3751+886A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671156 | ||||||
| chr11:77671160
|
T | A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3751+882A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671160 | ||||||
| chr11:77671199
|
A | G | 5 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0307others(2): Show | 5 | HG01891.hp2 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3751+843T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671199 | ||||||
| chr11:77671208
|
T | TATAC | 12 | a0001c0002t0010g0013a0001c0002t0010g0350a0001c0002t0010g0351others(9): Show | 12 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.3751+833_3751+834i others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671208 | ||||||
| chr11:77671208
|
T | TATATAC | 68 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.3751+833_3751+834i others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671208 | ||||||
| chr11:77671241
|
A | G | 2 | a0002c0003t0002g0208a0002c0003t0002g0227 | 2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.3751+801T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671241 | ||||||
| chr11:77671318
|
T | C | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3751+724A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671318 | ||||||
| chr11:77671402
|
T | C | 1 | a0001c0001t0004g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3751+640A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671402 | ||||||
| chr11:77671634
|
AT | A | 258 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(255): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.3751+407delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671634 | ||||||
| chr11:77671782
|
G | A | 25 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(22): Show | 25 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.3751+260C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671782 | ||||||
| chr11:77671842
|
C | T | 1 | a0002c0003t0002g0220 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3751+200G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77671842 | ||||||
| chr11:77672019
|
T | C | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3751+23A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 15/15 | chr11 | 77672019 | ||||||
| chr11:77672307
|
A | G | 1 | a0002c0003t0002g0217 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3563-77T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672307 | ||||||
| chr11:77672379
|
G | C | 68 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.3563-149C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672379 | ||||||
| chr11:77672466
|
T | C | 270 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(267): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.3563-236A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672466 | ||||||
| chr11:77672579
|
TA | T | 82 | a0001c0001t0004g0152a0001c0002t0003g0018a0001c0002t0003g0019others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.3563-350delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672579 | ||||||
| chr11:77672594
|
T | C | 1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3563-364A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672594 | ||||||
| chr11:77672685
|
T | C | 1 | a0003c0004t0002g0232 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3563-455A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672685 | ||||||
| chr11:77672716
|
T | G | 1 | a0001c0001t0004g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3563-486A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672716 | ||||||
| chr11:77672721
|
C | T | 1 | a0001c0001t0027g0260 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3563-491G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672721 | ||||||
| chr11:77672722
|
G | A | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3563-492C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672722 | ||||||
| chr11:77672807
|
C | T | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3563-577G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672807 | ||||||
| chr11:77672924
|
C | T | 1 | a0003c0004t0002g0231 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3563-694G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77672924 | ||||||
| chr11:77673127
|
C | A | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3563-897G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673127 | ||||||
| chr11:77673194
|
T | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3563-964A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673194 | ||||||
| chr11:77673392
|
C | T | 4 | a0001c0002t0010g0013a0001c0002t0010g0350a0001c0002t0010g0351others(1): Show | 4 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3563-1162G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673392 | ||||||
| chr11:77673673
|
A | C | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3562+1363T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673673 | ||||||
| chr11:77673926
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3562+1110A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673926 | ||||||
| chr11:77673951
|
C | T | 1 | a0002c0003t0002g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3562+1085G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673951 | ||||||
| chr11:77673963
|
G | A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3562+1073C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77673963 | ||||||
| chr11:77674023
|
T | C | 1 | a0001c0002t0016g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3562+1013A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674023 | ||||||
| chr11:77674217
|
A | C | 1 | a0001c0001t0006g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3562+819T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674217 | ||||||
| chr11:77674666
|
G | A | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3562+370C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674666 | ||||||
| chr11:77674667
|
A | G | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3562+369T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674667 | ||||||
| chr11:77674789
|
C | T | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3562+247G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674789 | ||||||
| chr11:77674868
|
A | G | 270 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(267): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.3562+168T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674868 | ||||||
| chr11:77674895
|
A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3562+141T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674895 | ||||||
| chr11:77674923
|
C | G | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3562+113G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674923 | ||||||
| chr11:77674923
|
C | T | 67 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(64): Show | 67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.3562+113G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674923 | ||||||
| chr11:77674924
|
G | C | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3562+112C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674924 | ||||||
| chr11:77674979
|
A | G | 1 | a0001c0002t0003g0058 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3562+57T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77674979 | ||||||
| chr11:77675003
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3562+33A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77675003 | ||||||
| chr11:77675004
|
T | G | 1 | a0001c0001t0004g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3562+32A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77675004 | ||||||
| chr11:77675027
|
T | G | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3562+9A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 14/15 | chr11 | 77675027 | ||||||
| chr11:77675618
|
C | T | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3342-362G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77675618 | ||||||
| chr11:77675913
|
A | G | 1 | a0001c0001t0048g0159 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3342-657T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77675913 | ||||||
| chr11:77675978
|
C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3342-722G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77675978 | ||||||
| chr11:77676279
|
CT | C | 6 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0312others(3): Show | 6 | HG01069.hp1 HG02451.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.3341+512delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676279 | ||||||
| chr11:77676279
|
CTT | C | 80 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.3341+511_3341+512d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676279 | ||||||
| chr11:77676309
|
G | C | 1 | a0001c0001t0063g0289 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3341+483C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676309 | ||||||
| chr11:77676424
|
C | T | 1 | a0001c0002t0003g0028 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3341+368G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676424 | ||||||
| chr11:77676489
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3341+303G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676489 | ||||||
| chr11:77676747
|
T | C | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.3341+45A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676747 | ||||||
| chr11:77676768
|
G | A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3341+24C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 13/15 | chr11 | 77676768 | ||||||
| chr11:77677083
|
T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3134-84A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677083 | ||||||
| chr11:77677252
|
G | A | 1 | a0001c0001t0004g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3134-253C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677252 | ||||||
| chr11:77677316
|
C | A | 1 | a0001c0001t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3134-317G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677316 | ||||||
| chr11:77677599
|
T | C | 1 | a0001c0001t0062g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3133+487A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677599 | ||||||
| chr11:77677703
|
G | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3133+383C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677703 | ||||||
| chr11:77677800
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3133+286C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677800 | ||||||
| chr11:77677975
|
T | C | 80 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.3133+111A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677975 | ||||||
| chr11:77677988
|
G | A | 1 | a0001c0001t0011g0162 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3133+98C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77677988 | ||||||
| chr11:77678007
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3133+79A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 12/15 | chr11 | 77678007 | ||||||
| chr11:77678193
|
CT | C | 160 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(157): Show | 160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.3066-41delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678193 | ||||||
| chr11:77678193
|
CTT | C | 184 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.3066-42_3066-41del others(2): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678193 | ||||||
| chr11:77678193
|
CTTT | C | 6 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0312others(3): Show | 6 | HG01070.hp2 HG02027.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.3066-43_3066-41del others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678193 | ||||||
| chr11:77678228
|
T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3066-75A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678228 | ||||||
| chr11:77678240
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3066-87G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678240 | ||||||
| chr11:77678419
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3066-266C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678419 | ||||||
| chr11:77678506
|
C | T | 1 | a0002c0003t0002g0241 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3066-353G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678506 | ||||||
| chr11:77678610
|
G | C | 1 | a0001c0001t0004g0136 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3066-457C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678610 | ||||||
| chr11:77678724
|
T | C | 2 | a0002c0003t0002g0099a0002c0003t0002g0228 | 2 | HG01358.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3066-571A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678724 | ||||||
| chr11:77678812
|
A | G | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3066-659T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678812 | ||||||
| chr11:77678925
|
C | T | 1 | a0001c0001t0006g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3066-772G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77678925 | ||||||
| chr11:77679089
|
C | CA | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3066-937dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679089 | ||||||
| chr11:77679257
|
T | C | 3 | a0001c0001t0004g0182a0001c0001t0004g0184a0001c0001t0051g0183 | 3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.3066-1104A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679257 | ||||||
| chr11:77679586
|
T | C | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3066-1433A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679586 | ||||||
| chr11:77679606
|
G | C | 2 | a0001c0001t0019g0161a0001c0001t0019g0176 | 2 | NA18963.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3066-1453C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679606 | ||||||
| chr11:77679613
|
A | C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3066-1460T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679613 | ||||||
| chr11:77679659
|
C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3066-1506G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679659 | ||||||
| chr11:77679672
|
C | CA | 38 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0002g0003others(35): Show | 38 | HG00639.hp2 HG01516.hp2 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.3066-1520dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77679672 | ||||||
| chr11:77680060
|
T | C | 1 | a0001c0001t0042g0173 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3066-1907A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680060 | ||||||
| chr11:77680121
|
G | A | 4 | a0001c0001t0013g0271a0001c0001t0013g0272a0001c0001t0013g0273others(1): Show | 4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3066-1968C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680121 | ||||||
| chr11:77680162
|
A | G | 268 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(265): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.3066-2009T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680162 | ||||||
| chr11:77680639
|
C | A | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.3066-2486G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680639 | ||||||
| chr11:77680650
|
T | C | 3 | a0001c0001t0001g0279a0006c0007t0001g0349a0006c0007t0064g0321 | 3 | NA18988.hp2 NA19056.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3066-2497A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680650 | ||||||
| chr11:77680727
|
A | G | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3066-2574T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680727 | ||||||
| chr11:77680759
|
A | G | 4 | a0001c0001t0001g0317a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | NA18968.hp2 NA18979.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.3066-2606T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680759 | ||||||
| chr11:77680993
|
A | C | 1 | a0001c0001t0001g0338 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3065+2717T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77680993 | ||||||
| chr11:77681011
|
A | C | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3065+2699T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681011 | ||||||
| chr11:77681094
|
C | T | 13 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(10): Show | 13 | HG01975.hp2 HG02056.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.3065+2616G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681094 | ||||||
| chr11:77681121
|
T | G | 1 | a0004c0005t0020g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3065+2589A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681121 | ||||||
| chr11:77681150
|
T | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3065+2560A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681150 | ||||||
| chr11:77681258
|
G | A | 1 | a0001c0002t0037g0060 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3065+2452C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681258 | ||||||
| chr11:77681499
|
T | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3065+2211A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77681499 | ||||||
| chr11:77682059
|
T | C | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3065+1651A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682059 | ||||||
| chr11:77682093
|
T | G | 3 | a0001c0001t0001g0279a0006c0007t0001g0349a0006c0007t0064g0321 | 3 | NA18988.hp2 NA19056.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.3065+1617A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682093 | ||||||
| chr11:77682311
|
G | A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3065+1399C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682311 | ||||||
| chr11:77682354
|
T | G | 4 | a0001c0002t0010g0013a0001c0002t0010g0350a0001c0002t0010g0351others(1): Show | 4 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3065+1356A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682354 | ||||||
| chr11:77682495
|
G | A | 9 | a0001c0002t0010g0013a0001c0002t0010g0350a0001c0002t0010g0351others(6): Show | 9 | HG01074.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.3065+1215C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682495 | ||||||
| chr11:77682649
|
C | T | 1 | a0002c0003t0002g0214 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3065+1061G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682649 | ||||||
| chr11:77682673
|
C | T | 1 | a0002c0003t0002g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3065+1037G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682673 | ||||||
| chr11:77682714
|
G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3065+996C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682714 | ||||||
| chr11:77682873
|
AGCATGT | A | 4 | a0001c0002t0010g0013a0001c0002t0010g0350a0001c0002t0010g0351others(1): Show | 4 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3065+831_3065+836d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682873 | ||||||
| chr11:77682901
|
G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3065+809C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682901 | ||||||
| chr11:77682948
|
G | C | 79 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.3065+762C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77682948 | ||||||
| chr11:77683026
|
C | T | 6 | a0002c0003t0002g0207a0002c0003t0002g0211a0002c0003t0002g0345others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.3065+684G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683026 | ||||||
| chr11:77683173
|
C | T | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3065+537G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683173 | ||||||
| chr11:77683228
|
T | C | 1 | a0002c0003t0002g0228 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3065+482A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683228 | ||||||
| chr11:77683397
|
A | G | 1 | a0001c0001t0004g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3065+313T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683397 | ||||||
| chr11:77683426
|
G | A | 1 | a0001c0001t0005g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3065+284C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683426 | ||||||
| chr11:77683532
|
C | T | 9 | a0001c0002t0010g0013a0001c0002t0010g0350a0001c0002t0010g0351others(6): Show | 9 | HG01074.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.3065+178G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683532 | ||||||
| chr11:77683555
|
G | A | 159 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.3065+155C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683555 | ||||||
| chr11:77683556
|
G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3065+154C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 11/15 | chr11 | 77683556 | ||||||
| chr11:77683859
|
T | C | 1 | a0001c0001t0009g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2956-40A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77683859 | ||||||
| chr11:77684207
|
T | A | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2956-388A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684207 | ||||||
| chr11:77684324
|
A | G | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2956-505T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684324 | ||||||
| chr11:77684429
|
C | G | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | NA18981.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2956-610G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684429 | ||||||
| chr11:77684652
|
G | A | 67 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(64): Show | 67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.2955+453C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684652 | ||||||
| chr11:77684736
|
C | G | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2955+369G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684736 | ||||||
| chr11:77684790
|
C | T | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2955+315G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684790 | ||||||
| chr11:77684804
|
A | G | 1 | a0001c0001t0002g0116 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2955+301T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684804 | ||||||
| chr11:77684822
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+283A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684822 | ||||||
| chr11:77684844
|
C | T | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2955+261G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684844 | ||||||
| chr11:77684988
|
G | GAAAT | 9 | a0001c0001t0002g0120a0001c0001t0004g0156a0001c0001t0007g0164others(6): Show | 9 | HG00597.hp2 HG01074.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2955+113_2955+116d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684988 | ||||||
| chr11:77684988
|
G | GAAATAAA others(1): Show |
59 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(56): Show | 59 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.2955+109_2955+116d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684988 | ||||||
| chr11:77684988
|
G | GAAATAAA others(5): Show |
13 | a0001c0002t0003g0022a0001c0002t0003g0027a0001c0002t0003g0028others(10): Show | 13 | HG00423.hp2 HG00733.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2955+105_2955+116d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684988 | ||||||
| chr11:77684988
|
G | GAAATAAA others(9): Show |
4 | a0001c0002t0003g0032a0001c0002t0016g0005a0001c0002t0016g0008others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+101_2955+116d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 10/15 | chr11 | 77684988 | ||||||
| chr11:77685294
|
A | ATTAT | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2901-139_2901-136d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685294 | ||||||
| chr11:77685295
|
T | C | 1 | a0001c0002t0003g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2901-136A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685295 | ||||||
| chr11:77685356
|
C | T | 1 | a0001c0001t0005g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2901-197G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685356 | ||||||
| chr11:77685676
|
A | G | 2 | a0001c0001t0001g0326a0001c0001t0004g0188 | 2 | HG00140.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.2901-517T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685676 | ||||||
| chr11:77685695
|
T | C | 1 | a0001c0001t0004g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2901-536A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685695 | ||||||
| chr11:77685813
|
T | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2901-654A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685813 | ||||||
| chr11:77685843
|
T | A | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2901-684A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77685843 | ||||||
| chr11:77686014
|
A | G | 80 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2901-855T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686014 | ||||||
| chr11:77686068
|
A | G | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2901-909T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686068 | ||||||
| chr11:77686120
|
T | C | 1 | a0001c0002t0018g0065 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2901-961A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686120 | ||||||
| chr11:77686141
|
T | G | 2 | a0002c0003t0002g0223a0002c0003t0002g0229 | 2 | HG01070.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2901-982A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686141 | ||||||
| chr11:77686163
|
T | C | 1 | a0001c0001t0004g0196 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2901-1004A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686163 | ||||||
| chr11:77686234
|
T | C | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2901-1075A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686234 | ||||||
| chr11:77686408
|
C | CAAAAA | 6 | a0001c0002t0017g0006a0001c0002t0017g0007a0001c0002t0029g0017others(3): Show | 6 | HG01243.hp2 HG02895.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2901-1254_2901-125 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(1): Show |
51 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(48): Show | 51 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.2901-1257_2901-125 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(2): Show |
22 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0127others(19): Show | 22 | HG00423.hp2 HG00639.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.2901-1258_2901-125 others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0005g0263a0001c0001t0005g0302a0001c0001t0006g0123others(2): Show | 5 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2901-1259_2901-125 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0335a0001c0002t0033g0012 | 2 | HG00408.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2901-1260_2901-125 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(5): Show |
22 | a0001c0001t0001g0016a0001c0001t0001g0274a0001c0001t0001g0277others(19): Show | 22 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.2901-1261_2901-125 others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(6): Show |
36 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0092others(33): Show | 36 | HG00323.hp1 HG00423.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.2901-1262_2901-125 others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(7): Show |
20 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(17): Show | 20 | HG00741.hp2 HG01070.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.2901-1263_2901-125 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(8): Show |
8 | a0001c0001t0001g0093a0001c0001t0001g0276a0001c0001t0001g0317others(5): Show | 8 | HG01071.hp1 HG01109.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2901-1264_2901-125 others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0009g0243others(1): Show | 4 | HG01516.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2901-1265_2901-125 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(10): Show |
9 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0129others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.2901-1266_2901-125 others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(11): Show |
19 | a0001c0001t0002g0110a0001c0001t0002g0128a0001c0001t0002g0130others(16): Show | 19 | HG00140.hp1 HG01070.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.2901-1267_2901-125 others(22): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(12): Show |
9 | a0002c0003t0002g0099a0002c0003t0002g0217a0002c0003t0002g0220others(6): Show | 9 | HG00733.hp1 HG01515.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.2901-1268_2901-125 others(23): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(13): Show |
19 | a0001c0001t0001g0264a0001c0001t0002g0108a0001c0001t0002g0115others(16): Show | 19 | HG00558.hp2 HG00673.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2901-1269_2901-125 others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(14): Show |
16 | a0001c0001t0002g0109a0001c0001t0002g0111a0001c0001t0002g0116others(13): Show | 16 | HG01433.hp1 HG01975.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.2901-1250_2901-124 others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0002g0124a0001c0001t0005g0038 | 2 | NA18965.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.2901-1250_2901-124 others(26): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0008g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(27): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(28): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(19): Show |
2 | a0001c0001t0052g0265a0002c0003t0002g0238 | 2 | HG01167.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2901-1250_2901-124 others(30): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(20): Show |
3 | a0001c0001t0005g0252a0001c0001t0013g0271a0001c0001t0013g0272 | 3 | NA18906.hp1 NA19043.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2901-1250_2901-124 others(31): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(29): Show |
1 | a0001c0001t0009g0245 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(40): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(32): Show |
1 | a0001c0001t0013g0273 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(43): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(35): Show |
1 | a0001c0001t0006g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(46): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686408
|
C | CAAAAAAA others(37): Show |
1 | a0001c0001t0009g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2901-1250_2901-124 others(48): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686408 | ||||||
| chr11:77686452
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2901-1293G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686452 | ||||||
| chr11:77686678
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1519C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686678 | ||||||
| chr11:77686679
|
G | T | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1520C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686679 | ||||||
| chr11:77686680
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1521A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686680 | ||||||
| chr11:77686682
|
T | G | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1523A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686682 | ||||||
| chr11:77686683
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1524C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686683 | ||||||
| chr11:77686687
|
A | C | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1528T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686687 | ||||||
| chr11:77686688
|
A | T | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2901-1529T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686688 | ||||||
| chr11:77686816
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2901-1657A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77686816 | ||||||
| chr11:77687022
|
A | G | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2901-1863T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687022 | ||||||
| chr11:77687169
|
G | A | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2901-2010C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687169 | ||||||
| chr11:77687253
|
G | A | 1 | a0001c0001t0004g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2901-2094C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687253 | ||||||
| chr11:77687408
|
A | G | 268 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(265): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2901-2249T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687408 | ||||||
| chr11:77687523
|
T | C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2901-2364A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687523 | ||||||
| chr11:77687564
|
G | C | 108 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(105): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.2901-2405C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687564 | ||||||
| chr11:77687576
|
G | A | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2901-2417C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687576 | ||||||
| chr11:77687631
|
T | C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2901-2472A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687631 | ||||||
| chr11:77687742
|
A | G | 6 | a0001c0002t0003g0019a0001c0002t0003g0020a0001c0002t0003g0021others(3): Show | 6 | HG02523.hp1 NA18747.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2901-2583T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687742 | ||||||
| chr11:77687838
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2901-2679T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687838 | ||||||
| chr11:77687870
|
C | T | 266 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(263): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.2901-2711G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687870 | ||||||
| chr11:77687871
|
A | G | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2901-2712T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77687871 | ||||||
| chr11:77688292
|
T | C | 272 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(269): Show | 272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.2900+2867A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688292 | ||||||
| chr11:77688368
|
T | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | NA18981.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2900+2791A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688368 | ||||||
| chr11:77688429
|
T | C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2900+2730A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688429 | ||||||
| chr11:77688557
|
G | T | 44 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2900+2602C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688557 | ||||||
| chr11:77688838
|
A | C | 12 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(9): Show | 12 | HG01975.hp2 HG02056.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.2900+2321T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77688838 | ||||||
| chr11:77689018
|
C | T | 3 | a0001c0001t0004g0182a0001c0001t0004g0184a0001c0001t0051g0183 | 3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2900+2141G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689018 | ||||||
| chr11:77689240
|
C | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2900+1919G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689240 | ||||||
| chr11:77689252
|
A | T | 16 | a0001c0002t0003g0032a0001c0002t0003g0033a0001c0002t0003g0035others(13): Show | 16 | HG01081.hp1 HG02257.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.2900+1907T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689252 | ||||||
| chr11:77689333
|
T | C | 1 | a0001c0002t0003g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2900+1826A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689333 | ||||||
| chr11:77689485
|
C | T | 1 | a0001c0001t0001g0334 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2900+1674G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689485 | ||||||
| chr11:77689584
|
A | G | 3 | a0001c0001t0004g0153a0001c0001t0004g0169a0001c0001t0004g0174 | 3 | HG01167.hp1 HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2900+1575T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689584 | ||||||
| chr11:77689680
|
A | G | 1 | a0001c0001t0001g0286 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2900+1479T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689680 | ||||||
| chr11:77689958
|
T | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2900+1201A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77689958 | ||||||
| chr11:77690023
|
G | A | 1 | a0001c0001t0044g0138 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2900+1136C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690023 | ||||||
| chr11:77690161
|
C | CA | 36 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0264others(33): Show | 36 | HG00558.hp1 HG00741.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.2900+997dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690161 | ||||||
| chr11:77690161
|
CA | C | 81 | a0001c0001t0001g0338a0001c0002t0003g0018a0001c0002t0003g0019others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2900+997delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690161 | ||||||
| chr11:77690172
|
A | C | 2 | a0001c0002t0015g0074a0001c0002t0024g0031 | 2 | NA19056.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2900+987T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690172 | ||||||
| chr11:77690173
|
A | C | 80 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.2900+986T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690173 | ||||||
| chr11:77690175
|
A | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2900+984T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690175 | ||||||
| chr11:77690181
|
C | A | 2 | a0001c0001t0005g0252a0001c0001t0023g0251 | 2 | HG02630.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2900+978G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690181 | ||||||
| chr11:77690182
|
A | T | 76 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(73): Show | 76 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.2900+977T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690182 | ||||||
| chr11:77690353
|
