Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6905 |
|---|---|
| ensemblid | ENSG00000284770.2 |
| hgncid | 11582 |
| symbol | TBCE |
| name | tubulin folding cofactor E |
| refseq_nuc | NM_003193.5 |
| refseq_prot | NP_003184.1 |
| ensembl_nuc | ENST00000642610.2 |
| ensembl_prot | ENSP00000494796.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 235367427 |
| end | 235452443 |
| strand | + |
| ver | v1.2 |
| region | chr1:235367427-235452443 |
| region5000 | chr1:235362427-235457443 |
| regionname0 | TBCE_chr1_235367427_235452443 |
| regionname5000 | TBCE_chr1_235362427_235457443 |
| 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 | 527 | 261 | 70 | 60 | 85 | 8 | 36 | 67 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0002 | 0/0 | 527 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0003 | 0/0 | 527 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0004 | 0/0 | 527 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0005 | 0/0 | 527 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| 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 | 1584 | 254 | 66 | 57 | 85 | 8 | 36 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| c0002 | 0/0 | 1584 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| c0003 | 0/0 | 1584 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| c0004 | 0/0 | 1584 | 2 | 2 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| c0005 | 0/0 | 1584 | 2 | 1 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| c0006 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| c0007 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| c0008 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| c0009 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| 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 | 3790 | 70 | 10 | 22 | 25 | 1 | 11 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0002 | 1/0 | 3791 | 61 | 3 | 14 | 32 | 1 | 10 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0003 | 0/0 | 3789 | 32 | 5 | 9 | 11 | 5 | 2 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0004 | 0/0 | 3795 | 27 | 14 | 4 | 3 | 0 | 6 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0005 | 0/0 | 3788 | 14 | 10 | 3 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0006 | 0/0 | 3791 | 9 | 2 | 0 | 7 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0007 | 0/0 | 3791 | 7 | 4 | 1 | 2 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0008 | 0/0 | 3788 | 5 | 5 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0009 | 0/0 | 3795 | 3 | 2 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0010 | 0/0 | 3795 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0011 | 0/0 | 3792 | 3 | 0 | 0 | 1 | 0 | 2 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0012 | 0/0 | 3789 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0013 | 0/0 | 3790 | 3 | 1 | 2 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0014 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0015 | 0/0 | 3790 | 2 | 0 | 0 | 1 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0016 | 0/0 | 3787 | 2 | 1 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0017 | 0/0 | 3795 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0018 | 0/0 | 3788 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0019 | 0/0 | 3795 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0020 | 0/0 | 3790 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0021 | 0/0 | 3790 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0022 | 0/0 | 3791 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0023 | 0/0 | 3791 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0024 | 0/0 | 3791 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0025 | 0/0 | 3791 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0026 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0027 | 0/0 | 3778 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0028 | 0/0 | 3790 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0029 | 0/0 | 3790 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0030 | 0/0 | 3791 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0031 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0032 | 0/0 | 3789 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0033 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0034 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0035 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0036 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0037 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| t0038 | 0/0 | 3790 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| 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 | 2 | 0 | 2 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| 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 | 1584 | 254 | 66 | 57 | 85 | 8 | 36 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0003 | 0/0 | 1584 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0005 | 0/0 | 1584 | 2 | 1 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0007 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0009 | 0/0 | 1584 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0002c0002 | 0/0 | 1584 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0003c0004 | 0/0 | 1584 | 2 | 2 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0004c0006 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0005c0008 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5373 | 65 | 7 | 21 | 24 | 1 | 11 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0002 | 1/0 | 5374 | 60 | 2 | 14 | 32 | 1 | 10 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0003 | 0/0 | 5372 | 32 | 5 | 9 | 11 | 5 | 2 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0004 | 0/0 | 5378 | 27 | 14 | 4 | 3 | 0 | 6 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0005 | 0/0 | 5371 | 14 | 10 | 3 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0006 | 0/0 | 5374 | 9 | 2 | 0 | 7 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0007 | 0/0 | 5374 | 6 | 4 | 0 | 2 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0008 | 0/0 | 5371 | 5 | 5 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0009 | 0/0 | 5378 | 3 | 2 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0011 | 0/0 | 5375 | 3 | 0 | 0 | 1 | 0 | 2 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0012 | 0/0 | 5372 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0013 | 0/0 | 5373 | 3 | 1 | 2 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0014 | 0/0 | 5372 | 2 | 2 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0015 | 0/0 | 5373 | 2 | 0 | 0 | 1 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0016 | 0/0 | 5370 | 2 | 1 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0017 | 0/0 | 5378 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0018 | 0/0 | 5371 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0019 | 0/0 | 5378 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0020 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0021 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0022 | 0/0 | 5374 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0023 | 0/0 | 5374 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0024 | 0/0 | 5374 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0025 | 0/0 | 5374 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0026 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0027 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0028 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0029 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0030 | 0/0 | 5374 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0032 | 0/0 | 5372 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0033 | 0/0 | 5372 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0034 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0001t0036 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0003t0001 | 0/0 | 5373 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0005t0035 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0005t0038 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0007t0001 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0001c0009t0007 | 0/0 | 5374 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0002c0002t0010 | 0/0 | 5378 | 3 | 3 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0003c0004t0031 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0003c0004t0037 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0004c0006t0002 | 0/0 | 5374 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| a0005c0008t0001 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | copy fasta | chr1 | 235362427 | 235457443 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0009g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0011g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0011g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0013g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0014g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0014g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0015g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0015g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0016g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0017g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0018g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0019g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0020g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0021g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0022g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0023g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0024g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0025g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0026g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0027g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0028g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0029g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0030g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0032g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0033g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0034g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0001t0036g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0005t0035g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0005t0038g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0007t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0001c0009t0007g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0002c0002t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0002c0002t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0002c0002t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0003c0004t0031g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0003c0004t0037g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0004c0006t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| a0005c0008t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0069 | EUR | GBR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0015 | EUR | GBR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | GBR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0066 | EUR | FIN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0212 | EUR | FIN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00642 | hp2 | a0001 | c0001 | t0032 | g0065 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00733 | hp1 | a0001 | c0001 | t0020 | g0001 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0163 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01070 | hp2 | a0001 | c0005 | t0038 | g0155 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01099 | hp2 | a0001 | c0007 | t0001 | g0061 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0020 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01109 | hp2 | a0001 | c0001 | t0016 | g0183 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01168 | hp1 | a0001 | c0001 | t0013 | g0130 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0131 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01243 | hp1 | a0001 | c0009 | t0007 | g0264 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0162 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0111 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0169 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01891 | hp1 | a0002 | c0002 | t0010 | g0023 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02027 | hp1 | a0001 | c0001 | t0019 | g0157 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0072 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02071 | hp1 | a0001 | c0001 | t0025 | g0091 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0265 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | CDX | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0186 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0185 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0266 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02280 | hp2 | a0001 | c0001 | t0018 | g0009 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02622 | hp1 | a0001 | c0001 | t0014 | g0189 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0177 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0176 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0204 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02738 | hp1 | a0001 | c0001 | t0021 | g0199 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0170 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0173 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0013 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02922 | hp1 | a0002 | c0002 | t0010 | g0017 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02976 | hp2 | a0004 | c0006 | t0002 | g0123 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03017 | hp2 | a0001 | c0001 | t0022 | g0206 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0174 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0167 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03098 | hp1 | a0001 | c0001 | t0034 | g0031 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03130 | hp1 | a0001 | c0001 | t0033 | g0261 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03130 | hp2 | a0001 | c0001 | t0036 | g0175 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0168 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0203 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03491 | hp1 | a0001 | c0001 | t0011 | g0232 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03516 | hp2 | a0001 | c0001 | t0030 | g0154 | AFR | ESN | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03540 | hp2 | a0001 | c0001 | t0027 | g0128 | AFR | GWD | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0141 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03654 | hp2 | a0001 | c0001 | t0015 | g0254 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03669 | hp2 | a0001 | c0001 | t0023 | g0230 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03704 | hp2 | a0001 | c0001 | t0011 | g0247 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0197 | SAS | BEB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0184 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0159 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | STU | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18522 | hp2 | a0003 | c0004 | t0031 | g0016 | AFR | YRI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | YRI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18906 | hp2 | a0001 | c0001 | t0026 | g0129 | AFR | YRI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18951 | hp2 | a0001 | c0001 | t0007 | g0060 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19011 | hp1 | a0001 | c0001 | t0028 | g0070 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0084 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19012 | hp1 | a0005 | c0008 | t0001 | g0242 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19012 | hp2 | a0001 | c0001 | t0011 | g0223 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19057 | hp1 | a0001 | c0001 | t0015 | g0241 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19085 | hp2 | a0001 | c0001 | t0029 | g0081 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA20129 | hp1 | a0001 | c0001 | t0017 | g0021 | AFR | ASW | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | ASW | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA20805 | hp1 | a0001 | c0001 | t0024 | g0211 | EUR | TSI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0067 | EUR | TSI | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | GIH | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | GIH | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02559 | hp1 | a0001 | c0001 | t0013 | g0152 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03471 | hp1 | a0001 | c0005 | t0035 | g0260 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG06807 | hp1 | a0002 | c0002 | t0010 | g0019 | AFR | USA | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | USA | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA20300 | hp1 | a0003 | c0004 | t0037 | g0172 | AFR | USA | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | USA | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0087 | REF | REF | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0213 | REF | REF | TBCE_chr1_235362427_235457443 | TBCE | chr1 | 235362427 | 235457443 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:235430758
|
T | C | 1 | a0003 | 2 | NA18522.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.614T>C | p.Val205Ala | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/17 | 723/5374 | 614/1584 | 205/527 | chr1 | 235430758 | ||
| chr1:235434210
|
C | T | 1 | a0005 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.667C>T | p.Arg223Trp | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/17 | 776/5374 | 667/1584 | 223/527 | chr1 | 235434210 | ||
| chr1:235436560
|
G | C | 1 | a0004 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.915G>C | p.Met305Ile | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/17 | 1024/5374 | 915/1584 | 305/527 | chr1 | 235436560 | ||
| chr1:235437356
|
G | C | 1 | a0002 | 3 | HG01891.hp1 HG02922.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.998G>C | p.Ser333Thr | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/17 | 1107/5374 | 998/1584 | 333/527 | chr1 | 235437356 | ||
| chr1:235438878
|
A | G | 1 | a0003 | 2 | NA18522.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.1226A>G | p.Glu409Gly | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/17 | 1335/5374 | 1226/1584 | 409/527 | chr1 | 235438878 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:235430729
|
C | T | 1 | a0001c0009 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.585C>T | p.Ser195Ser | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/17 | 694/5374 | 585/1584 | 195/527 | chr1 | 235430729 | ||
| chr1:235436395
|
A | G | 1 | a0001c0007 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.843A>G | p.Gln281Gln | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 10/17 | 952/5374 | 843/1584 | 281/527 | chr1 | 235436395 | ||
| chr1:235437408
|
A | G | 1 | a0001c0003 | 3 | HG02809.hp2 HG03195.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.1050A>G | p.Glu350Glu | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/17 | 1159/5374 | 1050/1584 | 350/527 | chr1 | 235437408 | ||
| chr1:235437426
|
A | G | 2 | a0001c0005a0003c0004 | 4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.1068A>G | p.Leu356Leu | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/17 | 1177/5374 | 1068/1584 | 356/527 | chr1 | 235437426 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:235367443
|
T | A | 3 | a0001c0001t0009a0001c0001t0017a0001c0001t0018 | 5 | HG01109.hp1 HG02280.hp2 HG03195.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-93T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/17 | 12607 | chr1 | 235367443 | |||||
| chr1:235367487
|
T | C | 6 | a0001c0001t0008a0001c0001t0009a0001c0001t0014others(3): Show | 15 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-49T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/17 | 12563 | chr1 | 235367487 | |||||
| chr1:235448811
|
T | C | 1 | a0001c0001t0017 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*49T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 49 | chr1 | 235448811 | |||||
| chr1:235448904
|
T | A | 5 | a0001c0001t0004a0001c0001t0009a0001c0001t0017others(2): Show | 35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*142T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 142 | chr1 | 235448904 | |||||
| chr1:235448913
|
G | A | 1 | a0001c0001t0020 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*151G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 151 | chr1 | 235448913 | |||||
| chr1:235448991
|
A | G | 1 | a0001c0005t0038 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*229A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 229 | chr1 | 235448991 | |||||
| chr1:235449005
|
C | T | 34 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(31): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*243C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 243 | chr1 | 235449005 | |||||
| chr1:235449079
|
C | CAGTT | 5 | a0001c0001t0004a0001c0001t0009a0001c0001t0017others(2): Show | 35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*319_*322dupGTTA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 323 | INFO_REALIGN_3_PRIME | chr1 | 235449079 | ||||
| chr1:235449138
|
AAAGGGTT others(5): Show |
A | 2 | a0001c0001t0026a0001c0001t0027 | 2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*379_*390delGGGTTA others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 379 | INFO_REALIGN_3_PRIME | chr1 | 235449138 | ||||
| chr1:235449314
|
ATCT | A | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0016others(1): Show | 22 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*559_*561delTCT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 559 | INFO_REALIGN_3_PRIME | chr1 | 235449314 | ||||
| chr1:235449341
|
T | C | 1 | a0001c0001t0021 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*579T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 579 | chr1 | 235449341 | |||||
| chr1:235449512
|
T | C | 2 | a0001c0001t0026a0001c0001t0027 | 2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*750T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 750 | chr1 | 235449512 | |||||
| chr1:235449704
|
T | C | 1 | a0001c0001t0028 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*942T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 942 | chr1 | 235449704 | |||||
| chr1:235449933
|
G | T | 1 | a0001c0001t0025 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1171G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1171 | chr1 | 235449933 | |||||
| chr1:235449983
|
C | T | 1 | a0003c0004t0037 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1221C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1221 | chr1 | 235449983 | |||||
| chr1:235450009
|
T | G | 2 | a0001c0001t0026a0001c0001t0027 | 2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1247T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1247 | chr1 | 235450009 | |||||
| chr1:235450103
|
G | C | 1 | a0001c0001t0022 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1341G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1341 | chr1 | 235450103 | |||||
| chr1:235450114
|
C | T | 1 | a0001c0001t0036 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1352C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1352 | chr1 | 235450114 | |||||
| chr1:235450264
|
G | A | 1 | a0001c0001t0019 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1502G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1502 | chr1 | 235450264 | |||||
| chr1:235450412
|
A | G | 2 | a0001c0005t0035a0001c0005t0038 | 2 | HG01070.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1650A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1650 | chr1 | 235450412 | |||||
| chr1:235450599
|
C | T | 1 | a0001c0001t0034 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1837C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1837 | chr1 | 235450599 | |||||
| chr1:235450708
|
G | A | 2 | a0001c0001t0026a0001c0001t0027 | 2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 1946 | chr1 | 235450708 | |||||
| chr1:235450794
|
T | C | 2 | a0001c0001t0029a0001c0001t0036 | 2 | HG03130.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2032T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2032 | chr1 | 235450794 | |||||
| chr1:235450814
|
T | TA | 5 | a0001c0001t0004a0001c0001t0009a0001c0001t0017others(2): Show | 35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2058dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2059 | INFO_REALIGN_3_PRIME | chr1 | 235450814 | ||||
| chr1:235450926
|
A | G | 1 | a0001c0001t0027 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2164A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2164 | chr1 | 235450926 | |||||
| chr1:235451063
|
A | G | 32 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(29): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*2301A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2301 | chr1 | 235451063 | |||||
| chr1:235451090
|
G | A | 1 | a0001c0001t0012 | 3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2328G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2328 | chr1 | 235451090 | |||||
| chr1:235451350
|
G | T | 1 | a0001c0005t0035 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2588G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2588 | chr1 | 235451350 | |||||
| chr1:235451472
|
C | CA | 6 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(3): Show | 33 | HG00733.hp2 HG01255.hp1 HG01261.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2730dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2731 | INFO_REALIGN_3_PRIME | chr1 | 235451472 | ||||
| chr1:235451472
|
CA | C | 7 | a0001c0001t0003a0001c0001t0012a0001c0001t0014others(4): Show | 42 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2730delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2730 | INFO_REALIGN_3_PRIME | chr1 | 235451472 | ||||
| chr1:235451630
|
C | T | 1 | a0001c0001t0033 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2868C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2868 | chr1 | 235451630 | |||||
| chr1:235451690
|
T | C | 2 | a0001c0001t0026a0001c0001t0027 | 2 | HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2928T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 2928 | chr1 | 235451690 | |||||
| chr1:235452019
|
GT | G | 32 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(29): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*3268delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3268 | INFO_REALIGN_3_PRIME | chr1 | 235452019 | ||||
| chr1:235452103
|
C | A | 1 | a0001c0001t0013 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3341C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3341 | chr1 | 235452103 | |||||
| chr1:235452158
|
G | A | 1 | a0001c0001t0023 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3396G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3396 | chr1 | 235452158 | |||||
| chr1:235452260
|
C | T | 1 | a0001c0001t0036 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3498C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3498 | chr1 | 235452260 | |||||
| chr1:235452265
|
C | T | 1 | a0001c0001t0024 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3503C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3503 | chr1 | 235452265 | |||||
| chr1:235452345
|
G | C | 1 | a0001c0001t0032 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3583G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 17/17 | 3583 | chr1 | 235452345 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:235367549
|
G | C | 1 | a0001c0001t0006g0002 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-32+45G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235367549 | ||||||
| chr1:235367550
|
C | G | 1 | a0001c0001t0006g0002 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-32+46C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235367550 | ||||||
| chr1:235367740
|
T | A | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-32+236T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235367740 | ||||||
| chr1:235368053
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-32+549G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368053 | ||||||
| chr1:235368071
|
A | G | 8 | a0001c0001t0001g0262a0001c0001t0001g0267a0001c0001t0004g0263others(5): Show | 8 | HG01243.hp1 HG01981.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32+567A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368071 | ||||||
| chr1:235368136
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-32+632T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368136 | ||||||
| chr1:235368142
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-32+638A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368142 | ||||||
| chr1:235368262
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-32+758G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368262 | ||||||
| chr1:235368290
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-32+786C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368290 | ||||||
| chr1:235368414
|
C | T | 5 | a0001c0001t0002g0195a0001c0001t0004g0194a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+910C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368414 | ||||||
| chr1:235368442
|
C | CA | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+941dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368442 | |||||
| chr1:235368552
|
C | CT | 22 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0258others(19): Show | 22 | HG00140.hp1 HG01069.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32+1071dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | |||||
| chr1:235368552
|
C | CTT | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0025others(108): Show | 111 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.-32+1070_-32+1071d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | |||||
| chr1:235368552
|
C | CTTT | 22 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(19): Show | 22 | HG00099.hp2 HG00621.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32+1069_-32+1071d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | |||||
| chr1:235368552
|
C | CTTTT | 6 | a0001c0001t0002g0195a0001c0001t0003g0153a0001c0001t0004g0194others(3): Show | 6 | HG01070.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32+1068_-32+1071d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | |||||
| chr1:235368552
|
C | CTTTTTT | 21 | a0001c0001t0001g0171a0001c0001t0004g0156a0001c0001t0004g0158others(18): Show | 21 | HG00733.hp2 HG01255.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-32+1066_-32+1071d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | |||||
| chr1:235368552
|
C | CTTTTTTT | 15 | a0001c0001t0002g0179a0001c0001t0002g0190a0001c0001t0003g0188others(12): Show | 15 | HG00642.hp1 HG01109.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-32+1065_-32+1071d others(9): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235368552 | |||||
| chr1:235368596
|
C | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32+1092C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368596 | ||||||
| chr1:235368599
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1095C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368599 | ||||||
| chr1:235368643
|
C | T | 10 | a0001c0001t0008g0024a0001c0001t0009g0008a0001c0001t0009g0020others(7): Show | 10 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32+1139C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368643 | ||||||
| chr1:235368663
|
A | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1159A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368663 | ||||||
| chr1:235368791
|
C | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1287C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368791 | ||||||
| chr1:235368815
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1311T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368815 | ||||||
| chr1:235368837
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1333G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368837 | ||||||
| chr1:235368923
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1419T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368923 | ||||||
| chr1:235368924
|
A | T | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1420A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368924 | ||||||
| chr1:235368925
|
T | A | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1421T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368925 | ||||||
| chr1:235368930
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1426C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368930 | ||||||
| chr1:235368936
|
G | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1432G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368936 | ||||||
| chr1:235368948
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1444T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368948 | ||||||
| chr1:235368951
|
C | T | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1447C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368951 | ||||||
| chr1:235368960
|
T | TCCTAATC others(30): Show |
1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1456_-32+1457i others(39): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368960 | ||||||
| chr1:235368962
|
A | C | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1458A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368962 | ||||||
| chr1:235368984
|
A | C | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1480A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368984 | ||||||
| chr1:235368993
|
G | T | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-32+1489G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235368993 | ||||||
| chr1:235369040
|
C | G | 44 | a0001c0001t0001g0171a0001c0001t0002g0179a0001c0001t0002g0190others(41): Show | 44 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-32+1536C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369040 | ||||||
| chr1:235369062
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1558G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369062 | ||||||
| chr1:235369069
|
C | T | 5 | a0001c0001t0001g0262a0001c0001t0001g0267a0001c0001t0004g0263others(2): Show | 5 | HG01981.hp2 HG02109.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+1565C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369069 | ||||||
| chr1:235369161
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+1657T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369161 | ||||||
| chr1:235369202
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1698T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369202 | ||||||
| chr1:235369208
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.-32+1704T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369208 | ||||||
| chr1:235369266
|
T | G | 1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-32+1762T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369266 | ||||||
| chr1:235369335
|
C | T | 25 | a0001c0001t0001g0262a0001c0001t0001g0267a0001c0001t0002g0195others(22): Show | 25 | HG01070.hp2 HG01109.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.-32+1831C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369335 | ||||||
| chr1:235369437
|
