Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8729 |
|---|---|
| ensemblid | ENSG00000107862.7 |
| hgncid | 4181 |
| symbol | GBF1 |
| name | golgi brefeldin A resistant guanine nucleotide exchange factor 1 |
| refseq_nuc | NM_001377137.1 |
| refseq_prot | NP_001364066.1 |
| ensembl_nuc | ENST00000369983.5 |
| ensembl_prot | ENSP00000359000.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 102245532 |
| end | 102382896 |
| strand | + |
| ver | v1.2 |
| region | chr10:102245532-102382896 |
| region5000 | chr10:102240532-102387896 |
| regionname0 | GBF1_chr10_102245532_102382896 |
| regionname5000 | GBF1_chr10_102240532_102387896 |
| 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 | 1860 | 300 | 81 | 53 | 122 | 9 | 33 | 97 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0002 | 0/0 | 1860 | 12 | 0 | 7 | 2 | 3 | 0 | 2 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0003 | 0/0 | 1860 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0004 | 0/0 | 1860 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0005 | 0/0 | 1860 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0006 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0007 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0008 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0009 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0010 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0011 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0012 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0013 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 5583 | 274 | 67 | 49 | 120 | 8 | 29 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0002 | 0/0 | 5583 | 12 | 0 | 7 | 2 | 3 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0003 | 0/0 | 5583 | 11 | 6 | 1 | 0 | 1 | 3 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0004 | 0/0 | 5583 | 6 | 6 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0005 | 0/0 | 5583 | 5 | 0 | 0 | 5 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0006 | 0/0 | 5583 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0007 | 1/0 | 5583 | 2 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0008 | 0/0 | 5583 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0009 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0010 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0011 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0012 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0013 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0014 | 0/0 | 5583 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0015 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0016 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0017 | 0/0 | 5583 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0018 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0019 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0020 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0021 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0022 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0023 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| c0024 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 821 | 160 | 63 | 29 | 49 | 7 | 12 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| t0002 | 1/1 | 821 | 91 | 12 | 22 | 40 | 3 | 12 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| t0003 | 0/0 | 821 | 68 | 2 | 13 | 44 | 1 | 8 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| t0004 | 0/0 | 821 | 6 | 6 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| t0005 | 0/0 | 821 | 2 | 1 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| t0006 | 0/0 | 821 | 2 | 0 | 0 | 0 | 0 | 2 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| t0007 | 0/0 | 821 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| 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 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 5583 | 274 | 67 | 49 | 120 | 8 | 29 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0003 | 0/0 | 5583 | 11 | 6 | 1 | 0 | 1 | 3 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0004 | 0/0 | 5583 | 6 | 6 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0007 | 1/0 | 5583 | 2 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0013 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0014 | 0/0 | 5583 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0016 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0021 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0022 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0023 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0024 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0002c0002 | 0/0 | 5583 | 12 | 0 | 7 | 2 | 3 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0003c0005 | 0/0 | 5583 | 5 | 0 | 0 | 5 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0004c0008 | 0/0 | 5583 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0004c0020 | 0/0 | 5583 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0005c0006 | 0/0 | 5583 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0006c0011 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0007c0010 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0008c0012 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0009c0015 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0010c0017 | 0/0 | 5583 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0011c0019 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0012c0018 | 0/0 | 5583 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0013c0009 | 0/0 | 5583 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6403 | 124 | 54 | 18 | 42 | 3 | 7 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0001t0002 | 0/1 | 6403 | 80 | 10 | 19 | 35 | 3 | 12 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0001t0003 | 0/0 | 6403 | 65 | 2 | 12 | 42 | 1 | 8 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0001t0005 | 0/0 | 6403 | 2 | 1 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0001t0006 | 0/0 | 6403 | 2 | 0 | 0 | 0 | 0 | 2 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0001t0007 | 0/0 | 6403 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0003t0001 | 0/0 | 6403 | 11 | 6 | 1 | 0 | 1 | 3 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0004t0002 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0004t0004 | 0/0 | 6403 | 5 | 5 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0007t0001 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0007t0002 | 1/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0013t0002 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0014t0001 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0016t0001 | 0/0 | 6403 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0021t0004 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0022t0003 | 0/0 | 6403 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0023t0003 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0001c0024t0001 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0002c0002t0001 | 0/0 | 6403 | 12 | 0 | 7 | 2 | 3 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0003c0005t0002 | 0/0 | 6403 | 5 | 0 | 0 | 5 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0004c0008t0001 | 0/0 | 6403 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0004c0020t0003 | 0/0 | 6403 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0005c0006t0001 | 0/0 | 6403 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0006c0011t0001 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0007c0010t0001 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0008c0012t0002 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0009c0015t0002 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0010c0017t0001 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0011c0019t0002 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0012c0018t0001 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| a0013c0009t0001 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | copy fasta | chr10 | 102240532 | 102387896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0070 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0004t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0004t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0004t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0004t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0004t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0004t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0007t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0007t0002g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0013t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0014t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0016t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0021t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0022t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0023t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0001c0024t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0003c0005t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0003c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0003c0005t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0003c0005t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0003c0005t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0004c0008t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0004c0008t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0004c0020t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0005c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0005c0006t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0006c0011t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0007c0010t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0008c0012t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0009c0015t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0010c0017t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0011c0019t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0012c0018t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| a0013c0009t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0291 | EUR | GBR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | GBR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0156 | EUR | FIN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0063 | EUR | FIN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00544 | hp1 | a0005 | c0006 | t0001 | g0157 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00738 | hp1 | a0009 | c0015 | t0002 | g0062 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0210 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01074 | hp1 | a0006 | c0011 | t0001 | g0295 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01081 | hp1 | a0001 | c0024 | t0001 | g0229 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01106 | hp1 | a0001 | c0023 | t0003 | g0269 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01175 | hp1 | a0012 | c0018 | t0001 | g0205 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01192 | hp1 | a0001 | c0013 | t0002 | g0049 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0108 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0109 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0203 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01928 | hp2 | a0011 | c0019 | t0002 | g0043 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02071 | hp1 | a0003 | c0005 | t0002 | g0102 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02135 | hp2 | a0005 | c0006 | t0001 | g0158 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0226 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02280 | hp1 | a0001 | c0004 | t0004 | g0013 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0227 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0258 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0211 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0222 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02818 | hp2 | a0007 | c0010 | t0001 | g0113 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0228 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02965 | hp2 | a0001 | c0004 | t0004 | g0017 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03017 | hp1 | a0010 | c0017 | t0001 | g0193 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03195 | hp1 | a0013 | c0009 | t0001 | g0217 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03209 | hp1 | a0001 | c0007 | t0001 | g0329 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0207 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0212 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0165 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG04228 | hp1 | a0001 | c0014 | t0001 | g0167 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0260 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18522 | hp1 | a0001 | c0004 | t0004 | g0014 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18949 | hp2 | a0004 | c0008 | t0001 | g0195 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18951 | hp2 | a0001 | c0001 | t0007 | g0147 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18952 | hp1 | a0003 | c0005 | t0002 | g0077 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18957 | hp2 | a0004 | c0008 | t0001 | g0200 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18992 | hp2 | a0003 | c0005 | t0002 | g0079 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18994 | hp1 | a0001 | c0016 | t0001 | g0189 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18994 | hp2 | a0004 | c0020 | t0003 | g0312 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19007 | hp1 | a0001 | c0022 | t0003 | g0235 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19010 | hp1 | a0003 | c0005 | t0002 | g0078 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19030 | hp2 | a0001 | c0004 | t0004 | g0015 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ASW | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ASW | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0073 | EUR | TSI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0178 | EUR | TSI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0280 | SAS | GIH | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0166 | SAS | GIH | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02109 | hp2 | a0008 | c0012 | t0002 | g0031 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02486 | hp1 | a0001 | c0021 | t0004 | g0016 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG06807 | hp1 | a0001 | c0004 | t0002 | g0104 | AFR | USA | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | USA | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA18955 | hp2 | a0003 | c0005 | t0002 | g0061 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | USA | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA20300 | hp2 | a0001 | c0004 | t0004 | g0004 | AFR | USA | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0070 | REF | REF | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| homoSapiens_grch38 | hp1 | a0001 | c0007 | t0002 | g0099 | REF | REF | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102358061
|
T | C | 1 | a0013 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.662T>C | p.Met221Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 9/40 | 922/6403 | 662/5583 | 221/1860 | chr10 | 102358061 | ||
| chr10:102358118
|
T | C | 1 | a0005 | 2 | HG00544.hp1 HG02135.hp2 |
missense_variant | MODERATE | c.719T>C | p.Met240Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 9/40 | 979/6403 | 719/5583 | 240/1860 | chr10 | 102358118 | ||
| chr10:102359382
|
T | C | 1 | a0003 | 5 | HG02071.hp1 NA18952.hp1 NA18955.hp2 others(2): Show |
missense_variant | MODERATE | c.1127T>C | p.Met376Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/40 | 1387/6403 | 1127/5583 | 376/1860 | chr10 | 102359382 | ||
| chr10:102361741
|
G | C | 1 | a0006 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.1515G>C | p.Glu505Asp | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/40 | 1775/6403 | 1515/5583 | 505/1860 | chr10 | 102361741 | ||
| chr10:102366499
|
G | A | 1 | a0007 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.2426G>A | p.Arg809His | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/40 | 2686/6403 | 2426/5583 | 809/1860 | chr10 | 102366499 | ||
| chr10:102370789
|
G | A | 1 | a0008 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3589G>A | p.Val1197Met | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/40 | 3849/6403 | 3589/5583 | 1197/1860 | chr10 | 102370789 | ||
| chr10:102370816
|
C | T | 1 | a0004 | 3 | NA18949.hp2 NA18957.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.3616C>T | p.Arg1206Cys | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/40 | 3876/6403 | 3616/5583 | 1206/1860 | chr10 | 102370816 | ||
| chr10:102376430
|
G | A | 1 | a0009 | 1 | HG00738.hp1 | missense_variant&splice_region_variant | MODERATE | c.4045G>A | p.Val1349Met | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 31/40 | 4305/6403 | 4045/5583 | 1349/1860 | chr10 | 102376430 | ||
| chr10:102379548
|
G | A | 1 | a0010 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.4673G>A | p.Arg1558Gln | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 35/40 | 4933/6403 | 4673/5583 | 1558/1860 | chr10 | 102379548 | ||
| chr10:102380593
|
G | A | 2 | a0002a0012 | 13 | HG00735.hp2 HG01099.hp1 HG01123.hp1 others(10): Show |
missense_variant | MODERATE | c.5080G>A | p.Gly1694Ser | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 38/40 | 5340/6403 | 5080/5583 | 1694/1860 | chr10 | 102380593 | ||
| chr10:102381186
|
G | A | 1 | a0011 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.5233G>A | p.Ala1745Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/40 | 5493/6403 | 5233/5583 | 1745/1860 | chr10 | 102381186 | ||
| chr10:102382195
|
G | T | 1 | a0012 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.5442G>T | p.Leu1814Phe | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 5702/6403 | 5442/5583 | 1814/1860 | chr10 | 102382195 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102351860
|
G | T | 1 | a0001c0024 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.432G>T | p.Leu144Leu | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/40 | 692/6403 | 432/5583 | 144/1860 | chr10 | 102351860 | ||
| chr10:102358516
|
C | T | 1 | a0001c0023 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.798C>T | p.Pro266Pro | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/40 | 1058/6403 | 798/5583 | 266/1860 | chr10 | 102358516 | ||
| chr10:102358666
|
G | A | 1 | a0007c0010 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.948G>A | p.Gly316Gly | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/40 | 1208/6403 | 948/5583 | 316/1860 | chr10 | 102358666 | ||
| chr10:102363759
|
A | G | 1 | a0007c0010 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.2067A>G | p.Pro689Pro | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/40 | 2327/6403 | 2067/5583 | 689/1860 | chr10 | 102363759 | ||
| chr10:102365489
|
C | T | 1 | a0001c0022 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.2199C>T | p.Asp733Asp | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/40 | 2459/6403 | 2199/5583 | 733/1860 | chr10 | 102365489 | ||
| chr10:102367555
|
C | T | 1 | a0001c0021 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.2637C>T | p.Ala879Ala | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 21/40 | 2897/6403 | 2637/5583 | 879/1860 | chr10 | 102367555 | ||
| chr10:102376375
|
G | A | 1 | a0001c0013 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.3990G>A | p.Pro1330Pro | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 31/40 | 4250/6403 | 3990/5583 | 1330/1860 | chr10 | 102376375 | ||
| chr10:102376405
|
C | A | 1 | a0001c0014 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.4020C>A | p.Ala1340Ala | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 31/40 | 4280/6403 | 4020/5583 | 1340/1860 | chr10 | 102376405 | ||
| chr10:102376586
|
C | A | 1 | a0001c0016 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.4074C>A | p.Ser1358Ser | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 32/40 | 4334/6403 | 4074/5583 | 1358/1860 | chr10 | 102376586 | ||
| chr10:102376712
|
T | C | 23 | a0001c0001a0001c0003a0001c0004others(20): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
synonymous_variant | LOW | c.4200T>C | p.Ile1400Ile | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 32/40 | 4460/6403 | 4200/5583 | 1400/1860 | chr10 | 102376712 | ||
| chr10:102376972
|
A | G | 2 | a0001c0004a0001c0021 | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.4326A>G | p.Lys1442Lys | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/40 | 4586/6403 | 4326/5583 | 1442/1860 | chr10 | 102376972 | ||
| chr10:102377116
|
G | A | 2 | a0001c0004a0001c0021 | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.4470G>A | p.Thr1490Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/40 | 4730/6403 | 4470/5583 | 1490/1860 | chr10 | 102377116 | ||
| chr10:102380598
|
C | T | 2 | a0001c0003a0001c0024 | 12 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(9): Show |
synonymous_variant | LOW | c.5085C>T | p.Pro1695Pro | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 38/40 | 5345/6403 | 5085/5583 | 1695/1860 | chr10 | 102380598 | ||
| chr10:102382294
|
A | C | 1 | a0004c0020 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.5541A>C | p.Thr1847Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 5801/6403 | 5541/5583 | 1847/1860 | chr10 | 102382294 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102245629
|
G | A | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(18): Show | 233 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(230): Show |
5_prime_UTR_variant | MODIFIER | c.-163G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/40 | 13310 | chr10 | 102245629 | |||||
| chr10:102245653
|
T | C | 4 | a0001c0001t0003a0001c0022t0003a0001c0023t0003others(1): Show | 68 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(65): Show |
5_prime_UTR_variant | MODIFIER | c.-139T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/40 | 13286 | chr10 | 102245653 | |||||
| chr10:102382536
|
C | T | 1 | a0001c0001t0007 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*200C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 200 | chr10 | 102382536 | |||||
| chr10:102382537
|
G | A | 1 | a0001c0001t0005 | 2 | HG00280.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*201G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 201 | chr10 | 102382537 | |||||
| chr10:102382632
|
G | A | 1 | a0001c0001t0006 | 2 | HG03927.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 296 | chr10 | 102382632 | |||||
| chr10:102382810
|
G | A | 2 | a0001c0004t0004a0001c0021t0004 | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*474G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 474 | chr10 | 102382810 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:102246022
|
C | T | 6 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+241C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246022 | ||||||
| chr10:102246258
|
T | C | 1 | a0001c0001t0002g0002 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-11+477T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246258 | ||||||
| chr10:102246321
|
G | T | 1 | a0001c0003t0001g0323 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-11+540G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246321 | ||||||
| chr10:102246331
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-11+550G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246331 | ||||||
| chr10:102246410
|
T | C | 1 | a0001c0004t0004g0004 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-11+629T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246410 | ||||||
| chr10:102246527
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-11+746C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246527 | ||||||
| chr10:102246590
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-11+809T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246590 | ||||||
| chr10:102246817
|
A | G | 1 | a0001c0001t0001g0321 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11+1036A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246817 | ||||||
| chr10:102247028
|
T | C | 1 | a0001c0001t0003g0006 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-11+1247T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247028 | ||||||
| chr10:102247049
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-11+1268T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247049 | ||||||
| chr10:102247097
|
G | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-11+1316G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247097 | ||||||
| chr10:102247275
|
T | C | 1 | a0001c0001t0001g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-11+1494T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247275 | ||||||
| chr10:102247286
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-11+1505G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247286 | ||||||
| chr10:102247526
|
C | T | 1 | a0001c0001t0001g0320 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-11+1745C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247526 | ||||||
| chr10:102247735
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-11+1954T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247735 | ||||||
| chr10:102248278
|
C | CT | 17 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0003g0305others(14): Show | 17 | HG00673.hp2 HG02071.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-11+2509dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102248278 | |||||
| chr10:102248307
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+2526C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248307 | ||||||
| chr10:102248448
|
T | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+2667T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248448 | ||||||
| chr10:102248506
|
C | T | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+2725C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248506 | ||||||
| chr10:102248507
|
G | T | 1 | a0001c0001t0002g0300 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-11+2726G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248507 | ||||||
| chr10:102248523
|
A | C | 232 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.-11+2742A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248523 | ||||||
| chr10:102248771
|
A | C | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-11+2990A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248771 | ||||||
| chr10:102248870
|
A | C | 1 | a0001c0007t0001g0329 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+3089A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248870 | ||||||
| chr10:102248931
|
A | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+3150A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248931 | ||||||
| chr10:102248957
|
A | C | 1 | a0001c0001t0002g0103 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-11+3176A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248957 | ||||||
| chr10:102248964
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-11+3183C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248964 | ||||||
| chr10:102248994
|
G | A | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-11+3213G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248994 | ||||||
| chr10:102249113
|
G | C | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-11+3332G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249113 | ||||||
| chr10:102249423
|
G | T | 1 | a0001c0001t0001g0296 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-11+3642G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249423 | ||||||
| chr10:102249437
|
A | C | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-11+3656A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249437 | ||||||
| chr10:102249746
|
C | A | 58 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0018others(55): Show | 58 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-11+3965C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249746 | ||||||
| chr10:102249932
|
C | T | 2 | a0001c0001t0001g0294a0001c0001t0001g0320 | 2 | NA18963.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-11+4151C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249932 | ||||||
| chr10:102250092
|
GT | G | 232 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.-11+4316delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102250092 | |||||
| chr10:102250106
|
G | T | 1 | a0001c0001t0001g0293 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+4325G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250106 | ||||||
| chr10:102250176
|
A | G | 1 | a0001c0001t0003g0292 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-11+4395A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250176 | ||||||
| chr10:102250385
|
A | G | 86 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0231others(83): Show | 87 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-11+4604A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250385 | ||||||
| chr10:102250524
|
AT | A | 17 | a0001c0001t0001g0230a0001c0001t0001g0324a0001c0001t0001g0325others(14): Show | 17 | HG01069.hp2 HG01891.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.-11+4762delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102250524 | |||||
| chr10:102250524
|
ATT | A | 218 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(215): Show | 219 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.-11+4761_-11+4762d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102250524 | |||||
| chr10:102250524
|
ATTT | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG01516.hp1 HG01516.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+4760_-11+4762d others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102250524 | |||||
| chr10:102250880
|
C | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0070a0001c0001t0002g0071others(1): Show | 4 | HG01346.hp1 HG01361.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+5099C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250880 | ||||||
| chr10:102250926
|
C | T | 1 | a0001c0024t0001g0229 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-11+5145C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250926 | ||||||
| chr10:102250945
|
G | A | 140 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(137): Show | 141 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11+5164G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250945 | ||||||
| chr10:102251008
|
GA | G | 8 | a0001c0001t0003g0236a0001c0004t0002g0104a0001c0004t0004g0004others(5): Show | 8 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+5240delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102251008 | |||||
| chr10:102251008
|
GAA | G | 227 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(224): Show | 228 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.-11+5239_-11+5240d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102251008 | |||||
| chr10:102251214
|
G | C | 86 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0231others(83): Show | 87 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-11+5433G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251214 | ||||||