T | C | 1 | a0001c0001t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2900+806A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690353 | ||||||
| chr11:77690586
|
C | G | 1 | a0001c0001t0005g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2900+573G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690586 | ||||||
| chr11:77690629
|
A | C | 1 | a0001c0001t0001g0335 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2900+530T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690629 | ||||||
| chr11:77690815
|
C | T | 1 | a0001c0001t0004g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2900+344G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77690815 | ||||||
| chr11:77691069
|
C | A | 3 | a0001c0001t0001g0300a0001c0001t0001g0303a0011c0012t0001g0281 | 3 | HG00423.hp1 HG00558.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2900+90G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77691069 | ||||||
| chr11:77691127
|
C | T | 1 | a0001c0001t0067g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2900+32G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 9/15 | chr11 | 77691127 | ||||||
| chr11:77691367
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2821-129C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691367 | ||||||
| chr11:77691374
|
T | C | 72 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(69): Show | 72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.2821-136A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691374 | ||||||
| chr11:77691448
|
A | G | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2821-210T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691448 | ||||||
| chr11:77691644
|
T | A | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2821-406A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691644 | ||||||
| chr11:77691689
|
C | A | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2821-451G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691689 | ||||||
| chr11:77691744
|
A | G | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2821-506T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691744 | ||||||
| chr11:77691820
|
T | C | 1 | a0001c0001t0013g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2821-582A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77691820 | ||||||
| chr11:77692205
|
T | A | 4 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2821-967A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692205 | ||||||
| chr11:77692221
|
TACTACTT others(315): Show |
T | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2820+964_2821-984d others(2): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692221 | ||||||
| chr11:77692233
|
A | AT | 17 | a0001c0001t0004g0134a0001c0001t0004g0135a0001c0001t0004g0139others(14): Show | 17 | HG00609.hp1 HG01069.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2821-996dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATT | 11 | a0001c0001t0004g0140a0001c0001t0004g0142a0001c0001t0004g0147others(8): Show | 11 | HG00280.hp1 HG00323.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2821-997_2821-996d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTT | 21 | a0001c0001t0043g0157a0002c0003t0002g0099a0002c0003t0002g0208others(18): Show | 21 | HG00558.hp2 HG01070.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.2821-998_2821-996d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTT | 14 | a0002c0003t0002g0203a0002c0003t0002g0211a0002c0003t0002g0214others(11): Show | 14 | HG00673.hp2 HG00733.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2821-999_2821-996d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTT | 7 | a0001c0001t0002g0115a0001c0001t0002g0124a0002c0003t0002g0207others(4): Show | 7 | HG00140.hp1 HG01123.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2821-1000_2821-996 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTT | 7 | a0001c0001t0002g0109a0001c0001t0002g0111a0001c0001t0002g0116others(4): Show | 7 | HG02602.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2821-1001_2821-996 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT | 12 | a0001c0001t0002g0108a0001c0001t0002g0112a0001c0001t0002g0126others(9): Show | 12 | HG00639.hp2 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2821-1002_2821-996 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(1): Show |
6 | a0001c0001t0002g0110a0001c0001t0002g0113a0001c0001t0008g0267others(3): Show | 6 | HG02055.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2821-1003_2821-996 others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(2): Show |
9 | a0001c0001t0001g0311a0001c0001t0002g0003a0001c0001t0002g0004others(6): Show | 9 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.2821-1004_2821-996 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(3): Show |
32 | a0001c0001t0001g0016a0001c0001t0001g0088a0001c0001t0001g0274others(29): Show | 32 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.2821-1005_2821-996 others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(4): Show |
35 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(32): Show | 35 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.2821-1006_2821-996 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(5): Show |
9 | a0001c0001t0001g0277a0001c0001t0001g0285a0001c0001t0001g0288others(6): Show | 9 | HG01109.hp2 HG01175.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2821-1007_2821-996 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(6): Show |
6 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0094others(3): Show | 6 | HG01255.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.2821-1008_2821-996 others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(7): Show |
4 | a0001c0001t0001g0308a0001c0001t0001g0323a0001c0001t0001g0327others(1): Show | 4 | HG02132.hp2 HG02886.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.2821-1009_2821-996 others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0279a0001c0001t0001g0334 | 2 | NA18991.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2821-1010_2821-996 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2821-1012_2821-996 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(11): Show |
2 | a0001c0001t0001g0096a0001c0001t0001g0276 | 2 | HG03098.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2821-1013_2821-996 others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0307 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2821-1017_2821-996 others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
A | ATTTTTTT others(21): Show |
1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2821-1023_2821-996 others(31): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
AT | A | 7 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0196others(4): Show | 7 | HG01975.hp1 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2821-996delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692233
|
ATTTTTTT others(2): Show |
A | 15 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(12): Show | 15 | HG01975.hp2 HG02056.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.2821-1004_2821-996 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692233 | ||||||
| chr11:77692268
|
G | A | 46 | a0001c0001t0004g0247a0001c0001t0004g0248a0002c0003t0002g0099others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.2821-1030C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692268 | ||||||
| chr11:77692345
|
C | G | 1 | a0001c0001t0001g0307 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2821-1107G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692345 | ||||||
| chr11:77692370
|
A | G | 1 | a0001c0001t0040g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2821-1132T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692370 | ||||||
| chr11:77692495
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2820+1012G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692495 | ||||||
| chr11:77692656
|
C | G | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2820+851G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692656 | ||||||
| chr11:77692681
|
GT | G | 262 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(259): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.2820+825delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692681 | ||||||
| chr11:77692685
|
T | G | 1 | a0001c0002t0003g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2820+822A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692685 | ||||||
| chr11:77692686
|
T | G | 76 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(73): Show | 76 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.2820+821A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692686 | ||||||
| chr11:77692745
|
T | C | 4 | a0001c0002t0010g0013a0001c0002t0010g0350a0001c0002t0010g0351others(1): Show | 4 | HG01074.hp1 HG02055.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.2820+762A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692745 | ||||||
| chr11:77692820
|
G | C | 1 | a0001c0001t0001g0290 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2820+687C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692820 | ||||||
| chr11:77692878
|
A | G | 1 | a0001c0001t0001g0286 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2820+629T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77692878 | ||||||
| chr11:77693065
|
A | C | 1 | a0001c0002t0003g0072 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2820+442T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77693065 | ||||||
| chr11:77693229
|
C | G | 4 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2820+278G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77693229 | ||||||
| chr11:77693352
|
C | G | 4 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0005t0049g0202others(1): Show | 4 | HG02451.hp2 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2820+155G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 8/15 | chr11 | 77693352 | ||||||
| chr11:77693764
|
C | CATTT | 141 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(138): Show | 141 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.2716-157_2716-154d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | ||||||
| chr11:77693764
|
C | CATTTATT others(1): Show |
23 | a0001c0001t0001g0016a0001c0001t0001g0280a0001c0001t0001g0303others(20): Show | 23 | HG00099.hp2 HG00423.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2716-161_2716-154d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | ||||||
| chr11:77693764
|
C | CATTTATT others(5): Show |
18 | a0001c0001t0001g0300a0001c0001t0001g0319a0002c0003t0002g0211others(15): Show | 18 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.2716-165_2716-154d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | ||||||
| chr11:77693764
|
C | CATTTATT others(9): Show |
20 | a0001c0001t0001g0320a0002c0003t0002g0099a0002c0003t0002g0205others(17): Show | 20 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.2716-169_2716-154d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | ||||||
| chr11:77693764
|
CATTT | C | 6 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0119others(3): Show | 6 | HG02647.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2716-157_2716-154d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | ||||||
| chr11:77693764
|
CATTTATT others(5): Show |
C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2716-165_2716-154d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693764 | ||||||
| chr11:77693871
|
G | A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2716-260C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77693871 | ||||||
| chr11:77694096
|
A | T | 110 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(107): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2716-485T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694096 | ||||||
| chr11:77694147
|
G | T | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2716-536C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694147 | ||||||
| chr11:77694221
|
T | A | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2716-610A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694221 | ||||||
| chr11:77694417
|
C | G | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2716-806G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694417 | ||||||
| chr11:77694522
|
T | C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2716-911A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694522 | ||||||
| chr11:77694769
|
A | C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2716-1158T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694769 | ||||||
| chr11:77694798
|
A | C | 2 | a0001c0002t0003g0061a0001c0002t0003g0077 | 2 | NA18942.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.2716-1187T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77694798 | ||||||
| chr11:77695212
|
A | G | 2 | a0002c0003t0002g0208a0002c0003t0002g0227 | 2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2716-1601T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695212 | ||||||
| chr11:77695237
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0332 | 3 | NA19005.hp1 NA19068.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2716-1626T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695237 | ||||||
| chr11:77695667
|
C | T | 2 | a0001c0001t0004g0160a0001c0001t0004g0167 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2716-2056G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695667 | ||||||
| chr11:77695840
|
A | G | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2716-2229T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695840 | ||||||
| chr11:77695943
|
C | T | 22 | a0001c0002t0003g0018a0001c0002t0003g0053a0001c0002t0003g0054others(19): Show | 22 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.2716-2332G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77695943 | ||||||
| chr11:77696030
|
G | A | 1 | a0001c0001t0001g0311 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2716-2419C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696030 | ||||||
| chr11:77696081
|
A | G | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2715+2406T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696081 | ||||||
| chr11:77696489
|
A | G | 1 | a0001c0002t0034g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2715+1998T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696489 | ||||||
| chr11:77696554
|
CCCATTTT others(1): Show |
C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+1925_2715+193 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696554 | ||||||
| chr11:77696607
|
A | T | 269 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(266): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.2715+1880T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696607 | ||||||
| chr11:77696711
|
A | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2715+1776T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77696711 | ||||||
| chr11:77697234
|
G | A | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+1253C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697234 | ||||||
| chr11:77697288
|
C | T | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2715+1199G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697288 | ||||||
| chr11:77697381
|
T | C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+1106A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697381 | ||||||
| chr11:77697398
|
A | G | 1 | a0001c0002t0034g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2715+1089T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697398 | ||||||
| chr11:77697441
|
TATATATA others(39): Show |
T | 268 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(265): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2715+1000_2715+104 others(50): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697441 | ||||||
| chr11:77697600
|
T | G | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2715+887A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697600 | ||||||
| chr11:77697694
|
A | T | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+793T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697694 | ||||||
| chr11:77697695
|
T | A | 1 | a0001c0001t0004g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2715+792A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697695 | ||||||
| chr11:77697832
|
C | T | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2715+655G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697832 | ||||||
| chr11:77697849
|
A | G | 1 | a0001c0001t0004g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2715+638T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697849 | ||||||
| chr11:77697987
|
T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2715+500A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77697987 | ||||||
| chr11:77698073
|
T | G | 113 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(110): Show | 113 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.2715+414A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698073 | ||||||
| chr11:77698201
|
G | A | 268 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(265): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2715+286C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698201 | ||||||
| chr11:77698289
|
G | A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2715+198C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698289 | ||||||
| chr11:77698297
|
A | G | 2 | a0001c0001t0008g0267a0002c0003t0008g0266 | 2 | HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2715+190T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698297 | ||||||
| chr11:77698362
|
C | T | 67 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(64): Show | 67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.2715+125G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 7/15 | chr11 | 77698362 | ||||||
| chr11:77698787
|
C | T | 74 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.2509-94G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77698787 | ||||||
| chr11:77698814
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2509-121A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77698814 | ||||||
| chr11:77698908
|
C | T | 1 | a0009c0008t0003g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2509-215G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77698908 | ||||||
| chr11:77699003
|
C | T | 2 | a0001c0002t0003g0050a0001c0002t0003g0059 | 2 | HG00280.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.2509-310G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699003 | ||||||
| chr11:77699061
|
T | C | 2 | a0002c0003t0002g0208a0002c0003t0002g0227 | 2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2509-368A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699061 | ||||||
| chr11:77699062
|
A | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2509-369T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699062 | ||||||
| chr11:77699361
|
A | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2509-668T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699361 | ||||||
| chr11:77699421
|
G | GAAACTTA others(3): Show |
350 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.2509-729_2509-728i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699421 | ||||||
| chr11:77699471
|
A | T | 1 | a0002c0003t0002g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2509-778T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699471 | ||||||
| chr11:77699633
|
C | T | 268 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(265): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2509-940G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699633 | ||||||
| chr11:77699662
|
G | A | 4 | a0001c0001t0004g0137a0001c0001t0004g0154a0001c0001t0004g0185others(1): Show | 4 | HG00609.hp1 HG02523.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2509-969C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699662 | ||||||
| chr11:77699823
|
T | C | 1 | a0001c0002t0003g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2508+898A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699823 | ||||||
| chr11:77699858
|
A | G | 9 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111others(6): Show | 9 | HG02602.hp2 HG03654.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.2508+863T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77699858 | ||||||
| chr11:77700136
|
A | G | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.2508+585T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700136 | ||||||
| chr11:77700300
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2508+421C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700300 | ||||||
| chr11:77700328
|
C | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2508+393G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700328 | ||||||
| chr11:77700349
|
C | CA | 17 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0004g0104others(14): Show | 17 | HG00597.hp2 HG00741.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2508+371dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | ||||||
| chr11:77700349
|
C | CAA | 20 | a0001c0001t0001g0286a0001c0001t0001g0308a0001c0001t0001g0342others(17): Show | 20 | HG00609.hp1 HG01074.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.2508+370_2508+371d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | ||||||
| chr11:77700349
|
C | CAAA | 67 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0088others(64): Show | 67 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.2508+369_2508+371d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | ||||||
| chr11:77700349
|
C | CAAAA | 20 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0276others(17): Show | 20 | HG01123.hp2 HG01261.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2508+368_2508+371d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | ||||||
| chr11:77700349
|
C | CCA | 3 | a0001c0001t0013g0272a0001c0001t0013g0273a0001c0001t0052g0265 | 3 | HG02572.hp1 HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2508+371_2508+372i others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | ||||||
| chr11:77700349
|
CA | C | 118 | a0001c0001t0002g0111a0001c0001t0002g0114a0001c0001t0002g0115others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2508+371delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | ||||||
| chr11:77700349
|
CAA | C | 6 | a0001c0001t0006g0127a0001c0002t0003g0022a0001c0002t0017g0006others(3): Show | 6 | HG01168.hp2 HG01243.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2508+370_2508+371d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | ||||||
| chr11:77700349
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0013g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2508+361_2508+371d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700349 | ||||||
| chr11:77700361
|
A | C | 1 | a0001c0001t0013g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2508+360T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 6/15 | chr11 | 77700361 | ||||||
| chr11:77702552
|
T | C | 2 | a0001c0001t0004g0105a0001c0001t0004g0106 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.734-57A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77702552 | ||||||
| chr11:77702780
|
A | G | 1 | a0001c0002t0003g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.734-285T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77702780 | ||||||
| chr11:77703337
|
T | C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-842A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77703337 | ||||||
| chr11:77703466
|
A | T | 2 | a0001c0002t0014g0009a0001c0002t0014g0011 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.734-971T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77703466 | ||||||
| chr11:77703809
|
A | AAT | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-1315_734-1314i others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77703809 | ||||||
| chr11:77703887
|
C | T | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-1392G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77703887 | ||||||
| chr11:77704187
|
G | A | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-1692C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704187 | ||||||
| chr11:77704497
|
G | A | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-2002C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704497 | ||||||
| chr11:77704520
|
G | A | 112 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(109): Show | 112 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.734-2025C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704520 | ||||||
| chr11:77704529
|
T | C | 81 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-2034A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704529 | ||||||
| chr11:77704732
|
G | T | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-2237C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704732 | ||||||
| chr11:77704753
|
G | GT | 35 | a0001c0001t0001g0016a0001c0001t0001g0264a0001c0001t0001g0274others(32): Show | 35 | HG00408.hp1 HG00609.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.734-2259dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | ||||||
| chr11:77704753
|
G | GTT | 10 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0332others(7): Show | 10 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-2260_734-2259d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | ||||||
| chr11:77704753
|
G | GTTTTT | 57 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0021others(54): Show | 57 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.734-2263_734-2259d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | ||||||
| chr11:77704753
|
G | GTTTTTT | 6 | a0001c0002t0003g0020a0001c0002t0003g0069a0001c0002t0003g0083others(3): Show | 6 | NA18950.hp1 NA18991.hp1 NA19078.hp2 others(3): Show |
intron_variant | MODIFIER | c.734-2264_734-2259d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | ||||||
| chr11:77704753
|
GT | G | 70 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.734-2259delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704753 | ||||||
| chr11:77704775
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.734-2280C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704775 | ||||||
| chr11:77704964
|
G | A | 5 | a0001c0001t0004g0153a0001c0001t0004g0169a0001c0001t0004g0174others(2): Show | 5 | HG01167.hp1 HG01261.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.734-2469C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77704964 | ||||||
| chr11:77705046
|
T | C | 268 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(265): Show | 268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.734-2551A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705046 | ||||||
| chr11:77705234
|
G | T | 1 | a0001c0001t0004g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.734-2739C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705234 | ||||||
| chr11:77705247
|
G | C | 1 | a0001c0001t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.734-2752C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705247 | ||||||
| chr11:77705386
|
G | T | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.734-2891C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705386 | ||||||
| chr11:77705445
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0097others(1): Show | 4 | HG01261.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-2950G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705445 | ||||||
| chr11:77705471
|
T | C | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-2976A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705471 | ||||||
| chr11:77705825
|
T | C | 2 | a0001c0001t0004g0160a0001c0001t0004g0167 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.734-3330A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705825 | ||||||
| chr11:77705861
|
A | C | 192 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(189): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.734-3366T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705861 | ||||||
| chr11:77705879
|
C | A | 3 | a0002c0003t0002g0235a0002c0003t0002g0236a0002c0003t0002g0238 | 3 | HG00733.hp1 HG01167.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.734-3384G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705879 | ||||||
| chr11:77705915
|
A | C | 1 | a0001c0002t0016g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.734-3420T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77705915 | ||||||
| chr11:77706059
|
C | T | 1 | a0001c0001t0019g0176 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.734-3564G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706059 | ||||||
| chr11:77706089
|
A | G | 9 | a0001c0001t0062g0284a0001c0002t0014g0009a0001c0002t0014g0011others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.734-3594T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706089 | ||||||
| chr11:77706166
|
G | A | 1 | a0004c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.734-3671C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706166 | ||||||
| chr11:77706240
|
C | CA | 23 | a0001c0001t0001g0089a0001c0001t0001g0285a0001c0001t0001g0329others(20): Show | 23 | HG00741.hp2 HG01243.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.734-3746dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706240 | ||||||
| chr11:77706314
|
T | C | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.734-3819A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706314 | ||||||
| chr11:77706347
|
G | T | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.734-3852C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706347 | ||||||
| chr11:77706663
|
T | A | 80 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.734-4168A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706663 | ||||||
| chr11:77706699
|
C | T | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.734-4204G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706699 | ||||||
| chr11:77706864
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-4369A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77706864 | ||||||
| chr11:77707216
|
G | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-4721C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707216 | ||||||
| chr11:77707450
|
T | C | 1 | a0001c0001t0004g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.734-4955A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707450 | ||||||
| chr11:77707657
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-5162G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707657 | ||||||
| chr11:77707835
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-5340G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707835 | ||||||
| chr11:77707915
|
C | T | 2 | a0001c0002t0017g0006a0007c0018t0032g0014 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.734-5420G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77707915 | ||||||
| chr11:77708038
|
C | T | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.734-5543G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708038 | ||||||
| chr11:77708053
|
T | A | 3 | a0002c0003t0002g0210a0002c0003t0002g0224a0002c0003t0002g0233 | 3 | HG03491.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.734-5558A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708053 | ||||||
| chr11:77708190
|
T | C | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.734-5695A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708190 | ||||||
| chr11:77708330
|
G | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-5835C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708330 | ||||||
| chr11:77708399
|
C | T | 1 | a0001c0002t0030g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.734-5904G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708399 | ||||||
| chr11:77708511
|
A | T | 4 | a0002c0003t0002g0345a0002c0003t0002g0346a0002c0003t0002g0347others(1): Show | 4 | HG01891.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-6016T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708511 | ||||||
| chr11:77708754
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.734-6259G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708754 | ||||||
| chr11:77708758
|
C | G | 1 | a0001c0001t0057g0278 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.734-6263G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708758 | ||||||
| chr11:77708774
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-6279A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708774 | ||||||
| chr11:77708859
|
C | T | 2 | a0002c0003t0002g0240a0002c0003t0002g0241 | 2 | HG02027.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.734-6364G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708859 | ||||||
| chr11:77708919
|
G | A | 1 | a0004c0016t0045g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.734-6424C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708919 | ||||||
| chr11:77708943
|
T | C | 4 | a0001c0001t0002g0306a0001c0001t0023g0275a0005c0006t0012g0001others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-6448A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708943 | ||||||
| chr11:77708971
|
C | A | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.734-6476G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77708971 | ||||||
| chr11:77709143
|
T | G | 1 | a0001c0001t0007g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.734-6648A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709143 | ||||||
| chr11:77709269
|
C | T | 273 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(270): Show | 273 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.734-6774G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709269 | ||||||
| chr11:77709473
|
A | T | 2 | a0001c0001t0038g0170a0001c0001t0039g0166 | 2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.734-6978T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709473 | ||||||
| chr11:77709537
|
C | T | 6 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0123others(3): Show | 6 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-7042G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709537 | ||||||
| chr11:77709546
|
A | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.734-7051T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709546 | ||||||
| chr11:77709694
|
CT | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-7200delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709694 | ||||||
| chr11:77709867
|
G | C | 3 | a0001c0002t0010g0013a0001c0002t0033g0012a0007c0018t0032g0014 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.734-7372C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77709867 | ||||||
| chr11:77710159
|
TA | T | 6 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0002t0014g0009others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-7665delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710159 | ||||||
| chr11:77710160
|
A | T | 1 | a0001c0001t0055g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.734-7665T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710160 | ||||||
| chr11:77710196
|
G | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-7701C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710196 | ||||||
| chr11:77710231
|
T | C | 8 | a0001c0001t0001g0274a0001c0001t0001g0334a0001c0001t0001g0335others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-7736A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710231 | ||||||
| chr11:77710359
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-7864A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710359 | ||||||
| chr11:77710401
|
T | A | 1 | a0001c0002t0003g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.734-7906A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710401 | ||||||
| chr11:77710402
|
T | A | 1 | a0001c0002t0003g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.734-7907A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710402 | ||||||
| chr11:77710435
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.734-7940G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710435 | ||||||
| chr11:77710502
|
G | A | 1 | a0004c0005t0020g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.734-8007C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710502 | ||||||
| chr11:77710506
|
T | C | 1 | a0002c0003t0002g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.734-8011A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710506 | ||||||
| chr11:77710536
|
C | T | 1 | a0001c0001t0005g0253 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.734-8041G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77710536 | ||||||
| chr11:77711063
|
A | G | 1 | a0001c0002t0034g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.734-8568T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711063 | ||||||
| chr11:77711108
|
T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.734-8613A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711108 | ||||||
| chr11:77711119
|
C | A | 1 | a0001c0001t0004g0192 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.734-8624G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711119 | ||||||
| chr11:77711120
|
CT | C | 5 | a0001c0001t0001g0274a0001c0001t0001g0334a0001c0001t0001g0335others(2): Show | 5 | HG00408.hp1 HG00609.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-8626delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711120 | ||||||
| chr11:77711143
|
T | TA | 16 | a0001c0001t0001g0276a0001c0001t0001g0285a0001c0001t0001g0296others(13): Show | 16 | HG01256.hp2 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.734-8649dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711143 | ||||||
| chr11:77711143
|
T | TAA | 62 | a0001c0001t0002g0003a0001c0002t0003g0018a0001c0002t0003g0020others(59): Show | 62 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.734-8650_734-8649d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711143 | ||||||
| chr11:77711143
|
T | TAAA | 7 | a0001c0002t0003g0019a0001c0002t0014g0009a0001c0002t0014g0011others(4): Show | 7 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-8651_734-8649d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711143 | ||||||
| chr11:77711143
|
TA | T | 58 | a0001c0001t0001g0091a0001c0001t0001g0305a0001c0001t0002g0114others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.734-8649delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711143 | ||||||
| chr11:77711180
|
T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.734-8685A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711180 | ||||||
| chr11:77711287
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.734-8792T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711287 | ||||||
