| geneid | 140458 |
|---|---|
| ensemblid | ENSG00000164122.9 |
| hgncid | 17180 |
| symbol | ASB5 |
| name | ankyrin repeat and SOCS box containing 5 |
| refseq_nuc | NM_080874.4 |
| refseq_prot | NP_543150.1 |
| ensembl_nuc | ENST00000296525.7 |
| ensembl_prot | ENSP00000296525.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 176213673 |
| end | 176269222 |
| strand | - |
| ver | v1.2 |
| region | chr4:176213673-176269222 |
| region5000 | chr4:176208673-176274222 |
| regionname0 | ASB5_chr4_176213673_176269222 |
| regionname5000 | ASB5_chr4_176208673_176274222 |
| 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 | 329 | 404 | 88 | 70 | 188 | 18 | 38 | 145 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0002 | 0/0 | 329 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0003 | 0/0 | 329 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0004 | 0/0 | 329 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0005 | 0/0 | 329 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0006 | 0/0 | 329 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0007 | 0/0 | 329 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 990 | 214 | 48 | 30 | 106 | 11 | 19 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0002 | 1/1 | 990 | 172 | 36 | 32 | 76 | 7 | 19 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0003 | 0/0 | 990 | 6 | 0 | 6 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0004 | 0/0 | 990 | 6 | 0 | 0 | 6 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0005 | 0/0 | 990 | 3 | 3 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0006 | 0/0 | 990 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0007 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0008 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0009 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0010 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0011 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0012 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| c0013 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2042 | 307 | 78 | 40 | 148 | 14 | 26 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0002 | 0/0 | 2042 | 49 | 3 | 10 | 28 | 1 | 7 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0003 | 0/0 | 2042 | 21 | 0 | 16 | 0 | 3 | 2 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0004 | 0/0 | 2042 | 5 | 5 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0005 | 0/0 | 2042 | 5 | 0 | 0 | 4 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0006 | 1/0 | 2042 | 4 | 2 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0007 | 0/0 | 2042 | 3 | 3 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0008 | 0/0 | 2042 | 3 | 0 | 0 | 3 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0009 | 0/0 | 2042 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0010 | 0/0 | 2042 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0011 | 0/0 | 2042 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0012 | 0/0 | 2042 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0013 | 0/0 | 2042 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0014 | 0/0 | 2042 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0015 | 0/0 | 2042 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0016 | 0/0 | 2042 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0017 | 0/0 | 2042 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0018 | 0/0 | 2042 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0019 | 0/0 | 2042 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| t0020 | 0/0 | 2042 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| 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 | 3 | 3 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0357 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 990 | 214 | 48 | 30 | 106 | 11 | 19 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002 | 1/1 | 990 | 172 | 36 | 32 | 76 | 7 | 19 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0003 | 0/0 | 990 | 6 | 0 | 6 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0004 | 0/0 | 990 | 6 | 0 | 0 | 6 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0005 | 0/0 | 990 | 3 | 3 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0006 | 0/0 | 990 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0010 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0002c0013 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0003c0007 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0004c0008 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0005c0012 | 0/0 | 990 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0006c0009 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0007c0011 | 0/0 | 990 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3031 | 198 | 47 | 29 | 94 | 11 | 17 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0001t0005 | 0/0 | 3031 | 5 | 0 | 0 | 4 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0001t0008 | 0/0 | 3031 | 3 | 0 | 0 | 3 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0001t0009 | 0/0 | 3031 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0001t0014 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0001t0015 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0001t0016 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0001t0018 | 0/0 | 3031 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0001t0019 | 0/0 | 3031 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0001t0020 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002t0001 | 0/1 | 3031 | 94 | 23 | 11 | 47 | 3 | 9 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002t0002 | 0/0 | 3031 | 44 | 3 | 5 | 28 | 1 | 7 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002t0003 | 0/0 | 3031 | 19 | 0 | 14 | 0 | 3 | 2 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002t0004 | 0/0 | 3031 | 5 | 5 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002t0006 | 1/0 | 3031 | 4 | 2 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002t0007 | 0/0 | 3031 | 3 | 3 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002t0012 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002t0013 | 0/0 | 3031 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0002t0017 | 0/0 | 3031 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0003t0002 | 0/0 | 3031 | 5 | 0 | 5 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0003t0011 | 0/0 | 3031 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0004t0001 | 0/0 | 3031 | 6 | 0 | 0 | 6 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0005t0001 | 0/0 | 3031 | 3 | 3 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0006t0003 | 0/0 | 3031 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0001c0010t0001 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0002c0013t0010 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0003c0007t0001 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0004c0008t0001 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0005c0012t0001 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0006c0009t0001 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| a0007c0011t0001 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | copy fasta | chr4 | 176208673 | 176274222 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0008g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0014g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0015g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0016g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0018g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0019g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0001t0020g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0029 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0006g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0006g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0006g0357 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0006g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0012g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0013g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0002t0017g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0003t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0003t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0003t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0003t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0003t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0003t0011g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0004t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0004t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0005t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0005t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0006t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0001c0010t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0002c0013t0010g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0003c0007t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0004c0008t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0005c0012t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0006c0009t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| a0007c0011t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0251 | EUR | GBR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0265 | EUR | GBR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0056 | EUR | FIN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0335 | EUR | FIN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0046 | EUR | FIN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0340 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0371 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0370 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0354 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00639 | hp2 | a0001 | c0006 | t0003 | g0017 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00642 | hp2 | a0001 | c0003 | t0002 | g0342 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00735 | hp1 | a0001 | c0002 | t0003 | g0044 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00738 | hp2 | a0001 | c0002 | t0006 | g0356 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0284 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0232 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0258 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0045 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0050 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01099 | hp1 | a0001 | c0006 | t0003 | g0017 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0351 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0231 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0285 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0059 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0043 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0104 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01258 | hp2 | a0001 | c0002 | t0003 | g0099 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0337 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0140 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0300 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0047 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0255 | EUR | IBS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01891 | hp2 | a0001 | c0002 | t0006 | g0358 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01928 | hp1 | a0001 | c0001 | t0019 | g0213 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0058 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0336 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0052 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01975 | hp1 | a0001 | c0003 | t0011 | g0338 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01978 | hp1 | a0001 | c0002 | t0017 | g0282 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0237 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0051 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02040 | hp1 | a0001 | c0001 | t0020 | g0375 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0276 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0228 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02074 | hp1 | a0005 | c0012 | t0001 | g0361 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02135 | hp2 | a0001 | c0002 | t0012 | g0066 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0332 | EAS | CDX | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0350 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02280 | hp2 | a0004 | c0008 | t0001 | g0095 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02523 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | KHV | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0038 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0306 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0278 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0305 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0348 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0160 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02723 | hp1 | a0001 | c0002 | t0007 | g0065 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02735 | hp1 | a0001 | c0001 | t0018 | g0048 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02738 | hp2 | a0001 | c0002 | t0013 | g0233 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0328 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0302 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02970 | hp1 | a0006 | c0009 | t0001 | g0186 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02976 | hp1 | a0001 | c0010 | t0001 | g0157 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02976 | hp2 | a0003 | c0007 | t0001 | g0034 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0341 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0041 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03225 | hp2 | a0001 | c0002 | t0007 | g0064 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0333 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0355 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0039 | AFR | ESN | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0249 | AFR | GWD | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0367 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0334 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0279 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0029 | SAS | STU | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0229 | SAS | PJL | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0307 | SAS | BEB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0329 | SAS | BEB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | BEB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0049 | SAS | BEB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0310 | SAS | STU | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0353 | SAS | STU | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0368 | SAS | BEB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | STU | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | CHB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0347 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18945 | hp1 | a0001 | c0004 | t0001 | g0365 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0360 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0359 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0102 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18953 | hp1 | a0001 | c0001 | t0009 | g0125 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18966 | hp2 | a0001 | c0001 | t0014 | g0111 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18972 | hp2 | a0001 | c0001 | t0009 | g0126 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0203 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18977 | hp2 | a0001 | c0001 | t0015 | g0112 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0373 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0330 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0322 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0331 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19001 | hp1 | a0002 | c0013 | t0010 | g0033 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0372 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0374 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0362 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0040 | AFR | LWK | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0304 | AFR | LWK | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0192 | AFR | LWK | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19058 | hp1 | a0001 | c0004 | t0001 | g0117 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0366 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19074 | hp1 | a0001 | c0001 | t0008 | g0083 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0349 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19085 | hp1 | a0001 | c0001 | t0008 | g0101 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0345 | AFR | YRI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ASW | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0004 | EUR | TSI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0369 | EUR | TSI | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0303 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0352 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0042 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG02486 | hp2 | a0007 | c0011 | t0001 | g0152 | AFR | ACB | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | USA | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | USA | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA18955 | hp2 | a0001 | c0004 | t0001 | g0200 | EAS | JPT | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | USA | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA20300 | hp2 | a0001 | c0002 | t0007 | g0035 | AFR | USA | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0269 | REF | REF | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0006 | g0357 | REF | REF | ASB5_chr4_176208673_176274222 | ASB5 | chr4 | 176208673 | 176274222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:176215604
|
C | T | 1 | a0006 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.986G>A | p.Arg329Gln | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 1100/3031 | 986/990 | 329/329 | chr4 | 176215604 | ||
| chr4:176221453
|
T | C | 1 | a0005 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.532A>G | p.Lys178Glu | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 4/7 | 646/3031 | 532/990 | 178/329 | chr4 | 176221453 | ||
| chr4:176221495
|
G | T | 1 | a0007 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.490C>A | p.Leu164Met | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 4/7 | 604/3031 | 490/990 | 164/329 | chr4 | 176221495 | ||
| chr4:176225293
|
C | T | 1 | a0004 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.245G>A | p.Arg82His | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/7 | 359/3031 | 245/990 | 82/329 | chr4 | 176225293 | ||
| chr4:176268966
|
C | T | 1 | a0003 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.143G>A | p.Arg48His | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/7 | 257/3031 | 143/990 | 48/329 | chr4 | 176268966 | ||
| chr4:176269072
|
G | T | 1 | a0002 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.37C>A | p.Gln13Lys | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/7 | 151/3031 | 37/990 | 13/329 | chr4 | 176269072 | ||
| chr4:176269073
|
T | G | 1 | a0002 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.36A>C | p.Gln12His | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/7 | 150/3031 | 36/990 | 12/329 | chr4 | 176269073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:176215708
|
G | A | 1 | a0001c0004 | 6 | NA18945.hp1 NA18955.hp2 NA18977.hp1 others(3): Show |
synonymous_variant | LOW | c.882C>T | p.Tyr294Tyr | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 996/3031 | 882/990 | 294/329 | chr4 | 176215708 | ||
| chr4:176216837
|
C | T | 6 | a0001c0001a0001c0004a0001c0010others(3): Show | 224 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(221): Show |
synonymous_variant | LOW | c.843G>A | p.Arg281Arg | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/7 | 957/3031 | 843/990 | 281/329 | chr4 | 176216837 | ||
| chr4:176221460
|
G | A | 1 | a0001c0006 | 2 | HG00639.hp2 HG01099.hp1 |
synonymous_variant | LOW | c.525C>T | p.Ala175Ala | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 4/7 | 639/3031 | 525/990 | 175/329 | chr4 | 176221460 | ||
| chr4:176221469
|
C | T | 1 | a0001c0003 | 6 | HG00642.hp2 HG01109.hp2 HG01358.hp2 others(3): Show |
synonymous_variant | LOW | c.516G>A | p.Thr172Thr | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 4/7 | 630/3031 | 516/990 | 172/329 | chr4 | 176221469 | ||
| chr4:176221580
|
A | G | 1 | a0001c0010 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.405T>C | p.Asp135Asp | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 4/7 | 519/3031 | 405/990 | 135/329 | chr4 | 176221580 | ||
| chr4:176222397
|
G | T | 2 | a0001c0005a0006c0009 | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.300C>A | p.Thr100Thr | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/7 | 414/3031 | 300/990 | 100/329 | chr4 | 176222397 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:176213844
|
G | T | 1 | a0001c0001t0016 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1756C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 1756 | chr4 | 176213844 | |||||
| chr4:176213923
|
G | C | 1 | a0001c0002t0017 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1677C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 1677 | chr4 | 176213923 | |||||
| chr4:176214010
|
A | G | 1 | a0001c0002t0012 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1590T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 1590 | chr4 | 176214010 | |||||
| chr4:176214329
|
G | A | 1 | a0001c0001t0018 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1271C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 1271 | chr4 | 176214329 | |||||
| chr4:176214345
|
A | C | 1 | a0001c0003t0011 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1255T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 1255 | chr4 | 176214345 | |||||
| chr4:176214469
|
G | A | 26 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(23): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
3_prime_UTR_variant | MODIFIER | c.*1131C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 1131 | chr4 | 176214469 | |||||
| chr4:176214480
|
C | T | 1 | a0001c0002t0007 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1120G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 1120 | chr4 | 176214480 | |||||
| chr4:176214595
|
C | T | 1 | a0001c0002t0013 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 1005 | chr4 | 176214595 | |||||
| chr4:176214604
|
T | G | 1 | a0001c0001t0009 | 2 | NA18953.hp1 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*996A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 996 | chr4 | 176214604 | |||||
| chr4:176214633
|
T | C | 1 | a0001c0001t0019 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*967A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 967 | chr4 | 176214633 | |||||
| chr4:176214776
|
A | C | 1 | a0001c0001t0015 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*824T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 824 | chr4 | 176214776 | |||||
| chr4:176214800
|
A | G | 1 | a0001c0001t0014 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*800T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 800 | chr4 | 176214800 | |||||
| chr4:176214803
|
A | G | 1 | a0001c0001t0014 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*797T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 797 | chr4 | 176214803 | |||||
| chr4:176214998
|
A | G | 3 | a0001c0002t0003a0001c0002t0013a0001c0006t0003 | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*602T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 602 | chr4 | 176214998 | |||||
| chr4:176215043
|
A | G | 30 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(27): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
3_prime_UTR_variant | MODIFIER | c.*557T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 557 | chr4 | 176215043 | |||||
| chr4:176215063
|
T | C | 1 | a0001c0001t0008 | 3 | NA18949.hp2 NA19074.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*537A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 537 | chr4 | 176215063 | |||||
| chr4:176215131
|
G | A | 1 | a0001c0001t0005 | 5 | HG02056.hp1 HG02523.hp2 HG03710.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*469C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 469 | chr4 | 176215131 | |||||
| chr4:176215361
|
G | A | 25 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(22): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
3_prime_UTR_variant | MODIFIER | c.*239C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 7/7 | 239 | chr4 | 176215361 | |||||
| chr4:176269172
|
T | A | 1 | a0001c0001t0020 | 1 | HG02040.hp1 | 5_prime_UTR_variant | MODIFIER | c.-64A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/7 | 64 | chr4 | 176269172 | |||||
| chr4:176269191
|
G | C | 1 | a0002c0013t0010 | 1 | NA19001.hp1 | 5_prime_UTR_variant | MODIFIER | c.-83C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/7 | 83 | chr4 | 176269191 | |||||
| chr4:176269192
|
C | G | 1 | a0002c0013t0010 | 1 | NA19001.hp1 | 5_prime_UTR_variant | MODIFIER | c.-84G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/7 | 84 | chr4 | 176269192 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:176215829
|
T | C | 1 | a0001c0010t0001g0157 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.863-102A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176215829 | ||||||
| chr4:176215850
|
A | G | 1 | a0001c0002t0001g0304 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.863-123T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176215850 | ||||||
| chr4:176215904
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.863-177A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176215904 | ||||||
| chr4:176215926
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(72): Show | 82 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.863-199T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176215926 | ||||||
| chr4:176216023
|
A | G | 1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.863-296T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216023 | ||||||
| chr4:176216222
|
G | A | 27 | a0001c0001t0001g0013a0001c0001t0001g0079a0001c0001t0001g0080others(24): Show | 28 | HG01123.hp1 HG01168.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.863-495C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216222 | ||||||
| chr4:176216233
|
A | G | 1 | a0001c0002t0001g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.863-506T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216233 | ||||||
| chr4:176216345
|
A | G | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.862+473T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216345 | ||||||
| chr4:176216399
|
G | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(69): Show | 79 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.862+419C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216399 | ||||||
| chr4:176216420
|
G | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(69): Show | 79 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.862+398C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216420 | ||||||
| chr4:176216443
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(69): Show | 79 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.862+375G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216443 | ||||||
| chr4:176216634
|
C | T | 86 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(83): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.862+184G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216634 | ||||||
| chr4:176216645
|
G | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(203): Show | 224 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.862+173C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216645 | ||||||
| chr4:176216672
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.862+146G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216672 | ||||||
| chr4:176216786
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.862+32A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 6/6 | chr4 | 176216786 | ||||||
| chr4:176217265
|
G | A | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.671-256C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217265 | ||||||
| chr4:176217298
|
A | C | 1 | a0001c0001t0001g0187 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.671-289T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217298 | ||||||
| chr4:176217303
|
C | A | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.671-294G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217303 | ||||||
| chr4:176217320
|
G | T | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-311C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217320 | ||||||
| chr4:176217393
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.671-384T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217393 | ||||||
| chr4:176217454
|
A | T | 2 | a0001c0001t0001g0107a0001c0001t0015g0112 | 2 | NA18950.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.671-445T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217454 | ||||||
| chr4:176217526
|
T | C | 1 | a0007c0011t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.671-517A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217526 | ||||||
| chr4:176217548
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.671-539A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217548 | ||||||
| chr4:176217584
|
C | T | 1 | a0001c0002t0002g0329 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.671-575G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217584 | ||||||
| chr4:176217585
|
C | A | 111 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.671-576G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217585 | ||||||
| chr4:176217600
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 7 | HG01081.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-591C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217600 | ||||||
| chr4:176217642
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0116 | 2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.671-633C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217642 | ||||||
| chr4:176217685
|
C | T | 112 | a0001c0001t0001g0119a0001c0002t0001g0019a0001c0002t0001g0021others(109): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.671-676G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217685 | ||||||
| chr4:176217758
|
T | C | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.671-749A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217758 | ||||||
| chr4:176217862
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.671-853G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217862 | ||||||
| chr4:176217867
|
C | A | 1 | a0001c0002t0002g0348 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.671-858G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217867 | ||||||
| chr4:176217884
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.671-875C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217884 | ||||||
| chr4:176217893
|
A | G | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.671-884T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217893 | ||||||
| chr4:176217990
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(60): Show | 69 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.671-981T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217990 | ||||||
| chr4:176217994
|
T | C | 40 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(37): Show | 41 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.671-985A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176217994 | ||||||
| chr4:176218030
|
A | G | 1 | a0001c0002t0002g0324 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.671-1021T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218030 | ||||||
| chr4:176218038
|
A | AGCATAAA others(72): Show |
1 | a0001c0002t0001g0261 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.671-1030_671-1029i others(81): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218038 | ||||||
| chr4:176218151
|
AATATATA others(68): Show |
A | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.671-1217_671-1143d others(77): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218151 | ||||||
| chr4:176218153
|
TATATACA others(231): Show |
T | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.671-1382_671-1145d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218153 | ||||||
| chr4:176218159
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(319): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.671-1150G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218159 | ||||||
| chr4:176218168
|
GATATATA others(1): Show |
G | 18 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(15): Show | 21 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.671-1167_671-1160d others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218168 | ||||||
| chr4:176218175
|
A | ATATTTGT others(27): Show |
1 | a0001c0002t0003g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.671-1167_671-1166i others(36): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218175 | ||||||
| chr4:176218176
|
A | G | 1 | a0001c0002t0003g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.671-1167T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218176 | ||||||
| chr4:176218201
|
A | AAT | 7 | a0001c0001t0001g0089a0001c0002t0001g0057a0001c0002t0001g0250others(4): Show | 7 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-1194_671-1193d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218201 | ||||||
| chr4:176218201
|
AATATATA others(18): Show |
A | 33 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(30): Show | 34 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.671-1217_671-1193d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218201 | ||||||
| chr4:176218201
|
AATATATA others(45): Show |
A | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(19): Show | 27 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.671-1244_671-1193d others(54): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218201 | ||||||
| chr4:176218203
|
T | TATATATA others(106): Show |
2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.671-1195_671-1194i others(115): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218203 | ||||||
| chr4:176218218
|
G | GAT | 145 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(142): Show | 158 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.671-1211_671-1210d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218218 | ||||||
| chr4:176218220
|
TATAA | T | 18 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(15): Show | 21 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.671-1215_671-1212d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218220 | ||||||
| chr4:176218222
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671-1213A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218222 | ||||||
| chr4:176218224
|
A | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(101): Show | 111 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.671-1215T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218224 | ||||||
| chr4:176218226
|
T | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(101): Show | 111 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.671-1217A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218226 | ||||||
| chr4:176218226
|
T | TATATATA others(110): Show |