| chr10:102251343
|
G | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+5562G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251343 | ||||||
| chr10:102251560
|
A | G | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0213others(22): Show | 25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11+5779A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251560 | ||||||
| chr10:102251573
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0152 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-11+5792A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251573 | ||||||
| chr10:102251643
|
T | G | 1 | a0001c0001t0001g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11+5862T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251643 | ||||||
| chr10:102251703
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-11+5922G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251703 | ||||||
| chr10:102251723
|
T | A | 3 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240 | 3 | HG01943.hp1 HG02004.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-11+5942T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251723 | ||||||
| chr10:102251750
|
C | G | 1 | a0001c0001t0002g0069 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-11+5969C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251750 | ||||||
| chr10:102251922
|
C | A | 1 | a0001c0003t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11+6141C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251922 | ||||||
| chr10:102251940
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+6159C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251940 | ||||||
| chr10:102251963
|
TCAGGAGT others(7): Show |
T | 1 | a0001c0001t0005g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-11+6200_-11+6213d others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102251963 | |||||
| chr10:102252196
|
C | T | 24 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(21): Show | 24 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11+6415C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252196 | ||||||
| chr10:102252208
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-11+6427G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252208 | ||||||
| chr10:102252331
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0003g0303a0001c0001t0003g0304 | 3 | HG02071.hp2 HG02074.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+6550G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252331 | ||||||
| chr10:102252378
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-10-6551A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252378 | ||||||
| chr10:102252485
|
A | G | 1 | a0003c0005t0002g0102 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-10-6444A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252485 | ||||||
| chr10:102252528
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-6401G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252528 | ||||||
| chr10:102252568
|
G | A | 1 | a0001c0001t0003g0236 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-10-6361G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252568 | ||||||
| chr10:102252671
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-10-6258G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252671 | ||||||
| chr10:102252825
|
C | T | 3 | a0001c0003t0001g0227a0001c0003t0001g0228a0001c0024t0001g0229 | 3 | HG01081.hp1 HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-10-6104C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252825 | ||||||
| chr10:102252920
|
T | C | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-10-6009T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252920 | ||||||
| chr10:102252921
|
G | A | 2 | a0001c0001t0001g0241a0006c0011t0001g0295 | 2 | HG01074.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-10-6008G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252921 | ||||||
| chr10:102253040
|
C | A | 1 | a0001c0001t0003g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5889C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253040 | ||||||
| chr10:102253041
|
C | T | 1 | a0001c0001t0003g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5888C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253041 | ||||||
| chr10:102253042
|
C | G | 1 | a0001c0001t0003g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5887C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253042 | ||||||
| chr10:102253043
|
T | A | 1 | a0001c0001t0003g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5886T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253043 | ||||||
| chr10:102253045
|
C | T | 1 | a0001c0001t0003g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5884C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253045 | ||||||
| chr10:102253046
|
C | A | 1 | a0001c0001t0003g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5883C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253046 | ||||||
| chr10:102253184
|
T | C | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-10-5745T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253184 | ||||||
| chr10:102253335
|
G | C | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-10-5594G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253335 | ||||||
| chr10:102253577
|
G | T | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5352G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253577 | ||||||
| chr10:102253765
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-5164C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253765 | ||||||
| chr10:102253783
|
G | C | 7 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076others(4): Show | 7 | HG02071.hp1 HG02135.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-5146G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253783 | ||||||
| chr10:102253838
|
C | G | 5 | a0002c0002t0001g0108a0002c0002t0001g0203a0002c0002t0001g0204others(2): Show | 5 | HG00735.hp2 HG01123.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-5091C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253838 | ||||||
| chr10:102253947
|
C | T | 3 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0067 | 3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-10-4982C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253947 | ||||||
| chr10:102254134
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10-4795A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254134 | ||||||
| chr10:102254198
|
T | C | 3 | a0001c0001t0001g0115a0001c0001t0005g0153a0001c0001t0005g0156 | 3 | HG00280.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-10-4731T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254198 | ||||||
| chr10:102254463
|
G | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-4466G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254463 | ||||||
| chr10:102254483
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-10-4446T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254483 | ||||||
| chr10:102254666
|
G | A | 1 | a0001c0001t0003g0001 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-4263G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254666 | ||||||
| chr10:102254775
|
T | TATTTCTC others(461): Show |
2 | a0001c0001t0003g0232a0001c0001t0003g0233 | 2 | NA18959.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-10-4138_-10-4137i others(470): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102254775 | |||||
| chr10:102254775
|
T | TATTTCTC others(462): Show |
2 | a0001c0001t0003g0234a0001c0022t0003g0235 | 2 | HG00609.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-10-4138_-10-4137i others(471): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102254775 | |||||
| chr10:102255056
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-3873T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255056 | ||||||
| chr10:102255101
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-3828C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255101 | ||||||
| chr10:102255114
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-3815C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255114 | ||||||
| chr10:102255150
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-10-3779C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255150 | ||||||
| chr10:102255241
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-10-3688A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255241 | ||||||
| chr10:102255497
|
A | G | 5 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-3432A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255497 | ||||||
| chr10:102255522
|
A | G | 78 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0231others(75): Show | 79 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.-10-3407A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255522 | ||||||
| chr10:102255955
|
TATTATTT others(4): Show |
T | 1 | a0001c0001t0003g0251 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-10-2972_-10-2962d others(13): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102255955 | |||||
| chr10:102255967
|
A | G | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-10-2962A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255967 | ||||||
| chr10:102255980
|
C | T | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-2949C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255980 | ||||||
| chr10:102256061
|
G | T | 239 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(236): Show | 240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-10-2868G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256061 | ||||||
| chr10:102256076
|
A | G | 1 | a0002c0002t0001g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-10-2853A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256076 | ||||||
| chr10:102256165
|
G | A | 1 | a0001c0003t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10-2764G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256165 | ||||||
| chr10:102256423
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-10-2506T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256423 | ||||||
| chr10:102256508
|
T | TA | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-2409dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102256508 | |||||
| chr10:102256558
|
C | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-2371C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256558 | ||||||
| chr10:102256562
|
CTGGA | C | 326 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(323): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.-10-2362_-10-2359d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102256562 | |||||
| chr10:102256773
|
A | T | 1 | a0001c0001t0002g0098 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-10-2156A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256773 | ||||||
| chr10:102256834
|
T | C | 2 | a0005c0006t0001g0157a0005c0006t0001g0158 | 2 | HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-10-2095T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256834 | ||||||
| chr10:102257121
|
G | A | 5 | a0001c0001t0001g0231a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-1808G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257121 | ||||||
| chr10:102257289
|
T | G | 4 | a0001c0001t0001g0231a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-1640T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257289 | ||||||
| chr10:102257365
|
G | A | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-10-1564G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257365 | ||||||
| chr10:102257384
|
C | G | 1 | a0001c0001t0002g0300 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-10-1545C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257384 | ||||||
| chr10:102257421
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-1508G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257421 | ||||||
| chr10:102257616
|
G | C | 1 | a0001c0001t0005g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-1313G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257616 | ||||||
| chr10:102257864
|
G | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-1065G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257864 | ||||||
| chr10:102257877
|
G | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-10-1052G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257877 | ||||||
| chr10:102257988
|
G | A | 5 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-941G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257988 | ||||||
| chr10:102258150
|
A | AT | 6 | a0001c0001t0002g0012a0001c0001t0002g0020a0001c0001t0002g0063others(3): Show | 6 | HG00280.hp2 HG00738.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-757dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258150 | |||||
| chr10:102258150
|
AT | A | 128 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(125): Show | 128 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.-10-757delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258150 | |||||
| chr10:102258150
|
ATT | A | 93 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(90): Show | 94 | HG00609.hp1 HG00673.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.-10-758_-10-757del others(2): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258150 | |||||
| chr10:102258150
|
ATTT | A | 16 | a0001c0001t0001g0118a0001c0001t0001g0297a0001c0001t0003g0238others(13): Show | 16 | HG00642.hp2 HG01943.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-759_-10-757del others(3): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258150 | |||||
| chr10:102258228
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-701T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102258228 | ||||||
| chr10:102258275
|
C | T | 5 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-654C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102258275 | ||||||
| chr10:102258384
|
G | A | 1 | a0001c0001t0003g0261 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10-545G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102258384 | ||||||
| chr10:102258774
|
C | CAA | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-136_-10-135dup others(2): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258774 | |||||
| chr10:102258774
|
CA | C | 19 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0197others(16): Show | 19 | HG01074.hp1 HG01258.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-135delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258774 | |||||
| chr10:102258774
|
CAAAAAAA others(5): Show |
C | 86 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0231others(83): Show | 87 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-10-146_-10-135del others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258774 | |||||
| chr10:102258889
|
C | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-10-40C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102258889 | ||||||
| chr10:102259279
|
T | G | 1 | a0001c0001t0002g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.96+245T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259279 | ||||||
| chr10:102259452
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.96+418A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259452 | ||||||
| chr10:102259690
|
C | A | 297 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(294): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.97-360C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259690 | ||||||
| chr10:102259732
|
A | G | 9 | a0001c0001t0001g0241a0001c0001t0001g0243a0001c0001t0001g0244others(6): Show | 9 | HG01169.hp1 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-318A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259732 | ||||||
| chr10:102259767
|
T | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-283T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259767 | ||||||
| chr10:102259999
|
T | C | 4 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(1): Show | 4 | HG02280.hp1 NA18522.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-51T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259999 | ||||||
| chr10:102260473
|
C | CTT | 11 | a0001c0001t0001g0010a0001c0001t0001g0161a0001c0001t0001g0213others(8): Show | 11 | HG01070.hp2 HG01109.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+358_163+359dup others(2): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | |||||
| chr10:102260473
|
C | CTTT | 163 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 163 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.163+359_163+360ins others(3): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | |||||
| chr10:102260473
|
C | CTTTT | 46 | a0001c0001t0001g0009a0001c0001t0001g0114a0001c0001t0001g0117others(43): Show | 47 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.163+359_163+360ins others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | |||||
| chr10:102260473
|
C | CTTTTTTT others(2): Show |
6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG01074.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+359_163+360ins others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | |||||
| chr10:102260473
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0293others(3): Show | 6 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+359_163+360ins others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | |||||
| chr10:102260473
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0112a0007c0010t0001g0113 | 2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.163+359_163+360ins others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | |||||
| chr10:102260476
|
C | CT | 11 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0091others(8): Show | 11 | HG02027.hp1 HG02970.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+383dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260476 | |||||
| chr10:102260476
|
C | T | 237 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(234): Show | 238 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(235): Show |
intron_variant | MODIFIER | c.163+360C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260476 | ||||||
| chr10:102260566
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163+450C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260566 | ||||||
| chr10:102260600
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.163+484C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260600 | ||||||
| chr10:102260635
|
A | G | 2 | a0001c0003t0001g0207a0001c0003t0001g0225 | 2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.163+519A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260635 | ||||||
| chr10:102260743
|
C | T | 1 | a0001c0001t0003g0001 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.163+627C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260743 | ||||||
| chr10:102261231
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.163+1115A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261231 | ||||||
| chr10:102261235
|
TTG | T | 269 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(266): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.163+1141_163+1142d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261235 | |||||
| chr10:102261235
|
TTGTGTGT others(7): Show |
T | 27 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0208others(24): Show | 27 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.163+1129_163+1142d others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261235 | |||||
| chr10:102261277
|
T | C | 18 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0118others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.163+1161T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261277 | ||||||
| chr10:102261277
|
T | TAC | 3 | a0001c0001t0001g0208a0001c0001t0002g0064a0001c0001t0003g0242 | 3 | HG01099.hp2 HG04115.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.163+1177_163+1178d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261277 | |||||
| chr10:102261328
|
A | G | 59 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(56): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.163+1212A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261328 | ||||||
| chr10:102261352
|
G | C | 26 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0209others(23): Show | 26 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.163+1236G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261352 | ||||||
| chr10:102261581
|
C | CT | 4 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(1): Show | 4 | HG00558.hp1 HG00621.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+1466dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261581 | |||||
| chr10:102261615
|
C | CT | 15 | a0001c0001t0002g0022a0001c0001t0002g0053a0001c0001t0002g0054others(12): Show | 15 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.163+1517dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261615 | |||||
| chr10:102261615
|
CT | C | 223 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(220): Show | 224 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(221): Show |
intron_variant | MODIFIER | c.163+1517delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261615 | |||||
| chr10:102261620
|
T | C | 6 | a0001c0001t0001g0231a0001c0001t0001g0237a0001c0001t0001g0252others(3): Show | 6 | HG02258.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+1504T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261620 | ||||||
| chr10:102261633
|
T | G | 1 | a0001c0001t0003g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.163+1517T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261633 | ||||||
| chr10:102261748
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.163+1632A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261748 | ||||||
| chr10:102261784
|
A | G | 297 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(294): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.163+1668A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261784 | ||||||
| chr10:102261911
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+1795C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261911 | ||||||
| chr10:102261951
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.163+1835C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261951 | ||||||
| chr10:102261955
|
GCT | G | 7 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(4): Show | 7 | HG02027.hp1 NA18953.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+1841_163+1842d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261955 | |||||
| chr10:102261960
|
C | G | 7 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(4): Show | 7 | HG02027.hp1 NA18953.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+1844C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261960 | ||||||
| chr10:102262000
|
T | C | 2 | a0001c0001t0003g0232a0001c0001t0003g0234 | 2 | HG00609.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.163+1884T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262000 | ||||||
| chr10:102262253
|
C | A | 1 | a0001c0001t0003g0263 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.163+2137C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262253 | ||||||
| chr10:102262543
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0112 | 2 | HG01106.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.163+2427G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262543 | ||||||
| chr10:102262621
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163+2505C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262621 | ||||||
| chr10:102262656
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.163+2540T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262656 | ||||||
| chr10:102262849
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0112 | 2 | HG01106.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.163+2733C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262849 | ||||||
| chr10:102262956
|
A | G | 1 | a0001c0001t0003g0315 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.163+2840A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262956 | ||||||
| chr10:102263054
|
G | T | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.163+2938G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102263054 | ||||||
| chr10:102263208
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0050a0001c0001t0002g0090 | 3 | HG00621.hp2 HG00673.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.163+3092C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102263208 | ||||||
| chr10:102263541
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163+3425C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102263541 | ||||||
| chr10:102263542
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163+3426A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102263542 | ||||||
| chr10:102264114
|
C | T | 123 | a0001c0001t0001g0155a0001c0001t0001g0208a0001c0001t0001g0209others(120): Show | 123 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.163+3998C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102264114 | ||||||
| chr10:102264230
|
C | T | 1 | a0010c0017t0001g0193 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.163+4114C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102264230 | ||||||
| chr10:102264269
|
G | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.163+4153G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102264269 | ||||||
| chr10:102265589
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+5473G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102265589 | ||||||
| chr10:102265626
|
A | G | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.163+5510A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102265626 | ||||||
| chr10:102265653
|
C | G | 56 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(53): Show | 56 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.163+5537C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102265653 | ||||||
| chr10:102265683
|
C | CAATG | 3 | a0001c0001t0003g0262a0001c0001t0003g0319a0006c0011t0001g0295 | 3 | HG01074.hp1 NA18963.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.163+5594_163+5597d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102265683 | |||||
| chr10:102266021
|
A | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+5905A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266021 | ||||||
| chr10:102266050
|
A | C | 1 | a0001c0001t0001g0131 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.163+5934A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266050 | ||||||
| chr10:102266112
|
G | A | 1 | a0001c0001t0002g0060 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.163+5996G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266112 | ||||||
| chr10:102266195
|
T | C | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.163+6079T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266195 | ||||||
| chr10:102266217
|
T | G | 1 | a0001c0001t0002g0090 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.163+6101T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266217 | ||||||
| chr10:102267418
|
T | C | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | NA19002.hp1 NA19005.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+7302T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102267418 | ||||||
| chr10:102267502
|
T | TCAA | 90 | a0001c0001t0001g0254a0001c0001t0002g0002a0001c0001t0002g0003others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.163+7411_163+7413d others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102267502 | |||||
| chr10:102267546
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.163+7430T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102267546 | ||||||
| chr10:102267737
|
G | T | 1 | a0001c0001t0002g0057 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.163+7621G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102267737 | ||||||
| chr10:102268181
|
G | A | 328 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(325): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.163+8065G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102268181 | ||||||
| chr10:102268294
|
C | G | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.163+8178C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102268294 | ||||||
| chr10:102268365
|
A | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+8249A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102268365 | ||||||
| chr10:102268750
|
C | A | 88 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(85): Show | 88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+8634C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102268750 | ||||||
| chr10:102268945
|
T | C | 3 | a0001c0001t0006g0165a0001c0001t0006g0166a0010c0017t0001g0193 | 3 | HG03017.hp1 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.163+8829T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102268945 | ||||||
| chr10:102269180
|
G | A | 1 | a0001c0014t0001g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163+9064G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269180 | ||||||
| chr10:102269289
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+9173G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269289 | ||||||
| chr10:102269371
|
G | T | 1 | a0001c0001t0001g0255 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.163+9255G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269371 | ||||||
| chr10:102269428
|
C | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+9312C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269428 | ||||||
| chr10:102269550
|
A | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0132others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.163+9434A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269550 | ||||||
| chr10:102269709
|
C | T | 5 | a0001c0003t0001g0109a0001c0003t0001g0210a0001c0003t0001g0211others(2): Show | 5 | HG01070.hp2 HG01516.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+9593C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269709 | ||||||
| chr10:102269880
|
A | AT | 6 | a0001c0001t0001g0192a0001c0001t0002g0025a0001c0001t0002g0048others(3): Show | 6 | HG01123.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+9780dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102269880 | |||||
| chr10:102269965
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+9849G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269965 | ||||||
| chr10:102270035
|
T | C | 90 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.163+9919T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270035 | ||||||
| chr10:102270046
|
T | C | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+9930T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270046 | ||||||
| chr10:102270253
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.163+10137T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270253 | ||||||
| chr10:102270361
|
G | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0152 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.163+10245G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270361 | ||||||
| chr10:102270437
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+10321T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270437 | ||||||