| chr11:77711290
|
C | T | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.734-8795G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711290 | ||||||
| chr11:77711483
|
AT | A | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-8989delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711483 | ||||||
| chr11:77711485
|
G | A | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-8990C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711485 | ||||||
| chr11:77711540
|
G | T | 1 | a0003c0004t0002g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.734-9045C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711540 | ||||||
| chr11:77711590
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.734-9095G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711590 | ||||||
| chr11:77711671
|
A | AAAAC | 80 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.734-9180_734-9177d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711671 | ||||||
| chr11:77711759
|
C | T | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.734-9264G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711759 | ||||||
| chr11:77711790
|
T | G | 13 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(10): Show | 13 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.734-9295A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711790 | ||||||
| chr11:77711939
|
C | T | 4 | a0001c0001t0002g0306a0001c0001t0023g0275a0005c0006t0012g0001others(1): Show | 4 | HG02451.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-9444G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77711939 | ||||||
| chr11:77712002
|
AGATT | A | 80 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.734-9511_734-9508d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712002 | ||||||
| chr11:77712142
|
T | C | 1 | a0001c0001t0004g0192 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.734-9647A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712142 | ||||||
| chr11:77712675
|
T | C | 1 | a0001c0001t0007g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.734-10180A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712675 | ||||||
| chr11:77712806
|
T | A | 1 | a0001c0001t0004g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.734-10311A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712806 | ||||||
| chr11:77712906
|
C | T | 1 | a0001c0002t0003g0020 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.734-10411G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712906 | ||||||
| chr11:77712981
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-10486A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77712981 | ||||||
| chr11:77713201
|
T | G | 2 | a0001c0001t0038g0170a0001c0001t0039g0166 | 2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.734-10706A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713201 | ||||||
| chr11:77713223
|
G | A | 9 | a0001c0001t0004g0100a0001c0001t0004g0193a0001c0001t0004g0194others(6): Show | 9 | HG01975.hp1 HG02040.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.734-10728C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713223 | ||||||
| chr11:77713315
|
G | C | 1 | a0001c0001t0005g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.734-10820C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713315 | ||||||
| chr11:77713476
|
T | C | 1 | a0001c0001t0004g0189 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.734-10981A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713476 | ||||||
| chr11:77713573
|
A | G | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.734-11078T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713573 | ||||||
| chr11:77713576
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.734-11081C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77713576 | ||||||
| chr11:77714040
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0004g0175others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.733+11505G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714040 | ||||||
| chr11:77714114
|
A | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0004g0175others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.733+11431T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714114 | ||||||
| chr11:77714272
|
T | C | 1 | a0001c0002t0003g0049 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.733+11273A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714272 | ||||||
| chr11:77714552
|
G | C | 2 | a0001c0001t0004g0105a0001c0001t0004g0106 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.733+10993C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714552 | ||||||
| chr11:77714660
|
G | C | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.733+10885C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714660 | ||||||
| chr11:77714710
|
C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.733+10835G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714710 | ||||||
| chr11:77714711
|
G | A | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+10834C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714711 | ||||||
| chr11:77714745
|
G | C | 22 | a0001c0001t0001g0264a0001c0001t0005g0038a0001c0001t0005g0252others(19): Show | 22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.733+10800C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714745 | ||||||
| chr11:77714842
|
T | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+10703A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714842 | ||||||
| chr11:77714943
|
A | C | 68 | a0001c0001t0004g0175a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.733+10602T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77714943 | ||||||
| chr11:77715050
|
G | A | 109 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(106): Show | 109 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.733+10495C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715050 | ||||||
| chr11:77715109
|
G | A | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.733+10436C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715109 | ||||||
| chr11:77715148
|
G | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.733+10397C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715148 | ||||||
| chr11:77715206
|
T | C | 3 | a0001c0001t0002g0110a0001c0001t0002g0112a0001c0001t0002g0113 | 3 | HG02055.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.733+10339A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715206 | ||||||
| chr11:77715227
|
T | C | 9 | a0001c0001t0001g0274a0001c0001t0001g0334a0001c0001t0001g0335others(6): Show | 9 | HG00408.hp1 HG00609.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.733+10318A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715227 | ||||||
| chr11:77715230
|
C | CA | 72 | a0001c0001t0004g0175a0001c0002t0003g0018a0001c0002t0003g0019others(69): Show | 72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.733+10314dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715230 | ||||||
| chr11:77715300
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.733+10245A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715300 | ||||||
| chr11:77715379
|
ATGT | A | 4 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0130others(1): Show | 4 | HG02622.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+10163_733+1016 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715379 | ||||||
| chr11:77715400
|
T | C | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+10145A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715400 | ||||||
| chr11:77715457
|
TA | T | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+10087delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715457 | ||||||
| chr11:77715499
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+10046C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715499 | ||||||
| chr11:77715508
|
C | T | 2 | a0002c0003t0002g0345a0002c0003t0002g0347 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.733+10037G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715508 | ||||||
| chr11:77715551
|
G | A | 2 | a0001c0001t0004g0105a0001c0001t0004g0106 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.733+9994C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715551 | ||||||
| chr11:77715670
|
A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.733+9875T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715670 | ||||||
| chr11:77715694
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+9851G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715694 | ||||||
| chr11:77715779
|
T | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0004g0175others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.733+9766A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77715779 | ||||||
| chr11:77716531
|
T | G | 1 | a0003c0004t0002g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.733+9014A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716531 | ||||||
| chr11:77716701
|
C | T | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.733+8844G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716701 | ||||||
| chr11:77716722
|
T | C | 1 | a0001c0002t0003g0036 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733+8823A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716722 | ||||||
| chr11:77716732
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0094 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.733+8813A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716732 | ||||||
| chr11:77716933
|
T | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+8612A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77716933 | ||||||
| chr11:77717119
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733+8426T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717119 | ||||||
| chr11:77717156
|
CA | C | 79 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0004g0175others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.733+8388delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717156 | ||||||
| chr11:77717166
|
A | C | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.733+8379T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717166 | ||||||
| chr11:77717181
|
CA | C | 260 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(257): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.733+8363delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717181 | ||||||
| chr11:77717627
|
T | C | 1 | a0002c0003t0002g0346 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.733+7918A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717627 | ||||||
| chr11:77717794
|
A | T | 1 | a0002c0003t0002g0221 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.733+7751T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717794 | ||||||
| chr11:77717888
|
C | T | 43 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.733+7657G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77717888 | ||||||
| chr11:77718260
|
C | T | 1 | a0001c0001t0004g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.733+7285G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718260 | ||||||
| chr11:77718263
|
G | A | 2 | a0001c0001t0002g0116a0001c0001t0002g0126 | 2 | NA18963.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.733+7282C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718263 | ||||||
| chr11:77718302
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.733+7243C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718302 | ||||||
| chr11:77718350
|
T | C | 1 | a0001c0001t0002g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.733+7195A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718350 | ||||||
| chr11:77718534
|
T | C | 1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.733+7011A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718534 | ||||||
| chr11:77718879
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+6666A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718879 | ||||||
| chr11:77718908
|
A | G | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+6637T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718908 | ||||||
| chr11:77718987
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+6558C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77718987 | ||||||
| chr11:77719015
|
G | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+6530C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719015 | ||||||
| chr11:77719134
|
C | T | 3 | a0001c0001t0022g0144a0001c0001t0022g0145a0001c0001t0054g0146 | 3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.733+6411G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719134 | ||||||
| chr11:77719147
|
T | C | 3 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0016t0045g0201 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.733+6398A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719147 | ||||||
| chr11:77719405
|
A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.733+6140T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719405 | ||||||
| chr11:77719555
|
A | C | 2 | a0001c0002t0010g0013a0001c0002t0033g0012 | 2 | HG01074.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.733+5990T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719555 | ||||||
| chr11:77719607
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+5938G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719607 | ||||||
| chr11:77719608
|
A | T | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.733+5937T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77719608 | ||||||
| chr11:77720013
|
G | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0094 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.733+5532C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720013 | ||||||
| chr11:77720123
|
A | G | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.733+5422T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720123 | ||||||
| chr11:77720146
|
C | T | 1 | a0002c0003t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.733+5399G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720146 | ||||||
| chr11:77720175
|
G | T | 6 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0123others(3): Show | 6 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+5370C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720175 | ||||||
| chr11:77720184
|
G | A | 76 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(73): Show | 76 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.733+5361C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720184 | ||||||
| chr11:77720261
|
C | T | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+5284G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720261 | ||||||
| chr11:77720289
|
G | A | 158 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(155): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.733+5256C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720289 | ||||||
| chr11:77720590
|
G | A | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.733+4955C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720590 | ||||||
| chr11:77720822
|
T | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+4723A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77720822 | ||||||
| chr11:77721039
|
T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.733+4506A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77721039 | ||||||
| chr11:77721459
|
G | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+4086C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77721459 | ||||||
| chr11:77721816
|
C | CTGAA | 6 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0016g0005others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.733+3725_733+3728d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77721816 | ||||||
| chr11:77721932
|
G | A | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.733+3613C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77721932 | ||||||
| chr11:77722019
|
A | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+3526T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77722019 | ||||||
| chr11:77722444
|
T | C | 1 | a0001c0001t0004g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.733+3101A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77722444 | ||||||
| chr11:77722482
|
T | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+3063A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77722482 | ||||||
| chr11:77722899
|
C | G | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+2646G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77722899 | ||||||
| chr11:77723080
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+2465G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723080 | ||||||
| chr11:77723216
|
T | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+2329A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723216 | ||||||
| chr11:77723239
|
G | A | 3 | a0001c0001t0004g0182a0001c0001t0004g0184a0001c0001t0051g0183 | 3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.733+2306C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723239 | ||||||
| chr11:77723341
|
G | A | 2 | a0001c0001t0004g0105a0001c0001t0004g0106 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.733+2204C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723341 | ||||||
| chr11:77723368
|
GGCTGGGA others(33): Show |
G | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.733+2137_733+2176d others(42): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723368 | ||||||
| chr11:77723393
|
T | C | 1 | a0001c0001t0063g0289 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.733+2152A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723393 | ||||||
| chr11:77723420
|
A | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+2125T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723420 | ||||||
| chr11:77723441
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+2104G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723441 | ||||||
| chr11:77723497
|
G | A | 265 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(262): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.733+2048C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723497 | ||||||
| chr11:77723717
|
T | C | 1 | a0001c0001t0001g0330 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.733+1828A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723717 | ||||||
| chr11:77723886
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0094 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.733+1659A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77723886 | ||||||
| chr11:77724110
|
T | C | 1 | a0001c0001t0002g0115 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.733+1435A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724110 | ||||||
| chr11:77724633
|
T | C | 2 | a0002c0003t0002g0208a0002c0003t0002g0227 | 2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.733+912A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724633 | ||||||
| chr11:77724659
|
T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.733+886A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724659 | ||||||
| chr11:77724786
|
G | A | 109 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(106): Show | 109 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.733+759C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724786 | ||||||
| chr11:77724890
|
G | C | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+655C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724890 | ||||||
| chr11:77724931
|
C | A | 3 | a0002c0003t0002g0218a0002c0003t0002g0223a0002c0003t0002g0229 | 3 | HG01070.hp2 HG01168.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.733+614G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77724931 | ||||||
| chr11:77725154
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.733+391A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77725154 | ||||||
| chr11:77725435
|
C | T | 3 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0016t0045g0201 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.733+110G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77725435 | ||||||
| chr11:77725472
|
T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.733+73A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 5/15 | chr11 | 77725472 | ||||||
| chr11:77725966
|
T | G | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.579-267A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77725966 | ||||||
| chr11:77726943
|
A | C | 1 | a0001c0001t0051g0183 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.579-1244T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77726943 | ||||||
| chr11:77726953
|
A | C | 2 | a0001c0002t0014g0009a0001c0002t0014g0011 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.579-1254T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77726953 | ||||||
| chr11:77727014
|
A | G | 71 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.579-1315T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727014 | ||||||
| chr11:77727042
|
C | A | 2 | a0001c0001t0005g0263a0001c0001t0060g0257 | 2 | NA18951.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.579-1343G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727042 | ||||||
| chr11:77727329
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.579-1630G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727329 | ||||||
| chr11:77727473
|
C | CT | 175 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(172): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.579-1775dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727473 | ||||||
| chr11:77727473
|
C | CTT | 16 | a0001c0001t0009g0243a0001c0001t0009g0244a0001c0002t0003g0019others(13): Show | 16 | HG01074.hp1 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.579-1776_579-1775d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727473 | ||||||
| chr11:77727473
|
C | CTTT | 68 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.579-1777_579-1775d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727473 | ||||||
| chr11:77727692
|
C | T | 1 | a0001c0001t0001g0318 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.579-1993G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727692 | ||||||
| chr11:77727759
|
C | T | 1 | a0001c0001t0007g0178 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.579-2060G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727759 | ||||||
| chr11:77727867
|
T | C | 6 | a0002c0003t0002g0207a0002c0003t0002g0211a0002c0003t0002g0345others(3): Show | 6 | HG01109.hp1 HG01891.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.579-2168A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727867 | ||||||
| chr11:77727947
|
A | G | 1 | a0001c0001t0004g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579-2248T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77727947 | ||||||
| chr11:77728049
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-2350A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728049 | ||||||
| chr11:77728450
|
A | G | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-2751T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728450 | ||||||
| chr11:77728464
|
C | T | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.579-2765G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728464 | ||||||
| chr11:77728465
|
G | A | 3 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0048g0159 | 3 | HG02895.hp2 HG02897.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.579-2766C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728465 | ||||||
| chr11:77728500
|
C | CAGGAA | 6 | a0001c0001t0002g0108a0001c0001t0009g0242a0001c0001t0009g0243others(3): Show | 6 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.579-2806_579-2802d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728500 | ||||||
| chr11:77728500
|
CAGGAA | C | 3 | a0001c0001t0002g0110a0001c0001t0002g0112a0001c0001t0002g0113 | 3 | HG02055.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.579-2806_579-2802d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728500 | ||||||
| chr11:77728866
|
T | TAA | 77 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(74): Show | 77 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.579-3169_579-3168d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77728866 | ||||||
| chr11:77729027
|
G | T | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.579-3328C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729027 | ||||||
| chr11:77729061
|
A | G | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-3362T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729061 | ||||||
| chr11:77729163
|
T | A | 81 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(78): Show | 81 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.579-3464A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729163 | ||||||
| chr11:77729163
|
T | G | 33 | a0001c0001t0001g0264a0001c0001t0001g0276a0001c0001t0001g0277others(30): Show | 33 | HG01074.hp2 HG01433.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.579-3464A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729163 | ||||||
| chr11:77729574
|
C | A | 1 | a0001c0001t0066g0172 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.579-3875G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729574 | ||||||
| chr11:77729607
|
T | G | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579-3908A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729607 | ||||||
| chr11:77729641
|
C | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.579-3942G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729641 | ||||||
| chr11:77729776
|
T | G | 2 | a0001c0001t0001g0317a0001c0001t0001g0324 | 2 | NA18979.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.579-4077A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729776 | ||||||
| chr11:77729895
|
C | CA | 14 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0135others(11): Show | 14 | HG00609.hp1 HG01175.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.579-4197dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(2): Show |
29 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0088others(26): Show | 29 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.579-4205_579-4197d others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(3): Show |
47 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0094others(44): Show | 47 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.579-4206_579-4197d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(4): Show |
30 | a0001c0001t0001g0274a0001c0001t0001g0287a0001c0001t0001g0290others(27): Show | 30 | HG00423.hp1 HG01070.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.579-4207_579-4197d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(5): Show |
15 | a0001c0001t0001g0332a0001c0001t0001g0344a0001c0001t0002g0110others(12): Show | 15 | HG00673.hp2 HG02027.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.579-4208_579-4197d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0002g0116a0001c0001t0002g0119a0001c0001t0009g0242others(4): Show | 7 | HG01516.hp1 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.579-4209_579-4197d others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0002t0010g0350others(1): Show | 4 | HG02055.hp2 NA18981.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-4210_579-4197d others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0279a0001c0001t0001g0333a0001c0001t0002g0115others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.579-4211_579-4197d others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0006g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.579-4212_579-4197d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(10): Show |
3 | a0001c0001t0006g0123a0001c0001t0006g0125a0001c0001t0006g0127 | 3 | HG02486.hp2 HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.579-4213_579-4197d others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0006g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.579-4214_579-4197d others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(13): Show |
1 | a0002c0003t0002g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.579-4216_579-4197d others(22): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(14): Show |
8 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(5): Show | 8 | HG00639.hp1 HG01975.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.579-4217_579-4197d others(23): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(15): Show |
4 | a0001c0001t0005g0261a0001c0001t0041g0249a0002c0003t0008g0266others(1): Show | 4 | HG02717.hp2 HG04228.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-4218_579-4197d others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(16): Show |
3 | a0001c0001t0005g0254a0001c0001t0008g0267a0001c0001t0025g0259 | 3 | HG03710.hp1 NA18977.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.579-4219_579-4197d others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0005g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.579-4220_579-4197d others(26): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(19): Show |
3 | a0001c0001t0005g0263a0001c0001t0008g0268a0001c0001t0009g0245 | 3 | HG01074.hp2 HG03209.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.579-4222_579-4197d others(28): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0008g0269 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.579-4224_579-4197d others(30): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
C | CAAAAAAA others(28): Show |
1 | a0001c0001t0008g0270 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.579-4197_579-4196i others(37): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
CA | C | 13 | a0001c0001t0002g0109a0001c0001t0002g0111a0001c0001t0004g0147others(10): Show | 13 | HG00140.hp1 HG00733.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.579-4197delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
CAAAAAA | C | 51 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(48): Show | 51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.579-4202_579-4197d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
CAAAAAAA | C | 25 | a0001c0002t0003g0032a0001c0002t0003g0035a0001c0002t0003g0036others(22): Show | 25 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.579-4203_579-4197d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77729895
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0002g0306a0001c0001t0023g0275a0001c0001t0040g0117others(2): Show | 5 | HG02451.hp1 HG02602.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.579-4208_579-4197d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77729895 | ||||||
| chr11:77730039
|
A | C | 1 | a0002c0003t0002g0206 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.579-4340T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730039 | ||||||
| chr11:77730257
|
T | C | 1 | a0001c0001t0008g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.579-4558A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730257 | ||||||
| chr11:77730276
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.579-4577A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730276 | ||||||
| chr11:77730285
|
T | G | 1 | a0001c0001t0007g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.579-4586A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730285 | ||||||
| chr11:77730295
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.579-4596A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730295 | ||||||
| chr11:77730337
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-4638G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730337 | ||||||
| chr11:77730546
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-4847G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730546 | ||||||
| chr11:77730673
|
A | C | 1 | a0001c0001t0001g0305 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.579-4974T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730673 | ||||||
| chr11:77730676
|
G | A | 79 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.579-4977C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730676 | ||||||
| chr11:77730758
|
G | A | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.579-5059C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730758 | ||||||
| chr11:77730803
|
G | A | 1 | a0002c0003t0021g0209 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.579-5104C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730803 | ||||||
| chr11:77730853
|
C | T | 1 | a0001c0001t0027g0260 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.579-5154G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730853 | ||||||
| chr11:77730928
|
A | G | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-5229T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730928 | ||||||
| chr11:77730939
|
G | A | 1 | a0001c0002t0003g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.579-5240C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77730939 | ||||||
| chr11:77731908
|
G | A | 7 | a0001c0002t0003g0048a0001c0002t0003g0052a0001c0002t0003g0055others(4): Show | 7 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.579-6209C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77731908 | ||||||
| chr11:77731979
|
G | A | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.579-6280C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77731979 | ||||||
| chr11:77732048
|
G | A | 3 | a0002c0003t0002g0204a0002c0003t0002g0205a0002c0003t0002g0206 | 3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.579-6349C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732048 | ||||||
| chr11:77732103
|
G | T | 1 | a0001c0001t0002g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.579-6404C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732103 | ||||||
| chr11:77732161
|
C | G | 2 | a0001c0001t0004g0153a0001c0001t0004g0174 | 2 | HG01167.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.579-6462G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732161 | ||||||
| chr11:77732224
|
T | C | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.579-6525A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732224 | ||||||
| chr11:77732339
|
AGTCTCAC others(36): Show |
A | 1 | a0001c0001t0004g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579-6683_579-6641d others(45): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732339 | ||||||
| chr11:77732383
|
T | A | 1 | a0001c0001t0004g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.579-6684A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732383 | ||||||
| chr11:77732582
|
G | A | 4 | a0001c0001t0013g0271a0001c0001t0013g0272a0001c0001t0013g0273others(1): Show | 4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.579-6883C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732582 | ||||||
| chr11:77732641
|
G | A | 8 | a0001c0001t0001g0285a0001c0001t0001g0296a0001c0001t0001g0297others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.579-6942C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732641 | ||||||
| chr11:77732661
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.579-6962T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732661 | ||||||
| chr11:77732671
|
C | T | 3 | a0001c0001t0005g0253a0001c0001t0005g0263a0001c0001t0060g0257 | 3 | HG01975.hp2 NA18951.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.579-6972G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732671 | ||||||
| chr11:77732859
|
T | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.579-7160A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77732859 | ||||||
| chr11:77733003
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.579-7304A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733003 | ||||||
| chr11:77733346
|
CTA | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+7383_578+7384d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733346 | ||||||
| chr11:77733424
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+7307G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733424 | ||||||
| chr11:77733434
|
T | TTC | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+7295_578+7296d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733434 | ||||||
| chr11:77733447
|
C | T | 2 | a0001c0001t0004g0136a0001c0001t0042g0173 | 2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.578+7284G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733447 | ||||||
| chr11:77733557
|
AT | A | 93 | a0001c0001t0001g0089a0001c0001t0001g0320a0001c0001t0001g0334others(90): Show | 93 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.578+7173delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733557 | ||||||
| chr11:77733557
|
ATT | A | 110 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(107): Show | 110 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.578+7172_578+7173d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733557 | ||||||
| chr11:77733852
|
A | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.578+6879T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733852 | ||||||
| chr11:77733865
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.578+6866G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77733865 | ||||||
| chr11:77734236
|
A | ATTCT | 79 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.578+6494_578+6495i others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734236 | ||||||
| chr11:77734239
|
A | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+6492T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734239 | ||||||
| chr11:77734246
|
A | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+6485T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734246 | ||||||
| chr11:77734301
|
CT | C | 87 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0253others(84): Show | 87 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.578+6429delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734301 | ||||||
| chr11:77734308
|
TG | T | 93 | a0001c0001t0001g0016a0001c0001t0001g0264a0001c0001t0001g0274others(90): Show | 93 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.578+6422delC | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734308 | ||||||
| chr11:77734309
|
G | T | 1 | a0002c0003t0002g0215 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.578+6422C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734309 | ||||||
| chr11:77734310
|
G | A | 51 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(48): Show | 51 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.578+6421C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734310 | ||||||
| chr11:77734354
|
A | G | 1 | a0002c0003t0002g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.578+6377T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734354 | ||||||