1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.671-1218_671-1217i others(119): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218226 | ||||||
| chr4:176218228
|
TATATATA others(273): Show |
T | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149 | 3 | HG02809.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.671-1499_671-1220d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218228 | ||||||
| chr4:176218230
|
T | A | 18 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(15): Show | 21 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.671-1221A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218230 | ||||||
| chr4:176218237
|
T | A | 18 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(15): Show | 21 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.671-1228A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218237 | ||||||
| chr4:176218243
|
GAT | G | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1236_671-1235d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218243 | ||||||
| chr4:176218247
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(62): Show | 70 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.671-1238A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218247 | ||||||
| chr4:176218247
|
T | TATATATT others(52): Show |
6 | a0001c0002t0001g0057a0001c0002t0001g0250a0001c0002t0001g0251others(3): Show | 6 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-1239_671-1238i others(61): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218247 | ||||||
| chr4:176218247
|
T | TATATATT others(52): Show |
1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671-1239_671-1238i others(61): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218247 | ||||||
| chr4:176218251
|
A | T | 7 | a0001c0001t0001g0089a0001c0002t0001g0057a0001c0002t0001g0250others(4): Show | 7 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-1242T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218251 | ||||||
| chr4:176218251
|
AAT | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(99): Show | 108 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.671-1244_671-1243d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218251 | ||||||
| chr4:176218251
|
AATAT | A | 18 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(15): Show | 21 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.671-1246_671-1243d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218251 | ||||||
| chr4:176218253
|
T | TATATATA others(18): Show |
68 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(65): Show | 75 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.671-1245_671-1244i others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218253
|
T | TATATATA others(8): Show |
9 | a0001c0002t0001g0025a0001c0002t0001g0084a0001c0002t0001g0085others(6): Show | 9 | HG01515.hp2 HG02258.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-1245_671-1244i others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218253
|
T | TATATATA others(358): Show |
1 | a0001c0002t0001g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.671-1245_671-1244i others(367): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218253
|
T | TATATATA others(362): Show |
1 | a0001c0002t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.671-1245_671-1244i others(371): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218253
|
T | TATATATA others(535): Show |
1 | a0001c0002t0001g0307 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.671-1245_671-1244i others(544): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218253
|
T | TATATATA others(492): Show |
2 | a0001c0002t0001g0238a0001c0002t0001g0240 | 2 | NA18971.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.671-1245_671-1244i others(501): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218253
|
T | TATATATA others(511): Show |
1 | a0003c0007t0001g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.671-1245_671-1244i others(520): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218253
|
T | TATATATA others(336): Show |
1 | a0001c0002t0001g0353 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.671-1245_671-1244i others(345): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218253
|
T | TATATATA others(100): Show |
4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-1245_671-1244i others(109): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218253
|
TATATATA others(248): Show |
T | 5 | a0001c0001t0001g0129a0001c0004t0001g0117a0001c0004t0001g0118others(2): Show | 5 | HG04184.hp1 NA18945.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-1499_671-1245d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218253 | ||||||
| chr4:176218255
|
T | A | 7 | a0001c0001t0001g0089a0001c0002t0001g0057a0001c0002t0001g0250others(4): Show | 7 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-1246A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218255 | ||||||
| chr4:176218255
|
T | TATATATA others(62): Show |
1 | a0001c0002t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.671-1247_671-1246i others(71): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218255 | ||||||
| chr4:176218255
|
T | TATATATT others(77): Show |
54 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0025others(51): Show | 58 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.671-1247_671-1246i others(86): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218255 | ||||||
| chr4:176218255
|
T | TATATGTA others(10): Show |
1 | a0001c0002t0003g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.671-1247_671-1246i others(19): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218255 | ||||||
| chr4:176218270
|
GATATATA others(3): Show |
G | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1271_671-1262d others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218270 | ||||||
| chr4:176218274
|
T | C | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0245 | 3 | HG02015.hp1 HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.671-1265A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218274 | ||||||
| chr4:176218278
|
AAT | A | 11 | a0001c0001t0001g0089a0001c0001t0001g0183a0001c0001t0001g0193others(8): Show | 11 | HG02015.hp1 HG02572.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.671-1271_671-1270d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218278 | ||||||
| chr4:176218280
|
T | TATATATA others(8): Show |
7 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(4): Show | 9 | NA18943.hp1 NA18947.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1272_671-1271i others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218280 | ||||||
| chr4:176218280
|
T | TATATATA others(344): Show |
1 | a0001c0002t0001g0302 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.671-1272_671-1271i others(353): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218280 | ||||||
| chr4:176218280
|
T | TATATATA others(346): Show |
1 | a0001c0002t0001g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671-1272_671-1271i others(355): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218280 | ||||||
| chr4:176218280
|
T | TATATATA others(271): Show |
1 | a0001c0002t0001g0025 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.671-1272_671-1271i others(280): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218280 | ||||||
| chr4:176218280
|
T | TATATATA others(321): Show |
2 | a0001c0002t0001g0084a0001c0002t0001g0085 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.671-1272_671-1271i others(330): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218280 | ||||||
| chr4:176218280
|
T | TATATATA others(346): Show |
3 | a0001c0002t0001g0283a0001c0002t0001g0288a0001c0002t0001g0289 | 3 | NA18973.hp2 NA18998.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.671-1272_671-1271i others(355): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218280 | ||||||
| chr4:176218280
|
T | TATATATA others(363): Show |
1 | a0001c0002t0001g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.671-1272_671-1271i others(372): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218280 | ||||||
| chr4:176218280
|
T | TATATATA others(388): Show |
6 | a0001c0002t0001g0024a0001c0002t0001g0252a0001c0002t0001g0258others(3): Show | 6 | HG01069.hp2 HG03704.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-1272_671-1271i others(397): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218280 | ||||||
| chr4:176218280
|
T | TATATATA others(413): Show |
1 | a0001c0002t0001g0260 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.671-1272_671-1271i others(422): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218280 | ||||||
| chr4:176218301
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 66 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.671-1292A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218301 | ||||||
| chr4:176218305
|
A | AAT | 66 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0025others(63): Show | 70 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.671-1298_671-1297d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218305 | ||||||
| chr4:176218307
|
TATATATA others(8): Show |
T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0245 | 3 | HG02015.hp1 HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.671-1313_671-1299d others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218307 | ||||||
| chr4:176218322
|
G | GATATATA others(1): Show |
37 | a0001c0002t0001g0024a0001c0002t0001g0025a0001c0002t0001g0084others(34): Show | 40 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.671-1314_671-1313i others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218322 | ||||||
| chr4:176218322
|
G | GATATATA others(3): Show |
3 | a0001c0001t0001g0089a0001c0001t0001g0323a0001c0001t0001g0325 | 3 | HG00597.hp1 HG06807.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.671-1314_671-1313i others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218322 | ||||||
| chr4:176218322
|
G | GATATATA others(162): Show |
7 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(4): Show | 9 | NA18943.hp1 NA18947.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1314_671-1313i others(171): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218322 | ||||||
| chr4:176218324
|
TATATATA others(16): Show |
T | 1 | a0001c0002t0002g0340 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.671-1338_671-1316d others(25): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218324 | ||||||
| chr4:176218326
|
T | TATAA | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1318_671-1317i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218326 | ||||||
| chr4:176218328
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.671-1319A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218328 | ||||||
| chr4:176218330
|
T | A | 5 | a0001c0002t0003g0044a0001c0002t0003g0047a0001c0002t0003g0049others(2): Show | 5 | HG00735.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1321A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218330 | ||||||
| chr4:176218332
|
TTTGTATG others(8): Show |
T | 5 | a0001c0002t0003g0044a0001c0002t0003g0047a0001c0002t0003g0049others(2): Show | 5 | HG00735.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1338_671-1324d others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218332 | ||||||
| chr4:176218333
|
T | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1324A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218333 | ||||||
| chr4:176218341
|
T | C | 7 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(4): Show | 9 | NA18943.hp1 NA18947.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1332A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218341 | ||||||
| chr4:176218345
|
T | C | 4 | a0001c0002t0001g0238a0001c0002t0001g0240a0001c0002t0001g0307others(1): Show | 4 | HG02976.hp2 HG03831.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-1336A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218345 | ||||||
| chr4:176218347
|
A | AAT | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 83 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.671-1340_671-1339d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218347 | ||||||
| chr4:176218347
|
A | AATATATA others(20): Show |
4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-1339_671-1338i others(29): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218347 | ||||||
| chr4:176218347
|
A | AATATATA others(66): Show |
12 | a0001c0002t0001g0026a0001c0002t0001g0057a0001c0002t0001g0250others(9): Show | 13 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.671-1339_671-1338i others(75): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218347 | ||||||
| chr4:176218347
|
A | AATATATA others(10): Show |
1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671-1355_671-1339d others(19): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218347 | ||||||
| chr4:176218347
|
A | AATATATA others(66): Show |
1 | a0001c0002t0001g0285 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.671-1339_671-1338i others(75): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218347 | ||||||
| chr4:176218354
|
ATT | A | 14 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(11): Show | 17 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.671-1347_671-1346d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218354 | ||||||
| chr4:176218356
|
T | A | 17 | a0001c0002t0001g0024a0001c0002t0001g0084a0001c0002t0001g0085others(14): Show | 17 | HG01069.hp2 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.671-1347A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218356 | ||||||
| chr4:176218364
|
T | C | 68 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(65): Show | 74 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.671-1355A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218364 | ||||||
| chr4:176218366
|
TATAA | T | 5 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0245others(2): Show | 5 | HG00597.hp1 HG02015.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1361_671-1358d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218366 | ||||||
| chr4:176218370
|
A | AATATATA others(237): Show |
3 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0303 | 3 | HG01433.hp1 HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.671-1362_671-1361i others(246): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218370 | ||||||
| chr4:176218377
|
A | ATATT | 26 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(23): Show | 27 | HG01069.hp2 HG01891.hp1 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.671-1369_671-1368i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATT | 14 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(11): Show | 17 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.671-1369_671-1368i others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATTTGTAT others(370): Show |
1 | a0001c0002t0001g0236 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.671-1369_671-1368i others(379): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATTTGTAT others(395): Show |
1 | a0001c0002t0001g0244 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.671-1369_671-1368i others(404): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATTTGTAT others(420): Show |
8 | a0001c0002t0001g0019a0001c0002t0001g0219a0001c0002t0001g0235others(5): Show | 9 | HG00544.hp2 HG01993.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1369_671-1368i others(429): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATTTGTAT others(214): Show |
1 | a0001c0002t0001g0025 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.671-1369_671-1368i others(223): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATTTGTAT others(414): Show |
5 | a0001c0002t0001g0262a0001c0002t0001g0267a0001c0002t0001g0290others(2): Show | 5 | HG00609.hp2 HG04184.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1369_671-1368i others(423): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATTTGTAT others(439): Show |
1 | a0001c0002t0001g0298 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.671-1369_671-1368i others(448): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATTTGTAT others(287): Show |
2 | a0001c0002t0001g0254a0001c0002t0001g0264 | 2 | HG01261.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.671-1369_671-1368i others(296): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATTTGTAT others(439): Show |
25 | a0001c0002t0001g0022a0001c0002t0001g0031a0001c0002t0001g0247others(22): Show | 27 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.671-1369_671-1368i others(448): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | ATTTGTAT others(437): Show |
1 | a0001c0002t0001g0078 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.671-1369_671-1368i others(446): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218377
|
A | T | 5 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0245others(2): Show | 5 | HG00597.hp1 HG02015.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1368T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218377 | ||||||
| chr4:176218391
|
A | AAT | 87 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(84): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.671-1384_671-1383d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218391 | ||||||
| chr4:176218391
|
AATATATA others(18): Show |
A | 1 | a0001c0002t0002g0341 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.671-1407_671-1383d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218391 | ||||||
| chr4:176218400
|
T | A | 1 | a0001c0002t0001g0025 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.671-1391A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218400 | ||||||
| chr4:176218400
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671-1391A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218400 | ||||||
| chr4:176218414
|
A | AAT | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1407_671-1406d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218414 | ||||||
| chr4:176218421
|
ATATT | A | 6 | a0001c0001t0001g0089a0001c0001t0001g0193a0001c0001t0001g0194others(3): Show | 6 | HG00597.hp1 HG02015.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-1416_671-1413d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218421 | ||||||
| chr4:176218439
|
A | AAT | 21 | a0001c0002t0001g0024a0001c0002t0001g0084a0001c0002t0001g0085others(18): Show | 21 | HG00140.hp1 HG01069.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.671-1432_671-1431d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218439 | ||||||
| chr4:176218439
|
AAT | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(26): Show | 34 | HG00280.hp2 HG00597.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.671-1432_671-1431d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218439 | ||||||
| chr4:176218439
|
AATATATA others(62): Show |
A | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.671-1499_671-1431d others(71): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218439 | ||||||
| chr4:176218441
|
TATATATA others(60): Show |
T | 13 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0090others(10): Show | 15 | HG00639.hp1 HG01993.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.671-1499_671-1433d others(69): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218441 | ||||||
| chr4:176218464
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1455T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218464 | ||||||
| chr4:176218464
|
AAT | A | 36 | a0001c0001t0001g0089a0001c0001t0001g0245a0001c0001t0001g0323others(33): Show | 39 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.671-1457_671-1456d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218464 | ||||||
| chr4:176218466
|
T | TATATATA others(265): Show |
1 | a0001c0005t0001g0306 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.671-1458_671-1457i others(274): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218466 | ||||||
| chr4:176218466
|
T | TATATATA others(240): Show |
2 | a0001c0005t0001g0305a0006c0009t0001g0186 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.671-1458_671-1457i others(249): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218466 | ||||||
| chr4:176218466
|
T | TTTGTATG others(75): Show |
4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1458_671-1457i others(84): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218466 | ||||||
| chr4:176218466
|
TATATATA others(35): Show |
T | 32 | a0001c0001t0001g0013a0001c0001t0001g0079a0001c0001t0001g0080others(29): Show | 33 | HG01123.hp1 HG01168.hp2 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.671-1499_671-1458d others(44): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218466 | ||||||
| chr4:176218487
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.671-1478A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218487 | ||||||
| chr4:176218489
|
T | C | 1 | a0001c0002t0001g0084 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.671-1480A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218489 | ||||||
| chr4:176218491
|
A | AAT | 46 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0025others(43): Show | 50 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.671-1484_671-1483d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218491 | ||||||
| chr4:176218493
|
TATATATA others(8): Show |
T | 6 | a0001c0001t0001g0137a0001c0002t0003g0044a0001c0002t0003g0047others(3): Show | 6 | HG00735.hp1 HG01496.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-1499_671-1485d others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218493 | ||||||
| chr4:176218500
|
A | G | 1 | a0001c0001t0001g0344 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.671-1491T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218500 | ||||||
| chr4:176218508
|
G | GATATATA others(1): Show |
65 | a0001c0001t0001g0245a0001c0002t0001g0019a0001c0002t0001g0021others(62): Show | 70 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.671-1500_671-1499i others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218508 | ||||||
| chr4:176218508
|
G | GATATATA others(3): Show |
8 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 9 | HG00597.hp1 HG01891.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-1500_671-1499i others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218508 | ||||||
| chr4:176218508
|
G | GATATATA others(355): Show |
2 | a0001c0002t0001g0026a0001c0002t0001g0304 | 3 | HG01884.hp2 HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.671-1500_671-1499i others(364): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218508 | ||||||
| chr4:176218508
|
G | GATATATA others(178): Show |
1 | a0001c0002t0001g0025 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.671-1500_671-1499i others(187): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218508 | ||||||
| chr4:176218510
|
T | TATACAA | 23 | a0001c0002t0001g0024a0001c0002t0001g0084a0001c0002t0001g0085others(20): Show | 23 | HG00140.hp1 HG01069.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.671-1502_671-1501i others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218510 | ||||||
| chr4:176218510
|
T | TATATAAA others(20): Show |
1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.671-1502_671-1501i others(29): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218510 | ||||||
| chr4:176218529
|
T | C | 8 | a0001c0001t0001g0129a0001c0001t0001g0146a0001c0001t0001g0147others(5): Show | 8 | HG02809.hp1 HG04184.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.671-1520A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218529 | ||||||
| chr4:176218529
|
TATAAATA others(676): Show |
T | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.670+1943_671-1521d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218529 | ||||||
| chr4:176218533
|
A | AAT | 46 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0031others(43): Show | 49 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.671-1526_671-1525d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218533 | ||||||
| chr4:176218533
|
AATATATA others(10): Show |
A | 3 | a0001c0001t0001g0159a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG01081.hp2 HG03209.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.671-1541_671-1525d others(19): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218533 | ||||||
| chr4:176218533
|
AATATATA others(37): Show |
A | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(40): Show | 48 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.671-1568_671-1525d others(46): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218533 | ||||||
| chr4:176218533
|
AATATATA others(252): Show |
A | 15 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0053others(12): Show | 15 | HG00735.hp2 HG01070.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.671-1783_671-1525d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218533 | ||||||
| chr4:176218544
|
TTGTATGA others(56): Show |
T | 76 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(73): Show | 84 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.671-1598_671-1536d others(65): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218544 | ||||||
| chr4:176218550
|
G | GATATACA others(207): Show |
1 | a0001c0002t0001g0025 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.671-1542_671-1541i others(216): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218550
|
G | GATATATA others(1): Show |
3 | a0001c0002t0001g0024a0001c0002t0001g0254a0001c0002t0001g0280 | 3 | HG03491.hp1 NA18952.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.671-1542_671-1541i others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218550
|
G | GATATATA others(3): Show |
46 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0031others(43): Show | 49 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.671-1542_671-1541i others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218550
|
G | GATATATA others(159): Show |
5 | a0001c0002t0001g0258a0001c0002t0001g0260a0001c0002t0001g0263others(2): Show | 5 | HG00140.hp1 HG01069.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1542_671-1541i others(168): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218550
|
G | GATATATA others(30): Show |
3 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0304 | 4 | HG01884.hp2 HG02809.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1542_671-1541i others(39): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218550
|
G | GATATATA others(128): Show |
7 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(4): Show | 9 | NA18943.hp1 NA18947.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1542_671-1541i others(137): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218550
|
G | GATATATA others(384): Show |
1 | a0001c0002t0001g0285 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.671-1542_671-1541i others(393): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218550
|
G | GATATATA others(80): Show |
1 | a0001c0002t0001g0252 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.671-1542_671-1541i others(89): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218550
|
G | GATATATA others(159): Show |
12 | a0001c0002t0001g0279a0001c0002t0001g0283a0001c0002t0001g0288others(9): Show | 12 | HG01433.hp1 HG02109.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.671-1542_671-1541i others(168): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218550
|
G | GATATATA others(161): Show |
2 | a0001c0002t0001g0084a0001c0002t0001g0085 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.671-1542_671-1541i others(170): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218550 | ||||||
| chr4:176218552
|
T | TATATAA | 10 | a0001c0002t0001g0057a0001c0002t0001g0250a0001c0002t0001g0251others(7): Show | 10 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.671-1544_671-1543i others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218552 | ||||||
| chr4:176218552
|
T | TATATAAA others(20): Show |
5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1544_671-1543i others(29): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218552 | ||||||
| chr4:176218554
|
T | TATAA | 16 | a0001c0001t0001g0081a0001c0001t0001g0309a0001c0002t0003g0004others(13): Show | 19 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.671-1546_671-1545i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218554 | ||||||
| chr4:176218554
|
TATATATT others(31): Show |
T | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.671-1583_671-1546d others(40): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218554 | ||||||
| chr4:176218561
|
T | A | 26 | a0001c0001t0001g0081a0001c0001t0001g0309a0001c0002t0001g0057others(23): Show | 29 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.671-1552A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218561 | ||||||
| chr4:176218575
|
AAT | A | 17 | a0001c0001t0001g0055a0001c0001t0001g0081a0001c0001t0001g0309others(14): Show | 20 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.671-1568_671-1567d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218575 | ||||||
| chr4:176218596
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.671-1587A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218596 | ||||||
| chr4:176218598
|
T | C | 7 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(4): Show | 9 | NA18943.hp1 NA18947.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1589A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218598 | ||||||
| chr4:176218600
|
A | T | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.671-1591T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218600 | ||||||
| chr4:176218607
|
A | ATATATT | 3 | a0001c0002t0001g0024a0001c0002t0001g0254a0001c0002t0001g0280 | 3 | HG03491.hp1 NA18952.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.671-1599_671-1598i others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218607 | ||||||
| chr4:176218607
|
A | ATATT | 4 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0309others(1): Show | 4 | HG00741.hp2 HG01515.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1599_671-1598i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218607 | ||||||
| chr4:176218607
|
A | ATATTTGT others(149): Show |
9 | a0001c0002t0001g0057a0001c0002t0001g0250a0001c0002t0001g0251others(6): Show | 9 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1599_671-1598i others(158): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218607 | ||||||
| chr4:176218607
|
A | ATT | 7 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(4): Show | 9 | NA18943.hp1 NA18947.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1599_671-1598i others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218607 | ||||||
| chr4:176218607
|
A | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0161 | 2 | NA18953.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.671-1598T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218607 | ||||||
| chr4:176218609
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1600C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218609 | ||||||
| chr4:176218612
|
TG | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1604delC | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218612 | ||||||
| chr4:176218614
|
A | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1605T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218614 | ||||||
| chr4:176218616
|
A | G | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1607T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218616 | ||||||
| chr4:176218619
|
T | TG | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1611_671-1610i others(3): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218619 | ||||||
| chr4:176218621
|
A | AAT | 10 | a0001c0001t0001g0089a0001c0001t0001g0159a0001c0002t0001g0057others(7): Show | 10 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.671-1614_671-1613d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218621 | ||||||
| chr4:176218621
|
A | AATAT | 3 | a0001c0002t0001g0024a0001c0002t0001g0254a0001c0002t0001g0280 | 3 | HG03491.hp1 NA18952.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.671-1616_671-1613d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218621 | ||||||
| chr4:176218621
|
A | AATATATA others(20): Show |
7 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(4): Show | 9 | NA18943.hp1 NA18947.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1613_671-1612i others(29): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218621 | ||||||
| chr4:176218621
|
A | AATATATA others(14): Show |
1 | a0001c0002t0001g0345 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.671-1633_671-1613d others(23): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218621 | ||||||
| chr4:176218621
|
A | AATATATA others(354): Show |
1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.671-1613_671-1612i others(363): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218621 | ||||||
| chr4:176218621
|
A | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1612T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218621 | ||||||
| chr4:176218626
|
A | G | 31 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0079others(28): Show | 32 | HG00140.hp2 HG01123.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.671-1617T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218626 | ||||||
| chr4:176218628
|
ATT | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(73): Show | 84 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.671-1621_671-1620d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218628 | ||||||
| chr4:176218630
|
T | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0309 | 2 | HG00741.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.671-1621A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218630 | ||||||
| chr4:176218632
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0309 | 2 | HG00741.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.671-1623C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218632 | ||||||
| chr4:176218634
|
A | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0309 | 2 | HG00741.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.671-1625T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218634 | ||||||
| chr4:176218644
|
A | AAT | 5 | a0001c0001t0001g0159a0001c0002t0001g0255a0001c0002t0007g0035others(2): Show | 5 | HG01515.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1637_671-1636d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218644 | ||||||
| chr4:176218644
|
A | AATATATA others(20): Show |
1 | a0001c0002t0002g0328 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.671-1662_671-1636d others(29): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218644 | ||||||
| chr4:176218644
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0309 | 2 | HG00741.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.671-1635T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218644 | ||||||
| chr4:176218644
|
AAT | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(74): Show | 85 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.671-1637_671-1636d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218644 | ||||||
| chr4:176218644
|
AATATATA others(20): Show |
A | 6 | a0001c0001t0001g0137a0001c0001t0001g0245a0001c0001t0001g0318others(3): Show | 6 | HG00597.hp1 HG02015.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-1662_671-1636d others(29): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218644 | ||||||
| chr4:176218646
|
TATATATA others(183): Show |
T | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(40): Show | 48 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.671-1827_671-1638d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218646 | ||||||
| chr4:176218651
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0172a0001c0010t0001g0157 | 4 | HG02004.hp1 HG02976.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-1642T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218651 | ||||||
| chr4:176218651
|