| chr10:102270444
|
G | A | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+10328G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270444 | ||||||
| chr10:102270845
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.163+10729T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270845 | ||||||
| chr10:102270857
|
C | T | 1 | a0001c0001t0005g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+10741C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270857 | ||||||
| chr10:102271035
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10919T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271035 | ||||||
| chr10:102271036
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10920T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271036 | ||||||
| chr10:102271038
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10922T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271038 | ||||||
| chr10:102271039
|
T | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10923T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271039 | ||||||
| chr10:102271040
|
A | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10924A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271040 | ||||||
| chr10:102271041
|
T | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10925T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271041 | ||||||
| chr10:102271042
|
T | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10926T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271042 | ||||||
| chr10:102271044
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10928T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271044 | ||||||
| chr10:102271046
|
A | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10930A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271046 | ||||||
| chr10:102271047
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10931T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271047 | ||||||
| chr10:102271050
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10934T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271050 | ||||||
| chr10:102271052
|
T | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10936T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271052 | ||||||
| chr10:102271053
|
T | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10937T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271053 | ||||||
| chr10:102271059
|
A | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10943A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271059 | ||||||
| chr10:102271065
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10949T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271065 | ||||||
| chr10:102271067
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10951T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271067 | ||||||
| chr10:102271068
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10952T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271068 | ||||||
| chr10:102271070
|
C | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10954C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271070 | ||||||
| chr10:102271071
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10955T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271071 | ||||||
| chr10:102271077
|
G | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10961G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271077 | ||||||
| chr10:102271079
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10963C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271079 | ||||||
| chr10:102271080
|
C | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10964C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271080 | ||||||
| chr10:102271082
|
G | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10966G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271082 | ||||||
| chr10:102271084
|
C | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10968C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271084 | ||||||
| chr10:102271088
|
A | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10972A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271088 | ||||||
| chr10:102271092
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10976C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271092 | ||||||
| chr10:102271099
|
G | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10983G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271099 | ||||||
| chr10:102271104
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10988C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271104 | ||||||
| chr10:102271111
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10995C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271111 | ||||||
| chr10:102271113
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10997C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271113 | ||||||
| chr10:102271118
|
A | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11002A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271118 | ||||||
| chr10:102271119
|
G | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11003G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271119 | ||||||
| chr10:102271121
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11005T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271121 | ||||||
| chr10:102271123
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11007C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271123 | ||||||
| chr10:102271126
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11010C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271126 | ||||||
| chr10:102271127
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11011T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271127 | ||||||
| chr10:102271128
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11012C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271128 | ||||||
| chr10:102271130
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11014T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271130 | ||||||
| chr10:102271130
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+11014T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271130 | ||||||
| chr10:102271131
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+11015G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271131 | ||||||
| chr10:102271132
|
G | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11016G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271132 | ||||||
| chr10:102271133
|
G | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11017G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271133 | ||||||
| chr10:102271138
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11022T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271138 | ||||||
| chr10:102271140
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11024C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271140 | ||||||
| chr10:102271141
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11025C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271141 | ||||||
| chr10:102271142
|
A | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11026A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271142 | ||||||
| chr10:102271144
|
T | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11028T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271144 | ||||||
| chr10:102271145
|
C | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11029C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271145 | ||||||
| chr10:102271146
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11030T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271146 | ||||||
| chr10:102271149
|
T | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11033T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271149 | ||||||
| chr10:102271150
|
G | C | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11034G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271150 | ||||||
| chr10:102271151
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11035C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271151 | ||||||
| chr10:102271152
|
C | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11036C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271152 | ||||||
| chr10:102271157
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11041C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271157 | ||||||
| chr10:102271161
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11045C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271161 | ||||||
| chr10:102271164
|
A | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11048A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271164 | ||||||
| chr10:102271165
|
G | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11049G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271165 | ||||||
| chr10:102271167
|
A | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11051A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271167 | ||||||
| chr10:102271171
|
G | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11055G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271171 | ||||||
| chr10:102271173
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11057G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271173 | ||||||
| chr10:102271175
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11059C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271175 | ||||||
| chr10:102271183
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11067G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271183 | ||||||
| chr10:102271186
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11070C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271186 | ||||||
| chr10:102271187
|
G | A | 1 | a0002c0002t0001g0105 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.163+11071G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271187 | ||||||
| chr10:102271189
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11073C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271189 | ||||||
| chr10:102271194
|
C | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11078C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271194 | ||||||
| chr10:102271195
|
G | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11079G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271195 | ||||||
| chr10:102271196
|
C | CAAAGATC others(6): Show |
1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11080_163+1108 others(17): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271196 | ||||||
| chr10:102271197
|
C | G | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11081C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271197 | ||||||
| chr10:102271199
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11083G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271199 | ||||||
| chr10:102271200
|
G | T | 1 | a0001c0001t0002g0091 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11084G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271200 | ||||||
| chr10:102271293
|
T | C | 5 | a0001c0001t0001g0160a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+11177T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271293 | ||||||
| chr10:102271317
|
G | A | 1 | a0001c0001t0003g0256 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.163+11201G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271317 | ||||||
| chr10:102271461
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.163+11345A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271461 | ||||||
| chr10:102271466
|
T | C | 328 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(325): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.163+11350T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271466 | ||||||
| chr10:102271514
|
C | CT | 87 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0191others(84): Show | 88 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.163+11413dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102271514 | |||||
| chr10:102271514
|
CT | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0134others(8): Show | 11 | HG01358.hp2 HG01496.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+11413delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102271514 | |||||
| chr10:102271532
|
T | C | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.163+11416T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271532 | ||||||
| chr10:102271604
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0068 | 2 | HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.163+11488C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271604 | ||||||
| chr10:102271641
|
G | A | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.163+11525G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271641 | ||||||
| chr10:102271704
|
T | G | 1 | a0001c0001t0003g0307 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.163+11588T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271704 | ||||||
| chr10:102272023
|
G | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+11907G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102272023 | ||||||
| chr10:102272112
|
A | AT | 140 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(137): Show | 141 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.163+12009dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102272112 | |||||
| chr10:102272112
|
AT | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+12009delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102272112 | |||||
| chr10:102272219
|
C | T | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.163+12103C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102272219 | ||||||
| chr10:102272455
|
A | C | 1 | a0001c0001t0002g0052 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.163+12339A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102272455 | ||||||
| chr10:102272526
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.163+12410G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102272526 | ||||||
| chr10:102273546
|
T | G | 3 | a0001c0001t0002g0024a0001c0001t0002g0026a0001c0001t0002g0048 | 3 | NA18944.hp2 NA18979.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.163+13430T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102273546 | ||||||
| chr10:102273658
|
C | T | 3 | a0001c0001t0003g0285a0001c0001t0003g0286a0001c0001t0003g0287 | 3 | NA18979.hp1 NA19002.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.163+13542C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102273658 | ||||||
| chr10:102274218
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+14102G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274218 | ||||||
| chr10:102274330
|
T | C | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.163+14214T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274330 | ||||||
| chr10:102274556
|
A | G | 1 | a0001c0001t0003g0277 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.163+14440A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274556 | ||||||
| chr10:102274699
|
A | AT | 11 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0134others(8): Show | 11 | HG00558.hp2 HG01175.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+14613dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | |||||
| chr10:102274699
|
A | ATT | 24 | a0001c0001t0001g0141a0001c0001t0001g0209a0001c0001t0001g0213others(21): Show | 24 | HG00673.hp1 HG01070.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.163+14612_163+1461 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | |||||
| chr10:102274699
|
A | ATTT | 31 | a0001c0001t0001g0214a0001c0001t0001g0220a0001c0001t0001g0224others(28): Show | 31 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.163+14611_163+1461 others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | |||||
| chr10:102274699
|
A | ATTTT | 20 | a0001c0001t0001g0221a0001c0001t0002g0012a0001c0001t0002g0020others(17): Show | 20 | HG01123.hp2 HG01346.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.163+14610_163+1461 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | |||||
| chr10:102274699
|
AT | A | 79 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(76): Show | 79 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.163+14613delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | |||||
| chr10:102274699
|
ATT | A | 66 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(63): Show | 67 | HG00099.hp1 HG00673.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.163+14612_163+1461 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | |||||
| chr10:102274699
|
ATTTTTTT others(3): Show |
A | 25 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0075others(22): Show | 25 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.163+14604_163+1461 others(14): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | |||||
| chr10:102274699
|
ATTTTTTT others(4): Show |
A | 3 | a0001c0001t0002g0003a0001c0001t0002g0092a0001c0001t0002g0093 | 3 | HG01069.hp1 NA18967.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.163+14603_163+1461 others(15): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | |||||
| chr10:102274699
|
ATTTTTTT others(5): Show |
A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+14602_163+1461 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | |||||
| chr10:102274701
|
T | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.163+14585T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274701 | ||||||
| chr10:102274793
|
C | T | 21 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0134others(18): Show | 21 | HG01169.hp1 HG01256.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.163+14677C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274793 | ||||||
| chr10:102274877
|
A | G | 1 | a0001c0001t0002g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.163+14761A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274877 | ||||||
| chr10:102275011
|
C | CT | 17 | a0001c0001t0001g0125a0001c0001t0001g0141a0001c0001t0001g0324others(14): Show | 17 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.163+14913dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102275011 | |||||
| chr10:102275011
|
CT | C | 85 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(82): Show | 85 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.163+14913delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102275011 | |||||
| chr10:102275023
|
T | C | 59 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(56): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.163+14907T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102275023 | ||||||
| chr10:102275901
|
G | C | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0039 | 3 | HG02523.hp2 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.163+15785G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102275901 | ||||||
| chr10:102276251
|
G | A | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+16135G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276251 | ||||||
| chr10:102276254
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG03041.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.163+16138C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276254 | ||||||
| chr10:102276394
|
C | T | 2 | a0001c0001t0003g0314a0001c0001t0003g0317 | 2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.163+16278C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276394 | ||||||
| chr10:102276525
|
CA | C | 196 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(193): Show | 197 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.163+16429delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276525 | |||||
| chr10:102276525
|
CAA | C | 82 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.163+16428_163+1642 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276525 | |||||
| chr10:102276525
|
CAAAA | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+16426_163+1642 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276525 | |||||
| chr10:102276540
|
A | T | 1 | a0001c0001t0005g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+16424A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276540 | ||||||
| chr10:102276593
|
C | T | 1 | a0001c0001t0002g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.163+16477C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276593 | ||||||
| chr10:102276598
|
G | A | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.163+16482G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276598 | ||||||
| chr10:102276692
|
T | A | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+16576T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276692 | ||||||
| chr10:102276958
|
T | G | 22 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(19): Show | 22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.163+16842T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276958 | ||||||
| chr10:102276965
|
T | TAC | 13 | a0001c0001t0001g0159a0001c0001t0001g0208a0001c0001t0002g0036others(10): Show | 13 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+16875_163+1687 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276965 | |||||
| chr10:102276965
|
T | TACAC | 48 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0154others(45): Show | 48 | HG00544.hp1 HG00609.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.163+16873_163+1687 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276965 | |||||
| chr10:102276965
|
TAC | T | 32 | a0001c0001t0001g0115a0001c0001t0001g0209a0001c0001t0001g0213others(29): Show | 32 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.163+16875_163+1687 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276965 | |||||
| chr10:102276965
|
TACAC | T | 4 | a0001c0001t0001g0185a0001c0001t0001g0192a0001c0001t0001g0196others(1): Show | 4 | HG01928.hp1 HG01934.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+16873_163+1687 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276965 | |||||
| chr10:102277330
|
G | T | 1 | a0001c0001t0002g0020 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.163+17214G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277330 | ||||||
| chr10:102277392
|
C | CT | 6 | a0001c0001t0001g0298a0001c0001t0002g0020a0001c0001t0003g0279others(3): Show | 6 | HG02055.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+17293dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102277392 | |||||
| chr10:102277392
|
CT | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(39): Show | 42 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.163+17293delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102277392 | |||||
| chr10:102277409
|
T | C | 5 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+17293T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277409 | ||||||
| chr10:102277437
|
T | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+17321T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277437 | ||||||
| chr10:102277527
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163+17411C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277527 | ||||||
| chr10:102277576
|
G | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+17460G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277576 | ||||||
| chr10:102277668
|
C | T | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0213others(22): Show | 25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+17552C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277668 | ||||||
| chr10:102277987
|
T | C | 6 | a0001c0001t0002g0019a0001c0001t0002g0052a0001c0001t0002g0059others(3): Show | 6 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+17871T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277987 | ||||||
| chr10:102278275
|
C | CT | 15 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0003g0232others(12): Show | 15 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.163+18173dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102278275 | |||||
| chr10:102278425
|
A | G | 11 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+18309A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102278425 | ||||||
| chr10:102278530
|
G | T | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+18414G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102278530 | ||||||
| chr10:102278660
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+18544G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102278660 | ||||||
| chr10:102278800
|
T | C | 12 | a0001c0001t0003g0303a0001c0001t0003g0304a0001c0001t0003g0305others(9): Show | 12 | HG00673.hp2 HG02071.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+18684T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102278800 | ||||||
| chr10:102279006
|
T | G | 22 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(19): Show | 22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.163+18890T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279006 | ||||||
| chr10:102279009
|
A | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+18893A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279009 | ||||||
| chr10:102279217
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.163+19101G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279217 | ||||||
| chr10:102279548
|
G | A | 5 | a0001c0001t0003g0263a0001c0001t0003g0284a0001c0001t0003g0285others(2): Show | 5 | NA18950.hp2 NA18979.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+19432G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279548 | ||||||
| chr10:102279717
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.163+19601C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279717 | ||||||
| chr10:102279750
|
G | A | 1 | a0001c0001t0002g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.163+19634G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279750 | ||||||
| chr10:102279958
|
A | AT | 7 | a0001c0001t0002g0065a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+19851dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102279958 | |||||
| chr10:102280130
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0137a0001c0001t0001g0148others(1): Show | 4 | NA18951.hp2 NA18964.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+20014A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102280130 | ||||||
| chr10:102280519
|
T | TAACAGAG others(614): Show |
1 | a0001c0001t0002g0020 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.163+20418_163+2041 others(625): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102280519 | |||||
| chr10:102280557
|
G | A | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+20441G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102280557 | ||||||
| chr10:102280639
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+20523G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102280639 | ||||||
| chr10:102281581
|
G | A | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.163+21465G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102281581 | ||||||
| chr10:102281949
|
C | T | 6 | a0001c0003t0001g0207a0001c0003t0001g0225a0001c0003t0001g0227others(3): Show | 6 | HG01081.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+21833C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102281949 | ||||||
| chr10:102281950
|
A | G | 5 | a0001c0001t0002g0025a0001c0001t0002g0036a0001c0001t0002g0064others(2): Show | 5 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+21834A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102281950 | ||||||
| chr10:102281966
|
G | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+21850G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102281966 | ||||||
| chr10:102282052
|
G | T | 1 | a0001c0001t0005g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+21936G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282052 | ||||||
| chr10:102282093
|
AT | A | 12 | a0001c0001t0001g0186a0001c0001t0001g0296a0001c0001t0002g0067others(9): Show | 12 | HG01256.hp2 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+21991delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102282093 | |||||
| chr10:102282093
|
ATT | A | 91 | a0001c0001t0001g0160a0001c0001t0002g0002a0001c0001t0002g0003others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.163+21990_163+2199 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102282093 | |||||
| chr10:102282187
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.163+22071G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282187 | ||||||
| chr10:102282264
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.163+22148C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282264 | ||||||
| chr10:102282357
|
G | A | 19 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.163+22241G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282357 | ||||||
| chr10:102282403
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163+22287G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282403 | ||||||
| chr10:102282404
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163+22288A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282404 | ||||||
| chr10:102282852
|
G | A | 26 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0213others(23): Show | 26 | HG01070.hp2 HG01074.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.163+22736G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282852 | ||||||
| chr10:102283258
|
A | G | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0213others(22): Show | 25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+23142A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102283258 | ||||||
| chr10:102283329
|
C | T | 1 | a0001c0001t0003g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163+23213C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102283329 | ||||||
| chr10:102283759
|
G | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(26): Show | 29 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.163+23643G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102283759 | ||||||
| chr10:102284061
|
A | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0051 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.163+23945A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284061 | ||||||
| chr10:102284088
|
A | ACT | 118 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(115): Show | 119 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.163+23973_163+2397 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102284088 | |||||
| chr10:102284216
|
AT | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+24102delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102284216 | |||||
| chr10:102284318
|
A | G | 2 | a0001c0004t0002g0104a0002c0002t0001g0105 | 2 | HG06807.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.163+24202A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284318 | ||||||
| chr10:102284580
|
A | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+24464A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284580 | ||||||
| chr10:102284664
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.163+24548C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284664 | ||||||
| chr10:102284892
|
G | T | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+24776G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284892 | ||||||