| chr11:77734386
|
A | T | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.578+6345T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734386 | ||||||
| chr11:77734556
|
G | C | 2 | a0001c0001t0009g0243a0001c0001t0009g0244 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.578+6175C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734556 | ||||||
| chr11:77734679
|
C | T | 1 | a0001c0001t0005g0291 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.578+6052G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734679 | ||||||
| chr11:77734797
|
C | T | 2 | a0001c0002t0003g0083a0001c0002t0003g0084 | 2 | NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.578+5934G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77734797 | ||||||
| chr11:77735006
|
T | C | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+5725A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735006 | ||||||
| chr11:77735049
|
C | T | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.578+5682G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735049 | ||||||
| chr11:77735072
|
C | T | 79 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.578+5659G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735072 | ||||||
| chr11:77735096
|
G | T | 1 | a0001c0002t0003g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.578+5635C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735096 | ||||||
| chr11:77735179
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.578+5552G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735179 | ||||||
| chr11:77735315
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0018others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.578+5416G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735315 | ||||||
| chr11:77735536
|
C | T | 1 | a0001c0002t0018g0065 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.578+5195G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735536 | ||||||
| chr11:77735810
|
G | C | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.578+4921C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735810 | ||||||
| chr11:77735943
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+4788A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77735943 | ||||||
| chr11:77736003
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+4728G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736003 | ||||||
| chr11:77736009
|
T | G | 71 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.578+4722A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736009 | ||||||
| chr11:77736023
|
C | T | 79 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.578+4708G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736023 | ||||||
| chr11:77736434
|
C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.578+4297G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736434 | ||||||
| chr11:77736617
|
T | C | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.578+4114A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736617 | ||||||
| chr11:77736693
|
T | C | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+4038A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77736693 | ||||||
| chr11:77737166
|
C | G | 269 | a0001c0001t0001g0264a0001c0001t0001g0277a0001c0001t0001g0307others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.578+3565G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737166 | ||||||
| chr11:77737323
|
C | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+3408G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737323 | ||||||
| chr11:77737454
|
C | CA | 13 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0001t0001g0305others(10): Show | 13 | HG01433.hp2 HG02055.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.578+3276dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737454 | ||||||
| chr11:77737467
|
C | A | 1 | a0001c0001t0068g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.578+3264G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737467 | ||||||
| chr11:77737469
|
A | C | 1 | a0001c0001t0068g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.578+3262T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737469 | ||||||
| chr11:77737472
|
A | AAAC | 71 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(68): Show | 71 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.578+3256_578+3258d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737472 | ||||||
| chr11:77737472
|
A | AAACAAC | 4 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+3253_578+3258d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737472 | ||||||
| chr11:77737472
|
AAACAAC | A | 7 | a0001c0001t0001g0285a0001c0001t0001g0296a0001c0001t0001g0297others(4): Show | 7 | HG01884.hp2 HG02630.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.578+3253_578+3258d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737472 | ||||||
| chr11:77737487
|
CAACAAA | C | 7 | a0001c0002t0003g0048a0001c0002t0003g0052a0001c0002t0003g0055others(4): Show | 7 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.578+3238_578+3243d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737487 | ||||||
| chr11:77737490
|
C | A | 2 | a0001c0001t0004g0160a0001c0001t0004g0167 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.578+3241G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737490 | ||||||
| chr11:77737493
|
A | C | 75 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(72): Show | 75 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.578+3238T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737493 | ||||||
| chr11:77737571
|
T | C | 78 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.578+3160A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737571 | ||||||
| chr11:77737606
|
T | G | 1 | a0012c0011t0007g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.578+3125A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737606 | ||||||
| chr11:77737607
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.578+3124A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737607 | ||||||
| chr11:77737616
|
TGG | T | 26 | a0001c0001t0001g0274a0001c0001t0001g0277a0001c0001t0001g0318others(23): Show | 26 | HG00140.hp2 HG00408.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.578+3113_578+3114d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737616 | ||||||
| chr11:77737619
|
G | GGT | 14 | a0001c0001t0001g0280a0001c0001t0001g0303a0001c0001t0001g0309others(11): Show | 14 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGGGTG others(3): Show |
2 | a0001c0001t0004g0133a0001c0001t0004g0165 | 2 | NA19007.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.578+3111_578+3112i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGGGTG others(9): Show |
1 | a0001c0001t0046g0171 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.578+3111_578+3112i others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGGGTG others(11): Show |
5 | a0001c0001t0004g0154a0001c0001t0004g0185a0001c0001t0011g0162others(2): Show | 5 | HG00609.hp1 HG01192.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGGGTG others(15): Show |
2 | a0001c0001t0004g0137a0001c0001t0004g0192 | 2 | HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.578+3111_578+3112i others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGGTGT others(4): Show |
1 | a0001c0001t0011g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.578+3111_578+3112i others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGT | 17 | a0001c0001t0001g0282a0001c0001t0001g0292a0001c0001t0001g0297others(14): Show | 17 | HG01081.hp1 HG01123.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGTGT | 16 | a0001c0001t0001g0286a0001c0001t0001g0298a0001c0001t0001g0334others(13): Show | 16 | HG00323.hp2 HG01074.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGTGTG others(1): Show |
17 | a0001c0001t0001g0279a0001c0001t0001g0293a0001c0001t0001g0299others(14): Show | 17 | HG00609.hp2 HG01346.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGTGTG others(3): Show |
8 | a0001c0001t0001g0296a0001c0001t0001g0342a0001c0001t0004g0104others(5): Show | 8 | HG01081.hp2 HG01243.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGTGTG others(5): Show |
26 | a0001c0001t0001g0016a0001c0001t0001g0288a0001c0001t0004g0136others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGTGTG others(7): Show |
16 | a0001c0001t0001g0264a0001c0001t0001g0295a0001c0001t0004g0103others(13): Show | 16 | HG01517.hp1 HG02015.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGTGTG others(9): Show |
9 | a0001c0001t0001g0283a0001c0001t0001g0294a0001c0001t0004g0101others(6): Show | 9 | HG02572.hp1 HG03225.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGTGTG others(11): Show |
2 | a0001c0001t0001g0300a0001c0001t0047g0102 | 2 | NA18967.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.578+3111_578+3112i others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GGTGTGTG others(13): Show |
4 | a0001c0001t0004g0180a0001c0001t0004g0250a0001c0001t0042g0173others(1): Show | 4 | HG03041.hp1 HG03669.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+3111_578+3112i others(22): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0004g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.578+3111_578+3112i others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
GGGGT | G | 66 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.578+3108_578+3111d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
GGGGTGT | G | 6 | a0001c0001t0001g0328a0001c0002t0003g0040a0001c0002t0003g0081others(3): Show | 6 | HG02132.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.578+3106_578+3111d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
GGGGTGTG others(3): Show |
G | 1 | a0001c0001t0001g0311 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.578+3102_578+3111d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
GGGGTGTG others(5): Show |
G | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+3100_578+3111d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
GGGGTGTG others(19): Show |
G | 3 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111 | 3 | NA18973.hp1 NA18994.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.578+3086_578+3111d others(28): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737619
|
GGGGTGTG others(21): Show |
G | 68 | a0001c0001t0002g0110a0001c0001t0002g0112a0001c0001t0002g0113others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.578+3084_578+3111d others(30): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737619 | ||||||
| chr11:77737621
|
G | GGTGTGTG others(5): Show |
1 | a0001c0001t0004g0197 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.578+3098_578+3109d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737621 | ||||||
| chr11:77737621
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0004g0100 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.578+3096_578+3109d others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737621 | ||||||
| chr11:77737621
|
G | T | 164 | a0001c0001t0001g0016a0001c0001t0001g0264a0001c0001t0001g0279others(161): Show | 164 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.578+3110C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737621 | ||||||
| chr11:77737667
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0066g0172 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.578+3063_578+3064i others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737667 | ||||||
| chr11:77737667
|
T | TGTGTGTG others(8): Show |
1 | a0001c0001t0004g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.578+3063_578+3064i others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737667 | ||||||
| chr11:77737686
|
C | G | 3 | a0001c0001t0001g0339a0001c0001t0001g0340a0001c0001t0001g0341 | 3 | HG02074.hp1 NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.578+3045G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737686 | ||||||
| chr11:77737728
|
TGAAAGCA | T | 238 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.578+2996_578+3002d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737728 | ||||||
| chr11:77737948
|
A | T | 238 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.578+2783T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77737948 | ||||||
| chr11:77738157
|
T | TAATTAAA others(1): Show |
3 | a0001c0002t0010g0013a0001c0002t0033g0012a0007c0018t0032g0014 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.578+2573_578+2574i others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738157 | ||||||
| chr11:77738157
|
T | TAGTTAAA others(1): Show |
79 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.578+2566_578+2573d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738157 | ||||||
| chr11:77738210
|
G | A | 1 | a0001c0001t0065g0150 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.578+2521C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738210 | ||||||
| chr11:77738280
|
G | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+2451C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738280 | ||||||
| chr11:77738314
|
A | AG | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.578+2416_578+2417i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738314 | ||||||
| chr11:77738318
|
GC | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.578+2412delG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738318 | ||||||
| chr11:77738359
|
A | G | 3 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0016t0045g0201 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.578+2372T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738359 | ||||||
| chr11:77738492
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+2239C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738492 | ||||||
| chr11:77738492
|
G | C | 1 | a0001c0001t0004g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.578+2239C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738492 | ||||||
| chr11:77738573
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.578+2158A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738573 | ||||||
| chr11:77738733
|
A | T | 261 | a0001c0001t0001g0264a0001c0001t0002g0003a0001c0001t0002g0004others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.578+1998T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738733 | ||||||
| chr11:77738915
|
C | T | 1 | a0002c0003t0021g0209 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.578+1816G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77738915 | ||||||
| chr11:77739084
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578+1647G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739084 | ||||||
| chr11:77739092
|
A | G | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+1639T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739092 | ||||||
| chr11:77739190
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.578+1541G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739190 | ||||||
| chr11:77739330
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.578+1401A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739330 | ||||||
| chr11:77739403
|
T | TA | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.578+1327_578+1328i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739403 | ||||||
| chr11:77739467
|
G | A | 1 | a0001c0001t0004g0101 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.578+1264C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739467 | ||||||
| chr11:77739542
|
T | C | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.578+1189A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739542 | ||||||
| chr11:77739827
|
C | T | 1 | a0001c0002t0003g0067 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.578+904G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739827 | ||||||
| chr11:77739849
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.578+882C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739849 | ||||||
| chr11:77739866
|
T | C | 1 | a0004c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.578+865A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739866 | ||||||
| chr11:77739913
|
T | TA | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.578+817dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77739913 | ||||||
| chr11:77740115
|
C | A | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.578+616G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740115 | ||||||
| chr11:77740158
|
C | A | 1 | a0001c0001t0001g0311 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.578+573G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740158 | ||||||
| chr11:77740288
|
T | C | 6 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0123others(3): Show | 6 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.578+443A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740288 | ||||||
| chr11:77740336
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.578+395A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740336 | ||||||
| chr11:77740370
|
C | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.578+361G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740370 | ||||||
| chr11:77740476
|
C | T | 1 | a0001c0001t0009g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.578+255G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740476 | ||||||
| chr11:77740688
|
C | T | 1 | a0001c0001t0007g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.578+43G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 4/15 | chr11 | 77740688 | ||||||
| chr11:77741015
|
T | C | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.373-79A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741015 | ||||||
| chr11:77741134
|
A | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.373-198T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741134 | ||||||
| chr11:77741323
|
G | A | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.373-387C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741323 | ||||||
| chr11:77741515
|
C | T | 2 | a0001c0001t0001g0300a0001c0001t0001g0303 | 2 | HG00423.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.373-579G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741515 | ||||||
| chr11:77741518
|
T | A | 23 | a0001c0002t0003g0018a0001c0002t0003g0053a0001c0002t0003g0054others(20): Show | 23 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.373-582A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741518 | ||||||
| chr11:77741552
|
AT | A | 73 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.373-617delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741552 | ||||||
| chr11:77741596
|
T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.373-660A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741596 | ||||||
| chr11:77741615
|
C | T | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.373-679G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741615 | ||||||
| chr11:77741745
|
T | C | 29 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0210others(26): Show | 29 | HG00673.hp2 HG00733.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.373-809A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741745 | ||||||
| chr11:77741903
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.373-967C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77741903 | ||||||
| chr11:77742067
|
C | G | 82 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.373-1131G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742067 | ||||||
| chr11:77742240
|
G | A | 3 | a0001c0002t0003g0019a0001c0002t0003g0020a0001c0002t0003g0021 | 3 | NA18747.hp2 NA18950.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.373-1304C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742240 | ||||||
| chr11:77742322
|
C | T | 75 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(72): Show | 75 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.373-1386G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742322 | ||||||
| chr11:77742341
|
G | A | 22 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(19): Show | 22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.373-1405C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742341 | ||||||
| chr11:77742355
|
C | G | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.373-1419G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742355 | ||||||
| chr11:77742441
|
A | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.373-1505T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742441 | ||||||
| chr11:77742624
|
T | G | 1 | a0001c0001t0004g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.373-1688A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742624 | ||||||
| chr11:77742671
|
C | T | 307 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.373-1735G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742671 | ||||||
| chr11:77742754
|
G | A | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.373-1818C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742754 | ||||||
| chr11:77742878
|
G | A | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.373-1942C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77742878 | ||||||
| chr11:77743028
|
C | T | 1 | a0001c0001t0009g0245 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.373-2092G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743028 | ||||||
| chr11:77743031
|
C | T | 155 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.373-2095G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743031 | ||||||
| chr11:77743034
|
C | T | 1 | a0001c0010t0001g0337 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.373-2098G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743034 | ||||||
| chr11:77743035
|
A | C | 1 | a0001c0010t0001g0337 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.373-2099T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743035 | ||||||
| chr11:77743191
|
C | G | 1 | a0001c0002t0003g0018 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.373-2255G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743191 | ||||||
| chr11:77743212
|
A | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.373-2276T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743212 | ||||||
| chr11:77743237
|
T | C | 80 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.373-2301A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743237 | ||||||
| chr11:77743312
|
G | C | 83 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0004g0100others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.373-2376C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743312 | ||||||
| chr11:77743330
|
G | A | 1 | a0001c0001t0059g0310 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.373-2394C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743330 | ||||||
| chr11:77743568
|
A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.373-2632T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77743568 | ||||||
| chr11:77744027
|
A | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.372+3009T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744027 | ||||||
| chr11:77744119
|
C | T | 1 | a0001c0010t0001g0337 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.372+2917G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744119 | ||||||
| chr11:77744121
|
C | T | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+2915G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744121 | ||||||
| chr11:77744384
|
G | A | 4 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+2652C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744384 | ||||||
| chr11:77744385
|
C | T | 3 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0016t0045g0201 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.372+2651G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744385 | ||||||
| chr11:77744448
|
G | A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.372+2588C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744448 | ||||||
| chr11:77744497
|
A | G | 238 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.372+2539T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744497 | ||||||
| chr11:77744538
|
A | G | 157 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(154): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.372+2498T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744538 | ||||||
| chr11:77744651
|
C | G | 1 | a0001c0001t0004g0189 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.372+2385G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744651 | ||||||
| chr11:77744693
|
T | C | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+2343A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744693 | ||||||
| chr11:77744859
|
A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.372+2177T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744859 | ||||||
| chr11:77744998
|
G | C | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.372+2038C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77744998 | ||||||
| chr11:77745000
|
T | C | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+2036A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745000 | ||||||
| chr11:77745056
|
A | AT | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.372+1979dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745056 | ||||||
| chr11:77745087
|
A | G | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.372+1949T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745087 | ||||||
| chr11:77745090
|
G | C | 1 | a0001c0001t0004g0189 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.372+1946C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745090 | ||||||
| chr11:77745115
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.372+1921G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745115 | ||||||
| chr11:77745298
|
T | C | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+1738A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745298 | ||||||
| chr11:77745328
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.372+1708G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745328 | ||||||
| chr11:77745509
|
A | ATT | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+1525_372+1526d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745509 | ||||||
| chr11:77745509
|
AT | A | 26 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(23): Show | 26 | HG00639.hp2 HG02055.hp1 HG02486.hp2 others(23): Show |
intron_variant | MODIFIER | c.372+1526delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745509 | ||||||
| chr11:77745592
|
C | T | 2 | a0001c0001t0009g0243a0001c0001t0009g0244 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.372+1444G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745592 | ||||||
| chr11:77745741
|
T | C | 21 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(18): Show | 21 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.372+1295A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745741 | ||||||
| chr11:77745764
|
T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.372+1272A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745764 | ||||||
| chr11:77745794
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.372+1242C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745794 | ||||||
| chr11:77745828
|
G | C | 1 | a0001c0010t0001g0337 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.372+1208C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745828 | ||||||
| chr11:77745829
|
C | G | 1 | a0001c0010t0001g0337 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.372+1207G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745829 | ||||||
| chr11:77745861
|
A | G | 54 | a0001c0001t0006g0121a0001c0001t0009g0242a0001c0001t0009g0243others(51): Show | 54 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.372+1175T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745861 | ||||||
| chr11:77745889
|
T | A | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.372+1147A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77745889 | ||||||
| chr11:77746007
|
A | G | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.372+1029T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746007 | ||||||
| chr11:77746348
|
C | A | 1 | a0001c0001t0001g0316 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.372+688G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746348 | ||||||
| chr11:77746356
|
T | C | 2 | a0002c0003t0002g0203a0002c0003t0002g0230 | 2 | NA18955.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.372+680A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746356 | ||||||
| chr11:77746490
|
A | G | 1 | a0002c0003t0002g0207 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.372+546T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746490 | ||||||
| chr11:77746571
|
C | T | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.372+465G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746571 | ||||||
| chr11:77746666
|
C | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.372+370G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746666 | ||||||
| chr11:77746712
|
A | G | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.372+324T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746712 | ||||||
| chr11:77746780
|
C | T | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+256G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 3/15 | chr11 | 77746780 | ||||||
| chr11:77747310
|
G | A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.280-182C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747310 | ||||||
| chr11:77747754
|
T | C | 13 | a0001c0002t0003g0033a0001c0002t0003g0035a0001c0002t0003g0036others(10): Show | 13 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.280-626A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747754 | ||||||
| chr11:77747831
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.280-703C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747831 | ||||||
| chr11:77747862
|
G | T | 80 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.280-734C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747862 | ||||||
| chr11:77747978
|
C | T | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.280-850G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77747978 | ||||||
| chr11:77748216
|
C | CT | 8 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(5): Show | 8 | HG01243.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-1089dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748216 | ||||||
| chr11:77748216
|
CT | C | 84 | a0001c0001t0001g0279a0001c0001t0001g0286a0001c0001t0004g0100others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.280-1089delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748216 | ||||||
| chr11:77748228
|
T | C | 1 | a0001c0001t0047g0102 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280-1100A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748228 | ||||||
| chr11:77748229
|
C | T | 1 | a0001c0001t0047g0102 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.280-1101G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748229 | ||||||
| chr11:77748349
|
C | T | 70 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.280-1221G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748349 | ||||||
| chr11:77748365
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.280-1237A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748365 | ||||||
| chr11:77748370
|
G | A | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-1242C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748370 | ||||||
| chr11:77748590
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-1462G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748590 | ||||||
| chr11:77748684
|
G | A | 2 | a0001c0001t0001g0311a0001c0001t0057g0278 | 2 | NA18962.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.280-1556C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748684 | ||||||
| chr11:77748841
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.280-1713C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77748841 | ||||||
| chr11:77749023
|
G | A | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280-1895C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749023 | ||||||
| chr11:77749234
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.280-2106A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749234 | ||||||
| chr11:77749277
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-2149A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749277 | ||||||
| chr11:77749325
|
A | G | 1 | a0001c0002t0003g0039 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.280-2197T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749325 | ||||||
| chr11:77749569
|
A | G | 80 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.280-2441T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749569 | ||||||
| chr11:77749702
|
T | C | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.280-2574A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749702 | ||||||
| chr11:77749716
|
C | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280-2588G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749716 | ||||||
| chr11:77749969
|
G | A | 1 | a0001c0002t0003g0028 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.280-2841C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77749969 | ||||||
| chr11:77750007
|
C | A | 261 | a0001c0001t0001g0264a0001c0001t0002g0003a0001c0001t0002g0004others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.280-2879G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750007 | ||||||
| chr11:77750014
|
T | C | 2 | a0002c0003t0002g0204a0002c0003t0002g0205 | 2 | HG00099.hp2 HG00639.hp1 |
intron_variant | MODIFIER | c.280-2886A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750014 | ||||||
| chr11:77750099
|
T | TA | 12 | a0001c0001t0001g0286a0001c0001t0004g0189a0001c0002t0003g0022others(9): Show | 12 | NA18939.hp1 NA18941.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.280-2972dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750099 | ||||||
| chr11:77750121
|
T | C | 3 | a0001c0001t0004g0182a0001c0001t0004g0184a0001c0001t0051g0183 | 3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.280-2993A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750121 | ||||||
| chr11:77750268
|
T | C | 1 | a0001c0001t0004g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.280-3140A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750268 | ||||||
| chr11:77750302
|
T | C | 4 | a0001c0001t0013g0271a0001c0001t0013g0272a0001c0001t0013g0273others(1): Show | 4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-3174A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750302 | ||||||
| chr11:77750502
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.280-3374A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750502 | ||||||
| chr11:77750608
|
T | C | 1 | a0001c0001t0005g0254 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.280-3480A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750608 | ||||||
| chr11:77750839
|
T | C | 1 | a0001c0001t0004g0189 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.280-3711A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77750839 | ||||||
| chr11:77751348
|
C | T | 2 | a0001c0002t0018g0046a0009c0008t0003g0034 | 2 | HG01081.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.280-4220G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751348 | ||||||
| chr11:77751377
|
A | C | 1 | a0001c0001t0043g0157 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.280-4249T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751377 | ||||||
| chr11:77751429
|
C | T | 1 | a0001c0002t0003g0018 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.280-4301G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751429 | ||||||
| chr11:77751457
|
CAA | C | 75 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.280-4331_280-4330d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751457 | ||||||
| chr11:77751637
|
G | C | 1 | a0001c0001t0001g0330 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.280-4509C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751637 | ||||||
| chr11:77751693
|
A | G | 1 | a0001c0002t0003g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-4565T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751693 | ||||||
| chr11:77751747
|
C | T | 74 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.280-4619G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77751747 | ||||||
| chr11:77752102
|
C | T | 1 | a0001c0001t0067g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.280-4974G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752102 | ||||||
| chr11:77752183
|
C | T | 11 | a0001c0001t0004g0140a0001c0001t0004g0142a0001c0001t0004g0147others(8): Show | 11 | HG00280.hp1 HG00323.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.280-5055G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752183 | ||||||
| chr11:77752332
|
G | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-5204C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752332 | ||||||
| chr11:77752410
|
C | A | 2 | a0001c0002t0014g0009a0001c0002t0014g0011 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.280-5282G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752410 | ||||||
| chr11:77752541
|
A | T | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.280-5413T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752541 | ||||||
| chr11:77752679
|
C | T | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.280-5551G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752679 | ||||||
| chr11:77752946
|
T | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.280-5818A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752946 | ||||||
| chr11:77752967
|
T | A | 1 | a0001c0001t0040g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.280-5839A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77752967 | ||||||
| chr11:77753108
|
T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.280-5980A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753108 | ||||||
| chr11:77753108
|
T | G | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.280-5980A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753108 | ||||||
| chr11:77753325
|
C | T | 43 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.280-6197G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753325 | ||||||
| chr11:77753381
|
T | C | 7 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111others(4): Show | 7 | NA18963.hp1 NA18965.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-6253A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753381 | ||||||
| chr11:77753485
|