A | G | 1 | a0001c0001t0002g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-32+1933A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369437 | ||||||
| chr1:235369461
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.-32+1957C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369461 | ||||||
| chr1:235369543
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-32+2039T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369543 | ||||||
| chr1:235369604
|
C | T | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-32+2100C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369604 | ||||||
| chr1:235369659
|
TA | T | 46 | a0001c0001t0001g0171a0001c0001t0002g0179a0001c0001t0002g0190others(43): Show | 46 | HG00642.hp1 HG00733.hp2 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.-32+2164delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235369659 | |||||
| chr1:235369659
|
TAA | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-32+2163_-32+2164d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235369659 | |||||
| chr1:235369790
|
C | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32+2286C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369790 | ||||||
| chr1:235369828
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-32+2324G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369828 | ||||||
| chr1:235369832
|
C | CA | 27 | a0001c0001t0001g0028a0001c0001t0002g0179a0001c0001t0002g0198others(24): Show | 27 | HG00621.hp1 HG00642.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.-32+2343dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235369832 | |||||
| chr1:235369832
|
CA | C | 32 | a0001c0001t0001g0171a0001c0001t0002g0190a0001c0001t0003g0188others(29): Show | 32 | HG00733.hp2 HG01109.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-32+2343delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235369832 | |||||
| chr1:235369859
|
C | T | 11 | a0001c0001t0002g0179a0001c0001t0004g0007a0001c0001t0004g0156others(8): Show | 11 | HG00642.hp1 HG01361.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.-32+2355C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369859 | ||||||
| chr1:235369867
|
A | T | 10 | a0001c0001t0008g0024a0001c0001t0009g0008a0001c0001t0009g0020others(7): Show | 10 | HG01109.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32+2363A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369867 | ||||||
| chr1:235369909
|
G | T | 5 | a0001c0001t0001g0262a0001c0001t0001g0267a0001c0001t0004g0263others(2): Show | 5 | HG01981.hp2 HG02109.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+2405G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235369909 | ||||||
| chr1:235370088
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.-32+2584G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370088 | ||||||
| chr1:235370121
|
G | A | 26 | a0001c0001t0001g0032a0001c0001t0001g0262a0001c0001t0001g0267others(23): Show | 26 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.-32+2617G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370121 | ||||||
| chr1:235370154
|
A | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG02738.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-32+2650A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370154 | ||||||
| chr1:235370252
|
C | CT | 6 | a0001c0001t0002g0122a0001c0001t0002g0249a0001c0001t0002g0250others(3): Show | 6 | HG02027.hp1 HG02300.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32+2765dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370252 | |||||
| chr1:235370252
|
C | CTT | 37 | a0001c0001t0001g0171a0001c0001t0001g0262a0001c0001t0001g0267others(34): Show | 37 | HG00733.hp2 HG01070.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.-32+2764_-32+2765d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370252 | |||||
| chr1:235370252
|
CT | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0033a0001c0001t0002g0034others(4): Show | 7 | HG01069.hp1 HG01069.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32+2765delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370252 | |||||
| chr1:235370269
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-32+2765T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370269 | ||||||
| chr1:235370276
|
C | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32+2772C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370276 | ||||||
| chr1:235370320
|
C | T | 3 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-32+2816C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370320 | ||||||
| chr1:235370339
|
T | C | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-32+2835T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370339 | ||||||
| chr1:235370465
|
T | C | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-32+2961T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370465 | ||||||
| chr1:235370530
|
C | T | 36 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0105others(33): Show | 36 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-32+3026C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370530 | ||||||
| chr1:235370534
|
A | G | 3 | a0001c0001t0008g0024a0001c0001t0012g0013a0001c0001t0012g0014 | 3 | HG02895.hp1 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-32+3030A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370534 | ||||||
| chr1:235370540
|
T | C | 3 | a0001c0001t0001g0037a0001c0005t0035g0260a0001c0005t0038g0155 | 3 | HG01070.hp2 HG02257.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-32+3036T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370540 | ||||||
| chr1:235370542
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-32+3038C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370542 | ||||||
| chr1:235370543
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0121a0001c0001t0002g0244others(1): Show | 4 | HG02015.hp1 HG02257.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32+3039A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370543 | ||||||
| chr1:235370546
|
C | T | 28 | a0001c0001t0001g0171a0001c0001t0003g0188a0001c0001t0005g0124others(25): Show | 28 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.-32+3042C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370546 | ||||||
| chr1:235370548
|
G | GC | 3 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-32+3045dupC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370548 | |||||
| chr1:235370550
|
A | AT | 10 | a0001c0001t0001g0037a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 10 | HG01981.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32+3062dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370550 | |||||
| chr1:235370550
|
A | T | 3 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-32+3046A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370550 | ||||||
| chr1:235370550
|
AT | A | 60 | a0001c0001t0001g0171a0001c0001t0002g0179a0001c0001t0003g0188others(57): Show | 60 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-32+3062delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370550 | |||||
| chr1:235370681
|
A | G | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-32+3177A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370681 | ||||||
| chr1:235370734
|
C | CCTTT | 37 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.-32+3233_-32+3234i others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370734 | |||||
| chr1:235370734
|
CCTTGT | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-32+3234_-32+3238d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370734 | |||||
| chr1:235370743
|
T | G | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.-32+3239T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370743 | ||||||
| chr1:235370745
|
C | CT | 66 | a0001c0001t0001g0171a0001c0001t0002g0179a0001c0001t0002g0256others(63): Show | 66 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.-32+3255dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235370745 | |||||
| chr1:235370808
|
G | C | 19 | a0001c0001t0001g0171a0001c0001t0005g0124a0001c0001t0005g0160others(16): Show | 19 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-32+3304G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370808 | ||||||
| chr1:235370810
|
C | T | 11 | a0001c0001t0004g0011a0001c0001t0004g0027a0001c0001t0004g0038others(8): Show | 11 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-32+3306C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370810 | ||||||
| chr1:235370835
|
G | T | 1 | a0001c0001t0002g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-32+3331G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370835 | ||||||
| chr1:235370861
|
T | C | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-32+3357T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235370861 | ||||||
| chr1:235371038
|
C | CT | 29 | a0001c0001t0001g0032a0001c0001t0001g0258a0001c0001t0002g0047others(26): Show | 29 | HG00140.hp2 HG01361.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.-32+3568dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
C | CTT | 16 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0121others(13): Show | 16 | HG00621.hp1 HG02148.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-32+3567_-32+3568d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
C | CTTT | 31 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0026others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.-32+3566_-32+3568d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
C | CTTTT | 56 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(53): Show | 56 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.-32+3565_-32+3568d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
C | CTTTTT | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0037others(26): Show | 29 | HG00544.hp1 HG00544.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-32+3564_-32+3568d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-32+3556_-32+3568d others(15): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
CTTTTT | C | 22 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0041others(19): Show | 22 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-32+3564_-32+3568d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
CTTTTTT | C | 24 | a0001c0001t0002g0179a0001c0001t0004g0011a0001c0001t0004g0027others(21): Show | 24 | HG00642.hp1 HG01261.hp2 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.-32+3563_-32+3568d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
CTTTTTTT | C | 13 | a0001c0001t0005g0124a0001c0001t0005g0162a0001c0001t0005g0163others(10): Show | 13 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-32+3562_-32+3568d others(9): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0005g0160a0001c0001t0022g0206 | 2 | HG02897.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-32+3557_-32+3568d others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
CTTTTTTT others(8): Show |
C | 3 | a0001c0003t0001g0051a0001c0003t0001g0052a0001c0003t0001g0135 | 3 | HG02809.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-32+3554_-32+3568d others(17): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+3551_-32+3568d others(20): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371038
|
CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-32+3548_-32+3568d others(23): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235371038 | |||||
| chr1:235371107
|
A | C | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-32+3603A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371107 | ||||||
| chr1:235371169
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+3665A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371169 | ||||||
| chr1:235371197
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+3693C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371197 | ||||||
| chr1:235371205
|
C | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32+3701C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371205 | ||||||
| chr1:235371435
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-32+3931A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371435 | ||||||
| chr1:235371527
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-32+4023A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371527 | ||||||
| chr1:235371564
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+4060T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371564 | ||||||
| chr1:235371830
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+4326A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371830 | ||||||
| chr1:235371838
|
A | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+4334A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371838 | ||||||
| chr1:235371963
|
T | C | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32+4459T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235371963 | ||||||
| chr1:235372002
|
A | T | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32+4498A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372002 | ||||||
| chr1:235372067
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+4563G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372067 | ||||||
| chr1:235372194
|
A | G | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-32+4690A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372194 | ||||||
| chr1:235372198
|
C | T | 1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-32+4694C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372198 | ||||||
| chr1:235372214
|
C | T | 1 | a0001c0001t0003g0098 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-32+4710C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372214 | ||||||
| chr1:235372250
|
A | G | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32+4746A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372250 | ||||||
| chr1:235372347
|
C | T | 1 | a0001c0001t0003g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-32+4843C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372347 | ||||||
| chr1:235372461
|
T | C | 1 | a0001c0001t0013g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-32+4957T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372461 | ||||||
| chr1:235372552
|
C | T | 1 | a0001c0001t0007g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-32+5048C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372552 | ||||||
| chr1:235372562
|
T | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5058T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372562 | ||||||
| chr1:235372589
|
C | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-32+5085C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372589 | ||||||
| chr1:235372664
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5160T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372664 | ||||||
| chr1:235372720
|
C | T | 3 | a0001c0001t0002g0195a0001c0001t0004g0194a0001c0005t0035g0260 | 3 | HG02559.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-32+5216C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372720 | ||||||
| chr1:235372750
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5246A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372750 | ||||||
| chr1:235372781
|
G | A | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+5277G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372781 | ||||||
| chr1:235372785
|
G | A | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-32+5281G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372785 | ||||||
| chr1:235372872
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5368T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372872 | ||||||
| chr1:235372881
|
A | G | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.-32+5377A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372881 | ||||||
| chr1:235372882
|
C | T | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.-32+5378C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372882 | ||||||
| chr1:235372922
|
T | TA | 47 | a0001c0001t0001g0094a0001c0001t0001g0125a0001c0001t0001g0192others(44): Show | 47 | HG00544.hp2 HG00642.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.-32+5441dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235372922 | |||||
| chr1:235372922
|
TA | T | 8 | a0001c0001t0001g0032a0001c0001t0002g0046a0001c0001t0002g0222others(5): Show | 8 | HG00099.hp1 HG01256.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-32+5441delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235372922 | |||||
| chr1:235372948
|
G | A | 1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-32+5444G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235372948 | ||||||
| chr1:235373071
|
A | G | 3 | a0001c0001t0026g0129a0001c0001t0027g0128a0003c0004t0031g0016 | 3 | HG03540.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-32+5567A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373071 | ||||||
| chr1:235373303
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+5799A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373303 | ||||||
| chr1:235373358
|
G | A | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32+5854G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373358 | ||||||
| chr1:235373523
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+6019A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373523 | ||||||
| chr1:235373570
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+6066A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373570 | ||||||
| chr1:235373604
|
C | T | 17 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(14): Show | 17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.-32+6100C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373604 | ||||||
| chr1:235373620
|
TTTTATTT others(3): Show |
T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32+6130_-32+6139d others(12): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235373620 | |||||
| chr1:235373630
|
ATTTATT | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.-32+6141_-32+6146d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235373630 | |||||
| chr1:235373671
|
C | T | 1 | a0001c0001t0011g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-32+6167C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373671 | ||||||
| chr1:235373750
|
GCCATTCT others(1265): Show |
G | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-31-6228_-31-4957d others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235373750 | |||||
| chr1:235373773
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-6246C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373773 | ||||||
| chr1:235373791
|
A | G | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6228A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373791 | ||||||
| chr1:235373794
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-31-6225G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373794 | ||||||
| chr1:235373795
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-31-6224C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373795 | ||||||
| chr1:235373797
|
C | T | 1 | a0001c0001t0034g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-31-6222C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373797 | ||||||
| chr1:235373803
|
C | T | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6216C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373803 | ||||||
| chr1:235373809
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-31-6210T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373809 | ||||||
| chr1:235373842
|
T | G | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6177T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373842 | ||||||
| chr1:235373843
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-6176G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373843 | ||||||
| chr1:235373853
|
G | T | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6166G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373853 | ||||||
| chr1:235373860
|
A | G | 1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31-6159A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373860 | ||||||
| chr1:235373892
|
T | G | 2 | a0001c0001t0008g0174a0001c0005t0035g0260 | 2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-31-6127T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373892 | ||||||
| chr1:235373929
|
G | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-31-6090G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235373929 | ||||||
| chr1:235374097
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5922C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374097 | ||||||
| chr1:235374103
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5916C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374103 | ||||||
| chr1:235374155
|
C | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31-5864C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374155 | ||||||
| chr1:235374165
|
A | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31-5854A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374165 | ||||||
| chr1:235374207
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-31-5812C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374207 | ||||||
| chr1:235374344
|
G | T | 40 | a0001c0001t0001g0058a0001c0001t0001g0105a0001c0001t0001g0113others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.-31-5675G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374344 | ||||||
| chr1:235374550
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5469A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374550 | ||||||
| chr1:235374557
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5462G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374557 | ||||||
| chr1:235374583
|
C | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31-5436C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374583 | ||||||
| chr1:235374584
|
T | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-31-5435T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374584 | ||||||
| chr1:235374680
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-31-5339T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374680 | ||||||
| chr1:235374690
|
G | A | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31-5329G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374690 | ||||||
| chr1:235374790
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-5229T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374790 | ||||||
| chr1:235374920
|
C | CT | 6 | a0001c0001t0001g0094a0001c0001t0002g0198a0001c0001t0005g0160others(3): Show | 6 | HG00544.hp2 HG00621.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-5081dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235374920 | |||||
| chr1:235374920
|
CT | C | 14 | a0001c0001t0001g0059a0001c0001t0002g0144a0001c0001t0002g0201others(11): Show | 14 | HG01069.hp1 HG01099.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31-5081delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235374920 | |||||
| chr1:235374924
|
T | C | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0141 | 3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-31-5095T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235374924 | ||||||
| chr1:235375001
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-31-5018A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375001 | ||||||
| chr1:235375110
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-4909T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375110 | ||||||
| chr1:235375118
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-4901T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375118 | ||||||
| chr1:235375143
|
A | G | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-31-4876A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375143 | ||||||
| chr1:235375152
|
C | T | 2 | a0001c0001t0003g0068a0001c0001t0003g0069 | 2 | HG00099.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.-31-4867C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375152 | ||||||
| chr1:235375253
|
T | TAAC | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.-31-4763_-31-4761d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235375253 | |||||
| chr1:235375257
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-31-4762A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375257 | ||||||
| chr1:235375705
|
A | G | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.-31-4314A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375705 | ||||||
| chr1:235375768
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-4251C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375768 | ||||||
| chr1:235375893
|
A | G | 3 | a0001c0001t0026g0129a0001c0001t0027g0128a0003c0004t0031g0016 | 3 | HG03540.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-31-4126A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375893 | ||||||
| chr1:235375904
|
C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31-4115C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375904 | ||||||
| chr1:235375986
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-4033T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235375986 | ||||||
| chr1:235376040
|
T | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-31-3979T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376040 | ||||||
| chr1:235376100
|
T | C | 2 | a0001c0001t0002g0195a0001c0001t0004g0194 | 2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-31-3919T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376100 | ||||||
| chr1:235376129
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-3890C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376129 | ||||||
| chr1:235376173
|
T | A | 1 | a0001c0001t0002g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-31-3846T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376173 | ||||||
| chr1:235376225
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-3794C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376225 | ||||||
| chr1:235376276
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-3743C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376276 | ||||||
| chr1:235376411
|
A | AG | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(2): Show | 5 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-3607dupG | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235376411 | |||||
| chr1:235376548
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-31-3471C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376548 | ||||||
| chr1:235376842
|
C | T | 35 | a0001c0001t0002g0179a0001c0001t0002g0216a0001c0001t0004g0006others(32): Show | 35 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.-31-3177C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376842 | ||||||
| chr1:235376873
|
G | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-3146G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235376873 | ||||||
| chr1:235376967
|
T | TAAAAAAA others(303): Show |
1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-31-3040_-31-3039i others(312): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235376967 | |||||
| chr1:235377094
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-31-2925G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377094 | ||||||
| chr1:235377350
|
T | A | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-31-2669T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377350 | ||||||
| chr1:235377389
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-2630T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377389 | ||||||
| chr1:235377400
|
C | T | 1 | a0001c0001t0007g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-31-2619C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377400 | ||||||
| chr1:235377478
|
C | G | 1 | a0001c0001t0013g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-31-2541C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377478 | ||||||
| chr1:235377478
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-31-2541C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377478 | ||||||
| chr1:235377501
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(51): Show | 54 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31-2518T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377501 | ||||||
| chr1:235377656
|
C | CT | 185 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.-31-2350dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235377656 | |||||
| chr1:235377744
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-31-2275C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377744 | ||||||
| chr1:235377773
|
T | A | 1 | a0001c0001t0003g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-31-2246T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377773 | ||||||
| chr1:235377802
|
G | A | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-31-2217G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377802 | ||||||
| chr1:235377841
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.-31-2178C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377841 | ||||||
| chr1:235377925
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-2094A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377925 | ||||||
| chr1:235377957
|
C | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0100others(1): Show | 4 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31-2062C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235377957 | ||||||
| chr1:235378110
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-31-1909A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378110 | ||||||
| chr1:235378189
|
G | A | 1 | a0001c0001t0003g0098 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-31-1830G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378189 | ||||||
| chr1:235378366
|
G | A | 2 | a0001c0001t0022g0206a0003c0004t0031g0016 | 2 | HG03017.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-31-1653G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378366 | ||||||
| chr1:235378395
|
AT | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-31-1615delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235378395 | |||||
| chr1:235378524
|
A | G | 3 | a0001c0001t0001g0028a0001c0001t0001g0063a0001c0001t0001g0086 | 3 | HG03710.hp1 NA18999.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-31-1495A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378524 | ||||||
| chr1:235378572
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-1447C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378572 | ||||||
| chr1:235378619
|
A | G | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.-31-1400A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378619 | ||||||
| chr1:235378708
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-31-1311A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378708 | ||||||
| chr1:235378735
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-31-1284C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378735 | ||||||
| chr1:235378848
|
G | A | 1 | a0001c0001t0022g0206 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-31-1171G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235378848 | ||||||
| chr1:235379088
|
C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-31-931C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379088 | ||||||
| chr1:235379249
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-31-770C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379249 | ||||||
| chr1:235379253
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-31-766C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379253 | ||||||
| chr1:235379275
|
C | T | 6 | a0001c0001t0006g0002a0001c0001t0006g0029a0001c0001t0006g0054others(3): Show | 6 | NA18956.hp1 NA18990.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31-744C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379275 | ||||||
| chr1:235379345
|
T | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-31-674T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379345 | ||||||
| chr1:235379566
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-31-453C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379566 | ||||||
| chr1:235379739
|
A | G | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-31-280A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379739 | ||||||
| chr1:235379818
|
G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-201G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379818 | ||||||
| chr1:235379834
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-31-185G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | chr1 | 235379834 | ||||||
| chr1:235379947
|
C | CA | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-31-55dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235379947 | |||||
| chr1:235379947
|
C | CAA | 14 | a0001c0001t0001g0097a0001c0001t0001g0125a0001c0001t0001g0243others(11): Show | 14 | HG01361.hp1 HG02109.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31-56_-31-55dupAA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr1 | 235379947 | |||||
| chr1:235380155
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.100+6C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380155 | ||||||
| chr1:235380161
|
T | TTG | 2 | a0001c0001t0002g0224a0001c0001t0002g0234 | 2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.100+64_100+65dupGT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTG | T | 27 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(24): Show | 27 | HG00621.hp1 HG01074.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.100+64_100+65delGT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTG | T | 19 | a0001c0001t0002g0106a0001c0001t0002g0144a0001c0001t0002g0195others(16): Show | 19 | HG00639.hp2 HG01168.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.100+62_100+65delGT others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTG | T | 11 | a0001c0001t0002g0047a0001c0001t0002g0122a0001c0001t0002g0200others(8): Show | 11 | HG00558.hp2 HG01256.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+60_100+65delGT others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTGT others(1): Show |
T | 15 | a0001c0001t0002g0088a0001c0001t0002g0209a0001c0001t0002g0225others(12): Show | 15 | HG00544.hp1 HG00733.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.100+58_100+65delGT others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTGT others(3): Show |
T | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100+56_100+65delGT others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTGT others(5): Show |
T | 5 | a0001c0001t0001g0117a0001c0001t0003g0067a0001c0001t0007g0265others(2): Show | 5 | HG02145.hp1 HG02280.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+54_100+65delGT others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTGT others(7): Show |
T | 34 | a0001c0001t0001g0058a0001c0001t0001g0105a0001c0001t0001g0113others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.100+52_100+65delGT others(12): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTGT others(9): Show |
T | 18 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0062others(15): Show | 18 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+50_100+65delGT others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTGT others(11): Show |
T | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 64 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.100+48_100+65delGT others(16): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTGT others(13): Show |