| chr10:102285175
|
C | T | 12 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0140others(9): Show | 12 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+25059C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102285175 | ||||||
| chr10:102285425
|
C | T | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+25309C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102285425 | ||||||
| chr10:102286067
|
G | C | 1 | a0001c0003t0001g0226 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.163+25951G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286067 | ||||||
| chr10:102286194
|
G | GT | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0116others(8): Show | 11 | HG01891.hp1 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+26101dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102286194 | |||||
| chr10:102286194
|
GT | G | 93 | a0001c0001t0001g0011a0001c0001t0001g0144a0001c0001t0001g0152others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.163+26101delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102286194 | |||||
| chr10:102286202
|
T | TG | 117 | a0001c0001t0001g0007a0001c0001t0001g0110a0001c0001t0001g0111others(114): Show | 118 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(115): Show |
intron_variant | MODIFIER | c.163+26086_163+2608 others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286202 | ||||||
| chr10:102286203
|
T | G | 97 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0106others(94): Show | 97 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.163+26087T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286203 | ||||||
| chr10:102286204
|
T | G | 93 | a0001c0001t0001g0011a0001c0001t0001g0144a0001c0001t0001g0152others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.163+26088T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286204 | ||||||
| chr10:102286405
|
T | G | 3 | a0001c0001t0003g0267a0001c0001t0003g0276a0001c0001t0003g0292 | 3 | NA18941.hp1 NA18967.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.163+26289T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286405 | ||||||
| chr10:102286662
|
G | A | 1 | a0001c0007t0001g0329 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.163+26546G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286662 | ||||||
| chr10:102286725
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.163+26609A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286725 | ||||||
| chr10:102286871
|
AGT | A | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+26757_163+2675 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102286871 | |||||
| chr10:102286969
|
T | G | 1 | a0001c0001t0003g0261 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.163+26853T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286969 | ||||||
| chr10:102287283
|
A | C | 1 | a0001c0001t0001g0162 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.163+27167A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287283 | ||||||
| chr10:102287339
|
A | C | 8 | a0001c0001t0003g0263a0001c0004t0002g0104a0001c0004t0004g0004others(5): Show | 8 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+27223A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287339 | ||||||
| chr10:102287344
|
CT | C | 142 | a0001c0001t0001g0009a0001c0001t0001g0110a0001c0001t0001g0111others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.163+27255delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102287344 | |||||
| chr10:102287344
|
CTT | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0106a0001c0001t0001g0159others(9): Show | 12 | HG01258.hp2 HG02615.hp2 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+27254_163+2725 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102287344 | |||||
| chr10:102287344
|
CTTTTTTT | C | 10 | a0001c0001t0001g0136a0001c0001t0001g0163a0001c0001t0001g0168others(7): Show | 10 | HG01358.hp2 HG01928.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+27249_163+2725 others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102287344 | |||||
| chr10:102287344
|
CTTTTTTT others(1): Show |
C | 76 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(73): Show | 76 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.163+27248_163+2725 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102287344 | |||||
| chr10:102287345
|
T | A | 2 | a0001c0001t0002g0012a0006c0011t0001g0295 | 2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.163+27229T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287345 | ||||||
| chr10:102287350
|
T | A | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+27234T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287350 | ||||||
| chr10:102287355
|
T | A | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+27239T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287355 | ||||||
| chr10:102287401
|
T | C | 1 | a0001c0001t0003g0277 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.163+27285T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287401 | ||||||
| chr10:102287472
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.163+27356G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287472 | ||||||
| chr10:102287795
|
C | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(26): Show | 29 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.163+27679C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287795 | ||||||
| chr10:102287862
|
C | T | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0213others(22): Show | 25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+27746C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287862 | ||||||
| chr10:102288079
|
G | T | 58 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0018others(55): Show | 58 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.163+27963G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288079 | ||||||
| chr10:102288254
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.163+28138T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288254 | ||||||
| chr10:102288327
|
TATATAAT others(1): Show |
T | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+28224_163+2823 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288327 | |||||
| chr10:102288438
|
G | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+28322G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288438 | ||||||
| chr10:102288480
|
G | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0293a0007c0010t0001g0113 | 3 | HG02615.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.163+28364G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288480 | ||||||
| chr10:102288482
|
C | A | 1 | a0001c0001t0003g0273 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.163+28366C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288482 | ||||||
| chr10:102288482
|
C | T | 1 | a0001c0001t0006g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.163+28366C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288482 | ||||||
| chr10:102288484
|
G | A | 4 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0094others(1): Show | 4 | NA18967.hp2 NA18977.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+28368G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288484 | ||||||
| chr10:102288507
|
C | T | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+28391C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288507 | ||||||
| chr10:102288565
|
GCCGGGCG others(20): Show |
G | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163+28452_163+2847 others(31): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288565 | |||||
| chr10:102288712
|
C | T | 1 | a0012c0018t0001g0205 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.163+28596C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288712 | ||||||
| chr10:102288722
|
G | GA | 42 | a0001c0001t0001g0118a0001c0001t0001g0120a0001c0001t0001g0136others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.163+28619dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288722 | |||||
| chr10:102288722
|
G | GAA | 56 | a0001c0001t0002g0012a0001c0001t0002g0019a0001c0001t0002g0020others(53): Show | 56 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.163+28618_163+2861 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288722 | |||||
| chr10:102288736
|
C | A | 93 | a0001c0001t0001g0214a0001c0001t0002g0002a0001c0001t0002g0003others(90): Show | 93 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.163+28620C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288736 | ||||||
| chr10:102288736
|
C | CA | 81 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(78): Show | 81 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.163+28632dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288736 | |||||
| chr10:102288738
|
A | AC | 3 | a0001c0001t0001g0140a0001c0001t0001g0230a0001c0001t0001g0322 | 3 | HG00621.hp1 HG02080.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.163+28622_163+2862 others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288738 | ||||||
| chr10:102288739
|
A | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0132others(10): Show | 13 | HG00544.hp2 HG00558.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+28623A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288739 | ||||||
| chr10:102288838
|
C | T | 4 | a0001c0001t0003g0232a0001c0001t0003g0233a0001c0001t0003g0234others(1): Show | 4 | HG00609.hp1 NA18959.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+28722C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288838 | ||||||
| chr10:102289105
|
GA | G | 59 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0019others(56): Show | 59 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.163+29005delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102289105 | |||||
| chr10:102289105
|
GAA | G | 37 | a0001c0001t0002g0003a0001c0001t0002g0018a0001c0001t0002g0029others(34): Show | 37 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.163+29004_163+2900 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102289105 | |||||
| chr10:102289393
|
G | A | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+29277G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102289393 | ||||||
| chr10:102289524
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.163+29408A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102289524 | ||||||
| chr10:102289922
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.163+29806C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102289922 | ||||||
| chr10:102289971
|
C | T | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+29855C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102289971 | ||||||
| chr10:102290027
|
C | G | 6 | a0001c0001t0002g0028a0001c0001t0002g0040a0001c0001t0002g0041others(3): Show | 6 | HG01934.hp2 HG01943.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+29911C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290027 | ||||||
| chr10:102290209
|
C | T | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.163+30093C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290209 | ||||||
| chr10:102290249
|
G | A | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+30133G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290249 | ||||||
| chr10:102290263
|
T | G | 1 | a0001c0001t0002g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.163+30147T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290263 | ||||||
| chr10:102290422
|
A | T | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+30306A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290422 | ||||||
| chr10:102290635
|
A | G | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0213others(22): Show | 25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+30519A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290635 | ||||||
| chr10:102291083
|
A | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+30967A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291083 | ||||||
| chr10:102291140
|
TTTTC | T | 25 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0213others(22): Show | 25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+31030_163+3103 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102291140 | |||||
| chr10:102291171
|
C | CTTTG | 13 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0149others(10): Show | 13 | HG00621.hp1 HG02027.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+31083_163+3108 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102291171 | |||||
| chr10:102291171
|
C | T | 1 | a0001c0001t0001g0182 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.163+31055C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291171 | ||||||
| chr10:102291345
|
T | C | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+31229T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291345 | ||||||
| chr10:102291408
|
G | T | 3 | a0001c0001t0003g0001a0001c0001t0003g0272a0001c0001t0003g0279 | 4 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+31292G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291408 | ||||||
| chr10:102291667
|
T | C | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.163+31551T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291667 | ||||||
| chr10:102291728
|
C | T | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+31612C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291728 | ||||||
| chr10:102291752
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+31636G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291752 | ||||||
| chr10:102291890
|
C | CT | 102 | a0001c0001t0001g0010a0001c0001t0001g0137a0001c0001t0001g0148others(99): Show | 102 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.163+31791dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102291890 | |||||
| chr10:102292141
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163+32025G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292141 | ||||||
| chr10:102292187
|
C | A | 1 | a0001c0001t0002g0064 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163+32071C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292187 | ||||||
| chr10:102292315
|
A | T | 1 | a0001c0001t0002g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.163+32199A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292315 | ||||||
| chr10:102292349
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.163+32233C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292349 | ||||||
| chr10:102292660
|
G | A | 1 | a0001c0001t0002g0300 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.163+32544G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292660 | ||||||
| chr10:102292811
|
G | A | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+32695G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292811 | ||||||
| chr10:102292936
|
A | G | 1 | a0001c0003t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.163+32820A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292936 | ||||||
| chr10:102293102
|
G | A | 3 | a0001c0001t0001g0111a0001c0001t0001g0293a0007c0010t0001g0113 | 3 | HG02615.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.163+32986G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293102 | ||||||
| chr10:102293400
|
TTATC | T | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+33288_163+3329 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293400 | |||||
| chr10:102293584
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.163+33468C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293584 | ||||||
| chr10:102293623
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163+33507C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293623 | ||||||
| chr10:102293762
|
ATGTTTTG | A | 5 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+33653_163+3365 others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293762 | |||||
| chr10:102293764
|
G | GT | 3 | a0001c0001t0001g0162a0005c0006t0001g0157a0005c0006t0001g0158 | 3 | HG00544.hp1 HG02135.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.163+33652dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTT | 11 | a0001c0001t0001g0011a0001c0001t0001g0132a0001c0001t0001g0144others(8): Show | 11 | HG00738.hp2 HG01192.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+33649_163+3365 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTT | 32 | a0001c0001t0001g0005a0001c0001t0001g0133a0001c0001t0001g0134others(29): Show | 32 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTT | 31 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0150others(28): Show | 31 | HG00280.hp2 HG00558.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT | 32 | a0001c0001t0001g0114a0001c0001t0001g0141a0001c0001t0001g0208others(29): Show | 32 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(1): Show |
18 | a0001c0001t0002g0035a0001c0001t0002g0039a0001c0001t0002g0042others(15): Show | 18 | HG00621.hp2 HG01516.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(2): Show |
12 | a0001c0001t0002g0028a0001c0001t0002g0040a0001c0001t0002g0041others(9): Show | 12 | HG01934.hp2 HG02027.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(13): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0148 | 2 | NA18964.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(14): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(5): Show |
1 | a0002c0002t0001g0105 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.163+33652_163+3365 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(6): Show |
3 | a0002c0002t0001g0108a0002c0002t0001g0172a0002c0002t0001g0203 | 3 | HG01099.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(17): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(7): Show |
6 | a0001c0001t0001g0107a0001c0001t0001g0168a0001c0001t0001g0182others(3): Show | 6 | HG01123.hp1 HG01981.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(8): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0164a0001c0001t0001g0177others(5): Show | 8 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(19): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(9): Show |
7 | a0001c0001t0001g0163a0001c0001t0001g0181a0001c0001t0001g0184others(4): Show | 7 | HG00609.hp2 HG02683.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(20): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(10): Show |
3 | a0001c0001t0001g0106a0001c0001t0001g0174a0001c0001t0005g0156 | 3 | HG00280.hp1 NA18945.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(21): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(11): Show |
2 | a0001c0001t0001g0161a0001c0001t0006g0165 | 2 | HG02293.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(22): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(14): Show |
4 | a0001c0001t0001g0007a0001c0001t0001g0171a0001c0001t0001g0183others(1): Show | 4 | HG03471.hp2 HG04204.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(25): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(15): Show |
2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(26): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(16): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0198a0002c0002t0001g0199 | 3 | HG01258.hp1 NA18982.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(27): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
G | GTTTTTTT others(17): Show |
1 | a0002c0002t0001g0178 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.163+33652_163+3365 others(28): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
GTTTTGTG others(4): Show |
G | 4 | a0001c0001t0003g0261a0001c0001t0003g0313a0001c0001t0003g0316others(1): Show | 4 | HG00741.hp1 HG02148.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+33653_163+3366 others(15): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
GTTTTGTG others(5): Show |
G | 103 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(100): Show | 104 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.163+33653_163+3366 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
GTTTTGTG others(6): Show |
G | 7 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0127others(4): Show | 7 | HG01169.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+33653_163+3366 others(17): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
GTTTTGTG others(7): Show |
G | 2 | a0004c0008t0001g0195a0004c0008t0001g0200 | 2 | NA18949.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.163+33653_163+3366 others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293764
|
GTTTTGTG others(8): Show |
G | 10 | a0001c0001t0001g0154a0001c0001t0001g0175a0001c0001t0001g0179others(7): Show | 10 | HG01928.hp1 HG01934.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+33653_163+3366 others(19): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | |||||
| chr10:102293765
|
TTTTGTG | T | 6 | a0001c0004t0002g0104a0001c0004t0004g0015a0003c0005t0002g0077others(3): Show | 6 | HG01074.hp1 HG06807.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+33653_163+3365 others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293765 | |||||
| chr10:102293769
|
G | T | 183 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(180): Show | 183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.163+33653G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293769 | ||||||
| chr10:102293771
|
G | T | 184 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(181): Show | 184 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.163+33655G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293771 | ||||||
| chr10:102293838
|
C | T | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+33722C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293838 | ||||||
| chr10:102293955
|
T | G | 2 | a0001c0001t0003g0202a0001c0023t0003g0269 | 2 | HG01106.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.163+33839T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293955 | ||||||
| chr10:102294152
|
A | G | 1 | a0001c0001t0002g0076 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.163+34036A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294152 | ||||||
| chr10:102294257
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163+34141G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294257 | ||||||
| chr10:102294386
|
C | CT | 87 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(84): Show | 87 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.163+34283dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102294386 | |||||
| chr10:102294526
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+34410C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294526 | ||||||
| chr10:102294621
|
C | T | 5 | a0001c0003t0001g0109a0001c0003t0001g0210a0001c0003t0001g0211others(2): Show | 5 | HG01070.hp2 HG01516.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+34505C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294621 | ||||||
| chr10:102294671
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.163+34555C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294671 | ||||||
| chr10:102294707
|
G | A | 1 | a0001c0001t0002g0103 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.163+34591G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294707 | ||||||
| chr10:102294848
|
T | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+34732T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294848 | ||||||
| chr10:102294860
|
C | T | 2 | a0001c0001t0002g0030a0001c0001t0002g0051 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.163+34744C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294860 | ||||||
| chr10:102295361
|
A | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+35245A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102295361 | ||||||
| chr10:102295799
|
C | T | 18 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.163+35683C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102295799 | ||||||
| chr10:102295831
|
A | AT | 5 | a0001c0001t0003g0251a0001c0001t0003g0267a0001c0001t0003g0276others(2): Show | 5 | NA18941.hp1 NA18967.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+35717dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102295831 | |||||
| chr10:102295955
|
T | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+35839T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102295955 | ||||||
| chr10:102296159
|
A | G | 1 | a0001c0001t0002g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163+36043A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296159 | ||||||
| chr10:102296226
|
A | G | 55 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(52): Show | 55 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.163+36110A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296226 | ||||||
| chr10:102296511
|
A | G | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.163+36395A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296511 | ||||||
| chr10:102296610
|
C | T | 4 | a0001c0001t0002g0018a0001c0001t0002g0035a0008c0012t0002g0031others(1): Show | 4 | HG01928.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+36494C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296610 | ||||||
| chr10:102296671
|
G | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(26): Show | 29 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.163+36555G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296671 | ||||||
| chr10:102296709
|
C | T | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+36593C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296709 | ||||||
| chr10:102297057
|
G | A | 1 | a0003c0005t0002g0102 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.163+36941G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297057 | ||||||
| chr10:102297057
|
G | GA | 87 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(84): Show | 87 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.163+36949dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102297057 | |||||
| chr10:102297153
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163+37037C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297153 | ||||||
| chr10:102297195
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0139others(1): Show | 4 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+37079T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297195 | ||||||
| chr10:102297335
|
T | C | 1 | a0001c0001t0002g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.163+37219T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297335 | ||||||
| chr10:102297494
|
A | C | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+37378A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297494 | ||||||
| chr10:102297724
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.163+37608A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297724 | ||||||
| chr10:102297916
|
A | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+37800A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297916 | ||||||
| chr10:102297931
|
G | T | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.163+37815G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297931 | ||||||
| chr10:102297939
|
G | T | 4 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0051others(1): Show | 4 | HG02258.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+37823G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297939 | ||||||
| chr10:102297959
|
G | A | 1 | a0005c0006t0001g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.163+37843G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297959 | ||||||
| chr10:102298007
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.163+37891T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298007 | ||||||
| chr10:102298030
|
T | G | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.163+37914T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298030 | ||||||
| chr10:102298037
|
T | C | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.163+37921T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298037 | ||||||
| chr10:102298042
|
C | G | 1 | a0002c0002t0001g0173 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.163+37926C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298042 | ||||||
| chr10:102298115
|
A | G | 1 | a0001c0003t0001g0225 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.163+37999A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298115 | ||||||
| chr10:102298441
|
G | A | 1 | a0001c0024t0001g0229 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.163+38325G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298441 | ||||||
| chr10:102298495
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.163+38379C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298495 | ||||||
| chr10:102298764
|
G | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0063 | 2 | HG00280.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.163+38648G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298764 | ||||||
| chr10:102298880
|
C | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+38764C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298880 | ||||||
| chr10:102299238
|
T | C | 5 | a0001c0001t0001g0231a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+39122T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299238 | ||||||
| chr10:102299382
|
A | G | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+39266A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299382 | ||||||
| chr10:102299409
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.163+39293G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299409 | ||||||
| chr10:102299545
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.163+39429C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299545 | ||||||
| chr10:102299636
|
G | A | 4 | a0001c0001t0002g0018a0001c0001t0002g0035a0008c0012t0002g0031others(1): Show | 4 | HG01928.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+39520G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299636 | ||||||
| chr10:102299659
|
G | A | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.163+39543G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299659 | ||||||
| chr10:102299741
|
G | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+39625G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299741 | ||||||
| chr10:102299983
|
A | G | 1 | a0001c0001t0002g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.163+39867A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299983 | ||||||
| chr10:102300303
|
G | C | 77 | a0001c0001t0001g0191a0001c0001t0001g0241a0001c0001t0001g0243others(74): Show | 78 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.163+40187G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102300303 | ||||||
| chr10:102300772
|
C | T | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+40656C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102300772 | ||||||
| chr10:102300976
|
C | CT | 227 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.163+40876dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102300976 | |||||
| chr10:102300976
|
C | CTT | 12 | a0001c0001t0001g0007a0001c0001t0001g0170a0001c0001t0002g0065others(9): Show | 12 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+40875_163+4087 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102300976 | |||||
| chr10:102300999
|
T | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0019others(47): Show | 50 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.163+40883T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102300999 | ||||||
| chr10:102301063
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.163+40947A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301063 | ||||||
| chr10:102301269
|
C | T | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+41153C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301269 | ||||||
| chr10:102301323
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163+41207C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301323 | ||||||
| chr10:102301339
|
T | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+41223T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301339 | ||||||
| chr10:102301368
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+41252T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301368 | ||||||
| chr10:102301461
|
C | T | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.163+41345C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301461 | ||||||
| chr10:102301462
|
G | A | 88 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0191others(85): Show | 89 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.163+41346G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301462 | ||||||
| chr10:102301521
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163+41405G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301521 | ||||||
| chr10:102301625
|
C | T | 1 | a0005c0006t0001g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.163+41509C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301625 | ||||||
| chr10:102301785
|
G | T | 1 | a0001c0013t0002g0049 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.163+41669G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301785 | ||||||
| chr10:102301853
|
C | T | 1 | a0001c0001t0003g0315 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.163+41737C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301853 | ||||||
| chr10:102301949
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.163+41833C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301949 | ||||||
| chr10:102302038
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.163+41922A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302038 | ||||||
| chr10:102302134
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.164-41917G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302134 | ||||||
| chr10:102302191
|
T | C | 1 | a0001c0001t0003g0285 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.164-41860T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302191 | ||||||
| chr10:102302251
|
TGTGGAAA others(5): Show |
T | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.164-41799_164-4178 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302251 | ||||||
| chr10:102302460
|
C | T | 1 | a0001c0001t0003g0272 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.164-41591C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302460 | ||||||
| chr10:102302657
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.164-41394A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302657 | ||||||
| chr10:102302678
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.164-41373A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302678 | ||||||
| chr10:102302735
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.164-41316A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302735 | ||||||
| chr10:102302737
|
A | G | 123 | a0001c0001t0001g0155a0001c0001t0001g0208a0001c0001t0001g0209others(120): Show | 123 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.164-41314A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302737 | ||||||
| chr10:102302847
|
G | A | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-41204G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302847 | ||||||
| chr10:102302931
|
A | G | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.164-41120A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302931 | ||||||
| chr10:102302986
|
C | CT | 44 | a0001c0001t0001g0124a0001c0001t0001g0133a0001c0001t0001g0137others(41): Show | 44 | HG00544.hp2 HG00558.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.164-41047dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102302986 | |||||
| chr10:102303005
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-41046G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303005 | ||||||
| chr10:102303118
|
G | A | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-40933G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303118 | ||||||
| chr10:102303458
|
G | A | 1 | a0001c0001t0002g0103 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.164-40593G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303458 | ||||||
| chr10:102303610
|
A | G | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.164-40441A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303610 | ||||||
| chr10:102303730
|
C | A | 5 | a0001c0001t0002g0022a0001c0001t0002g0053a0001c0001t0002g0055others(2): Show | 5 | NA18951.hp1 NA18968.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-40321C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303730 | ||||||
| chr10:102303796
|
A | G | 3 | a0001c0001t0006g0165a0001c0001t0006g0166a0010c0017t0001g0193 | 3 | HG03017.hp1 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.164-40255A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303796 | ||||||
| chr10:102303800
|
T | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-40251T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303800 | ||||||
| chr10:102303860
|
A | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-40191A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303860 | ||||||
| chr10:102303990
|
G | GT | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-40051dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102303990 | |||||
| chr10:102304094
|
T | C | 4 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(1): Show | 4 | HG00558.hp1 HG00621.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-39957T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304094 | ||||||
| chr10:102304287
|
C | T | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-39764C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304287 | ||||||
| chr10:102304345
|
C | T | 29 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(26): Show | 29 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.164-39706C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304345 | ||||||
| chr10:102304493
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.164-39558G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304493 | ||||||
| chr10:102304791
|
A | G | 113 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(110): Show | 114 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.164-39260A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304791 | ||||||
| chr10:102304989
|
AAAAG | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0001g0148others(2): Show | 5 | HG01175.hp2 HG02074.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-39034_164-3903 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102304989 | |||||
| chr10:102304989
|
AAAAGAAA others(1): Show |
A | 321 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(318): Show | 322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.164-39038_164-3903 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102304989 | |||||
| chr10:102305089
|
C | A | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.164-38962C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305089 | ||||||
| chr10:102305128
|
C | G | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.164-38923C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305128 | ||||||
| chr10:102305175
|
T | TTG | 20 | a0001c0001t0001g0123a0001c0001t0001g0209a0001c0001t0001g0218others(17): Show | 21 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.164-38832_164-3883 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305175
|
T | TTGTG | 5 | a0001c0001t0001g0118a0001c0001t0001g0219a0001c0001t0002g0041others(2): Show | 5 | HG01934.hp2 HG02698.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-38834_164-3883 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305175
|
T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0155a0001c0001t0001g0214a0001c0004t0004g0004others(3): Show | 6 | HG02055.hp1 HG02486.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-38838_164-3883 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305175
|
T | TTGTGTGT others(5): Show |
1 | a0001c0004t0004g0017 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-38842_164-3883 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305175
|
TTG | T | 66 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0115others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.164-38832_164-3883 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305175
|
TTGTG | T | 156 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0111others(153): Show | 156 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.164-38834_164-3883 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305175
|
TTGTGTG | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(33): Show | 36 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.164-38836_164-3883 others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305175
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0001g0137a0001c0001t0002g0086a0001c0001t0002g0097 | 3 | HG03942.hp2 HG04184.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.164-38838_164-3883 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305175
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0230 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.164-38840_164-3883 others(14): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305175
|
TTGTGTGT others(5): Show |
T | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-38842_164-3883 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | |||||
| chr10:102305472
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-38579T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305472 | ||||||
| chr10:102305488
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.164-38563T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305488 | ||||||
| chr10:102305540
|
G | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-38511G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305540 | ||||||
| chr10:102305610
|
C | CA | 10 | a0001c0001t0002g0037a0001c0001t0002g0046a0001c0004t0002g0104others(7): Show | 10 | HG01074.hp1 HG01358.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-38431dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305610 | |||||
| chr10:102305771
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.164-38280C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305771 | ||||||
| chr10:102305983
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.164-38068A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305983 | ||||||
| chr10:102306046
|
C | CTA | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.164-37994_164-3799 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102306046 | |||||
| chr10:102306360
|
C | A | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.164-37691C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306360 | ||||||
| chr10:102306463
|
G | A | 5 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-37588G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306463 | ||||||
| chr10:102306480
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164-37571A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306480 | ||||||
| chr10:102306482
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-37569G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306482 | ||||||
| chr10:102306615
|
G | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0152 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.164-37436G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306615 | ||||||
| chr10:102306650
|
C | T | 2 | a0001c0001t0002g0098a0001c0001t0002g0300 | 2 | NA18961.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.164-37401C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306650 | ||||||
| chr10:102306750
|
A | T | 55 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(52): Show | 55 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.164-37301A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306750 | ||||||
| chr10:102306883
|
A | G | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.164-37168A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306883 | ||||||
| chr10:102306945
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.164-37106T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306945 | ||||||
| chr10:102306951
|
ATC | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 5 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-37098_164-3709 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102306951 | |||||
| chr10:102307100
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.164-36951T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307100 | ||||||
| chr10:102307228
|
A | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-36823A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307228 | ||||||
| chr10:102307246
|
T | C | 4 | a0001c0001t0002g0018a0001c0001t0002g0035a0008c0012t0002g0031others(1): Show | 4 | HG01928.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-36805T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307246 | ||||||
| chr10:102307266
|
A | G | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.164-36785A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307266 | ||||||
| chr10:102307443
|
C | CA | 10 | a0001c0001t0001g0191a0001c0001t0001g0247a0001c0001t0001g0322others(7): Show | 10 | HG00609.hp1 HG01358.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-36592dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102307443 | |||||
| chr10:102307461
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.164-36590G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307461 | ||||||
| chr10:102307476
|
G | A | 2 | a0001c0001t0002g0021a0001c0001t0002g0038 | 2 | HG00099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.164-36575G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307476 | ||||||
| chr10:102307682
|
C | T | 6 | a0001c0001t0002g0028a0001c0001t0002g0040a0001c0001t0002g0041others(3): Show | 6 | HG01934.hp2 HG01943.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-36369C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307682 | ||||||
| chr10:102307734
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.164-36317G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307734 | ||||||
| chr10:102307829
|
A | G | 1 | a0002c0002t0001g0199 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.164-36222A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307829 | ||||||
| chr10:102307831
|
T | C | 4 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(1): Show | 4 | HG00558.hp1 HG00621.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-36220T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307831 | ||||||
| chr10:102307889
|
A | C | 1 | a0001c0001t0002g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.164-36162A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307889 | ||||||
| chr10:102308201
|
T | TA | 164 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(161): Show | 165 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.164-35832dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102308201 | |||||
| chr10:102308201
|
T | TAA | 66 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(63): Show | 66 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.164-35833_164-3583 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102308201 | |||||
| chr10:102308201
|
T | TAAA | 84 | a0001c0001t0001g0187a0001c0001t0002g0002a0001c0001t0002g0003others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.164-35834_164-3583 others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102308201 | |||||
| chr10:102308280
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.164-35771A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308280 | ||||||
| chr10:102308290
|
A | T | 5 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(2): Show | 5 | HG00099.hp2 HG01255.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-35761A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308290 | ||||||
| chr10:102308381
|
A | G | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.164-35670A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308381 | ||||||
| chr10:102308633
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.164-35418C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308633 | ||||||
| chr10:102308739
|
G | A | 83 | a0001c0001t0001g0191a0001c0001t0001g0231a0001c0001t0001g0237others(80): Show | 84 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.164-35312G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308739 | ||||||
| chr10:102309164
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.164-34887C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309164 | ||||||
| chr10:102309700
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-34351C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309700 | ||||||
| chr10:102309701
|
T | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-34350T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309701 | ||||||
| chr10:102309707
|
T | C | 1 | a0001c0001t0002g0065 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164-34344T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309707 | ||||||
| chr10:102309839
|
C | A | 1 | a0001c0001t0002g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.164-34212C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309839 | ||||||
| chr10:102310259
|
A | G | 22 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(19): Show | 22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.164-33792A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102310259 | ||||||
| chr10:102310927
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.164-33124G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102310927 | ||||||
| chr10:102311295
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-32756G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311295 | ||||||
| chr10:102311338
|
T | A | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-32713T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311338 | ||||||
| chr10:102311431
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.164-32620T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311431 | ||||||
| chr10:102311460
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.164-32591A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311460 | ||||||
| chr10:102311725
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.164-32326C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311725 | ||||||
| chr10:102312044
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.164-32007C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312044 | ||||||
| chr10:102312216
|
C | G | 58 | a0001c0001t0002g0002a0001c0001t0002g0012a0001c0001t0002g0018others(55): Show | 58 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.164-31835C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312216 | ||||||
| chr10:102312295
|
G | GA | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-31741dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102312295 | |||||
| chr10:102312295
|
GA | G | 32 | a0001c0001t0001g0127a0001c0001t0002g0003a0001c0001t0002g0027others(29): Show | 32 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.164-31741delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102312295 | |||||
| chr10:102312538
|
G | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.164-31513G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312538 | ||||||
| chr10:102312570
|
T | C | 98 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.164-31481T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312570 | ||||||
| chr10:102312609
|
GGTTAAAA others(7): Show |
G | 1 | a0001c0001t0005g0153 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-31424_164-3141 others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102312609 | |||||
| chr10:102312699
|
C | T | 3 | a0001c0001t0003g0261a0001c0001t0003g0268a0001c0001t0003g0270 | 3 | HG00735.hp1 HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.164-31352C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312699 | ||||||
| chr10:102313014
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.164-31037G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313014 | ||||||
| chr10:102313090
|
C | T | 2 | a0001c0001t0003g0275a0001c0001t0003g0282 | 2 | NA19079.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.164-30961C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313090 | ||||||
| chr10:102313207
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.164-30844G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313207 | ||||||
| chr10:102313358
|
AC | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0067 | 3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.164-30691delC | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102313358 | |||||
| chr10:102313363
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.164-30688C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313363 | ||||||
| chr10:102313692
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.164-30359C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313692 | ||||||
| chr10:102314020
|
A | G | 6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0029others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-30031A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314020 | ||||||
| chr10:102314075
|
A | G | 1 | a0001c0024t0001g0229 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.164-29976A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314075 | ||||||
| chr10:102314141
|
C | CT | 126 | a0001c0001t0001g0139a0001c0001t0001g0154a0001c0001t0001g0162others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.164-29891dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102314141 | |||||
| chr10:102314141
|
C | CTT | 17 | a0001c0001t0001g0007a0001c0001t0001g0159a0001c0001t0002g0037others(14): Show | 17 | HG00738.hp1 HG01358.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.164-29892_164-2989 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102314141 | |||||
| chr10:102314141
|
C | CTTTT | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-29894_164-2989 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102314141 | |||||
| chr10:102314301
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.164-29750C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314301 | ||||||
| chr10:102314302
|
A | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-29749A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314302 | ||||||
| chr10:102314308
|
C | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0132others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-29743C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314308 | ||||||
| chr10:102314318
|
A | AT | 8 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-29725dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102314318 | |||||
| chr10:102314394
|
G | A | 5 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 5 | HG02280.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-29657G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314394 | ||||||
| chr10:102314398
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.164-29653A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314398 | ||||||
| chr10:102314398
|
A | T | 91 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.164-29653A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314398 | ||||||
| chr10:102314519
|
G | A | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.164-29532G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314519 | ||||||
| chr10:102314565
|
T | A | 98 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.164-29486T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314565 | ||||||
| chr10:102314583
|
G | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0132others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-29468G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314583 | ||||||
| chr10:102314815
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.164-29236G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314815 | ||||||
| chr10:102314935
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.164-29116A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314935 | ||||||
| chr10:102315138
|
G | A | 1 | a0001c0004t0004g0017 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-28913G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315138 | ||||||
| chr10:102315308
|
C | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0067 | 3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.164-28743C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315308 | ||||||
| chr10:102315337
|
G | T | 1 | a0001c0001t0002g0025 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.164-28714G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315337 | ||||||
| chr10:102315460
|
A | G | 114 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(111): Show | 115 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.164-28591A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315460 | ||||||
| chr10:102315554
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.164-28497C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315554 | ||||||
| chr10:102315651
|
T | G | 1 | a0001c0001t0003g0290 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.164-28400T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315651 | ||||||
| chr10:102315784
|
T | G | 98 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.164-28267T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315784 | ||||||
| chr10:102315861
|
A | G | 6 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(3): Show | 6 | HG02559.hp2 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-28190A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315861 | ||||||
| chr10:102315863
|
TA | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0137a0001c0001t0001g0148 | 3 | NA18964.hp1 NA18992.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.164-28187delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315863 | ||||||
| chr10:102315964
|
T | C | 91 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.164-28087T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315964 | ||||||
| chr10:102316084
|
C | CT | 18 | a0001c0001t0001g0118a0001c0001t0001g0150a0001c0001t0001g0164others(15): Show | 18 | HG01099.hp1 HG01109.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-27947dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102316084 | |||||
| chr10:102316084
|
CT | C | 8 | a0001c0001t0001g0107a0001c0001t0001g0187a0001c0001t0001g0243others(5): Show | 8 | HG00099.hp2 HG01070.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-27947delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102316084 | |||||
| chr10:102316179
|
T | C | 100 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(97): Show | 100 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.164-27872T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316179 | ||||||
| chr10:102316188
|
G | A | 1 | a0001c0022t0003g0235 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.164-27863G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316188 | ||||||
| chr10:102316268
|
G | A | 91 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.164-27783G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316268 | ||||||
| chr10:102316277
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-27774G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316277 | ||||||
| chr10:102316282
|
T | C | 23 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(20): Show | 23 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.164-27769T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316282 | ||||||
| chr10:102316293
|
G | A | 4 | a0001c0001t0001g0106a0001c0001t0001g0159a0001c0001t0001g0161others(1): Show | 4 | HG02293.hp2 NA18954.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-27758G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316293 | ||||||
| chr10:102316335
|
C | T | 10 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-27716C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316335 | ||||||
| chr10:102316380
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-27671G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316380 | ||||||
| chr10:102316474
|
G | A | 60 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.164-27577G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316474 | ||||||
| chr10:102316480
|
C | T | 1 | a0001c0001t0002g0039 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.164-27571C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316480 | ||||||
| chr10:102316780
|
G | A | 2 | a0001c0001t0003g0303a0001c0001t0003g0304 | 2 | HG02071.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.164-27271G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316780 | ||||||
| chr10:102316802
|
C | A | 1 | a0001c0001t0002g0037 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.164-27249C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316802 | ||||||
| chr10:102317021
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.164-27030T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317021 | ||||||
| chr10:102317182
|
AGCTACTC others(5): Show |
A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-26865_164-2685 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102317182 | |||||
| chr10:102317199
|
A | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-26852A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317199 | ||||||
| chr10:102317211
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.164-26840C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317211 | ||||||
| chr10:102317285
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164-26766T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317285 | ||||||
| chr10:102317596
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.164-26455C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317596 | ||||||
| chr10:102317625
|
A | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-26426A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317625 | ||||||
| chr10:102317711
|
C | T | 1 | a0001c0001t0001g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.164-26340C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317711 | ||||||
| chr10:102317746
|
C | T | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-26305C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317746 | ||||||
| chr10:102317901
|
T | TTTTTA | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.164-26146_164-2614 others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102317901 | |||||
| chr10:102317904
|
T | A | 5 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-26147T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317904 | ||||||