G | A | 43 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.280-6357C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753485 | ||||||
| chr11:77753525
|
G | A | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280-6397C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753525 | ||||||
| chr11:77753526
|
GACGGTTT others(2): Show |
G | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-6407_280-6399d others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753526 | ||||||
| chr11:77753686
|
G | C | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.280-6558C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753686 | ||||||
| chr11:77753695
|
C | T | 1 | a0001c0002t0003g0025 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.280-6567G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753695 | ||||||
| chr11:77753721
|
G | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-6593C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753721 | ||||||
| chr11:77753789
|
A | G | 43 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.280-6661T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753789 | ||||||
| chr11:77753849
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.280-6721A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753849 | ||||||
| chr11:77753865
|
T | A | 1 | a0001c0002t0003g0050 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.280-6737A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753865 | ||||||
| chr11:77753891
|
C | T | 78 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.280-6763G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753891 | ||||||
| chr11:77753987
|
G | A | 2 | a0001c0001t0009g0243a0001c0001t0009g0244 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.280-6859C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77753987 | ||||||
| chr11:77754366
|
C | T | 1 | a0001c0001t0004g0104 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.280-7238G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754366 | ||||||
| chr11:77754408
|
C | A | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-7280G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754408 | ||||||
| chr11:77754451
|
A | G | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-7323T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754451 | ||||||
| chr11:77754584
|
A | G | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280-7456T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754584 | ||||||
| chr11:77754757
|
C | A | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280-7629G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754757 | ||||||
| chr11:77754762
|
A | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.280-7634T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754762 | ||||||
| chr11:77754831
|
T | C | 1 | a0001c0001t0004g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.280-7703A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754831 | ||||||
| chr11:77754835
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.280-7707C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754835 | ||||||
| chr11:77754839
|
C | A | 1 | a0001c0001t0001g0334 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.280-7711G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754839 | ||||||
| chr11:77754949
|
C | A | 83 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(80): Show | 83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.280-7821G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77754949 | ||||||
| chr11:77755289
|
G | A | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.280-8161C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755289 | ||||||
| chr11:77755304
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280-8176A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755304 | ||||||
| chr11:77755345
|
A | C | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-8217T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755345 | ||||||
| chr11:77755432
|
T | C | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.280-8304A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755432 | ||||||
| chr11:77755434
|
G | T | 1 | a0001c0001t0001g0287 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.280-8306C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755434 | ||||||
| chr11:77755584
|
A | AT | 162 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0004g0100others(159): Show | 162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.280-8457dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755584 | ||||||
| chr11:77755584
|
ATT | A | 17 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(14): Show | 17 | HG02055.hp1 HG02602.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.280-8458_280-8457d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755584 | ||||||
| chr11:77755605
|
A | G | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.280-8477T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755605 | ||||||
| chr11:77755657
|
G | A | 1 | a0001c0002t0003g0035 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280-8529C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755657 | ||||||
| chr11:77755726
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.280-8598G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755726 | ||||||
| chr11:77755740
|
T | C | 163 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0004g0100others(160): Show | 163 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.280-8612A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755740 | ||||||
| chr11:77755821
|
G | A | 3 | a0002c0003t0002g0204a0002c0003t0002g0205a0002c0003t0002g0206 | 3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.280-8693C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755821 | ||||||
| chr11:77755855
|
G | A | 1 | a0001c0002t0003g0077 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.280-8727C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77755855 | ||||||
| chr11:77756028
|
A | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.279+8570T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756028 | ||||||
| chr11:77756052
|
A | C | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+8546T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756052 | ||||||
| chr11:77756358
|
C | CA | 19 | a0001c0001t0002g0119a0001c0001t0004g0142a0001c0001t0004g0195others(16): Show | 19 | HG01074.hp1 HG01884.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.279+8239dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756358 | ||||||
| chr11:77756362
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0307 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.279+8236T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756362 | ||||||
| chr11:77756400
|
C | G | 351 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.279+8198G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756400 | ||||||
| chr11:77756528
|
T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.279+8070A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756528 | ||||||
| chr11:77756975
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.279+7623A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756975 | ||||||
| chr11:77756991
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.279+7607A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77756991 | ||||||
| chr11:77757021
|
C | T | 3 | a0001c0002t0010g0013a0001c0002t0033g0012a0007c0018t0032g0014 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.279+7577G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757021 | ||||||
| chr11:77757043
|
C | A | 70 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.279+7555G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757043 | ||||||
| chr11:77757354
|
C | T | 1 | a0004c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.279+7244G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757354 | ||||||
| chr11:77757507
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.279+7091C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757507 | ||||||
| chr11:77757666
|
A | G | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.279+6932T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757666 | ||||||
| chr11:77757937
|
C | T | 1 | a0001c0002t0003g0040 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.279+6661G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77757937 | ||||||
| chr11:77758003
|
T | C | 1 | a0002c0003t0050g0213 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.279+6595A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758003 | ||||||
| chr11:77758140
|
GA | G | 84 | a0001c0001t0001g0316a0001c0001t0002g0132a0001c0001t0004g0100others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.279+6457delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758140 | ||||||
| chr11:77758321
|
A | G | 1 | a0001c0001t0066g0172 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.279+6277T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758321 | ||||||
| chr11:77758381
|
C | T | 1 | a0001c0001t0059g0310 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.279+6217G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758381 | ||||||
| chr11:77758472
|
G | C | 1 | a0001c0001t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.279+6126C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758472 | ||||||
| chr11:77758559
|
T | G | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.279+6039A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758559 | ||||||
| chr11:77758621
|
A | T | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.279+5977T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758621 | ||||||
| chr11:77758858
|
AC | A | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.279+5739delG | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77758858 | ||||||
| chr11:77759022
|
A | C | 78 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.279+5576T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759022 | ||||||
| chr11:77759121
|
A | T | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.279+5477T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759121 | ||||||
| chr11:77759184
|
T | C | 1 | a0001c0001t0005g0255 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.279+5414A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759184 | ||||||
| chr11:77759298
|
C | T | 1 | a0002c0003t0002g0223 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.279+5300G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759298 | ||||||
| chr11:77759332
|
G | A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.279+5266C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759332 | ||||||
| chr11:77759482
|
G | A | 1 | a0001c0001t0008g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.279+5116C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759482 | ||||||
| chr11:77759541
|
A | T | 75 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(72): Show | 75 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.279+5057T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759541 | ||||||
| chr11:77759553
|
G | A | 4 | a0001c0001t0013g0271a0001c0001t0013g0272a0001c0001t0013g0273others(1): Show | 4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+5045C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759553 | ||||||
| chr11:77759598
|
C | A | 1 | a0001c0001t0004g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.279+5000G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759598 | ||||||
| chr11:77759728
|
G | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.279+4870C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759728 | ||||||
| chr11:77759768
|
C | G | 3 | a0001c0002t0003g0066a0001c0002t0003g0072a0001c0002t0003g0076 | 3 | NA18965.hp1 NA18967.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.279+4830G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759768 | ||||||
| chr11:77759855
|
T | TA | 245 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.279+4742dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759855 | ||||||
| chr11:77759855
|
TA | T | 77 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(74): Show | 77 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.279+4742delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759855 | ||||||
| chr11:77759906
|
T | C | 3 | a0001c0001t0002g0110a0001c0001t0002g0112a0001c0001t0002g0113 | 3 | HG02055.hp1 HG02976.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.279+4692A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759906 | ||||||
| chr11:77759997
|
C | T | 43 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.279+4601G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77759997 | ||||||
| chr11:77760102
|
C | T | 1 | a0001c0001t0004g0186 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.279+4496G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760102 | ||||||
| chr11:77760167
|
G | A | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.279+4431C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760167 | ||||||
| chr11:77760627
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.279+3971A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760627 | ||||||
| chr11:77760781
|
G | T | 25 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(22): Show | 25 | HG00639.hp2 HG02055.hp1 HG02486.hp2 others(22): Show |
intron_variant | MODIFIER | c.279+3817C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760781 | ||||||
| chr11:77760856
|
A | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+3742T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760856 | ||||||
| chr11:77760899
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.279+3699G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77760899 | ||||||
| chr11:77761076
|
C | G | 1 | a0001c0001t0001g0311 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.279+3522G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761076 | ||||||
| chr11:77761093
|
C | T | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.279+3505G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761093 | ||||||
| chr11:77761123
|
T | G | 1 | a0001c0002t0003g0049 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.279+3475A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761123 | ||||||
| chr11:77761130
|
G | A | 3 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0016t0045g0201 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.279+3468C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761130 | ||||||
| chr11:77761193
|
C | A | 1 | a0001c0001t0002g0108 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.279+3405G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761193 | ||||||
| chr11:77761504
|
C | CT | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+3093_279+3094i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761504 | ||||||
| chr11:77761574
|
T | C | 2 | a0001c0001t0038g0170a0001c0001t0039g0166 | 2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.279+3024A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761574 | ||||||
| chr11:77761577
|
G | A | 1 | a0001c0002t0003g0018 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.279+3021C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761577 | ||||||
| chr11:77761828
|
A | ACTTTTT | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+2769_279+2770i others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | ||||||
| chr11:77761828
|
A | AT | 246 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.279+2769dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | ||||||
| chr11:77761828
|
A | ATT | 15 | a0001c0001t0001g0088a0001c0001t0001g0288a0001c0001t0001g0312others(12): Show | 15 | HG01109.hp1 HG01192.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.279+2768_279+2769d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | ||||||
| chr11:77761828
|
A | ATTTTT | 7 | a0001c0002t0003g0041a0001c0002t0003g0078a0001c0002t0010g0013others(4): Show | 7 | HG01069.hp2 HG01074.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+2765_279+2769d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | ||||||
| chr11:77761828
|
A | ATTTTTT | 52 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0022others(49): Show | 52 | HG00280.hp2 HG00408.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.279+2764_279+2769d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | ||||||
| chr11:77761828
|
A | ATTTTTTT | 19 | a0001c0002t0003g0019a0001c0002t0003g0020a0001c0002t0003g0021others(16): Show | 19 | HG00423.hp2 HG00597.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.279+2763_279+2769d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77761828 | ||||||
| chr11:77762017
|
C | A | 17 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(14): Show | 17 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.279+2581G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762017 | ||||||
| chr11:77762022
|
C | CTTTTCTT | 23 | a0001c0001t0004g0160a0001c0001t0005g0252a0001c0001t0005g0254others(20): Show | 23 | HG01074.hp2 HG01433.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.279+2569_279+2575d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762022 | ||||||
| chr11:77762027
|
C | CTTTTT | 8 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0023others(5): Show | 8 | HG02280.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+2566_279+2570d others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTT | 61 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(58): Show | 61 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.279+2565_279+2570d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTTC others(1): Show |
66 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0133others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.279+2570_279+2571i others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTTC others(2): Show |
11 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(8): Show | 11 | HG00609.hp1 HG02080.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+2570_279+2571i others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTTC others(3): Show |
1 | a0001c0001t0004g0175 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.279+2570_279+2571i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTTC others(6): Show |
1 | a0001c0001t0002g0120 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.279+2570_279+2571i others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTTC others(7): Show |
22 | a0001c0001t0002g0109a0001c0001t0002g0110a0001c0001t0002g0111others(19): Show | 22 | HG02055.hp1 HG02486.hp2 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.279+2570_279+2571i others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTTC others(8): Show |
5 | a0001c0001t0002g0108a0001c0001t0002g0128a0001c0001t0006g0122others(2): Show | 5 | HG02647.hp2 HG03098.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2570_279+2571i others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTTC others(9): Show |
1 | a0004c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.279+2570_279+2571i others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTTT | 8 | a0001c0001t0005g0038a0001c0002t0003g0036a0001c0002t0003g0043others(5): Show | 8 | HG00733.hp2 HG02071.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.279+2564_279+2570d others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762027
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.279+2552_279+2570d others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762027 | ||||||
| chr11:77762033
|
T | TC | 41 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.279+2564_279+2565i others(3): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762033 | ||||||
| chr11:77762034
|
T | C | 1 | a0002c0003t0002g0235 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.279+2564A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762034 | ||||||
| chr11:77762035
|
T | C | 1 | a0001c0001t0006g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.279+2563A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762035 | ||||||
| chr11:77762089
|
G | C | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279+2509C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762089 | ||||||
| chr11:77762164
|
T | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+2434A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762164 | ||||||
| chr11:77762278
|
A | T | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.279+2320T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762278 | ||||||
| chr11:77762338
|
C | T | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.279+2260G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762338 | ||||||
| chr11:77762364
|
T | C | 1 | a0001c0001t0004g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.279+2234A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762364 | ||||||
| chr11:77762460
|
T | C | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.279+2138A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762460 | ||||||
| chr11:77762552
|
G | A | 2 | a0002c0003t0002g0099a0002c0003t0002g0228 | 2 | HG01358.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.279+2046C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762552 | ||||||
| chr11:77762753
|
T | C | 1 | a0001c0002t0003g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.279+1845A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77762753 | ||||||
| chr11:77763040
|
ATAAAAGA others(1): Show |
A | 10 | a0001c0002t0003g0022a0001c0002t0003g0023a0001c0002t0003g0024others(7): Show | 10 | NA18939.hp1 NA18941.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+1550_279+1557d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763040 | ||||||
| chr11:77763048
|
T | C | 7 | a0001c0002t0003g0048a0001c0002t0003g0052a0001c0002t0003g0055others(4): Show | 7 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+1550A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763048 | ||||||
| chr11:77763068
|
C | G | 7 | a0001c0002t0010g0013a0001c0002t0016g0005a0001c0002t0016g0008others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+1530G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763068 | ||||||
| chr11:77763116
|
G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.279+1482C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763116 | ||||||
| chr11:77763290
|
C | T | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.279+1308G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763290 | ||||||
| chr11:77763291
|
G | A | 2 | a0001c0001t0009g0243a0001c0001t0009g0244 | 2 | HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.279+1307C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763291 | ||||||
| chr11:77763340
|
T | TA | 159 | a0001c0001t0001g0264a0001c0001t0002g0003a0001c0001t0002g0004others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.279+1257dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763340 | ||||||
| chr11:77763340
|
TA | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0319a0001c0001t0001g0320others(6): Show | 9 | HG01256.hp1 HG01515.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.279+1257delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763340 | ||||||
| chr11:77763464
|
G | C | 2 | a0001c0001t0008g0269a0001c0001t0008g0270 | 2 | HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.279+1134C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77763464 | ||||||
| chr11:77764122
|
G | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+476C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77764122 | ||||||
| chr11:77764358
|
G | A | 13 | a0001c0002t0003g0033a0001c0002t0003g0035a0001c0002t0003g0036others(10): Show | 13 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.279+240C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77764358 | ||||||
| chr11:77764461
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.279+137G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 2/15 | chr11 | 77764461 | ||||||
| chr11:77764983
|
T | C | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.188-294A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77764983 | ||||||
| chr11:77765028
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-339G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765028 | ||||||
| chr11:77765135
|
TA | T | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-447delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765135 | ||||||
| chr11:77765638
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-949G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765638 | ||||||
| chr11:77765931
|
A | C | 3 | a0001c0001t0005g0254a0001c0001t0025g0259a0008c0014t0005g0258 | 3 | NA18942.hp1 NA18977.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.188-1242T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765931 | ||||||
| chr11:77765991
|
G | A | 9 | a0001c0002t0003g0048a0001c0002t0003g0050a0001c0002t0003g0052others(6): Show | 9 | HG00280.hp2 HG00733.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-1302C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77765991 | ||||||
| chr11:77766133
|
T | C | 4 | a0002c0003t0002g0345a0002c0003t0002g0346a0002c0003t0002g0347others(1): Show | 4 | HG01891.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-1444A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766133 | ||||||
| chr11:77766138
|
C | CA | 7 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0002t0010g0013others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-1450dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766138 | ||||||
| chr11:77766154
|
G | GT | 73 | a0001c0001t0001g0288a0001c0001t0005g0038a0001c0002t0003g0018others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.188-1466dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766154 | ||||||
| chr11:77766299
|
G | A | 1 | a0001c0002t0003g0052 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.188-1610C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766299 | ||||||
| chr11:77766697
|
A | C | 1 | a0002c0003t0002g0217 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.188-2008T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766697 | ||||||
| chr11:77766706
|
A | C | 1 | a0002c0003t0050g0213 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.188-2017T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766706 | ||||||
| chr11:77766783
|
T | C | 85 | a0001c0001t0001g0277a0001c0001t0001g0307a0001c0001t0001g0308others(82): Show | 85 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.188-2094A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766783 | ||||||
| chr11:77766825
|
GTTT | G | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-2139_188-2137d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766825 | ||||||
| chr11:77766867
|
C | T | 2 | a0001c0001t0002g0108a0001c0002t0003g0072 | 2 | NA18967.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.188-2178G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766867 | ||||||
| chr11:77766911
|
A | G | 265 | a0001c0001t0001g0264a0001c0001t0001g0316a0001c0001t0001g0318others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.188-2222T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766911 | ||||||
| chr11:77766938
|
T | C | 2 | a0001c0001t0004g0105a0001c0001t0004g0106 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.188-2249A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766938 | ||||||
| chr11:77766953
|
A | G | 2 | a0001c0001t0006g0121a0004c0005t0049g0202 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.188-2264T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77766953 | ||||||
| chr11:77767063
|
G | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-2374C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767063 | ||||||
| chr11:77767123
|
C | T | 1 | a0002c0003t0002g0215 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.188-2434G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767123 | ||||||
| chr11:77767163
|
T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.188-2474A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767163 | ||||||
| chr11:77767424
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-2735A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767424 | ||||||
| chr11:77767673
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-2984A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767673 | ||||||
| chr11:77767734
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-3045G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767734 | ||||||
| chr11:77767741
|
T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188-3052A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767741 | ||||||
| chr11:77767775
|
T | C | 19 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(16): Show | 19 | HG02055.hp1 HG02602.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-3086A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77767775 | ||||||
| chr11:77768020
|
T | C | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-3331A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768020 | ||||||
| chr11:77768045
|
C | T | 52 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(49): Show | 52 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.188-3356G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768045 | ||||||
| chr11:77768143
|
A | G | 9 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111others(6): Show | 9 | HG02602.hp2 HG03654.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-3454T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768143 | ||||||
| chr11:77768161
|
C | CT | 44 | a0001c0001t0001g0087a0001c0001t0001g0276a0001c0001t0001g0282others(41): Show | 44 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.188-3473dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768161 | ||||||
| chr11:77768161
|
C | CTT | 22 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0006g0118others(19): Show | 22 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.188-3474_188-3473d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768161 | ||||||
| chr11:77768161
|
C | CTTT | 58 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(55): Show | 58 | HG00280.hp2 HG00423.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.188-3475_188-3473d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768161 | ||||||
| chr11:77768161
|
C | CTTTT | 9 | a0001c0002t0003g0020a0001c0002t0003g0054a0001c0002t0003g0063others(6): Show | 9 | HG00408.hp2 HG00597.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-3476_188-3473d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768161 | ||||||
| chr11:77768193
|
C | T | 3 | a0001c0002t0010g0013a0001c0002t0033g0012a0007c0018t0032g0014 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.188-3504G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768193 | ||||||
| chr11:77768219
|
G | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-3530C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768219 | ||||||
| chr11:77768248
|
T | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-3559A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768248 | ||||||
| chr11:77768373
|
G | A | 1 | a0001c0002t0003g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.188-3684C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768373 | ||||||
| chr11:77768407
|
G | A | 3 | a0002c0003t0002g0204a0002c0003t0002g0205a0002c0003t0002g0206 | 3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.188-3718C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768407 | ||||||
| chr11:77768412
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.188-3723C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768412 | ||||||
| chr11:77768453
|
G | A | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG00544.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.188-3764C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768453 | ||||||
| chr11:77768792
|
T | C | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.188-4103A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768792 | ||||||
| chr11:77768873
|
C | A | 1 | a0002c0003t0002g0228 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.188-4184G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768873 | ||||||
| chr11:77768991
|
A | G | 1 | a0001c0001t0004g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.188-4302T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77768991 | ||||||
| chr11:77769017
|
G | A | 4 | a0001c0002t0029g0017a0002c0003t0012g0222a0002c0003t0021g0209others(1): Show | 4 | HG00140.hp1 HG01123.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-4328C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769017 | ||||||
| chr11:77769067
|
T | C | 1 | a0001c0001t0011g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.188-4378A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769067 | ||||||
| chr11:77769073
|
T | C | 1 | a0001c0001t0039g0166 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.188-4384A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769073 | ||||||
| chr11:77769119
|
G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.188-4430C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769119 | ||||||
| chr11:77769174
|
C | G | 1 | a0001c0001t0011g0143 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.188-4485G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769174 | ||||||
| chr11:77769204
|
C | T | 3 | a0001c0002t0003g0082a0001c0002t0003g0083a0001c0002t0003g0084 | 3 | HG02523.hp1 NA19084.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.188-4515G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769204 | ||||||
| chr11:77769403
|
A | G | 1 | a0001c0001t0005g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.188-4714T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769403 | ||||||
| chr11:77769498
|
T | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-4809A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769498 | ||||||
| chr11:77769897
|
T | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-5208A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77769897 | ||||||
| chr11:77770153
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-5464C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770153 | ||||||
| chr11:77770387
|
G | A | 2 | a0001c0001t0006g0121a0004c0005t0049g0202 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.188-5698C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770387 | ||||||
| chr11:77770510
|
T | C | 3 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111 | 3 | NA18973.hp1 NA18994.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.188-5821A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770510 | ||||||
| chr11:77770686
|
C | T | 1 | a0002c0003t0002g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.188-5997G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770686 | ||||||
| chr11:77770763
|
A | C | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-6074T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770763 | ||||||
| chr11:77770895
|
G | A | 4 | a0001c0001t0013g0271a0001c0001t0013g0272a0001c0001t0013g0273others(1): Show | 4 | HG02572.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-6206C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77770895 | ||||||
| chr11:77771001
|
T | C | 1 | a0002c0003t0002g0221 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.188-6312A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771001 | ||||||
| chr11:77771308
|
G | A | 1 | a0001c0001t0009g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.188-6619C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771308 | ||||||
| chr11:77771608
|
C | G | 6 | a0001c0001t0007g0155a0001c0001t0007g0164a0001c0001t0007g0178others(3): Show | 6 | HG00544.hp1 HG00597.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-6919G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771608 | ||||||
| chr11:77771646
|
C | T | 1 | a0001c0001t0004g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.188-6957G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771646 | ||||||
| chr11:77771728
|
A | G | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-7039T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771728 | ||||||
| chr11:77771737
|
C | T | 1 | a0001c0001t0007g0178 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.188-7048G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771737 | ||||||
| chr11:77771876
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-7187A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771876 | ||||||
| chr11:77771934
|
T | A | 1 | a0001c0001t0001g0322 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.188-7245A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77771934 | ||||||
| chr11:77772084
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.188-7395C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772084 | ||||||
| chr11:77772417
|
G | A | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.188-7728C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772417 | ||||||
| chr11:77772831
|
A | G | 1 | a0001c0001t0053g0191 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.188-8142T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772831 | ||||||
| chr11:77772848
|
G | GA | 141 | a0001c0001t0001g0292a0001c0001t0001g0311a0001c0001t0001g0316others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.188-8160dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772848 | ||||||
| chr11:77772848
|
G | GAA | 19 | a0001c0001t0002g0113a0001c0001t0002g0126a0001c0001t0002g0131others(16): Show | 19 | HG00733.hp1 HG01074.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-8161_188-8160d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772848 | ||||||
| chr11:77772848
|
GA | G | 70 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(67): Show | 70 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.188-8160delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77772848 | ||||||
| chr11:77773272
|
C | T | 2 | a0001c0001t0006g0123a0001c0001t0006g0127 | 2 | HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.188-8583G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773272 | ||||||
| chr11:77773339
|
C | T | 9 | a0001c0001t0001g0274a0001c0001t0001g0334a0001c0001t0001g0335others(6): Show | 9 | HG00408.hp1 HG00609.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-8650G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773339 | ||||||
| chr11:77773413
|
G | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0089a0001c0001t0001g0092others(4): Show | 7 | HG00323.hp1 HG00741.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-8724C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773413 | ||||||
| chr11:77773670
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.188-8981A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773670 | ||||||