T | 16 | a0001c0001t0001g0071a0001c0001t0001g0136a0001c0001t0002g0179others(13): Show | 16 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+46_100+65delGT others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTGT others(15): Show |
T | 28 | a0001c0001t0002g0048a0001c0001t0004g0007a0001c0001t0004g0011others(25): Show | 28 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.100+44_100+65delGT others(20): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380161
|
TTGTGTGT others(17): Show |
T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+42_100+65delGT others(22): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235380161 | |||||
| chr1:235380202
|
T | C | 1 | a0001c0001t0004g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.100+53T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380202 | ||||||
| chr1:235380255
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+106T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380255 | ||||||
| chr1:235380400
|
A | G | 4 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+251A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380400 | ||||||
| chr1:235380496
|
G | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+347G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380496 | ||||||
| chr1:235380680
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+531A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380680 | ||||||
| chr1:235380807
|
C | T | 1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100+658C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380807 | ||||||
| chr1:235380808
|
A | G | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.100+659A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380808 | ||||||
| chr1:235380825
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+676A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380825 | ||||||
| chr1:235380838
|
T | G | 1 | a0001c0001t0004g0134 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.100+689T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235380838 | ||||||
| chr1:235381003
|
TCGAA | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+856_100+859del others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381003 | |||||
| chr1:235381022
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+873T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381022 | ||||||
| chr1:235381150
|
A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+1001A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381150 | ||||||
| chr1:235381407
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+1258G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381407 | ||||||
| chr1:235381430
|
T | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+1281T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381430 | ||||||
| chr1:235381542
|
G | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+1393G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381542 | ||||||
| chr1:235381557
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+1408A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381557 | ||||||
| chr1:235381624
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+1475G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381624 | ||||||
| chr1:235381664
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+1515G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381664 | ||||||
| chr1:235381672
|
G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.100+1523G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381672 | ||||||
| chr1:235381685
|
C | CA | 21 | a0001c0001t0001g0086a0001c0001t0002g0046a0001c0001t0002g0047others(18): Show | 21 | HG00280.hp2 HG00558.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+1563dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381685 | |||||
| chr1:235381685
|
CA | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.100+1563delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381685 | |||||
| chr1:235381685
|
CAA | C | 31 | a0001c0001t0002g0179a0001c0001t0003g0066a0001c0001t0004g0011others(28): Show | 31 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.100+1562_100+1563d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381685 | |||||
| chr1:235381733
|
A | G | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.100+1584A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381733 | ||||||
| chr1:235381750
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+1601T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381750 | ||||||
| chr1:235381779
|
CT | C | 6 | a0001c0001t0002g0253a0001c0001t0002g0259a0001c0001t0007g0045others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+1638delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235381779 | |||||
| chr1:235381959
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100+1810C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381959 | ||||||
| chr1:235381965
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100+1816T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235381965 | ||||||
| chr1:235382109
|
C | T | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+1960C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382109 | ||||||
| chr1:235382220
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2071G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382220 | ||||||
| chr1:235382264
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2115A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382264 | ||||||
| chr1:235382285
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2136G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382285 | ||||||
| chr1:235382308
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2159G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382308 | ||||||
| chr1:235382354
|
G | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.100+2205G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382354 | ||||||
| chr1:235382384
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2235C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382384 | ||||||
| chr1:235382431
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.100+2282A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382431 | ||||||
| chr1:235382454
|
C | T | 1 | a0005c0008t0001g0242 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.100+2305C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382454 | ||||||
| chr1:235382641
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+2492C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382641 | ||||||
| chr1:235382740
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.100+2591G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382740 | ||||||
| chr1:235382776
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.100+2627T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382776 | ||||||
| chr1:235382890
|
C | T | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.100+2741C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382890 | ||||||
| chr1:235382897
|
A | G | 25 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(22): Show | 25 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.100+2748A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382897 | ||||||
| chr1:235382983
|
A | C | 7 | a0001c0001t0001g0058a0001c0001t0001g0117a0001c0001t0001g0120others(4): Show | 7 | HG00558.hp1 NA18975.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+2834A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235382983 | ||||||
| chr1:235383011
|
T | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.100+2862T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383011 | ||||||
| chr1:235383153
|
C | T | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100+3004C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383153 | ||||||
| chr1:235383189
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+3040A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383189 | ||||||
| chr1:235383291
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0057others(4): Show | 7 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+3142C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383291 | ||||||
| chr1:235383296
|
C | T | 1 | a0001c0001t0002g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.100+3147C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383296 | ||||||
| chr1:235383443
|
C | T | 2 | a0001c0001t0003g0188a0001c0001t0014g0018 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.100+3294C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383443 | ||||||
| chr1:235383582
|
T | C | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+3433T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383582 | ||||||
| chr1:235383725
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+3576G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383725 | ||||||
| chr1:235383735
|
C | G | 1 | a0001c0001t0003g0068 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100+3586C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383735 | ||||||
| chr1:235383843
|
C | G | 1 | a0001c0001t0002g0215 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.100+3694C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383843 | ||||||
| chr1:235383878
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(50): Show | 53 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.100+3729C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235383878 | ||||||
| chr1:235384076
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+3927T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384076 | ||||||
| chr1:235384119
|
T | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+3970T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384119 | ||||||
| chr1:235384301
|
G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4152G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384301 | ||||||
| chr1:235384336
|
G | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+4187G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384336 | ||||||
| chr1:235384363
|
A | G | 2 | a0001c0001t0001g0083a0004c0006t0002g0123 | 2 | HG02976.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.100+4214A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384363 | ||||||
| chr1:235384424
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4275C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384424 | ||||||
| chr1:235384467
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4318G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384467 | ||||||
| chr1:235384637
|
G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4488G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384637 | ||||||
| chr1:235384731
|
G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.100+4582G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384731 | ||||||
| chr1:235384822
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4673C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384822 | ||||||
| chr1:235384971
|
C | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+4822C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235384971 | ||||||
| chr1:235385178
|
G | A | 1 | a0001c0001t0005g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100+5029G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385178 | ||||||
| chr1:235385202
|
T | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.100+5053T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385202 | ||||||
| chr1:235385330
|
C | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5181C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385330 | ||||||
| chr1:235385365
|
C | G | 2 | a0001c0005t0035g0260a0001c0005t0038g0155 | 2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.100+5216C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385365 | ||||||
| chr1:235385373
|
G | A | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+5224G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385373 | ||||||
| chr1:235385384
|
G | C | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.100+5235G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385384 | ||||||
| chr1:235385388
|
C | T | 2 | a0001c0001t0004g0208a0001c0001t0022g0206 | 2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.100+5239C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385388 | ||||||
| chr1:235385395
|
C | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+5246C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385395 | ||||||
| chr1:235385436
|
C | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+5287C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385436 | ||||||
| chr1:235385438
|
T | A | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+5289T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385438 | ||||||
| chr1:235385518
|
A | G | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+5369A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385518 | ||||||
| chr1:235385561
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5412T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385561 | ||||||
| chr1:235385669
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5520G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385669 | ||||||
| chr1:235385687
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5538T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385687 | ||||||
| chr1:235385809
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.100+5660C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385809 | ||||||
| chr1:235385838
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+5689G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385838 | ||||||
| chr1:235385960
|
G | C | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+5811G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235385960 | ||||||
| chr1:235386185
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100+6036C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386185 | ||||||
| chr1:235386197
|
G | C | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.100+6048G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386197 | ||||||
| chr1:235386255
|
G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6106G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386255 | ||||||
| chr1:235386286
|
C | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.100+6137C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386286 | ||||||
| chr1:235386387
|
A | G | 1 | a0001c0001t0003g0080 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.100+6238A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386387 | ||||||
| chr1:235386469
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+6320C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386469 | ||||||
| chr1:235386551
|
A | C | 1 | a0001c0001t0011g0223 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.100+6402A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386551 | ||||||
| chr1:235386558
|
A | C | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.100+6409A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386558 | ||||||
| chr1:235386566
|
T | C | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.100+6417T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386566 | ||||||
| chr1:235386592
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6443A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386592 | ||||||
| chr1:235386760
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+6611C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386760 | ||||||
| chr1:235386796
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6647A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386796 | ||||||
| chr1:235386799
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6650T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386799 | ||||||
| chr1:235386815
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6666T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386815 | ||||||
| chr1:235386838
|
G | A | 1 | a0001c0001t0005g0163 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.100+6689G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386838 | ||||||
| chr1:235386845
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6696G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386845 | ||||||
| chr1:235386872
|
G | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100+6723G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386872 | ||||||
| chr1:235386887
|
G | A | 21 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(18): Show | 21 | HG00544.hp1 HG00738.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.100+6738G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386887 | ||||||
| chr1:235386936
|
A | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0033others(7): Show | 10 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+6787A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386936 | ||||||
| chr1:235386988
|
C | A | 17 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(14): Show | 17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.100+6839C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235386988 | ||||||
| chr1:235387094
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+6945A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387094 | ||||||
| chr1:235387102
|
C | T | 2 | a0001c0001t0002g0198a0001c0001t0015g0241 | 2 | HG00621.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.100+6953C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387102 | ||||||
| chr1:235387111
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0004g0007 | 2 | HG00642.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.100+6962G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387111 | ||||||
| chr1:235387197
|
G | T | 6 | a0001c0001t0003g0143a0001c0001t0003g0149a0001c0001t0012g0013others(3): Show | 6 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+7048G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387197 | ||||||
| chr1:235387236
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7087A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387236 | ||||||
| chr1:235387287
|
A | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.100+7138A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387287 | ||||||
| chr1:235387299
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7150A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387299 | ||||||
| chr1:235387338
|
G | A | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.100+7189G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387338 | ||||||
| chr1:235387436
|
A | C | 1 | a0001c0001t0002g0255 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.100+7287A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387436 | ||||||
| chr1:235387489
|
A | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7340A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387489 | ||||||
| chr1:235387524
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7375G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387524 | ||||||
| chr1:235387531
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7382T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387531 | ||||||
| chr1:235387583
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+7434A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387583 | ||||||
| chr1:235387605
|
G | T | 1 | a0001c0001t0002g0231 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.100+7456G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387605 | ||||||
| chr1:235387635
|
T | G | 1 | a0001c0001t0002g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.100+7486T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387635 | ||||||
| chr1:235387644
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7495T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387644 | ||||||
| chr1:235387680
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7531C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387680 | ||||||
| chr1:235387738
|
C | A | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.100+7589C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387738 | ||||||
| chr1:235387806
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+7657G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387806 | ||||||
| chr1:235387818
|
C | T | 5 | a0001c0001t0005g0165a0001c0001t0005g0166a0001c0001t0005g0167others(2): Show | 5 | HG02622.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+7669C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387818 | ||||||
| chr1:235387841
|
A | C | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+7692A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235387841 | ||||||
| chr1:235388210
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8061T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388210 | ||||||
| chr1:235388271
|
T | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8122T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388271 | ||||||
| chr1:235388283
|
C | CT | 13 | a0001c0001t0001g0097a0001c0001t0001g0145a0001c0001t0002g0179others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.100+8156dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235388283 | |||||
| chr1:235388283
|
CT | C | 29 | a0001c0001t0001g0108a0001c0001t0002g0122a0001c0001t0002g0127others(26): Show | 29 | HG00733.hp2 HG01099.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.100+8156delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235388283 | |||||
| chr1:235388607
|
G | A | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.100+8458G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388607 | ||||||
| chr1:235388645
|
A | G | 1 | a0001c0001t0003g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.100+8496A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388645 | ||||||
| chr1:235388649
|
T | A | 1 | a0001c0001t0008g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+8500T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388649 | ||||||
| chr1:235388658
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8509C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388658 | ||||||
| chr1:235388664
|
A | G | 4 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+8515A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388664 | ||||||
| chr1:235388665
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8516G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388665 | ||||||
| chr1:235388847
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8698T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388847 | ||||||
| chr1:235388970
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+8821A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235388970 | ||||||
| chr1:235389004
|
T | C | 5 | a0001c0001t0006g0044a0001c0001t0007g0045a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+8855T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389004 | ||||||
| chr1:235389045
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+8896C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389045 | ||||||
| chr1:235389242
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100+9093C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389242 | ||||||
| chr1:235389396
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9247C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389396 | ||||||
| chr1:235389505
|
G | GT | 6 | a0001c0001t0001g0073a0001c0001t0001g0125a0001c0001t0002g0233others(3): Show | 6 | HG01361.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+9363dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235389505 | |||||
| chr1:235389521
|
C | T | 17 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(14): Show | 17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.100+9372C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389521 | ||||||
| chr1:235389638
|
A | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9489A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389638 | ||||||
| chr1:235389920
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9771T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389920 | ||||||
| chr1:235389983
|
G | A | 24 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(21): Show | 24 | HG00642.hp1 HG01109.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.100+9834G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235389983 | ||||||
| chr1:235390050
|
C | T | 3 | a0001c0001t0002g0209a0001c0001t0002g0225a0001c0001t0002g0251 | 3 | NA19005.hp2 NA19056.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.100+9901C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390050 | ||||||
| chr1:235390058
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9909A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390058 | ||||||
| chr1:235390123
|
C | CA | 11 | a0001c0001t0002g0195a0001c0001t0004g0194a0001c0001t0006g0029others(8): Show | 11 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+9985dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235390123 | |||||
| chr1:235390135
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+9986G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390135 | ||||||
| chr1:235390155
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100+10006A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390155 | ||||||
| chr1:235390214
|
C | T | 1 | a0001c0001t0011g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.100+10065C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390214 | ||||||
| chr1:235390376
|
A | G | 2 | a0001c0001t0013g0130a0001c0001t0013g0131 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.100+10227A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390376 | ||||||
| chr1:235390578
|
C | A | 1 | a0001c0001t0002g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.100+10429C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390578 | ||||||
| chr1:235390638
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.100+10489A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390638 | ||||||
| chr1:235390754
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+10605G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390754 | ||||||
| chr1:235390758
|
C | CA | 27 | a0001c0001t0001g0059a0001c0001t0001g0126a0001c0001t0003g0107others(24): Show | 27 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.100+10629dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235390758 | |||||
| chr1:235390758
|
CA | C | 45 | a0001c0001t0001g0136a0001c0001t0001g0171a0001c0001t0001g0193others(42): Show | 45 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.100+10629delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235390758 | |||||
| chr1:235390863
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.101-10640G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235390863 | ||||||
| chr1:235391009
|
G | T | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-10494G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391009 | ||||||
| chr1:235391057
|
G | A | 1 | a0001c0001t0002g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.101-10446G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391057 | ||||||
| chr1:235391102
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-10401T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391102 | ||||||
| chr1:235391280
|
G | A | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-10223G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391280 | ||||||
| chr1:235391302
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.101-10201C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391302 | ||||||
| chr1:235391434
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.101-10069G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391434 | ||||||
| chr1:235391480
|
C | CA | 6 | a0001c0001t0001g0064a0001c0001t0002g0195a0001c0001t0002g0251others(3): Show | 6 | HG00140.hp1 HG01257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-10011dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391480 | |||||
| chr1:235391546
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9957T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391546 | ||||||
| chr1:235391600
|
C | CT | 36 | a0001c0001t0002g0049a0001c0001t0002g0089a0001c0001t0002g0179others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.101-9879dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | |||||
| chr1:235391600
|
C | CTT | 7 | a0001c0001t0004g0041a0001c0001t0004g0050a0001c0001t0004g0159others(4): Show | 7 | HG01243.hp2 HG02027.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-9880_101-9879d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | |||||
| chr1:235391600
|
CT | C | 27 | a0001c0001t0001g0217a0001c0001t0002g0202a0001c0001t0005g0124others(24): Show | 27 | HG00733.hp2 HG01255.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-9879delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | |||||
| chr1:235391600
|
CTTTTT | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0096others(12): Show | 15 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.101-9883_101-9879d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | |||||
| chr1:235391600
|
CTTTTTT | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.101-9884_101-9879d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235391600 | |||||
| chr1:235391803
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9700T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391803 | ||||||
| chr1:235391806
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9697C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391806 | ||||||
| chr1:235391830
|
C | A | 1 | a0001c0001t0003g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.101-9673C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391830 | ||||||
| chr1:235391848
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.101-9655C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391848 | ||||||
| chr1:235391902
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-9601C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235391902 | ||||||
| chr1:235392045
|
G | C | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-9458G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392045 | ||||||
| chr1:235392171
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9332A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392171 | ||||||
| chr1:235392219
|
G | A | 1 | a0001c0001t0005g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.101-9284G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392219 | ||||||
| chr1:235392277
|
C | G | 5 | a0001c0001t0003g0036a0001c0001t0003g0102a0001c0001t0003g0103others(2): Show | 5 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-9226C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392277 | ||||||
| chr1:235392408
|
T | TTC | 5 | a0001c0001t0001g0078a0001c0001t0001g0125a0001c0001t0003g0067others(2): Show | 5 | HG02055.hp2 HG02071.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-9094_101-9093i others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235392408 | |||||
| chr1:235392409
|
T | TC | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.101-9094_101-9093i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392409 | ||||||
| chr1:235392410
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0003g0068a0001c0001t0008g0024 | 3 | HG00639.hp1 NA19062.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-9093T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392410 | ||||||
| chr1:235392433
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-9070A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392433 | ||||||
| chr1:235392505
|
G | T | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.101-8998G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392505 | ||||||
| chr1:235392591
|
G | A | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8912G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392591 | ||||||
| chr1:235392701
|
A | T | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8802A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392701 | ||||||
| chr1:235392702
|
C | T | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8801C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392702 | ||||||
| chr1:235392757
|
T | G | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8746T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392757 | ||||||
| chr1:235392780
|
T | C | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8723T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392780 | ||||||
| chr1:235392802
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-8701A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392802 | ||||||
| chr1:235392804
|
T | C | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-8699T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235392804 | ||||||
| chr1:235393015
|
A | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.101-8488A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393015 | ||||||
| chr1:235393021
|
A | T | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-8482A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393021 | ||||||
| chr1:235393168
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(7): Show | 10 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-8335T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393168 | ||||||
| chr1:235393260
|
C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.101-8243C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393260 | ||||||
| chr1:235393274
|
C | T | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-8229C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393274 | ||||||
| chr1:235393355
|
G | A | 1 | a0001c0009t0007g0264 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.101-8148G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393355 | ||||||
| chr1:235393408
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-8095C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393408 | ||||||
| chr1:235393479
|
G | A | 4 | a0001c0001t0034g0031a0001c0003t0001g0051a0001c0003t0001g0052others(1): Show | 4 | HG02809.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-8024G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393479 | ||||||
| chr1:235393608
|
GT | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.101-7886delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235393608 | |||||
| chr1:235393794
|
T | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.101-7709T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235393794 | ||||||
| chr1:235394105
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.101-7398C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394105 | ||||||
| chr1:235394165
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-7338G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394165 | ||||||
| chr1:235394176
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-7327G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394176 | ||||||
| chr1:235394343
|
G | C | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-7160G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394343 | ||||||
| chr1:235394353
|
C | T | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG02015.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.101-7150C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394353 | ||||||
| chr1:235394418
|
C | CT | 20 | a0001c0001t0001g0033a0001c0001t0001g0053a0001c0001t0001g0077others(17): Show | 20 | HG01168.hp1 HG01256.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.101-7060dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | |||||
| chr1:235394418
|