| chr10:102317906
|
A | T | 5 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-26145A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317906 | ||||||
| chr10:102318118
|
G | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-25933G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318118 | ||||||
| chr10:102318287
|
A | G | 11 | a0002c0002t0001g0108a0002c0002t0001g0172a0002c0002t0001g0173others(8): Show | 11 | HG00735.hp2 HG01099.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-25764A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318287 | ||||||
| chr10:102318475
|
G | GC | 98 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.164-25575dupC | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102318475 | |||||
| chr10:102318535
|
T | C | 1 | a0001c0003t0001g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164-25516T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318535 | ||||||
| chr10:102318677
|
C | A | 5 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 5 | HG02280.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-25374C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318677 | ||||||
| chr10:102318830
|
G | A | 1 | a0001c0001t0005g0156 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.164-25221G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318830 | ||||||
| chr10:102318894
|
C | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0121others(2): Show | 5 | HG01109.hp2 HG02451.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-25157C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318894 | ||||||
| chr10:102319003
|
G | C | 98 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.164-25048G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319003 | ||||||
| chr10:102319151
|
A | C | 24 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0214others(21): Show | 24 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.164-24900A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319151 | ||||||
| chr10:102319181
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-24870G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319181 | ||||||
| chr10:102319245
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.164-24806G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319245 | ||||||
| chr10:102319261
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.164-24790A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319261 | ||||||
| chr10:102319277
|
G | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0039 | 3 | HG02523.hp2 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.164-24774G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319277 | ||||||
| chr10:102319318
|
TCAA | T | 56 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(53): Show | 56 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.164-24717_164-2471 others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102319318 | |||||
| chr10:102319334
|
C | A | 96 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.164-24717C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319334 | ||||||
| chr10:102319374
|
T | TA | 106 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0115others(103): Show | 107 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.164-24668dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102319374 | |||||
| chr10:102319728
|
C | CT | 15 | a0001c0001t0001g0107a0001c0001t0001g0162a0001c0001t0001g0163others(12): Show | 15 | HG00544.hp1 HG00609.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.164-24306dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102319728 | |||||
| chr10:102319728
|
CT | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0134others(10): Show | 13 | HG01169.hp1 HG01496.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.164-24306delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102319728 | |||||
| chr10:102319814
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.164-24237C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319814 | ||||||
| chr10:102320061
|
T | C | 58 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(55): Show | 58 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.164-23990T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320061 | ||||||
| chr10:102320099
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.164-23952A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320099 | ||||||
| chr10:102320196
|
A | G | 4 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(1): Show | 4 | HG02280.hp1 NA18522.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-23855A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320196 | ||||||
| chr10:102320275
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.164-23776T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320275 | ||||||
| chr10:102320368
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.164-23683G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320368 | ||||||
| chr10:102320471
|
A | G | 28 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-23580A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320471 | ||||||
| chr10:102320560
|
G | C | 2 | a0001c0001t0003g0280a0001c0001t0003g0290 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.164-23491G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320560 | ||||||
| chr10:102320826
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0005g0156 | 2 | HG00280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.164-23225C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320826 | ||||||
| chr10:102321011
|
G | C | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.164-23040G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321011 | ||||||
| chr10:102321056
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0252 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.164-22995G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321056 | ||||||
| chr10:102321085
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0185a0001c0001t0001g0190others(6): Show | 9 | HG01928.hp1 HG01934.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-22966G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321085 | ||||||
| chr10:102321356
|
ATCTT | A | 7 | a0002c0002t0001g0108a0002c0002t0001g0178a0002c0002t0001g0199others(4): Show | 7 | HG00735.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-22689_164-2268 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102321356 | |||||
| chr10:102321592
|
C | T | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0012others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.164-22459C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321592 | ||||||
| chr10:102321624
|
T | C | 4 | a0001c0001t0002g0012a0001c0001t0002g0070a0001c0001t0002g0071others(1): Show | 4 | HG01346.hp1 HG01361.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-22427T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321624 | ||||||
| chr10:102321632
|
C | T | 87 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0191others(84): Show | 88 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.164-22419C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321632 | ||||||
| chr10:102321759
|
G | A | 6 | a0001c0003t0001g0207a0001c0003t0001g0225a0001c0003t0001g0227others(3): Show | 6 | HG01081.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-22292G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321759 | ||||||
| chr10:102321789
|
T | G | 3 | a0004c0008t0001g0195a0004c0008t0001g0200a0004c0020t0003g0312 | 3 | NA18949.hp2 NA18957.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.164-22262T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321789 | ||||||
| chr10:102321879
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-22172G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321879 | ||||||
| chr10:102322032
|
G | T | 1 | a0001c0024t0001g0229 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.164-22019G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322032 | ||||||
| chr10:102322369
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.164-21682A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322369 | ||||||
| chr10:102322440
|
T | C | 2 | a0001c0001t0002g0036a0009c0015t0002g0062 | 2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.164-21611T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322440 | ||||||
| chr10:102322545
|
C | T | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-21506C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322545 | ||||||
| chr10:102322718
|
CA | C | 173 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(170): Show | 174 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.164-21307delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102322718 | |||||
| chr10:102322718
|
CAA | C | 95 | a0001c0001t0001g0011a0001c0001t0001g0132a0001c0001t0001g0133others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.164-21308_164-2130 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102322718 | |||||
| chr10:102322718
|
CAAAAAAA | C | 21 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(18): Show | 21 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.164-21313_164-2130 others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102322718 | |||||
| chr10:102322882
|
A | G | 2 | a0001c0001t0001g0324a0001c0001t0001g0327 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.164-21169A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322882 | ||||||
| chr10:102322931
|
T | G | 123 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(120): Show | 123 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.164-21120T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322931 | ||||||
| chr10:102322934
|
G | T | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-21117G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322934 | ||||||
| chr10:102323010
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.164-21041G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323010 | ||||||
| chr10:102323117
|
A | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-20934A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323117 | ||||||
| chr10:102323121
|
C | A | 1 | a0001c0003t0001g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164-20930C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323121 | ||||||
| chr10:102323167
|
CT | C | 91 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.164-20880delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323167 | |||||
| chr10:102323196
|
G | A | 1 | a0001c0001t0005g0156 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.164-20855G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323196 | ||||||
| chr10:102323239
|
G | GA | 16 | a0001c0001t0001g0155a0001c0001t0001g0168a0001c0001t0001g0191others(13): Show | 16 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-20790dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323239 | |||||
| chr10:102323239
|
G | GAA | 23 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(20): Show | 23 | HG00544.hp2 HG00621.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.164-20791_164-2079 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323239 | |||||
| chr10:102323239
|
GA | G | 11 | a0001c0001t0001g0183a0001c0001t0002g0036a0001c0003t0001g0210others(8): Show | 11 | HG01070.hp2 HG01074.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-20790delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323239 | |||||
| chr10:102323259
|
A | G | 3 | a0001c0001t0002g0037a0001c0001t0002g0046a0001c0004t0002g0104 | 3 | HG01358.hp1 HG03942.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.164-20792A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323259 | ||||||
| chr10:102323388
|
C | T | 2 | a0001c0001t0001g0155a0006c0011t0001g0295 | 2 | HG01074.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.164-20663C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323388 | ||||||
| chr10:102323431
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.164-20620G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323431 | ||||||
| chr10:102323575
|
CT | C | 9 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0324others(6): Show | 9 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-20461delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323575 | |||||
| chr10:102324151
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-19900T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324151 | ||||||
| chr10:102324193
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164-19858A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324193 | ||||||
| chr10:102324269
|
C | A | 1 | a0003c0005t0002g0078 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.164-19782C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324269 | ||||||
| chr10:102324371
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.164-19680A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324371 | ||||||
| chr10:102324411
|
G | T | 1 | a0001c0001t0002g0048 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.164-19640G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324411 | ||||||
| chr10:102324610
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.164-19441G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324610 | ||||||
| chr10:102324700
|
C | T | 1 | a0001c0001t0003g0283 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.164-19351C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324700 | ||||||
| chr10:102324978
|
A | G | 5 | a0003c0005t0002g0061a0003c0005t0002g0077a0003c0005t0002g0078others(2): Show | 5 | HG02071.hp1 NA18952.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-19073A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324978 | ||||||
| chr10:102325132
|
A | G | 56 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(53): Show | 56 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.164-18919A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325132 | ||||||
| chr10:102325148
|
C | CTCCCCGA others(7): Show |
1 | a0001c0001t0001g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.164-18898_164-1888 others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102325148 | |||||
| chr10:102325154
|
G | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0201a0004c0008t0001g0195others(2): Show | 5 | HG02074.hp2 NA18612.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-18897G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325154 | ||||||
| chr10:102325324
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.164-18727G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325324 | ||||||
| chr10:102325378
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-18673C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325378 | ||||||
| chr10:102325550
|
C | CA | 95 | a0001c0001t0001g0155a0001c0001t0001g0320a0001c0001t0001g0324others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.164-18485dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102325550 | |||||
| chr10:102325550
|
C | CAA | 10 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0018others(7): Show | 10 | HG01109.hp1 HG01928.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-18486_164-1848 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102325550 | |||||
| chr10:102325550
|
CA | C | 6 | a0001c0001t0001g0252a0001c0001t0001g0293a0001c0001t0001g0296others(3): Show | 6 | HG00099.hp1 HG02895.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-18485delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102325550 | |||||
| chr10:102325610
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.164-18441G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325610 | ||||||
| chr10:102325726
|
T | C | 31 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0074others(28): Show | 31 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.164-18325T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325726 | ||||||
| chr10:102325727
|
G | T | 3 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0067 | 3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.164-18324G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325727 | ||||||
| chr10:102326164
|
C | T | 82 | a0001c0001t0001g0191a0001c0001t0001g0231a0001c0001t0001g0237others(79): Show | 83 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-17887C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102326164 | ||||||
| chr10:102326319
|
T | C | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-17732T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102326319 | ||||||
| chr10:102326323
|
A | G | 4 | a0001c0001t0002g0018a0001c0001t0002g0035a0008c0012t0002g0031others(1): Show | 4 | HG01928.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-17728A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102326323 | ||||||
| chr10:102327151
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.164-16900G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327151 | ||||||
| chr10:102327153
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.164-16898G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327153 | ||||||
| chr10:102327199
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.164-16852G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327199 | ||||||
| chr10:102327339
|
A | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-16712A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327339 | ||||||
| chr10:102327457
|
G | A | 5 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0023others(2): Show | 5 | HG00099.hp2 HG01255.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-16594G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327457 | ||||||
| chr10:102327472
|
A | G | 19 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(16): Show | 19 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.164-16579A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327472 | ||||||
| chr10:102327560
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.164-16491C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327560 | ||||||
| chr10:102327599
|
T | C | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.164-16452T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327599 | ||||||
| chr10:102327959
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.164-16092C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327959 | ||||||
| chr10:102328107
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-15944G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328107 | ||||||
| chr10:102328174
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164-15877T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328174 | ||||||
| chr10:102328340
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.164-15711A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328340 | ||||||
| chr10:102328373
|
G | A | 1 | a0001c0001t0003g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.164-15678G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328373 | ||||||
| chr10:102328543
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0152 | 2 | HG01175.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.164-15508A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328543 | ||||||
| chr10:102328545
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-15506G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328545 | ||||||
| chr10:102329184
|
C | T | 1 | a0002c0002t0001g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.164-14867C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329184 | ||||||
| chr10:102329269
|
C | T | 9 | a0001c0001t0001g0106a0001c0001t0001g0159a0001c0001t0001g0160others(6): Show | 9 | HG02293.hp2 NA18954.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-14782C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329269 | ||||||
| chr10:102329357
|
T | A | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-14694T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329357 | ||||||
| chr10:102329554
|
C | G | 1 | a0001c0001t0002g0052 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.164-14497C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329554 | ||||||
| chr10:102329658
|
T | G | 112 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(109): Show | 113 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.164-14393T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329658 | ||||||
| chr10:102329664
|
C | T | 112 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(109): Show | 113 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.164-14387C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329664 | ||||||
| chr10:102330512
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164-13539C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330512 | ||||||
| chr10:102330554
|
C | T | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-13497C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330554 | ||||||
| chr10:102330555
|
A | G | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.164-13496A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330555 | ||||||
| chr10:102330579
|
A | G | 18 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 18 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.164-13472A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330579 | ||||||
| chr10:102330596
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.164-13455G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330596 | ||||||
| chr10:102330686
|
C | CA | 9 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(6): Show | 9 | HG01516.hp1 HG01517.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-13355dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102330686 | |||||
| chr10:102330693
|
A | T | 1 | a0001c0001t0002g0083 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.164-13358A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330693 | ||||||
| chr10:102330788
|
G | C | 1 | a0001c0001t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-13263G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330788 | ||||||
| chr10:102331065
|
G | T | 1 | a0012c0018t0001g0205 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.164-12986G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331065 | ||||||
| chr10:102331161
|
G | A | 10 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0018others(7): Show | 10 | HG01109.hp1 HG01928.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-12890G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331161 | ||||||
| chr10:102331328
|
C | T | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-12723C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331328 | ||||||
| chr10:102331339
|
A | T | 1 | a0001c0001t0005g0156 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.164-12712A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331339 | ||||||
| chr10:102331851
|
A | AT | 46 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0119others(43): Show | 46 | HG00280.hp1 HG00558.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.164-12174dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | |||||
| chr10:102331851
|
A | ATT | 33 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0003others(30): Show | 33 | HG00621.hp2 HG01069.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.164-12175_164-1217 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | |||||
| chr10:102331851
|
A | ATTT | 37 | a0001c0001t0002g0012a0001c0001t0002g0020a0001c0001t0002g0021others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.164-12176_164-1217 others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | |||||
| chr10:102331851
|
A | ATTTT | 9 | a0001c0001t0002g0002a0001c0001t0002g0022a0001c0001t0002g0036others(6): Show | 9 | HG00673.hp1 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-12177_164-1217 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | |||||
| chr10:102331851
|
A | ATTTTT | 8 | a0001c0001t0002g0027a0001c0001t0002g0053a0001c0001t0002g0054others(5): Show | 8 | NA18955.hp1 NA18959.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-12178_164-1217 others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | |||||
| chr10:102331851
|
A | ATTTTTTT others(13): Show |
3 | a0001c0004t0004g0013a0001c0004t0004g0014a0001c0004t0004g0017 | 3 | HG02280.hp1 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.164-12193_164-1217 others(24): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | |||||
| chr10:102331851
|
A | ATTTTTTT others(14): Show |
2 | a0001c0004t0004g0004a0001c0004t0004g0015 | 2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.164-12194_164-1217 others(25): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | |||||
| chr10:102331851
|
AT | A | 22 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0155others(19): Show | 22 | HG01070.hp2 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.164-12174delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | |||||
| chr10:102331925
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-12126T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331925 | ||||||
| chr10:102332080
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.164-11971G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332080 | ||||||
| chr10:102332139
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-11912T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332139 | ||||||
| chr10:102332235
|
C | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0039 | 3 | HG02523.hp2 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.164-11816C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332235 | ||||||
| chr10:102332279
|
C | T | 5 | a0001c0001t0001g0231a0001c0001t0001g0252a0001c0001t0001g0253others(2): Show | 5 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-11772C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332279 | ||||||
| chr10:102332387
|
C | CT | 89 | a0001c0001t0001g0142a0001c0001t0001g0186a0001c0001t0001g0213others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.164-11651dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102332387 | |||||
| chr10:102332487
|
G | A | 1 | a0001c0001t0003g0236 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.164-11564G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332487 | ||||||
| chr10:102333110
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.164-10941G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333110 | ||||||
| chr10:102333196
|
A | G | 3 | a0002c0002t0001g0172a0002c0002t0001g0180a0002c0002t0001g0188 | 3 | HG01099.hp1 HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.164-10855A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333196 | ||||||
| chr10:102333331
|
A | G | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-10720A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333331 | ||||||
| chr10:102333885
|
T | G | 2 | a0003c0005t0002g0061a0003c0005t0002g0102 | 2 | HG02071.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.164-10166T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333885 | ||||||
| chr10:102333901
|
C | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-10150C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333901 | ||||||
| chr10:102334176
|
A | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-9875A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334176 | ||||||
| chr10:102334367
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.164-9684A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334367 | ||||||
| chr10:102334722
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.164-9329G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334722 | ||||||
| chr10:102334741
|
C | T | 22 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(19): Show | 22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.164-9310C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334741 | ||||||
| chr10:102334773
|
G | A | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-9278G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334773 | ||||||
| chr10:102334848
|
CA | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-9187delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102334848 | |||||
| chr10:102334861
|
A | G | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-9190A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334861 | ||||||
| chr10:102334881
|
A | G | 1 | a0001c0001t0003g0313 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.164-9170A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334881 | ||||||
| chr10:102334971
|
C | G | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | NA18953.hp1 NA18967.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-9080C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334971 | ||||||
| chr10:102335200
|
A | G | 1 | a0002c0002t0001g0173 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.164-8851A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335200 | ||||||
| chr10:102335244
|
TGACTGGC others(15): Show |
T | 4 | a0001c0001t0003g0284a0001c0001t0003g0285a0001c0001t0003g0286others(1): Show | 4 | NA18950.hp2 NA18979.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-8803_164-8782d others(24): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102335244 | |||||
| chr10:102335289
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-8762T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335289 | ||||||
| chr10:102335383
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-8668G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335383 | ||||||
| chr10:102335773
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164-8278C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335773 | ||||||
| chr10:102335891
|
A | G | 1 | a0001c0001t0002g0025 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.164-8160A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335891 | ||||||
| chr10:102335986
|
A | G | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-8065A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335986 | ||||||
| chr10:102336043
|
T | C | 1 | a0001c0001t0003g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.164-8008T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336043 | ||||||
| chr10:102336054
|
C | G | 31 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0074others(28): Show | 31 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.164-7997C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336054 | ||||||
| chr10:102336199
|
G | A | 5 | a0001c0003t0001g0109a0001c0003t0001g0210a0001c0003t0001g0211others(2): Show | 5 | HG01070.hp2 HG01516.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-7852G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336199 | ||||||
| chr10:102336226
|
G | C | 1 | a0001c0001t0003g0276 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.164-7825G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336226 | ||||||
| chr10:102336299
|
CA | C | 7 | a0001c0001t0002g0047a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-7737delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102336299 | |||||
| chr10:102336302
|
AAAAAAAA others(6): Show |
A | 13 | a0001c0001t0001g0107a0001c0001t0001g0186a0001c0001t0001g0209others(10): Show | 13 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.164-7732_164-7720d others(15): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102336302 | |||||
| chr10:102336316
|