ATATT | A | 5 | a0001c0002t0003g0044a0001c0002t0003g0047a0001c0002t0003g0049others(2): Show | 5 | HG00735.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1646_671-1643d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218651 | ||||||
| chr4:176218661
|
GATATATA others(3): Show |
G | 1 | a0001c0001t0001g0159 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.671-1662_671-1653d others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218661 | ||||||
| chr4:176218669
|
AAT | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(111): Show | 126 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.671-1662_671-1661d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218669 | ||||||
| chr4:176218669
|
AATAT | A | 5 | a0001c0002t0003g0044a0001c0002t0003g0047a0001c0002t0003g0049others(2): Show | 5 | HG00735.hp1 HG01496.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1664_671-1661d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218669 | ||||||
| chr4:176218671
|
T | TATATATA others(16): Show |
60 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0025others(57): Show | 63 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.671-1663_671-1662i others(25): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218671 | ||||||
| chr4:176218671
|
T | TATATATA others(41): Show |
1 | a0001c0002t0001g0084 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.671-1663_671-1662i others(50): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218671 | ||||||
| chr4:176218671
|
TATATATA others(584): Show |
T | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149 | 3 | HG02809.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.670+1893_671-1663d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218671 | ||||||
| chr4:176218673
|
T | TATATATA others(41): Show |
1 | a0001c0002t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.671-1665_671-1664i others(50): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218673 | ||||||
| chr4:176218690
|
TATATAAA others(471): Show |
T | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.670+1987_671-1682d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218690 | ||||||
| chr4:176218696
|
A | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0062others(39): Show | 45 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.671-1687T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218696 | ||||||
| chr4:176218696
|
AAT | A | 85 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0141others(82): Show | 90 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.671-1689_671-1688d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218696 | ||||||
| chr4:176218698
|
TATATATA others(154): Show |
T | 1 | a0001c0001t0018g0048 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.671-1850_671-1690d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218698 | ||||||
| chr4:176218699
|
A | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0062others(39): Show | 45 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.671-1690T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218699 | ||||||
| chr4:176218701
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0062others(39): Show | 45 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.671-1692T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218701 | ||||||
| chr4:176218704
|
T | TG | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0062others(39): Show | 45 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.671-1696_671-1695i others(3): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218704 | ||||||
| chr4:176218704
|
TATATTTG others(12): Show |
T | 5 | a0001c0001t0001g0159a0001c0001t0001g0309a0001c0002t0003g0044others(2): Show | 5 | HG00735.hp1 HG00741.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-1714_671-1696d others(21): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218704 | ||||||
| chr4:176218706
|
TATTTGTA others(10): Show |
T | 20 | a0001c0001t0001g0081a0001c0001t0001g0129a0001c0001t0001g0141others(17): Show | 22 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.671-1714_671-1698d others(19): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218706 | ||||||
| chr4:176218709
|
T | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0062others(39): Show | 45 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.671-1700A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218709 | ||||||
| chr4:176218710
|
TGTA | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0062others(39): Show | 45 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.671-1704_671-1702d others(5): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218710 | ||||||
| chr4:176218714
|
T | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0062others(39): Show | 45 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.671-1705A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218714 | ||||||
| chr4:176218715
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0062others(39): Show | 45 | HG00140.hp2 HG00639.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.671-1706C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218715 | ||||||
| chr4:176218715
|
G | GATATATA others(1): Show |
90 | a0001c0001t0001g0142a0001c0002t0001g0019a0001c0002t0001g0021others(87): Show | 97 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.671-1707_671-1706i others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218715 | ||||||
| chr4:176218715
|
G | GATATATA others(70): Show |
2 | a0001c0002t0001g0024a0001c0002t0001g0280 | 2 | NA18952.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.671-1707_671-1706i others(79): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218715 | ||||||
| chr4:176218715
|
G | GATATATA others(197): Show |
1 | a0001c0002t0001g0254 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.671-1707_671-1706i others(206): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218715 | ||||||
| chr4:176218723
|
C | A | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1714G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218723 | ||||||
| chr4:176218723
|
C | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(229): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.671-1714G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218723 | ||||||
| chr4:176218726
|
T | A | 6 | a0001c0001t0001g0089a0001c0001t0001g0150a0001c0002t0003g0018others(3): Show | 6 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-1717A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218726 | ||||||
| chr4:176218728
|
G | A | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1719C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218728 | ||||||
| chr4:176218731
|
TG | T | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1723delC | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218731 | ||||||
| chr4:176218735
|
A | T | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1726T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218735 | ||||||
| chr4:176218737
|
A | G | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1728T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218737 | ||||||
| chr4:176218739
|
A | AT | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1731_671-1730i others(3): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218739 | ||||||
| chr4:176218740
|
A | AAT | 83 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(80): Show | 88 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.671-1733_671-1732d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218740 | ||||||
| chr4:176218740
|
A | G | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1731T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218740 | ||||||
| chr4:176218740
|
AAT | A | 3 | a0001c0001t0001g0089a0001c0001t0001g0142a0001c0001t0001g0150 | 3 | HG02615.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.671-1733_671-1732d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218740 | ||||||
| chr4:176218751
|
T | TTGTATGA others(33): Show |
1 | a0001c0005t0001g0305 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.671-1743_671-1742i others(42): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218751 | ||||||
| chr4:176218757
|
G | GATATATA others(17): Show |
1 | a0001c0002t0001g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.671-1749_671-1748i others(26): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218757 | ||||||
| chr4:176218757
|
GATATATA others(1): Show |
G | 15 | a0001c0001t0001g0129a0001c0002t0003g0004a0001c0002t0003g0018others(12): Show | 17 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.671-1756_671-1749d others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218757 | ||||||
| chr4:176218765
|
A | AAT | 20 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(17): Show | 22 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.671-1758_671-1757d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218765 | ||||||
| chr4:176218765
|
A | AATATATA others(101): Show |
1 | a0001c0002t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.671-1757_671-1756i others(110): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218765 | ||||||
| chr4:176218765
|
A | AATATATA others(37): Show |
5 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0238others(2): Show | 6 | HG01884.hp2 HG02809.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-1757_671-1756i others(46): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218765 | ||||||
| chr4:176218765
|
A | AATATATA others(10): Show |
66 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0025others(63): Show | 69 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.671-1773_671-1757d others(19): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218765 | ||||||
| chr4:176218765
|
A | AATATATA others(62): Show |
1 | a0001c0002t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.671-1757_671-1756i others(71): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218765 | ||||||
| chr4:176218765
|
A | T | 2 | a0001c0005t0001g0306a0006c0009t0001g0186 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.671-1756T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218765 | ||||||
| chr4:176218765
|
AAT | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-1758_671-1757d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218765 | ||||||
| chr4:176218767
|
T | TATTTGTA others(31): Show |
2 | a0001c0005t0001g0306a0006c0009t0001g0186 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.671-1759_671-1758i others(40): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218767 | ||||||
| chr4:176218790
|
A | AAT | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1783_671-1782d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218790 | ||||||
| chr4:176218790
|
AAT | A | 12 | a0001c0001t0001g0081a0001c0001t0001g0129a0001c0001t0001g0141others(9): Show | 12 | HG00741.hp2 HG01884.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.671-1783_671-1782d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218790 | ||||||
| chr4:176218792
|
T | TATATATG others(12): Show |
5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1784_671-1783i others(21): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218792 | ||||||
| chr4:176218801
|
TTGTATGA others(14): Show |
T | 1 | a0001c0001t0001g0216 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.671-1813_671-1793d others(23): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218801 | ||||||
| chr4:176218807
|
GATATATA others(22): Show |
G | 1 | a0001c0002t0003g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.671-1827_671-1799d others(31): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218807 | ||||||
| chr4:176218811
|
TATAA | T | 3 | a0001c0002t0003g0044a0001c0002t0003g0047a0001c0002t0003g0049 | 3 | HG00735.hp1 HG01496.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.671-1806_671-1803d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218811 | ||||||
| chr4:176218817
|
TATATATG others(12): Show |
T | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.671-1827_671-1809d others(21): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218817 | ||||||
| chr4:176218822
|
A | ATATATT | 9 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(6): Show | 11 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-1814_671-1813i others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218822 | ||||||
| chr4:176218822
|
A | ATATT | 29 | a0001c0001t0001g0032a0001c0001t0001g0079a0001c0001t0001g0081others(26): Show | 30 | HG00741.hp2 HG01123.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.671-1814_671-1813i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218822 | ||||||
| chr4:176218822
|
A | ATT | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(111): Show | 124 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.671-1814_671-1813i others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218822 | ||||||
| chr4:176218822
|
A | T | 3 | a0001c0002t0003g0044a0001c0002t0003g0047a0001c0002t0003g0049 | 3 | HG00735.hp1 HG01496.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.671-1813T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218822 | ||||||
| chr4:176218824
|
G | A | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1815C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218824 | ||||||
| chr4:176218826
|
A | T | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1817T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218826 | ||||||
| chr4:176218828
|
GATA | G | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1822_671-1820d others(5): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218828 | ||||||
| chr4:176218834
|
TA | T | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1826delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218834 | ||||||
| chr4:176218836
|
A | AAT | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(143): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.671-1829_671-1828d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218836 | ||||||
| chr4:176218836
|
A | AATAT | 3 | a0001c0002t0001g0024a0001c0002t0001g0280a0001c0002t0003g0051 | 3 | HG02004.hp2 NA18952.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.671-1831_671-1828d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218836 | ||||||
| chr4:176218836
|
A | AATATATA others(18): Show |
1 | a0001c0002t0002g0328 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.671-1852_671-1828d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218836 | ||||||
| chr4:176218836
|
A | AATATATA others(43): Show |
1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.671-1877_671-1828d others(52): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218836 | ||||||
| chr4:176218836
|
A | G | 4 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0059others(1): Show | 4 | HG00323.hp2 HG01169.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1827T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218836 | ||||||
| chr4:176218851
|
GATATATA others(3): Show |
G | 10 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(7): Show | 12 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.671-1852_671-1843d others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218851 | ||||||
| chr4:176218859
|
A | AAT | 3 | a0001c0002t0003g0044a0001c0002t0003g0047a0001c0002t0003g0049 | 3 | HG00735.hp1 HG01496.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.671-1852_671-1851d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218859 | ||||||
| chr4:176218876
|
GATATATA others(3): Show |
G | 2 | a0001c0002t0003g0051a0001c0002t0003g0058 | 2 | HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.671-1877_671-1868d others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218876 | ||||||
| chr4:176218883
|
A | ATATTTGT others(173): Show |
2 | a0001c0002t0001g0024a0001c0002t0001g0280 | 2 | NA18952.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.671-1875_671-1874i others(182): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218883 | ||||||
| chr4:176218884
|
A | AAT | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(51): Show | 59 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.671-1877_671-1876d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218884 | ||||||
| chr4:176218884
|
A | AATATATA others(37): Show |
7 | a0001c0002t0001g0078a0001c0002t0001g0283a0001c0002t0001g0286others(4): Show | 7 | HG00673.hp1 HG02083.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.671-1876_671-1875i others(46): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218884 | ||||||
| chr4:176218884
|
A | AATATATA others(62): Show |
55 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0025others(52): Show | 60 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.671-1876_671-1875i others(71): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218884 | ||||||
| chr4:176218884
|
A | G | 2 | a0001c0002t0001g0024a0001c0002t0001g0280 | 2 | NA18952.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.671-1875T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218884 | ||||||
| chr4:176218886
|
T | TATATATA others(8): Show |
1 | a0001c0002t0003g0047 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.671-1892_671-1878d others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218886 | ||||||
| chr4:176218891
|
ATATT | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0150a0001c0001t0001g0318 | 3 | HG01123.hp1 HG03098.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.671-1886_671-1883d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218891 | ||||||
| chr4:176218901
|
GATATATA others(3): Show |
G | 2 | a0001c0002t0003g0044a0001c0002t0003g0049 | 2 | HG00735.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.671-1902_671-1893d others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218901 | ||||||
| chr4:176218909
|
A | AAT | 26 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0053others(23): Show | 28 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.671-1902_671-1901d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218909 | ||||||
| chr4:176218909
|
AAT | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0150a0001c0001t0001g0318 | 3 | HG01123.hp1 HG03098.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.671-1902_671-1901d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218909 | ||||||
| chr4:176218916
|
ATATT | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(67): Show | 77 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.671-1911_671-1908d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218916 | ||||||
| chr4:176218926
|
GATATATA others(22): Show |
G | 5 | a0001c0002t0003g0018a0001c0002t0003g0046a0001c0002t0003g0050others(2): Show | 5 | HG00323.hp2 HG01081.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1946_671-1918d others(31): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218926 | ||||||
| chr4:176218928
|
TATATAAA others(20): Show |
T | 49 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(46): Show | 54 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.671-1946_671-1920d others(29): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218928 | ||||||
| chr4:176218936
|
TATATATG others(12): Show |
T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.671-1946_671-1928d others(21): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218936 | ||||||
| chr4:176218941
|
A | ATATATT | 13 | a0001c0002t0001g0254a0001c0002t0001g0258a0001c0002t0001g0260others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.671-1933_671-1932i others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218941 | ||||||
| chr4:176218941
|
A | ATATT | 23 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(20): Show | 26 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.671-1933_671-1932i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218941 | ||||||
| chr4:176218941
|
A | ATT | 71 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(68): Show | 78 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.671-1933_671-1932i others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218941 | ||||||
| chr4:176218943
|
G | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0053others(23): Show | 28 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.671-1934C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218943 | ||||||
| chr4:176218945
|
A | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0053others(23): Show | 28 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.671-1936T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218945 | ||||||
| chr4:176218947
|
GA | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0053others(14): Show | 17 | HG00735.hp2 HG01070.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.671-1939delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218947 | ||||||
| chr4:176218947
|
GATA | G | 9 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(6): Show | 11 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-1941_671-1939d others(5): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218947 | ||||||
| chr4:176218949
|
TATATAA | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0164a0001c0001t0001g0212others(1): Show | 4 | HG01346.hp2 HG01928.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1946_671-1941d others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218949 | ||||||
| chr4:176218951
|
TA | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0053others(14): Show | 17 | HG00735.hp2 HG01070.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.671-1943delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218951 | ||||||
| chr4:176218953
|
T | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0053others(14): Show | 17 | HG00735.hp2 HG01070.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.671-1944A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218953 | ||||||
| chr4:176218953
|
TA | T | 9 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(6): Show | 11 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-1945delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218953 | ||||||
| chr4:176218955
|
A | AAT | 75 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(72): Show | 83 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.671-1948_671-1947d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | AATATATA others(12): Show |
9 | a0001c0002t0001g0254a0001c0002t0001g0258a0001c0002t0001g0260others(6): Show | 9 | HG00140.hp1 HG01069.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.671-1947_671-1946i others(21): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | AATATATA others(64): Show |
2 | a0001c0002t0001g0255a0001c0002t0001g0274 | 2 | HG01515.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.671-1947_671-1946i others(73): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | AATATATA others(252): Show |
12 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(9): Show | 14 | HG00099.hp1 HG00741.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.671-1947_671-1946i others(261): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | AATATATA others(277): Show |
2 | a0001c0002t0001g0272a0001c0002t0001g0273 | 2 | HG00642.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.671-1947_671-1946i others(286): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | AATATATA others(251): Show |
1 | a0001c0002t0001g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.671-1947_671-1946i others(260): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | AATATATA others(33): Show |
5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1986_671-1947d others(42): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | AATATATA others(35): Show |
1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671-1988_671-1947d others(44): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | AATATATA others(794): Show |
1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.671-1947_671-1946i others(803): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | G | 9 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(6): Show | 11 | HG00639.hp2 HG01069.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-1946T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218955
|
A | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0053others(14): Show | 17 | HG00735.hp2 HG01070.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.671-1946T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218955 | ||||||
| chr4:176218970
|
GATATATA others(1): Show |
G | 67 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(64): Show | 74 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.671-1969_671-1962d others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218970 | ||||||
| chr4:176218970
|
GATATATA others(3): Show |
G | 4 | a0001c0002t0003g0047a0001c0002t0003g0051a0001c0002t0003g0056others(1): Show | 4 | HG00280.hp1 HG01496.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1971_671-1962d others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218970 | ||||||
| chr4:176218978
|
A | AATATATA others(31): Show |
4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-1970_671-1969i others(40): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218978 | ||||||
| chr4:176218980
|
T | TATATATA others(8): Show |
2 | a0001c0002t0003g0044a0001c0002t0003g0049 | 2 | HG00735.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.671-1986_671-1972d others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218980 | ||||||
| chr4:176218989
|
T | TTGTATGA others(56): Show |
3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.671-1981_671-1980i others(65): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218989 | ||||||
| chr4:176218999
|
TATAA | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0032others(56): Show | 63 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.671-1994_671-1991d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176218999 | ||||||
| chr4:176219010
|
A | ATATATT | 63 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0024others(60): Show | 68 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.671-2002_671-2001i others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219010 | ||||||
| chr4:176219010
|
A | ATATT | 79 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(76): Show | 87 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.671-2002_671-2001i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219010 | ||||||
| chr4:176219010
|
A | ATT | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.671-2002_671-2001i others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219010 | ||||||
| chr4:176219010
|
A | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0032others(56): Show | 63 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.671-2001T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219010 | ||||||
| chr4:176219024
|
A | AAT | 64 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0032others(61): Show | 68 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.671-2017_671-2016d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219024 | ||||||
| chr4:176219024
|
A | AATAT | 64 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0024others(61): Show | 69 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.671-2019_671-2016d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219024 | ||||||
| chr4:176219024
|
AATATATA others(18): Show |
A | 13 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(10): Show | 16 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.671-2040_671-2016d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219024 | ||||||
| chr4:176219031
|
ATT | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(74): Show | 85 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.671-2024_671-2023d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219031 | ||||||
| chr4:176219047
|
A | AAT | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.671-2040_671-2039d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219047 | ||||||
| chr4:176219047
|
AAT | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(74): Show | 85 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.671-2040_671-2039d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219047 | ||||||
| chr4:176219049
|
T | TATATATA others(79): Show |
62 | a0001c0002t0001g0019a0001c0002t0001g0022a0001c0002t0001g0024others(59): Show | 67 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.671-2041_671-2040i others(88): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219049 | ||||||
| chr4:176219049
|
T | TATATATG others(12): Show |
59 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0032others(56): Show | 63 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.671-2041_671-2040i others(21): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219049 | ||||||
| chr4:176219072
|
A | T | 2 | a0001c0002t0001g0252a0001c0002t0001g0307 | 2 | HG03831.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.671-2063T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219072 | ||||||
| chr4:176219072
|
AAT | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(131): Show | 146 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.671-2065_671-2064d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219072 | ||||||
| chr4:176219072
|
AATATATA others(22): Show |
A | 5 | a0001c0001t0001g0079a0001c0001t0001g0164a0001c0001t0001g0212others(2): Show | 5 | HG01123.hp1 HG01346.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+2054_671-2064d others(31): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219072 | ||||||
| chr4:176219074
|
T | TTTGTATG others(8): Show |
1 | a0001c0002t0001g0252 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.671-2066_671-2065i others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219074 | ||||||
| chr4:176219099
|
A | ATATATAT others(155): Show |
1 | a0001c0002t0001g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.670+2055_670+2056i others(164): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219099 | ||||||
| chr4:176219099
|
AAT | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(213): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.670+2054_670+2055d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219099 | ||||||
| chr4:176219101
|
T | A | 1 | a0001c0002t0001g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.670+2054A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219101 | ||||||
| chr4:176219101
|
T | TATATATA others(156): Show |
20 | a0001c0002t0001g0021a0001c0002t0001g0023a0001c0002t0001g0024others(17): Show | 22 | HG00099.hp1 HG00140.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.670+2053_670+2054i others(165): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219101 | ||||||
| chr4:176219101
|
T | TATATATA others(87): Show |
1 | a0001c0002t0001g0307 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.670+2053_670+2054i others(96): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219101 | ||||||
| chr4:176219103
|
T | TATATATA others(16): Show |
3 | a0001c0002t0001g0256a0001c0002t0001g0272a0001c0002t0001g0273 | 3 | HG00642.hp1 HG01169.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.670+2051_670+2052i others(25): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219103 | ||||||
| chr4:176219103
|
T | TATATATA others(206): Show |
1 | a0001c0002t0001g0274 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.670+2051_670+2052i others(215): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219103 | ||||||
| chr4:176219103
|
T | TATATATT others(41): Show |
1 | a0001c0002t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.670+2051_670+2052i others(50): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219103 | ||||||
| chr4:176219105
|
T | TATGTATG others(62): Show |
1 | a0001c0002t0001g0252 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.670+2049_670+2050i others(71): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219105 | ||||||
| chr4:176219108
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+2047T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219108 | ||||||
| chr4:176219113
|
T | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+2042A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219113 | ||||||
| chr4:176219114
|
T | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+2041A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219114 | ||||||
| chr4:176219116
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+2039C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219116 | ||||||
| chr4:176219122
|
T | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+2033A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219122 | ||||||
| chr4:176219145
|
A | AAT | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0001g0255 | 3 | HG01081.hp2 HG01515.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+2008_670+2009d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219145 | ||||||
| chr4:176219145
|
A | AATATATA others(110): Show |
4 | a0001c0002t0001g0256a0001c0002t0001g0272a0001c0002t0001g0273others(1): Show | 4 | HG00642.hp1 HG01169.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+2009_670+2010i others(119): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219145 | ||||||
| chr4:176219156
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(60): Show | 69 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.670+1999C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219156 | ||||||
| chr4:176219162
|
C | T | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0001g0255others(4): Show | 7 | HG00642.hp1 HG01081.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1993G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219162 | ||||||
| chr4:176219164
|
T | C | 1 | a0001c0002t0001g0293 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.670+1991A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219164 | ||||||
| chr4:176219168
|
A | AATATATA others(18): Show |
1 | a0001c0002t0001g0259 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.670+1962_670+1986d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219168 | ||||||
| chr4:176219177
|
T | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+1978A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219177 | ||||||
| chr4:176219179
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+1976C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219179 | ||||||
| chr4:176219184
|
A | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+1971T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219184 | ||||||
| chr4:176219185
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0001g0255 | 3 | HG01081.hp2 HG01515.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+1970G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219185 | ||||||
| chr4:176219185
|
CATATAAA others(87): Show |
C | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.670+1876_670+1969d others(96): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219185 | ||||||
| chr4:176219186
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+1969T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219186 | ||||||
| chr4:176219187
|
TATAAATA others(18): Show |
T | 2 | a0001c0002t0007g0035a0001c0002t0007g0065 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.670+1943_670+1967d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219187 | ||||||
| chr4:176219191
|
A | AATATATA others(113): Show |
1 | a0001c0002t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.670+1963_670+1964i others(122): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219191 | ||||||
| chr4:176219191
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+1964T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219191 | ||||||
| chr4:176219191
|
AAT | A | 4 | a0001c0002t0001g0256a0001c0002t0001g0272a0001c0002t0001g0273others(1): Show | 4 | HG00642.hp1 HG01169.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+1962_670+1963d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219191 | ||||||
| chr4:176219202
|
TTGTATGA others(39): Show |