C | CTT | 100 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.101-7061_101-7060d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | |||||
| chr1:235394418
|
C | CTTT | 28 | a0001c0001t0001g0079a0001c0001t0001g0125a0001c0001t0001g0126others(25): Show | 28 | HG00733.hp2 HG01255.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.101-7062_101-7060d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | |||||
| chr1:235394418
|
CT | C | 6 | a0001c0001t0002g0202a0001c0001t0002g0226a0001c0001t0002g0229others(3): Show | 6 | HG02055.hp2 HG03704.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-7060delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | |||||
| chr1:235394418
|
CTT | C | 31 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(28): Show | 31 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.101-7061_101-7060d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | |||||
| chr1:235394418
|
CTTTT | C | 6 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0187others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-7063_101-7060d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | |||||
| chr1:235394418
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-7070_101-7060d others(13): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235394418 | |||||
| chr1:235394429
|
T | C | 1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.101-7074T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394429 | ||||||
| chr1:235394620
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.101-6883G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394620 | ||||||
| chr1:235394910
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-6593G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394910 | ||||||
| chr1:235394910
|
G | C | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.101-6593G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394910 | ||||||
| chr1:235394963
|
C | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-6540C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235394963 | ||||||
| chr1:235395191
|
A | T | 34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-6312A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395191 | ||||||
| chr1:235395344
|
G | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-6159G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395344 | ||||||
| chr1:235395391
|
C | T | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-6112C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395391 | ||||||
| chr1:235395489
|
C | G | 26 | a0001c0001t0001g0058a0001c0001t0001g0105a0001c0001t0001g0113others(23): Show | 26 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.101-6014C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395489 | ||||||
| chr1:235395548
|
C | CT | 27 | a0001c0001t0002g0207a0001c0001t0002g0214a0001c0001t0004g0006others(24): Show | 27 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-5941dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235395548 | |||||
| chr1:235395548
|
CT | C | 5 | a0001c0001t0002g0055a0001c0001t0002g0144a0001c0001t0002g0201others(2): Show | 5 | HG01069.hp1 HG02451.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-5941delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235395548 | |||||
| chr1:235395575
|
C | T | 4 | a0001c0001t0034g0031a0001c0003t0001g0051a0001c0003t0001g0052others(1): Show | 4 | HG02809.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-5928C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395575 | ||||||
| chr1:235395905
|
A | G | 1 | a0001c0001t0011g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.101-5598A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395905 | ||||||
| chr1:235395955
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5548C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235395955 | ||||||
| chr1:235396203
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-5300T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235396203 | ||||||
| chr1:235396275
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-5228G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235396275 | ||||||
| chr1:235396349
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.101-5154T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235396349 | ||||||
| chr1:235396473
|
A | G | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-5030A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235396473 | ||||||
| chr1:235396954
|
G | GTTTA | 108 | a0001c0001t0001g0058a0001c0001t0001g0117a0001c0001t0001g0120others(105): Show | 108 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.101-4521_101-4518d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | |||||
| chr1:235396954
|
G | GTTTATTT others(1): Show |
15 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(12): Show | 15 | HG00642.hp1 HG01106.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.101-4525_101-4518d others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | |||||
| chr1:235396954
|
G | GTTTATTT others(5): Show |
4 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-4529_101-4518d others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | |||||
| chr1:235396954
|
G | GTTTGTTT others(5): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-4546_101-4545i others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | |||||
| chr1:235396954
|
GTTTA | G | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.101-4521_101-4518d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235396954 | |||||
| chr1:235397035
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.101-4468C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397035 | ||||||
| chr1:235397071
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.101-4432C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397071 | ||||||
| chr1:235397123
|
C | T | 1 | a0001c0001t0027g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.101-4380C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397123 | ||||||
| chr1:235397196
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.101-4307A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397196 | ||||||
| chr1:235397200
|
CT | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.101-4284delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235397200 | |||||
| chr1:235397200
|
CTT | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0003g0137others(4): Show | 7 | HG02451.hp1 HG02922.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-4285_101-4284d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235397200 | |||||
| chr1:235397343
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.101-4160G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397343 | ||||||
| chr1:235397410
|
C | T | 1 | a0005c0008t0001g0242 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.101-4093C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397410 | ||||||
| chr1:235397491
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-4012G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397491 | ||||||
| chr1:235397512
|
A | G | 2 | a0001c0001t0002g0198a0001c0001t0015g0241 | 2 | HG00621.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.101-3991A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397512 | ||||||
| chr1:235397649
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-3854A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397649 | ||||||
| chr1:235397741
|
C | T | 36 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(33): Show | 36 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.101-3762C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397741 | ||||||
| chr1:235397917
|
G | A | 3 | a0001c0001t0004g0158a0001c0001t0004g0180a0001c0001t0004g0181 | 3 | NA18943.hp2 NA18954.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.101-3586G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235397917 | ||||||
| chr1:235398142
|
CT | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.101-3346delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235398142 | |||||
| chr1:235398311
|
A | G | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-3192A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398311 | ||||||
| chr1:235398442
|
G | A | 6 | a0001c0001t0003g0030a0001c0001t0003g0066a0001c0001t0003g0067others(3): Show | 6 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-3061G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398442 | ||||||
| chr1:235398680
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2823A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398680 | ||||||
| chr1:235398734
|
C | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-2769C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398734 | ||||||
| chr1:235398753
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2750C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398753 | ||||||
| chr1:235398754
|
T | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2749T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398754 | ||||||
| chr1:235398755
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2748A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398755 | ||||||
| chr1:235398796
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-2707G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398796 | ||||||
| chr1:235398905
|
A | G | 1 | a0001c0001t0002g0210 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.101-2598A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398905 | ||||||
| chr1:235398935
|
G | A | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.101-2568G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235398935 | ||||||
| chr1:235399387
|
G | C | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.101-2116G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399387 | ||||||
| chr1:235399497
|
C | T | 1 | a0001c0001t0007g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.101-2006C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399497 | ||||||
| chr1:235399723
|
C | T | 1 | a0001c0001t0004g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.101-1780C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399723 | ||||||
| chr1:235399869
|
A | C | 1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.101-1634A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399869 | ||||||
| chr1:235399902
|
A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1601A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399902 | ||||||
| chr1:235399903
|
A | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1600A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399903 | ||||||
| chr1:235399904
|
A | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1599A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399904 | ||||||
| chr1:235399905
|
A | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1598A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399905 | ||||||
| chr1:235399906
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1597C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399906 | ||||||
| chr1:235399944
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.101-1559C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399944 | ||||||
| chr1:235399977
|
A | G | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.101-1526A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235399977 | ||||||
| chr1:235400153
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-1350G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400153 | ||||||
| chr1:235400226
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.101-1277C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400226 | ||||||
| chr1:235400408
|
C | CTTTTTTT others(1): Show |
34 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(31): Show | 34 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-1092_101-1085d others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | |||||
| chr1:235400408
|
C | CTTTTTTT others(6): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-1085_101-1084i others(15): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | |||||
| chr1:235400408
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0002g0195a0004c0006t0002g0123 | 2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.101-1085_101-1084i others(16): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | |||||
| chr1:235400408
|
C | CTTTTTTT others(8): Show |
33 | a0001c0001t0001g0032a0001c0001t0001g0075a0001c0001t0003g0036others(30): Show | 33 | HG00733.hp2 HG01070.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.101-1085_101-1084i others(17): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | |||||
| chr1:235400408
|
C | CTTTTTTT others(9): Show |
99 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.101-1085_101-1084i others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | |||||
| chr1:235400408
|
C | CTTTTTTT others(10): Show |
23 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0062others(20): Show | 23 | HG00621.hp2 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.101-1085_101-1084i others(19): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400408 | |||||
| chr1:235400432
|
G | A | 17 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(14): Show | 17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-1071G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400432 | ||||||
| chr1:235400493
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-1010C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400493 | ||||||
| chr1:235400525
|
G | A | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-978G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400525 | ||||||
| chr1:235400624
|
A | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-879A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400624 | ||||||
| chr1:235400658
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.101-845T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400658 | ||||||
| chr1:235400660
|
A | G | 2 | a0001c0001t0002g0207a0001c0001t0002g0214 | 2 | HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.101-843A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400660 | ||||||
| chr1:235400671
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101-832G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400671 | ||||||
| chr1:235400679
|
C | T | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG02015.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.101-824C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400679 | ||||||
| chr1:235400787
|
C | T | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.101-716C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400787 | ||||||
| chr1:235400905
|
GCCAGTCT others(3): Show |
G | 25 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(22): Show | 25 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.101-587_101-578del others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr1 | 235400905 | |||||
| chr1:235400939
|
G | A | 39 | a0001c0001t0001g0058a0001c0001t0001g0105a0001c0001t0001g0113others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.101-564G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400939 | ||||||
| chr1:235400983
|
C | T | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-520C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235400983 | ||||||
| chr1:235401065
|
C | T | 4 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-438C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401065 | ||||||
| chr1:235401075
|
A | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.101-428A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401075 | ||||||
| chr1:235401097
|
G | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.101-406G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401097 | ||||||
| chr1:235401416
|
C | T | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.101-87C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401416 | ||||||
| chr1:235401448
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-55G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401448 | ||||||
| chr1:235401498
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.101-5G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 2/16 | chr1 | 235401498 | ||||||
| chr1:235401609
|
G | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0003g0119 | 3 | HG01123.hp1 HG02300.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.185+22G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235401609 | ||||||
| chr1:235401806
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+219A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235401806 | ||||||
| chr1:235401811
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+224G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235401811 | ||||||
| chr1:235401826
|
C | CT | 10 | a0001c0001t0002g0048a0001c0001t0002g0195a0001c0001t0002g0245others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+262dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235401826 | |||||
| chr1:235401826
|
C | CTTT | 31 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(28): Show | 31 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.185+260_185+262dup others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235401826 | |||||
| chr1:235401826
|
CT | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.185+262delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235401826 | |||||
| chr1:235401826
|
CTT | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0075a0001c0001t0001g0100others(6): Show | 9 | HG01070.hp1 HG01167.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+261_185+262del others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235401826 | |||||
| chr1:235402000
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.185+413T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402000 | ||||||
| chr1:235402065
|
C | CT | 7 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0002g0207others(4): Show | 7 | HG00738.hp2 HG01074.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+495dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235402065 | |||||
| chr1:235402156
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+569T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402156 | ||||||
| chr1:235402171
|
C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.185+584C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402171 | ||||||
| chr1:235402282
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+695C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402282 | ||||||
| chr1:235402357
|
C | T | 6 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0110others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+770C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402357 | ||||||
| chr1:235402394
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+807C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402394 | ||||||
| chr1:235402511
|
G | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+924G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402511 | ||||||
| chr1:235402587
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+1000G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402587 | ||||||
| chr1:235402589
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0097 | 2 | NA18953.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.185+1002G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402589 | ||||||
| chr1:235402597
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.185+1010C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402597 | ||||||
| chr1:235402624
|
T | G | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.185+1037T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402624 | ||||||
| chr1:235402770
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+1183G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402770 | ||||||
| chr1:235402808
|
T | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+1221T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402808 | ||||||
| chr1:235402888
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+1301C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402888 | ||||||
| chr1:235402948
|
A | G | 1 | a0001c0001t0002g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.185+1361A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402948 | ||||||
| chr1:235402976
|
C | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.185+1389C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235402976 | ||||||
| chr1:235403542
|
T | G | 1 | a0001c0001t0002g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.185+1955T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235403542 | ||||||
| chr1:235403637
|
C | T | 4 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0110others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+2050C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235403637 | ||||||
| chr1:235403690
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.185+2103C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235403690 | ||||||
| chr1:235403786
|
G | C | 1 | a0001c0001t0023g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.185+2199G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235403786 | ||||||
| chr1:235404001
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+2414G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404001 | ||||||
| chr1:235404071
|
G | C | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.185+2484G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404071 | ||||||
| chr1:235404131
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.185+2544G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404131 | ||||||
| chr1:235404231
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.185+2644C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404231 | ||||||
| chr1:235404247
|
A | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0097 | 2 | NA18953.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.185+2660A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404247 | ||||||
| chr1:235404254
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+2667G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404254 | ||||||
| chr1:235404271
|
C | T | 2 | a0001c0001t0001g0097a0001c0005t0035g0260 | 2 | HG03471.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.185+2684C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404271 | ||||||
| chr1:235404289
|
AAATT | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.185+2705_185+2708d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235404289 | |||||
| chr1:235404319
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+2732T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404319 | ||||||
| chr1:235404385
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+2798C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404385 | ||||||
| chr1:235404853
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3266G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404853 | ||||||
| chr1:235404877
|
G | C | 1 | a0001c0001t0002g0090 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.185+3290G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404877 | ||||||
| chr1:235404939
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3352C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404939 | ||||||
| chr1:235404958
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3371T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235404958 | ||||||
| chr1:235404960
|
C | CT | 6 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0002g0195others(3): Show | 6 | HG00621.hp2 HG01106.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+3392dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235404960 | |||||
| chr1:235404960
|
CT | C | 38 | a0001c0001t0002g0179a0001c0001t0003g0153a0001c0001t0004g0006others(35): Show | 38 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.185+3392delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235404960 | |||||
| chr1:235405107
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3520C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405107 | ||||||
| chr1:235405205
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3618T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405205 | ||||||
| chr1:235405207
|
C | T | 8 | a0001c0001t0002g0179a0001c0001t0004g0007a0001c0001t0004g0158others(5): Show | 8 | HG00642.hp1 HG01361.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+3620C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405207 | ||||||
| chr1:235405212
|
C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.185+3625C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405212 | ||||||
| chr1:235405266
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3679G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405266 | ||||||
| chr1:235405320
|
CT | C | 18 | a0001c0001t0001g0117a0001c0001t0001g0145a0001c0001t0002g0202others(15): Show | 18 | HG00639.hp2 HG01256.hp1 HG02976.hp2 others(15): Show |
intron_variant | MODIFIER | c.185+3752delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235405320 | |||||
| chr1:235405320
|
CTT | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.185+3751_185+3752d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235405320 | |||||
| chr1:235405320
|
CTTT | C | 8 | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0086others(5): Show | 8 | HG01167.hp1 HG01496.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+3750_185+3752d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235405320 | |||||
| chr1:235405336
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+3749T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405336 | ||||||
| chr1:235405446
|
G | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3859G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405446 | ||||||
| chr1:235405457
|
T | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3870T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405457 | ||||||
| chr1:235405498
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+3911T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405498 | ||||||
| chr1:235405831
|
G | A | 3 | a0001c0001t0001g0136a0001c0001t0001g0171a0003c0004t0037g0172 | 3 | HG01106.hp1 HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.185+4244G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405831 | ||||||
| chr1:235405918
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4331C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235405918 | ||||||
| chr1:235406072
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4485C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406072 | ||||||
| chr1:235406124
|
A | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4537A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406124 | ||||||
| chr1:235406487
|
C | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4900C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406487 | ||||||
| chr1:235406543
|
A | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4956A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406543 | ||||||
| chr1:235406556
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4969G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406556 | ||||||
| chr1:235406559
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+4972T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406559 | ||||||
| chr1:235406571
|
G | A | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.185+4984G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406571 | ||||||
| chr1:235406645
|
C | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+5058C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406645 | ||||||
| chr1:235406676
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.185+5089C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406676 | ||||||
| chr1:235406762
|
A | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+5175A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406762 | ||||||
| chr1:235406829
|
C | CT | 13 | a0001c0001t0001g0145a0001c0001t0002g0144a0001c0001t0002g0229others(10): Show | 13 | HG00733.hp2 HG01361.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+5264dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235406829 | |||||
| chr1:235406829
|
CT | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.185+5264delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235406829 | |||||
| chr1:235406829
|
CTT | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0071a0001c0001t0001g0171others(4): Show | 7 | HG00738.hp1 HG01081.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+5263_185+5264d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235406829 | |||||
| chr1:235406857
|
G | A | 2 | a0001c0001t0002g0229a0001c0001t0002g0239 | 2 | NA19082.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.185+5270G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406857 | ||||||
| chr1:235406975
|
T | C | 2 | a0001c0001t0013g0130a0001c0001t0013g0131 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.185+5388T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235406975 | ||||||
| chr1:235407118
|
T | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.185+5531T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407118 | ||||||
| chr1:235407118
|
T | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.185+5531T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407118 | ||||||
| chr1:235407131
|
C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.185+5544C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407131 | ||||||
| chr1:235407134
|
C | CT | 31 | a0001c0001t0001g0125a0001c0001t0001g0145a0001c0001t0001g0147others(28): Show | 31 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.185+5563dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235407134 | |||||
| chr1:235407155
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.185+5568G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407155 | ||||||
| chr1:235407188
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.185+5601C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407188 | ||||||
| chr1:235407208
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.185+5621G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407208 | ||||||
| chr1:235407319
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.185+5732T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407319 | ||||||
| chr1:235407636
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.185+6049G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407636 | ||||||
| chr1:235407819
|
T | A | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.185+6232T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235407819 | ||||||
| chr1:235407878
|
G | GT | 39 | a0001c0001t0002g0179a0001c0001t0002g0198a0001c0001t0004g0006others(36): Show | 39 | HG00621.hp1 HG00642.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.185+6301dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235407878 | |||||
| chr1:235408028
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.186-6405C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408028 | ||||||
| chr1:235408087
|
T | A | 37 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-6346T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408087 | ||||||
| chr1:235408097
|
C | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-6336C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408097 | ||||||
| chr1:235408098
|
C | G | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.186-6335C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408098 | ||||||
| chr1:235408113
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.186-6320G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408113 | ||||||
| chr1:235408251
|
T | C | 1 | a0001c0001t0002g0220 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.186-6182T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408251 | ||||||
| chr1:235408264
|
A | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-6169A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408264 | ||||||
| chr1:235408347
|
A | T | 37 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-6086A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408347 | ||||||
| chr1:235408432
|
A | AT | 38 | a0001c0001t0001g0071a0001c0001t0001g0145a0001c0001t0002g0179others(35): Show | 38 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.186-5986dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235408432 | |||||
| chr1:235408432
|
AT | A | 8 | a0001c0001t0001g0117a0001c0001t0002g0048a0001c0001t0002g0055others(5): Show | 8 | HG02559.hp2 HG02895.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-5986delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235408432 | |||||
| chr1:235408502
|
T | TTAC | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-5931_186-5930i others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408502 | ||||||
| chr1:235408719
|
G | A | 37 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-5714G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408719 | ||||||
| chr1:235408722
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(52): Show | 55 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.186-5711C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408722 | ||||||
| chr1:235408767
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.186-5666C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235408767 | ||||||
| chr1:235409009
|
CT | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.186-5406delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409009 | |||||
| chr1:235409009
|
CTT | C | 33 | a0001c0001t0002g0179a0001c0001t0003g0098a0001c0001t0004g0007others(30): Show | 33 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.186-5407_186-5406d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409009 | |||||
| chr1:235409031
|
A | G | 32 | a0001c0001t0002g0179a0001c0001t0004g0007a0001c0001t0004g0011others(29): Show | 32 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.186-5402A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409031 | ||||||
| chr1:235409079
|
T | C | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-5354T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409079 | ||||||
| chr1:235409354
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.186-5079T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409354 | ||||||
| chr1:235409440
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4993C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409440 | ||||||
| chr1:235409499
|
G | A | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-4934G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409499 | ||||||
| chr1:235409803
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.186-4630C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409803 | ||||||
| chr1:235409824
|
T | TTCGAGAC others(3814): Show |
1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3823): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3815): Show |
1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3824): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3828): Show |
1 | a0001c0001t0003g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3837): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3831): Show |
1 | a0005c0008t0001g0242 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3829): Show |
1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3839): Show |
1 | a0001c0001t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3848): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3829): Show |