A | G | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-7735A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336316 | ||||||
| chr10:102336839
|
A | ATGAT | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-7212_164-7211i others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336839 | ||||||
| chr10:102336975
|
A | T | 59 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(56): Show | 59 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.164-7076A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336975 | ||||||
| chr10:102337104
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.164-6947C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337104 | ||||||
| chr10:102337165
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.164-6886T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337165 | ||||||
| chr10:102337295
|
G | GCGAACCC others(1): Show |
327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.164-6754_164-6753i others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102337295 | |||||
| chr10:102337298
|
T | A | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.164-6753T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337298 | ||||||
| chr10:102337301
|
G | C | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.164-6750G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337301 | ||||||
| chr10:102337369
|
C | CA | 165 | a0001c0001t0001g0110a0001c0001t0001g0120a0001c0001t0001g0129others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.164-6665dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102337369 | |||||
| chr10:102337369
|
C | CAA | 10 | a0001c0001t0001g0213a0001c0001t0001g0247a0001c0001t0002g0055others(7): Show | 10 | HG00609.hp1 HG01109.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-6666_164-6665d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102337369 | |||||
| chr10:102337381
|
A | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-6670A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337381 | ||||||
| chr10:102337501
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-6550A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337501 | ||||||
| chr10:102337604
|
C | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-6447C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337604 | ||||||
| chr10:102337615
|
G | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-6436G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337615 | ||||||
| chr10:102337806
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.164-6245G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337806 | ||||||
| chr10:102337858
|
AAAAG | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-6173_164-6170d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102337858 | |||||
| chr10:102337961
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.164-6090T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337961 | ||||||
| chr10:102337977
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.164-6074C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337977 | ||||||
| chr10:102338237
|
C | CT | 47 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 47 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.164-5793dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102338237 | |||||
| chr10:102338237
|
C | CTTTT | 9 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(6): Show | 9 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-5796_164-5793d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102338237 | |||||
| chr10:102338237
|
C | CTTTTT | 9 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-5797_164-5793d others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102338237 | |||||
| chr10:102338239
|
T | TC | 6 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-5812_164-5811i others(3): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338239 | ||||||
| chr10:102338240
|
T | C | 1 | a0001c0004t0004g0017 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-5811T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338240 | ||||||
| chr10:102338407
|
A | T | 5 | a0001c0001t0002g0025a0001c0001t0002g0036a0001c0001t0002g0064others(2): Show | 5 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-5644A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338407 | ||||||
| chr10:102338470
|
G | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-5581G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338470 | ||||||
| chr10:102338554
|
A | G | 2 | a0001c0004t0004g0004a0001c0004t0004g0015 | 2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.164-5497A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338554 | ||||||
| chr10:102338932
|
A | G | 11 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-5119A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338932 | ||||||
| chr10:102339085
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0298others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-4966G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339085 | ||||||
| chr10:102339129
|
G | A | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-4922G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339129 | ||||||
| chr10:102339192
|
G | A | 91 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.164-4859G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339192 | ||||||
| chr10:102339425
|
G | A | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-4626G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339425 | ||||||
| chr10:102339470
|
T | C | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-4581T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339470 | ||||||
| chr10:102339530
|
G | A | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-4521G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339530 | ||||||
| chr10:102339552
|
A | G | 1 | a0001c0001t0007g0147 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.164-4499A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339552 | ||||||
| chr10:102339695
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA19002.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.164-4356A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339695 | ||||||
| chr10:102339700
|
T | C | 1 | a0001c0001t0002g0046 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164-4351T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339700 | ||||||
| chr10:102339953
|
A | AT | 222 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(219): Show | 223 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(220): Show |
intron_variant | MODIFIER | c.164-4080dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102339953 | |||||
| chr10:102339953
|
A | ATT | 22 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0119others(19): Show | 22 | HG00609.hp1 HG01109.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.164-4081_164-4080d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102339953 | |||||
| chr10:102340060
|
T | C | 1 | a0001c0001t0003g0251 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.164-3991T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340060 | ||||||
| chr10:102340101
|
G | A | 3 | a0001c0001t0003g0001a0001c0001t0003g0272a0001c0001t0003g0279 | 4 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-3950G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340101 | ||||||
| chr10:102340263
|
A | G | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-3788A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340263 | ||||||
| chr10:102340267
|
C | CT | 93 | a0001c0001t0001g0010a0001c0001t0001g0110a0001c0001t0001g0117others(90): Show | 93 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.164-3761dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102340267 | |||||
| chr10:102340267
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.164-3784C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340267 | ||||||
| chr10:102340352
|
A | C | 23 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(20): Show | 23 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.164-3699A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340352 | ||||||
| chr10:102340482
|
C | T | 3 | a0001c0001t0003g0232a0001c0001t0003g0233a0001c0001t0003g0234 | 3 | HG00609.hp1 NA18959.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.164-3569C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340482 | ||||||
| chr10:102340878
|
G | A | 1 | a0002c0002t0001g0173 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.164-3173G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340878 | ||||||
| chr10:102340976
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0139others(1): Show | 4 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-3075G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340976 | ||||||
| chr10:102341056
|
T | C | 6 | a0001c0001t0002g0019a0001c0001t0002g0052a0001c0001t0002g0059others(3): Show | 6 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-2995T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341056 | ||||||
| chr10:102341264
|
A | G | 1 | a0001c0001t0003g0242 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.164-2787A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341264 | ||||||
| chr10:102341382
|
G | A | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2669G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341382 | ||||||
| chr10:102341658
|
A | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2393A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341658 | ||||||
| chr10:102341800
|
A | C | 1 | a0001c0001t0001g0196 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.164-2251A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341800 | ||||||
| chr10:102341899
|
C | T | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2152C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341899 | ||||||
| chr10:102341900
|
G | T | 1 | a0001c0001t0002g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.164-2151G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341900 | ||||||
| chr10:102341903
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.164-2148T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341903 | ||||||
| chr10:102341927
|
C | A | 1 | a0001c0001t0001g0328 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.164-2124C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341927 | ||||||
| chr10:102342038
|
C | CT | 28 | a0001c0001t0001g0190a0001c0001t0001g0208a0001c0001t0001g0209others(25): Show | 28 | HG01070.hp2 HG01074.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-1997dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102342038 | |||||
| chr10:102342259
|
G | C | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164-1792G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342259 | ||||||
| chr10:102342361
|
G | A | 57 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(54): Show | 57 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.164-1690G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342361 | ||||||
| chr10:102342387
|
ACG | A | 11 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-1662_164-1661d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102342387 | |||||
| chr10:102342389
|
G | GCA | 18 | a0001c0001t0001g0208a0001c0003t0001g0109a0001c0003t0001g0207others(15): Show | 18 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.164-1644_164-1643d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102342389 | |||||
| chr10:102342389
|
GCA | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0255a0001c0001t0002g0030 | 3 | HG02258.hp2 HG03516.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.164-1644_164-1643d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102342389 | |||||
| chr10:102342574
|
G | A | 98 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.164-1477G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342574 | ||||||
| chr10:102342746
|
T | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-1305T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342746 | ||||||
| chr10:102342854
|
A | G | 8 | a0001c0001t0001g0007a0001c0001t0001g0168a0001c0001t0001g0181others(5): Show | 8 | HG02040.hp2 HG02683.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-1197A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342854 | ||||||
| chr10:102343547
|
G | C | 2 | a0001c0001t0001g0294a0001c0001t0001g0320 | 2 | NA18963.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.164-504G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102343547 | ||||||
| chr10:102343588
|
C | T | 2 | a0001c0001t0002g0019a0001c0001t0002g0066 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.164-463C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102343588 | ||||||
| chr10:102343597
|
T | C | 1 | a0001c0001t0003g0262 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.164-454T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102343597 | ||||||
| chr10:102343799
|
C | CA | 21 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0296others(18): Show | 21 | HG00735.hp2 HG01099.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.164-235dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102343799 | |||||
| chr10:102343799
|
CA | C | 226 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(223): Show | 227 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.164-235delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102343799 | |||||
| chr10:102344465
|
G | GGTTT | 102 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(99): Show | 103 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.295+308_295+311dup others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102344465 | |||||
| chr10:102344601
|
C | T | 1 | a0001c0001t0003g0303 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.295+419C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344601 | ||||||
| chr10:102344680
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.295+498C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344680 | ||||||
| chr10:102344812
|
A | G | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.295+630A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344812 | ||||||
| chr10:102344908
|
T | C | 2 | a0001c0001t0003g0280a0001c0001t0003g0290 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.295+726T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344908 | ||||||
| chr10:102344940
|
G | T | 2 | a0001c0003t0001g0227a0001c0003t0001g0228 | 2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.295+758G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344940 | ||||||
| chr10:102345065
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0139 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.295+883C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345065 | ||||||
| chr10:102345066
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.295+884G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345066 | ||||||
| chr10:102345112
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0132others(13): Show | 16 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.295+930T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345112 | ||||||
| chr10:102345281
|
C | CA | 9 | a0001c0001t0001g0322a0001c0001t0003g0290a0001c0003t0001g0222others(6): Show | 9 | HG02280.hp1 HG02738.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.295+1115dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345281 | |||||
| chr10:102345281
|
CA | C | 91 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.295+1115delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345281 | |||||
| chr10:102345424
|
G | A | 1 | a0001c0003t0001g0323 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295+1242G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345424 | ||||||
| chr10:102345639
|
TC | T | 30 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0074others(27): Show | 30 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.295+1459delC | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345639 | |||||
| chr10:102345642
|
G | A | 5 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0121others(2): Show | 5 | HG01109.hp2 HG02451.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1460G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345642 | ||||||
| chr10:102345646
|
C | CA | 71 | a0001c0001t0001g0005a0001c0001t0001g0112a0001c0001t0001g0115others(68): Show | 71 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.295+1490dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345646 | |||||
| chr10:102345646
|
CA | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01496.hp2 HG01515.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.295+1490delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345646 | |||||
| chr10:102345646
|
CAAAA | C | 9 | a0001c0001t0002g0027a0001c0001t0002g0054a0001c0004t0002g0104others(6): Show | 9 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.295+1487_295+1490d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345646 | |||||
| chr10:102345646
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0294 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.295+1478_295+1490d others(15): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345646 | |||||
| chr10:102345794
|
T | C | 6 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG00558.hp2 HG01978.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+1612T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345794 | ||||||
| chr10:102345822
|
G | C | 1 | a0001c0004t0004g0017 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295+1640G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345822 | ||||||
| chr10:102345968
|
G | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0001g0138 | 3 | HG01496.hp2 HG01515.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.295+1786G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345968 | ||||||
| chr10:102346085
|
TTTTTTTA | T | 56 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(53): Show | 56 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.295+1904_295+1910d others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346085 | ||||||
| chr10:102346113
|
C | T | 1 | a0001c0001t0003g0284 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.295+1931C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346113 | ||||||
| chr10:102346323
|
T | G | 1 | a0001c0004t0004g0017 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295+2141T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346323 | ||||||
| chr10:102346443
|
T | C | 122 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0213others(119): Show | 122 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.295+2261T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346443 | ||||||
| chr10:102346545
|
G | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.295+2363G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346545 | ||||||
| chr10:102346577
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295+2395C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346577 | ||||||
| chr10:102346601
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.295+2419G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346601 | ||||||
| chr10:102347434
|
C | T | 2 | a0001c0001t0005g0153a0001c0001t0005g0156 | 2 | HG00280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.295+3252C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102347434 | ||||||
| chr10:102347497
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+3315T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102347497 | ||||||
| chr10:102347983
|
T | C | 5 | a0001c0003t0001g0109a0001c0003t0001g0210a0001c0003t0001g0211others(2): Show | 5 | HG01070.hp2 HG01516.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3273T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102347983 | ||||||
| chr10:102347990
|
G | A | 1 | a0001c0001t0002g0018 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.296-3266G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102347990 | ||||||
| chr10:102348571
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.296-2685G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102348571 | ||||||
| chr10:102348657
|
G | A | 3 | a0001c0001t0003g0001a0001c0001t0003g0272a0001c0001t0003g0279 | 4 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2599G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102348657 | ||||||
| chr10:102349118
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.296-2138C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349118 | ||||||
| chr10:102349179
|
T | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.296-2077T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349179 | ||||||
| chr10:102349349
|
A | G | 113 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(110): Show | 114 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.296-1907A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349349 | ||||||
| chr10:102349482
|
A | T | 1 | a0001c0007t0001g0329 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.296-1774A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349482 | ||||||
| chr10:102349813
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.296-1443A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349813 | ||||||
| chr10:102350250
|
T | C | 1 | a0001c0001t0001g0297 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.296-1006T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350250 | ||||||
| chr10:102350350
|
C | CA | 6 | a0001c0001t0001g0186a0001c0001t0001g0224a0001c0001t0003g0274others(3): Show | 6 | HG01123.hp1 HG02145.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-891dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102350350 | |||||
| chr10:102350350
|
CA | C | 7 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(4): Show | 7 | HG01081.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-891delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102350350 | |||||
| chr10:102350395
|
G | A | 1 | a0002c0002t0001g0204 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.296-861G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350395 | ||||||
| chr10:102350648
|
T | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0054a0001c0001t0002g0069 | 3 | NA18959.hp1 NA18980.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.296-608T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350648 | ||||||
| chr10:102350738
|
A | C | 1 | a0001c0001t0002g0029 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.296-518A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350738 | ||||||
| chr10:102350849
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.296-407C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350849 | ||||||
| chr10:102350959
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.296-297C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350959 | ||||||
| chr10:102350977
|
C | G | 1 | a0001c0001t0003g0261 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.296-279C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350977 | ||||||
| chr10:102350981
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.296-275G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350981 | ||||||
| chr10:102351086
|
C | CA | 35 | a0001c0001t0001g0005a0001c0001t0001g0208a0001c0001t0001g0215others(32): Show | 35 | HG01070.hp2 HG01081.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.296-152dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102351086 | |||||
| chr10:102351086
|
C | CAAAA | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-155_296-152dup others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102351086 | |||||
| chr10:102351592
|
TTAAA | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0135a0001c0001t0001g0138 | 3 | HG01496.hp2 HG01515.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.414+221_414+224del others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 5/39 | INFO_REALIGN_3_PRIME | chr10 | 102351592 | |||||
| chr10:102351776
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-67T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 5/39 | chr10 | 102351776 | ||||||
| chr10:102351783
|
T | TACC | 31 | a0001c0001t0002g0003a0001c0001t0002g0073a0001c0001t0002g0074others(28): Show | 31 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.415-59_415-57dupAC others(1): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 5/39 | INFO_REALIGN_3_PRIME | chr10 | 102351783 | |||||
| chr10:102351813
|
A | G | 12 | a0001c0001t0001g0107a0001c0001t0001g0162a0001c0001t0001g0163others(9): Show | 12 | HG00544.hp1 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-30A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 5/39 | chr10 | 102351813 | ||||||
| chr10:102352054
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.523+103C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352054 | ||||||
| chr10:102352077
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0046 | 2 | HG01358.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.523+126T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352077 | ||||||
| chr10:102352137
|
C | T | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.523+186C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352137 | ||||||
| chr10:102352232
|
C | A | 2 | a0001c0001t0003g0314a0001c0001t0003g0317 | 2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.524-226C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352232 | ||||||
| chr10:102352246
|
A | G | 2 | a0001c0001t0003g0280a0001c0001t0003g0290 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.524-212A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352246 | ||||||
| chr10:102352451
|
T | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.524-7T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352451 | ||||||
| chr10:102352570
|
G | C | 1 | a0001c0001t0002g0048 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.584+52G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102352570 | ||||||
| chr10:102352980
|
T | C | 98 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.584+462T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102352980 | ||||||
| chr10:102353059
|
A | G | 23 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(20): Show | 23 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.584+541A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102353059 | ||||||
| chr10:102353184
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.585-416G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102353184 | ||||||
| chr10:102353213
|
A | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.585-387A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102353213 | ||||||
| chr10:102353784
|
C | T | 4 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0094others(1): Show | 4 | NA18967.hp2 NA18977.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.639+130C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102353784 | ||||||
| chr10:102353944
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.639+290A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102353944 | ||||||
| chr10:102354179
|
C | T | 1 | a0001c0001t0002g0003 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.639+525C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354179 | ||||||
| chr10:102354275
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0003g0274 | 2 | NA18974.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.639+621C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354275 | ||||||
| chr10:102354473
|
C | T | 1 | a0001c0001t0002g0075 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.639+819C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354473 | ||||||
| chr10:102354478
|
CCT | C | 7 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(4): Show | 7 | HG01891.hp2 HG02145.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.639+829_639+830del others(2): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102354478 | |||||
| chr10:102354571
|
T | C | 98 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.639+917T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354571 | ||||||
| chr10:102354715
|
G | A | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.639+1061G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354715 | ||||||
| chr10:102354729
|
T | C | 1 | a0001c0003t0001g0225 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.639+1075T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354729 | ||||||
| chr10:102354767
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.639+1113C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354767 | ||||||
| chr10:102354855
|
T | A | 1 | a0001c0001t0002g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.639+1201T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354855 | ||||||
| chr10:102354856
|
C | A | 1 | a0001c0001t0002g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.639+1202C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354856 | ||||||
| chr10:102354913
|
CT | C | 120 | a0001c0001t0001g0107a0001c0001t0001g0121a0001c0001t0001g0143others(117): Show | 120 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.639+1277delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102354913 | |||||
| chr10:102355129
|
C | T | 122 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(119): Show | 123 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(120): Show |
intron_variant | MODIFIER | c.639+1475C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355129 | ||||||
| chr10:102355277
|
C | T | 5 | a0001c0001t0002g0022a0001c0001t0002g0053a0001c0001t0002g0055others(2): Show | 5 | NA18951.hp1 NA18968.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+1623C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355277 | ||||||
| chr10:102355409
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.639+1755T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355409 | ||||||
| chr10:102355505
|
G | A | 2 | a0002c0002t0001g0178a0002c0002t0001g0199 | 2 | HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.639+1851G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355505 | ||||||
| chr10:102355638
|
A | T | 60 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.639+1984A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355638 | ||||||
| chr10:102355687
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.639+2033A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355687 | ||||||
| chr10:102356122
|
G | A | 4 | a0001c0001t0003g0284a0001c0001t0003g0285a0001c0001t0003g0286others(1): Show | 4 | NA18950.hp2 NA18979.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-1917G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356122 | ||||||
| chr10:102356138
|
G | A | 3 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0067 | 3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.640-1901G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356138 | ||||||
| chr10:102356314
|
C | T | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.640-1725C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356314 | ||||||
| chr10:102356562
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.640-1477G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356562 | ||||||
| chr10:102356692
|
A | G | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.640-1347A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356692 | ||||||