T | 1 | a0001c0002t0007g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.670+1907_670+1952d others(48): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219202 | ||||||
| chr4:176219210
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0001g0255 | 3 | HG01081.hp2 HG01515.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+1945G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219210 | ||||||
| chr4:176219212
|
G | T | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(308): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.670+1943C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219212 | ||||||
| chr4:176219216
|
A | T | 1 | a0001c0002t0003g0047 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.670+1939T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219216 | ||||||
| chr4:176219235
|
T | C | 7 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0325others(4): Show | 7 | HG00597.hp1 HG00642.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.670+1920A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219235 | ||||||
| chr4:176219241
|
AATATATA others(16): Show |
A | 1 | a0001c0001t0001g0309 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.670+1891_670+1913d others(25): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219241 | ||||||
| chr4:176219243
|
TATATATG others(12): Show |
T | 3 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0325 | 3 | HG00597.hp1 NA18939.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.670+1893_670+1911d others(21): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219243 | ||||||
| chr4:176219248
|
A | ATATT | 4 | a0001c0002t0001g0256a0001c0002t0001g0272a0001c0002t0001g0273others(1): Show | 4 | HG00642.hp1 HG01169.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+1906_670+1907i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219248 | ||||||
| chr4:176219256
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+1899A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219256 | ||||||
| chr4:176219262
|
A | AATATATA others(18): Show |
2 | a0001c0002t0002g0330a0001c0002t0002g0362 | 2 | NA18980.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.670+1868_670+1892d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219262 | ||||||
| chr4:176219262
|
AATATATA others(18): Show |
A | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(25): Show | 33 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.670+1868_670+1892d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219262 | ||||||
| chr4:176219269
|
ATT | A | 5 | a0001c0002t0001g0256a0001c0002t0001g0272a0001c0002t0001g0273others(2): Show | 5 | HG00642.hp1 HG01169.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+1884_670+1885d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219269 | ||||||
| chr4:176219279
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.670+1876A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219279 | ||||||
| chr4:176219279
|
T | TATATAAA others(135): Show |
1 | a0001c0002t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.670+1875_670+1876i others(144): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219279 | ||||||
| chr4:176219285
|
AAT | A | 5 | a0001c0002t0001g0256a0001c0002t0001g0272a0001c0002t0001g0273others(2): Show | 5 | HG00642.hp1 HG01169.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+1868_670+1869d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219285 | ||||||
| chr4:176219287
|
T | TATATATA others(37): Show |
1 | a0001c0002t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.670+1867_670+1868i others(46): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219287 | ||||||
| chr4:176219292
|
ATATT | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0325 | 3 | HG00597.hp1 NA18939.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.670+1859_670+1862d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219292 | ||||||
| chr4:176219293
|
T | A | 1 | a0001c0002t0001g0304 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.670+1862A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219293 | ||||||
| chr4:176219310
|
AAT | A | 5 | a0001c0001t0001g0124a0001c0001t0001g0127a0001c0001t0001g0190others(2): Show | 5 | HG00597.hp1 HG01081.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+1843_670+1844d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219310 | ||||||
| chr4:176219317
|
ATATT | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149others(1): Show | 4 | HG02809.hp1 HG03098.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+1834_670+1837d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219317 | ||||||
| chr4:176219327
|
G | T | 4 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0303others(1): Show | 4 | HG01433.hp1 HG02109.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+1828C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219327 | ||||||
| chr4:176219335
|
AAT | A | 7 | a0001c0001t0001g0081a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.670+1818_670+1819d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219335 | ||||||
| chr4:176219342
|
ATATTTGT others(95): Show |
A | 1 | a0001c0001t0001g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.670+1711_670+1812d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219342 | ||||||
| chr4:176219356
|
T | G | 85 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(82): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.670+1799A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219356 | ||||||
| chr4:176219360
|
AATATATA others(45): Show |
A | 15 | a0001c0001t0001g0020a0001c0001t0001g0194a0001c0001t0001g0202others(12): Show | 15 | HG01928.hp1 HG02015.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+1743_670+1794d others(54): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219360 | ||||||
| chr4:176219367
|
ATATT | A | 18 | a0001c0001t0001g0016a0001c0001t0001g0098a0001c0001t0001g0119others(15): Show | 18 | HG00673.hp2 HG01123.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.670+1784_670+1787d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219367 | ||||||
| chr4:176219367
|
ATATTTG | A | 12 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0061others(9): Show | 12 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.670+1782_670+1787d others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219367 | ||||||
| chr4:176219367
|
ATATTTGT others(24): Show |
A | 1 | a0001c0001t0008g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.670+1757_670+1787d others(33): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219367 | ||||||
| chr4:176219367
|
ATATTTGT others(47): Show |
A | 23 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0055others(20): Show | 24 | HG00408.hp1 HG01358.hp1 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.670+1734_670+1787d others(56): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219367 | ||||||
| chr4:176219367
|
ATATTTGT others(70): Show |
A | 38 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(35): Show | 42 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.670+1711_670+1787d others(79): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219367 | ||||||
| chr4:176219371
|
T | TTGTATGA others(16): Show |
1 | a0001c0002t0001g0368 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.670+1761_670+1783d others(25): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219371 | ||||||
| chr4:176219371
|
TTGTATGA others(41): Show |
T | 3 | a0001c0002t0004g0040a0001c0002t0007g0035a0001c0002t0007g0065 | 3 | HG02723.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.670+1736_670+1783d others(50): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219371 | ||||||
| chr4:176219381
|
T | G | 5 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0272others(2): Show | 5 | HG00642.hp1 HG01169.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+1774A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219381 | ||||||
| chr4:176219392
|
ATATT | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0227others(1): Show | 4 | HG01069.hp2 HG01891.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+1759_670+1762d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219392 | ||||||
| chr4:176219392
|
ATATTTGT others(22): Show |
A | 2 | a0001c0001t0001g0116a0001c0001t0005g0228 | 2 | HG02056.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.670+1734_670+1762d others(31): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219392 | ||||||
| chr4:176219392
|
ATATTTGT others(45): Show |
A | 3 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0088 | 3 | HG02280.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.670+1711_670+1762d others(54): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219392 | ||||||
| chr4:176219394
|
ATT | A | 105 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0136others(102): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.670+1759_670+1760d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219394 | ||||||
| chr4:176219396
|
TTGTATGA others(16): Show |
T | 22 | a0001c0001t0001g0016a0001c0001t0001g0098a0001c0001t0001g0109others(19): Show | 22 | HG00673.hp2 HG01123.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+1736_670+1758d others(25): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219396 | ||||||
| chr4:176219406
|
T | G | 7 | a0001c0002t0001g0057a0001c0002t0001g0250a0001c0002t0001g0251others(4): Show | 7 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1749A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219406 | ||||||
| chr4:176219410
|
A | AATATATA others(16): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.670+1744_670+1745i others(25): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219410 | ||||||
| chr4:176219410
|
AAT | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0309a0001c0001t0001g0325others(1): Show | 4 | HG00597.hp1 HG00741.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+1743_670+1744d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219410 | ||||||
| chr4:176219417
|
ATATGTAT others(20): Show |
A | 1 | a0001c0001t0001g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.670+1711_670+1737d others(29): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219417 | ||||||
| chr4:176219417
|
ATATGTAT others(45): Show |
A | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+1686_670+1737d others(54): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219417 | ||||||
| chr4:176219419
|
A | ATATT | 3 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0136 | 4 | HG01099.hp2 HG02738.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+1735_670+1736i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219419 | ||||||
| chr4:176219419
|
A | ATGTATGA others(18): Show |
1 | a0001c0002t0002g0322 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.670+1711_670+1735d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219419 | ||||||
| chr4:176219419
|
A | ATGTATGA others(43): Show |
1 | a0001c0002t0002g0329 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.670+1686_670+1735d others(52): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219419 | ||||||
| chr4:176219419
|
A | ATT | 163 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0032others(160): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.670+1735_670+1736i others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219419 | ||||||
| chr4:176219419
|
A | ATTTGTAT others(41): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 9 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+1735_670+1736i others(50): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219419 | ||||||
| chr4:176219419
|
A | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0150 | 3 | HG02717.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.670+1736T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219419 | ||||||
| chr4:176219419
|
ATGTATGA others(18): Show |
A | 3 | a0001c0002t0007g0064a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.670+1711_670+1735d others(27): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219419 | ||||||
| chr4:176219429
|
T | G | 83 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(80): Show | 91 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.670+1726A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219429 | ||||||
| chr4:176219433
|
A | AAT | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0149 | 3 | HG02809.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.670+1720_670+1721d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219433 | ||||||
| chr4:176219433
|
AAT | A | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+1720_670+1721d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219433 | ||||||
| chr4:176219435
|
TATATATA others(133): Show |
T | 2 | a0001c0001t0001g0012a0001c0001t0001g0075 | 3 | HG01099.hp2 HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.670+1580_670+1719d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219435 | ||||||
| chr4:176219437
|
TATATATT others(131): Show |
T | 1 | a0001c0001t0001g0136 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.670+1580_670+1717d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219437 | ||||||
| chr4:176219440
|
ATATT | A | 33 | a0001c0001t0001g0032a0001c0001t0001g0062a0001c0001t0001g0079others(30): Show | 34 | HG00140.hp2 HG01081.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.670+1711_670+1714d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219440 | ||||||
| chr4:176219444
|
T | TTGTATGA others(16): Show |
1 | a0001c0005t0001g0305 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.670+1688_670+1710d others(25): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219444 | ||||||
| chr4:176219454
|
T | G | 6 | a0001c0002t0001g0255a0001c0002t0001g0256a0001c0002t0001g0272others(3): Show | 6 | HG00642.hp1 HG01169.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+1701A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219454 | ||||||
| chr4:176219455
|
A | G | 4 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG00639.hp1 HG02280.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+1700T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219455 | ||||||
| chr4:176219458
|
AAT | A | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+1695_670+1696d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219458 | ||||||
| chr4:176219458
|
AATATATA others(110): Show |
A | 2 | a0001c0001t0001g0146a0001c0001t0001g0149 | 2 | NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.670+1580_670+1696d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219458 | ||||||
| chr4:176219460
|
TATATATA others(108): Show |
T | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.670+1580_670+1694d others(2): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219460 | ||||||
| chr4:176219465
|
ATATT | A | 8 | a0001c0001t0001g0013a0001c0001t0001g0103a0001c0001t0001g0155others(5): Show | 9 | HG02886.hp1 HG03130.hp1 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.670+1686_670+1689d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219465 | ||||||
| chr4:176219467
|
ATT | A | 4 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0223others(1): Show | 4 | HG01934.hp1 NA18987.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+1686_670+1687d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219467 | ||||||
| chr4:176219469
|
T | TTGTATGA others(14): Show |
4 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0176others(1): Show | 4 | NA18946.hp1 NA18965.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+1665_670+1685d others(23): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219469 | ||||||
| chr4:176219483
|
A | AAT | 10 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0100others(7): Show | 10 | HG00735.hp2 HG01175.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.670+1670_670+1671d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219483 | ||||||
| chr4:176219492
|
ATT | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0087others(20): Show | 23 | HG00673.hp2 HG00741.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.670+1661_670+1662d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219492 | ||||||
| chr4:176219494
|
T | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0061others(5): Show | 8 | HG00733.hp1 HG00735.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+1661A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219494 | ||||||
| chr4:176219508
|
A | AAT | 32 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0037others(29): Show | 32 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.670+1645_670+1646d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219508 | ||||||
| chr4:176219511
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.670+1644T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219511 | ||||||
| chr4:176219512
|
TATATATT others(14): Show |
T | 2 | a0001c0001t0001g0110a0001c0004t0001g0366 | 2 | HG02683.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.670+1622_670+1642d others(23): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219512 | ||||||
| chr4:176219512
|
TATATATT others(56): Show |
T | 1 | a0001c0001t0001g0215 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.670+1580_670+1642d others(65): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219512 | ||||||
| chr4:176219514
|
T | A | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+1641A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219514 | ||||||
| chr4:176219514
|
TATATTTG others(54): Show |
T | 1 | a0001c0001t0001g0343 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.670+1580_670+1640d others(63): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219514 | ||||||
| chr4:176219516
|
TATTTGTA others(52): Show |
T | 2 | a0001c0001t0001g0217a0001c0001t0001g0223 | 2 | NA18987.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.670+1580_670+1638d others(61): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219516 | ||||||
| chr4:176219517
|
ATT | A | 34 | a0001c0001t0001g0020a0001c0001t0001g0032a0001c0001t0001g0062others(31): Show | 35 | HG00140.hp2 HG00597.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.670+1636_670+1637d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219517 | ||||||
| chr4:176219519
|
T | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0129a0001c0001t0008g0101others(1): Show | 4 | HG04184.hp1 NA18945.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+1636A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219519 | ||||||
| chr4:176219519
|
T | TTGTATGA others(16): Show |
1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.670+1613_670+1635d others(25): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219519 | ||||||
| chr4:176219533
|
A | AATAT | 26 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0055others(23): Show | 27 | HG00408.hp1 HG01358.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.670+1618_670+1621d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219533 | ||||||
| chr4:176219533
|
AATATATA others(35): Show |
A | 6 | a0001c0001t0001g0016a0001c0001t0001g0098a0001c0001t0001g0105others(3): Show | 6 | HG01975.hp2 HG02717.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+1580_670+1621d others(44): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219533 | ||||||
| chr4:176219533
|
AATATATA others(37): Show |
A | 6 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0100others(3): Show | 6 | HG00735.hp2 HG01175.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+1578_670+1621d others(46): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219533 | ||||||
| chr4:176219533
|
AATATATA others(39): Show |
A | 1 | a0001c0001t0001g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.670+1576_670+1621d others(48): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219533 | ||||||
| chr4:176219533
|
AATATATA others(63): Show |
A | 1 | a0001c0001t0001g0218 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.670+1552_670+1621d others(72): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219533 | ||||||
| chr4:176219535
|
TATATATA others(33): Show |
T | 4 | a0001c0001t0001g0087a0001c0001t0001g0164a0001c0001t0001g0243others(1): Show | 4 | HG01346.hp2 NA18972.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+1580_670+1619d others(42): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219535 | ||||||
| chr4:176219537
|
TATATATG others(31): Show |
T | 5 | a0001c0001t0001g0009a0001c0001t0001g0224a0001c0001t0001g0309others(2): Show | 5 | HG00741.hp2 HG01891.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+1580_670+1617d others(40): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219537 | ||||||
| chr4:176219539
|
TATATGTA others(29): Show |
T | 2 | a0001c0001t0001g0133a0001c0001t0001g0193 | 2 | HG01123.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.670+1580_670+1615d others(38): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219539 | ||||||
| chr4:176219541
|
TATGTATG others(27): Show |
T | 2 | a0001c0001t0001g0227a0001c0001t0001g0346 | 2 | NA18961.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.670+1580_670+1613d others(36): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219541 | ||||||
| chr4:176219542
|
A | ATATT | 41 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0020others(38): Show | 44 | HG00140.hp2 HG00597.hp1 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.670+1612_670+1613i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219542 | ||||||
| chr4:176219542
|
A | ATT | 23 | a0001c0002t0001g0255a0001c0002t0001g0272a0001c0002t0001g0273others(20): Show | 26 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.670+1612_670+1613i others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219542 | ||||||
| chr4:176219544
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0178 | 2 | HG00673.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.670+1611C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219544 | ||||||
| chr4:176219545
|
TATGATAT others(23): Show |
T | 2 | a0001c0001t0001g0119a0001c0001t0001g0178 | 2 | HG00673.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.670+1580_670+1609d others(32): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219545 | ||||||
| chr4:176219556
|
AATATGTA others(8): Show |
A | 1 | a0001c0001t0001g0173 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.670+1584_670+1598d others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219556 | ||||||
| chr4:176219556
|
AATATGTA others(11): Show |
A | 1 | a0001c0001t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.670+1581_670+1598d others(20): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219556 | ||||||
| chr4:176219556
|
AATATGTA others(12): Show |
A | 7 | a0001c0001t0001g0129a0001c0001t0001g0225a0001c0001t0001g0226others(4): Show | 7 | HG00597.hp1 HG01928.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1580_670+1598d others(21): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219556 | ||||||
| chr4:176219556
|
AATATGTA others(14): Show |
A | 1 | a0001c0001t0001g0109 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.670+1578_670+1598d others(23): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219556 | ||||||
| chr4:176219556
|
AATATGTA others(44): Show |
A | 1 | a0001c0001t0001g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.670+1548_670+1598d others(53): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219556 | ||||||
| chr4:176219558
|
TATGTATA others(10): Show |
T | 14 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0032others(11): Show | 16 | HG02129.hp1 HG02145.hp2 HG03490.hp1 others(13): Show |
intron_variant | MODIFIER | c.670+1580_670+1596d others(19): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219558 | ||||||
| chr4:176219560
|
TGTATATA others(8): Show |
T | 9 | a0001c0001t0001g0006a0001c0001t0001g0062a0001c0001t0001g0067others(6): Show | 10 | HG00140.hp2 HG02074.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.670+1580_670+1594d others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219560 | ||||||
| chr4:176219561
|
G | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(250): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.670+1594C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219561 | ||||||
| chr4:176219562
|
TATATATT others(6): Show |
T | 3 | a0001c0001t0001g0079a0001c0001t0001g0177a0001c0001t0001g0194 | 3 | HG01123.hp1 HG02027.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.670+1580_670+1592d others(15): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219562 | ||||||
| chr4:176219564
|
TATATTTG others(4): Show |
T | 1 | a0001c0001t0001g0145 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.670+1580_670+1590d others(13): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219564 | ||||||
| chr4:176219569
|
T | A | 1 | a0001c0002t0001g0274 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.670+1586A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219569 | ||||||
| chr4:176219569
|
T | C | 1 | a0001c0002t0001g0298 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.670+1586A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219569 | ||||||
| chr4:176219575
|
G | GATATAT | 5 | a0001c0002t0002g0140a0001c0002t0002g0248a0001c0002t0002g0321others(2): Show | 5 | HG01361.hp2 HG01975.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+1574_670+1579d others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(1): Show |
35 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0027others(32): Show | 38 | HG00099.hp2 HG00408.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.670+1579_670+1580i others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(5): Show |
1 | a0001c0001t0001g0158 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.670+1579_670+1580i others(14): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(3): Show |
25 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(22): Show | 29 | HG00544.hp1 HG00558.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.670+1579_670+1580i others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(5): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0183 | 3 | HG02280.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.670+1579_670+1580i others(14): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(7): Show |
4 | a0001c0001t0001g0068a0001c0001t0001g0077a0001c0001t0001g0088others(1): Show | 4 | HG03139.hp1 NA18966.hp2 NA19089.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+1579_670+1580i others(16): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(11): Show |
6 | a0001c0001t0001g0103a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+1579_670+1580i others(20): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(1): Show |
6 | a0001c0001t0001g0363a0001c0002t0002g0326a0001c0002t0002g0329others(3): Show | 6 | HG00323.hp1 HG01358.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+1572_670+1579d others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(3): Show |
17 | a0001c0002t0002g0003a0001c0002t0002g0010a0001c0002t0002g0028others(14): Show | 21 | HG00597.hp2 HG01109.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.670+1570_670+1579d others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(5): Show |
4 | a0001c0002t0002g0104a0001c0002t0002g0115a0001c0002t0002g0197others(1): Show | 4 | HG01256.hp2 HG01433.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+1568_670+1579d others(14): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(7): Show |
2 | a0001c0002t0002g0324a0001c0002t0002g0370 | 2 | HG00621.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.670+1566_670+1579d others(16): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | GATATATA others(13): Show |
2 | a0001c0002t0002g0348a0001c0003t0002g0342 | 2 | HG00642.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.670+1560_670+1579d others(22): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
G | T | 1 | a0001c0001t0001g0175 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.670+1580C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
GAT | G | 6 | a0001c0001t0001g0072a0001c0001t0001g0093a0001c0001t0001g0151others(3): Show | 6 | HG00280.hp2 HG00738.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+1578_670+1579d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
GATAT | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 11 | HG00639.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+1576_670+1579d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
GATATAT | G | 6 | a0001c0001t0001g0150a0001c0002t0004g0038a0001c0002t0004g0039others(3): Show | 6 | HG02486.hp1 HG02615.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+1574_670+1579d others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
GATATATA others(1): Show |
G | 8 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0189others(5): Show | 8 | HG02886.hp1 HG03130.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+1572_670+1579d others(10): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
GATATATA others(3): Show |
G | 79 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(76): Show | 87 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.670+1570_670+1579d others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
GATATATA others(5): Show |
G | 6 | a0001c0001t0005g0122a0001c0002t0001g0084a0001c0002t0001g0085others(3): Show | 6 | HG01433.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+1568_670+1579d others(14): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
GATATATA others(7): Show |
G | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.670+1566_670+1579d others(16): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
GATATATA others(11): Show |
G | 4 | a0001c0002t0002g0030a0001c0002t0002g0340a0001c0002t0002g0354others(1): Show | 5 | HG00423.hp2 HG00621.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+1562_670+1579d others(20): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219575
|
GATATATA others(13): Show |
G | 2 | a0001c0001t0001g0081a0001c0001t0001g0221 | 2 | HG03453.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.670+1560_670+1579d others(22): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219575 | ||||||
| chr4:176219577
|
T | TATATAA | 22 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0106others(19): Show | 23 | HG00408.hp1 HG01934.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.670+1577_670+1578i others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219577 | ||||||
| chr4:176219577
|
T | TATATAAA others(7): Show |
1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.670+1577_670+1578i others(16): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219577 | ||||||
| chr4:176219579
|
T | TATAA | 5 | a0001c0001t0001g0014a0001c0001t0001g0180a0001c0001t0001g0196others(2): Show | 6 | HG00609.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+1575_670+1576i others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219579 | ||||||
| chr4:176219581
|
T | TAA | 4 | a0001c0001t0001g0181a0001c0001t0001g0195a0001c0001t0005g0228others(1): Show | 4 | HG02056.hp1 HG03579.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+1573_670+1574i others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219581 | ||||||
| chr4:176219583
|
T | A | 22 | a0001c0001t0001g0074a0001c0001t0001g0137a0001c0002t0001g0274others(19): Show | 25 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.670+1572A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219583 | ||||||
| chr4:176219585
|
T | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0093a0001c0001t0001g0151 | 3 | HG00280.hp2 HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.670+1570A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219585 | ||||||
| chr4:176219586
|
A | G | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+1569T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219586 | ||||||
| chr4:176219587
|
T | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0091others(5): Show | 10 | HG00639.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.670+1568A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219587 | ||||||
| chr4:176219589
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.670+1566A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219589 | ||||||
| chr4:176219591
|
T | A | 7 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0189others(4): Show | 7 | HG02886.hp1 HG03130.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1564A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219591 | ||||||
| chr4:176219591
|
T | TG | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.670+1563_670+1564i others(3): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219591 | ||||||
| chr4:176219593
|
T | A | 79 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(76): Show | 87 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.670+1562A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219593 | ||||||
| chr4:176219593
|
T | TATTTGTA others(2): Show |
19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+1561_670+1562i others(11): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219593 | ||||||
| chr4:176219593
|
T | TATTTGTA others(10): Show |
1 | a0001c0002t0001g0274 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.670+1561_670+1562i others(19): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219593 | ||||||
| chr4:176219595
|
T | A | 6 | a0001c0001t0005g0122a0001c0002t0001g0084a0001c0002t0001g0085others(3): Show | 6 | HG01433.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+1560A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219595 | ||||||
| chr4:176219597
|
T | A | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.670+1558A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219597 | ||||||
| chr4:176219601
|
T | A | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+1554A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219601 | ||||||
| chr4:176219601
|
T | TG | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.670+1553_670+1554i others(3): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219601 | ||||||
| chr4:176219603
|
T | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0221 | 2 | HG03453.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.670+1552A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219603 | ||||||
| chr4:176219618
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.670+1537T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219618 | ||||||
| chr4:176219619
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.670+1536C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219619 | ||||||
| chr4:176219648
|
C | T | 1 | a0001c0002t0001g0219 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.670+1507G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219648 | ||||||
| chr4:176219667
|
C | T | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.670+1488G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219667 | ||||||
| chr4:176219723
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.670+1432A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219723 | ||||||
| chr4:176219725
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+1430G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219725 | ||||||
| chr4:176219809
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.670+1346G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219809 | ||||||
| chr4:176219879
|
G | T | 89 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(86): Show | 97 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.670+1276C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219879 | ||||||
| chr4:176219897
|
T | C | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(323): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.670+1258A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176219897 | ||||||
| chr4:176220023
|
G | A | 111 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.670+1132C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220023 | ||||||
| chr4:176220045
|
C | A | 111 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.670+1110G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220045 | ||||||
| chr4:176220061
|