| chr11:77773689
|
T | C | 261 | a0001c0001t0001g0264a0001c0001t0002g0003a0001c0001t0002g0004others(258): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.188-9000A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773689 | ||||||
| chr11:77773701
|
C | T | 3 | a0001c0001t0022g0144a0001c0001t0022g0145a0001c0001t0054g0146 | 3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.188-9012G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773701 | ||||||
| chr11:77773868
|
C | T | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-9179G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77773868 | ||||||
| chr11:77774155
|
T | C | 3 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0016t0045g0201 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.188-9466A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774155 | ||||||
| chr11:77774164
|
T | A | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.188-9475A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774164 | ||||||
| chr11:77774231
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.188-9542G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774231 | ||||||
| chr11:77774395
|
G | A | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.188-9706C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774395 | ||||||
| chr11:77774573
|
A | AAAAT | 20 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(17): Show | 20 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.188-9888_188-9885d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | ||||||
| chr11:77774573
|
AAAAT | A | 137 | a0001c0001t0001g0309a0001c0001t0002g0003a0001c0001t0002g0004others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.188-9888_188-9885d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | ||||||
| chr11:77774573
|
AAAATAAA others(1): Show |
A | 7 | a0001c0001t0001g0264a0001c0001t0004g0180a0001c0001t0006g0122others(4): Show | 7 | HG01074.hp1 HG03098.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-9892_188-9885d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | ||||||
| chr11:77774573
|
AAAATAAA others(5): Show |
A | 3 | a0001c0002t0010g0350a0001c0002t0010g0351a0001c0002t0033g0012 | 3 | HG02055.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-9896_188-9885d others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | ||||||
| chr11:77774573
|
AAAATAAA others(9): Show |
A | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.188-9900_188-9885d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774573 | ||||||
| chr11:77774617
|
T | A | 3 | a0001c0001t0001g0292a0001c0001t0004g0160a0001c0001t0004g0167 | 3 | HG01123.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.188-9928A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774617 | ||||||
| chr11:77774677
|
A | T | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188-9988T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774677 | ||||||
| chr11:77774721
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.188-10032C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774721 | ||||||
| chr11:77774773
|
C | CT | 78 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(75): Show | 78 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.188-10085dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774773 | ||||||
| chr11:77774826
|
G | T | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10137C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774826 | ||||||
| chr11:77774924
|
G | C | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10235C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774924 | ||||||
| chr11:77774925
|
C | G | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10236G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77774925 | ||||||
| chr11:77775204
|
C | T | 3 | a0002c0003t0002g0204a0002c0003t0002g0205a0002c0003t0002g0206 | 3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.188-10515G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775204 | ||||||
| chr11:77775324
|
A | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-10635T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775324 | ||||||
| chr11:77775434
|
G | T | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10745C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775434 | ||||||
| chr11:77775679
|
A | T | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-10990T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775679 | ||||||
| chr11:77775811
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-11122A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775811 | ||||||
| chr11:77775811
|
T | G | 1 | a0001c0001t0023g0275 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.188-11122A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775811 | ||||||
| chr11:77775812
|
A | T | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-11123T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775812 | ||||||
| chr11:77775940
|
T | C | 13 | a0001c0002t0003g0033a0001c0002t0003g0035a0001c0002t0003g0036others(10): Show | 13 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-11251A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77775940 | ||||||
| chr11:77776117
|
A | G | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-11428T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776117 | ||||||
| chr11:77776204
|
C | A | 2 | a0001c0001t0004g0101a0001c0001t0004g0103 | 2 | HG02083.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.188-11515G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776204 | ||||||
| chr11:77776229
|
CA | C | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-11541delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776229 | ||||||
| chr11:77776323
|
C | G | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-11634G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776323 | ||||||
| chr11:77776371
|
C | A | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-11682G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776371 | ||||||
| chr11:77776372
|
A | T | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-11683T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776372 | ||||||
| chr11:77776375
|
T | C | 1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-11686A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776375 | ||||||
| chr11:77776698
|
C | A | 1 | a0001c0002t0014g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.188-12009G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77776698 | ||||||
| chr11:77777011
|
T | A | 350 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.188-12322A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777011 | ||||||
| chr11:77777029
|
G | A | 1 | a0001c0001t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.188-12340C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777029 | ||||||
| chr11:77777033
|
G | C | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.188-12344C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777033 | ||||||
| chr11:77777034
|
A | T | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.188-12345T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777034 | ||||||
| chr11:77777041
|
C | A | 1 | a0002c0003t0050g0213 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.188-12352G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777041 | ||||||
| chr11:77777056
|
A | T | 4 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0307others(1): Show | 4 | HG01891.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-12367T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777056 | ||||||
| chr11:77777132
|
A | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-12443T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777132 | ||||||
| chr11:77777384
|
G | A | 3 | a0002c0003t0002g0218a0002c0003t0002g0223a0002c0003t0002g0229 | 3 | HG01070.hp2 HG01168.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.188-12695C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777384 | ||||||
| chr11:77777448
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.188-12759G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777448 | ||||||
| chr11:77777763
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-13074G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777763 | ||||||
| chr11:77777779
|
G | A | 69 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.188-13090C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777779 | ||||||
| chr11:77777937
|
G | C | 1 | a0002c0003t0002g0208 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.188-13248C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777937 | ||||||
| chr11:77777950
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.188-13261A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77777950 | ||||||
| chr11:77778095
|
T | C | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.188-13406A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778095 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(102): Show |
1 | a0001c0002t0031g0075 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.188-13427_188-1342 others(113): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(104): Show |
1 | a0001c0001t0004g0184 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(104): Show |
1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(102): Show |
1 | a0001c0001t0002g0109 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(113): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(103): Show |
326 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(323): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.188-13427_188-1342 others(114): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(104): Show |
1 | a0001c0001t0053g0191 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(102): Show |
1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(113): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(105): Show |
1 | a0001c0001t0068g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.188-13427_188-1342 others(116): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(104): Show |
15 | a0001c0001t0001g0276a0001c0001t0001g0316a0001c0001t0002g0116others(12): Show | 15 | HG01358.hp2 HG02027.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.188-13427_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778115
|
A | AGGAGGAG others(105): Show |
1 | a0001c0001t0002g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.188-13427_188-1342 others(116): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778115 | ||||||
| chr11:77778118
|
A | AGGAGGGG others(104): Show |
1 | a0001c0001t0001g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.188-13430_188-1342 others(115): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778118 | ||||||
| chr11:77778118
|
A | AGGAGGGG others(107): Show |
1 | a0001c0001t0054g0146 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.188-13430_188-1342 others(118): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778118 | ||||||
| chr11:77778144
|
G | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-13455C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778144 | ||||||
| chr11:77778179
|
AGGGGAGG others(4): Show |
A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-13501_188-1349 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778179 | ||||||
| chr11:77778201
|
G | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-13512C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778201 | ||||||
| chr11:77778219
|
G | A | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-13530C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778219 | ||||||
| chr11:77778227
|
T | G | 1 | a0001c0002t0003g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.188-13538A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778227 | ||||||
| chr11:77778329
|
G | A | 3 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111 | 3 | NA18973.hp1 NA18994.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.188-13640C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778329 | ||||||
| chr11:77778430
|
T | G | 3 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0126 | 3 | NA18963.hp1 NA18975.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.188-13741A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778430 | ||||||
| chr11:77778470
|
G | A | 1 | a0001c0001t0004g0198 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.188-13781C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778470 | ||||||
| chr11:77778562
|
T | G | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-13873A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778562 | ||||||
| chr11:77778679
|
C | T | 72 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(69): Show | 72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.188-13990G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778679 | ||||||
| chr11:77778704
|
T | G | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-14015A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778704 | ||||||
| chr11:77778805
|
C | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-14116G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77778805 | ||||||
| chr11:77779185
|
C | T | 2 | a0001c0001t0004g0136a0001c0001t0042g0173 | 2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.188-14496G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779185 | ||||||
| chr11:77779349
|
A | AGCCG | 6 | a0001c0001t0007g0155a0001c0001t0007g0164a0001c0001t0007g0178others(3): Show | 6 | HG00544.hp1 HG00597.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-14661_188-1466 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779349 | ||||||
| chr11:77779384
|
A | AT | 20 | a0001c0001t0001g0277a0001c0001t0001g0287a0001c0001t0001g0342others(17): Show | 20 | HG00544.hp2 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.188-14696dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779384 | ||||||
| chr11:77779384
|
A | ATT | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.188-14697_188-1469 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779384 | ||||||
| chr11:77779384
|
A | T | 1 | a0001c0001t0001g0334 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.188-14695T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779384 | ||||||
| chr11:77779384
|
AT | A | 6 | a0001c0001t0001g0322a0001c0001t0004g0147a0001c0001t0004g0167others(3): Show | 6 | HG01070.hp2 HG01081.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-14696delA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779384 | ||||||
| chr11:77779385
|
T | A | 2 | a0001c0001t0001g0334a0001c0001t0007g0155 | 2 | HG00544.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.188-14696A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779385 | ||||||
| chr11:77779404
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.188-14715A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779404 | ||||||
| chr11:77779405
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.188-14716C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779405 | ||||||
| chr11:77779804
|
T | C | 265 | a0001c0001t0001g0264a0001c0001t0001g0276a0001c0001t0001g0277others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.188-15115A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779804 | ||||||
| chr11:77779912
|
G | A | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-15223C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779912 | ||||||
| chr11:77779957
|
C | G | 1 | a0001c0002t0003g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.188-15268G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77779957 | ||||||
| chr11:77780035
|
G | A | 1 | a0001c0002t0003g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.188-15346C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780035 | ||||||
| chr11:77780210
|
T | C | 4 | a0003c0004t0002g0231a0003c0004t0002g0232a0003c0004t0002g0234others(1): Show | 4 | HG00673.hp2 HG02015.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-15521A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780210 | ||||||
| chr11:77780366
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.188-15677T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780366 | ||||||
| chr11:77780548
|
G | A | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-15859C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780548 | ||||||
| chr11:77780599
|
G | A | 1 | a0004c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.188-15910C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780599 | ||||||
| chr11:77780682
|
G | A | 1 | a0001c0001t0004g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.188-15993C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780682 | ||||||
| chr11:77780757
|
A | G | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-16068T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780757 | ||||||
| chr11:77780818
|
C | A | 80 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.188-16129G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780818 | ||||||
| chr11:77780824
|
C | CA | 154 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(151): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.188-16136dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780824 | ||||||
| chr11:77780824
|
C | CAA | 109 | a0001c0001t0001g0097a0001c0001t0001g0299a0001c0001t0002g0108others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.188-16137_188-1613 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780824 | ||||||
| chr11:77780824
|
C | CAAA | 6 | a0001c0001t0002g0110a0001c0001t0009g0243a0001c0001t0009g0244others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-16138_188-1613 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780824 | ||||||
| chr11:77780824
|
CA | C | 7 | a0001c0002t0010g0013a0001c0002t0016g0005a0001c0002t0016g0008others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-16136delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780824 | ||||||
| chr11:77780854
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.188-16165T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77780854 | ||||||
| chr11:77781100
|
T | C | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.188-16411A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781100 | ||||||
| chr11:77781103
|
T | C | 1 | a0001c0002t0003g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-16414A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781103 | ||||||
| chr11:77781104
|
C | CT | 80 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.188-16416dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781104 | ||||||
| chr11:77781113
|
T | G | 2 | a0004c0005t0020g0199a0004c0005t0020g0200 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.188-16424A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781113 | ||||||
| chr11:77781114
|
T | A | 3 | a0001c0002t0035g0057a0004c0005t0020g0199a0004c0005t0020g0200 | 3 | HG02451.hp2 HG03041.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.188-16425A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781114 | ||||||
| chr11:77781180
|
A | C | 1 | a0001c0002t0003g0030 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.188-16491T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781180 | ||||||
| chr11:77781243
|
C | T | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188-16554G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781243 | ||||||
| chr11:77781371
|
T | C | 2 | a0001c0001t0002g0114a0001c0001t0040g0117 | 2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.188-16682A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781371 | ||||||
| chr11:77781536
|
T | C | 1 | a0001c0001t0038g0170 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.188-16847A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781536 | ||||||
| chr11:77781548
|
A | G | 43 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.188-16859T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781548 | ||||||
| chr11:77781689
|
A | T | 1 | a0001c0001t0002g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.188-17000T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781689 | ||||||
| chr11:77781789
|
T | G | 1 | a0001c0001t0004g0186 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.188-17100A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781789 | ||||||
| chr11:77781895
|
C | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-17206G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781895 | ||||||
| chr11:77781896
|
A | G | 1 | a0001c0001t0004g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.188-17207T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77781896 | ||||||
| chr11:77782060
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-17371A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782060 | ||||||
| chr11:77782171
|
TAATTAC | T | 4 | a0003c0004t0002g0231a0003c0004t0002g0232a0003c0004t0002g0234others(1): Show | 4 | HG00673.hp2 HG02015.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-17488_188-1748 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782171 | ||||||
| chr11:77782208
|
T | C | 1 | a0001c0001t0004g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.188-17519A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782208 | ||||||
| chr11:77782257
|
G | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG01884.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.188-17568C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782257 | ||||||
| chr11:77782307
|
G | T | 2 | a0001c0002t0010g0013a0001c0002t0033g0012 | 2 | HG01074.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.188-17618C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782307 | ||||||
| chr11:77782412
|
G | A | 1 | a0002c0003t0002g0217 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.188-17723C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782412 | ||||||
| chr11:77782473
|
G | A | 1 | a0002c0003t0002g0215 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.188-17784C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782473 | ||||||
| chr11:77782538
|
C | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-17849G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782538 | ||||||
| chr11:77782540
|
C | CA | 8 | a0001c0001t0001g0016a0001c0001t0001g0319a0001c0001t0001g0320others(5): Show | 8 | HG01070.hp2 HG01168.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-17852dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782540 | ||||||
| chr11:77782958
|
T | C | 22 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(19): Show | 22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.188-18269A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782958 | ||||||
| chr11:77782960
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-18271G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77782960 | ||||||
| chr11:77783091
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-18402A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783091 | ||||||
| chr11:77783287
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-18598C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783287 | ||||||
| chr11:77783474
|
C | T | 1 | a0001c0001t0005g0038 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.188-18785G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783474 | ||||||
| chr11:77783493
|
T | C | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188-18804A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783493 | ||||||
| chr11:77783564
|
G | A | 1 | a0001c0001t0023g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.188-18875C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783564 | ||||||
| chr11:77783617
|
G | A | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.188-18928C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783617 | ||||||
| chr11:77783663
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-18974C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783663 | ||||||
| chr11:77783708
|
G | A | 39 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0207others(36): Show | 39 | HG00140.hp1 HG00673.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.188-19019C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783708 | ||||||
| chr11:77783809
|
T | A | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.188-19120A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783809 | ||||||
| chr11:77783811
|
C | T | 1 | a0002c0003t0002g0219 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.188-19122G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783811 | ||||||
| chr11:77783833
|
C | A | 1 | a0002c0003t0002g0216 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.188-19144G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783833 | ||||||
| chr11:77783863
|
G | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-19174C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77783863 | ||||||
| chr11:77784022
|
T | A | 1 | a0003c0004t0002g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.188-19333A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784022 | ||||||
| chr11:77784102
|
G | C | 73 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.188-19413C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784102 | ||||||
| chr11:77784110
|
C | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-19421G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784110 | ||||||
| chr11:77784206
|
T | A | 1 | a0001c0002t0003g0058 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.188-19517A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784206 | ||||||
| chr11:77784427
|
T | C | 1 | a0002c0003t0002g0205 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.188-19738A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784427 | ||||||
| chr11:77784599
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-19910G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784599 | ||||||
| chr11:77784680
|
G | A | 1 | a0002c0003t0002g0207 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.188-19991C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784680 | ||||||
| chr11:77784850
|
A | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-20161T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784850 | ||||||
| chr11:77784978
|
C | T | 5 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(2): Show | 5 | HG01884.hp2 HG02630.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-20289G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77784978 | ||||||
| chr11:77785059
|
TTC | T | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-20372_188-2037 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785059 | ||||||
| chr11:77785126
|
C | T | 52 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(49): Show | 52 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.188-20437G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785126 | ||||||
| chr11:77785480
|
C | T | 1 | a0001c0001t0008g0270 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.188-20791G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785480 | ||||||
| chr11:77785521
|
C | T | 69 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.188-20832G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785521 | ||||||
| chr11:77785645
|
A | T | 42 | a0002c0003t0002g0099a0002c0003t0002g0203a0002c0003t0002g0204others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.188-20956T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785645 | ||||||
| chr11:77785718
|
G | A | 5 | a0001c0001t0006g0118a0001c0001t0006g0123a0001c0001t0006g0125others(2): Show | 5 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-21029C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785718 | ||||||
| chr11:77785754
|
GA | G | 86 | a0001c0001t0001g0287a0001c0001t0001g0290a0001c0001t0001g0332others(83): Show | 86 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.188-21066delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785754 | ||||||
| chr11:77785791
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-21102G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785791 | ||||||
| chr11:77785874
|
C | T | 1 | a0001c0001t0004g0154 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.188-21185G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785874 | ||||||
| chr11:77785894
|
C | T | 3 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0016t0045g0201 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.188-21205G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785894 | ||||||
| chr11:77785904
|
C | T | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.188-21215G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785904 | ||||||
| chr11:77785917
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.188-21228A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785917 | ||||||
| chr11:77785925
|
C | CA | 62 | a0001c0001t0001g0089a0001c0001t0001g0094a0001c0001t0001g0277others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.188-21237dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | ||||||
| chr11:77785925
|
C | CAA | 75 | a0001c0001t0001g0285a0001c0001t0001g0298a0001c0001t0002g0109others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.188-21238_188-2123 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | ||||||
| chr11:77785925
|
C | CAAA | 24 | a0001c0001t0002g0108a0001c0001t0002g0115a0001c0001t0002g0120others(21): Show | 24 | HG00609.hp1 HG01175.hp1 HG02071.hp2 others(21): Show |
intron_variant | MODIFIER | c.188-21239_188-2123 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | ||||||
| chr11:77785925
|
C | CAAAA | 17 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0300others(14): Show | 17 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-21240_188-2123 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | ||||||
| chr11:77785925
|
C | CAAAAA | 7 | a0001c0001t0001g0303a0001c0001t0004g0135a0001c0001t0005g0302others(4): Show | 7 | HG00423.hp1 HG02027.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-21241_188-2123 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | ||||||
| chr11:77785925
|
CAAAA | C | 8 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0019others(5): Show | 8 | HG01081.hp1 HG02809.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-21240_188-2123 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | ||||||
| chr11:77785925
|
CAAAAA | C | 70 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0021others(67): Show | 70 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.188-21241_188-2123 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | ||||||
| chr11:77785925
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.188-21250_188-2123 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785925 | ||||||
| chr11:77785957
|
A | T | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-21268T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785957 | ||||||
| chr11:77785992
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-21303C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77785992 | ||||||
| chr11:77786008
|
C | CA | 351 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.188-21320dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786008 | ||||||
| chr11:77786024
|
C | T | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.188-21335G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786024 | ||||||
| chr11:77786073
|
T | C | 4 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-21384A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786073 | ||||||
| chr11:77786349
|
C | G | 236 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.188-21660G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786349 | ||||||
| chr11:77786701
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-22012G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786701 | ||||||
| chr11:77786828
|
A | T | 2 | a0001c0002t0003g0033a0001c0002t0003g0047 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.188-22139T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786828 | ||||||
| chr11:77786841
|
C | T | 1 | a0001c0001t0009g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.188-22152G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786841 | ||||||
| chr11:77786887
|
G | A | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-22198C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77786887 | ||||||
| chr11:77787006
|
G | A | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-22317C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787006 | ||||||
| chr11:77787014
|
G | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-22325C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787014 | ||||||
| chr11:77787118
|
G | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188-22429C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787118 | ||||||
| chr11:77787195
|
C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.188-22506G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787195 | ||||||
| chr11:77787228
|
C | T | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.188-22539G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787228 | ||||||
| chr11:77787440
|
T | C | 73 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.188-22751A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787440 | ||||||
| chr11:77787489
|
G | A | 1 | a0001c0002t0003g0056 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.188-22800C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787489 | ||||||
| chr11:77787521
|
T | G | 1 | a0001c0001t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.188-22832A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787521 | ||||||
| chr11:77787562
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-22873G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787562 | ||||||
| chr11:77787569
|
T | C | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.188-22880A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787569 | ||||||
| chr11:77787628
|
A | T | 1 | a0001c0002t0003g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-22939T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787628 | ||||||
| chr11:77787722
|
T | C | 236 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.188-23033A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787722 | ||||||
| chr11:77787833
|
T | TA | 8 | a0001c0001t0001g0089a0001c0001t0001g0344a0001c0001t0004g0182others(5): Show | 8 | HG00544.hp1 HG00741.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-23145dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | ||||||
| chr11:77787833
|
T | TAAAAAAA others(3): Show |
61 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(58): Show | 61 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.188-23154_188-2314 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | ||||||
| chr11:77787833
|
T | TAAAAAAA others(4): Show |
14 | a0001c0002t0003g0020a0001c0002t0003g0040a0001c0002t0003g0052others(11): Show | 14 | HG01192.hp2 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.188-23155_188-2314 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | ||||||
| chr11:77787833
|
T | TAAAAAAA others(5): Show |
1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188-23156_188-2314 others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | ||||||
| chr11:77787833
|
T | TAAAAAAA others(9): Show |
1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-23145_188-2314 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787833 | ||||||
| chr11:77787856
|
G | A | 10 | a0002c0003t0002g0099a0002c0003t0002g0218a0002c0003t0002g0219others(7): Show | 10 | HG00733.hp1 HG01070.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-23167C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787856 | ||||||
| chr11:77787881
|
G | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-23192C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787881 | ||||||
| chr11:77787887
|
T | C | 13 | a0001c0002t0003g0033a0001c0002t0003g0035a0001c0002t0003g0036others(10): Show | 13 | HG02257.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-23198A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787887 | ||||||
| chr11:77787897
|
A | G | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188-23208T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787897 | ||||||
| chr11:77787932
|
G | A | 1 | a0002c0003t0002g0207 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.188-23243C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77787932 | ||||||
| chr11:77788035
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.188-23346C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788035 | ||||||
| chr11:77788142
|
C | CA | 36 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0264others(33): Show | 36 | HG00558.hp1 HG00558.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.188-23454dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
C | CAA | 36 | a0001c0001t0001g0090a0001c0001t0001g0277a0001c0001t0001g0280others(33): Show | 36 | HG00544.hp2 HG00639.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.188-23455_188-2345 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
C | CAAA | 37 | a0001c0001t0001g0285a0001c0001t0001g0303a0001c0001t0002g0108others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.188-23456_188-2345 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
C | CAAAA | 51 | a0001c0001t0001g0297a0001c0001t0002g0109a0001c0001t0002g0124others(48): Show | 51 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.188-23457_188-2345 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
C | CAAAAA | 24 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0139others(21): Show | 24 | HG00099.hp1 HG00597.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.188-23458_188-2345 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
C | CAAAAAA | 9 | a0001c0001t0004g0136a0001c0001t0004g0188a0001c0001t0004g0194others(6): Show | 9 | HG00741.hp1 HG01256.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-23459_188-2345 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
C | CAAAAAAA others(3): Show |
2 | a0001c0001t0004g0187a0001c0001t0042g0173 | 2 | HG03688.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.188-23463_188-2345 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0006g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.188-23469_188-2345 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
CA | C | 25 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0313others(22): Show | 25 | HG01070.hp1 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.188-23454delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