2 | a0001c0001t0003g0188a0001c0001t0014g0018 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3828): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0100 | 2 | HG01070.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3837): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3829): Show |
40 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3830): Show |
40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0037others(37): Show | 40 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3831): Show |
13 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0073others(10): Show | 13 | HG00544.hp2 HG01099.hp2 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3831): Show |
3 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
16 | a0001c0001t0005g0124a0001c0001t0005g0165a0001c0001t0005g0166others(13): Show | 16 | HG01109.hp2 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3833): Show |
1 | a0001c0001t0005g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3842): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0160 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3833): Show |
1 | a0001c0001t0005g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3842): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0163 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3833): Show |
1 | a0001c0001t0006g0002 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3842): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3830): Show |
1 | a0001c0001t0001g0071 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3832): Show |
1 | a0001c0001t0005g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3841): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3830): Show |
1 | a0001c0001t0003g0015 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3829): Show |
5 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0003g0104others(2): Show | 5 | HG01081.hp1 HG01123.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3830): Show |
1 | a0001c0001t0003g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3833): Show |
1 | a0001c0001t0003g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3842): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3817): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3826): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3843): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3852): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3821): Show |
3 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266 | 3 | HG02145.hp1 HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3830): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3822): Show |
1 | a0001c0009t0007g0264 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3831): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3822): Show |
1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-4600_186-4599i others(3831): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3830): Show |
2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTCGAGAC others(3831): Show |
2 | a0001c0001t0003g0102a0001c0001t0003g0103 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.186-4600_186-4599i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3838): Show |
1 | a0001c0001t0004g0006 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3847): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3831): Show |
4 | a0001c0001t0009g0008a0001c0001t0009g0020a0001c0001t0009g0022others(1): Show | 4 | HG01109.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-4608_186-4607i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3815): Show |
2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4608_186-4607i others(3824): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3830): Show |
22 | a0001c0001t0004g0011a0001c0001t0004g0027a0001c0001t0004g0038others(19): Show | 22 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-4608_186-4607i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3831): Show |
1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3829): Show |
1 | a0001c0001t0004g0158 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3838): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3830): Show |
2 | a0001c0001t0004g0180a0001c0001t0019g0157 | 2 | HG02027.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.186-4608_186-4607i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3830): Show |
1 | a0001c0001t0004g0181 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3831): Show |
1 | a0001c0001t0004g0159 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3840): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3830): Show |
1 | a0001c0001t0004g0007 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3839): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409824
|
T | TTGGAGAC others(3826): Show |
1 | a0001c0001t0002g0179 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.186-4608_186-4607i others(3835): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235409824 | |||||
| chr1:235409838
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.186-4595A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409838 | ||||||
| chr1:235409875
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4558A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409875 | ||||||
| chr1:235409891
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-4542G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409891 | ||||||
| chr1:235409978
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4455C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235409978 | ||||||
| chr1:235410029
|
CAAACAAA others(5): Show |
C | 1 | a0001c0001t0027g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.186-4394_186-4383d others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235410029 | |||||
| chr1:235410074
|
G | C | 1 | a0001c0001t0003g0103 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.186-4359G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410074 | ||||||
| chr1:235410075
|
C | G | 1 | a0001c0001t0003g0103 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.186-4358C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410075 | ||||||
| chr1:235410080
|
T | G | 1 | a0001c0001t0013g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.186-4353T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410080 | ||||||
| chr1:235410139
|
CGGGAGGC others(25): Show |
C | 3 | a0001c0001t0026g0129a0001c0001t0027g0128a0003c0004t0031g0016 | 3 | HG03540.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-4281_186-4250d others(34): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235410139 | |||||
| chr1:235410163
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.186-4270C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410163 | ||||||
| chr1:235410171
|
A | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.186-4262A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410171 | ||||||
| chr1:235410312
|
CTGGGTGC others(46): Show |
C | 1 | a0001c0001t0006g0054 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.186-4119_186-4067d others(55): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235410312 | |||||
| chr1:235410361
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.186-4072G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410361 | ||||||
| chr1:235410434
|
G | T | 1 | a0001c0001t0003g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.186-3999G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410434 | ||||||
| chr1:235410460
|
G | C | 4 | a0001c0001t0004g0197a0001c0001t0004g0203a0001c0001t0004g0204others(1): Show | 4 | HG02735.hp1 HG03490.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-3973G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410460 | ||||||
| chr1:235410648
|
T | C | 3 | a0001c0001t0003g0109a0001c0001t0003g0151a0001c0001t0003g0191 | 3 | HG00741.hp2 HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.186-3785T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410648 | ||||||
| chr1:235410711
|
T | A | 1 | a0001c0001t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.186-3722T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410711 | ||||||
| chr1:235410782
|
A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-3651A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235410782 | ||||||
| chr1:235411082
|
T | G | 3 | a0001c0001t0026g0129a0001c0001t0027g0128a0003c0004t0031g0016 | 3 | HG03540.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-3351T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411082 | ||||||
| chr1:235411162
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0267 | 2 | HG01981.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.186-3271C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411162 | ||||||
| chr1:235411188
|
G | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-3245G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411188 | ||||||
| chr1:235411292
|
C | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-3141C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411292 | ||||||
| chr1:235411330
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-3103A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411330 | ||||||
| chr1:235411404
|
A | T | 1 | a0001c0001t0016g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.186-3029A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411404 | ||||||
| chr1:235411436
|
G | C | 1 | a0001c0001t0005g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.186-2997G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411436 | ||||||
| chr1:235411603
|
G | GAATAATA others(6): Show |
1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.186-2829_186-2817d others(15): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235411603 | |||||
| chr1:235411659
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(57): Show | 60 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.186-2774C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411659 | ||||||
| chr1:235411809
|
A | G | 3 | a0001c0003t0001g0051a0001c0003t0001g0052a0001c0003t0001g0135 | 3 | HG02809.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.186-2624A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411809 | ||||||
| chr1:235411814
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.186-2619A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411814 | ||||||
| chr1:235411866
|
C | T | 5 | a0001c0001t0002g0055a0001c0001t0004g0197a0001c0001t0004g0203others(2): Show | 5 | HG02735.hp1 HG03490.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-2567C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411866 | ||||||
| chr1:235411891
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.186-2542C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411891 | ||||||
| chr1:235411902
|
C | G | 1 | a0001c0001t0003g0015 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.186-2531C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411902 | ||||||
| chr1:235411960
|
C | T | 1 | a0001c0001t0008g0176 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.186-2473C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235411960 | ||||||
| chr1:235412006
|
C | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.186-2427C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412006 | ||||||
| chr1:235412092
|
G | GTTTCCCT others(9): Show |
2 | a0001c0001t0002g0239a0001c0001t0006g0044 | 2 | HG06807.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.186-2315_186-2300d others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | |||||
| chr1:235412092
|
G | GTTTCCCT others(25): Show |
107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.186-2331_186-2300d others(34): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | |||||
| chr1:235412092
|
G | GTTTCCCT others(41): Show |
6 | a0001c0001t0001g0058a0001c0001t0001g0117a0001c0001t0003g0115others(3): Show | 6 | HG00558.hp1 NA18975.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-2300_186-2299i others(50): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | |||||
| chr1:235412092
|
G | GTTTCCCT others(57): Show |
3 | a0001c0001t0005g0162a0001c0001t0006g0161a0001c0001t0016g0183 | 3 | HG01109.hp2 HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.186-2300_186-2299i others(66): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | |||||
| chr1:235412092
|
G | GTTTCCCT others(89): Show |
1 | a0001c0001t0003g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.186-2300_186-2299i others(98): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412092 | |||||
| chr1:235412101
|
C | CCCATCCC others(24): Show |
1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-2330_186-2300d others(33): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412101 | |||||
| chr1:235412112
|
C | CCTTCCCA others(23): Show |
1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-2320_186-2319i others(32): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412112 | |||||
| chr1:235412115
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-2318T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412115 | ||||||
| chr1:235412117
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-2316C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412117 | ||||||
| chr1:235412118
|
C | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-2315C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412118 | ||||||
| chr1:235412120
|
A | C | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-2313A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412120 | ||||||
| chr1:235412122
|
CCCTTT | C | 20 | a0001c0001t0002g0179a0001c0001t0004g0011a0001c0001t0004g0027others(17): Show | 20 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.186-2308_186-2304d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412122 | |||||
| chr1:235412125
|
T | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0041others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-2308T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412125 | ||||||
| chr1:235412131
|
T | C | 15 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0041others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-2302T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412131 | ||||||
| chr1:235412134
|
T | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0073others(72): Show | 75 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.186-2299T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412134 | ||||||
| chr1:235412135
|
C | CATCCCTT others(301): Show |
1 | a0001c0001t0016g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.186-2298_186-2297i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | ||||||
| chr1:235412135
|
C | CATCCCTT others(318): Show |
2 | a0001c0001t0008g0024a0001c0001t0018g0009 | 2 | HG02280.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.186-2298_186-2297i others(327): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | ||||||
| chr1:235412135
|
C | CATCCCTT others(298): Show |
12 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0163others(9): Show | 12 | HG00733.hp2 HG01261.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.186-2298_186-2297i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | ||||||
| chr1:235412135
|
C | CATCCCTT others(282): Show |
4 | a0001c0001t0005g0187a0001c0001t0008g0173a0001c0001t0008g0176others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-2298_186-2297i others(291): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | ||||||
| chr1:235412135
|
C | CATCCCTT others(287): Show |
1 | a0001c0001t0008g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.186-2298_186-2297i others(296): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | ||||||
| chr1:235412135
|
C | CATCCCTT others(381): Show |
1 | a0001c0001t0015g0241 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.186-2298_186-2297i others(390): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | ||||||
| chr1:235412135
|
C | CATCCCTT others(379): Show |
1 | a0001c0001t0002g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.186-2298_186-2297i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412135 | ||||||
| chr1:235412136
|
C | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0073others(15): Show | 18 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.186-2297C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412136 | ||||||
| chr1:235412137
|
T | C | 22 | a0001c0001t0002g0198a0001c0001t0005g0124a0001c0001t0005g0160others(19): Show | 22 | HG00621.hp1 HG00733.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-2296T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412137 | ||||||
| chr1:235412141
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0073others(15): Show | 18 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.186-2292C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412141 | ||||||
| chr1:235412141
|
CT | C | 25 | a0001c0001t0002g0179a0001c0001t0004g0011a0001c0001t0004g0027others(22): Show | 25 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.186-2290delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412141 | |||||
| chr1:235412142
|
T | G | 22 | a0001c0001t0002g0198a0001c0001t0005g0124a0001c0001t0005g0160others(19): Show | 22 | HG00621.hp1 HG00733.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-2291T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | ||||||
| chr1:235412142
|
T | TCCCC | 3 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0203 | 3 | HG01361.hp1 HG02572.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.186-2291_186-2290i others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | ||||||
| chr1:235412142
|
T | TCCCCTCC others(2): Show |
4 | a0001c0001t0009g0008a0001c0001t0009g0020a0001c0001t0009g0022others(1): Show | 4 | HG01109.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2291_186-2290i others(11): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | ||||||
| chr1:235412142
|
T | TCCCCTCC others(5): Show |
1 | a0001c0001t0004g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186-2291_186-2290i others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | ||||||
| chr1:235412142
|
T | TCCCCTCC others(10): Show |
1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.186-2291_186-2290i others(19): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | ||||||
| chr1:235412142
|
T | TCCCCTCC others(36): Show |
1 | a0001c0001t0004g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.186-2291_186-2290i others(45): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412142 | ||||||
| chr1:235412143
|
T | C | 1 | a0001c0001t0004g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186-2290T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412143 | ||||||
| chr1:235412143
|
T | TCCCTTCC others(355): Show |
1 | a0001c0001t0001g0073 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.186-2287_186-2286i others(364): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412143 | |||||
| chr1:235412143
|
T | TCCCTTCC others(343): Show |
1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.186-2287_186-2286i others(352): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412143 | |||||
| chr1:235412146
|
C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-2287C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412146 | ||||||
| chr1:235412147
|
C | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0073 | 2 | HG03017.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.186-2286C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412147 | ||||||
| chr1:235412147
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(13): Show | 16 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-2286C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412147 | ||||||
| chr1:235412148
|
T | C | 4 | a0001c0001t0009g0008a0001c0001t0009g0020a0001c0001t0009g0022others(1): Show | 4 | HG01109.hp1 HG03195.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2285T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412148 | ||||||
| chr1:235412151
|
C | T | 22 | a0001c0001t0002g0198a0001c0001t0005g0124a0001c0001t0005g0160others(19): Show | 22 | HG00621.hp1 HG00733.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.186-2282C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412151 | ||||||
| chr1:235412152
|
C | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(13): Show | 16 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-2281C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412152 | ||||||
| chr1:235412156
|
C | CG | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.186-2277_186-2276i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412156 | ||||||
| chr1:235412156
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0073 | 2 | HG03017.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.186-2277C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412156 | ||||||
| chr1:235412157
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(12): Show | 15 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.186-2276C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412157 | ||||||
| chr1:235412157
|
CT | C | 4 | a0001c0001t0004g0050a0001c0001t0004g0133a0001c0001t0004g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2275delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412157 | ||||||
| chr1:235412158
|
T | C | 1 | a0001c0001t0004g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.186-2275T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412158 | ||||||
| chr1:235412158
|
T | TC | 23 | a0001c0001t0002g0198a0001c0001t0005g0124a0001c0001t0005g0160others(20): Show | 23 | HG00621.hp1 HG00733.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.186-2271dupC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412158 | |||||
| chr1:235412159
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(13): Show | 16 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-2274C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412159 | ||||||
| chr1:235412161
|
C | T | 1 | a0001c0001t0004g0197 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.186-2272C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412161 | ||||||
| chr1:235412163
|
T | C | 45 | a0001c0001t0001g0097a0001c0001t0002g0179a0001c0001t0002g0198others(42): Show | 45 | HG00621.hp1 HG00642.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.186-2270T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
T | TCCCCCTC others(270): Show |
1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.186-2270_186-2269i others(279): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
T | TCCCCCTC others(292): Show |
1 | a0001c0001t0001g0053 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.186-2270_186-2269i others(301): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
T | TCCCCCTC others(292): Show |
1 | a0001c0001t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.186-2270_186-2269i others(301): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
T | TCCCCCTC others(309): Show |
1 | a0001c0001t0006g0084 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.186-2270_186-2269i others(318): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
T | TCCCCCTC others(251): Show |
2 | a0001c0001t0013g0130a0001c0001t0013g0131 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.186-2270_186-2269i others(260): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
T | TCCCCCTC others(289): Show |
1 | a0001c0001t0001g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.186-2270_186-2269i others(298): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
T | TCCCCCTC others(308): Show |
1 | a0001c0001t0001g0025 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.186-2270_186-2269i others(317): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
T | TCCCCCTC others(307): Show |
1 | a0001c0001t0001g0026 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.186-2270_186-2269i others(316): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
T | TTCCCCTC others(375): Show |
1 | a0001c0001t0002g0246 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(384): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412163 | |||||
| chr1:235412163
|
TTC | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.186-2269_186-2268d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412163
|
TTCC | T | 4 | a0001c0001t0004g0050a0001c0001t0004g0133a0001c0001t0004g0158others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2269_186-2267d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412163 | ||||||
| chr1:235412164
|
T | C | 37 | a0001c0001t0001g0012a0001c0001t0001g0073a0001c0001t0001g0145others(34): Show | 37 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-2269T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412164 | ||||||
| chr1:235412165
|
C | CTCCT | 14 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(11): Show | 14 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.186-2268_186-2267i others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412165 | ||||||
| chr1:235412166
|
C | CCATCACC others(382): Show |
1 | a0001c0001t0006g0054 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.186-2266_186-2265i others(391): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCATCCCT others(343): Show |
1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.186-2266_186-2265i others(352): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCCCTCC others(3): Show |
3 | a0001c0001t0002g0198a0001c0001t0002g0246a0001c0001t0015g0241 | 3 | HG00621.hp1 NA18983.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.186-2257_186-2248d others(12): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCT | 9 | a0001c0001t0002g0190a0001c0001t0002g0227a0001c0001t0002g0228others(6): Show | 9 | HG01243.hp2 HG02071.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-2265_186-2264i others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(376): Show |
1 | a0001c0001t0002g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(385): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(374): Show |
1 | a0001c0001t0002g0055 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(383): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(374): Show |
1 | a0001c0001t0002g0233 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(383): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(364): Show |
1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(373): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(411): Show |
1 | a0001c0001t0011g0223 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(420): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(397): Show |
1 | a0001c0001t0002g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(406): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(384): Show |
1 | a0001c0001t0002g0226 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(393): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(417): Show |
1 | a0001c0001t0002g0210 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(426): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(384): Show |
1 | a0001c0001t0002g0244 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(393): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(380): Show |
1 | a0001c0001t0002g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(420): Show |
1 | a0001c0001t0011g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(429): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(436): Show |
1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(445): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(393): Show |
1 | a0001c0001t0001g0258 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(402): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(375): Show |
1 | a0001c0001t0002g0106 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(384): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(367): Show |
5 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(2): Show | 5 | HG01346.hp1 HG02523.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-2265_186-2264i others(376): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(379): Show |
1 | a0001c0001t0002g0245 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(380): Show |
1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(380): Show |
1 | a0001c0001t0021g0199 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(374): Show |
2 | a0001c0001t0002g0090a0001c0001t0002g0216 | 2 | HG00639.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.186-2265_186-2264i others(383): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(380): Show |
1 | a0001c0001t0002g0236 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(379): Show |
25 | a0001c0001t0002g0046a0001c0001t0002g0088a0001c0001t0002g0092others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(384): Show |
1 | a0001c0001t0002g0237 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(393): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(372): Show |
1 | a0001c0001t0002g0209 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(381): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(379): Show |
1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(378): Show |
1 | a0001c0001t0002g0220 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.186-2265_186-2264i others(387): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(378): Show |
1 | a0001c0001t0002g0201 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(387): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(379): Show |
2 | a0001c0001t0002g0255a0001c0001t0002g0256 | 2 | HG01496.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(367): Show |
1 | a0001c0001t0002g0222 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(376): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(301): Show |
1 | a0001c0001t0002g0231 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(380): Show |
1 | a0001c0001t0002g0202 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(389): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(379): Show |
2 | a0001c0001t0002g0034a0001c0001t0002g0093 | 2 | NA18950.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.186-2265_186-2264i others(388): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCCTCCCC others(294): Show |
1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-2265_186-2264i others(303): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCTCCTCC others(69): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2266_186-2265i others(78): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCTCCTCC others(52): Show |
2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-2266_186-2265i others(61): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | CCTCCTCC others(35): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-2266_186-2265i others(44): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412166 | |||||
| chr1:235412166
|
C | T | 21 | a0001c0001t0002g0179a0001c0001t0004g0011a0001c0001t0004g0027others(18): Show | 21 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.186-2267C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412166 | ||||||
| chr1:235412169
|
C | CCTCCCCT others(23): Show |
2 | a0001c0001t0013g0130a0001c0001t0013g0131 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.186-2253_186-2252i others(32): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412169 | |||||
| chr1:235412169
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0006g0054 | 2 | NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.186-2264C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412169 | ||||||
| chr1:235412170
|
C | T | 15 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0136others(12): Show | 15 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.186-2263C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412170 | ||||||
| chr1:235412171
|
T | C | 1 | a0001c0001t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.186-2262T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412171 | ||||||
| chr1:235412172
|
C | CCCGCTCC others(401): Show |
1 | a0001c0001t0002g0228 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.186-2259_186-2258i others(410): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412172 | |||||
| chr1:235412174
|
C | CG | 5 | a0001c0001t0002g0190a0001c0001t0002g0227a0001c0001t0002g0249others(2): Show | 5 | HG02071.hp1 HG02300.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-2259_186-2258i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412174 | ||||||
| chr1:235412174
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.186-2259C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412174 | ||||||
| chr1:235412176
|
T | TCCCCATC others(302): Show |
1 | a0001c0001t0014g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-2253_186-2252i others(311): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412176 | |||||
| chr1:235412181
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0006g0054a0003c0004t0031g0016 | 3 | NA18522.hp2 NA18994.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.186-2252T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412181 | ||||||
| chr1:235412181
|
TC | T | 20 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0163others(17): Show | 20 | HG00733.hp2 HG01261.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.186-2247delC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412181 | |||||
| chr1:235412182
|
C | CCCCATCC others(309): Show |
1 | a0001c0001t0003g0103 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(318): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(358): Show |
1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(367): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(316): Show |
1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(325): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(301): Show |
1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(301): Show |
1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
1 | a0001c0001t0003g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(302): Show |
1 | a0001c0001t0003g0015 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(311): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(296): Show |
1 | a0001c0001t0001g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(305): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(300): Show |
1 | a0001c0001t0003g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(301): Show |
1 | a0001c0001t0003g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(301): Show |
1 | a0001c0001t0003g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(310): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(300): Show |
2 | a0001c0001t0001g0062a0001c0001t0003g0035 | 2 | HG04199.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(300): Show |
1 | a0001c0001t0001g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(300): Show |
1 | a0001c0001t0001g0078 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
1 | a0001c0001t0003g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
1 | a0001c0001t0001g0032 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(300): Show |
1 | a0001c0001t0028g0070 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(300): Show |
1 | a0001c0001t0001g0221 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
53 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0037others(50): Show | 53 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(300): Show |
1 | a0001c0001t0001g0192 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(309): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(298): Show |
1 | a0001c0001t0003g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(270): Show |