| chr10:102356723
|
C | T | 9 | a0001c0001t0001g0106a0001c0001t0001g0159a0001c0001t0001g0160others(6): Show | 9 | HG02293.hp2 NA18954.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.640-1316C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356723 | ||||||
| chr10:102356766
|
C | CA | 45 | a0001c0001t0001g0118a0001c0001t0001g0124a0001c0001t0001g0125others(42): Show | 45 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.640-1253dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102356766 | |||||
| chr10:102356766
|
CA | C | 51 | a0001c0001t0001g0007a0001c0001t0001g0155a0001c0001t0001g0168others(48): Show | 51 | HG00558.hp1 HG00621.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.640-1253delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102356766 | |||||
| chr10:102356766
|
CAA | C | 32 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0154others(29): Show | 32 | HG00609.hp2 HG01928.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.640-1254_640-1253d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102356766 | |||||
| chr10:102357042
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.640-997A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357042 | ||||||
| chr10:102357252
|
T | C | 98 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.640-787T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357252 | ||||||
| chr10:102357486
|
C | CA | 6 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.640-536dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102357486 | |||||
| chr10:102357647
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.640-392T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357647 | ||||||
| chr10:102357685
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG00558.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.640-354C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357685 | ||||||
| chr10:102357716
|
T | C | 2 | a0001c0001t0003g0232a0001c0001t0003g0234 | 2 | HG00609.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.640-323T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357716 | ||||||
| chr10:102357921
|
T | A | 3 | a0002c0002t0001g0172a0002c0002t0001g0180a0002c0002t0001g0188 | 3 | HG01099.hp1 HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.640-118T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357921 | ||||||
| chr10:102358438
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.788-68C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 9/39 | chr10 | 102358438 | ||||||
| chr10:102358877
|
T | C | 2 | a0001c0001t0005g0153a0001c0001t0005g0156 | 2 | HG00280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1011+148T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/39 | chr10 | 102358877 | ||||||
| chr10:102359128
|
G | A | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012-139G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/39 | chr10 | 102359128 | ||||||
| chr10:102359226
|
G | C | 3 | a0002c0002t0001g0172a0002c0002t0001g0180a0002c0002t0001g0188 | 3 | HG01099.hp1 HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1012-41G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/39 | chr10 | 102359226 | ||||||
| chr10:102359615
|
C | T | 4 | a0001c0001t0003g0284a0001c0001t0003g0285a0001c0001t0003g0286others(1): Show | 4 | NA18950.hp2 NA18979.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+180C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | chr10 | 102359615 | ||||||
| chr10:102359757
|
A | G | 1 | a0001c0014t0001g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1180+322A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | chr10 | 102359757 | ||||||
| chr10:102359778
|
C | CT | 72 | a0001c0001t0001g0137a0001c0001t0001g0213a0001c0001t0001g0214others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.1180+358dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | INFO_REALIGN_3_PRIME | chr10 | 102359778 | |||||
| chr10:102359947
|
G | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0063 | 2 | HG00280.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1181-237G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | chr10 | 102359947 | ||||||
| chr10:102360058
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1181-126G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | chr10 | 102360058 | ||||||
| chr10:102360461
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1392+66G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360461 | ||||||
| chr10:102360631
|
C | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0039 | 3 | HG02523.hp2 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1392+236C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360631 | ||||||
| chr10:102360728
|
A | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-294A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360728 | ||||||
| chr10:102360765
|
C | G | 58 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(55): Show | 58 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1393-257C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360765 | ||||||
| chr10:102360929
|
T | C | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1393-93T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360929 | ||||||
| chr10:102360974
|
C | CA | 15 | a0001c0001t0001g0155a0001c0001t0001g0214a0001c0001t0001g0255others(12): Show | 15 | HG00544.hp1 HG00738.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1393-30dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | INFO_REALIGN_3_PRIME | chr10 | 102360974 | |||||
| chr10:102361282
|
T | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491+162T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 13/39 | chr10 | 102361282 | ||||||
| chr10:102361345
|
T | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491+225T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 13/39 | chr10 | 102361345 | ||||||
| chr10:102361364
|
G | A | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1491+244G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 13/39 | chr10 | 102361364 | ||||||
| chr10:102361374
|
C | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0152 | 2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1491+254C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 13/39 | chr10 | 102361374 | ||||||
| chr10:102362050
|
C | CT | 34 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0111others(31): Show | 34 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1686+162dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | INFO_REALIGN_3_PRIME | chr10 | 102362050 | |||||
| chr10:102362050
|
CT | C | 97 | a0001c0001t0001g0127a0001c0001t0001g0208a0001c0001t0001g0209others(94): Show | 97 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.1686+162delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | INFO_REALIGN_3_PRIME | chr10 | 102362050 | |||||
| chr10:102362050
|
CTT | C | 8 | a0001c0001t0002g0029a0001c0004t0002g0104a0001c0004t0004g0004others(5): Show | 8 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1686+161_1686+162d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | INFO_REALIGN_3_PRIME | chr10 | 102362050 | |||||
| chr10:102362055
|
T | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0063 | 2 | HG00280.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1686+143T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362055 | ||||||
| chr10:102362057
|
T | C | 1 | a0001c0001t0002g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1686+145T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362057 | ||||||
| chr10:102362098
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+186C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362098 | ||||||
| chr10:102362158
|
A | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1686+246A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362158 | ||||||
| chr10:102362182
|
G | A | 1 | a0001c0007t0001g0329 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1686+270G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362182 | ||||||
| chr10:102362217
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1687-258C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362217 | ||||||
| chr10:102362355
|
C | T | 1 | a0012c0018t0001g0205 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1687-120C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362355 | ||||||
| chr10:102362682
|
C | A | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1876+18C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 15/39 | chr10 | 102362682 | ||||||
| chr10:102362918
|
T | G | 1 | a0001c0001t0003g0265 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1876+254T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 15/39 | chr10 | 102362918 | ||||||
| chr10:102363085
|
A | G | 60 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1877-171A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 15/39 | chr10 | 102363085 | ||||||
| chr10:102363144
|
C | T | 4 | a0001c0001t0002g0019a0001c0001t0002g0059a0001c0001t0002g0066others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1877-112C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 15/39 | chr10 | 102363144 | ||||||
| chr10:102364012
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2106+214C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364012 | ||||||
| chr10:102364123
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2106+325A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364123 | ||||||
| chr10:102364166
|
TTAGTAAG others(7): Show |
T | 1 | a0009c0015t0002g0062 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2106+385_2106+398d others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364166 | |||||
| chr10:102364217
|
C | CT | 138 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 139 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.2106+444dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364217 | |||||
| chr10:102364217
|
C | CTT | 14 | a0001c0001t0001g0106a0001c0001t0001g0191a0001c0001t0001g0231others(11): Show | 14 | HG00609.hp1 HG00735.hp2 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.2106+443_2106+444d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364217 | |||||
| chr10:102364217
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0259 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2106+434_2106+444d others(13): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364217 | |||||
| chr10:102364228
|
T | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2106+430T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364228 | ||||||
| chr10:102364298
|
C | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0154others(46): Show | 49 | HG00280.hp1 HG00544.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.2106+500C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364298 | ||||||
| chr10:102364317
|
CG | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2106+522delG | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364317 | |||||
| chr10:102364320
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2106+522G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364320 | ||||||
| chr10:102364438
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0248a0001c0001t0002g0012 | 3 | HG01256.hp1 HG01258.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2106+640G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364438 | ||||||
| chr10:102364517
|
T | C | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.2106+719T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364517 | ||||||
| chr10:102364614
|
C | T | 13 | a0001c0001t0001g0208a0001c0003t0001g0109a0001c0003t0001g0207others(10): Show | 13 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.2107-783C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364614 | ||||||
| chr10:102364848
|
C | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0106a0001c0001t0001g0107others(55): Show | 58 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.2107-549C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364848 | ||||||
| chr10:102364961
|
G | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0297others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107-436G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364961 | ||||||
| chr10:102364980
|
C | T | 12 | a0001c0003t0001g0109a0001c0003t0001g0207a0001c0003t0001g0210others(9): Show | 12 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.2107-417C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364980 | ||||||
| chr10:102365130
|
A | G | 328 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(325): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.2107-267A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102365130 | ||||||
| chr10:102365264
|
C | G | 1 | a0001c0001t0002g0092 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2107-133C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102365264 | ||||||
| chr10:102365648
|
T | C | 1 | a0002c0002t0001g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2309+49T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365648 | ||||||
| chr10:102365874
|
GTGATAGA others(32): Show |
G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+276_2309+314d others(41): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365874 | ||||||
| chr10:102365918
|
G | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+319G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365918 | ||||||
| chr10:102365919
|
T | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+320T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365919 | ||||||
| chr10:102365920
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+321G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365920 | ||||||
| chr10:102365923
|
A | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+324A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365923 | ||||||
| chr10:102365924
|
G | C | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+325G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365924 | ||||||
| chr10:102365925
|
A | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+326A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365925 | ||||||
| chr10:102365926
|
GCT | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+328_2309+329d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365926 | ||||||
| chr10:102365951
|
C | CA | 7 | a0001c0001t0001g0208a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2309+364dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | INFO_REALIGN_3_PRIME | chr10 | 102365951 | |||||
| chr10:102366017
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2310-366G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102366017 | ||||||
| chr10:102366097
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2310-286G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102366097 | ||||||
| chr10:102366584
|
C | CT | 23 | a0001c0001t0001g0005a0001c0001t0001g0115a0001c0001t0001g0119others(20): Show | 23 | HG00099.hp1 HG00642.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.2433+98dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/39 | INFO_REALIGN_3_PRIME | chr10 | 102366584 | |||||
| chr10:102366584
|
CT | C | 94 | a0001c0001t0001g0132a0001c0001t0001g0160a0001c0001t0001g0213others(91): Show | 94 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.2433+98delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/39 | INFO_REALIGN_3_PRIME | chr10 | 102366584 | |||||
| chr10:102366680
|
G | A | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2433+174G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/39 | chr10 | 102366680 | ||||||
| chr10:102366829
|
G | A | 1 | a0001c0003t0001g0225 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2434-256G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/39 | chr10 | 102366829 | ||||||
| chr10:102367257
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2559+47G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 20/39 | chr10 | 102367257 | ||||||
| chr10:102367414
|
G | A | 199 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(196): Show | 200 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(197): Show |
intron_variant | MODIFIER | c.2560-64G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 20/39 | chr10 | 102367414 | ||||||
| chr10:102367979
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2643-239A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 21/39 | chr10 | 102367979 | ||||||
| chr10:102368183
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2643-35G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 21/39 | chr10 | 102368183 | ||||||
| chr10:102368633
|
T | C | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2880-106T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 22/39 | chr10 | 102368633 | ||||||
| chr10:102369197
|
T | A | 322 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.2974-14T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 23/39 | chr10 | 102369197 | ||||||
| chr10:102369398
|
G | A | 1 | a0002c0002t0001g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3150+11G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 24/39 | chr10 | 102369398 | ||||||
| chr10:102370112
|
T | G | 1 | a0001c0001t0003g0260 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3340-62T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 26/39 | chr10 | 102370112 | ||||||
| chr10:102370551
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3506+73G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 28/39 | chr10 | 102370551 | ||||||
| chr10:102370942
|
C | A | 1 | a0001c0001t0003g0283 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3660+82C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102370942 | ||||||
| chr10:102370986
|
C | T | 1 | a0001c0001t0003g0268 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3660+126C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102370986 | ||||||
| chr10:102371017
|
C | T | 1 | a0001c0001t0002g0034 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3660+157C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371017 | ||||||
| chr10:102371329
|
G | T | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3660+469G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371329 | ||||||
| chr10:102371387
|
A | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3660+527A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371387 | ||||||
| chr10:102371546
|
G | C | 2 | a0001c0001t0006g0165a0001c0001t0006g0166 | 2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3660+686G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371546 | ||||||
| chr10:102371727
|
A | G | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.3660+867A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371727 | ||||||
| chr10:102371952
|
G | C | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3660+1092G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371952 | ||||||
| chr10:102371994
|
G | C | 123 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0110others(120): Show | 124 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(121): Show |
intron_variant | MODIFIER | c.3660+1134G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371994 | ||||||
| chr10:102372032
|
G | T | 1 | a0001c0001t0003g0236 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3660+1172G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372032 | ||||||
| chr10:102372142
|
C | T | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3660+1282C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372142 | ||||||
| chr10:102372496
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3660+1636C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372496 | ||||||
| chr10:102372716
|
T | C | 1 | a0001c0001t0003g0284 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3660+1856T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372716 | ||||||
| chr10:102372778
|
A | G | 82 | a0001c0001t0001g0191a0001c0001t0001g0231a0001c0001t0001g0237others(79): Show | 83 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.3660+1918A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372778 | ||||||
| chr10:102373044
|
A | G | 1 | a0002c0002t0001g0173 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3660+2184A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102373044 | ||||||
| chr10:102373435
|
G | A | 1 | a0001c0001t0003g0266 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3661-1924G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102373435 | ||||||
| chr10:102373498
|
C | T | 1 | a0002c0002t0001g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3661-1861C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102373498 | ||||||
| chr10:102374347
|
C | CA | 89 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.3661-1001dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | INFO_REALIGN_3_PRIME | chr10 | 102374347 | |||||
| chr10:102374695
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3661-664A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102374695 | ||||||
| chr10:102374827
|
T | G | 7 | a0001c0004t0002g0104a0001c0004t0004g0004a0001c0004t0004g0013others(4): Show | 7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3661-532T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102374827 | ||||||
| chr10:102375202
|
G | GA | 6 | a0001c0001t0001g0136a0001c0001t0002g0018a0001c0001t0002g0035others(3): Show | 6 | HG01358.hp2 HG01928.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3661-143dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | INFO_REALIGN_3_PRIME | chr10 | 102375202 | |||||
| chr10:102375693
|
C | T | 22 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(19): Show | 22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.3886+109C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375693 | ||||||
| chr10:102375826
|
C | T | 3 | a0002c0002t0001g0172a0002c0002t0001g0180a0002c0002t0001g0188 | 3 | HG01099.hp1 HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.3886+242C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375826 | ||||||
| chr10:102375896
|
T | TACTCGGG others(3): Show |
1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+313_3886+314i others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | INFO_REALIGN_3_PRIME | chr10 | 102375896 | |||||
| chr10:102375898
|
G | T | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+314G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375898 | ||||||
| chr10:102375901
|
T | A | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+317T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375901 | ||||||
| chr10:102375912
|
G | C | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+328G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375912 | ||||||
| chr10:102375927
|
A | G | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+343A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375927 | ||||||
| chr10:102375929
|
T | G | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3887-343T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375929 | ||||||
| chr10:102375937
|
T | G | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3887-335T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375937 | ||||||
| chr10:102375939
|
A | T | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3887-333A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375939 | ||||||
| chr10:102375945
|
T | A | 1 | a0003c0005t0002g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3887-327T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375945 | ||||||
| chr10:102376029
|
A | G | 1 | a0001c0001t0003g0279 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3887-243A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102376029 | ||||||
| chr10:102376222
|
C | T | 2 | a0001c0003t0001g0227a0001c0003t0001g0228 | 2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3887-50C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102376222 | ||||||
| chr10:102376245
|
C | T | 10 | a0001c0001t0002g0022a0001c0001t0002g0027a0001c0001t0002g0053others(7): Show | 10 | NA18951.hp1 NA18955.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.3887-27C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102376245 | ||||||
| chr10:102376859
|
G | T | 2 | a0001c0001t0002g0086a0001c0001t0002g0097 | 2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.4288+59G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 32/39 | chr10 | 102376859 | ||||||
| chr10:102377200
|
C | T | 6 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0029others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.4494+60C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377200 | ||||||
| chr10:102377318
|
AATTTATT others(25): Show |
A | 91 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(88): Show | 91 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.4494+201_4494+232d others(34): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | INFO_REALIGN_3_PRIME | chr10 | 102377318 | |||||
| chr10:102377340
|
T | A | 1 | a0001c0001t0003g0319 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4494+200T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377340 | ||||||
| chr10:102377371
|
T | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4494+231T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377371 | ||||||
| chr10:102377383
|
TCTCTCTG others(9): Show |
T | 3 | a0001c0001t0002g0024a0001c0001t0002g0026a0001c0001t0002g0048 | 3 | NA18944.hp2 NA18979.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.4494+246_4494+261d others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | INFO_REALIGN_3_PRIME | chr10 | 102377383 | |||||
| chr10:102377456
|
C | T | 5 | a0001c0001t0002g0028a0001c0001t0002g0040a0001c0001t0002g0041others(2): Show | 5 | HG01934.hp2 HG01943.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.4494+316C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377456 | ||||||
| chr10:102377457
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4494+317G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377457 | ||||||
| chr10:102377994
|
T | C | 327 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.4494+854T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377994 | ||||||
| chr10:102378090
|
C | T | 1 | a0003c0005t0002g0077 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4494+950C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378090 | ||||||
| chr10:102378135
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0187 | 2 | NA19062.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.4494+995G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378135 | ||||||
| chr10:102378174
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.4494+1034T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378174 | ||||||
| chr10:102378217
|
C | CA | 13 | a0001c0001t0002g0034a0001c0001t0002g0092a0001c0001t0002g0093others(10): Show | 13 | HG02071.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.4495-1053dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | INFO_REALIGN_3_PRIME | chr10 | 102378217 | |||||
| chr10:102378410
|
G | T | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4495-874G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378410 | ||||||
| chr10:102378589
|
G | T | 1 | a0006c0011t0001g0295 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4495-695G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378589 | ||||||
| chr10:102378639
|
AATAAAAT | A | 10 | a0001c0001t0001g0209a0001c0001t0001g0215a0001c0001t0001g0216others(7): Show | 10 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.4495-643_4495-637d others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | INFO_REALIGN_3_PRIME | chr10 | 102378639 | |||||
| chr10:102378899
|
A | T | 1 | a0002c0002t0001g0173 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4495-385A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378899 | ||||||
| chr10:102378975
|
A | G | 1 | a0001c0001t0006g0166 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4495-309A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378975 | ||||||
| chr10:102379239
|
C | T | 7 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(4): Show | 7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4495-45C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102379239 | ||||||
| chr10:102380774
|
G | A | 1 | a0001c0004t0002g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5173+88G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 38/39 | chr10 | 102380774 | ||||||
| chr10:102380845
|
G | A | 90 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0002g0002others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.5173+159G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 38/39 | chr10 | 102380845 | ||||||
| chr10:102381540
|
C | T | 1 | a0001c0001t0003g0316 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5302+285C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381540 | ||||||
| chr10:102381814
|
C | A | 1 | a0001c0001t0001g0293 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5303-242C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381814 | ||||||
| chr10:102381815
|
C | T | 1 | a0001c0001t0002g0034 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5303-241C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381815 | ||||||
| chr10:102381822
|
C | CGA | 73 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0129others(70): Show | 74 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.5303-233_5303-232d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381822 | |||||
| chr10:102381823
|
G | GA | 89 | a0001c0001t0001g0117a0001c0001t0001g0155a0001c0001t0001g0162others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.5303-207dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381823 | |||||
| chr10:102381823
|
G | GAGA | 12 | a0001c0001t0003g0242a0001c0001t0003g0251a0001c0001t0003g0266others(9): Show | 12 | HG01981.hp2 HG02738.hp1 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.5303-232_5303-231i others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381823 | |||||
| chr10:102381823
|
GAA | G | 6 | a0001c0004t0004g0004a0001c0004t0004g0013a0001c0004t0004g0014others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.5303-208_5303-207d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381823 | |||||
| chr10:102381823
|
GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0003g0268 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5303-216_5303-207d others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381823 | |||||
| chr10:102381824
|
A | AG | 3 | a0001c0001t0001g0007a0001c0001t0003g0202a0001c0001t0003g0308 | 3 | HG04204.hp1 NA19009.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.5303-232_5303-231i others(3): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381824 | ||||||
| chr10:102381835
|
A | G | 1 | a0001c0001t0003g0268 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5303-221A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381835 | ||||||
| chr10:102381976
|
T | G | 1 | a0001c0003t0001g0225 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5303-80T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381976 | ||||||
| chr10:102381994
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5303-62A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381994 |