T | G | 1 | a0001c0002t0001g0057 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.670+1094A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220061 | ||||||
| chr4:176220114
|
G | T | 89 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(86): Show | 97 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.670+1041C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220114 | ||||||
| chr4:176220178
|
C | G | 1 | a0001c0002t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.670+977G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220178 | ||||||
| chr4:176220264
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.670+891C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220264 | ||||||
| chr4:176220385
|
G | A | 111 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.670+770C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220385 | ||||||
| chr4:176220485
|
G | A | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.670+670C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220485 | ||||||
| chr4:176220508
|
A | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 26 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.670+647T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220508 | ||||||
| chr4:176220528
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.670+627C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220528 | ||||||
| chr4:176220544
|
T | A | 1 | a0001c0001t0001g0204 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.670+611A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220544 | ||||||
| chr4:176220644
|
G | T | 2 | a0001c0002t0001g0261a0001c0002t0001g0270 | 2 | HG02523.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.670+511C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220644 | ||||||
| chr4:176220684
|
A | G | 1 | a0001c0002t0001g0277 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.670+471T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220684 | ||||||
| chr4:176220782
|
T | C | 111 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.670+373A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220782 | ||||||
| chr4:176220889
|
A | C | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.670+266T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220889 | ||||||
| chr4:176220968
|
C | T | 92 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(89): Show | 100 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.670+187G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220968 | ||||||
| chr4:176220980
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.670+175A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176220980 | ||||||
| chr4:176221052
|
CA | C | 16 | a0001c0001t0001g0013a0001c0001t0001g0158a0001c0001t0001g0159others(13): Show | 17 | HG02080.hp1 HG02083.hp1 NA18942.hp1 others(14): Show |
intron_variant | MODIFIER | c.670+102delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 5/6 | chr4 | 176221052 | ||||||
| chr4:176221321
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.536-32T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 4/6 | chr4 | 176221321 | ||||||
| chr4:176221337
|
C | T | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.536-48G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 4/6 | chr4 | 176221337 | ||||||
| chr4:176221374
|
T | C | 1 | a0001c0010t0001g0157 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.535+76A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 4/6 | chr4 | 176221374 | ||||||
| chr4:176221397
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.535+53T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 4/6 | chr4 | 176221397 | ||||||
| chr4:176221625
|
C | A | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(318): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.385-25G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176221625 | ||||||
| chr4:176221626
|
A | C | 111 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.385-26T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176221626 | ||||||
| chr4:176221718
|
T | G | 92 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(89): Show | 100 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.385-118A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176221718 | ||||||
| chr4:176221748
|
T | C | 1 | a0001c0002t0003g0058 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.385-148A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176221748 | ||||||
| chr4:176222056
|
T | C | 1 | a0001c0002t0001g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.384+257A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176222056 | ||||||
| chr4:176222122
|
T | C | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.384+191A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176222122 | ||||||
| chr4:176222158
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.384+155C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176222158 | ||||||
| chr4:176222162
|
A | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | NA18978.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.384+151T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176222162 | ||||||
| chr4:176222227
|
T | A | 40 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(37): Show | 41 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.384+86A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176222227 | ||||||
| chr4:176222247
|
T | G | 1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.384+66A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176222247 | ||||||
| chr4:176222266
|
C | T | 111 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.384+47G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 3/6 | chr4 | 176222266 | ||||||
| chr4:176222467
|
A | T | 1 | a0001c0001t0001g0187 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.277-47T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222467 | ||||||
| chr4:176222513
|
C | G | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.277-93G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222513 | ||||||
| chr4:176222535
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0019g0213 | 2 | HG01346.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.277-115C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222535 | ||||||
| chr4:176222576
|
G | T | 92 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(89): Show | 100 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.277-156C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222576 | ||||||
| chr4:176222577
|
G | C | 92 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(89): Show | 100 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.277-157C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222577 | ||||||
| chr4:176222585
|
C | T | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.277-165G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222585 | ||||||
| chr4:176222699
|
T | C | 16 | a0001c0002t0002g0248a0001c0002t0002g0316a0001c0002t0002g0326others(13): Show | 16 | HG00597.hp2 HG00621.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.277-279A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222699 | ||||||
| chr4:176222711
|
A | G | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.277-291T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222711 | ||||||
| chr4:176222750
|
GT | G | 92 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(89): Show | 100 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.277-331delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222750 | ||||||
| chr4:176222762
|
T | G | 1 | a0001c0002t0001g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.277-342A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222762 | ||||||
| chr4:176222817
|
A | G | 1 | a0007c0011t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.277-397T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222817 | ||||||
| chr4:176222822
|
A | G | 1 | a0007c0011t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.277-402T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222822 | ||||||
| chr4:176222847
|
G | T | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.277-427C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222847 | ||||||
| chr4:176222878
|
T | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(322): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.277-458A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222878 | ||||||
| chr4:176222885
|
C | G | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.277-465G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222885 | ||||||
| chr4:176222909
|
C | T | 92 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(89): Show | 100 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.277-489G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222909 | ||||||
| chr4:176222944
|
A | AT | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(207): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.277-525dupA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222944 | ||||||
| chr4:176222980
|
G | A | 1 | a0001c0002t0002g0332 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.277-560C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222980 | ||||||
| chr4:176222999
|
T | C | 1 | a0001c0002t0002g0248 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.277-579A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176222999 | ||||||
| chr4:176223029
|
T | C | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(328): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.277-609A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223029 | ||||||
| chr4:176223030
|
G | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(319): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.277-610C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223030 | ||||||
| chr4:176223031
|
G | A | 112 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(109): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.277-611C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223031 | ||||||
| chr4:176223076
|
C | T | 9 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(6): Show | 9 | HG02486.hp1 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-656G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223076 | ||||||
| chr4:176223096
|
C | T | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.277-676G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223096 | ||||||
| chr4:176223213
|
T | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(318): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.277-793A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223213 | ||||||
| chr4:176223230
|
A | G | 111 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.277-810T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223230 | ||||||
| chr4:176223273
|
A | G | 111 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.277-853T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223273 | ||||||
| chr4:176223280
|
A | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(207): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.277-860T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223280 | ||||||
| chr4:176223519
|
A | G | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.277-1099T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223519 | ||||||
| chr4:176223587
|
T | C | 1 | a0001c0002t0007g0065 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.277-1167A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223587 | ||||||
| chr4:176223624
|
T | A | 88 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(85): Show | 96 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.277-1204A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223624 | ||||||
| chr4:176223673
|
T | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(207): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.277-1253A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223673 | ||||||
| chr4:176223779
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(317): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.277-1359T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223779 | ||||||
| chr4:176223781
|
C | T | 88 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(85): Show | 96 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.277-1361G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223781 | ||||||
| chr4:176223782
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.277-1362C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223782 | ||||||
| chr4:176223803
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(317): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.277-1383T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223803 | ||||||
| chr4:176223861
|
C | T | 1 | a0001c0002t0002g0197 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.276+1401G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223861 | ||||||
| chr4:176223967
|
C | T | 1 | a0001c0001t0001g0363 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.276+1295G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223967 | ||||||
| chr4:176223981
|
G | A | 2 | a0001c0002t0007g0035a0001c0002t0007g0065 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.276+1281C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176223981 | ||||||
| chr4:176224002
|
C | A | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+1260G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224002 | ||||||
| chr4:176224085
|
A | G | 1 | a0001c0002t0002g0348 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.276+1177T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224085 | ||||||
| chr4:176224142
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.276+1120G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224142 | ||||||
| chr4:176224191
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.276+1071C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224191 | ||||||
| chr4:176224221
|
A | AT | 56 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(53): Show | 60 | HG00280.hp2 HG00741.hp2 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.276+1040dupA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224221 | ||||||
| chr4:176224221
|
A | ATT | 108 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(105): Show | 119 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.276+1039_276+1040d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224221 | ||||||
| chr4:176224221
|
A | ATTT | 29 | a0001c0001t0001g0037a0001c0001t0001g0053a0001c0001t0001g0075others(26): Show | 29 | HG00673.hp2 HG00735.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.276+1038_276+1040d others(5): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224221 | ||||||
| chr4:176224221
|
A | ATTTT | 29 | a0001c0001t0001g0161a0001c0002t0002g0003a0001c0002t0002g0029others(26): Show | 32 | HG00323.hp1 HG00423.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.276+1037_276+1040d others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224221 | ||||||
| chr4:176224221
|
A | ATTTTT | 11 | a0001c0002t0002g0028a0001c0002t0002g0030a0001c0002t0002g0248others(8): Show | 13 | HG00642.hp2 HG02071.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.276+1036_276+1040d others(7): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224221 | ||||||
| chr4:176224221
|
AT | A | 14 | a0001c0002t0001g0241a0001c0002t0001g0255a0001c0002t0001g0259others(11): Show | 14 | HG00423.hp1 HG00642.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.276+1040delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224221 | ||||||
| chr4:176224221
|
ATT | A | 73 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(70): Show | 81 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.276+1039_276+1040d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224221 | ||||||
| chr4:176224221
|
ATTTTTT | A | 18 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(15): Show | 21 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.276+1035_276+1040d others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224221 | ||||||
| chr4:176224253
|
G | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(317): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.276+1009C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224253 | ||||||
| chr4:176224296
|
G | A | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+966C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224296 | ||||||
| chr4:176224396
|
G | A | 1 | a0001c0002t0001g0250 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.276+866C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224396 | ||||||
| chr4:176224487
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.276+775G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224487 | ||||||
| chr4:176224512
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(207): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.276+750C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224512 | ||||||
| chr4:176224534
|
T | TA | 87 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(84): Show | 95 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.276+727dupT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224534 | ||||||
| chr4:176224535
|
AT | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(207): Show | 229 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.276+726delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224535 | ||||||
| chr4:176224536
|
T | A | 23 | a0001c0002t0001g0274a0001c0002t0003g0004a0001c0002t0003g0018others(20): Show | 26 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.276+726A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224536 | ||||||
| chr4:176224561
|
T | C | 110 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(107): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.276+701A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224561 | ||||||
| chr4:176224562
|
G | A | 88 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(85): Show | 96 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.276+700C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224562 | ||||||
| chr4:176224688
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(129): Show | 143 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.276+574A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224688 | ||||||
| chr4:176224703
|
CA | C | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(307): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.276+558delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224703 | ||||||
| chr4:176224739
|
T | C | 88 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(85): Show | 96 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.276+523A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224739 | ||||||
| chr4:176224779
|
T | A | 1 | a0001c0002t0001g0239 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.276+483A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224779 | ||||||
| chr4:176224899
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.276+363A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224899 | ||||||
| chr4:176224941
|
T | A | 1 | a0001c0002t0003g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.276+321A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224941 | ||||||
| chr4:176224953
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.276+309C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176224953 | ||||||
| chr4:176225026
|
G | A | 1 | a0001c0004t0001g0117 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.276+236C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176225026 | ||||||
| chr4:176225044
|
C | T | 2 | a0001c0002t0001g0241a0001c0002t0001g0246 | 2 | NA18940.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.276+218G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176225044 | ||||||
| chr4:176225108
|
A | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0243 | 5 | HG00544.hp1 HG02080.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+154T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 2/6 | chr4 | 176225108 | ||||||
| chr4:176225421
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.197-80G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176225421 | ||||||
| chr4:176225476
|
T | C | 110 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(107): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.197-135A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176225476 | ||||||
| chr4:176225512
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197-171T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176225512 | ||||||
| chr4:176225591
|
A | AT | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(326): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.197-251dupA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176225591 | ||||||
| chr4:176225841
|
T | C | 110 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(107): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.197-500A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176225841 | ||||||
| chr4:176225879
|
T | C | 110 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(107): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.197-538A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176225879 | ||||||
| chr4:176225886
|
G | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-545C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176225886 | ||||||
| chr4:176225925
|
A | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(321): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.197-584T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176225925 | ||||||
| chr4:176225976
|
G | A | 1 | a0001c0002t0001g0302 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.197-635C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176225976 | ||||||
| chr4:176226095
|
G | A | 1 | a0001c0002t0002g0321 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.197-754C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226095 | ||||||
| chr4:176226267
|
C | T | 110 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(107): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.197-926G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226267 | ||||||
| chr4:176226352
|
G | A | 1 | a0001c0002t0002g0316 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.197-1011C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226352 | ||||||
| chr4:176226354
|
T | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(317): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.197-1013A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226354 | ||||||
| chr4:176226440
|
C | T | 88 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(85): Show | 96 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.197-1099G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226440 | ||||||
| chr4:176226441
|
G | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0176others(1): Show | 4 | NA18946.hp1 NA18965.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-1100C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226441 | ||||||
| chr4:176226537
|
T | C | 1 | a0007c0011t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.197-1196A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226537 | ||||||
| chr4:176226545
|
C | T | 111 | a0001c0001t0001g0089a0001c0002t0001g0019a0001c0002t0001g0021others(108): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.197-1204G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226545 | ||||||
| chr4:176226654
|
C | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(326): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.197-1313G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226654 | ||||||
| chr4:176226747
|
G | C | 1 | a0001c0002t0001g0271 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.197-1406C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226747 | ||||||
| chr4:176226846
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197-1505T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226846 | ||||||
| chr4:176226892
|
G | A | 20 | a0001c0001t0001g0151a0001c0002t0003g0004a0001c0002t0003g0018others(17): Show | 23 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-1551C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176226892 | ||||||
| chr4:176227188
|
A | C | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.197-1847T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227188 | ||||||
| chr4:176227292
|
A | T | 1 | a0006c0009t0001g0186 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.197-1951T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227292 | ||||||
| chr4:176227308
|
A | G | 1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-1967T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227308 | ||||||
| chr4:176227369
|
T | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(129): Show | 143 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.197-2028A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227369 | ||||||
| chr4:176227428
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-2087G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227428 | ||||||
| chr4:176227470
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.197-2129C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227470 | ||||||
| chr4:176227524
|
C | T | 1 | a0001c0001t0005g0120 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.197-2183G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227524 | ||||||
| chr4:176227742
|
G | A | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-2401C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227742 | ||||||
| chr4:176227895
|
G | A | 326 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(323): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.197-2554C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227895 | ||||||
| chr4:176227971
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.197-2630C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176227971 | ||||||
| chr4:176228197
|
A | G | 1 | a0001c0002t0001g0291 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.197-2856T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228197 | ||||||
| chr4:176228222
|
A | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 11 | HG01081.hp2 HG01891.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-2881T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228222 | ||||||
| chr4:176228367
|
C | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(63): Show | 73 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.197-3026G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228367 | ||||||
| chr4:176228452
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.197-3111T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228452 | ||||||
| chr4:176228460
|
C | G | 1 | a0001c0001t0001g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.197-3119G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228460 | ||||||
| chr4:176228650
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197-3309A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228650 | ||||||
| chr4:176228691
|
G | A | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(326): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.197-3350C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228691 | ||||||
| chr4:176228856
|
T | C | 6 | a0001c0002t0001g0057a0001c0002t0001g0250a0001c0002t0001g0251others(3): Show | 6 | HG00099.hp1 HG00733.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-3515A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228856 | ||||||
| chr4:176228893
|
C | T | 1 | a0001c0002t0001g0353 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.197-3552G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228893 | ||||||
| chr4:176228911
|
A | G | 20 | a0001c0002t0002g0140a0001c0002t0003g0004a0001c0002t0003g0018others(17): Show | 23 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-3570T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228911 | ||||||
| chr4:176228953
|
C | T | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.197-3612G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176228953 | ||||||
| chr4:176229117
|
T | C | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | NA18961.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.197-3776A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229117 | ||||||
| chr4:176229166
|
C | T | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 28 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.197-3825G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229166 | ||||||
| chr4:176229316
|
T | C | 1 | a0001c0002t0003g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.197-3975A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229316 | ||||||
| chr4:176229340
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.197-3999G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229340 | ||||||
| chr4:176229349
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.197-4008G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229349 | ||||||
| chr4:176229362
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.197-4021A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229362 | ||||||
| chr4:176229441
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-4100A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229441 | ||||||
| chr4:176229576
|
A | G | 1 | a0001c0002t0003g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.197-4235T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229576 | ||||||
| chr4:176229591
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197-4250A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229591 | ||||||
| chr4:176229594
|
C | T | 20 | a0001c0002t0002g0140a0001c0002t0003g0004a0001c0002t0003g0018others(17): Show | 23 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-4253G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229594 | ||||||
| chr4:176229658
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-4317G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229658 | ||||||
| chr4:176229676
|
GA | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(259): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.197-4336delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229676 | ||||||
| chr4:176229705
|
G | A | 1 | a0001c0002t0002g0335 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.197-4364C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229705 | ||||||
| chr4:176229774
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(221): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.197-4433T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229774 | ||||||
| chr4:176229796
|
T | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-4455A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229796 | ||||||
| chr4:176229811
|
C | A | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.197-4470G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229811 | ||||||
| chr4:176229818
|
C | A | 1 | a0001c0001t0001g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.197-4477G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229818 | ||||||
| chr4:176229872
|
G | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 28 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.197-4531C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229872 | ||||||
| chr4:176229905
|
C | T | 20 | a0001c0002t0002g0140a0001c0002t0003g0004a0001c0002t0003g0018others(17): Show | 23 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-4564G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229905 | ||||||
| chr4:176229929
|
G | T | 32 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(29): Show | 35 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.197-4588C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176229929 | ||||||
| chr4:176230027
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 7 | HG01081.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-4686G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176230027 | ||||||
| chr4:176230171
|
A | C | 32 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(29): Show | 35 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.197-4830T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176230171 | ||||||
| chr4:176230252
|
C | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(216): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.197-4911G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176230252 | ||||||
| chr4:176230288
|
A | T | 1 | a0001c0002t0001g0294 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.197-4947T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176230288 | ||||||
| chr4:176230308
|
A | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 7 | HG01081.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-4967T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176230308 | ||||||
| chr4:176230512
|
T | C | 1 | a0001c0001t0001g0327 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.197-5171A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176230512 | ||||||
| chr4:176230670
|
C | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0216others(1): Show | 6 | HG02129.hp1 NA18943.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-5329G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176230670 | ||||||
| chr4:176230807
|
C | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(3): Show | 7 | HG01081.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-5466G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176230807 | ||||||
| chr4:176230923
|
T | G | 1 | a0001c0004t0001g0366 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.197-5582A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176230923 | ||||||
| chr4:176231013
|
C | A | 84 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(81): Show | 92 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.197-5672G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231013 | ||||||
| chr4:176231047
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.197-5706G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231047 | ||||||
| chr4:176231083
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-5742A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231083 | ||||||
| chr4:176231223
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.197-5882A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231223 | ||||||
| chr4:176231225
|
A | AT | 42 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(39): Show | 44 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.197-5885dupA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231225 | ||||||
| chr4:176231225
|
AT | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(22): Show | 30 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.197-5885delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231225 | ||||||
| chr4:176231225
|
ATT | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(136): Show | 150 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.197-5886_197-5885d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231225 | ||||||
| chr4:176231225
|
ATTT | A | 84 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(81): Show | 92 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.197-5887_197-5885d others(5): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231225 | ||||||
| chr4:176231271
|
T | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(221): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.197-5930A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231271 | ||||||
| chr4:176231289
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0225 | 3 | HG02071.hp2 HG04199.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.197-5948G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231289 | ||||||
| chr4:176231433
|