1 | a0001c0001t0013g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(279): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(320): Show |
1 | a0001c0001t0003g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(329): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(298): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0105a0001c0001t0007g0142 | 3 | HG02300.hp1 NA18950.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(302): Show |
1 | a0001c0001t0032g0065 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(311): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(298): Show |
3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0114 | 3 | HG01070.hp1 HG01071.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(297): Show |
1 | a0001c0001t0003g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(306): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(297): Show |
1 | a0001c0001t0001g0087 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(306): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(296): Show |
1 | a0001c0001t0001g0148 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(305): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(298): Show |
1 | a0001c0001t0001g0028 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(297): Show |
1 | a0001c0001t0001g0064 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(306): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
1 | a0001c0001t0003g0151 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(298): Show |
1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(245): Show |
1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(254): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
1 | a0001c0001t0001g0003 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(298): Show |
1 | a0001c0001t0001g0097 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(307): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCATCC others(299): Show |
1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.186-2248_186-2247i others(308): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCTCCC others(105): Show |
4 | a0001c0001t0004g0006a0001c0001t0009g0008a0001c0001t0009g0020others(1): Show | 4 | HG01109.hp1 HG02572.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-2248_186-2247i others(114): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | CCCCTCCC others(115): Show |
1 | a0001c0001t0017g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.186-2248_186-2247i others(124): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412182 | |||||
| chr1:235412182
|
C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-2251C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412182 | ||||||
| chr1:235412185
|
C | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(11): Show | 14 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.186-2248C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412185 | ||||||
| chr1:235412186
|
C | A | 10 | a0001c0001t0001g0121a0001c0001t0005g0162a0001c0001t0006g0161others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-2247C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412186 | ||||||
| chr1:235412192
|
T | C | 1 | a0001c0001t0011g0223 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.186-2241T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412192 | ||||||
| chr1:235412192
|
T | TCCCTTCC others(283): Show |
1 | a0001c0001t0034g0031 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.186-2238_186-2237i others(292): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412192 | |||||
| chr1:235412192
|
T | TCCCTTCC others(282): Show |
1 | a0001c0001t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.186-2238_186-2237i others(291): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412192 | |||||
| chr1:235412192
|
T | TCCCTTCC others(212): Show |
1 | a0001c0001t0006g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-2238_186-2237i others(221): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412192 | |||||
| chr1:235412192
|
TC | T | 5 | a0001c0001t0004g0006a0001c0001t0009g0008a0001c0001t0009g0020others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-2236delC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412192 | |||||
| chr1:235412193
|
C | CCCCCTCC others(106): Show |
1 | a0001c0001t0004g0041 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(115): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(351): Show |
1 | a0001c0001t0002g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(360): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(358): Show |
1 | a0001c0001t0002g0227 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(367): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(343): Show |
1 | a0001c0001t0002g0249 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.186-2237_186-2236i others(352): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(348): Show |
1 | a0001c0001t0011g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(357): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(357): Show |
1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(366): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(33): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(42): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(38): Show |
2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-2237_186-2236i others(47): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(126): Show |
2 | a0001c0001t0004g0197a0001c0001t0004g0204 | 2 | HG02735.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.186-2237_186-2236i others(135): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(105): Show |
1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(114): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(110): Show |
11 | a0001c0001t0002g0179a0001c0001t0004g0039a0001c0001t0004g0040others(8): Show | 11 | HG00642.hp1 HG01891.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.186-2237_186-2236i others(119): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(126): Show |
1 | a0001c0001t0004g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(135): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(110): Show |
1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(119): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(115): Show |
2 | a0001c0001t0004g0042a0001c0001t0004g0134 | 2 | HG01106.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.186-2237_186-2236i others(124): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(120): Show |
2 | a0001c0001t0004g0027a0001c0001t0004g0194 | 2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.186-2237_186-2236i others(129): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(166): Show |
1 | a0001c0001t0004g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.186-2237_186-2236i others(175): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(125): Show |
1 | a0001c0001t0004g0043 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(134): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(145): Show |
1 | a0001c0001t0004g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.186-2237_186-2236i others(154): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(115): Show |
1 | a0001c0001t0004g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.186-2237_186-2236i others(124): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(74): Show |
1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(83): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCCTCCC others(79): Show |
1 | a0001c0001t0004g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.186-2237_186-2236i others(88): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCTTCCC others(215): Show |
1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-2238_186-2237i others(224): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCTTCCC others(208): Show |
4 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-2238_186-2237i others(217): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCTTCCC others(231): Show |
1 | a0001c0001t0016g0183 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.186-2238_186-2237i others(240): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412193
|
C | CCCTTCCC others(219): Show |
1 | a0001c0001t0005g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.186-2238_186-2237i others(228): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412193 | |||||
| chr1:235412197
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0006g0044 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.186-2236C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412197 | ||||||
| chr1:235412198
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0006g0044 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.186-2235T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412198 | ||||||
| chr1:235412198
|
T | TCCCCTC | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.186-2231_186-2226d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412198
|
T | TCCCCTCC others(322): Show |
1 | a0001c0001t0012g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(331): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412198
|
T | TCCCCTCC others(322): Show |
1 | a0001c0001t0003g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(331): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412198
|
T | TCCCCTCC others(327): Show |
1 | a0005c0008t0001g0242 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.186-2221_186-2220i others(336): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412198
|
T | TCCCCTCC others(319): Show |
1 | a0001c0001t0007g0060 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(328): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412198
|
T | TCCCCTCC others(319): Show |
1 | a0001c0001t0012g0014 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(328): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412198
|
T | TCCCCTCC others(318): Show |
1 | a0001c0001t0001g0136 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.186-2221_186-2220i others(327): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412198
|
T | TCCCCTCC others(323): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0138a0001c0001t0001g0140others(4): Show | 7 | HG01891.hp2 HG01981.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-2221_186-2220i others(332): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412198
|
T | TCCCCTCC others(316): Show |
1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.186-2221_186-2220i others(325): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412198
|
T | TCCTCCCC others(3): Show |
1 | a0001c0001t0014g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-2233_186-2232i others(12): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412198 | |||||
| chr1:235412203
|
T | C | 1 | a0001c0001t0016g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.186-2230T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412203 | ||||||
| chr1:235412204
|
C | CCCCTCCC others(19): Show |
1 | a0001c0001t0011g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.186-2210_186-2209i others(28): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412204 | |||||
| chr1:235412208
|
T | TCCCTCCC others(4): Show |
1 | a0001c0001t0014g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-2222_186-2221i others(13): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412208 | |||||
| chr1:235412213
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.186-2220C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412213 | ||||||
| chr1:235412214
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.186-2219T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412214 | ||||||
| chr1:235412214
|
T | TCCCCTCC others(21): Show |
1 | a0001c0001t0002g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.186-2210_186-2209i others(30): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412214 | |||||
| chr1:235412219
|
T | C | 1 | a0001c0001t0014g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.186-2214T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412219 | ||||||
| chr1:235412223
|
C | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-2210C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412223 | ||||||
| chr1:235412224
|
T | TCCCCCTC others(10): Show |
1 | a0001c0001t0002g0227 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.186-2198_186-2197i others(19): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412224 | |||||
| chr1:235412224
|
TCCCCC | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0013g0130others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-2208_186-2204d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412224 | ||||||
| chr1:235412225
|
C | CCCCTCCC others(15): Show |
1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-2205_186-2204i others(24): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412225 | |||||
| chr1:235412225
|
C | CCCCTCCC others(123): Show |
1 | a0001c0001t0004g0203 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.186-2205_186-2204i others(132): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412225 | |||||
| chr1:235412228
|
C | CTCCCCTC others(118): Show |
1 | a0001c0001t0004g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.186-2205_186-2204i others(127): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412228 | ||||||
| chr1:235412229
|
C | CTCCCCTC others(4): Show |
26 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0121others(23): Show | 26 | HG01106.hp1 HG01109.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.186-2198_186-2197i others(13): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412229 | |||||
| chr1:235412229
|
C | CTCCCCTC others(19): Show |
1 | a0001c0001t0006g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-2198_186-2197i others(28): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412229 | |||||
| chr1:235412229
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.186-2204C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412229 | ||||||
| chr1:235412230
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.186-2203T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412230 | ||||||
| chr1:235412230
|
T | TCCCCCCT others(11): Show |
32 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0011others(29): Show | 32 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.186-2199_186-2198i others(20): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412230 | |||||
| chr1:235412230
|
T | TCCCCTCC others(32): Show |
2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.186-2198_186-2197i others(41): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412230 | |||||
| chr1:235412230
|
T | TCCCCTCC others(32): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-2198_186-2197i others(41): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412230 | |||||
| chr1:235412230
|
T | TCCCCTGC others(105): Show |
1 | a0001c0001t0004g0007 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.186-2198_186-2197i others(114): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412230 | |||||
| chr1:235412234
|
C | CTCCCCTC others(9): Show |
1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.186-2198_186-2197i others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412234 | |||||
| chr1:235412236
|
T | A | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(1): Show | 4 | HG02523.hp1 NA18943.hp1 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-2197T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412236 | ||||||
| chr1:235412236
|
T | C | 1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.186-2197T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412236 | ||||||
| chr1:235412237
|
C | A | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.186-2196C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412237 | ||||||
| chr1:235412269
|
C | T | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.186-2164C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412269 | ||||||
| chr1:235412270
|
G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.186-2163G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412270 | ||||||
| chr1:235412506
|
A | C | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.186-1927A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412506 | ||||||
| chr1:235412519
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.186-1914C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412519 | ||||||
| chr1:235412558
|
C | T | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0122others(1): Show | 4 | HG02523.hp1 HG02809.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-1875C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412558 | ||||||
| chr1:235412567
|
C | T | 3 | a0001c0003t0001g0051a0001c0003t0001g0052a0001c0003t0001g0135 | 3 | HG02809.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.186-1866C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412567 | ||||||
| chr1:235412633
|
T | C | 1 | a0001c0001t0011g0247 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.186-1800T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412633 | ||||||
| chr1:235412745
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-1688C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412745 | ||||||
| chr1:235412797
|
AATTATT | A | 39 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(36): Show | 39 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.186-1623_186-1618d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235412797 | |||||
| chr1:235412857
|
G | A | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-1576G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235412857 | ||||||
| chr1:235413007
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-1426T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413007 | ||||||
| chr1:235413172
|
G | A | 39 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(36): Show | 39 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.186-1261G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413172 | ||||||
| chr1:235413335
|
G | A | 1 | a0001c0001t0027g0128 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.186-1098G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413335 | ||||||
| chr1:235413363
|
T | TA | 24 | a0001c0001t0001g0078a0001c0001t0001g0136a0001c0001t0001g0146others(21): Show | 24 | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.186-1052dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413363 | |||||
| chr1:235413363
|
TA | T | 16 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0074others(13): Show | 16 | HG01070.hp2 HG01168.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.186-1052delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413363 | |||||
| chr1:235413499
|
TA | T | 3 | a0001c0001t0001g0028a0001c0001t0003g0103a0001c0001t0006g0161 | 3 | HG01169.hp1 HG02451.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.186-929delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413499 | |||||
| chr1:235413569
|
A | G | 17 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(14): Show | 17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.186-864A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413569 | ||||||
| chr1:235413634
|
G | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.186-799G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413634 | ||||||
| chr1:235413662
|
C | CA | 43 | a0001c0001t0001g0073a0001c0001t0002g0179a0001c0001t0002g0200others(40): Show | 43 | HG00558.hp2 HG00642.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.186-759dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413662 | |||||
| chr1:235413676
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.186-757A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413676 | ||||||
| chr1:235413752
|
CT | C | 38 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(35): Show | 38 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.186-672delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413752 | |||||
| chr1:235413846
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-587C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413846 | ||||||
| chr1:235413848
|
A | AT | 11 | a0001c0001t0002g0106a0001c0001t0002g0179a0001c0001t0002g0190others(8): Show | 11 | HG00642.hp1 HG01106.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.186-560dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413848 | |||||
| chr1:235413848
|
AT | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.186-560delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413848 | |||||
| chr1:235413848
|
ATT | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0058a0001c0001t0001g0071others(16): Show | 19 | HG01070.hp1 HG01243.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.186-561_186-560del others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr1 | 235413848 | |||||
| chr1:235413893
|
C | T | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.186-540C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235413893 | ||||||
| chr1:235414327
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.186-106T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 3/16 | chr1 | 235414327 | ||||||
| chr1:235414953
|
T | C | 6 | a0001c0001t0008g0024a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.371+335T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235414953 | ||||||
| chr1:235415140
|
T | G | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.371+522T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415140 | ||||||
| chr1:235415448
|
CTGGCCAG others(4): Show |
C | 2 | a0001c0001t0002g0201a0001c0001t0002g0233 | 2 | HG01069.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.371+833_371+843del others(11): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235415448 | |||||
| chr1:235415491
|
C | T | 1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.371+873C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415491 | ||||||
| chr1:235415548
|
T | C | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.371+930T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415548 | ||||||
| chr1:235415879
|
G | A | 35 | a0001c0001t0002g0179a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00642.hp1 HG00741.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.371+1261G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415879 | ||||||
| chr1:235415926
|
T | C | 1 | a0001c0001t0003g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+1308T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235415926 | ||||||
| chr1:235416104
|
C | T | 2 | a0001c0001t0001g0057a0001c0005t0038g0155 | 2 | HG01070.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.371+1486C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416104 | ||||||
| chr1:235416168
|
C | CA | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.371+1568dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416168 | |||||
| chr1:235416168
|
C | CAA | 27 | a0001c0001t0001g0026a0001c0001t0001g0073a0001c0001t0001g0078others(24): Show | 27 | HG00558.hp1 HG00621.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.371+1567_371+1568d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416168 | |||||
| chr1:235416168
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.371+1558_371+1568d others(13): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416168 | |||||
| chr1:235416168
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0262 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.371+1555_371+1568d others(16): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416168 | |||||
| chr1:235416412
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.371+1794A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416412 | ||||||
| chr1:235416523
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.371+1905C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416523 | ||||||
| chr1:235416541
|
CA | C | 15 | a0001c0001t0001g0053a0001c0001t0001g0073a0001c0001t0001g0095others(12): Show | 15 | HG01106.hp2 HG01168.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.371+1935delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416541 | |||||
| chr1:235416541
|
CAA | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.371+1934_371+1935d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235416541 | |||||
| chr1:235416554
|
C | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.371+1936C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416554 | ||||||
| chr1:235416597
|
T | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.371+1979T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416597 | ||||||
| chr1:235416876
|
G | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.371+2258G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235416876 | ||||||
| chr1:235417067
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.372-2406A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417067 | ||||||
| chr1:235417284
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.372-2189C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417284 | ||||||
| chr1:235417331
|
G | C | 34 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(31): Show | 34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.372-2142G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417331 | ||||||
| chr1:235417356
|
T | C | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.372-2117T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417356 | ||||||
| chr1:235417412
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.372-2061A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417412 | ||||||
| chr1:235417462
|
A | G | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.372-2011A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417462 | ||||||
| chr1:235417506
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.372-1967A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417506 | ||||||
| chr1:235417514
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.372-1959C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417514 | ||||||
| chr1:235417613
|
G | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.372-1860G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417613 | ||||||
| chr1:235417760
|
C | CT | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.372-1705dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235417760 | |||||
| chr1:235417845
|
C | T | 1 | a0001c0001t0003g0066 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.372-1628C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417845 | ||||||
| chr1:235417951
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.372-1522T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235417951 | ||||||
| chr1:235418096
|
C | T | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.372-1377C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418096 | ||||||
| chr1:235418168
|
C | T | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.372-1305C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418168 | ||||||
| chr1:235418186
|
C | T | 1 | a0001c0001t0004g0178 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.372-1287C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418186 | ||||||
| chr1:235418207
|
T | C | 1 | a0001c0001t0002g0234 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.372-1266T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418207 | ||||||
| chr1:235418222
|
G | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.372-1251G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418222 | ||||||
| chr1:235418487
|
TTAACAAA others(15): Show |
T | 1 | a0001c0001t0002g0256 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.372-984_372-963del others(22): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr1 | 235418487 | |||||
| chr1:235418558
|
G | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | NA18954.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.372-915G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418558 | ||||||
| chr1:235418643
|
G | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.372-830G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418643 | ||||||
| chr1:235418957
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.372-516A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235418957 | ||||||
| chr1:235419073
|
A | G | 2 | a0001c0005t0035g0260a0001c0005t0038g0155 | 2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.372-400A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235419073 | ||||||
| chr1:235419131
|
T | C | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.372-342T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235419131 | ||||||
| chr1:235419145
|
T | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.372-328T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235419145 | ||||||
| chr1:235419228
|
C | T | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.372-245C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 4/16 | chr1 | 235419228 | ||||||
| chr1:235419609
|
T | G | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+48T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419609 | ||||||
| chr1:235419761
|
C | G | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+200C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419761 | ||||||
| chr1:235419818
|
T | G | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+257T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419818 | ||||||
| chr1:235419869
|
C | T | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+308C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419869 | ||||||
| chr1:235419888
|
A | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.460+327A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235419888 | ||||||
| chr1:235420039
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.460+478C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420039 | ||||||
| chr1:235420079
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0003g0076a0001c0001t0003g0080 | 3 | HG02155.hp1 NA18982.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.460+518T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420079 | ||||||
| chr1:235420109
|
T | G | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+548T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420109 | ||||||
| chr1:235420169
|
C | T | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.460+608C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420169 | ||||||
| chr1:235420274
|
T | C | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+713T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420274 | ||||||
| chr1:235420296
|
T | C | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.460+735T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420296 | ||||||
| chr1:235420318
|
C | CT | 39 | a0001c0001t0001g0171a0001c0001t0002g0246a0001c0001t0002g0257others(36): Show | 39 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.460+771dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235420318 | |||||
| chr1:235420375
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.460+814C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420375 | ||||||
| chr1:235420400
|
C | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 84 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.460+839C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420400 | ||||||
| chr1:235420458
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.460+897G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420458 | ||||||
| chr1:235420463
|
C | T | 34 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(31): Show | 34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.460+902C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420463 | ||||||
| chr1:235420464
|
G | A | 31 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(28): Show | 31 | HG00733.hp2 HG01070.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.460+903G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420464 | ||||||
| chr1:235420481
|
A | AT | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.460+940dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235420481 | |||||
| chr1:235420481
|
A | ATT | 15 | a0001c0001t0001g0062a0001c0001t0001g0073a0001c0001t0001g0117others(12): Show | 15 | HG01109.hp1 HG02027.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.460+939_460+940dup others(2): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235420481 | |||||
| chr1:235420617
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.460+1056G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420617 | ||||||
| chr1:235420619
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.460+1058G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420619 | ||||||
| chr1:235420735
|
C | A | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1174C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420735 | ||||||
| chr1:235420740
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+1179C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420740 | ||||||
| chr1:235420878
|
G | A | 34 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(31): Show | 34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.460+1317G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235420878 | ||||||
| chr1:235421043
|
G | T | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1482G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421043 | ||||||
| chr1:235421078
|
T | C | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.460+1517T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421078 | ||||||
| chr1:235421085
|
T | C | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1524T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421085 | ||||||
| chr1:235421108
|
G | A | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1547G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421108 | ||||||
| chr1:235421228
|
C | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.460+1667C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421228 | ||||||
| chr1:235421233
|
C | CTTG | 2 | a0001c0001t0002g0201a0001c0001t0002g0233 | 2 | HG01069.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.460+1674_460+1676d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235421233 | |||||
| chr1:235421245
|
A | C | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.460+1684A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421245 | ||||||
| chr1:235421399
|
C | T | 3 | a0001c0001t0006g0044a0001c0001t0026g0129a0001c0001t0027g0128 | 3 | HG03540.hp2 HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+1838C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421399 | ||||||
| chr1:235421460
|
T | C | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1899T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421460 | ||||||
| chr1:235421524
|
C | A | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+1963C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421524 | ||||||
| chr1:235421640
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+2079C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421640 | ||||||
| chr1:235421642
|
G | A | 1 | a0001c0001t0005g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.460+2081G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421642 | ||||||
| chr1:235421772
|
C | T | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+2211C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421772 | ||||||
| chr1:235421802
|
C | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+2241C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235421802 | ||||||
| chr1:235422093
|