CAA | C | 49 | a0001c0001t0001g0307a0001c0002t0003g0018a0001c0002t0003g0019others(46): Show | 49 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.188-23455_188-2345 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0004g0246a0007c0018t0032g0014 | 2 | HG04115.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.188-23465_188-2345 others(16): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0002g0004 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.188-23467_188-2345 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0002g0003a0001c0002t0010g0013a0001c0002t0014g0011others(2): Show | 5 | HG01074.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-23468_188-2345 others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788142
|
CAAAAAAA others(9): Show |
C | 5 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-23469_188-2345 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788142 | ||||||
| chr11:77788185
|
T | TA | 53 | a0001c0001t0001g0322a0001c0001t0005g0038a0001c0002t0003g0018others(50): Show | 53 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.188-23497dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788185 | ||||||
| chr11:77788217
|
G | A | 7 | a0002c0003t0002g0203a0002c0003t0002g0230a0002c0003t0002g0239others(4): Show | 7 | HG00673.hp2 HG02015.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-23528C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788217 | ||||||
| chr11:77788341
|
C | T | 69 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.188-23652G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788341 | ||||||
| chr11:77788488
|
A | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-23799T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788488 | ||||||
| chr11:77788497
|
TA | T | 109 | a0001c0001t0001g0091a0001c0001t0001g0307a0001c0001t0002g0108others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.188-23809delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788497 | ||||||
| chr11:77788497
|
TAA | T | 123 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0004g0174others(120): Show | 123 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.188-23810_188-2380 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788497 | ||||||
| chr11:77788499
|
A | T | 1 | a0001c0001t0004g0156 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.188-23810T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788499 | ||||||
| chr11:77788515
|
G | A | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.188-23826C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788515 | ||||||
| chr11:77788533
|
T | G | 1 | a0001c0002t0017g0007 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.188-23844A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788533 | ||||||
| chr11:77788541
|
T | C | 1 | a0001c0001t0004g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.188-23852A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788541 | ||||||
| chr11:77788632
|
G | C | 1 | a0001c0002t0017g0007 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.188-23943C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788632 | ||||||
| chr11:77788632
|
G | T | 1 | a0001c0001t0004g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.188-23943C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788632 | ||||||
| chr11:77788861
|
A | C | 1 | a0001c0001t0001g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-24172T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77788861 | ||||||
| chr11:77789183
|
A | G | 1 | a0001c0001t0007g0155 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.188-24494T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789183 | ||||||
| chr11:77789316
|
T | C | 2 | a0001c0001t0001g0293a0001c0001t0001g0342 | 2 | NA18973.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.188-24627A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789316 | ||||||
| chr11:77789405
|
G | T | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-24716C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789405 | ||||||
| chr11:77789439
|
C | T | 1 | a0001c0001t0041g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.188-24750G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789439 | ||||||
| chr11:77789457
|
G | C | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-24768C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789457 | ||||||
| chr11:77789544
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-24855G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789544 | ||||||
| chr11:77789568
|
G | T | 1 | a0001c0001t0002g0115 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.188-24879C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789568 | ||||||
| chr11:77789586
|
C | T | 3 | a0001c0001t0004g0186a0001c0002t0003g0041a0001c0002t0003g0042 | 3 | HG02886.hp2 HG03041.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.188-24897G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789586 | ||||||
| chr11:77789596
|
C | T | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-24907G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789596 | ||||||
| chr11:77789647
|
T | C | 2 | a0001c0001t0001g0089a0001c0017t0001g0095 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.188-24958A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789647 | ||||||
| chr11:77789690
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-25001G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789690 | ||||||
| chr11:77789719
|
A | C | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188-25030T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77789719 | ||||||
| chr11:77790057
|
A | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-25368T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790057 | ||||||
| chr11:77790216
|
T | C | 80 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(77): Show | 80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.188-25527A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790216 | ||||||
| chr11:77790230
|
G | A | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188-25541C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790230 | ||||||
| chr11:77790376
|
C | T | 1 | a0001c0001t0004g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.188-25687G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790376 | ||||||
| chr11:77790402
|
T | A | 69 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(66): Show | 69 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.188-25713A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790402 | ||||||
| chr11:77790502
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.188-25813A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790502 | ||||||
| chr11:77790619
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.188-25930T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790619 | ||||||
| chr11:77790937
|
A | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-26248T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77790937 | ||||||
| chr11:77791017
|
C | T | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188-26328G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791017 | ||||||
| chr11:77791086
|
C | T | 80 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.188-26397G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791086 | ||||||
| chr11:77791124
|
C | G | 1 | a0001c0001t0004g0136 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.188-26435G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791124 | ||||||
| chr11:77791303
|
T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188-26614A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791303 | ||||||
| chr11:77791424
|
C | G | 52 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(49): Show | 52 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.188-26735G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791424 | ||||||
| chr11:77791473
|
A | C | 78 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(75): Show | 78 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.188-26784T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791473 | ||||||
| chr11:77791473
|
A | T | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-26784T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791473 | ||||||
| chr11:77791498
|
A | C | 2 | a0001c0001t0009g0242a0001c0001t0009g0245 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.188-26809T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791498 | ||||||
| chr11:77791586
|
T | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.188-26897A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791586 | ||||||
| chr11:77791634
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.188-26945G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791634 | ||||||
| chr11:77791905
|
C | T | 2 | a0001c0001t0001g0283a0001c0001t0001g0286 | 2 | NA18981.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.188-27216G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791905 | ||||||
| chr11:77791971
|
C | T | 7 | a0001c0001t0006g0118a0001c0001t0006g0121a0001c0001t0006g0122others(4): Show | 7 | HG00639.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-27282G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77791971 | ||||||
| chr11:77792166
|
G | C | 8 | a0001c0001t0001g0285a0001c0001t0001g0296a0001c0001t0001g0297others(5): Show | 8 | HG01884.hp2 HG02145.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-27477C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792166 | ||||||
| chr11:77792256
|
C | G | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188-27567G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792256 | ||||||
| chr11:77792367
|
C | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.188-27678G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792367 | ||||||
| chr11:77792429
|
G | A | 19 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(16): Show | 19 | HG02055.hp1 HG02602.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-27740C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792429 | ||||||
| chr11:77792547
|
C | G | 1 | a0003c0004t0002g0232 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.188-27858G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792547 | ||||||
| chr11:77792616
|
G | T | 1 | a0001c0002t0035g0057 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.187+27912C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792616 | ||||||
| chr11:77792672
|
A | G | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.187+27856T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792672 | ||||||
| chr11:77792707
|
G | A | 13 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(10): Show | 13 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.187+27821C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792707 | ||||||
| chr11:77792749
|
A | C | 1 | a0004c0005t0020g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.187+27779T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792749 | ||||||
| chr11:77792752
|
C | A | 83 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0120others(80): Show | 83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.187+27776G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792752 | ||||||
| chr11:77792753
|
T | A | 12 | a0001c0002t0003g0033a0001c0002t0003g0041a0001c0002t0003g0042others(9): Show | 12 | HG01243.hp2 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+27775A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792753 | ||||||
| chr11:77792840
|
C | T | 3 | a0002c0003t0002g0204a0002c0003t0002g0205a0002c0003t0002g0206 | 3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.187+27688G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792840 | ||||||
| chr11:77792906
|
C | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+27622G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792906 | ||||||
| chr11:77792914
|
C | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+27614G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77792914 | ||||||
| chr11:77793058
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+27470C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793058 | ||||||
| chr11:77793239
|
A | C | 1 | a0001c0001t0001g0288 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.187+27289T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793239 | ||||||
| chr11:77793328
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+27200T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793328 | ||||||
| chr11:77793447
|
G | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+27081C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793447 | ||||||
| chr11:77793491
|
A | C | 1 | a0001c0002t0003g0041 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.187+27037T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793491 | ||||||
| chr11:77793663
|
C | T | 60 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(57): Show | 60 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.187+26865G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793663 | ||||||
| chr11:77793685
|
C | T | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.187+26843G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793685 | ||||||
| chr11:77793816
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+26712C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793816 | ||||||
| chr11:77793950
|
T | C | 22 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(19): Show | 22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+26578A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793950 | ||||||
| chr11:77793995
|
A | T | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.187+26533T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77793995 | ||||||
| chr11:77794041
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.187+26487T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794041 | ||||||
| chr11:77794052
|
T | C | 1 | a0001c0002t0035g0057 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.187+26476A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794052 | ||||||
| chr11:77794172
|
T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.187+26356A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794172 | ||||||
| chr11:77794310
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.187+26218G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794310 | ||||||
| chr11:77794433
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+26095G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794433 | ||||||
| chr11:77794491
|
C | T | 2 | a0001c0001t0001g0097a0004c0016t0045g0201 | 2 | HG01261.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.187+26037G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794491 | ||||||
| chr11:77794553
|
A | C | 1 | a0001c0001t0001g0334 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.187+25975T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794553 | ||||||
| chr11:77794897
|
AAAG | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+25628_187+2563 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794897 | ||||||
| chr11:77794914
|
T | G | 1 | a0001c0002t0031g0075 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.187+25614A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794914 | ||||||
| chr11:77794926
|
C | T | 1 | a0001c0002t0003g0018 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.187+25602G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794926 | ||||||
| chr11:77794998
|
C | T | 79 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.187+25530G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77794998 | ||||||
| chr11:77795423
|
A | T | 1 | a0002c0003t0002g0214 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.187+25105T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795423 | ||||||
| chr11:77795453
|
C | T | 3 | a0002c0003t0002g0204a0002c0003t0002g0205a0002c0003t0002g0206 | 3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.187+25075G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795453 | ||||||
| chr11:77795489
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+25039G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795489 | ||||||
| chr11:77795649
|
T | A | 237 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.187+24879A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795649 | ||||||
| chr11:77795662
|
A | G | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187+24866T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795662 | ||||||
| chr11:77795892
|
A | C | 14 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0300others(11): Show | 14 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.187+24636T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795892 | ||||||
| chr11:77795943
|
G | A | 1 | a0001c0001t0008g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.187+24585C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77795943 | ||||||
| chr11:77796152
|
G | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+24376C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796152 | ||||||
| chr11:77796165
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+24363G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796165 | ||||||
| chr11:77796286
|
G | C | 124 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.187+24242C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796286 | ||||||
| chr11:77796374
|
G | T | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+24154C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796374 | ||||||
| chr11:77796399
|
A | G | 5 | a0001c0001t0001g0317a0001c0001t0001g0323a0001c0001t0001g0324others(2): Show | 5 | HG02132.hp2 NA18968.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+24129T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796399 | ||||||
| chr11:77796495
|
T | G | 2 | a0002c0003t0002g0221a0002c0003t0008g0266 | 2 | HG01515.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.187+24033A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796495 | ||||||
| chr11:77796504
|
A | C | 1 | a0001c0001t0051g0183 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.187+24024T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796504 | ||||||
| chr11:77796864
|
AACAG | A | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.187+23660_187+2366 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796864 | ||||||
| chr11:77796892
|
G | GTGAACTC others(16): Show |
1 | a0001c0001t0005g0254 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.187+23613_187+2363 others(27): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77796892 | ||||||
| chr11:77797083
|
C | T | 1 | a0001c0001t0005g0255 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.187+23445G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797083 | ||||||
| chr11:77797108
|
C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+23420G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797108 | ||||||
| chr11:77797167
|
C | T | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+23361G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797167 | ||||||
| chr11:77797510
|
C | T | 1 | a0001c0002t0017g0006 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.187+23018G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797510 | ||||||
| chr11:77797546
|
G | A | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+22982C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797546 | ||||||
| chr11:77797773
|
G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.187+22755C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797773 | ||||||
| chr11:77797800
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.187+22728A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797800 | ||||||
| chr11:77797833
|
CAA | C | 68 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.187+22693_187+2269 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797833 | ||||||
| chr11:77797853
|
T | C | 1 | a0001c0001t0006g0121 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.187+22675A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797853 | ||||||
| chr11:77797936
|
C | T | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.187+22592G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77797936 | ||||||
| chr11:77798307
|
G | A | 1 | a0001c0001t0040g0117 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.187+22221C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798307 | ||||||
| chr11:77798364
|
C | G | 1 | a0001c0001t0004g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.187+22164G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798364 | ||||||
| chr11:77798371
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+22157G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798371 | ||||||
| chr11:77798440
|
C | T | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.187+22088G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798440 | ||||||
| chr11:77798581
|
T | TAAAA | 7 | a0001c0001t0001g0098a0001c0001t0001g0299a0001c0001t0001g0328others(4): Show | 7 | HG02132.hp2 HG02965.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+21943_187+2194 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
T | TAAAAAAA others(6): Show |
1 | a0001c0002t0010g0350 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.187+21934_187+2194 others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
T | TAAAAAAA others(7): Show |
2 | a0001c0001t0005g0261a0001c0002t0010g0351 | 2 | HG02055.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.187+21933_187+2194 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TA | T | 29 | a0001c0001t0001g0087a0001c0001t0001g0091a0001c0001t0001g0092others(26): Show | 29 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.187+21946delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAA | T | 46 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0090others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.187+21945_187+2194 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAA | T | 28 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0300others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.187+21944_187+2194 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAA | T | 56 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111others(53): Show | 56 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.187+21943_187+2194 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAA | T | 25 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0124others(22): Show | 25 | HG00673.hp2 HG01255.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.187+21942_187+2194 others(9): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAA | T | 19 | a0001c0001t0002g0110a0001c0001t0002g0114a0001c0001t0004g0180others(16): Show | 19 | HG00639.hp1 HG01168.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.187+21941_187+2194 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA | T | 10 | a0001c0001t0002g0113a0001c0001t0002g0119a0001c0001t0002g0120others(7): Show | 10 | HG00099.hp2 HG00639.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+21940_187+2194 others(11): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(1): Show |
T | 7 | a0001c0001t0002g0112a0001c0001t0002g0129a0001c0001t0002g0130others(4): Show | 7 | HG00741.hp1 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+21939_187+2194 others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(3): Show |
T | 61 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(58): Show | 61 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.187+21937_187+2194 others(14): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(4): Show |
T | 7 | a0001c0002t0003g0022a0001c0002t0003g0035a0001c0002t0003g0061others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+21936_187+2194 others(15): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(6): Show |
T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0010g0013others(1): Show | 4 | HG01074.hp1 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+21934_187+2194 others(17): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(7): Show |
T | 5 | a0001c0001t0028g0149a0001c0002t0016g0005a0001c0002t0016g0008others(2): Show | 5 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+21933_187+2194 others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0004g0105a0001c0001t0004g0106a0004c0016t0045g0201 | 3 | HG03195.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.187+21932_187+2194 others(19): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(9): Show |
T | 4 | a0001c0001t0001g0280a0001c0001t0001g0285a0004c0005t0020g0199others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+21931_187+2194 others(20): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0002g0306 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.187+21930_187+2194 others(21): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(12): Show |
T | 5 | a0001c0001t0001g0311a0001c0001t0004g0135a0001c0001t0005g0253others(2): Show | 5 | HG01975.hp2 HG02602.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+21928_187+2194 others(23): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(13): Show |
T | 1 | a0001c0001t0002g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.187+21927_187+2194 others(24): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798581
|
TAAAAAAA others(14): Show |
T | 2 | a0001c0002t0003g0036a0001c0002t0003g0037 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.187+21926_187+2194 others(25): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798581 | ||||||
| chr11:77798619
|
A | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+21909T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798619 | ||||||
| chr11:77798928
|
C | T | 3 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0111 | 3 | NA18973.hp1 NA18994.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.187+21600G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798928 | ||||||
| chr11:77798964
|
TAA | T | 78 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(75): Show | 78 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.187+21562_187+2156 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77798964 | ||||||
| chr11:77799344
|
T | C | 1 | a0001c0009t0036g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187+21184A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799344 | ||||||
| chr11:77799501
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+21027G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799501 | ||||||
| chr11:77799504
|
C | CA | 81 | a0001c0001t0001g0328a0001c0001t0002g0003a0001c0001t0002g0004others(78): Show | 81 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+21023dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799504 | ||||||
| chr11:77799561
|
A | G | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.187+20967T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799561 | ||||||
| chr11:77799848
|
T | C | 1 | a0001c0001t0004g0177 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.187+20680A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77799848 | ||||||
| chr11:77800106
|
G | A | 1 | a0001c0001t0009g0242 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.187+20422C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800106 | ||||||
| chr11:77800198
|
A | G | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.187+20330T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800198 | ||||||
| chr11:77800250
|
G | A | 1 | a0001c0001t0004g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.187+20278C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800250 | ||||||
| chr11:77800337
|
C | G | 1 | a0002c0003t0050g0213 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.187+20191G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800337 | ||||||
| chr11:77800356
|
T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+20172A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800356 | ||||||
| chr11:77800366
|
C | T | 1 | a0009c0008t0003g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.187+20162G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800366 | ||||||
| chr11:77800431
|
G | A | 1 | a0004c0005t0049g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187+20097C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800431 | ||||||
| chr11:77800434
|
G | T | 2 | a0001c0001t0002g0109a0001c0001t0002g0111 | 2 | NA18973.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.187+20094C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800434 | ||||||
| chr11:77800436
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+20092C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800436 | ||||||
| chr11:77800742
|
C | A | 1 | a0001c0001t0009g0244 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187+19786G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800742 | ||||||
| chr11:77800927
|
C | T | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.187+19601G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77800927 | ||||||
| chr11:77801012
|
CA | C | 79 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.187+19515delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801012 | ||||||
| chr11:77801139
|
T | C | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+19389A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801139 | ||||||
| chr11:77801321
|
G | A | 1 | a0001c0002t0016g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.187+19207C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801321 | ||||||
| chr11:77801360
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+19168C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801360 | ||||||
| chr11:77801377
|
G | A | 3 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0016t0045g0201 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.187+19151C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801377 | ||||||
| chr11:77801381
|
G | A | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+19147C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801381 | ||||||
| chr11:77801433
|
A | G | 4 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+19095T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801433 | ||||||
| chr11:77801453
|
G | A | 1 | a0001c0002t0003g0030 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.187+19075C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801453 | ||||||
| chr11:77801573
|
G | C | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.187+18955C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801573 | ||||||
| chr11:77801617
|
G | A | 1 | a0001c0002t0018g0046 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.187+18911C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801617 | ||||||
| chr11:77801805
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.187+18723G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77801805 | ||||||
| chr11:77802052
|
G | A | 1 | a0001c0001t0059g0310 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.187+18476C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802052 | ||||||
| chr11:77802095
|
C | T | 5 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0130others(2): Show | 5 | HG02622.hp2 HG02965.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+18433G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802095 | ||||||
| chr11:77802179
|
G | A | 1 | a0001c0001t0004g0196 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.187+18349C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802179 | ||||||
| chr11:77802342
|
T | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+18186A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802342 | ||||||
| chr11:77802427
|
G | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+18101C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802427 | ||||||
| chr11:77802787
|
G | A | 12 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0300others(9): Show | 12 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+17741C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802787 | ||||||
| chr11:77802793
|
C | T | 1 | a0001c0001t0055g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.187+17735G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802793 | ||||||
| chr11:77802905
|
T | C | 1 | a0001c0002t0003g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.187+17623A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77802905 | ||||||
| chr11:77803170
|
G | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+17358C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803170 | ||||||
| chr11:77803311
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+17217G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803311 | ||||||
| chr11:77803384
|
C | T | 3 | a0001c0002t0010g0013a0001c0002t0033g0012a0007c0018t0032g0014 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.187+17144G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803384 | ||||||
| chr11:77803385
|
G | A | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+17143C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803385 | ||||||
| chr11:77803388
|
T | G | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+17140A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803388 | ||||||
| chr11:77803458
|
C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+17070G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803458 | ||||||
| chr11:77803460
|
A | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+17068T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803460 | ||||||
| chr11:77803606
|
C | T | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+16922G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803606 | ||||||
| chr11:77803713
|
G | C | 1 | a0001c0001t0002g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.187+16815C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77803713 | ||||||
| chr11:77804184
|
T | C | 114 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(111): Show | 114 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.187+16344A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804184 | ||||||
| chr11:77804286
|
G | A | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+16242C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804286 | ||||||
| chr11:77804325
|
G | A | 1 | a0010c0013t0007g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.187+16203C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804325 | ||||||
| chr11:77804590
|
A | T | 3 | a0001c0001t0022g0144a0001c0001t0022g0145a0001c0001t0054g0146 | 3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.187+15938T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804590 | ||||||
| chr11:77804683
|
A | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+15845T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804683 | ||||||
| chr11:77804916
|
A | C | 2 | a0001c0002t0016g0005a0001c0002t0016g0008 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.187+15612T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77804916 | ||||||
| chr11:77805190
|
G | C | 72 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(69): Show | 72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.187+15338C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805190 | ||||||
| chr11:77805217
|
C | T | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.187+15311G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805217 | ||||||
| chr11:77805442
|
A | G | 17 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0110others(14): Show | 17 | HG02055.hp1 HG02602.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+15086T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805442 | ||||||
| chr11:77805625
|
A | G | 1 | a0001c0001t0004g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.187+14903T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805625 | ||||||
| chr11:77805726
|
G | A | 2 | a0001c0001t0008g0269a0001c0001t0008g0270 | 2 | HG01433.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.187+14802C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805726 | ||||||
| chr11:77805727
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+14801A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77805727 | ||||||
| chr11:77806341
|
G | A | 1 | a0012c0011t0007g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.187+14187C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806341 | ||||||
| chr11:77806345
|
T | G | 1 | a0001c0001t0001g0308 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.187+14183A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806345 | ||||||
| chr11:77806372
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+14156C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806372 | ||||||
| chr11:77806467
|
T | C | 1 | a0001c0001t0004g0186 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.187+14061A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806467 | ||||||
| chr11:77806474
|
A | T | 22 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(19): Show | 22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+14054T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806474 | ||||||
| chr11:77806493
|
T | C | 1 | a0001c0001t0004g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.187+14035A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806493 | ||||||
| chr11:77806699
|
G | C | 114 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(111): Show | 114 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.187+13829C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806699 | ||||||
| chr11:77806766
|
C | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+13762G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806766 | ||||||
| chr11:77806798
|
A | G | 1 | a0001c0001t0004g0147 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.187+13730T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806798 | ||||||
| chr11:77806927
|
T | G | 43 | a0001c0002t0003g0018a0001c0002t0003g0022a0001c0002t0003g0023others(40): Show | 43 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.187+13601A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806927 | ||||||
| chr11:77806952
|
T | C | 3 | a0002c0003t0002g0204a0002c0003t0002g0205a0002c0003t0002g0206 | 3 | HG00099.hp2 HG00639.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.187+13576A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77806952 | ||||||
| chr11:77807039
|
A | G | 351 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.187+13489T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807039 | ||||||
| chr11:77807209
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+13319A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807209 | ||||||
| chr11:77807572
|
G | A | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.187+12956C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807572 | ||||||
| chr11:77807582
|