AT | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(222): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.197-6093delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231433 | ||||||
| chr4:176231641
|
A | G | 43 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(40): Show | 45 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-6300T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231641 | ||||||
| chr4:176231659
|
C | CA | 10 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 12 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-6319dupT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231659 | ||||||
| chr4:176231659
|
C | CAA | 11 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(8): Show | 11 | HG02630.hp1 HG02647.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-6320_197-6319d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231659 | ||||||
| chr4:176231659
|
C | CAAA | 19 | a0001c0001t0001g0150a0001c0002t0003g0004a0001c0002t0003g0018others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-6321_197-6319d others(5): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231659 | ||||||
| chr4:176231659
|
CA | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(213): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.197-6319delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231659 | ||||||
| chr4:176231684
|
AT | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(222): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.197-6344delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231684 | ||||||
| chr4:176231701
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-6360C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231701 | ||||||
| chr4:176231716
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(257): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.197-6375G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231716 | ||||||
| chr4:176231757
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.197-6416T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231757 | ||||||
| chr4:176231772
|
G | A | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(63): Show | 73 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.197-6431C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231772 | ||||||
| chr4:176231842
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.197-6501G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231842 | ||||||
| chr4:176231843
|
T | TCAAAACA others(3): Show |
369 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(366): Show | 404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.197-6512_197-6503d others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231843 | ||||||
| chr4:176231843
|
T | TCAAAACA others(8): Show |
1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197-6517_197-6503d others(17): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231843 | ||||||
| chr4:176231854
|
C | CAAAACAA others(3): Show |
1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-6514_197-6513i others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231854 | ||||||
| chr4:176231891
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-6550T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176231891 | ||||||
| chr4:176232031
|
G | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-6690C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232031 | ||||||
| chr4:176232109
|
T | TTA | 6 | a0001c0001t0001g0089a0001c0002t0004g0038a0001c0002t0004g0039others(3): Show | 6 | HG02273.hp1 HG02486.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-6770_197-6769d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232109 | ||||||
| chr4:176232126
|
TAC | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(25): Show | 34 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.197-6787_197-6786d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232126 | ||||||
| chr4:176232127
|
ACT | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(50): Show | 55 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.197-6788_197-6787d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232127 | ||||||
| chr4:176232128
|
C | A | 1 | a0001c0002t0004g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.197-6787G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232128 | ||||||
| chr4:176232128
|
C | T | 20 | a0001c0001t0001g0150a0001c0002t0003g0004a0001c0002t0003g0018others(17): Show | 23 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-6787G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232128 | ||||||
| chr4:176232129
|
T | C | 1 | a0001c0002t0004g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.197-6788A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232129 | ||||||
| chr4:176232131
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.197-6790A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232131 | ||||||
| chr4:176232344
|
C | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(324): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.197-7003G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232344 | ||||||
| chr4:176232400
|
T | C | 6 | a0001c0003t0002g0336a0001c0003t0002g0337a0001c0003t0002g0342others(3): Show | 6 | HG00642.hp2 HG01109.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-7059A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232400 | ||||||
| chr4:176232411
|
G | A | 1 | a0001c0002t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.197-7070C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232411 | ||||||
| chr4:176232445
|
C | T | 26 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(23): Show | 30 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.197-7104G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232445 | ||||||
| chr4:176232708
|
T | C | 86 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(83): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.197-7367A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232708 | ||||||
| chr4:176232718
|
G | A | 1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-7377C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232718 | ||||||
| chr4:176232732
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.197-7391C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232732 | ||||||
| chr4:176232802
|
T | A | 1 | a0001c0002t0002g0339 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.197-7461A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232802 | ||||||
| chr4:176232855
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-7514G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232855 | ||||||
| chr4:176232911
|
G | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG02630.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-7570C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232911 | ||||||
| chr4:176232996
|
A | G | 1 | a0001c0002t0002g0313 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.197-7655T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176232996 | ||||||
| chr4:176233045
|
A | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0032others(53): Show | 60 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.197-7704T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233045 | ||||||
| chr4:176233071
|
A | T | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-7730T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233071 | ||||||
| chr4:176233102
|
A | T | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0189 | 3 | HG02886.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.197-7761T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233102 | ||||||
| chr4:176233172
|
T | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(83): Show | 96 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.197-7831A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233172 | ||||||
| chr4:176233270
|
T | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG03225.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.197-7929A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233270 | ||||||
| chr4:176233283
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-7942G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233283 | ||||||
| chr4:176233448
|
TA | T | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-8108delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233448 | ||||||
| chr4:176233457
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(324): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.197-8116C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233457 | ||||||
| chr4:176233480
|
A | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(4): Show | 8 | HG01891.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-8139T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233480 | ||||||
| chr4:176233515
|
T | C | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-8174A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233515 | ||||||
| chr4:176233567
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.197-8226C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233567 | ||||||
| chr4:176233804
|
G | T | 1 | a0001c0004t0001g0365 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.197-8463C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233804 | ||||||
| chr4:176233864
|
C | T | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-8523G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233864 | ||||||
| chr4:176233902
|
G | A | 26 | a0001c0001t0001g0013a0001c0001t0001g0079a0001c0001t0001g0080others(23): Show | 27 | HG01123.hp1 HG01168.hp2 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.197-8561C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233902 | ||||||
| chr4:176233988
|
G | C | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-8647C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176233988 | ||||||
| chr4:176234046
|
G | A | 29 | a0001c0001t0001g0089a0001c0001t0001g0146a0001c0001t0001g0147others(26): Show | 32 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.197-8705C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234046 | ||||||
| chr4:176234126
|
T | C | 1 | a0001c0002t0013g0233 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.197-8785A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234126 | ||||||
| chr4:176234139
|
C | T | 20 | a0001c0001t0001g0089a0001c0002t0003g0004a0001c0002t0003g0018others(17): Show | 23 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-8798G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234139 | ||||||
| chr4:176234198
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0067 | 5 | HG03491.hp2 HG03492.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-8857T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234198 | ||||||
| chr4:176234205
|
G | A | 9 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 11 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-8864C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234205 | ||||||
| chr4:176234299
|
G | C | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-8958C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234299 | ||||||
| chr4:176234328
|
C | T | 2 | a0001c0002t0013g0233a0001c0006t0003g0017 | 3 | HG00639.hp2 HG01099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.197-8987G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234328 | ||||||
| chr4:176234355
|
CT | C | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.197-9015delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234355 | ||||||
| chr4:176234412
|
T | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 9 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.197-9071A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234412 | ||||||
| chr4:176234449
|
T | A | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.197-9108A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234449 | ||||||
| chr4:176234475
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.197-9134G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234475 | ||||||
| chr4:176234502
|
G | A | 1 | a0001c0002t0001g0308 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.197-9161C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234502 | ||||||
| chr4:176234583
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(72): Show | 82 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.197-9242C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234583 | ||||||
| chr4:176234634
|
T | A | 7 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(4): Show | 8 | HG01891.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-9293A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234634 | ||||||
| chr4:176234637
|
C | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0012others(218): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.197-9296G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234637 | ||||||
| chr4:176234700
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-9359G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234700 | ||||||
| chr4:176234749
|
A | C | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.197-9408T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234749 | ||||||
| chr4:176234804
|
C | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-9463G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176234804 | ||||||
| chr4:176235017
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(258): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.197-9676G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235017 | ||||||
| chr4:176235025
|
T | G | 81 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(78): Show | 89 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.197-9684A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235025 | ||||||
| chr4:176235075
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.197-9734G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235075 | ||||||
| chr4:176235142
|
C | A | 3 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0303 | 3 | HG01433.hp1 HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.197-9801G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235142 | ||||||
| chr4:176235176
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0016g0160 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.197-9835C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235176 | ||||||
| chr4:176235213
|
T | A | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197-9872A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235213 | ||||||
| chr4:176235341
|
G | A | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(325): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.197-10000C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235341 | ||||||
| chr4:176235686
|
C | T | 43 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(40): Show | 45 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-10345G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235686 | ||||||
| chr4:176235743
|
C | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-10402G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235743 | ||||||
| chr4:176235790
|
G | T | 86 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(83): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.197-10449C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235790 | ||||||
| chr4:176235792
|
CT | C | 60 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0037others(57): Show | 64 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.197-10452delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235792 | ||||||
| chr4:176235851
|
C | A | 1 | a0001c0002t0001g0271 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.197-10510G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235851 | ||||||
| chr4:176235980
|
A | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 29 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.197-10639T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176235980 | ||||||
| chr4:176236041
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 29 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.197-10700C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236041 | ||||||
| chr4:176236043
|
C | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 29 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.197-10702G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236043 | ||||||
| chr4:176236167
|
AT | A | 83 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0037others(80): Show | 89 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.197-10827delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236167 | ||||||
| chr4:176236295
|
T | C | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.197-10954A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236295 | ||||||
| chr4:176236377
|
C | A | 1 | a0001c0001t0018g0048 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.197-11036G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236377 | ||||||
| chr4:176236377
|
C | T | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-11036G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236377 | ||||||
| chr4:176236447
|
T | C | 1 | a0001c0002t0003g0099 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.197-11106A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236447 | ||||||
| chr4:176236644
|
A | G | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-11303T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236644 | ||||||
| chr4:176236654
|
T | C | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-11313A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236654 | ||||||
| chr4:176236679
|
G | A | 82 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0037others(79): Show | 88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.197-11338C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236679 | ||||||
| chr4:176236698
|
C | A | 82 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0037others(79): Show | 88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.197-11357G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236698 | ||||||
| chr4:176236797
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.197-11456T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236797 | ||||||
| chr4:176236872
|
G | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-11531C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236872 | ||||||
| chr4:176236918
|
A | C | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-11577T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236918 | ||||||
| chr4:176236943
|
T | A | 1 | a0001c0001t0014g0111 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.197-11602A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176236943 | ||||||
| chr4:176237190
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.197-11849G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237190 | ||||||
| chr4:176237194
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.197-11853A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237194 | ||||||
| chr4:176237209
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-11868C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237209 | ||||||
| chr4:176237239
|
G | T | 3 | a0001c0002t0001g0249a0001c0002t0001g0257a0001c0002t0017g0282 | 3 | HG00738.hp1 HG01978.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.197-11898C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237239 | ||||||
| chr4:176237339
|
A | T | 1 | a0001c0002t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.197-11998T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237339 | ||||||
| chr4:176237536
|
A | T | 43 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(40): Show | 45 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-12195T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237536 | ||||||
| chr4:176237582
|
A | C | 43 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(40): Show | 45 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-12241T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237582 | ||||||
| chr4:176237600
|
C | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0127 | 2 | NA18939.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.197-12259G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237600 | ||||||
| chr4:176237630
|
G | A | 1 | a0001c0002t0002g0313 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.197-12289C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237630 | ||||||
| chr4:176237731
|
T | G | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.197-12390A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237731 | ||||||
| chr4:176237772
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197-12431C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237772 | ||||||
| chr4:176237777
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-12436T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237777 | ||||||
| chr4:176237840
|
A | G | 1 | a0001c0002t0002g0360 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.197-12499T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237840 | ||||||
| chr4:176237988
|
G | A | 3 | a0001c0002t0002g0030a0001c0002t0002g0340a0001c0002t0002g0354 | 4 | HG00423.hp2 HG00621.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-12647C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237988 | ||||||
| chr4:176237988
|
G | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(72): Show | 82 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.197-12647C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176237988 | ||||||
| chr4:176238050
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0206a0001c0001t0001g0225 | 3 | HG02071.hp2 HG04199.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.197-12709G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238050 | ||||||
| chr4:176238055
|
T | C | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.197-12714A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238055 | ||||||
| chr4:176238084
|
T | C | 1 | a0001c0002t0001g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.197-12743A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238084 | ||||||
| chr4:176238206
|
C | CA | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 93 | HG00280.hp2 HG00408.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.197-12866dupT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238206 | ||||||
| chr4:176238206
|
C | CAA | 26 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0089others(23): Show | 30 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.197-12867_197-1286 others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238206 | ||||||
| chr4:176238206
|
CA | C | 190 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(187): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.197-12866delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238206 | ||||||
| chr4:176238206
|
CAA | C | 13 | a0001c0001t0001g0138a0001c0001t0001g0195a0001c0001t0001g0196others(10): Show | 13 | HG00597.hp1 HG00609.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.197-12867_197-1286 others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238206 | ||||||
| chr4:176238300
|
T | C | 27 | a0001c0001t0001g0013a0001c0001t0001g0079a0001c0001t0001g0080others(24): Show | 28 | HG01123.hp1 HG01168.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.197-12959A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238300 | ||||||
| chr4:176238438
|
G | A | 1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-13097C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238438 | ||||||
| chr4:176238523
|
G | C | 3 | a0001c0002t0003g0018a0001c0002t0003g0231a0001c0002t0003g0232 | 4 | HG01069.hp1 HG01071.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-13182C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238523 | ||||||
| chr4:176238594
|
G | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0116 | 2 | HG03017.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.197-13253C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238594 | ||||||
| chr4:176238620
|
T | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0075a0001c0001t0001g0136 | 4 | HG01099.hp2 HG02738.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-13279A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238620 | ||||||
| chr4:176238648
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197-13307A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238648 | ||||||
| chr4:176238654
|
T | A | 1 | a0001c0002t0002g0115 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.197-13313A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238654 | ||||||
| chr4:176238754
|
GA | G | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-13414delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238754 | ||||||
| chr4:176238812
|
C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(72): Show | 82 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.197-13471G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238812 | ||||||
| chr4:176238846
|
G | A | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.197-13505C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238846 | ||||||
| chr4:176238999
|
A | G | 1 | a0001c0002t0001g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.197-13658T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176238999 | ||||||
| chr4:176239032
|
C | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(4): Show | 8 | HG01891.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-13691G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239032 | ||||||
| chr4:176239111
|
A | G | 48 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(45): Show | 50 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.197-13770T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239111 | ||||||
| chr4:176239114
|
G | T | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-13773C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239114 | ||||||
| chr4:176239166
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-13825G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239166 | ||||||
| chr4:176239247
|
C | G | 71 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(68): Show | 76 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.197-13906G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239247 | ||||||
| chr4:176239339
|
T | G | 1 | a0001c0001t0001g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.197-13998A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239339 | ||||||
| chr4:176239597
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-14256C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239597 | ||||||
| chr4:176239757
|
G | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-14416C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239757 | ||||||
| chr4:176239840
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.197-14499G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239840 | ||||||
| chr4:176239943
|
A | T | 3 | a0001c0005t0001g0305a0001c0005t0001g0306a0006c0009t0001g0186 | 3 | HG02630.hp1 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.197-14602T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176239943 | ||||||
| chr4:176240011
|
T | C | 1 | a0001c0002t0001g0271 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.197-14670A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240011 | ||||||
| chr4:176240042
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.197-14701G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240042 | ||||||
| chr4:176240043
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.197-14702C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240043 | ||||||
| chr4:176240098
|
C | G | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-14757G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240098 | ||||||
| chr4:176240158
|
A | G | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-14817T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240158 | ||||||
| chr4:176240261
|
A | T | 19 | a0001c0002t0003g0004a0001c0002t0003g0018a0001c0002t0003g0043others(16): Show | 22 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-14920T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240261 | ||||||
| chr4:176240273
|
T | C | 1 | a0001c0002t0001g0292 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.197-14932A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240273 | ||||||
| chr4:176240288
|
C | T | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-14947G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240288 | ||||||
| chr4:176240298
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0015others(72): Show | 82 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.197-14957C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240298 | ||||||
| chr4:176240467
|
G | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-15126C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240467 | ||||||
| chr4:176240539
|
C | T | 3 | a0001c0002t0001g0299a0001c0002t0001g0300a0001c0002t0001g0303 | 3 | HG01433.hp1 HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.197-15198G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240539 | ||||||
| chr4:176240572
|
G | A | 1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-15231C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240572 | ||||||
| chr4:176240675
|
C | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-15334G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240675 | ||||||
| chr4:176240687
|
A | G | 1 | a0001c0001t0001g0165 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.197-15346T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240687 | ||||||
| chr4:176240697
|
A | T | 20 | a0001c0002t0002g0140a0001c0002t0003g0004a0001c0002t0003g0018others(17): Show | 23 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-15356T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240697 | ||||||
| chr4:176240755
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-15414G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240755 | ||||||
| chr4:176240824
|
G | A | 1 | a0001c0002t0001g0287 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.197-15483C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240824 | ||||||
| chr4:176240966
|
G | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(301): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.197-15625C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176240966 | ||||||
| chr4:176241158
|
G | A | 2 | a0001c0002t0002g0030a0001c0002t0002g0354 | 3 | HG00621.hp2 NA18959.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.197-15817C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176241158 | ||||||
| chr4:176241395
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197-16054C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176241395 | ||||||
| chr4:176241784
|
G | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093 | 5 | HG02055.hp2 HG03195.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-16443C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176241784 | ||||||
| chr4:176241811
|
T | C | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(325): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.197-16470A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176241811 | ||||||
| chr4:176241848
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0364a0001c0001t0001g0367 | 4 | HG02145.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-16507C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176241848 | ||||||
| chr4:176241931
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.197-16590G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176241931 | ||||||
| chr4:176241937
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197-16596A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176241937 | ||||||
| chr4:176242019
|
T | C | 1 | a0001c0001t0001g0008 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.197-16678A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176242019 | ||||||
| chr4:176242137
|
C | CTGCCATC others(1199): Show |
1 | a0001c0002t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.197-16797_197-1679 others(1210): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176242137 | ||||||
| chr4:176242263
|
G | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(286): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.197-16922C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176242263 | ||||||
| chr4:176242385
|
T | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 29 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.197-17044A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176242385 | ||||||
| chr4:176242390
|
T | C | 1 | a0001c0005t0001g0305 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.197-17049A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176242390 | ||||||
| chr4:176242561
|
T | C | 1 | a0001c0002t0001g0296 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.197-17220A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176242561 | ||||||
| chr4:176242785
|
T | C | 1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-17444A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176242785 | ||||||
| chr4:176242875
|
A | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(211): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.197-17534T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176242875 | ||||||
| chr4:176242913
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(211): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.197-17572A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176242913 | ||||||
| chr4:176243134
|
G | T | 75 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(72): Show | 80 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.197-17793C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243134 | ||||||
| chr4:176243151
|
T | C | 86 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(83): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.197-17810A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243151 | ||||||
| chr4:176243152
|
T | C | 3 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | HG03225.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.197-17811A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243152 | ||||||
| chr4:176243181
|
G | A | 43 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(40): Show | 45 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-17840C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243181 | ||||||
| chr4:176243274
|
GGTCT | G | 3 | a0001c0002t0001g0255a0001c0002t0001g0272a0001c0002t0001g0273 | 3 | HG00642.hp1 HG01169.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.197-17937_197-1793 others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243274 | ||||||
| chr4:176243275
|
GTCTA | G | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(207): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.197-17938_197-1793 others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243275 | ||||||
| chr4:176243344
|
T | C | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-18003A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243344 | ||||||
| chr4:176243558
|
G | A | 2 | a0001c0002t0001g0288a0001c0002t0001g0293 | 2 | NA18973.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.197-18217C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243558 | ||||||
| chr4:176243580
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-18239C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243580 | ||||||
| chr4:176243602
|
A | T | 1 | a0001c0001t0001g0346 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.197-18261T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243602 | ||||||
| chr4:176243651
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-18310G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243651 | ||||||
| chr4:176243794
|