A | G | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+2532A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422093 | ||||||
| chr1:235422123
|
A | G | 4 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.460+2562A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422123 | ||||||
| chr1:235422299
|
G | C | 2 | a0001c0005t0035g0260a0001c0005t0038g0155 | 2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.460+2738G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422299 | ||||||
| chr1:235422328
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.460+2767A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422328 | ||||||
| chr1:235422409
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.460+2848A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422409 | ||||||
| chr1:235422543
|
G | A | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+2982G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422543 | ||||||
| chr1:235422783
|
C | T | 1 | a0001c0001t0004g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.460+3222C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422783 | ||||||
| chr1:235422831
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.460+3270A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235422831 | ||||||
| chr1:235423015
|
T | A | 2 | a0001c0005t0035g0260a0001c0005t0038g0155 | 2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.460+3454T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423015 | ||||||
| chr1:235423016
|
T | A | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+3455T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423016 | ||||||
| chr1:235423061
|
C | T | 31 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(28): Show | 31 | HG00733.hp2 HG01070.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.460+3500C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423061 | ||||||
| chr1:235423116
|
T | G | 31 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(28): Show | 31 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.460+3555T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423116 | ||||||
| chr1:235423195
|
G | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.460+3634G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423195 | ||||||
| chr1:235423229
|
C | T | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.460+3668C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423229 | ||||||
| chr1:235423298
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.460+3737C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423298 | ||||||
| chr1:235423428
|
G | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.461-3712G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423428 | ||||||
| chr1:235423482
|
T | A | 1 | a0001c0001t0002g0255 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.461-3658T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423482 | ||||||
| chr1:235423578
|
T | C | 29 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(26): Show | 29 | HG00733.hp2 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.461-3562T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423578 | ||||||
| chr1:235423626
|
C | G | 1 | a0001c0001t0005g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.461-3514C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423626 | ||||||
| chr1:235423659
|
A | G | 26 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(23): Show | 26 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.461-3481A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423659 | ||||||
| chr1:235423757
|
C | T | 2 | a0001c0001t0013g0130a0001c0001t0013g0131 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.461-3383C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423757 | ||||||
| chr1:235423797
|
A | G | 6 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-3343A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423797 | ||||||
| chr1:235423833
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.461-3307G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423833 | ||||||
| chr1:235423858
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.461-3282A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423858 | ||||||
| chr1:235423946
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.461-3194G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423946 | ||||||
| chr1:235423955
|
C | G | 6 | a0001c0001t0003g0036a0001c0001t0003g0102a0001c0001t0003g0103others(3): Show | 6 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.461-3185C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235423955 | ||||||
| chr1:235424094
|
G | T | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-3046G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424094 | ||||||
| chr1:235424193
|
G | A | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.461-2947G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424193 | ||||||
| chr1:235424202
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.461-2938G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424202 | ||||||
| chr1:235424230
|
T | G | 3 | a0001c0001t0005g0187a0003c0004t0031g0016a0003c0004t0037g0172 | 3 | HG02109.hp1 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-2910T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424230 | ||||||
| chr1:235424322
|
C | CT | 7 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0227others(4): Show | 7 | NA18949.hp1 NA18951.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.461-2798dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235424322 | |||||
| chr1:235424322
|
CT | C | 8 | a0001c0001t0001g0262a0001c0001t0003g0076a0001c0001t0003g0102others(5): Show | 8 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.461-2798delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr1 | 235424322 | |||||
| chr1:235424388
|
G | A | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-2752G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424388 | ||||||
| chr1:235424427
|
G | GC | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.461-2713_461-2712i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424427 | ||||||
| chr1:235424502
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.461-2638G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235424502 | ||||||
| chr1:235425094
|
C | A | 34 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(31): Show | 34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.461-2046C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425094 | ||||||
| chr1:235425096
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.461-2044C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425096 | ||||||
| chr1:235425200
|
C | T | 2 | a0001c0001t0004g0042a0001c0001t0004g0134 | 2 | HG01106.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.461-1940C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425200 | ||||||
| chr1:235425485
|
G | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.461-1655G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425485 | ||||||
| chr1:235425616
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.461-1524C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425616 | ||||||
| chr1:235425617
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.461-1523G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425617 | ||||||
| chr1:235425650
|
C | T | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.461-1490C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425650 | ||||||
| chr1:235425799
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.461-1341G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425799 | ||||||
| chr1:235425987
|
T | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-1153T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235425987 | ||||||
| chr1:235426088
|
C | A | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0141 | 3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.461-1052C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426088 | ||||||
| chr1:235426133
|
G | A | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-1007G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426133 | ||||||
| chr1:235426166
|
G | C | 4 | a0001c0001t0003g0102a0001c0001t0003g0103a0001c0001t0003g0110others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.461-974G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426166 | ||||||
| chr1:235426184
|
T | C | 1 | a0001c0001t0001g0087 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.461-956T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426184 | ||||||
| chr1:235426464
|
A | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-676A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426464 | ||||||
| chr1:235426533
|
C | T | 1 | a0001c0001t0028g0070 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.461-607C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426533 | ||||||
| chr1:235426793
|
G | A | 1 | a0001c0007t0001g0061 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.461-347G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426793 | ||||||
| chr1:235426919
|
T | C | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-221T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426919 | ||||||
| chr1:235426936
|
G | A | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.461-204G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426936 | ||||||
| chr1:235426950
|
A | T | 1 | a0001c0001t0004g0007 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.461-190A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426950 | ||||||
| chr1:235426963
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.461-177G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 5/16 | chr1 | 235426963 | ||||||
| chr1:235427244
|
G | A | 34 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(31): Show | 34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
splice_region_variant&intron_variant | LOW | c.560+5G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427244 | ||||||
| chr1:235427447
|
A | G | 1 | a0001c0001t0002g0239 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.560+208A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427447 | ||||||
| chr1:235427470
|
G | A | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+231G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427470 | ||||||
| chr1:235427471
|
C | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+232C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427471 | ||||||
| chr1:235427504
|
A | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+265A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427504 | ||||||
| chr1:235427530
|
A | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+291A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427530 | ||||||
| chr1:235427622
|
A | T | 58 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(55): Show | 58 | HG00733.hp2 HG00741.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.560+383A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427622 | ||||||
| chr1:235427645
|
A | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+406A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427645 | ||||||
| chr1:235427740
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.560+501G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427740 | ||||||
| chr1:235427828
|
T | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+589T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427828 | ||||||
| chr1:235427945
|
G | T | 1 | a0001c0001t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.560+706G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235427945 | ||||||
| chr1:235428024
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0114 | 2 | HG01123.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.560+785C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428024 | ||||||
| chr1:235428025
|
G | A | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.560+786G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428025 | ||||||
| chr1:235428047
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.560+808A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428047 | ||||||
| chr1:235428050
|
C | T | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+811C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428050 | ||||||
| chr1:235428095
|
C | T | 1 | a0001c0001t0003g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.560+856C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428095 | ||||||
| chr1:235428184
|
C | T | 1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.560+945C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428184 | ||||||
| chr1:235428197
|
A | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+958A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428197 | ||||||
| chr1:235428217
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0114 | 2 | HG01123.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.560+978G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428217 | ||||||
| chr1:235428310
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.560+1071C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428310 | ||||||
| chr1:235428370
|
C | T | 2 | a0001c0001t0002g0253a0001c0001t0002g0259 | 2 | NA18951.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.560+1131C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428370 | ||||||
| chr1:235428380
|
C | T | 2 | a0001c0001t0002g0198a0001c0001t0015g0241 | 2 | HG00621.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.560+1141C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428380 | ||||||
| chr1:235428488
|
T | A | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.560+1249T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428488 | ||||||
| chr1:235428586
|
T | A | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.560+1347T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428586 | ||||||
| chr1:235428595
|
C | A | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.560+1356C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428595 | ||||||
| chr1:235428631
|
C | CTTTA | 25 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0163others(22): Show | 25 | HG00733.hp2 HG01109.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.560+1420_560+1423d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | |||||
| chr1:235428631
|
C | CTTTATTT others(1): Show |
100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0010others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.560+1416_560+1423d others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | |||||
| chr1:235428631
|
C | CTTTATTT others(5): Show |
20 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0037others(17): Show | 20 | HG01167.hp1 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.560+1412_560+1423d others(14): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | |||||
| chr1:235428631
|
C | CTTTATTT others(9): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0064others(1): Show | 4 | HG00738.hp1 HG01099.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.560+1408_560+1423d others(18): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | |||||
| chr1:235428631
|
C | CTTTATTT others(13): Show |
5 | a0001c0001t0001g0057a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01070.hp1 HG01071.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.560+1404_560+1423d others(22): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | |||||
| chr1:235428631
|
C | CTTTATTT others(17): Show |
1 | a0001c0003t0001g0052 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.560+1400_560+1423d others(26): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | |||||
| chr1:235428631
|
CTTTATTT others(1): Show |
C | 34 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(31): Show | 34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.560+1416_560+1423d others(10): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428631 | |||||
| chr1:235428800
|
C | T | 2 | a0001c0005t0035g0260a0001c0005t0038g0155 | 2 | HG01070.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.560+1561C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428800 | ||||||
| chr1:235428830
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.560+1591G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428830 | ||||||
| chr1:235428844
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.560+1605A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428844 | ||||||
| chr1:235428873
|
A | T | 1 | a0001c0001t0003g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.560+1634A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428873 | ||||||
| chr1:235428969
|
G | GTATATA | 4 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-1724_561-1719d others(8): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428969 | |||||
| chr1:235428969
|
G | GTGTGTGT others(25): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.560+1731_560+1732i others(34): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428969 | |||||
| chr1:235428969
|
G | GTGTGTGT others(27): Show |
1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.560+1731_560+1732i others(36): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428969 | |||||
| chr1:235428971
|
A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.560+1732A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428971 | ||||||
| chr1:235428983
|
A | AT | 17 | a0001c0001t0004g0006a0001c0001t0004g0027a0001c0001t0004g0038others(14): Show | 17 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.561-1721dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428983 | |||||
| chr1:235428983
|
ATAT | A | 14 | a0001c0001t0005g0124a0001c0001t0005g0162a0001c0001t0005g0163others(11): Show | 14 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.561-1720_561-1718d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428983 | |||||
| chr1:235428985
|
A | AT | 12 | a0001c0001t0002g0198a0001c0001t0002g0227a0001c0001t0004g0007others(9): Show | 12 | HG00621.hp1 HG01361.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.561-1700dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428985 | |||||
| chr1:235428985
|
A | T | 24 | a0001c0001t0002g0195a0001c0001t0002g0207a0001c0001t0002g0214others(21): Show | 24 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.561-1720A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428985 | ||||||
| chr1:235428985
|
AT | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.561-1700delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428985 | |||||
| chr1:235428985
|
ATT | A | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0006g0161others(2): Show | 5 | HG01099.hp2 HG02451.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-1701_561-1700d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428985 | |||||
| chr1:235428985
|
ATTT | A | 8 | a0001c0001t0005g0160a0001c0001t0005g0184a0001c0001t0008g0024others(5): Show | 8 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.561-1702_561-1700d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235428985 | |||||
| chr1:235428986
|
T | TA | 4 | a0001c0001t0002g0046a0001c0001t0004g0158a0001c0001t0004g0180others(1): Show | 4 | HG02976.hp2 HG04228.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-1719_561-1718i others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428986 | ||||||
| chr1:235428986
|
T | TATA | 4 | a0001c0001t0006g0044a0001c0001t0026g0129a0001c0001t0027g0128others(1): Show | 4 | HG01070.hp2 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.561-1719_561-1718i others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428986 | ||||||
| chr1:235428987
|
T | A | 50 | a0001c0001t0001g0105a0001c0001t0001g0113a0001c0001t0001g0117others(47): Show | 50 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.561-1718T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428987 | ||||||
| chr1:235428988
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.561-1717T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428988 | ||||||
| chr1:235428989
|
T | A | 36 | a0001c0001t0001g0105a0001c0001t0001g0113a0001c0001t0001g0117others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.561-1716T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428989 | ||||||
| chr1:235428990
|
T | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0032others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.561-1715T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428990 | ||||||
| chr1:235428991
|
T | A | 3 | a0001c0001t0003g0112a0001c0001t0003g0151a0001c0005t0035g0260 | 3 | HG01433.hp1 HG03471.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.561-1714T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428991 | ||||||
| chr1:235428992
|
T | A | 2 | a0001c0001t0001g0012a0001c0001t0003g0137 | 2 | HG03017.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.561-1713T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235428992 | ||||||
| chr1:235429004
|
T | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1701T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429004 | ||||||
| chr1:235429135
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.561-1570C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429135 | ||||||
| chr1:235429180
|
G | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.561-1525G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429180 | ||||||
| chr1:235429488
|
A | G | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.561-1217A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429488 | ||||||
| chr1:235429545
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1160G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429545 | ||||||
| chr1:235429580
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.561-1125A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429580 | ||||||
| chr1:235429722
|
A | AT | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.561-970dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235429722 | |||||
| chr1:235429790
|
T | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-915T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429790 | ||||||
| chr1:235429803
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.561-902C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429803 | ||||||
| chr1:235429997
|
C | T | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-708C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235429997 | ||||||
| chr1:235430007
|
C | T | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-698C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430007 | ||||||
| chr1:235430058
|
ATGTGAG | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.561-643_561-638del others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | 235430058 | |||||
| chr1:235430122
|
G | A | 2 | a0001c0001t0003g0067a0001c0001t0032g0065 | 2 | HG00642.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.561-583G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430122 | ||||||
| chr1:235430163
|
G | A | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-542G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430163 | ||||||
| chr1:235430201
|
C | T | 5 | a0001c0001t0005g0165a0001c0001t0005g0166a0001c0001t0005g0167others(2): Show | 5 | HG02622.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-504C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430201 | ||||||
| chr1:235430210
|
T | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-495T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430210 | ||||||
| chr1:235430383
|
A | G | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.561-322A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430383 | ||||||
| chr1:235430443
|
A | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-262A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430443 | ||||||
| chr1:235430457
|
G | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.561-248G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 6/16 | chr1 | 235430457 | ||||||
| chr1:235430867
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.660+63A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235430867 | ||||||
| chr1:235430935
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.660+131A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235430935 | ||||||
| chr1:235431101
|
A | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+297A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431101 | ||||||
| chr1:235431176
|
G | C | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.660+372G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431176 | ||||||
| chr1:235431213
|
C | T | 34 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(31): Show | 34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.660+409C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431213 | ||||||
| chr1:235431214
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.660+410G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431214 | ||||||
| chr1:235431301
|
T | G | 1 | a0001c0001t0032g0065 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.660+497T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431301 | ||||||
| chr1:235431321
|
T | C | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.660+517T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431321 | ||||||
| chr1:235431363
|
CT | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0057a0001c0001t0001g0071others(6): Show | 9 | HG01069.hp2 HG01168.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+574delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr1 | 235431363 | |||||
| chr1:235431515
|
T | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+711T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431515 | ||||||
| chr1:235431521
|
C | T | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+717C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431521 | ||||||
| chr1:235431572
|
G | A | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.660+768G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431572 | ||||||
| chr1:235431580
|
C | T | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.660+776C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431580 | ||||||
| chr1:235431636
|
G | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.660+832G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431636 | ||||||
| chr1:235431650
|
C | T | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+846C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431650 | ||||||
| chr1:235431719
|
G | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+915G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431719 | ||||||
| chr1:235431828
|
A | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1024A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431828 | ||||||
| chr1:235431903
|
T | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1099T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431903 | ||||||
| chr1:235431961
|
C | T | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.660+1157C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431961 | ||||||
| chr1:235431962
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.660+1158G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235431962 | ||||||
| chr1:235432014
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.660+1210C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432014 | ||||||
| chr1:235432068
|
C | T | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.660+1264C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432068 | ||||||
| chr1:235432107
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0138others(5): Show | 8 | HG01106.hp1 HG01891.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+1303C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432107 | ||||||
| chr1:235432108
|
A | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1304A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432108 | ||||||
| chr1:235432128
|
C | T | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1324C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432128 | ||||||
| chr1:235432223
|
A | C | 58 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(55): Show | 58 | HG00733.hp2 HG00741.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.660+1419A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432223 | ||||||
| chr1:235432275
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.660+1471T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432275 | ||||||
| chr1:235432298
|
T | G | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1494T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432298 | ||||||
| chr1:235432390
|
C | T | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.660+1586C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432390 | ||||||
| chr1:235432391
|
C | T | 1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.660+1587C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432391 | ||||||
| chr1:235432505
|
C | T | 4 | a0001c0001t0004g0197a0001c0001t0004g0203a0001c0001t0004g0204others(1): Show | 4 | HG02735.hp1 HG03490.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-1699C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432505 | ||||||
| chr1:235432680
|
G | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-1524G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432680 | ||||||
| chr1:235432738
|
C | T | 1 | a0001c0001t0003g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.661-1466C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432738 | ||||||
| chr1:235432739
|
T | C | 1 | a0001c0001t0003g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.661-1465T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432739 | ||||||
| chr1:235432755
|
C | T | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.661-1449C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235432755 | ||||||
| chr1:235432916
|
AT | A | 6 | a0001c0001t0001g0138a0001c0001t0007g0045a0001c0001t0007g0132others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.661-1277delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr1 | 235432916 | |||||
| chr1:235433008
|
C | T | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-1196C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433008 | ||||||
| chr1:235433081
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.661-1123C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433081 | ||||||
| chr1:235433089
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.661-1115C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433089 | ||||||
| chr1:235433312
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.661-892C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433312 | ||||||
| chr1:235433366
|
G | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.661-838G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433366 | ||||||
| chr1:235433466
|
T | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-738T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433466 | ||||||
| chr1:235433508
|
A | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-696A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433508 | ||||||
| chr1:235433567
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.661-637C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433567 | ||||||
| chr1:235433652
|
G | A | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.661-552G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433652 | ||||||
| chr1:235433883
|
T | C | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-321T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433883 | ||||||
| chr1:235433937
|
T | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.661-267T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235433937 | ||||||
| chr1:235434008
|
T | G | 1 | a0001c0001t0007g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.661-196T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235434008 | ||||||
| chr1:235434085
|
G | A | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.661-119G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 7/16 | chr1 | 235434085 | ||||||
| chr1:235434520
|
T | C | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.737+240T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235434520 | ||||||
| chr1:235434549
|
C | CTTTCTT | 5 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0164others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.737+272_737+273ins others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235434549 | |||||
| chr1:235434549
|
C | CTTTTT | 7 | a0001c0001t0001g0117a0001c0001t0005g0167a0001c0001t0007g0045others(4): Show | 7 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.737+272_737+276dup others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235434549 | |||||
| chr1:235434549
|
C | CTTTTTT | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.737+271_737+276dup others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235434549 | |||||
| chr1:235434578
|
G | A | 3 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.737+298G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235434578 | ||||||
| chr1:235434604
|
T | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.737+324T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235434604 | ||||||
| chr1:235434777
|
C | T | 1 | a0001c0001t0005g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.737+497C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235434777 | ||||||
| chr1:235435075
|
C | T | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0141 | 3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.738-670C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435075 | ||||||
| chr1:235435107
|
G | GT | 36 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(33): Show | 36 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.738-628dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235435107 | |||||
| chr1:235435107
|
G | T | 2 | a0001c0001t0004g0180a0001c0001t0004g0181 | 2 | NA18943.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.738-638G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435107 | ||||||
| chr1:235435122
|
T | TAGAGTTT others(9): Show |
1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-608_738-607ins others(16): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235435122 | |||||
| chr1:235435290
|
G | C | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-455G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435290 | ||||||
| chr1:235435310
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-435C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435310 | ||||||
| chr1:235435311
|
G | C | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.738-434G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435311 | ||||||
| chr1:235435348
|
G | A | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.738-397G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435348 | ||||||
| chr1:235435406
|
G | A | 3 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.738-339G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435406 | ||||||
| chr1:235435437
|
TAATC | T | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.738-306_738-303del others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr1 | 235435437 | |||||
| chr1:235435438
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.738-307A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435438 | ||||||
| chr1:235435529
|
A | G | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.738-216A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435529 | ||||||
| chr1:235435556