T | C | 1 | a0001c0001t0001g0330 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.187+12946A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807582 | ||||||
| chr11:77807616
|
CATAAAT | C | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.187+12906_187+1291 others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807616 | ||||||
| chr11:77807634
|
A | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+12894T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807634 | ||||||
| chr11:77807663
|
G | T | 3 | a0001c0001t0022g0144a0001c0001t0022g0145a0001c0001t0054g0146 | 3 | HG02615.hp1 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.187+12865C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807663 | ||||||
| chr11:77807764
|
G | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+12764C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807764 | ||||||
| chr11:77807787
|
G | C | 90 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(87): Show | 90 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.187+12741C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807787 | ||||||
| chr11:77807823
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+12705C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807823 | ||||||
| chr11:77807963
|
G | C | 1 | a0001c0001t0004g0136 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.187+12565C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77807963 | ||||||
| chr11:77808031
|
A | T | 22 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(19): Show | 22 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+12497T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808031 | ||||||
| chr11:77808353
|
A | C | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+12175T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808353 | ||||||
| chr11:77808355
|
A | C | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+12173T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808355 | ||||||
| chr11:77808356
|
C | A | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+12172G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808356 | ||||||
| chr11:77808356
|
C | CACA | 350 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.187+12169_187+1217 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808356 | ||||||
| chr11:77808413
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0319a0001c0001t0001g0320others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+12115G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808413 | ||||||
| chr11:77808463
|
C | T | 2 | a0002c0003t0021g0209a0002c0003t0021g0212 | 2 | HG00140.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.187+12065G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808463 | ||||||
| chr11:77808469
|
G | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+12059C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808469 | ||||||
| chr11:77808513
|
TTCAAATA others(312): Show |
T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+11696_187+1201 others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808513 | ||||||
| chr11:77808527
|
C | CT | 41 | a0001c0001t0004g0136a0001c0001t0004g0197a0001c0001t0004g0198others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.187+12000dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808527 | ||||||
| chr11:77808527
|
C | CTT | 127 | a0001c0001t0001g0264a0001c0001t0001g0307a0001c0001t0001g0308others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.187+11999_187+1200 others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808527 | ||||||
| chr11:77808527
|
C | CTTT | 77 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0090others(74): Show | 77 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.187+11998_187+1200 others(7): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808527 | ||||||
| chr11:77808527
|
C | CTTTT | 18 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(15): Show | 18 | HG00408.hp1 HG00609.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.187+11997_187+1200 others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808527 | ||||||
| chr11:77808565
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.187+11963C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808565 | ||||||
| chr11:77808626
|
C | T | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+11902G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808626 | ||||||
| chr11:77808908
|
G | A | 1 | a0001c0002t0003g0059 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.187+11620C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77808908 | ||||||
| chr11:77809020
|
C | T | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | NA18969.hp2 NA19074.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.187+11508G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809020 | ||||||
| chr11:77809086
|
A | G | 1 | a0001c0002t0033g0012 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.187+11442T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809086 | ||||||
| chr11:77809165
|
T | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+11363A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809165 | ||||||
| chr11:77809327
|
T | C | 1 | a0001c0001t0004g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.187+11201A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809327 | ||||||
| chr11:77809410
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+11118C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809410 | ||||||
| chr11:77809827
|
T | A | 1 | a0007c0018t0032g0014 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.187+10701A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77809827 | ||||||
| chr11:77810344
|
A | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+10184T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810344 | ||||||
| chr11:77810358
|
A | G | 4 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+10170T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810358 | ||||||
| chr11:77810400
|
C | T | 1 | a0002c0003t0002g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.187+10128G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810400 | ||||||
| chr11:77810494
|
C | A | 1 | a0001c0002t0003g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.187+10034G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810494 | ||||||
| chr11:77810495
|
C | G | 1 | a0001c0002t0003g0033 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.187+10033G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810495 | ||||||
| chr11:77810570
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.187+9958C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810570 | ||||||
| chr11:77810682
|
T | C | 1 | a0001c0002t0010g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.187+9846A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77810682 | ||||||
| chr11:77811079
|
T | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+9449A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811079 | ||||||
| chr11:77811142
|
A | T | 237 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0108others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.187+9386T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811142 | ||||||
| chr11:77811144
|
T | C | 1 | a0001c0001t0007g0181 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.187+9384A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811144 | ||||||
| chr11:77811173
|
G | A | 1 | a0002c0003t0002g0348 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.187+9355C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811173 | ||||||
| chr11:77811188
|
C | T | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+9340G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811188 | ||||||
| chr11:77811338
|
A | G | 3 | a0001c0001t0004g0182a0001c0001t0004g0184a0001c0001t0051g0183 | 3 | NA18954.hp2 NA18988.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.187+9190T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811338 | ||||||
| chr11:77811587
|
G | A | 114 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(111): Show | 114 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.187+8941C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811587 | ||||||
| chr11:77811631
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8897G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811631 | ||||||
| chr11:77811750
|
A | G | 4 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0312others(1): Show | 4 | HG00558.hp1 NA18982.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+8778T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811750 | ||||||
| chr11:77811790
|
G | T | 1 | a0001c0001t0004g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.187+8738C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811790 | ||||||
| chr11:77811931
|
G | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8597C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77811931 | ||||||
| chr11:77812038
|
T | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8490A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812038 | ||||||
| chr11:77812039
|
G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+8489C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812039 | ||||||
| chr11:77812149
|
A | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+8379T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812149 | ||||||
| chr11:77812187
|
A | G | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+8341T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812187 | ||||||
| chr11:77812270
|
T | C | 1 | a0001c0002t0037g0060 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.187+8258A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812270 | ||||||
| chr11:77812381
|
A | G | 6 | a0001c0002t0003g0019a0001c0002t0003g0020a0001c0002t0003g0021others(3): Show | 6 | HG02523.hp1 NA18747.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+8147T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812381 | ||||||
| chr11:77812419
|
T | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8109A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812419 | ||||||
| chr11:77812438
|
C | T | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+8090G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812438 | ||||||
| chr11:77812690
|
C | A | 2 | a0002c0003t0002g0208a0002c0003t0002g0227 | 2 | HG02486.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.187+7838G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812690 | ||||||
| chr11:77812751
|
G | A | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+7777C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812751 | ||||||
| chr11:77812884
|
C | CA | 23 | a0001c0002t0003g0018a0001c0002t0003g0061a0001c0002t0003g0062others(20): Show | 23 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.187+7643dupT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812884 | ||||||
| chr11:77812884
|
CA | C | 88 | a0001c0001t0001g0276a0001c0001t0001g0342a0001c0001t0002g0004others(85): Show | 88 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.187+7643delT | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812884 | ||||||
| chr11:77812884
|
CAA | C | 108 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(105): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.187+7642_187+7643d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812884 | ||||||
| chr11:77812988
|
A | G | 1 | a0001c0002t0003g0032 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.187+7540T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812988 | ||||||
| chr11:77812997
|
A | G | 1 | a0001c0001t0004g0137 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.187+7531T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77812997 | ||||||
| chr11:77813305
|
T | C | 6 | a0001c0002t0010g0013a0001c0002t0014g0009a0001c0002t0014g0011others(3): Show | 6 | HG01074.hp1 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+7223A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813305 | ||||||
| chr11:77813469
|
C | T | 1 | a0001c0001t0005g0253 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.187+7059G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813469 | ||||||
| chr11:77813622
|
G | A | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.187+6906C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813622 | ||||||
| chr11:77813676
|
T | G | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+6852A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813676 | ||||||
| chr11:77813714
|
C | T | 6 | a0001c0002t0010g0013a0001c0002t0014g0009a0001c0002t0014g0011others(3): Show | 6 | HG01074.hp1 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+6814G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813714 | ||||||
| chr11:77813752
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.187+6776C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813752 | ||||||
| chr11:77813808
|
A | T | 10 | a0001c0002t0003g0022a0001c0002t0003g0023a0001c0002t0003g0024others(7): Show | 10 | NA18939.hp1 NA18941.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.187+6720T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813808 | ||||||
| chr11:77813820
|
G | GAC | 78 | a0001c0001t0001g0087a0001c0001t0001g0279a0001c0001t0001g0334others(75): Show | 78 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.187+6706_187+6707d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | ||||||
| chr11:77813820
|
G | GACAC | 61 | a0001c0001t0001g0274a0001c0001t0001g0280a0001c0001t0001g0282others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.187+6704_187+6707d others(6): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | ||||||
| chr11:77813820
|
G | GACACAC | 57 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0088others(54): Show | 57 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.187+6702_187+6707d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | ||||||
| chr11:77813820
|
G | GACACACA others(1): Show |
8 | a0001c0001t0001g0096a0001c0001t0001g0264a0001c0001t0001g0276others(5): Show | 8 | HG01109.hp2 HG02572.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+6700_187+6707d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | ||||||
| chr11:77813820
|
G | GACACACA others(3): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG01261.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.187+6698_187+6707d others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | ||||||
| chr11:77813820
|
GAC | G | 6 | a0001c0001t0002g0108a0001c0001t0004g0135a0001c0001t0009g0242others(3): Show | 6 | HG01928.hp2 HG02602.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+6706_187+6707d others(4): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | ||||||
| chr11:77813820
|
GACACAC | G | 9 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0002t0003g0019others(6): Show | 9 | HG02523.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.187+6702_187+6707d others(8): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | ||||||
| chr11:77813820
|
GACACACA others(1): Show |
G | 72 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0022others(69): Show | 72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.187+6700_187+6707d others(10): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | ||||||
| chr11:77813820
|
GACACACA others(9): Show |
G | 1 | a0001c0001t0004g0134 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.187+6692_187+6707d others(18): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77813820 | ||||||
| chr11:77814157
|
G | A | 115 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(112): Show | 115 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.187+6371C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814157 | ||||||
| chr11:77814208
|
A | AAAG | 305 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.187+6317_187+6319d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814208 | ||||||
| chr11:77814263
|
C | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+6265G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814263 | ||||||
| chr11:77814264
|
G | A | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+6264C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814264 | ||||||
| chr11:77814280
|
C | T | 1 | a0001c0001t0004g0100 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.187+6248G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814280 | ||||||
| chr11:77814356
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6172T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814356 | ||||||
| chr11:77814358
|
C | G | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+6170G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814358 | ||||||
| chr11:77814364
|
A | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6164T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814364 | ||||||
| chr11:77814373
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6155A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814373 | ||||||
| chr11:77814375
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6153A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814375 | ||||||
| chr11:77814379
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6149A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814379 | ||||||
| chr11:77814381
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6147A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814381 | ||||||
| chr11:77814382
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6146T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814382 | ||||||
| chr11:77814384
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6144A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814384 | ||||||
| chr11:77814385
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6143A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814385 | ||||||
| chr11:77814386
|
C | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6142G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814386 | ||||||
| chr11:77814389
|
A | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6139T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814389 | ||||||
| chr11:77814390
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6138G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814390 | ||||||
| chr11:77814391
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6137A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814391 | ||||||
| chr11:77814395
|
C | CGGGGGGG others(3): Show |
1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6132_187+6133i others(12): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814395 | ||||||
| chr11:77814399
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6129T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814399 | ||||||
| chr11:77814402
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6126A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814402 | ||||||
| chr11:77814403
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6125A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814403 | ||||||
| chr11:77814412
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6116T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814412 | ||||||
| chr11:77814419
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6109G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814419 | ||||||
| chr11:77814420
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6108A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814420 | ||||||
| chr11:77814421
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6107A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814421 | ||||||
| chr11:77814423
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6105T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814423 | ||||||
| chr11:77814425
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6103G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814425 | ||||||
| chr11:77814426
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6102G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814426 | ||||||
| chr11:77814427
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6101G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814427 | ||||||
| chr11:77814428
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6100T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814428 | ||||||
| chr11:77814431
|
A | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6097T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814431 | ||||||
| chr11:77814432
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6096T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814432 | ||||||
| chr11:77814433
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6095A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814433 | ||||||
| chr11:77814434
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6094A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814434 | ||||||
| chr11:77814435
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6093G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814435 | ||||||
| chr11:77814436
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6092T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814436 | ||||||
| chr11:77814437
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6091T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814437 | ||||||
| chr11:77814440
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6088G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814440 | ||||||
| chr11:77814441
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6087G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814441 | ||||||
| chr11:77814442
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6086G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814442 | ||||||
| chr11:77814443
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6085A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814443 | ||||||
| chr11:77814444
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6084T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814444 | ||||||
| chr11:77814445
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6083T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814445 | ||||||
| chr11:77814446
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6082G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814446 | ||||||
| chr11:77814447
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6081A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814447 | ||||||
| chr11:77814448
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6080G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814448 | ||||||
| chr11:77814449
|
T | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6079A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814449 | ||||||
| chr11:77814457
|
A | G | 3 | a0004c0005t0020g0199a0004c0005t0020g0200a0004c0016t0045g0201 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.187+6071T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814457 | ||||||
| chr11:77814471
|
AGTCTCGC others(4): Show |
A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6046_187+6056d others(13): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814471 | ||||||
| chr11:77814476
|
C | A | 1 | a0001c0001t0004g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.187+6052G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814476 | ||||||
| chr11:77814510
|
A | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6018T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814510 | ||||||
| chr11:77814515
|
G | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6013C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814515 | ||||||
| chr11:77814516
|
G | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6012C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814516 | ||||||
| chr11:77814525
|
A | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+6003T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814525 | ||||||
| chr11:77814538
|
C | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5990G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814538 | ||||||
| chr11:77814539
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5989T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814539 | ||||||
| chr11:77814542
|
T | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5986A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814542 | ||||||
| chr11:77814549
|
G | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5979C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814549 | ||||||
| chr11:77814563
|
G | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5965C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814563 | ||||||
| chr11:77814579
|
G | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5949C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814579 | ||||||
| chr11:77814583
|
T | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5945A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814583 | ||||||
| chr11:77814595
|
G | A | 9 | a0001c0001t0001g0274a0001c0001t0001g0334a0001c0001t0001g0335others(6): Show | 9 | HG00408.hp1 HG00609.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+5933C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814595 | ||||||
| chr11:77814602
|
G | T | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5926C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814602 | ||||||
| chr11:77814604
|
T | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5924A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814604 | ||||||
| chr11:77814606
|
T | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5922A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814606 | ||||||
| chr11:77814608
|
A | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0005g0038others(79): Show | 82 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+5920T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814608 | ||||||
| chr11:77814609
|
C | A | 1 | a0001c0002t0003g0080 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.187+5919G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814609 | ||||||
| chr11:77814618
|
G | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5910C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814618 | ||||||
| chr11:77814619
|
T | A | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5909A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814619 | ||||||
| chr11:77814626
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5902T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814626 | ||||||
| chr11:77814644
|
C | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5884G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814644 | ||||||
| chr11:77814646
|
A | C | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5882T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814646 | ||||||
| chr11:77814661
|
G | C | 2 | a0001c0002t0017g0006a0001c0002t0017g0007 | 2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.187+5867C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814661 | ||||||
| chr11:77814666
|
A | G | 1 | a0002c0003t0002g0203 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.187+5862T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814666 | ||||||
| chr11:77814689
|
G | A | 1 | a0001c0002t0003g0081 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.187+5839C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814689 | ||||||
| chr11:77814692
|
G | A | 72 | a0001c0001t0002g0128a0001c0001t0002g0129a0001c0001t0002g0130others(69): Show | 72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.187+5836C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814692 | ||||||
| chr11:77814699
|
C | A | 1 | a0004c0016t0045g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.187+5829G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814699 | ||||||
| chr11:77814881
|
C | A | 1 | a0001c0001t0001g0342 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.187+5647G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814881 | ||||||
| chr11:77814890
|
G | GT | 70 | a0001c0001t0001g0276a0001c0001t0005g0038a0001c0001t0023g0275others(67): Show | 70 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.187+5637dupA | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814890 | ||||||
| chr11:77814890
|
G | T | 17 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(14): Show | 17 | HG01074.hp2 HG01433.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+5638C>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77814890 | ||||||
| chr11:77815016
|
A | C | 1 | a0001c0001t0001g0274 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.187+5512T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815016 | ||||||
| chr11:77815121
|
T | G | 1 | a0001c0001t0002g0132 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187+5407A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815121 | ||||||
| chr11:77815158
|
T | A | 6 | a0001c0002t0003g0019a0001c0002t0003g0020a0001c0002t0003g0021others(3): Show | 6 | HG02523.hp1 NA18747.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+5370A>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815158 | ||||||
| chr11:77815179
|
C | T | 1 | a0001c0001t0052g0265 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.187+5349G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815179 | ||||||
| chr11:77815389
|
C | A | 1 | a0001c0002t0030g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.187+5139G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815389 | ||||||
| chr11:77815428
|
C | A | 90 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(87): Show | 90 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.187+5100G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815428 | ||||||
| chr11:77815490
|
A | C | 1 | a0001c0001t0004g0133 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.187+5038T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815490 | ||||||
| chr11:77815538
|
T | C | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+4990A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815538 | ||||||
| chr11:77815616
|
T | C | 1 | a0002c0003t0002g0239 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.187+4912A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815616 | ||||||
| chr11:77815748
|
A | T | 78 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.187+4780T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815748 | ||||||
| chr11:77815760
|
CCCA | C | 81 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+4765_187+4767d others(5): Show |
RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815760 | ||||||
| chr11:77815769
|
T | G | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+4759A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815769 | ||||||
| chr11:77815857
|
C | T | 1 | a0001c0001t0005g0252 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.187+4671G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815857 | ||||||
| chr11:77815993
|
C | T | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+4535G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77815993 | ||||||
| chr11:77816687
|
C | T | 13 | a0001c0001t0001g0264a0001c0001t0005g0252a0001c0001t0005g0253others(10): Show | 13 | HG01975.hp2 HG02056.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.187+3841G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77816687 | ||||||
| chr11:77816909
|
A | C | 6 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(3): Show | 6 | HG01243.hp2 HG02559.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+3619T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77816909 | ||||||
| chr11:77816986
|
T | C | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG00544.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.187+3542A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77816986 | ||||||
| chr11:77817077
|
A | G | 3 | a0001c0002t0014g0009a0001c0002t0014g0011a0001c0002t0034g0010 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.187+3451T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817077 | ||||||
| chr11:77817115
|
C | G | 281 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(278): Show | 281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.187+3413G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817115 | ||||||
| chr11:77817293
|
T | C | 82 | a0001c0001t0004g0100a0001c0001t0004g0101a0001c0001t0004g0103others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.187+3235A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817293 | ||||||
| chr11:77817741
|
A | G | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+2787T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817741 | ||||||
| chr11:77817804
|
A | T | 1 | a0001c0001t0004g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.187+2724T>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817804 | ||||||
| chr11:77817882
|
T | C | 1 | a0001c0002t0016g0008 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.187+2646A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77817882 | ||||||
| chr11:77818062
|
C | T | 2 | a0001c0001t0004g0105a0001c0001t0004g0106 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.187+2466G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818062 | ||||||
| chr11:77818071
|
G | A | 1 | a0001c0002t0029g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.187+2457C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818071 | ||||||
| chr11:77818180
|
G | C | 2 | a0002c0003t0002g0240a0002c0003t0002g0241 | 2 | HG02027.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.187+2348C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818180 | ||||||
| chr11:77818393
|
A | G | 4 | a0001c0001t0004g0101a0001c0001t0004g0103a0001c0001t0004g0104others(1): Show | 4 | HG02083.hp2 NA18612.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+2135T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818393 | ||||||
| chr11:77818482
|
C | T | 308 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(305): Show | 308 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.187+2046G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818482 | ||||||
| chr11:77818631
|
T | C | 1 | a0001c0001t0009g0245 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.187+1897A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818631 | ||||||
| chr11:77818650
|
A | G | 1 | a0001c0001t0023g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.187+1878T>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818650 | ||||||
| chr11:77818919
|
A | C | 4 | a0001c0002t0016g0005a0001c0002t0016g0008a0001c0002t0017g0006others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1609T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77818919 | ||||||
| chr11:77819001
|
T | G | 4 | a0001c0001t0009g0242a0001c0001t0009g0243a0001c0001t0009g0244others(1): Show | 4 | HG02647.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1527A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819001 | ||||||
| chr11:77819092
|
G | A | 1 | a0001c0001t0004g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.187+1436C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819092 | ||||||
| chr11:77819249
|
C | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0004 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+1279G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819249 | ||||||
| chr11:77819256
|
G | C | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.187+1272C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819256 | ||||||
| chr11:77819409
|
G | C | 1 | a0006c0007t0001g0349 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.187+1119C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819409 | ||||||
| chr11:77819524
|
A | C | 4 | a0001c0002t0003g0018a0001c0002t0003g0019a0001c0002t0003g0020others(1): Show | 4 | HG02132.hp1 NA18747.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1004T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819524 | ||||||
| chr11:77819814
|
T | C | 1 | a0001c0001t0041g0249 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.187+714A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819814 | ||||||
| chr11:77819820
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.187+708G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819820 | ||||||
| chr11:77819825
|
C | A | 83 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0004others(80): Show | 83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.187+703G>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819825 | ||||||
| chr11:77819907
|
T | C | 83 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0004others(80): Show | 83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.187+621A>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819907 | ||||||
| chr11:77819953
|
A | C | 1 | a0001c0001t0004g0100 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.187+575T>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819953 | ||||||
| chr11:77819997
|
G | C | 68 | a0001c0001t0005g0038a0001c0002t0003g0018a0001c0002t0003g0019others(65): Show | 68 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.187+531C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77819997 | ||||||
| chr11:77820008
|
C | G | 1 | a0002c0003t0002g0099 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.187+520G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820008 | ||||||
| chr11:77820010
|
G | A | 1 | a0001c0001t0004g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.187+518C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820010 | ||||||
| chr11:77820112
|
G | A | 2 | a0001c0002t0010g0350a0001c0002t0010g0351 | 2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.187+416C>T | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820112 | ||||||
| chr11:77820235
|
G | C | 117 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(114): Show | 117 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.187+293C>G | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820235 | ||||||
| chr11:77820269
|
T | G | 1 | a0001c0001t0068g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.187+259A>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820269 | ||||||
| chr11:77820297
|
C | T | 13 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(10): Show | 13 | HG00323.hp1 HG00741.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.187+231G>A | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820297 | ||||||
| chr11:77820480
|
C | G | 83 | a0001c0001t0001g0016a0001c0001t0002g0003a0001c0001t0002g0004others(80): Show | 83 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.187+48G>C | RSF1 | ENSG00000048649.14 | transcript | ENST00000308488.11 | protein_coding | 1/15 | chr11 | 77820480 |