A | G | 86 | a0001c0002t0001g0019a0001c0002t0001g0021a0001c0002t0001g0022others(83): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.197-18453T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243794 | ||||||
| chr4:176243796
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0149 | 2 | NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.197-18455C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243796 | ||||||
| chr4:176243851
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 10 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-18510C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176243851 | ||||||
| chr4:176244030
|
C | T | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-18689G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244030 | ||||||
| chr4:176244031
|
A | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(310): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.197-18690T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244031 | ||||||
| chr4:176244122
|
T | C | 3 | a0001c0002t0001g0241a0001c0002t0001g0242a0001c0002t0001g0246 | 3 | NA18940.hp2 NA19054.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.197-18781A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244122 | ||||||
| chr4:176244138
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.197-18797T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244138 | ||||||
| chr4:176244321
|
T | G | 1 | a0001c0002t0002g0313 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.197-18980A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244321 | ||||||
| chr4:176244405
|
T | G | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(310): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.197-19064A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244405 | ||||||
| chr4:176244437
|
T | C | 43 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(40): Show | 45 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-19096A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244437 | ||||||
| chr4:176244494
|
T | C | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(310): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.197-19153A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244494 | ||||||
| chr4:176244601
|
C | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-19260G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244601 | ||||||
| chr4:176244634
|
G | A | 1 | a0001c0002t0001g0353 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.197-19293C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244634 | ||||||
| chr4:176244800
|
A | C | 370 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(367): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.197-19459T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244800 | ||||||
| chr4:176244818
|
C | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 11 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-19477G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244818 | ||||||
| chr4:176244966
|
A | T | 44 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0062others(41): Show | 46 | HG00140.hp2 HG00741.hp2 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.197-19625T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176244966 | ||||||
| chr4:176245027
|
C | T | 1 | a0001c0001t0008g0083 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.197-19686G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245027 | ||||||
| chr4:176245057
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0190a0001c0001t0001g0191 | 3 | HG01081.hp2 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.197-19716G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245057 | ||||||
| chr4:176245238
|
A | T | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-19897T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245238 | ||||||
| chr4:176245251
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0181 | 4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-19910G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245251 | ||||||
| chr4:176245438
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(205): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.197-20097G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245438 | ||||||
| chr4:176245490
|
G | A | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-20149C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245490 | ||||||
| chr4:176245527
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-20186G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245527 | ||||||
| chr4:176245553
|
A | G | 20 | a0001c0002t0002g0140a0001c0002t0003g0004a0001c0002t0003g0018others(17): Show | 23 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-20212T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245553 | ||||||
| chr4:176245598
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.197-20257C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245598 | ||||||
| chr4:176245664
|
C | T | 5 | a0001c0001t0001g0150a0001c0005t0001g0192a0001c0005t0001g0305others(2): Show | 5 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-20323G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245664 | ||||||
| chr4:176245671
|
G | C | 1 | a0001c0001t0008g0102 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.197-20330C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245671 | ||||||
| chr4:176245682
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-20341A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245682 | ||||||
| chr4:176245683
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-20342C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245683 | ||||||
| chr4:176245745
|
C | T | 313 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(310): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.197-20404G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245745 | ||||||
| chr4:176245753
|
T | C | 1 | a0001c0002t0001g0274 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.197-20412A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245753 | ||||||
| chr4:176245774
|
A | G | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-20433T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245774 | ||||||
| chr4:176245840
|
T | A | 1 | a0001c0002t0001g0353 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.197-20499A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245840 | ||||||
| chr4:176245906
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(221): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.197-20565C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245906 | ||||||
| chr4:176245960
|
C | T | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(311): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.197-20619G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245960 | ||||||
| chr4:176245971
|
A | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(287): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.197-20630T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245971 | ||||||
| chr4:176245993
|
A | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(279): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.197-20652T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176245993 | ||||||
| chr4:176246005
|
C | A | 1 | a0001c0001t0016g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.197-20664G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246005 | ||||||
| chr4:176246008
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(308): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.197-20667C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246008 | ||||||
| chr4:176246021
|
A | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 28 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.197-20680T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246021 | ||||||
| chr4:176246045
|
TA | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(309): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.197-20705delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246045 | ||||||
| chr4:176246111
|
T | A | 1 | a0001c0002t0001g0303 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.197-20770A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246111 | ||||||
| chr4:176246176
|
G | C | 1 | a0001c0001t0001g0204 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.197-20835C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246176 | ||||||
| chr4:176246177
|
T | G | 1 | a0001c0001t0001g0204 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.197-20836A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246177 | ||||||
| chr4:176246178
|
G | T | 1 | a0001c0001t0001g0204 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.197-20837C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246178 | ||||||
| chr4:176246212
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-20871T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246212 | ||||||
| chr4:176246589
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.197-21248G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246589 | ||||||
| chr4:176246688
|
A | G | 3 | a0001c0002t0001g0026a0001c0002t0001g0298a0001c0002t0001g0304 | 4 | HG01884.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-21347T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246688 | ||||||
| chr4:176246760
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.197-21419G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246760 | ||||||
| chr4:176246793
|
T | G | 5 | a0001c0001t0001g0129a0001c0004t0001g0117a0001c0004t0001g0118others(2): Show | 5 | HG04184.hp1 NA18945.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-21452A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246793 | ||||||
| chr4:176246936
|
TA | T | 4 | a0001c0005t0001g0192a0001c0005t0001g0305a0001c0005t0001g0306others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-21596delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246936 | ||||||
| chr4:176246937
|
A | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-21596T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176246937 | ||||||
| chr4:176247001
|
T | C | 1 | a0001c0002t0001g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.197-21660A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247001 | ||||||
| chr4:176247042
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.197-21701C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247042 | ||||||
| chr4:176247043
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.197-21702G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247043 | ||||||
| chr4:176247066
|
G | A | 50 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0053others(47): Show | 52 | HG00408.hp1 HG00733.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.197-21725C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247066 | ||||||
| chr4:176247124
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197-21783T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247124 | ||||||
| chr4:176247161
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.196+21752C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247161 | ||||||
| chr4:176247286
|
G | T | 204 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0012others(201): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.196+21627C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247286 | ||||||
| chr4:176247454
|
A | G | 1 | a0001c0004t0001g0365 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.196+21459T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247454 | ||||||
| chr4:176247471
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.196+21442A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247471 | ||||||
| chr4:176247573
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.196+21340A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247573 | ||||||
| chr4:176247619
|
C | T | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | NA18947.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.196+21294G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247619 | ||||||
| chr4:176247907
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.196+21006A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247907 | ||||||
| chr4:176247950
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.196+20963A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247950 | ||||||
| chr4:176247972
|
G | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(16): Show | 23 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.196+20941C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176247972 | ||||||
| chr4:176248279
|
T | C | 38 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(35): Show | 44 | HG00280.hp2 HG00639.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.196+20634A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176248279 | ||||||
| chr4:176248330
|
G | A | 4 | a0001c0002t0003g0043a0001c0002t0003g0044a0001c0002t0003g0056others(1): Show | 4 | HG00280.hp1 HG00735.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+20583C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176248330 | ||||||
| chr4:176248426
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.196+20487A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176248426 | ||||||
| chr4:176248537
|
A | G | 1 | a0001c0002t0002g0360 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.196+20376T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176248537 | ||||||
| chr4:176248555
|
C | T | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+20358G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176248555 | ||||||
| chr4:176248928
|
G | A | 2 | a0001c0001t0001g0116a0001c0002t0002g0362 | 2 | HG03017.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.196+19985C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176248928 | ||||||
| chr4:176248996
|
T | A | 1 | a0001c0001t0001g0133 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.196+19917A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176248996 | ||||||
| chr4:176249130
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.196+19783G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249130 | ||||||
| chr4:176249153
|
G | A | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+19760C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249153 | ||||||
| chr4:176249337
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.196+19576G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249337 | ||||||
| chr4:176249338
|
G | A | 2 | a0001c0002t0001g0084a0001c0002t0001g0085 | 2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.196+19575C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249338 | ||||||
| chr4:176249341
|
G | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG02486.hp2 HG02809.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+19572C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249341 | ||||||
| chr4:176249344
|
T | C | 1 | a0001c0002t0003g0056 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.196+19569A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249344 | ||||||
| chr4:176249347
|
T | G | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 24 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.196+19566A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249347 | ||||||
| chr4:176249393
|
A | G | 1 | a0001c0002t0004g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+19520T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249393 | ||||||
| chr4:176249510
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.196+19403C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249510 | ||||||
| chr4:176249653
|
A | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0153a0001c0001t0001g0198 | 4 | NA18951.hp2 NA18981.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+19260T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249653 | ||||||
| chr4:176249690
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0016g0160 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.196+19223A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249690 | ||||||
| chr4:176249717
|
TG | T | 31 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0062others(28): Show | 33 | HG00140.hp2 HG01123.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.196+19195delC | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249717 | ||||||
| chr4:176249798
|
G | C | 1 | a0001c0002t0001g0353 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.196+19115C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249798 | ||||||
| chr4:176249801
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.196+19112G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249801 | ||||||
| chr4:176249826
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.196+19087C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249826 | ||||||
| chr4:176249834
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 10 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+19079C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249834 | ||||||
| chr4:176249836
|
C | T | 135 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0037others(132): Show | 146 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.196+19077G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249836 | ||||||
| chr4:176249840
|
T | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(309): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.196+19073A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249840 | ||||||
| chr4:176249841
|
G | A | 1 | a0001c0002t0001g0290 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.196+19072C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249841 | ||||||
| chr4:176249842
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(167): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.196+19071C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249842 | ||||||
| chr4:176249861
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.196+19052C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249861 | ||||||
| chr4:176249861
|
G | T | 1 | a0001c0001t0001g0227 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.196+19052C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249861 | ||||||
| chr4:176249871
|
C | T | 7 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0162others(4): Show | 7 | HG01346.hp2 NA18953.hp2 NA18978.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+19042G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249871 | ||||||
| chr4:176249872
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.196+19041A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249872 | ||||||
| chr4:176249881
|
C | T | 28 | a0001c0001t0001g0009a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 32 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.196+19032G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249881 | ||||||
| chr4:176249882
|
A | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0004t0001g0117others(1): Show | 4 | HG02717.hp1 HG02895.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+19031T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249882 | ||||||
| chr4:176249892
|
C | T | 2 | a0001c0001t0001g0323a0001c0001t0001g0325 | 2 | HG00597.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.196+19021G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249892 | ||||||
| chr4:176249907
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(215): Show | 238 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.196+19006G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249907 | ||||||
| chr4:176249909
|
C | CA | 21 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(18): Show | 24 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.196+19003dupT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249909 | ||||||
| chr4:176249911
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(12): Show | 17 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.196+19002T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249911 | ||||||
| chr4:176249916
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.196+18997A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249916 | ||||||
| chr4:176249931
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.196+18982C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249931 | ||||||
| chr4:176249932
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(221): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.196+18981T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249932 | ||||||
| chr4:176249934
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.196+18979C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249934 | ||||||
| chr4:176249937
|
C | A | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.196+18976G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249937 | ||||||
| chr4:176249968
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 10 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+18945C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249968 | ||||||
| chr4:176249977
|
A | C | 11 | a0001c0001t0001g0001a0001c0001t0001g0092a0001c0001t0001g0093others(8): Show | 13 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+18936T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249977 | ||||||
| chr4:176249977
|
A | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 225 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.196+18936T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249977 | ||||||
| chr4:176249994
|
G | A | 7 | a0001c0002t0001g0256a0001c0002t0001g0275a0001c0002t0001g0276others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+18919C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176249994 | ||||||
| chr4:176250020
|
A | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 48 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.196+18893T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250020 | ||||||
| chr4:176250022
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.196+18891T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250022 | ||||||
| chr4:176250028
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.196+18885C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250028 | ||||||
| chr4:176250043
|
T | C | 4 | a0001c0001t0001g0060a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG00099.hp2 HG00741.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+18870A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250043 | ||||||
| chr4:176250056
|
C | A | 42 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0082others(39): Show | 44 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.196+18857G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250056 | ||||||
| chr4:176250056
|
C | T | 1 | a0001c0002t0001g0345 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.196+18857G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250056 | ||||||
| chr4:176250064
|
CAAAA | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(170): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.196+18845_196+1884 others(8): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250064 | ||||||
| chr4:176250095
|
A | C | 1 | a0001c0002t0001g0256 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.196+18818T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250095 | ||||||
| chr4:176250378
|
C | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 48 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.196+18535G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250378 | ||||||
| chr4:176250495
|
T | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+18418A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250495 | ||||||
| chr4:176250748
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(216): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.196+18165A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250748 | ||||||
| chr4:176250936
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.196+17977G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250936 | ||||||
| chr4:176250948
|
C | T | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0189 | 3 | HG02886.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.196+17965G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250948 | ||||||
| chr4:176250985
|
T | C | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196+17928A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176250985 | ||||||
| chr4:176251213
|
G | T | 1 | a0001c0002t0003g0046 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.196+17700C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251213 | ||||||
| chr4:176251232
|
A | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.196+17681T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251232 | ||||||
| chr4:176251280
|
A | ACAGAAAG others(642): Show |
1 | a0001c0001t0001g0068 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.196+17632_196+1763 others(653): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251280 | ||||||
| chr4:176251280
|
A | ACAGAAAG others(643): Show |
1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.196+17632_196+1763 others(654): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251280 | ||||||
| chr4:176251280
|
A | ACAGAAAG others(643): Show |
1 | a0001c0001t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.196+17632_196+1763 others(654): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251280 | ||||||
| chr4:176251280
|
A | ACAGAAAG others(643): Show |
2 | a0001c0001t0001g0089a0001c0005t0001g0192 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196+17632_196+1763 others(654): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251280 | ||||||
| chr4:176251280
|
A | ACAGAAAG others(643): Show |
2 | a0001c0001t0001g0309a0007c0011t0001g0152 | 2 | HG00741.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.196+17632_196+1763 others(654): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251280 | ||||||
| chr4:176251280
|
A | ACAGAAAG others(643): Show |
166 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(163): Show | 181 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.196+17632_196+1763 others(654): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251280 | ||||||
| chr4:176251280
|
A | ACAGAAAG others(643): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG00099.hp2 HG01123.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.196+17632_196+1763 others(654): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251280 | ||||||
| chr4:176251280
|
A | ACAGAAAG others(643): Show |
44 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 48 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.196+17632_196+1763 others(654): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251280 | ||||||
| chr4:176251280
|
A | ACAGAAAG others(643): Show |
1 | a0001c0001t0001g0218 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.196+17632_196+1763 others(654): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251280 | ||||||
| chr4:176251281
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0223 | 2 | NA18987.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.196+17632C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251281 | ||||||
| chr4:176251287
|
G | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17626C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251287 | ||||||
| chr4:176251288
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17625G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251288 | ||||||
| chr4:176251291
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17622C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251291 | ||||||
| chr4:176251296
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17617G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251296 | ||||||
| chr4:176251301
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17612C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251301 | ||||||
| chr4:176251302
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17611G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251302 | ||||||
| chr4:176251317
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17596G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251317 | ||||||
| chr4:176251328
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17585G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251328 | ||||||
| chr4:176251334
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17579C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251334 | ||||||
| chr4:176251336
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17577C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251336 | ||||||
| chr4:176251339
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17574C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251339 | ||||||
| chr4:176251344
|
C | CTT | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17568_196+1756 others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251344 | ||||||
| chr4:176251356
|
A | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17557T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251356 | ||||||
| chr4:176251359
|
G | T | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196+17554C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251359 | ||||||
| chr4:176251361
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17552C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251361 | ||||||
| chr4:176251366
|
T | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17547A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251366 | ||||||
| chr4:176251369
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17544G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251369 | ||||||
| chr4:176251373
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17540A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251373 | ||||||
| chr4:176251376
|
A | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17537T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251376 | ||||||
| chr4:176251381
|
T | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17532A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251381 | ||||||
| chr4:176251390
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17523C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251390 | ||||||
| chr4:176251391
|
T | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17522A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251391 | ||||||
| chr4:176251394
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17519G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251394 | ||||||
| chr4:176251406
|
CA | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17506delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251406 | ||||||
| chr4:176251418
|
C | T | 23 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(20): Show | 26 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.196+17495G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251418 | ||||||
| chr4:176251423
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17490C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251423 | ||||||
| chr4:176251424
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17489A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251424 | ||||||
| chr4:176251425
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17488T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251425 | ||||||
| chr4:176251431
|
G | A | 2 | a0001c0001t0001g0309a0007c0011t0001g0152 | 2 | HG00741.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.196+17482C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251431 | ||||||
| chr4:176251431
|
G | C | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196+17482C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251431 | ||||||
| chr4:176251432
|
G | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17481C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251432 | ||||||
| chr4:176251434
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17479G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251434 | ||||||
| chr4:176251442
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17471C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251442 | ||||||
| chr4:176251454
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17459A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251454 | ||||||
| chr4:176251455
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17458C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251455 | ||||||
| chr4:176251461
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17452G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251461 | ||||||
| chr4:176251476
|
G | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17437C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251476 | ||||||
| chr4:176251479
|
G | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17434C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251479 | ||||||
| chr4:176251487
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17426C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251487 | ||||||
| chr4:176251494
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17419C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251494 | ||||||
| chr4:176251498
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17415G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251498 | ||||||
| chr4:176251505
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17408A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251505 | ||||||
| chr4:176251508
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17405C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251508 | ||||||
| chr4:176251511
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17402C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251511 | ||||||
| chr4:176251512
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17401T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251512 | ||||||
| chr4:176251517
|
C | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17396G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251517 | ||||||
| chr4:176251518
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.196+17395G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251518 | ||||||
| chr4:176251541
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(218): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.196+17372C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251541 | ||||||
| chr4:176251564
|
T | TA | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(108): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.196+17348dupT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251564
|
T | TAA | 45 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0074others(42): Show | 49 | HG00673.hp1 HG00741.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.196+17347_196+1734 others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251564
|
T | TAAA | 7 | a0001c0001t0001g0243a0001c0002t0001g0024a0001c0002t0001g0026others(4): Show | 9 | HG01884.hp2 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+17346_196+1734 others(7): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251564
|
T | TAAAAAAA | 26 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0098others(23): Show | 29 | HG00408.hp2 HG00741.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.196+17342_196+1734 others(11): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251564
|
T | TAAAAAAA others(1): Show |
11 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00609.hp1 HG01943.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+17341_196+1734 others(12): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251564
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0224 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.196+17339_196+1734 others(14): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251564
|
T | TAAAAAAA others(5): Show |