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.738-189G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435556 | ||||||
| chr1:235435571
|
C | T | 17 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(14): Show | 17 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.738-174C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435571 | ||||||
| chr1:235435572
|
G | A | 2 | a0003c0004t0031g0016a0003c0004t0037g0172 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.738-173G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435572 | ||||||
| chr1:235435585
|
G | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.738-160G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435585 | ||||||
| chr1:235435656
|
A | G | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.738-89A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435656 | ||||||
| chr1:235435658
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.738-87C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 8/16 | chr1 | 235435658 | ||||||
| chr1:235435990
|
G | C | 1 | a0001c0001t0023g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.833+150G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235435990 | ||||||
| chr1:235435993
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.833+153T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235435993 | ||||||
| chr1:235436113
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.833+273C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436113 | ||||||
| chr1:235436177
|
C | G | 1 | a0001c0001t0005g0162 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.834-209C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436177 | ||||||
| chr1:235436180
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.834-206G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436180 | ||||||
| chr1:235436309
|
T | G | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.834-77T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436309 | ||||||
| chr1:235436316
|
C | T | 6 | a0001c0001t0008g0024a0001c0001t0008g0173a0001c0001t0008g0174others(3): Show | 6 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.834-70C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 9/16 | chr1 | 235436316 | ||||||
| chr1:235436507
|
T | A | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.899-37T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 10/16 | chr1 | 235436507 | ||||||
| chr1:235436734
|
A | C | 4 | a0001c0005t0035g0260a0001c0005t0038g0155a0003c0004t0031g0016others(1): Show | 4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+126A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436734 | ||||||
| chr1:235436738
|
A | AC | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(62): Show | 65 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.963+130_963+131ins others(1): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436738 | ||||||
| chr1:235436741
|
C | T | 5 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0139others(2): Show | 5 | HG00621.hp2 HG02027.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+133C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436741 | ||||||
| chr1:235436814
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.963+206T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436814 | ||||||
| chr1:235436841
|
G | A | 3 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.963+233G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436841 | ||||||
| chr1:235436893
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.963+285C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436893 | ||||||
| chr1:235436916
|
C | G | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.963+308C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436916 | ||||||
| chr1:235436951
|
T | TCTA | 5 | a0001c0001t0008g0024a0001c0001t0008g0174a0001c0001t0008g0176others(2): Show | 5 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+347_963+349dup others(3): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr1 | 235436951 | |||||
| chr1:235436956
|
T | TA | 14 | a0001c0001t0001g0097a0001c0001t0001g0136a0001c0001t0001g0145others(11): Show | 14 | HG00621.hp1 HG01106.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.964-351dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr1 | 235436956 | |||||
| chr1:235436990
|
G | A | 2 | a0001c0001t0005g0168a0001c0001t0005g0170 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-332G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235436990 | ||||||
| chr1:235437086
|
G | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.964-236G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235437086 | ||||||
| chr1:235437129
|
AAAAAC | A | 3 | a0001c0001t0006g0044a0003c0004t0031g0016a0003c0004t0037g0172 | 3 | HG06807.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.964-173_964-169del others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr1 | 235437129 | |||||
| chr1:235437275
|
G | A | 4 | a0001c0005t0035g0260a0001c0005t0038g0155a0003c0004t0031g0016others(1): Show | 4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-47G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235437275 | ||||||
| chr1:235437290
|
C | T | 2 | a0001c0001t0003g0151a0001c0001t0003g0191 | 2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.964-32C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 11/16 | chr1 | 235437290 | ||||||
| chr1:235437496
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1116+22A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437496 | ||||||
| chr1:235437498
|
A | C | 4 | a0001c0005t0035g0260a0001c0005t0038g0155a0003c0004t0031g0016others(1): Show | 4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+24A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437498 | ||||||
| chr1:235437538
|
G | A | 2 | a0001c0001t0004g0180a0001c0001t0004g0181 | 2 | NA18943.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1116+64G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437538 | ||||||
| chr1:235437596
|
C | G | 4 | a0001c0005t0035g0260a0001c0005t0038g0155a0003c0004t0031g0016others(1): Show | 4 | HG01070.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+122C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437596 | ||||||
| chr1:235437601
|
C | A | 1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1116+127C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437601 | ||||||
| chr1:235437654
|
A | C | 1 | a0001c0001t0025g0091 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1116+180A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437654 | ||||||
| chr1:235437781
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1116+307C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437781 | ||||||
| chr1:235437847
|
A | G | 2 | a0001c0001t0002g0236a0001c0001t0002g0240 | 2 | NA18975.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1116+373A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437847 | ||||||
| chr1:235437899
|
G | T | 1 | a0001c0001t0004g0156 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1116+425G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437899 | ||||||
| chr1:235437987
|
T | C | 3 | a0001c0001t0004g0038a0001c0001t0004g0043a0001c0001t0004g0133 | 3 | HG00741.hp1 HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1116+513T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235437987 | ||||||
| chr1:235438025
|
A | T | 1 | a0001c0001t0001g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1116+551A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438025 | ||||||
| chr1:235438181
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1117-588G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438181 | ||||||
| chr1:235438237
|
C | T | 8 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0164others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-532C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438237 | ||||||
| chr1:235438366
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1117-403C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438366 | ||||||
| chr1:235438518
|
A | C | 7 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(4): Show | 7 | HG01070.hp2 HG01243.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-251A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438518 | ||||||
| chr1:235438552
|
T | TAAA | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1117-208_1117-206d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr1 | 235438552 | |||||
| chr1:235438564
|
G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1117-205G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438564 | ||||||
| chr1:235438643
|
G | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1117-126G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438643 | ||||||
| chr1:235438646
|
C | G | 2 | a0001c0001t0012g0013a0001c0001t0012g0014 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1117-123C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 12/16 | chr1 | 235438646 | ||||||
| chr1:235438989
|
G | A | 27 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(24): Show | 27 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1270+67G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235438989 | ||||||
| chr1:235439085
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1270+163G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439085 | ||||||
| chr1:235439089
|
G | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1270+167G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439089 | ||||||
| chr1:235439214
|
G | A | 3 | a0001c0001t0001g0140a0003c0004t0031g0016a0003c0004t0037g0172 | 3 | HG03471.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1270+292G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439214 | ||||||
| chr1:235439229
|
G | C | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+307G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439229 | ||||||
| chr1:235439235
|
T | A | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1270+313T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439235 | ||||||
| chr1:235439238
|
T | C | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1270+316T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439238 | ||||||
| chr1:235439246
|
T | C | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+324T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439246 | ||||||
| chr1:235439257
|
T | C | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+335T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439257 | ||||||
| chr1:235439258
|
G | A | 23 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1270+336G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439258 | ||||||
| chr1:235439266
|
T | C | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+344T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439266 | ||||||
| chr1:235439267
|
G | T | 1 | a0001c0001t0008g0024 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1270+345G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439267 | ||||||
| chr1:235439277
|
G | C | 22 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0163others(19): Show | 22 | HG00733.hp2 HG01109.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1270+355G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439277 | ||||||
| chr1:235439299
|
A | G | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+377A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439299 | ||||||
| chr1:235439315
|
C | G | 7 | a0001c0001t0008g0024a0001c0001t0008g0173a0001c0001t0008g0174others(4): Show | 7 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1270+393C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439315 | ||||||
| chr1:235439322
|
C | T | 7 | a0001c0001t0008g0024a0001c0001t0008g0173a0001c0001t0008g0174others(4): Show | 7 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1270+400C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439322 | ||||||
| chr1:235439335
|
C | CA | 6 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(3): Show | 6 | HG01243.hp1 HG02071.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270+424dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 235439335 | |||||
| chr1:235439335
|
C | CAA | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.1270+423_1270+424d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 235439335 | |||||
| chr1:235439335
|
CAAAAA | C | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+420_1270+424d others(7): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 235439335 | |||||
| chr1:235439348
|
G | T | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+426G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439348 | ||||||
| chr1:235439352
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1270+430C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439352 | ||||||
| chr1:235439357
|
G | A | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+435G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439357 | ||||||
| chr1:235439359
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0003g0116a0001c0001t0003g0118others(1): Show | 4 | NA18975.hp1 NA19005.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+437G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439359 | ||||||
| chr1:235439369
|
A | G | 4 | a0001c0001t0001g0117a0001c0001t0003g0116a0001c0001t0003g0118others(1): Show | 4 | NA18975.hp1 NA19005.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+447A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439369 | ||||||
| chr1:235439424
|
G | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1270+502G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439424 | ||||||
| chr1:235439569
|
C | T | 1 | a0001c0001t0005g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1270+647C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439569 | ||||||
| chr1:235439616
|
TAG | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1270+695_1270+696d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439616 | ||||||
| chr1:235439636
|
C | T | 1 | a0001c0001t0002g0252 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1270+714C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439636 | ||||||
| chr1:235439710
|
A | G | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(1): Show | 4 | HG02523.hp1 NA18943.hp1 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+788A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439710 | ||||||
| chr1:235439739
|
C | T | 1 | a0004c0006t0002g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1270+817C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439739 | ||||||
| chr1:235439805
|
C | A | 8 | a0001c0001t0002g0034a0001c0001t0002g0088a0001c0001t0002g0089others(5): Show | 8 | HG00544.hp1 HG01081.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1270+883C>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439805 | ||||||
| chr1:235439846
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1270+924G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439846 | ||||||
| chr1:235439903
|
G | A | 4 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1270+981G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235439903 | ||||||
| chr1:235440009
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1270+1087C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440009 | ||||||
| chr1:235440026
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1270+1104A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440026 | ||||||
| chr1:235440080
|
C | T | 3 | a0001c0001t0004g0158a0001c0001t0004g0180a0001c0001t0004g0181 | 3 | NA18943.hp2 NA18954.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1270+1158C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440080 | ||||||
| chr1:235440100
|
G | A | 1 | a0001c0005t0038g0155 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1270+1178G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440100 | ||||||
| chr1:235440108
|
C | T | 2 | a0001c0001t0002g0253a0001c0001t0002g0259 | 2 | NA18951.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1270+1186C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440108 | ||||||
| chr1:235440120
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1270+1198A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440120 | ||||||
| chr1:235440172
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1270+1250G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440172 | ||||||
| chr1:235440217
|
A | G | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+1295A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440217 | ||||||
| chr1:235440231
|
G | A | 2 | a0001c0001t0008g0173a0001c0001t0008g0177 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1270+1309G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440231 | ||||||
| chr1:235440262
|
G | A | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1270+1340G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440262 | ||||||
| chr1:235440266
|
A | G | 6 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(3): Show | 6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1270+1344A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440266 | ||||||
| chr1:235440377
|
G | C | 38 | a0001c0001t0004g0006a0001c0001t0004g0011a0001c0001t0004g0027others(35): Show | 38 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1271-1437G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440377 | ||||||
| chr1:235440380
|
T | C | 38 | a0001c0001t0004g0006a0001c0001t0004g0011a0001c0001t0004g0027others(35): Show | 38 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1271-1434T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440380 | ||||||
| chr1:235440390
|
G | GTA | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-1412_1271-141 others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr1 | 235440390 | |||||
| chr1:235440402
|
A | T | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.1271-1412A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440402 | ||||||
| chr1:235440417
|
T | A | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1271-1397T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440417 | ||||||
| chr1:235440483
|
C | G | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-1331C>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440483 | ||||||
| chr1:235440636
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1271-1178C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440636 | ||||||
| chr1:235440784
|
G | GTGTAGTT others(8): Show |
1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1271-1030_1271-102 others(19): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440784 | ||||||
| chr1:235440785
|
G | A | 1 | a0001c0001t0030g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1271-1029G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440785 | ||||||
| chr1:235440959
|
A | G | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1271-855A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235440959 | ||||||
| chr1:235441028
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1271-786A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441028 | ||||||
| chr1:235441065
|
A | G | 4 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(1): Show | 4 | HG02145.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1271-749A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441065 | ||||||
| chr1:235441238
|
G | T | 1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1271-576G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441238 | ||||||
| chr1:235441405
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1271-409C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441405 | ||||||
| chr1:235441520
|
C | T | 1 | a0001c0001t0006g0044 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1271-294C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441520 | ||||||
| chr1:235441573
|
C | T | 4 | a0001c0001t0026g0129a0001c0001t0027g0128a0001c0001t0030g0154others(1): Show | 4 | HG03516.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1271-241C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441573 | ||||||
| chr1:235441680
|
A | G | 1 | a0001c0001t0003g0149 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1271-134A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 13/16 | chr1 | 235441680 | ||||||
| chr1:235442008
|
A | T | 26 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(23): Show | 26 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1339+126A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442008 | ||||||
| chr1:235442008
|
AT | A | 6 | a0001c0001t0001g0097a0001c0001t0001g0117a0001c0001t0002g0089others(3): Show | 6 | HG01070.hp2 HG02897.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1339+143delT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr1 | 235442008 | |||||
| chr1:235442009
|
T | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0003g0107 | 3 | HG01257.hp2 HG02135.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1339+127T>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442009 | ||||||
| chr1:235442146
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.1339+264C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442146 | ||||||
| chr1:235442169
|
C | T | 1 | a0001c0001t0004g0011 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1339+287C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442169 | ||||||
| chr1:235442248
|
G | A | 3 | a0001c0005t0035g0260a0001c0005t0038g0155a0003c0004t0037g0172 | 3 | HG01070.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1339+366G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442248 | ||||||
| chr1:235442280
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1339+398C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442280 | ||||||
| chr1:235442416
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1340-436C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442416 | ||||||
| chr1:235442446
|
C | T | 1 | a0001c0001t0012g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1340-406C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442446 | ||||||
| chr1:235442480
|
A | C | 1 | a0001c0001t0036g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1340-372A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442480 | ||||||
| chr1:235442604
|
G | A | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1340-248G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442604 | ||||||
| chr1:235442663
|
A | G | 4 | a0001c0001t0026g0129a0001c0001t0027g0128a0001c0001t0030g0154others(1): Show | 4 | HG03516.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1340-189A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442663 | ||||||
| chr1:235442666
|
G | A | 4 | a0001c0001t0026g0129a0001c0001t0027g0128a0001c0001t0030g0154others(1): Show | 4 | HG03516.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1340-186G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 14/16 | chr1 | 235442666 | ||||||
| chr1:235443087
|
G | GC | 7 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(4): Show | 7 | HG01070.hp2 HG01243.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1399+181dupC | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443087 | |||||
| chr1:235443110
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1399+199C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443110 | ||||||
| chr1:235443177
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1399+266C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443177 | ||||||
| chr1:235443183
|
C | CAT | 7 | a0001c0001t0008g0024a0001c0001t0008g0173a0001c0001t0008g0174others(4): Show | 7 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1399+273_1399+274i others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443183 | |||||
| chr1:235443183
|
C | CATAT | 34 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(31): Show | 34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1399+273_1399+274i others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443183 | |||||
| chr1:235443185
|
C | CATAT | 16 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(13): Show | 16 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.1399+282_1399+285d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443185 | |||||
| chr1:235443185
|
C | T | 41 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(38): Show | 41 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1399+274C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443185 | ||||||
| chr1:235443185
|
CAT | C | 4 | a0001c0001t0007g0045a0001c0001t0007g0265a0001c0001t0007g0266others(1): Show | 4 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1399+284_1399+285d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443185 | |||||
| chr1:235443195
|
T | TAC | 60 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(57): Show | 60 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1399+298_1399+299d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443195 | |||||
| chr1:235443398
|
C | T | 5 | a0001c0001t0007g0045a0001c0001t0007g0132a0001c0001t0007g0265others(2): Show | 5 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1399+487C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443398 | ||||||
| chr1:235443450
|
G | A | 4 | a0001c0001t0026g0129a0001c0001t0027g0128a0001c0001t0030g0154others(1): Show | 4 | HG03516.hp2 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399+539G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443450 | ||||||
| chr1:235443579
|
GCTGTTTC others(8): Show |
G | 3 | a0001c0001t0013g0130a0001c0001t0013g0131a0001c0001t0013g0152 | 3 | HG01168.hp1 HG01169.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1399+673_1399+687d others(17): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235443579 | |||||
| chr1:235443915
|
A | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1399+1004A>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235443915 | ||||||
| chr1:235444218
|
A | C | 3 | a0001c0001t0002g0210a0001c0001t0002g0228a0001c0001t0011g0223 | 3 | NA18956.hp2 NA18962.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1399+1307A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444218 | ||||||
| chr1:235444241
|
A | C | 3 | a0001c0005t0035g0260a0001c0005t0038g0155a0003c0004t0037g0172 | 3 | HG01070.hp2 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1399+1330A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444241 | ||||||
| chr1:235444304
|
G | A | 1 | a0003c0004t0037g0172 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1399+1393G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444304 | ||||||
| chr1:235444437
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1399+1526C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444437 | ||||||
| chr1:235444704
|
A | G | 58 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(55): Show | 58 | HG00733.hp2 HG00741.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.1399+1793A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444704 | ||||||
| chr1:235444707
|
C | T | 3 | a0001c0001t0004g0011a0001c0001t0004g0042a0001c0001t0004g0134 | 3 | HG01106.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1399+1796C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444707 | ||||||
| chr1:235444844
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1399+1933T>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235444844 | ||||||
| chr1:235445002
|
A | G | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1399+2091A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445002 | ||||||
| chr1:235445128
|
A | G | 1 | a0001c0001t0007g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1399+2217A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445128 | ||||||
| chr1:235445297
|
G | T | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1399+2386G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445297 | ||||||
| chr1:235445410
|
C | T | 2 | a0001c0001t0003g0068a0001c0001t0003g0069 | 2 | HG00099.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.1399+2499C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445410 | ||||||
| chr1:235445434
|
G | A | 34 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(31): Show | 34 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1399+2523G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445434 | ||||||
| chr1:235445503
|
G | A | 17 | a0001c0001t0002g0034a0001c0001t0002g0088a0001c0001t0002g0089others(14): Show | 17 | HG00544.hp1 HG01081.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1399+2592G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445503 | ||||||
| chr1:235445560
|
T | C | 2 | a0001c0001t0026g0129a0001c0001t0027g0128 | 2 | HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1399+2649T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445560 | ||||||
| chr1:235445602
|
A | G | 24 | a0001c0001t0005g0124a0001c0001t0005g0160a0001c0001t0005g0162others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1399+2691A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445602 | ||||||
| chr1:235445967
|
A | G | 1 | a0002c0002t0010g0023 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1400-2382A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235445967 | ||||||
| chr1:235446183
|
C | CT | 35 | a0001c0001t0002g0127a0001c0001t0004g0006a0001c0001t0004g0007others(32): Show | 35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1400-2156dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235446183 | |||||
| chr1:235446326
|
G | A | 2 | a0001c0001t0001g0058a0001c0001t0001g0120 | 2 | NA18982.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1400-2023G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235446326 | ||||||
| chr1:235446420
|
G | A | 1 | a0001c0001t0006g0054 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1400-1929G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235446420 | ||||||
| chr1:235446429
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1400-1920G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235446429 | ||||||
| chr1:235446695
|
G | GT | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 61 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1400-1638dupT | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235446695 | |||||
| chr1:235446695
|
G | GTT | 5 | a0001c0001t0001g0012a0001c0001t0001g0073a0001c0001t0001g0218others(2): Show | 5 | HG00738.hp2 HG01074.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1400-1639_1400-163 others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235446695 | |||||
| chr1:235446829
|
C | T | 1 | a0001c0005t0035g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1400-1520C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235446829 | ||||||
| chr1:235447253
|
G | T | 1 | a0001c0001t0001g0004 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1400-1096G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447253 | ||||||
| chr1:235447333
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1400-1016C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447333 | ||||||
| chr1:235447629
|
A | G | 2 | a0001c0001t0030g0154a0003c0004t0031g0016 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1400-720A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447629 | ||||||
| chr1:235447778
|
A | G | 35 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(32): Show | 35 | HG00741.hp1 HG01106.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1400-571A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447778 | ||||||
| chr1:235447893
|
T | TACTTGGG others(21): Show |
1 | a0003c0004t0031g0016 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1400-431_1400-430i others(30): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235447893 | |||||
| chr1:235447951
|
T | C | 1 | a0001c0001t0002g0248 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1400-398T>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447951 | ||||||
| chr1:235447970
|
G | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1400-379G>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447970 | ||||||
| chr1:235447978
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1400-371G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235447978 | ||||||
| chr1:235448014
|
G | T | 4 | a0001c0001t0004g0158a0001c0001t0004g0180a0001c0001t0004g0181others(1): Show | 4 | HG02027.hp1 NA18943.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1400-335G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448014 | ||||||
| chr1:235448018
|
G | A | 13 | a0001c0001t0004g0027a0001c0001t0004g0039a0001c0001t0004g0040others(10): Show | 13 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1400-331G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448018 | ||||||
| chr1:235448019
|
G | T | 1 | a0001c0001t0003g0036 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1400-330G>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448019 | ||||||
| chr1:235448085
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0003g0119 | 2 | HG02300.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1400-264A>G | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448085 | ||||||
| chr1:235448125
|
G | A | 2 | a0001c0001t0007g0132a0001c0005t0038g0155 | 2 | HG01070.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1400-224G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448125 | ||||||
| chr1:235448206
|
A | C | 3 | a0001c0001t0001g0140a0001c0005t0035g0260a0001c0005t0038g0155 | 3 | HG01070.hp2 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1400-143A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448206 | ||||||
| chr1:235448210
|
A | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0071others(6): Show | 9 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1400-139A>C | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448210 | ||||||
| chr1:235448220
|
C | CA | 11 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0073others(8): Show | 11 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1400-109dupA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | |||||
| chr1:235448220
|
C | CAA | 8 | a0001c0001t0002g0195a0001c0001t0002g0240a0001c0001t0004g0038others(5): Show | 8 | HG01070.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1400-110_1400-109d others(4): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | |||||
| chr1:235448220
|
C | CAAA | 25 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0011others(22): Show | 25 | HG00741.hp1 HG01243.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.1400-111_1400-109d others(5): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | |||||
| chr1:235448220
|
C | CAAAA | 6 | a0001c0001t0004g0042a0001c0001t0004g0050a0001c0001t0004g0133others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1400-112_1400-109d others(6): Show |
TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | |||||
| chr1:235448220
|
CA | C | 13 | a0001c0001t0001g0193a0001c0001t0002g0179a0001c0001t0002g0222others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1400-109delA | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr1 | 235448220 | |||||
| chr1:235448322
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1400-27G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 15/16 | chr1 | 235448322 | ||||||
| chr1:235448588
|
C | T | 1 | a0001c0001t0005g0163 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1492-82C>T | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 16/16 | chr1 | 235448588 | ||||||
| chr1:235448612
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1492-58G>A | TBCE | ENSG00000284770.2 | transcript | ENST00000642610.2 | protein_coding | 16/16 | chr1 | 235448612 |