2 | a0001c0001t0001g0199a0001c0001t0001g0225 | 2 | HG02071.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.196+17337_196+1734 others(16): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251564
|
TA | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0037others(43): Show | 50 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.196+17348delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251564
|
TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0001g0015a0001c0002t0001g0078a0003c0007t0001g0034 | 4 | HG00544.hp1 HG02080.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+17338_196+1734 others(15): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251564
|
TAAAAAAA others(7): Show |
T | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+17335_196+1734 others(18): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251564 | ||||||
| chr4:176251804
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.196+17109G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251804 | ||||||
| chr4:176251838
|
G | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0067 | 3 | NA18951.hp1 NA18982.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.196+17075C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251838 | ||||||
| chr4:176251863
|
A | C | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196+17050T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251863 | ||||||
| chr4:176251877
|
G | A | 43 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0082others(40): Show | 45 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.196+17036C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251877 | ||||||
| chr4:176251878
|
C | A | 43 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0082others(40): Show | 45 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.196+17035G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176251878 | ||||||
| chr4:176252082
|
AAG | A | 7 | a0001c0001t0001g0158a0001c0001t0001g0179a0001c0001t0001g0323others(4): Show | 7 | HG00099.hp1 HG03041.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+16829_196+1683 others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252082 | ||||||
| chr4:176252084
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(62): Show | 70 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.196+16829C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252084 | ||||||
| chr4:176252084
|
GA | G | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.196+16828delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252084 | ||||||
| chr4:176252084
|
GAA | G | 9 | a0001c0001t0001g0089a0001c0002t0001g0084a0001c0002t0001g0085others(6): Show | 9 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+16827_196+1682 others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252084 | ||||||
| chr4:176252085
|
A | AG | 13 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0091others(10): Show | 15 | HG00639.hp1 HG01358.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.196+16827_196+1682 others(5): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252085 | ||||||
| chr4:176252085
|
A | G | 61 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0037others(58): Show | 64 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.196+16828T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252085 | ||||||
| chr4:176252093
|
A | G | 1 | a0001c0002t0001g0244 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.196+16820T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252093 | ||||||
| chr4:176252108
|
C | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(42): Show | 49 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.196+16805G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252108 | ||||||
| chr4:176252132
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196+16781G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252132 | ||||||
| chr4:176252262
|
AT | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+16650delA | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252262 | ||||||
| chr4:176252341
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0315 | 2 | HG00558.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.196+16572G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252341 | ||||||
| chr4:176252461
|
T | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 6 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+16452A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252461 | ||||||
| chr4:176252466
|
G | A | 42 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0082others(39): Show | 44 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.196+16447C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252466 | ||||||
| chr4:176252628
|
C | T | 86 | a0001c0001t0001g0020a0001c0001t0001g0243a0001c0001t0001g0253others(83): Show | 95 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.196+16285G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252628 | ||||||
| chr4:176252873
|
C | A | 1 | a0001c0002t0002g0354 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.196+16040G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176252873 | ||||||
| chr4:176253048
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(124): Show | 138 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.196+15865G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253048 | ||||||
| chr4:176253049
|
A | G | 371 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(368): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.196+15864T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253049 | ||||||
| chr4:176253131
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196+15782C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253131 | ||||||
| chr4:176253166
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(42): Show | 49 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.196+15747A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253166 | ||||||
| chr4:176253340
|
G | A | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196+15573C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253340 | ||||||
| chr4:176253347
|
C | A | 1 | a0001c0002t0001g0244 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.196+15566G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253347 | ||||||
| chr4:176253378
|
C | T | 1 | a0001c0010t0001g0157 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196+15535G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253378 | ||||||
| chr4:176253407
|
C | G | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+15506G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253407 | ||||||
| chr4:176253526
|
T | C | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+15387A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253526 | ||||||
| chr4:176253817
|
GCAA | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(42): Show | 49 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.196+15093_196+1509 others(7): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253817 | ||||||
| chr4:176253919
|
C | T | 78 | a0001c0001t0001g0020a0001c0001t0001g0243a0001c0001t0001g0253others(75): Show | 87 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.196+14994G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253919 | ||||||
| chr4:176253984
|
A | G | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.196+14929T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176253984 | ||||||
| chr4:176254134
|
C | T | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+14779G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254134 | ||||||
| chr4:176254268
|
G | A | 1 | a0001c0002t0002g0248 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.196+14645C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254268 | ||||||
| chr4:176254537
|
C | CA | 26 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(23): Show | 29 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.196+14375dupT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254537 | ||||||
| chr4:176254537
|
CA | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 159 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.196+14375delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254537 | ||||||
| chr4:176254598
|
A | G | 1 | a0007c0011t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.196+14315T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254598 | ||||||
| chr4:176254600
|
C | T | 86 | a0001c0001t0001g0020a0001c0001t0001g0243a0001c0001t0001g0253others(83): Show | 95 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.196+14313G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254600 | ||||||
| chr4:176254601
|
G | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(213): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.196+14312C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254601 | ||||||
| chr4:176254671
|
G | A | 1 | a0001c0002t0001g0304 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.196+14242C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254671 | ||||||
| chr4:176254720
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(216): Show | 238 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.196+14193A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254720 | ||||||
| chr4:176254859
|
C | T | 1 | a0001c0001t0008g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.196+14054G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254859 | ||||||
| chr4:176254943
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.196+13970T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176254943 | ||||||
| chr4:176255030
|
T | C | 1 | a0001c0002t0002g0360 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.196+13883A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255030 | ||||||
| chr4:176255054
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0062a0001c0001t0001g0364others(1): Show | 5 | HG00140.hp2 HG02145.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+13859G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255054 | ||||||
| chr4:176255150
|
C | A | 7 | a0001c0001t0001g0014a0001c0001t0001g0154a0001c0001t0001g0179others(4): Show | 8 | HG02622.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.196+13763G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255150 | ||||||
| chr4:176255157
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.196+13756G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255157 | ||||||
| chr4:176255234
|
C | T | 1 | a0001c0002t0002g0322 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.196+13679G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255234 | ||||||
| chr4:176255334
|
C | T | 1 | a0001c0002t0002g0321 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.196+13579G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255334 | ||||||
| chr4:176255389
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.196+13524A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255389 | ||||||
| chr4:176255627
|
G | T | 1 | a0001c0002t0012g0066 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.196+13286C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255627 | ||||||
| chr4:176255659
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.196+13254C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255659 | ||||||
| chr4:176255685
|
G | A | 1 | a0001c0002t0002g0316 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.196+13228C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255685 | ||||||
| chr4:176255716
|
G | A | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+13197C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255716 | ||||||
| chr4:176255732
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.196+13181G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255732 | ||||||
| chr4:176255991
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(42): Show | 49 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.196+12922A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176255991 | ||||||
| chr4:176256095
|
C | T | 5 | a0001c0002t0004g0038a0001c0002t0004g0039a0001c0002t0004g0040others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+12818G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176256095 | ||||||
| chr4:176256213
|
A | G | 1 | a0001c0002t0001g0236 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.196+12700T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176256213 | ||||||
| chr4:176256314
|
TATAATGG others(4): Show |
T | 1 | a0001c0002t0001g0021 | 2 | NA18947.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.196+12588_196+1259 others(15): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176256314 | ||||||
| chr4:176256384
|
C | A | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196+12529G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176256384 | ||||||
| chr4:176256537
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.196+12376T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176256537 | ||||||
| chr4:176256672
|
C | T | 2 | a0001c0001t0001g0309a0007c0011t0001g0152 | 2 | HG00741.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.196+12241G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176256672 | ||||||
| chr4:176257076
|
A | G | 1 | a0001c0002t0001g0249 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.196+11837T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257076 | ||||||
| chr4:176257118
|
G | T | 2 | a0001c0002t0003g0043a0001c0002t0003g0044 | 2 | HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.196+11795C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257118 | ||||||
| chr4:176257333
|
C | G | 50 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0082others(47): Show | 52 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.196+11580G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257333 | ||||||
| chr4:176257333
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.196+11580G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257333 | ||||||
| chr4:176257340
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.196+11573C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257340 | ||||||
| chr4:176257341
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.196+11572T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257341 | ||||||
| chr4:176257447
|
G | T | 1 | a0002c0013t0010g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.196+11466C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257447 | ||||||
| chr4:176257501
|
C | A | 46 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(43): Show | 50 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.196+11412G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257501 | ||||||
| chr4:176257507
|
T | C | 23 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(20): Show | 26 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.196+11406A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257507 | ||||||
| chr4:176257557
|
C | G | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0189 | 3 | HG02886.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.196+11356G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257557 | ||||||
| chr4:176257609
|
T | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(82): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.196+11304A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257609 | ||||||
| chr4:176257670
|
T | A | 86 | a0001c0001t0001g0020a0001c0001t0001g0243a0001c0001t0001g0253others(83): Show | 95 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.196+11243A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257670 | ||||||
| chr4:176257845
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.196+11068T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257845 | ||||||
| chr4:176257860
|
A | T | 3 | a0001c0002t0004g0039a0001c0002t0004g0040a0001c0002t0004g0042 | 3 | HG02486.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.196+11053T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176257860 | ||||||
| chr4:176258173
|
A | G | 1 | a0001c0001t0001g0364 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.196+10740T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258173 | ||||||
| chr4:176258403
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.196+10510A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258403 | ||||||
| chr4:176258441
|
A | T | 1 | a0002c0013t0010g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.196+10472T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258441 | ||||||
| chr4:176258515
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.196+10398A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258515 | ||||||
| chr4:176258657
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.196+10256A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258657 | ||||||
| chr4:176258671
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0317a0001c0001t0001g0318others(2): Show | 6 | NA18952.hp1 NA18961.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+10242G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258671 | ||||||
| chr4:176258690
|
A | G | 1 | a0003c0007t0001g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.196+10223T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258690 | ||||||
| chr4:176258802
|
TAA | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 11 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+10109_196+1011 others(6): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258802 | ||||||
| chr4:176258834
|
T | C | 1 | a0001c0002t0001g0296 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.196+10079A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258834 | ||||||
| chr4:176258950
|
A | T | 1 | a0002c0013t0010g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.196+9963T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258950 | ||||||
| chr4:176258968
|
G | T | 1 | a0001c0002t0003g0099 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.196+9945C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258968 | ||||||
| chr4:176258998
|
T | A | 1 | a0002c0013t0010g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.196+9915A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176258998 | ||||||
| chr4:176259052
|
T | C | 1 | a0001c0002t0002g0362 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.196+9861A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259052 | ||||||
| chr4:176259077
|
A | G | 1 | a0001c0002t0002g0316 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.196+9836T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259077 | ||||||
| chr4:176259090
|
G | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG01891.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+9823C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259090 | ||||||
| chr4:176259093
|
G | A | 1 | a0003c0007t0001g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.196+9820C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259093 | ||||||
| chr4:176259121
|
A | T | 1 | a0002c0013t0010g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.196+9792T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259121 | ||||||
| chr4:176259152
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.196+9761G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259152 | ||||||
| chr4:176259153
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196+9760A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259153 | ||||||
| chr4:176259370
|
C | T | 42 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0082others(39): Show | 44 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.196+9543G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259370 | ||||||
| chr4:176259424
|
A | G | 42 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0082others(39): Show | 44 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.196+9489T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259424 | ||||||
| chr4:176259941
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.196+8972A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176259941 | ||||||
| chr4:176260206
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(217): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.196+8707C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176260206 | ||||||
| chr4:176260467
|
C | G | 2 | a0001c0001t0001g0089a0001c0005t0001g0192 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.196+8446G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176260467 | ||||||
| chr4:176260623
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.196+8290C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176260623 | ||||||
| chr4:176260659
|
T | G | 1 | a0001c0002t0003g0059 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.196+8254A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176260659 | ||||||
| chr4:176260666
|
G | C | 85 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.196+8247C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176260666 | ||||||
| chr4:176260691
|
T | G | 42 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0082others(39): Show | 44 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.196+8222A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176260691 | ||||||
| chr4:176260701
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.196+8212G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176260701 | ||||||
| chr4:176260738
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.196+8175G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176260738 | ||||||
| chr4:176260811
|
G | T | 3 | a0001c0002t0007g0035a0001c0002t0007g0064a0001c0002t0007g0065 | 3 | HG02723.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196+8102C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176260811 | ||||||
| chr4:176261099
|
T | C | 1 | a0001c0001t0001g0367 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.196+7814A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176261099 | ||||||
| chr4:176261116
|
G | C | 1 | a0001c0002t0001g0368 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.196+7797C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176261116 | ||||||
| chr4:176261137
|
T | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 11 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+7776A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176261137 | ||||||
| chr4:176261157
|
C | T | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+7756G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176261157 | ||||||
| chr4:176261367
|
T | A | 1 | a0001c0002t0004g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196+7546A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176261367 | ||||||
| chr4:176261414
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(7): Show | 12 | HG00639.hp1 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.196+7499A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176261414 | ||||||
| chr4:176261463
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.196+7450T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176261463 | ||||||
| chr4:176261804
|
A | C | 1 | a0001c0002t0001g0247 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.196+7109T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176261804 | ||||||
| chr4:176261935
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.196+6978T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176261935 | ||||||
| chr4:176262135
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.196+6778A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176262135 | ||||||
| chr4:176262224
|
G | A | 1 | a0001c0002t0001g0297 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.196+6689C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176262224 | ||||||
| chr4:176262567
|
G | C | 1 | a0001c0002t0001g0078 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.196+6346C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176262567 | ||||||
| chr4:176262796
|
C | T | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+6117G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176262796 | ||||||
| chr4:176262886
|
T | G | 76 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 82 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.196+6027A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176262886 | ||||||
| chr4:176263077
|
C | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG01123.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.196+5836G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263077 | ||||||
| chr4:176263125
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.196+5788G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263125 | ||||||
| chr4:176263176
|
T | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(39): Show | 46 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.196+5737A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263176 | ||||||
| chr4:176263372
|
GTC | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.196+5539_196+5540d others(4): Show |
ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263372 | ||||||
| chr4:176263482
|
C | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG01884.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+5431G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263482 | ||||||
| chr4:176263512
|
G | C | 1 | a0001c0001t0001g0185 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.196+5401C>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263512 | ||||||
| chr4:176263565
|
C | T | 12 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0130others(9): Show | 13 | HG01099.hp2 HG01123.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+5348G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263565 | ||||||
| chr4:176263584
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196+5329C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263584 | ||||||
| chr4:176263616
|
T | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(40): Show | 47 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.196+5297A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263616 | ||||||
| chr4:176263929
|
C | T | 1 | a0001c0002t0001g0235 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.196+4984G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176263929 | ||||||
| chr4:176264034
|
G | A | 1 | a0001c0001t0001g0369 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.196+4879C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264034 | ||||||
| chr4:176264041
|
C | CA | 7 | a0001c0001t0001g0187a0001c0002t0004g0038a0001c0002t0004g0039others(4): Show | 7 | HG02486.hp1 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+4871dupT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264041 | ||||||
| chr4:176264041
|
CA | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(161): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.196+4871delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264041 | ||||||
| chr4:176264134
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.196+4779T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264134 | ||||||
| chr4:176264161
|
C | T | 1 | a0001c0005t0001g0192 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196+4752G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264161 | ||||||
| chr4:176264395
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0130others(9): Show | 13 | HG01099.hp2 HG01123.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.196+4518A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264395 | ||||||
| chr4:176264404
|
TA | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0086others(13): Show | 19 | HG00639.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.196+4508delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264404 | ||||||
| chr4:176264517
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.196+4396T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264517 | ||||||
| chr4:176264534
|
A | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0086others(13): Show | 19 | HG00639.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.196+4379T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264534 | ||||||
| chr4:176264554
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.196+4359C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264554 | ||||||
| chr4:176264631
|
C | A | 2 | a0001c0002t0002g0370a0001c0002t0002g0371 | 2 | HG00597.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.196+4282G>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264631 | ||||||
| chr4:176264834
|
TA | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG01884.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+4078delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264834 | ||||||
| chr4:176264965
|
T | C | 1 | a0001c0002t0001g0307 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.196+3948A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176264965 | ||||||
| chr4:176265220
|
T | C | 1 | a0001c0002t0001g0308 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.196+3693A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176265220 | ||||||
| chr4:176265288
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.196+3625G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176265288 | ||||||
| chr4:176265337
|
T | C | 25 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(22): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.196+3576A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176265337 | ||||||
| chr4:176265731
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(215): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.196+3182A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176265731 | ||||||
| chr4:176265776
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(133): Show | 149 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.196+3137G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176265776 | ||||||
| chr4:176266250
|
A | G | 14 | a0001c0001t0001g0020a0001c0001t0001g0243a0001c0001t0001g0245others(11): Show | 16 | HG00544.hp2 HG01993.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.196+2663T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176266250 | ||||||
| chr4:176266362
|
A | G | 1 | a0001c0001t0008g0083 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.196+2551T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176266362 | ||||||
| chr4:176266592
|
G | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0004g0038 | 3 | HG01081.hp2 HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.196+2321C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176266592 | ||||||
| chr4:176266680
|
T | A | 1 | a0001c0001t0001g0188 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.196+2233A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176266680 | ||||||
| chr4:176266782
|
A | G | 1 | a0001c0002t0002g0310 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.196+2131T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176266782 | ||||||
| chr4:176266793
|
C | G | 1 | a0003c0007t0001g0034 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.196+2120G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176266793 | ||||||
| chr4:176266897
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+2016A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176266897 | ||||||
| chr4:176266957
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(215): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.196+1956T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176266957 | ||||||
| chr4:176267047
|
C | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG00609.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.196+1866G>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267047 | ||||||
| chr4:176267056
|
T | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.196+1857A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267056 | ||||||
| chr4:176267141
|
T | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 44 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.196+1772A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267141 | ||||||
| chr4:176267330
|
T | G | 86 | a0001c0001t0001g0020a0001c0001t0001g0243a0001c0001t0001g0245others(83): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.196+1583A>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267330 | ||||||
| chr4:176267491
|
G | T | 1 | a0002c0013t0010g0033 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.196+1422C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267491 | ||||||
| chr4:176267512
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01081.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.196+1401C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267512 | ||||||
| chr4:176267513
|
G | T | 1 | a0001c0001t0001g0082 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.196+1400C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267513 | ||||||
| chr4:176267567
|
A | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(40): Show | 47 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.196+1346T>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267567 | ||||||
| chr4:176267579
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.196+1334A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267579 | ||||||
| chr4:176267730
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.196+1183A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267730 | ||||||
| chr4:176267757
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.196+1156T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267757 | ||||||
| chr4:176267853
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(23): Show | 30 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.196+1060G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176267853 | ||||||
| chr4:176268110
|
GA | G | 24 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(21): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.196+802delT | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268110 | ||||||
| chr4:176268170
|
G | T | 85 | a0001c0001t0001g0020a0001c0001t0001g0243a0001c0001t0001g0245others(82): Show | 93 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.196+743C>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268170 | ||||||
| chr4:176268245
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(210): Show | 232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.196+668A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268245 | ||||||
| chr4:176268381
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(40): Show | 47 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.196+532C>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268381 | ||||||
| chr4:176268430
|
T | C | 5 | a0001c0002t0003g0018a0001c0002t0003g0231a0001c0002t0003g0232others(2): Show | 7 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+483A>G | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268430 | ||||||
| chr4:176268554
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.196+359G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268554 | ||||||
| chr4:176268591
|
A | T | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.196+322T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268591 | ||||||
| chr4:176268597
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.196+316G>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268597 | ||||||
| chr4:176268659
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(215): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.196+254T>C | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268659 | ||||||
| chr4:176268710
|
T | A | 3 | a0001c0002t0001g0372a0001c0002t0001g0373a0001c0002t0001g0374 | 3 | NA18979.hp2 NA19004.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.196+203A>T | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268710 | ||||||
| chr4:176268743
|
A | T | 1 | a0001c0002t0007g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196+170T>A | ASB5 | ENSG00000164122.9 | transcript | ENST00000296525.7 | protein_coding | 1/6 | chr4 | 176268743 |